Three-dimensional structure of bovine rhodopsin

Abstract

The present invention discloses a three-dimensional structure of bovine rhodopsin. There is provided a G protein-coupled receptor selected from the group consisting of the following (a) and (b):

Description

TECHNICAL FIELD OF THE INVENTION

[0001] The present invention relates to three-dimensional structures of G protein-coupled receptors, especially rhodopsin, and derived structures therefrom.

BACKGROUND OF THE INVENTION

[0002] Most eukaryotic organisms utilize guanine nucleotide-binding regulatory protein (hereinafter, referred to as “G protein”)-coupled receptors (G protein-coupled receptors; hereinafter, frequently referred to as “GPCRs”) to respond to a variety of stimuli such as Ca2+, amines, hormones, peptides, and even large proteins. Each GPCR is composed of an extracellular region, an intracellular region and a transmembrane bundle of seven α-helices. The binding of specific ligands to the extracellular or transmembrane domain evokes conformational changes that are transmitted to the intracellular region. The conformational switch from inactive to active state in the intracellular region produces a catalytically competent receptor that is responsible for binding and nucleotide exchange (GDP ⇄GTP) on α-subunits of several hundreds of G proteins of a specific subtype. α-and/or A′-subunit of the G proteins activates the next target protein(s) to evoke further intracellular responses. Because all of several hundreds of members in the GPCR family appear to share a common motif in their transmembrane structure and a common topology, it is generally accepted that a similar switching mechanism functions in all of these receptors.

[0003] The largest GPCR subfamily constituting about 90% of the total GPCRs include rhodopsin, cone pigment, and adrenergic or other receptors (Y. Shichida et al., Cell. Mol. Life Sci. 54, 1299 (1998)). Rhodopsin is recognized to be a member of the GPCR family because of its importance in the visual excitation (G. Wald et al., Science, 111, 179 (1950)), and its molecular and chemical characterization has been carried out for more than 50 years. The structural feature of rhodopsin is that it is composed of two molecules, i.e., opsin (˜40 kDa) and a cofactor 11-cis-retinal (a derivative of vitamin A). These two molecules are covalently linked through Lys296 (i.e., lysine at position 296 of the amino acid sequence of rhodopsin) located in the transmembrane region of the receptor (Y. A. Ovchinnikov, FEBS Lett. 148, 179 (1982); P. A. Hargrave et al., Biophys. Struct. Mech. 9, 235 (1983); J. Nathans & T. Hogness, Cell 34, 807 (1983)), and give a characteristic maximum absorption at ˜500 nm. However, when the 11-cis-retinylidene group is located in a similar environment in homologous cone opsins, the maximum absorption of these pigments ranges between 380-580 nm. This spectral tuning allows the perception of colors.

[0004] Key residues in the binding pocket of the 11-cis-retinylidene group appear to be critical in interactions with the chromophore and are responsible for the spectral tuning (T. Yoshizawa, Photochem. Photobiol. 56, 859 (1992); G. G. Kochendoerfer et al., Trends Biochem. Sci. 24, 300 (1999); S. W. Lin et al., J. Biol. Chem. 273, 24583 (1998); A.B. Asenjo et al., Neuron 12, 1131 (1994); G. G. Kochendoerfer et al., Biochemistry 36, 6577 (1997); S. L. Merbs & J. Nathans, Photochem. Photobiol. 56, 869 (1992)). Rhodopsin has also been extensively investigated from a clinical view point since mutations in the human rhodopsin gene lead to retinal pathologies (T. P. Dryja et al., Nature 343, 364-366 (1990); P. Humphries et al., Science 256, 804 (1992); A. Ratter et al., Annu. Rev. Genet. 33, 89 (1999)).

[0005] Absorption of a photon by the 11-cis-retinal chromophore covalently linked to transmembrane helix H-VII (“H” denotes helix, and the subsequent number denotes the order in the primary sequence) of rhodopsin causes its isomerization to all-trans-retinal (T. Yoshizawa & G. Wald, Nature 197, 1279 (1963); R. W. Schoenlein et al., Science 254, 412 (1991); Kandori et al., J. Am. Chem. Soc. 118, 1002 (1996)), leading to a conformational change of the protein moiety including the cytoplasmic surface.

[0006] The structural change of the chromophore as a result of absorption of photon only transiently activates opsin, and subsequently the all-trans-retinal is hydrolyzed and dissociated from the opsin. Rhodopsin is regenerated by newly synthesized 11-cis-retinal from adjacent retinal epithelial cells. This transient photoactivation of rhodopsin is especially remarkable because the absorption of a single photon results in the activaton of 100-1000 G protein molecules, whereas the 11-cis-retinal-bound rhodopsin is extremely low in activity (B. K. K. Fung & L. Stryer, Proc. Natl. Acad. Sci. USA 77, 2500 (1980); H. Kuhn et al., Proc. Natl. Acad. Sci. USA 78, 6873 (1983)). These two properties are the molecular roots of high sensitivity in the human scotopic visual system and enable detection of as few as five photons (S. Hecht et al., J. Gen. Physiol. 25, 819 (1942)). These features put rhodopsin in a class of its own, as the most sophisticated molecular device among GPCRs.

[0007] With respect to three-dimensional structural information on GPCRs, several reports as described below have been made in addition to biochemical approaches and computational prediction studies.

[0008] A cryo-electron microscopic study of frog rhodopsin has revealed the organization of this receptor at 7.5 Å in the plane of the membrane and at 16.5 Å in the perpendicular direction to the membrane (V. M. Unger et al., Nature 389, 203 (1997)). This study permitted the prediction of the locations of seven rods of density that correspond to the transmembrane helices. The electron density map also allowed an estimation of the tilt angles for these seven helices. Many additional approaches have been employed to explore the structure of rhodopsin, and have also provided valuable information (J. Klein-Seetharaman et al., Proc. Natl. Acad. Sci. USA 96, 13744 (1999); O. P. Ernst et al., J. Biol. Chem. 275, 1937 (2000); C. Altenbach et al., Biochemistry 38, 7945 (1999); J. Hwa et al., Proc. Natl. Acad. Sci. USA 96, 1932 (1999); J.-M. Kim et al., Proc. Natl. Acad. Sci. USA 94, 14273 (1997); Z. T. Farahbakhsh et al., Biochemistry 34, 8812 (1995); H. Yu et al., Biochemistry 38, 12028 (1995)). At present, several theoretical models of rhodopsin are available (T. Shieh et al., J. Mol. Biol. 269, 3737 (1997); P. Herzyk & R. E. Hubbard, J. Mol. Biol. 281, 741 (1998); I. D. Pogozheva et al., Biophys. J. 72, 1963 (1997); J. M. Baldwin, EMBO J. 12, 1693, (1993); T. A. Nakayama & H. G. Khoranam, J. Biol. Chem. 266,4269 (1991)).

[0009] Although these studies have provided a starting point for structural studies of the other members in the rhodopsin family, higher resolution three-dimensional accurate experimental models at the atomic level are needed to obtain further insight into the mechanisms of receptor activation, and the source of interactions between specific ligands and G proteins. Atomic models are also vital for understanding how specific mutations of the members of the GPCR superfamily can lead to genetic disorders.

[0010] Seven times transmembrane type GPCRs (7TMRs) are a major cellular receptor. They are important targets for developing pharmaceuticals. Many research groups have attempted production and crystallization of 7TMRs and even preparation of heavy atom derivatives from their crystals for the purpose of crystallographic analysis. However, no group has ever succeeded since these attempts have been extremely difficult.

SUMMARY OF THE INVENTION

[0011] It is an object of the invention to elucidate the three-dimensional structure of bovine rhodopsin and to provide the fundamental structure of seven times transmembrane type GPCRs.

[0012] As a result of intensive and extensive researches toward the solution of the above problem, the present inventors have succeeded in analyzing the crystal structure of a GPCR at atomic resolution by crystallizing a rhodopsin prepared from bovine eyes, preparing a mercury derivative from the crystal taking a long period of time, and collecting six diffraction data from the single crystal by multi-wavelength anomalous diffraction methods (especially, a method in which the crystal was measured with varied wavelengths using synchrotron radiation and a beamline equipped with a trichrometer at SPring-8 Station). Thus, the present invention has been achieved.

[0013] The present invention relates to the following (1) to (6).

[0014] (1) A peptide fragment consisting of an amino acid sequence of positions 36-64, positions 71-100, positions 107-139, positions 151-173, positions 200-225, positions 247-277 or positions 286-306 of the amino acid sequence as shown in SEQ ID NO: 1, or a salt of the peptide fragment.

[0015] (2) A protein selected from the group consisting of the following (a), (b) and (c):

[0016] (a) an isolated protein consisting of an amino acid sequence of positions 36-306 of the amino acid sequence as shown in SEQ ID NO: 1;

[0017] (b) an isolated protein which consists of a part of an amino acid sequence of positions 36-306 of the amino acid sequence as shown in SEQ ID NO: 1, said part comprising at least positions 107-277, and which has G protein-coupled receptor activity;

[0018] (c) an isolated protein which consists of an amino acid sequence of positions 36-306 or 107-277 of the amino acid sequence as shown in SEQ ID NO: 1 having a deletion(s), substitution(s) or addition(s) of one or more amino acids, and which has G protein-coupled receptor activity.

[0019] (3) A G protein-coupled receptor selected from the group consisting of the following (a) and (b):

[0020] (a) a G protein-coupled receptor having three-dimensional structure I defined by the atomic coordinates as shown in Table 1;

[0021] (b) a G protein-coupled receptor having three-dimensional structure II defined by derived coordinates from the atomic coordinates as shown in Table 1, wherein the mean residual of the discrepancies between the positions of the α carbon atoms in the amino acid residues of seven helix sites H-I (36-64), H-II (71-100), H-III (107-139), H-IV (151-173), H-V (200-225), H-VI (247-277) and H-VII (286-306) in the amino acid sequence as shown in SEQ ID NO: 1 of the three-dimensional structure I and the positions of the corresponding α carbon atoms in the amino acid residues of the corresponding seven helix sites of the three-dimensional structure II is 1.5 Å or less when an image of the three-dimensional structure I obtained by computer-processing the atomic coordinates of Table 1 and an image of the three-dimensional structure II obtained by computer-processing the derived coordinates are superposed.

[0022] As a specific example of the G protein-coupled receptor, bovine rhodopsin may be given. Preferably, this bovine rhodopsin is a metal derivative of its crystal. The metal is, for example, a mercury compound.

[0023] (4) A method of virtual screening for drugs, comprising computer-processing the following atomic coordinates (a) or (b), or derived coordinates therefrom, inputting the resultant computer-processed data into a virtual compound library and searching for useful drugs through the library:

[0024] (a) a part of the atomic coordinates as shown in Table 1, the part corresponding to the amino acid residues of at least the three helix sites of H-III (107-139), H-V (200-225) and H-VI (247-277) selected from seven helix sites H-I (36-64), H-II (71-100), H-III (107-139), H-IV (151-173), H-V (200-225), H-VI (247-277) and H-VII (286-306) in the amino acid sequence as shown in SEQ ID NO: 1;

[0025] (b) the atomic coordinates as shown in Table 1.

[0026] In the above-described method, one example of the derived coordinates is derived coordinates generated by homology modeling based on the atomic coordinates as shown in Table 1, the mean residual of the discrepancies between the positions of the α carbon atoms in the amino acid residues of the three helix sites H-III (107-139), H-V (200-225) and H-VI (247-277) in the amino acid sequence as shown in SEQ ID NO: 1 and the positions of the corresponding α carbon atoms in the amino acid residues of the corresponding three helix sites in the derived coordinates being 1.5 Å or less.

[0027] (5) A method of drug design, comprising imaging three-dimensional structures of G protein-coupled receptors using the following atomic coordinates (a) or (b), or derived coordinates therefrom, analyzing the resultant images by computer graphics and designing structures of useful drugs based on the resultant analysis data:

[0028] (a) a part of the atomic coordinates as shown in Table 1, the part corresponding to the amino acid residues of at least the three helix sites of H-III (107-139), H-V (200-225) and H-VI (247-277) selected from seven helix sites H-I (36-64), H-II (71-100), H-III (107-139), H-IV (151-173), H-V (200-225), H-VI (247-277) and H-VII (286-306) in the amino acid sequence as shown in SEQ ID NO: 1;

[0029] (b) the atomic coordinates as shown in Table 1.

[0030] The derived coordinates are as described in (4) above. (6) A method of screening for target substances that influence the effect of the G protein-coupled receptor described in (3) above, comprising comparing the three-dimensional structure of the receptor with three-dimensional structures of test substances.

[0031] The present specification encompasses the contents of the specification and drawings of Japanese Patent Application No. 2000-236288 based on which the present application claims priority.

BRIEF DESCRIPTION OF THE DRAWINGS

[0032] FIG. 1 shows the molecular packing viewed along the x-axis of the crystal (Panel A); the electrostatic potentials of two rhodopsin molecules within the asymmetric unit expressed with MolScript (Panel B); and the crystal packing interface showing interactions between the N-terminal regions of neighboring rhodopsin molecules (Panel C).

[0033] FIG. 2 shows ribbon drawings of rhodopsin.

[0034] FIG. 3 shows a stereoview of the C α-trace of rhodopsin and residues involved in the hydrogen bonds between transmembrane segments (Panel A) and a ribbon drawing of the structure shadow-coded by average thermal parameters, with the same orientation as Panel A (Panel B). The darker the shadow, the lower the thermal parameter.

[0035] FIG. 4A shows the lengths of transmembrane α-helices and an alignment of rhodopsin sequences.

[0036] FIG. 4B shows a two-dimensional model of rhodopsin.

[0037] FIG. 5 shows stereoviews of the C α-traces on the intradiscal side of the transmembrane helices (Panel A) and on the cytoplasmic side of the molecule (Panel B).

[0038] FIG. 6 shows four regions characteristic of rhodopsin. The E-II loop near the disulfide bridge connecting Cys110 and Cys187, viewed from extracellular side (Panel A). The C-IV cytoplasmic loop from Lys311 to Leu321 forming a short amphiphilic helix (H-VIII) (Panel B). Interhelical hydrogen bonds mediated by a highly conserved Asn55, connecting H-I, H-II, and H-VII, and by Asn78 for H-II, H-III, and H-IV (Panel C). The (D/E)R(Y/W) motif region located near the cytoplasmic end of H-III (Panel D).

[0039] FIG. 7 shows an electron density map surrounding the 11-cis-retinal chromophore using experimental phases (Panel A); an electron density map surrounding the 11-cis-retinal chromophore using calculated phases based on the final model (Panel B); a schematic showing the side chains surrounding the 11-cis-retinylidene group (Panel C); and a schematic presenting side chains within 4.5 Å distance from the 11-cis-retinylidene group (Panel D).

[0040] FIG. 8 shows a three-dimensional structure of an AT-II receptor homology model that was created using the atomic coordinates of bovine rhodopsin.

DETAILED DESCRIPTION OF THE INVENTION

[0041] Hereinbelow, the present invention will be described in detail.

[0042] G protein-coupled receptors (GPCRs) function in a number of signaling pathways, converting a variety of external stimuli to activate multiple copies of G protein subtypes specific to the relevant G protein-coupled receptor. GPCRs, including the prototypical member of this family, rhodopsin, share many structural features, including a bundle of seven transmembrane α-helices connected by six loops of varying lengths. In the present invention, diffraction data were collected from a crystal of bovine rhodopsin in the ground state at 2.8 Å resolution in order to obtain detailed information on the three-dimensional structure of rhodopsin. X-ray crystallographic analysis of bovine rhodopsin using the multi-wavelength anomalous diffraction method has elucidated for the first time the structure of GPCR (crystallographic R-factor: 19.98%; Rfree:25.55%). The highly organized structure in the extracellular region (including a conserved disulfide bridge) forms a lid for the extracellular moiety of the seven-helix transmembrane motif.

[0043] The intrinsic chromophore to bovine rhodopsin, 11-cis-retinal, is a key cofactor for holding the transmembrane region of the protein in the inactive conformation. The chromophore also interacts with a cluster of key residues that give the wavelength of the maximum absorption. The site of a set of residues that mediate interactions between the transmembrane helices and the cytoplasmic surface, where G-protein activation is induced, suggests a possible structural change upon photoactivation.

[0044] Hereinbelow, the preparation and crystallization of rhodopsin, the structural analysis of the resultant crystal and applications of the obtained structure will be described taking bovine rhodopsin as an example of GPCR.

[0045] 1. Preparation of Bovine Rhodopsin

[0046] In the present invention, bovine rhodopsin (hereinafter, sometimes just referred to as “rhodopsin”) for use in crystallographic analysis may be collected from bovine eyes. Alternatively, commercial retinas may be used.

[0047] For example, rod outer segments (ROSs) are purified from bovine retinas (purchased from Schenk Packing Co., Inc., Stanwood, Wash.) using alkyl-thio-glycoside and divalent metal ions by conventional methods (e.g., Okada, T., Takeda, K. and Tokuyama, T., Photochem. Photobiol. 67: (5) 495499 (1998); or Papermaster, D. S. Methods Enzymol. 81, 48-52 (1982)). These ROSs are solubilized with a surfactant nonyl glucoside and zinc acetate, and then concentrated by centrifugation to prepare a sample.

[0048] 2. Crystallization of Bovine Rhodopsin

[0049] In the present invention, the crystallization of bovine rhodopsin may be carried out based on commonly used crystallization methods for X-ray crystallographic analysis. For example, a precipitant is added to a bovine rhodopsin solution of a specific concentration to change the concentration. As a result, the solubility of rhodopsin molecules lowers gradually and they are deposited as crystals.

[0050] The purity of rhodopsin is important for crystallization. It is essential to purify rhodopsin from highly pure ROSs. The concentration of rhodopsin is 5 mg/ml to 20 mg/ml, preferably ˜10 mg/ml. As a precipitant, ammonium sulfate may be used, for example.

[0051] A suitable pH range for crystallization is 5.5-7.5, preferably 6.0-6.1. A suitable temperature range is 4-25° C., preferably 4-15° C. In the crystallization of membrane proteins, the type of surfactant and the concentration of the protein are most important. In the crystallization of rhodopsin, nonylglucoside and heptane-1,2,3-triol may be used preferably. In the present invention, pH is also an important parameter. For examining three parameters including pH (e.g., surfactant, pH and protein concentration) efficiently, it is desirable to prepare a phase diagram. Once crystals have begun to deposit, these parameters should be changed further finely to determine the optimal crystallization conditions under which best crystals are generated.

[0052] In crystallization, it is preferable to equilibrate a sample solution with a solution of the optimal crystallization conditions. In that case, a technique such as vapor diffusion or dialysis may be used.

[0053] Since rhodopsin is unique in structure and has poor resemblance with structures of other proteins, the molecular replacement method cannot be used in the structural analysis in the present invention. Phase information on each diffraction spot must be obtained directly from experiments and used in the analysis. Thus, the present invention has employed a technique called multi-wavelength anomalous diffraction (MAD) method that allows phase determination with only one heavy atom derivative by using variable wavelength synchrotron radiation. According to MAD method, phase information can be obtained using only one heavy atom derivative. Thus, this method is advantageous in a point that structure determination is possible even for those protein crystals, such as bovine rhodopsin crystal, whose lattice changes easily. However, measurement accuracy must be higher than other methods.

[0054] For introducing a heavy atom into crystals, the soaking method is generally used. In this method, already grown crystals are soaked in a solution containing a heavy atom reagent, which permeates into crystals spontaneously by diffusion.

[0055] Examples of heavy atom reagents useful in the invention include mercury compounds, platinum compounds, uranium compounds and gold compounds. Since bovine rhodopsin crystals are easily destroyed, a sufficient time is needed for soaking. Therefore, soaking for the preparation of a heavy atom derivative of rhodopsin crystal is carried out at 4-25°C., preferably 4-6° C., for two weeks to six months, preferably two to three months.

[0056] 3. Structural Analysis of the Crystal

[0057] In the present invention, the structural analysis of the resultant crystal can be performed by the so-called MAD method. In the present invention, X-ray diffraction of the crystal is measured using synchrotron radiation on a beamline equipped with a trichrometer with varied wavelengths. Synchrotron radiation useful in the present invention may be generated by RIKEN Beamline I (BL45XU) at SPring-8 station, which is a large scale synchrotron radiation laboratory. In particular, RIKEN Beamline I (BL45XU) is a beamline optimized for the MAD method and suitable for collecting diffraction data for phase determination with varied wavelengths, even from those crystals, such as rhodopsin crystals, that are bad in reproducibility and have little isomorphism among crystals. The range of X-ray wavelengths used is 0.09-0.12 nm, preferably 0.07-0.15 nm. When using synchrotron radiation, it should be noted that the XANES spectrum of the test crystal must be measured in advance in order to determine exactly the X-ray wavelength corresponding to the absorption edge of the heavy atom.

[0058] As a result of the above structural analysis, the three-dimensional structure of bovine rhodopsin can be obtained as three-dimensional coordinates. The atomic coordinates obtained by the invention are shown in Table 1 below.

TABLE 1
Column:
1	2	3	4	5	6	7	8	9	10	11	12
ATOM	1	CA	ACE	A	0	42.692	−7.910	−28.406	1.00	58.37	A
ATOM	2	C	ACE	A	0	43.697	−7.215	−27.535	1.00	58.09	A
ATOM	3	O	ACE	A	0	44.386	−7.856	−26.737	1.00	56.65	A
ATOM	4	N	MET	A	1	43.789	−5.895	−27.702	1.00	58.70	A
ATOM	5	CA	MET	A	1	44.707	−5.048	−26.931	1.00	58.56	A
ATOM	6	CB	MET	A	1	44.894	−3.702	−27.636	1.00	59.31	A
ATOM	7	CG	MET	A	1	46.319	−3.408	−28.061	1.00	59.50	A
ATOM	8	SD	MET	A	1	46.951	−4.694	−29.133	1.00	58.62	A
ATOM	9	CE	MET	A	1	48.475	−5.135	−28.302	1.00	59.39	A
ATOM	10	C	MET	A	1	44.160	−4.807	−25.526	1.00	57.96	A
ATOM	11	O	MET	A	1	42.977	−4.475	−25.374	1.00	58.24	A
ATOM	12	N	ASN	A	2	45.029	−4.949	−24.518	1.00	56.79	A
ATOM	13	CA	ASN	A	2	44.666	−4.775	−23.096	1.00	54.67	A
ATOM	14	CB	ASN	A	2	45.640	−5.537	−22.195	1.00	57.29	A
ATOM	15	CG	ASN	A	2	45.749	−6.998	−22.546	1.00	58.49	A
ATOM	16	OD1	ASN	A	2	44.879	−7.795	−22.198	1.00	57.12	A
ATOM	17	ND2	ASN	A	2	46.841	−7.354	−23.215	1.00	62.99	A
ATOM	18	C	ASN	A	2	44.657	−3.320	−22.645	1.00	51.53	A
ATOM	19	O	ASN	A	2	44.350	−3.010	−21.495	1.00	49.90	A
ATOM	20	N	GLY	A	3	45.077	−2.447	−23.546	1.00	49.81	A
ATOM	21	CA	GLY	A	3	45.117	−1.037	−23.251	1.00	48.69	A
ATOM	22	C	GLY	A	3	44.897	−0.233	−24.511	1.00	48.17	A
ATOM	23	O	GLY	A	3	45.179	−0.680	−25.628	1.00	48.57	A
ATOM	24	N	THR	A	4	44.357	0.958	−24.328	1.00	46.74	A
ATOM	25	CA	THR	A	4	44.102	1.835	−25.441	1.00	45.97	A
ATOM	26	CB	THR	A	4	42.803	2.622	−25.218	1.00	44.14	A
ATOM	27	OG1	THR	A	4	41.719	1.705	−25.043	1.00	43.79	A
ATOM	28	CG2	THR	A	4	42.499	3.507	−26.395	1.00	42.35	A
ATOM	29	C	THR	A	4	45.286	2.780	−25.546	1.00	47.50	A
ATOM	30	O	THR	A	4	45.460	3.643	−24.686	1.00	48.20	A
ATOM	31	N	GLU	A	5	46.146	2.554	−26.542	1.00	48.98	A
ATOM	32	CA	GLU	A	5	47.303	3.425	−26.763	1.00	50.20	A
ATOM	33	CB	GLU	A	5	48.471	2.695	−27.448	1.00	50.08	A
ATOM	35	CG	GLU	A	5	49.682	3.624	−27.697	1.00	51.17	A
ATOM	35	CD	GLU	A	5	50.903	2.942	−28.316	1.00	53.77	A
ATOM	36	OE1	GLU	A	5	50.953	1.692	−28.362	1.00	56.13	A
ATOM	37	OE2	GLU	A	5	51.833	3.665	−28.748	1.00	53.09	A
ATOM	38	C	GLU	A	5	46.892	4.610	−27.630	1.00	51.17	A
ATOM	39	O	GLU	A	5	46.112	4.457	−28.579	1.00	52.54	A
ATOM	40	N	GLY	A	6	47.411	5.787	−27.287	1.00	50.76	A
ATOM	41	CA	GLY	A	6	47.120	6.994	−28.037	1.00	48.54	A
ATOM	42	C	GLY	A	6	48.422	7.622	−28.486	1.00	48.35	A
ATOM	43	O	GLY	A	6	49.496	7.083	−28.210	1.00	47.71	A
ATOM	44	N	PRO	A	7	48.365	8.779	−29.159	1.00	48.51	A
ATOM	45	CD	PRO	A	7	47.128	9.506	−29.486	1.00	49.71	A
ATOM	46	CA	PRO	A	7	49.543	9.500	−29.658	1.00	48.79	A
ATOM	47	CB	PRO	A	7	48.927	10.664	−30.435	1.00	49.17	A
ATOM	48	CG	PRO	A	7	47.640	10.909	−29.711	1.00	51.01	A
ATOM	49	C	PRO	A	7	50.486	9.989	−28.566	1.00	48.79	A
ATOM	50	O	PRO	A	7	51.686	10.165	−28.801	1.00	49.71	A
ATOM	51	N	ASN	A	8	49.935	10.186	−27.372	1.00	48.52	A
ATOM	52	CA	ASN	A	8	50.699	10.659	−26.221	1.00	46.90	A
ATOM	53	CB	ASN	A	8	50.780	12.191	−26.237	1.00	44.50	A
ATOM	54	CG	ASN	A	8	49.414	12.859	−26.212	1.00	42.02	A
ATOM	55	OD1	ASN	A	8	48.373	12.214	−26.354	1.00	41.82	A
ATOM	56	ND2	ASN	A	8	49.417	14.168	−26.038	1.00	41.53	A
ATOM	57	C	ASN	A	8	50.150	10.164	−24.873	1.00	46.71	A
ATOM	58	O	ASN	A	8	50.259	10.858	−23.860	1.00	46.87	A
ATOM	59	N	PHE	A	9	49.593	8.951	−24.867	1.00	46.38	A
ATOM	60	CA	PHE	A	9	49.039	8.351	−23.656	1.00	45.07	A
ATOM	61	CB	PHE	A	9	47.708	9.002	−23.304	1.00	43.55	A
ATOM	62	CG	PHE	A	9	46.616	8.727	−24.291	1.00	41.97	A
ATOM	63	CD1	PHE	A	9	45.856	7.572	−24.198	1.00	42.00	A
ATOM	64	CD2	PHE	A	9	46.307	9.653	−25.275	1.00	42.21	A
ATOM	65	CE1	PHE	A	9	44.802	7.350	−25.063	1.00	42.06	A
ATOM	66	CE2	PHE	A	9	45.255	9.438	−26.145	1.00	41.43	A
ATOM	67	CZ	PHE	A	9	44.499	8.285	−26.039	1.00	40.93	A
ATOM	68	C	PHE	A	9	48.853	6.837	−23.732	1.00	44.99	A
ATOM	69	O	PHE	A	9	49.107	6.210	−24.754	1.00	46.12	A
ATOM	70	N	TYR	A	10	48.402	6.261	−22.627	1.00	44.13	A
ATOM	71	CA	TYR	A	10	48.158	4.833	−22.542	1.00	42.99	A
ATOM	72	CB	TYR	A	10	49.473	4.063	−22.300	1.00	43.47	A
ATOM	73	CG	TYR	A	10	49.322	2.553	−22.376	1.00	45.26	A
ATOM	74	CD1	TYR	A	10	48.954	1.808	−21.256	1.00	46.30	A
ATOM	75	CE1	TYR	A	10	48.741	0.435	−21.338	1.00	47.80	A
ATOM	76	CD2	TYR	A	10	49.483	1.879	−23.583	1.00	47.13	A
ATOM	77	CE2	TYR	A	10	49.272	0.503	−23.678	1.00	47.87	A
ATOM	78	CZ	TYR	A	10	48.900	−0.211	−22.554	1.00	48.99	A
ATOM	79	OH	TYR	A	10	48.680	−1.567	−22.653	1.00	50.18	A
ATOM	80	C	TYR	A	10	47.168	4.589	−21.402	1.00	42.43	A
ATOM	81	O	TYR	A	10	47.544	4.633	−20.230	1.00	41.33	A
ATOM	82	N	VAL	A	11	45.891	4.425	−21.746	1.00	41.03	A
ATOM	83	CA	VAL	A	11	44.855	4.153	−20.747	1.00	39.70	A
ATOM	84	CB	VAL	A	11	43.451	4.588	−21.236	1.00	38.18	A
ATOM	85	CG1	VAL	A	11	42.415	4.307	−20.175	1.00	36.36	A
ATOM	86	CG2	VAL	A	11	43.442	6.052	−21.598	1.00	36.33	A
ATOM	87	C	VAL	A	11	44.860	2.638	−20.561	1.00	39.64	A
ATOM	88	O	VAL	A	11	44.689	1.903	−21.531	1.00	40.35	A
ATOM	89	N	PRO	A	12	45.117	2.152	−19.330	1.00	39.18	A
ATOM	90	CD	PRO	A	12	45.558	2.904	−18.149	1.00	36.83	A
ATOM	91	CA	PRO	A	12	45.146	0.711	−19.047	1.00	40.46	A
ATOM	92	CB	PRO	A	12	45.801	0.657	−17.663	1.00	38.51	A
ATOM	93	CG	PRO	A	12	46.531	1.953	−17.553	1.00	36.31	A
ATOM	94	C	PRO	A	12	43.731	0.117	−19.020	1.00	42.67	A
ATOM	95	O	PRO	A	12	43.357	−0.559	−18.064	1.00	42.99	A
ATOM	96	N	PHE	A	13	42.980	0.351	−20.097	1.00	45.27	A
ATOM	97	CA	PHE	A	13	41.590	−0.096	−20.237	1.00	46.73	A
ATOM	98	CB	PHE	A	13	40.663	1.069	−19.862	1.00	46.22	A
ATOM	99	CG	PHE	A	13	39.292	0.656	−19.387	1.00	45.70	A
ATOM	100	CD1	PHE	A	13	38.177	0.833	−20.201	1.00	43.82	A
ATOM	101	CD2	PHE	A	13	39.106	0.164	−18.093	1.00	44.88	A
ATOM	102	CE1	PHE	A	13	36.902	0.535	−19.732	1.00	42.05	A
ATOM	103	CE2	PHE	A	13	37.835	−0.135	−17.619	1.00	42.65	A
ATOM	104	CZ	PHE	A	13	36.733	0.052	−18.439	1.00	42.24	A
ATOM	105	C	PHE	A	13	41.365	−0.436	−21.706	1.00	48.19	A
ATOM	106	O	PHE	A	13	41.814	0.303	−22.582	1.00	48.79	A
ATOM	107	N	SER	A	14	40.651	−1.524	−21.984	1.00	49.86	A
ATOM	108	CA	SER	A	14	40.402	−1.897	−23.370	1.00	51.43	A
ATOM	109	CB	SER	A	14	40.085	−3.382	−23.499	1.00	51.26	A
ATOM	110	OG	SER	A	14	40.183	−3.774	−24.864	1.00	54.09	A
ATOM	111	C	SER	A	14	39.296	−1.074	−24.018	1.00	52.82	A
ATOM	112	O	SER	A	14	38.220	−0.875	−23.442	1.00	52.39	A
ATOM	113	N	ASN	A	15	39.567	−0.618	−25.235	1.00	54.06	A
ATOM	114	CA	ASN	A	15	38.613	0.184	−25.973	1.00	55.84	A
ATOM	115	CB	ASN	A	15	39.352	1.225	−26.794	1.00	57.15	A
ATOM	116	CG	ASN	A	15	38.463	2.371	−27.138	1.00	58.84	A
ATOM	117	OD1	ASN	A	15	37.585	2.722	−26.354	1.00	57.21	A
ATOM	118	ND2	ASN	A	15	38.657	2.948	−28.315	1.00	60.52	A
ATOM	119	C	ASN	A	15	37.721	−0.651	−26.879	1.00	57.35	A
ATOM	120	O	ASN	A	15	37.147	−0.153	−27.852	1.00	57.21	A
ATOM	121	N	LYS	A	16	37.619	−1.935	−26.565	1.00	59.76	A
ATOM	122	CA	LYS	A	16	36.783	−2.839	−27.337	1.00	62.14	A
ATOM	123	CB	LYS	A	16	37.090	−4.295	−26.981	1.00	65.26	A
ATOM	124	CG	LYS	A	16	38.378	−4.812	−27.617	1.00	68.18	A
ATOM	125	CD	LYS	A	16	38.259	−4.804	−29.132	1.00	68.88	A
ATOM	126	CE	LYS	A	16	39.571	−5.145	−29.796	1.00	69.87	A
ATOM	127	NZ	LYS	A	16	39.385	−5.280	−31.265	1.00	70.07	A
ATOM	128	C	LYS	A	16	35.325	−2.520	−27.076	1.00	61.59	A
ATOM	129	O	LYS	A	16	35.430	−3.187	−27.588	1.00	61.19	A
ATOM	130	N	THR	A	17	35.110	−1.502	−26.249	1.00	61.93	A
ATOM	131	CA	THR	A	17	33.779	−1.012	−25.900	1.00	61.52	A
ATOM	132	CB	THR	A	17	33.549	−1.028	−24.373	1.00	61.66	A
ATOM	133	OG1	THR	A	17	35.154	−2.197	−23.805	1.00	60.58	A
ATOM	135	CG2	THR	A	17	32.047	−1.024	−24.064	1.00	61.50	A
ATOM	135	C	THR	A	17	33.691	0.444	−26.377	1.00	60.86	A
ATOM	136	O	THR	A	17	32.635	1.074	−26.289	1.00	60.20	A
ATOM	137	N	GLY	A	18	35.821	0.972	−26.855	1.00	59.85	A
ATOM	138	CA	GLY	A	18	35.875	2.350	−27.333	1.00	58.66	A
ATOM	139	C	GLY	A	18	35.730	3.363	−26.220	1.00	58.05	A
ATOM	140	O	GLY	A	18	35.839	4.564	−26.459	1.00	58.70	A
ATOM	141	N	VAL	A	19	35.527	2.882	−24.997	1.00	56.90	A
ATOM	142	CA	VAL	A	19	35.355	3.736	−23.825	1.00	55.72	A
ATOM	143	CB	VAL	A	19	33.898	2.895	−22.608	1.00	56.73	A
ATOM	144	CG1	VAL	A	19	35.049	2.028	−22.111	1.00	58.03	A
ATOM	145	CG2	VAL	A	19	33.353	3.788	−21.502	1.00	57.66	A
ATOM	146	C	VAL	A	19	35.575	4.563	−23.451	1.00	54.16	A
ATOM	147	O	VAL	A	19	35.460	5.581	−22.772	1.00	55.02	A
ATOM	148	N	VAL	A	20	36.749	4.125	−23.889	1.00	52.88	A
ATOM	149	CA	VAL	A	20	37.975	4.846	−23.588	1.00	51.10	A
ATOM	150	CB	VAL	A	20	39.235	4.009	−23.905	1.00	49.57	A
ATOM	151	CG1	VAL	A	20	40.481	4.806	−23.579	1.00	48.43	A
ATOM	152	CG2	VAL	A	20	39.220	2.710	−23.122	1.00	47.78	A
ATOM	153	C	VAL	A	20	38.038	6.144	−24.372	1.00	51.08	A
ATOM	154	O	VAL	A	20	37.753	6.182	−25.560	1.00	50.63	A
ATOM	155	N	ARG	A	21	38.394	7.217	−23.685	1.00	53.23	A
ATOM	156	CA	ARG	A	21	38.518	8.521	−24.318	1.00	55.42	A
ATOM	157	CB	ARG	A	21	37.273	9.372	−24.033	1.00	58.74	A
ATOM	158	CG	ARG	A	21	36.974	10.418	−25.107	1.00	63.20	A
ATOM	159	CD	ARG	A	21	37.077	9.811	−26.508	1.00	67.31	A
ATOM	160	NE	ARG	A	21	36.395	8.517	−26.595	1.00	70.83	A
ATOM	161	CZ	ARG	A	21	35.373	8.257	−27.406	1.00	72.69	A
ATOM	162	NH1	ARG	A	21	35.905	9.203	−28.213	1.00	74.26	A
ATOM	163	NH2	ARG	A	21	35.811	7.053	−27.408	1.00	72.56	A
ATOM	164	C	ARG	A	21	39.787	9.193	−23.788	1.00	54.36	A
ATOM	165	O	ARG	A	21	40.067	9.135	−22.592	1.00	54.83	A
ATOM	166	N	SER	A	22	40.554	9.810	−24.685	1.00	53.47	A
ATOM	167	CA	SER	A	22	41.808	10.468	−24.326	1.00	52.57	A
ATOM	168	CB	SER	A	22	42.235	11.457	−25.407	1.00	51.00	A
ATOM	169	OG	SER	A	22	43.508	12.010	−25.117	1.00	47.83	A
ATOM	170	C	SER	A	22	41.742	11.187	−22.996	1.00	54.30	A
ATOM	171	O	SER	A	22	40.798	11.924	−22.735	1.00	53.49	A
ATOM	172	N	PRO	A	23	42.723	10.928	−22.113	1.00	56.74	A
ATOM	173	CD	PRO	A	23	43.730	9.867	−22.282	1.00	57.82	A
ATOM	174	CA	PRO	A	23	42.836	11.527	−20.777	1.00	56.74	A
ATOM	175	CB	PRO	A	23	43.970	10.726	−20.132	1.00	57.71	A
ATOM	176	CG	PRO	A	23	43.948	9.426	−20.862	1.00	58.98	A
ATOM	177	C	PRO	A	23	43.205	13.006	−20.850	1.00	56.91	A
ATOM	178	O	PRO	A	23	43.664	13.579	−19.867	1.00	57.91	A
ATOM	179	N	PHE	A	24	43.045	13.600	−22.030	1.00	56.66	A
ATOM	180	CA	PHE	A	24	43.332	15.015	−22.254	1.00	55.58	A
ATOM	181	CB	PHE	A	24	44.502	15.169	−23.231	1.00	55.30	A
ATOM	182	CG	PHE	A	24	45.816	14.667	−22.698	1.00	54.57	A
ATOM	183	CD1	PHE	A	24	46.464	15.332	−21.665	1.00	54.43	A
ATOM	184	CD2	PHE	A	24	46.408	13.531	−23.227	1.00	54.79	A
ATOM	185	CE1	PHE	A	24	47.683	14.872	−21.167	1.00	53.44	A
ATOM	186	CE2	PHE	A	24	47.628	13.066	−22.731	1.00	54.53	A
ATOM	187	CZ	PHE	A	24	48.262	13.740	−21.700	1.00	52.84	A
ATOM	188	C	PHE	A	24	42.094	15.716	−22.823	1.00	55.93	A
ATOM	189	O	PHE	A	24	42.059	16.947	−22.940	1.00	55.94	A
ATOM	190	N	GLN	A	25	41.075	14.920	−23.149	1.00	55.86	A
ATOM	191	CA	GLN	A	25	39.831	15.421	−23.727	1.00	56.04	A
ATOM	192	CB	GLN	A	25	39.643	14.848	−25.146	1.00	57.04	A
ATOM	193	CG	GLN	A	25	40.805	15.044	−26.129	1.00	59.85	A
ATOM	194	CD	GLN	A	25	40.779	14.038	−27.302	1.00	62.89	A
ATOM	195	OE1	GLN	A	25	39.872	13.199	−27.413	1.00	63.17	A
ATOM	196	NE2	GLN	A	25	41.796	14.109	−28.162	1.00	63.39	A
ATOM	197	C	GLN	A	25	38.562	15.114	−22.903	1.00	54.84	A
ATOM	198	O	GLN	A	25	37.546	15.791	−23.081	1.00	55.15	A
ATOM	199	N	ALA	A	26	38.608	14.116	−22.013	1.00	52.77	A
ATOM	200	CA	ALA	A	26	37.420	13.741	−21.226	1.00	51.75	A
ATOM	201	CB	ALA	A	26	36.414	13.024	−22.143	1.00	52.35	A
ATOM	202	C	ALA	A	26	37.653	12.892	−19.958	1.00	50.19	A
ATOM	203	O	ALA	A	26	38.606	12.122	−19.888	1.00	50.55	A
ATOM	204	N	PRO	A	27	36.743	12.989	−18.960	1.00	48.72	A
ATOM	205	CD	PRO	A	27	35.541	13.841	−18.929	1.00	48.24	A
ATOM	206	CA	PRO	A	27	36.846	12.235	−17.705	1.00	48.18	A
ATOM	207	CB	PRO	A	27	35.553	12.616	−16.968	1.00	47.65	A
ATOM	208	CG	PRO	A	27	35.626	13.041	−18.054	1.00	46.86	A
ATOM	209	C	PRO	A	27	36.995	10.713	−17.846	1.00	47.75	A
ATOM	210	O	PRO	A	27	36.351	10.079	−18.684	1.00	48.12	A
ATOM	211	N	GLN	A	28	37.846	10.148	−16.990	1.00	45.86	A
ATOM	212	CA	GLN	A	28	38.136	8.722	−16.965	1.00	45.53	A
ATOM	213	CB	GLN	A	28	39.593	8.517	−16.587	1.00	42.65	A
ATOM	214	CG	GLN	A	28	40.538	9.306	−17.441	1.00	39.97	A
ATOM	215	CD	GLN	A	28	40.440	8.928	−18.896	1.00	38.43	A
ATOM	216	OE1	GLN	A	28	39.831	9.639	−19.688	1.00	38.10	A
ATOM	217	NE2	GLN	A	28	41.037	7.800	−19.259	1.00	37.92	A
ATOM	218	C	GLN	A	28	37.247	7.956	−15.992	1.00	47.57	A
ATOM	219	O	GLN	A	28	37.649	6.933	−15.438	1.00	47.46	A
ATOM	220	N	TYR	A	29	36.030	8.451	−15.803	1.00	50.16	A
ATOM	221	CA	TYR	A	29	35.057	7.837	−14.904	1.00	52.07	A
ATOM	222	CB	TYR	A	29	33.796	8.696	−14.841	1.00	54.49	A
ATOM	223	CG	TYR	A	29	35.028	10.052	−14.217	1.00	56.18	A
ATOM	224	CD1	TYR	A	29	35.109	10.272	−13.365	1.00	56.35	A
ATOM	225	CE1	TYR	A	29	35.311	11.501	−12.761	1.00	57.44	A
ATOM	226	CD2	TYR	A	29	33.153	11.104	−14.454	1.00	58.05	A
ATOM	227	CE2	TYR	A	29	33.355	12.350	−13.853	1.00	59.89	A
ATOM	228	CZ	TYR	A	29	35.425	12.529	−13.006	1.00	59.52	A
ATOM	229	OH	TYR	A	29	35.599	13.744	−12.386	1.00	61.93	A
ATOM	230	C	TYR	A	29	35.694	6.421	−15.312	1.00	52.01	A
ATOM	231	O	TYR	A	29	33.991	5.717	−14.589	1.00	51.86	A
ATOM	232	N	TYR	A	30	35.135	6.024	−16.495	1.00	52.13	A
ATOM	233	CA	TYR	A	30	35.869	4.684	−16.973	1.00	53.48	A
ATOM	235	CB	TYR	A	30	35.857	4.670	−18.503	1.00	51.86	A
ATOM	235	CG	TYR	A	30	36.144	5.124	−19.140	1.00	49.90	A
ATOM	236	CD1	TYR	A	30	37.206	4.243	−19.288	1.00	49.78	A
ATOM	237	CE1	TYR	A	30	38.386	4.633	−19.889	1.00	49.52	A
ATOM	238	CD2	TYR	A	30	36.296	6.424	−19.613	1.00	49.21	A
ATOM	239	CE2	TYR	A	30	37.482	6.829	−20.225	1.00	48.45	A
ATOM	240	CZ	TYR	A	30	38.524	5.920	−20.357	1.00	49.12	A
ATOM	241	OH	TYR	A	30	39.714	6.269	−20.956	1.00	49.53	A
ATOM	242	C	TYR	A	30	35.926	3.731	−16.396	1.00	54.93	A
ATOM	243	O	TYR	A	30	35.750	2.511	−16.404	1.00	55.10	A
ATOM	244	N	LEU	A	31	37.007	4.311	−15.870	1.00	56.77	A
ATOM	245	CA	LEU	A	31	38.108	3.558	−15.262	1.00	58.98	A
ATOM	246	CB	LEU	A	31	39.399	4.383	−15.288	1.00	57.98	A
ATOM	247	CG	LEU	A	31	40.083	4.658	−16.624	1.00	57.81	A
ATOM	248	CD1	LEU	A	31	41.409	5.356	−16.386	1.00	57.24	A
ATOM	249	CD2	LEU	A	31	40.321	3.357	−17.354	1.00	57.12	A
ATOM	250	C	LEU	A	31	37.814	3.169	−13.812	1.00	60.84	A
ATOM	251	O	LEU	A	31	38.395	2.213	−13.282	1.00	61.51	A
ATOM	252	N	ALA	A	32	36.953	3.958	−13.172	1.00	62.90	A
ATOM	253	CA	ALA	A	32	36.537	3.764	−11.781	1.00	64.61	A
ATOM	254	CB	ALA	A	32	37.742	3.828	−10.855	1.00	64.59	A
ATOM	255	C	ALA	A	32	35.517	4.851	−11.407	1.00	66.21	A
ATOM	256	O	ALA	A	32	35.466	5.908	−12.045	1.00	67.09	A
ATOM	257	N	GLU	A	33	35.729	4.600	−10.363	1.00	66.91	A
ATOM	258	CA	GLU	A	33	33.692	5.536	−9.909	1.00	67.99	A
ATOM	259	CB	GLU	A	33	32.953	4.952	−8.697	1.00	69.11	A
ATOM	260	CG	GLU	A	33	31.857	3.932	−9.030	1.00	70.98	A
ATOM	261	CD	GLU	A	33	32.387	2.623	−9.605	1.00	71.82	A
ATOM	262	OE1	GLU	A	33	31.692	2.021	−10.456	1.00	71.74	A
ATOM	263	OE2	GLU	A	33	33.488	2.189	−9.198	1.00	73.40	A
ATOM	264	C	GLU	A	33	35.139	6.975	−9.599	1.00	68.12	A
ATOM	265	O	GLU	A	33	35.315	7.229	−9.335	1.00	69.00	A
ATOM	266	N	PRO	A	35	33.198	7.941	−9.668	1.00	68.22	A
ATOM	267	CD	PRO	A	35	31.866	7.756	−10.281	1.00	69.30	A
ATOM	268	CA	PRO	A	35	33.438	9.367	−9.401	1.00	67.84	A
ATOM	269	CB	PRO	A	35	32.071	9.997	−9.687	1.00	68.35	A
ATOM	270	CG	PRO	A	35	31.546	9.144	−10.798	1.00	68.37	A
ATOM	271	C	PRO	A	35	33.930	9.714	−7.987	1.00	66.46	A
ATOM	272	O	PRO	A	35	35.545	10.764	−7.780	1.00	67.29	A
ATOM	273	N	TRP	A	35	33.648	8.850	−7.018	1.00	64.20	A
ATOM	274	CA	TRP	A	35	35.071	9.098	−5.645	1.00	61.58	A
ATOM	275	CB	TRP	A	35	33.171	8.357	−4.661	1.00	63.00	A
ATOM	276	CG	TRP	A	35	33.279	6.849	−4.719	1.00	63.73	A
ATOM	277	CD2	TRP	A	35	35.129	6.022	−3.915	1.00	64.23	A
ATOM	278	CE2	TRP	A	35	33.849	4.679	−4.255	1.00	63.97	A
ATOM	279	CE3	TRP	A	35	35.101	6.288	−2.935	1.00	64.19	A
ATOM	280	CD1	TRP	A	35	32.546	6.000	−5.501	1.00	63.86	A
ATOM	281	NE1	TRP	A	35	32.881	4.693	−5.224	1.00	63.51	A
ATOM	282	CZ2	TRP	A	35	35.504	3.601	−3.649	1.00	64.18	A
ATOM	283	CZ3	TRP	A	35	35.753	5.219	−2.335	1.00	63.97	A
ATOM	284	CH2	TRP	A	35	35.450	3.890	−2.694	1.00	64.70	A
ATOM	285	C	TRP	A	35	35.545	8.749	−5.426	1.00	58.79	A
ATOM	286	O	TRP	A	35	36.222	9.359	−4.589	1.00	58.48	A
ATOM	287	N	GLN	A	36	36.037	7.767	−6.172	1.00	55.09	A
ATOM	288	CA	GLN	A	36	37.433	7.376	−6.068	1.00	52.73	A
ATOM	289	CB	GLN	A	36	37.711	6.182	−6.966	1.00	52.01	A
ATOM	290	CG	GLN	A	36	36.674	5.109	−6.819	1.00	52.45	A
ATOM	291	CD	GLN	A	36	37.221	3.744	−7.105	1.00	53.55	A
ATOM	292	OE1	GLN	A	36	36.829	3.094	−8.075	1.00	55.20	A
ATOM	293	NE2	GLN	A	36	38.130	3.286	−6.252	1.00	54.05	A
ATOM	294	C	GLN	A	36	38.235	8.582	−6.524	1.00	51.36	A
ATOM	295	O	GLN	A	36	39.209	8.969	−5.881	1.00	51.76	A
ATOM	296	N	PHE	A	37	37.788	9.186	−7.625	1.00	48.47	A
ATOM	297	CA	PHE	A	37	38.414	10.385	−8.159	1.00	45.29	A
ATOM	298	CB	PHE	A	37	37.733	10.813	−9.469	1.00	44.44	A
ATOM	299	CG	PHE	A	37	38.174	10.018	−10.677	1.00	43.06	A
ATOM	300	CD1	PHE	A	37	39.306	10.392	−11.395	1.00	40.60	A
ATOM	301	CD2	PHE	A	37	37.478	8.880	−11.077	1.00	43.60	A
ATOM	302	CE1	PHE	A	37	39.745	9.645	−12.489	1.00	41.10	A
ATOM	303	CE2	PHE	A	37	37.909	8.121	−12.175	1.00	43.01	A
ATOM	304	CZ	PHE	A	37	39.047	8.507	−12.879	1.00	42.77	A
ATOM	305	C	PHE	A	37	38.270	11.478	−7.104	1.00	44.14	A
ATOM	306	O	PHE	A	37	39.228	12.179	−6.783	1.00	44.00	A
ATOM	307	N	SER	A	38	37.077	11.571	−6.522	1.00	43.46	A
ATOM	308	CA	SER	A	38	36.798	12.558	−5.486	1.00	43.76	A
ATOM	309	CB	SER	A	38	35.313	12.530	−5.098	1.00	46.04	A
ATOM	310	OG	SER	A	38	35.486	12.970	−6.169	1.00	49.09	A
ATOM	311	C	SER	A	38	37.681	12.355	−4.255	1.00	42.43	A
ATOM	312	O	SER	A	38	37.879	13.264	−3.465	1.00	41.74	A
ATOM	313	N	MET	A	39	38.190	11.126	−4.086	1.00	41.51	A
ATOM	314	CA	MET	A	39	39.074	10.815	−2.967	1.00	41.18	A
ATOM	315	CB	MET	A	39	39.029	9.329	−2.623	1.00	44.09	A
ATOM	316	CG	MET	A	39	37.852	8.962	−1.737	1.00	49.61	A
ATOM	317	SD	MET	A	39	37.752	9.986	−0.228	1.00	57.49	A
ATOM	318	CE	MET	A	39	36.203	10.897	−0.537	1.00	56.18	A
ATOM	319	C	MET	A	39	40.504	11.269	−3.249	1.00	39.31	A
ATOM	320	O	MET	A	39	41.224	11.689	−2.335	1.00	38.29	A
ATOM	321	N	LEU	A	40	40.910	11.177	−4.514	1.00	36.67	A
ATOM	322	CA	LEU	A	40	42.233	11.621	−4.927	1.00	35.61	A
ATOM	323	CB	LEU	A	40	42.465	11.338	−6.406	1.00	30.36	A
ATOM	324	CG	LEU	A	40	42.357	9.891	−6.846	1.00	27.35	A
ATOM	325	CD1	LEU	A	40	42.836	9.766	−8.273	1.00	23.69	A
ATOM	326	CD2	LEU	A	40	43.160	9.015	−5.921	1.00	25.37	A
ATOM	327	C	LEU	A	40	42.251	13.123	−4.710	1.00	35.88	A
ATOM	328	O	LEU	A	40	43.225	13.668	−4.188	1.00	35.88	A
ATOM	329	N	ALA	A	41	41.152	13.773	−5.106	1.00	36.04	A
ATOM	330	CA	ALA	A	41	40.982	15.213	−4.961	1.00	36.09	A
ATOM	331	CB	ALA	A	41	39.669	15.639	−5.555	1.00	35.79	A
ATOM	332	C	ALA	A	41	41.066	15.610	−3.481	1.00	38.21	A
ATOM	333	O	ALA	A	41	41.877	16.464	−3.123	1.00	40.99	A
ATOM	335	N	ALA	A	42	40.266	14.972	−2.618	1.00	37.61	A
ATOM	335	CA	ALA	A	42	40.288	15.255	−1.176	1.00	35.01	A
ATOM	336	CB	ALA	A	42	39.303	14.381	−0.447	1.00	32.92	A
ATOM	337	C	ALA	A	42	41.694	15.003	−0.649	1.00	35.26	A
ATOM	338	O	ALA	A	42	42.280	15.859	0.004	1.00	36.19	A
ATOM	339	N	TYR	A	43	42.246	13.838	−0.973	1.00	35.30	A
ATOM	350	CA	TYR	A	43	43.597	13.473	−0.561	1.00	32.52	A
ATOM	351	CB	TYR	A	43	43.986	12.171	−1.242	1.00	30.14	A
ATOM	352	CG	TYR	A	43	45.439	11.797	−1.114	1.00	27.43	A
ATOM	353	CD1	TYR	A	43	46.227	11.630	−2.245	1.00	27.24	A
ATOM	354	CE1	TYR	A	43	47.541	11.223	−2.147	1.00	25.54	A
ATOM	355	CD2	TYR	A	43	46.013	11.555	0.128	1.00	26.96	A
ATOM	356	CE2	TYR	A	43	47.329	11.148	0.237	1.00	25.16	A
ATOM	357	CZ	TYR	A	43	48.080	10.980	−0.908	1.00	25.93	A
ATOM	358	OH	TYR	A	43	49.363	10.517	−0.821	1.00	31.19	A
ATOM	359	C	TYR	A	43	44.613	14.560	−0.917	1.00	33.46	A
ATOM	350	O	TYR	A	43	45.398	14.988	−0.072	1.00	32.85	A
ATOM	351	N	MET	A	44	44.591	15.000	−2.174	1.00	35.67	A
ATOM	352	CA	MET	A	44	45.509	16.044	−2.660	1.00	35.92	A
ATOM	353	CB	MET	A	44	45.381	16.231	−4.182	1.00	33.16	A
ATOM	354	CG	MET	A	44	45.923	15.069	−5.003	1.00	31.07	A
ATOM	355	SD	MET	A	44	47.576	14.506	−4.491	1.00	29.27	A
ATOM	356	CE	MET	A	44	48.506	16.035	−4.521	1.00	28.35	A
ATOM	357	C	MET	A	44	45.296	17.377	−1.952	1.00	35.20	A
ATOM	358	O	MET	A	44	46.244	18.094	−1.663	1.00	33.71	A
ATOM	359	N	PHE	A	45	44.039	17.699	−1.686	1.00	36.29	A
ATOM	360	CA	PHE	A	45	43.693	18.921	−0.993	1.00	37.83	A
ATOM	361	CB	PHE	A	45	42.171	19.029	−0.906	1.00	41.69	A
ATOM	362	CG	PHE	A	45	41.691	20.205	−0.113	1.00	46.82	A
ATOM	363	CD1	PHE	A	45	40.926	20.016	1.035	1.00	49.30	A
ATOM	364	CD2	PHE	A	45	42.024	21.503	−0.494	1.00	48.89	A
ATOM	365	CE1	PHE	A	45	40.500	21.105	1.796	1.00	50.21	A
ATOM	366	CE2	PHE	A	45	41.604	22.600	0.259	1.00	49.91	A
ATOM	367	CZ	PHE	A	45	40.841	22.399	1.408	1.00	50.54	A
ATOM	368	C	PHE	A	45	44.335	18.910	0.403	1.00	37.13	A
ATOM	369	O	PHE	A	45	44.783	19.944	0.894	1.00	37.22	A
ATOM	370	N	LEU	A	46	44.419	17.726	1.010	1.00	36.48	A
ATOM	371	CA	LEU	A	46	45.014	17.553	2.338	1.00	35.63	A
ATOM	372	CB	LEU	A	46	44.572	16.225	2.954	1.00	35.19	A
ATOM	373	CG	LEU	A	46	43.267	16.208	3.764	1.00	35.37	A
ATOM	374	CD1	LEU	A	46	42.486	17.503	3.575	1.00	35.98	A
ATOM	375	CD2	LEU	A	46	42.409	14.986	3.410	1.00	35.74	A
ATOM	376	C	LEU	A	46	46.535	17.629	2.320	1.00	35.49	A
ATOM	377	O	LEU	A	46	47.142	18.015	3.311	1.00	35.21	A
ATOM	378	N	LEU	A	47	47.144	17.227	1.205	1.00	35.51	A
ATOM	379	CA	LEU	A	47	48.604	17.270	1.059	1.00	35.31	A
ATOM	380	CB	LEU	A	47	49.070	16.401	−0.110	1.00	32.89	A
ATOM	381	CG	LEU	A	47	49.162	14.892	0.037	1.00	30.45	A
ATOM	382	CD1	LEU	A	47	49.863	14.355	−1.197	1.00	29.73	A
ATOM	383	CD2	LEU	A	47	49.942	14.551	1.284	1.00	27.83	A
ATOM	384	C	LEU	A	47	49.071	18.694	0.802	1.00	35.79	A
ATOM	385	O	LEU	A	47	50.189	19.071	1.154	1.00	35.35	A
ATOM	386	N	ILE	A	48	48.230	19.448	0.101	1.00	35.66	A
ATOM	387	CA	ILE	A	48	48.514	20.835	−0.228	1.00	35.75	A
ATOM	388	CB	ILE	A	48	47.578	21.332	−1.350	1.00	32.51	A
ATOM	389	CG2	ILE	A	48	47.705	22.831	−1.532	1.00	32.60	A
ATOM	390	CG1	ILE	A	48	47.909	20.591	−2.650	1.00	30.84	A
ATOM	391	CD1	ILE	A	48	47.261	21.168	−3.895	1.00	27.15	A
ATOM	392	C	ILE	A	48	48.354	21.668	1.036	1.00	35.45	A
ATOM	393	O	ILE	A	48	49.064	22.657	1.242	1.00	36.90	A
ATOM	394	N	MET	A	49	47.468	21.214	1.914	1.00	35.64	A
ATOM	395	CA	MET	A	49	47.227	21.904	3.171	1.00	36.72	A
ATOM	396	CB	MET	A	49	45.873	21.482	3.744	1.00	36.36	A
ATOM	397	CG	MET	A	49	45.282	22.480	4.708	1.00	36.93	A
ATOM	398	SD	MET	A	49	43.584	22.085	5.115	1.00	38.55	A
ATOM	399	CE	MET	A	49	42.721	23.522	4.353	1.00	36.69	A
ATOM	400	C	MET	A	49	48.373	21.639	4.164	1.00	36.73	A
ATOM	401	O	MET	A	49	48.669	22.470	5.019	1.00	38.01	A
ATOM	402	N	LEU	A	50	49.026	20.490	4.032	1.00	36.47	A
ATOM	403	CA	LEU	A	50	50.151	20.139	4.895	1.00	37.55	A
ATOM	404	CB	LEU	A	50	50.183	18.633	5.154	1.00	38.09	A
ATOM	405	CG	LEU	A	50	49.177	17.996	6.104	1.00	37.57	A
ATOM	406	CD1	LEU	A	50	49.373	16.479	6.139	1.00	33.82	A
ATOM	407	CD2	LEU	A	50	49.369	18.607	7.481	1.00	37.68	A
ATOM	408	C	LEU	A	50	51.492	20.552	4.271	1.00	38.43	A
ATOM	409	O	LEU	A	50	52.317	21.202	4.919	1.00	39.85	A
ATOM	410	N	GLY	A	51	51.706	20.155	3.017	1.00	36.98	A
ATOM	411	CA	GLY	A	51	52.942	20.470	2.327	1.00	35.24	A
ATOM	412	C	GLY	A	51	53.256	21.944	2.313	1.00	32.66	A
ATOM	413	O	GLY	A	51	54.415	22.332	2.278	1.00	30.63	A
ATOM	414	N	PHE	A	52	52.222	22.773	2.350	1.00	33.26	A
ATOM	415	CA	PHE	A	52	52.449	24.204	2.329	1.00	35.51	A
ATOM	416	CB	PHE	A	52	51.192	24.965	1.916	1.00	35.53	A
ATOM	417	CG	PHE	A	52	51.373	26.442	1.928	1.00	39.37	A
ATOM	418	CD1	PHE	A	52	52.602	27.004	1.583	1.00	40.99	A
ATOM	419	CD2	PHE	A	52	50.351	27.278	2.324	1.00	42.26	A
ATOM	420	CE1	PHE	A	52	52.808	28.378	1.636	1.00	42.29	A
ATOM	421	CE2	PHE	A	52	50.533	28.659	2.382	1.00	43.24	A
ATOM	422	CZ	PHE	A	52	51.774	29.208	2.037	1.00	42.87	A
ATOM	423	C	PHE	A	52	53.064	24.754	3.636	1.00	36.49	A
ATOM	424	O	PHE	A	52	54.252	25.098	3.649	1.00	37.53	A
ATOM	425	N	PRO	A	53	52.294	24.787	4.756	1.00	35.79	A
ATOM	426	CD	PRO	A	53	50.929	24.264	4.935	1.00	36.08	A
ATOM	427	CA	PRO	A	53	52.794	25.292	6.038	1.00	33.97	A
ATOM	428	CB	PRO	A	53	51.659	24.963	6.996	1.00	33.32	A
ATOM	429	CG	PRO	A	53	50.467	25.004	6.142	1.00	35.39	A
ATOM	430	C	PRO	A	53	54.077	24.606	6.481	1.00	35.16	A
ATOM	431	O	PRO	A	53	55.122	25.235	6.535	1.00	36.65	A
ATOM	432	N	ILE	A	54	53.996	23.315	6.776	1.00	32.27	A
ATOM	433	CA	ILE	A	54	55.151	22.546	7.222	1.00	31.91	A
ATOM	435	CB	ILE	A	54	54.912	21.040	7.051	1.00	31.67	A
ATOM	435	CG2	ILE	A	54	56.101	20.262	7.552	1.00	30.45	A
ATOM	436	CG1	ILE	A	54	53.658	20.618	7.816	1.00	30.45	A
ATOM	437	CD1	ILE	A	54	53.166	19.244	7.463	1.00	29.57	A
ATOM	438	C	ILE	A	54	56.413	22.915	6.463	1.00	32.63	A
ATOM	439	O	ILE	A	54	57.421	23.255	7.070	1.00	32.03	A
ATOM	440	N	ASN	A	55	56.335	22.888	5.135	1.00	35.43	A
ATOM	441	CA	ASN	A	55	57.480	23.220	4.293	1.00	36.06	A
ATOM	442	CB	ASN	A	55	57.237	22.816	2.838	1.00	35.75	A
ATOM	443	CG	ASN	A	55	57.371	21.333	2.627	1.00	33.05	A
ATOM	444	OD1	ASN	A	55	58.465	20.785	2.705	1.00	35.94	A
ATOM	445	ND2	ASN	A	55	56.260	20.668	2.384	1.00	31.71	A
ATOM	446	C	ASN	A	55	57.818	24.686	4.361	1.00	36.90	A
ATOM	447	O	ASN	A	55	58.986	25.049	4.462	1.00	36.68	A
ATOM	448	N	PHE	A	56	56.789	25.525	4.313	1.00	38.75	A
ATOM	449	CA	PHE	A	56	56.982	26.968	4.376	1.00	40.68	A
ATOM	450	CB	PHE	A	56	55.705	27.699	3.981	1.00	43.46	A
ATOM	451	CG	PHE	A	56	55.866	29.185	3.937	1.00	46.85	A
ATOM	452	CD1	PHE	A	56	56.449	29.797	2.828	1.00	48.01	A
ATOM	453	CD2	PHE	A	56	55.489	29.970	5.024	1.00	46.41	A
ATOM	454	CE1	PHE	A	56	56.659	31.168	2.803	1.00	47.15	A
ATOM	455	CE2	PHE	A	56	55.694	31.350	5.009	1.00	46.24	A
ATOM	456	CZ	PHE	A	56	56.281	31.941	3.898	1.00	47.56	A
ATOM	457	C	PHE	A	56	57.465	27.461	5.749	1.00	39.97	A
ATOM	458	O	PHE	A	56	58.181	28.455	5.835	1.00	39.35	A
ATOM	459	N	LEU	A	57	57.015	26.808	6.818	1.00	39.36	A
ATOM	460	CA	LEU	A	57	57.431	27.154	8.173	1.00	37.23	A
ATOM	461	CB	LEU	A	57	56.573	26.426	9.201	1.00	35.80	A
ATOM	462	CG	LEU	A	57	57.150	26.466	10.617	1.00	35.39	A
ATOM	463	CD1	LEU	A	57	56.976	27.862	11.157	1.00	35.37	A
ATOM	464	CD2	LEU	A	57	56.490	25.435	11.531	1.00	35.88	A
ATOM	465	C	LEU	A	57	58.876	26.692	8.317	1.00	38.17	A
ATOM	466	O	LEU	A	57	59.684	27.351	8.970	1.00	38.21	A
ATOM	467	N	THR	A	58	59.180	25.539	7.729	1.00	38.57	A
ATOM	468	CA	THR	A	58	60.530	24.995	7.760	1.00	39.20	A
ATOM	469	CB	THR	A	58	60.595	23.657	6.989	1.00	36.63	A
ATOM	470	OG1	THR	A	58	59.770	22.690	7.645	1.00	35.10	A
ATOM	471	CG2	THR	A	58	62.015	23.138	6.917	1.00	33.97	A
ATOM	472	C	THR	A	58	61.427	26.018	7.066	1.00	42.25	A
ATOM	473	O	THR	A	58	62.541	26.316	7.507	1.00	42.64	A
ATOM	474	N	LEU	A	59	60.887	26.587	5.996	1.00	44.91	A
ATOM	475	CA	LEU	A	59	61.576	27.582	5.193	1.00	46.80	A
ATOM	476	CB	LEU	A	59	60.719	27.902	3.968	1.00	48.20	A
ATOM	477	CG	LEU	A	59	61.397	28.570	2.783	1.00	48.78	A
ATOM	478	CD1	LEU	A	59	62.101	27.504	1.983	1.00	49.35	A
ATOM	479	CD2	LEU	A	59	60.352	29.261	1.930	1.00	49.92	A
ATOM	480	C	LEU	A	59	61.859	28.865	5.986	1.00	46.86	A
ATOM	481	O	LEU	A	59	63.019	29.220	6.198	1.00	45.89	A
ATOM	482	N	TYR	A	60	60.796	29.523	6.454	1.00	47.35	A
ATOM	483	CA	TYR	A	60	60.915	30.768	7.206	1.00	48.92	A
ATOM	484	CB	TYR	A	60	59.536	31.317	7.611	1.00	52.88	A
ATOM	485	CG	TYR	A	60	59.580	32.745	8.155	1.00	58.10	A
ATOM	486	CD1	TYR	A	60	58.726	33.162	9.186	1.00	58.93	A
ATOM	487	CE1	TYR	A	60	58.798	35.480	9.704	1.00	61.99	A
ATOM	488	CD2	TYR	A	60	60.504	33.675	7.651	1.00	61.33	A
ATOM	489	CE2	TYR	A	60	60.589	35.985	8.159	1.00	63.16	A
ATOM	490	CZ	TYR	A	60	59.738	35.384	9.182	1.00	63.60	A
ATOM	491	OH	TYR	A	60	59.852	36.675	9.668	1.00	63.39	A
ATOM	492	C	TYR	A	60	61.817	30.674	8.432	1.00	48.21	A
ATOM	493	O	TYR	A	60	62.502	31.632	8.774	1.00	48.22	A
ATOM	494	N	VAL	A	61	61.837	29.528	9.094	1.00	47.56	A
ATOM	495	CA	VAL	A	61	62.683	29.398	10.267	1.00	48.19	A
ATOM	496	CB	VAL	A	61	62.394	28.087	11.047	1.00	48.28	A
ATOM	497	CG1	VAL	A	61	63.332	27.965	12.244	1.00	47.74	A
ATOM	498	CG2	VAL	A	61	60.947	28.057	11.526	1.00	46.86	A
ATOM	499	C	VAL	A	61	64.166	29.478	9.885	1.00	49.97	A
ATOM	500	O	VAL	A	61	64.871	30.386	10.336	1.00	49.43	A
ATOM	501	N	THR	A	62	64.602	28.586	8.989	1.00	51.64	A
ATOM	502	CA	THR	A	62	66.006	28.504	8.544	1.00	51.75	A
ATOM	503	CB	THR	A	62	66.199	27.429	7.412	1.00	49.98	A
ATOM	504	OG1	THR	A	62	65.582	26.190	7.793	1.00	47.83	A
ATOM	505	CG2	THR	A	62	67.677	27.163	7.169	1.00	47.16	A
ATOM	506	C	THR	A	62	66.624	29.843	8.100	1.00	53.25	A
ATOM	507	O	THR	A	62	67.791	30.129	8.400	1.00	53.15	A
ATOM	508	N	VAL	A	63	65.826	30.669	7.425	1.00	54.32	A
ATOM	509	CA	VAL	A	63	66.282	31.969	6.928	1.00	56.47	A
ATOM	510	CB	VAL	A	63	65.335	32.518	5.843	1.00	55.74	A
ATOM	511	CG1	VAL	A	63	65.972	33.709	5.150	1.00	55.35	A
ATOM	512	CG2	VAL	A	63	64.973	31.429	4.853	1.00	54.49	A
ATOM	513	C	VAL	A	63	66.391	33.038	8.016	1.00	58.18	A
ATOM	514	O	VAL	A	63	67.326	33.846	8.014	1.00	59.55	A
ATOM	515	N	GLN	A	64	65.409	33.046	8.917	1.00	59.07	A
ATOM	516	CA	GLN	A	64	65.322	35.004	10.020	1.00	58.87	A
ATOM	517	CB	GLN	A	64	63.963	33.870	10.709	1.00	59.45	A
ATOM	518	CG	GLN	A	64	63.812	35.708	11.962	1.00	60.94	A
ATOM	519	CD	GLN	A	64	62.433	35.594	12.581	1.00	61.16	A
ATOM	520	OE1	GLN	A	64	61.480	35.209	12.108	1.00	62.42	A
ATOM	521	NE2	GLN	A	64	62.324	33.820	13.654	1.00	60.83	A
ATOM	522	C	GLN	A	64	66.420	33.856	11.058	1.00	58.59	A
ATOM	523	O	GLN	A	64	66.851	35.845	11.661	1.00	58.39	A
ATOM	524	N	HIS	A	65	66.836	32.612	11.281	1.00	58.81	A
ATOM	525	CA	HIS	A	65	67.870	32.289	12.255	1.00	59.29	A
ATOM	526	CB	HIS	A	65	67.462	31.033	13.022	1.00	61.19	A
ATOM	527	CG	HIS	A	65	66.174	31.187	13.777	1.00	63.64	A
ATOM	528	CD2	HIS	A	65	65.455	32.289	14.099	1.00	65.30	A
ATOM	529	ND1	HIS	A	65	65.479	30.117	14.300	1.00	65.61	A
ATOM	530	CE1	HIS	A	65	64.390	30.553	14.909	1.00	63.68	A
ATOM	531	NE2	HIS	A	65	64.352	31.867	14.803	1.00	63.66	A
ATOM	532	C	HIS	A	65	69.235	32.145	11.585	1.00	58.91	A
ATOM	533	O	HIS	A	65	69.645	31.049	11.197	1.00	58.21	A
ATOM	535	N	LYS	A	66	69.936	33.279	11.506	1.00	58.73	A
ATOM	535	CA	LYS	A	66	71.246	33.426	10.858	1.00	58.41	A
ATOM	536	CB	LYS	A	66	71.738	35.886	10.989	1.00	58.14	A
ATOM	537	CG	LYS	A	66	70.894	35.910	10.205	1.00	57.41	A
ATOM	538	CD	LYS	A	66	71.012	35.660	8.703	1.00	57.50	A
ATOM	539	CE	LYS	A	66	69.881	36.286	7.907	1.00	56.75	A
ATOM	540	NZ	LYS	A	66	69.920	35.804	6.489	1.00	56.63	A
ATOM	541	C	LYS	A	66	72.386	32.431	11.142	1.00	57.56	A
ATOM	542	O	LYS	A	66	73.302	32.298	10.317	1.00	57.85	A
ATOM	543	N	LYS	A	67	72.329	31.719	12.268	1.00	56.19	A
ATOM	544	CA	LYS	A	67	73.376	30.747	12.601	1.00	54.53	A
ATOM	545	CB	LYS	A	67	73.819	30.867	14.074	1.00	55.11	A
ATOM	546	CG	LYS	A	67	74.545	32.169	14.470	1.00	55.63	A
ATOM	547	CD	LYS	A	67	75.470	31.952	15.684	1.00	56.05	A
ATOM	548	CE	LYS	A	67	74.708	31.497	16.935	1.00	55.98	A
ATOM	549	NZ	LYS	A	67	75.593	31.064	18.070	1.00	55.20	A
ATOM	550	C	LYS	A	67	72.954	29.304	12.310	1.00	53.05	A
ATOM	551	O	LYS	A	67	73.706	28.367	12.567	1.00	54.24	A
ATOM	552	N	LEU	A	68	71.748	29.126	11.785	1.00	51.46	A
ATOM	553	CA	LEU	A	68	71.235	27.791	11.462	1.00	50.99	A
ATOM	554	CB	LEU	A	68	69.698	27.809	11.577	1.00	48.86	A
ATOM	555	CG	LEU	A	68	68.853	26.645	12.119	1.00	44.80	A
ATOM	556	CD1	LEU	A	68	69.327	26.196	13.482	1.00	43.96	A
ATOM	557	CD2	LEU	A	68	67.410	27.095	12.211	1.00	42.39	A
ATOM	558	C	LEU	A	68	71.684	27.461	10.026	1.00	51.57	A
ATOM	559	O	LEU	A	68	70.859	27.187	9.147	1.00	51.25	A
ATOM	560	N	ARG	A	69	73.001	27.459	9.806	1.00	51.26	A
ATOM	561	CA	ARG	A	69	73.551	27.225	8.476	1.00	50.50	A
ATOM	562	CB	ARG	A	69	74.076	28.554	7.919	1.00	49.06	A
ATOM	563	CG	ARG	A	69	73.106	29.711	8.025	1.00	47.95	A
ATOM	564	CD	ARG	A	69	71.860	29.450	7.208	1.00	50.65	A
ATOM	565	NE	ARG	A	69	70.815	30.435	7.455	1.00	53.72	A
ATOM	566	CZ	ARG	A	69	70.922	31.732	7.173	1.00	57.64	A
ATOM	567	NH1	ARG	A	69	72.040	32.216	6.629	1.00	58.63	A
ATOM	568	NH2	ARG	A	69	69.902	32.548	7.429	1.00	57.82	A
ATOM	569	C	ARG	A	69	74.632	26.143	8.318	1.00	51.47	A
ATOM	570	O	ARG	A	69	75.779	26.449	8.003	1.00	51.90	A
ATOM	571	N	THR	A	70	74.268	24.879	8.498	1.00	53.05	A
ATOM	572	CA	THR	A	70	75.235	23.787	8.324	1.00	54.84	A
ATOM	573	CB	THR	A	70	75.383	22.923	9.611	1.00	54.96	A
ATOM	574	OG1	THR	A	70	74.280	22.015	9.735	1.00	54.48	A
ATOM	575	CG2	THR	A	70	75.445	23.814	10.840	1.00	56.71	A
ATOM	576	C	THR	A	70	74.778	22.896	7.160	1.00	55.57	A
ATOM	577	O	THR	A	70	73.633	23.010	6.709	1.00	55.90	A
ATOM	578	N	PRO	A	71	75.674	22.029	6.630	1.00	55.72	A
ATOM	579	CD	PRO	A	71	77.115	21.909	6.922	1.00	55.61	A
ATOM	580	CA	PRO	A	71	75.306	21.140	5.518	1.00	55.36	A
ATOM	581	CB	PRO	A	71	76.479	20.174	5.464	1.00	55.09	A
ATOM	582	CG	PRO	A	71	77.620	21.096	5.745	1.00	55.44	A
ATOM	583	C	PRO	A	71	73.968	20.429	5.728	1.00	54.31	A
ATOM	584	O	PRO	A	71	73.242	20.192	4.768	1.00	55.07	A
ATOM	585	N	LEU	A	72	73.636	20.110	6.979	1.00	52.30	A
ATOM	586	CA	LEU	A	72	72.356	19.479	7.279	1.00	49.51	A
ATOM	587	CB	LEU	A	72	72.350	18.859	8.671	1.00	49.57	A
ATOM	588	CG	LEU	A	72	70.936	18.390	9.028	1.00	49.23	A
ATOM	589	CD1	LEU	A	72	70.600	17.176	8.190	1.00	50.64	A
ATOM	590	CD2	LEU	A	72	70.806	18.067	10.500	1.00	50.16	A
ATOM	591	C	LEU	A	72	71.247	20.522	7.214	1.00	47.98	A
ATOM	592	O	LEU	A	72	70.209	20.297	6.606	1.00	47.58	A
ATOM	593	N	ASN	A	73	71.474	21.658	7.864	1.00	47.73	A
ATOM	594	CA	ASN	A	73	70.498	22.742	7.901	1.00	47.16	A
ATOM	595	CB	ASN	A	73	70.948	23.843	8.873	1.00	45.92	A
ATOM	596	CG	ASN	A	73	71.078	23.352	10.309	1.00	45.35	A
ATOM	597	OD1	ASN	A	73	72.047	22.677	10.668	1.00	45.25	A
ATOM	598	ND2	ASN	A	73	70.095	23.654	11.130	1.00	45.35	A
ATOM	599	C	ASN	A	73	70.233	23.317	6.514	1.00	47.25	A
ATOM	600	O	ASN	A	73	69.128	23.788	6.248	1.00	48.96	A
ATOM	601	N	TYR	A	74	71.235	23.252	5.636	1.00	46.18	A
ATOM	602	CA	TYR	A	74	71.129	23.748	4.257	1.00	46.67	A
ATOM	603	CB	TYR	A	74	72.520	23.866	3.626	1.00	46.82	A
ATOM	604	CG	TYR	A	74	73.050	25.271	3.540	1.00	47.01	A
ATOM	605	CD1	TYR	A	74	72.590	26.153	2.562	1.00	47.17	A
ATOM	606	CE1	TYR	A	74	73.040	27.474	2.520	1.00	47.64	A
ATOM	607	CD2	TYR	A	74	73.979	25.738	4.469	1.00	47.79	A
ATOM	608	CE2	TYR	A	74	74.433	27.051	4.437	1.00	47.35	A
ATOM	609	CZ	TYR	A	74	73.960	27.914	3.467	1.00	47.78	A
ATOM	610	OH	TYR	A	74	74.394	29.219	3.467	1.00	49.58	A
ATOM	611	C	TYR	A	74	70.307	22.808	3.383	1.00	47.78	A
ATOM	612	O	TYR	A	74	69.376	23.227	2.689	1.00	47.65	A
ATOM	613	N	ILE	A	75	70.722	21.540	3.380	1.00	48.75	A
ATOM	614	CA	ILE	A	75	70.086	20.475	2.605	1.00	47.99	A
ATOM	615	CB	ILE	A	75	70.776	19.098	2.870	1.00	47.66	A
ATOM	616	CG2	ILE	A	75	69.763	17.981	2.951	1.00	46.32	A
ATOM	617	CG1	ILE	A	75	71.796	18.793	1.772	1.00	49.02	A
ATOM	618	CD1	ILE	A	75	72.952	19.778	1.685	1.00	50.80	A
ATOM	619	C	ILE	A	75	68.604	20.378	2.906	1.00	47.42	A
ATOM	620	O	ILE	A	75	67.823	19.962	2.055	1.00	47.68	A
ATOM	621	N	LEU	A	76	68.221	20.738	4.124	1.00	47.15	A
ATOM	622	CA	LEU	A	76	66.818	20.679	4.485	1.00	47.88	A
ATOM	623	CB	LEU	A	76	66.631	20.288	5.949	1.00	46.29	A
ATOM	624	CG	LEU	A	76	66.540	18.758	6.002	1.00	46.02	A
ATOM	625	CD1	LEU	A	76	67.633	18.161	6.850	1.00	45.18	A
ATOM	626	CD2	LEU	A	76	65.164	18.329	6.468	1.00	45.07	A
ATOM	627	C	LEU	A	76	66.027	21.915	4.094	1.00	48.19	A
ATOM	628	O	LEU	A	76	64.797	21.903	4.116	1.00	49.14	A
ATOM	629	N	LEU	A	77	66.735	22.970	3.699	1.00	48.02	A
ATOM	630	CA	LEU	A	77	66.081	24.189	3.243	1.00	47.27	A
ATOM	631	CB	LEU	A	77	67.006	25.399	3.422	1.00	47.76	A
ATOM	632	CG	LEU	A	77	66.379	26.791	3.288	1.00	47.63	A
ATOM	633	CD1	LEU	A	77	66.360	27.240	1.847	1.00	48.32	A
ATOM	635	CD2	LEU	A	77	64.976	26.790	3.875	1.00	48.71	A
ATOM	635	C	LEU	A	77	65.802	23.925	1.768	1.00	47.10	A
ATOM	636	O	LEU	A	77	64.790	24.367	1.217	1.00	46.95	A
ATOM	637	N	ASN	A	78	66.702	23.146	1.164	1.00	46.56	A
ATOM	638	CA	ASN	A	78	66.632	22.736	−0.238	1.00	45.64	A
ATOM	639	CB	ASN	A	78	67.860	21.861	−0.574	1.00	47.42	A
ATOM	640	CG	ASN	A	78	67.948	21.473	−2.056	1.00	47.49	A
ATOM	641	OD1	ASN	A	78	67.505	22.213	−2.938	1.00	46.97	A
ATOM	642	ND2	ASN	A	78	68.556	20.318	−2.328	1.00	46.72	A
ATOM	643	C	ASN	A	78	65.353	21.939	−0.445	1.00	44.05	A
ATOM	644	O	ASN	A	78	64.573	22.220	−1.350	1.00	44.31	A
ATOM	645	N	LEU	A	79	65.128	20.979	0.445	1.00	42.80	A
ATOM	646	CA	LEU	A	79	63.965	20.113	0.385	1.00	41.37	A
ATOM	647	CB	LEU	A	79	64.167	18.932	1.330	1.00	40.19	A
ATOM	648	CG	LEU	A	79	65.427	18.129	0.979	1.00	39.85	A
ATOM	649	CD1	LEU	A	79	65.593	16.964	1.918	1.00	38.99	A
ATOM	650	CD2	LEU	A	79	65.357	17.636	−0.457	1.00	38.87	A
ATOM	651	C	LEU	A	79	62.644	20.835	0.655	1.00	42.07	A
ATOM	652	O	LEU	A	79	61.626	20.507	0.041	1.00	43.09	A
ATOM	653	N	ALA	A	80	62.661	21.830	1.541	1.00	41.12	A
ATOM	654	CA	ALA	A	80	61.454	22.596	1.851	1.00	39.86	A
ATOM	655	CB	ALA	A	80	61.736	23.591	2.954	1.00	38.62	A
ATOM	656	C	ALA	A	80	60.971	23.318	0.585	1.00	40.35	A
ATOM	657	O	ALA	A	80	59.768	23.401	0.320	1.00	41.58	A
ATOM	658	N	VAL	A	81	61.924	23.815	−0.201	1.00	39.33	A
ATOM	659	CA	VAL	A	81	61.641	24.510	−1.459	1.00	37.70	A
ATOM	660	CB	VAL	A	81	62.911	25.220	−1.992	1.00	36.48	A
ATOM	661	CG1	VAL	A	81	62.694	25.724	−3.413	1.00	35.73	A
ATOM	662	CG2	VAL	A	81	63.288	26.363	−1.072	1.00	35.76	A
ATOM	663	C	VAL	A	81	61.125	23.533	−2.523	1.00	36.93	A
ATOM	664	O	VAL	A	81	60.098	23.783	−3.158	1.00	35.47	A
ATOM	665	N	ALA	A	82	61.859	22.436	−2.717	1.00	36.04	A
ATOM	666	CA	ALA	A	82	61.497	21.408	−3.686	1.00	35.47	A
ATOM	667	CB	ALA	A	82	62.491	20.252	−3.638	1.00	33.67	A
ATOM	668	C	ALA	A	82	60.087	20.918	−3.382	1.00	36.09	A
ATOM	669	O	ALA	A	82	59.315	20.637	−4.307	1.00	37.02	A
ATOM	670	N	ASP	A	83	59.753	20.849	−2.088	1.00	35.02	A
ATOM	671	CA	ASP	A	83	58.427	20.421	−1.646	1.00	35.37	A
ATOM	672	CB	ASP	A	83	58.433	20.018	−0.168	1.00	33.07	A
ATOM	673	CG	ASP	A	83	59.230	18.738	0.107	1.00	35.24	A
ATOM	674	OD1	ASP	A	83	60.058	18.319	−0.735	1.00	35.14	A
ATOM	675	OD2	ASP	A	83	59.043	18.146	1.196	1.00	35.83	A
ATOM	676	C	ASP	A	83	57.407	21.543	−1.903	1.00	35.33	A
ATOM	677	O	ASP	A	83	56.245	21.270	−2.198	1.00	36.97	A
ATOM	678	N	LEU	A	84	57.839	22.802	−1.811	1.00	35.83	A
ATOM	679	CA	LEU	A	84	56.941	23.925	−2.085	1.00	32.53	A
ATOM	680	CB	LEU	A	84	57.518	25.250	−1.570	1.00	32.03	A
ATOM	681	CG	LEU	A	84	57.497	25.481	−0.054	1.00	30.64	A
ATOM	682	OD1	LEU	A	84	58.223	26.754	0.271	1.00	29.76	A
ATOM	683	CD2	LEU	A	84	56.077	25.544	0.463	1.00	30.26	A
ATOM	684	C	LEU	A	84	56.689	23.983	−3.591	1.00	31.54	A
ATOM	685	O	LEU	A	84	55.614	24.375	−4.016	1.00	31.37	A
ATOM	686	N	PHE	A	85	57.680	23.580	−4.386	1.00	31.79	A
ATOM	687	CA	PHE	A	85	57.547	23.533	−5.848	1.00	32.99	A
ATOM	688	CB	PHE	A	85	58.888	23.292	−6.532	1.00	32.58	A
ATOM	689	CG	PHE	A	85	59.610	24.542	−6.867	1.00	35.24	A
ATOM	690	CD1	PHE	A	85	58.904	25.675	−7.266	1.00	36.55	A
ATOM	691	CD2	PHE	A	85	60.997	24.607	−6.775	1.00	36.35	A
ATOM	692	CE1	PHE	A	85	59.568	26.863	−7.569	1.00	37.42	A
ATOM	693	CE2	PHE	A	85	61.674	25.788	−7.075	1.00	36.51	A
ATOM	694	CZ	PHE	A	85	60.957	26.920	−7.473	1.00	37.03	A
ATOM	695	C	PHE	A	85	56.600	22.416	−6.235	1.00	32.88	A
ATOM	696	O	PHE	A	85	55.899	22.495	−7.240	1.00	32.01	A
ATOM	697	N	MET	A	86	56.626	21.355	−5.458	1.00	32.13	A
ATOM	698	CA	MET	A	86	55.725	20.247	−5.712	1.00	33.85	A
ATOM	699	CB	MET	A	86	56.061	19.063	−4.802	1.00	33.64	A
ATOM	700	CG	MET	A	86	57.468	18.522	−4.962	1.00	31.95	A
ATOM	701	SD	MET	A	86	57.610	16.797	−4.461	1.00	29.61	A
ATOM	702	CE	MET	A	86	58.500	16.953	−3.048	1.00	32.77	A
ATOM	703	C	MET	A	86	54.299	20.758	−5.428	1.00	35.87	A
ATOM	704	O	MET	A	86	53.450	20.784	−6.323	1.00	35.21	A
ATOM	705	N	VAL	A	87	54.087	21.247	−4.204	1.00	35.00	A
ATOM	706	CA	VAL	A	87	52.792	21.756	−3.761	1.00	33.71	A
ATOM	707	CB	VAL	A	87	52.908	22.457	−2.379	1.00	33.26	A
ATOM	708	CG1	VAL	A	87	51.547	22.935	−1.904	1.00	31.72	A
ATOM	709	CG2	VAL	A	87	53.503	21.527	−1.357	1.00	32.17	A
ATOM	710	C	VAL	A	87	52.161	22.741	−4.740	1.00	35.69	A
ATOM	711	O	VAL	A	87	50.963	22.695	−4.999	1.00	35.07	A
ATOM	712	N	PHE	A	88	52.976	23.631	−5.287	1.00	38.23	A
ATOM	713	CA	PHE	A	88	52.473	24.640	−6.203	1.00	39.32	A
ATOM	714	CB	PHE	A	88	53.123	25.993	−5.898	1.00	42.10	A
ATOM	715	CG	PHE	A	88	52.998	26.418	−4.461	1.00	44.23	A
ATOM	716	CD1	PHE	A	88	51.788	26.286	−3.782	1.00	45.24	A
ATOM	717	CD2	PHE	A	88	54.099	26.931	−3.778	1.00	46.54	A
ATOM	718	CE1	PHE	A	88	51.672	26.656	−2.438	1.00	46.03	A
ATOM	719	CE2	PHE	A	88	53.994	27.305	−2.430	1.00	48.18	A
ATOM	720	CZ	PHE	A	88	52.774	27.164	−1.763	1.00	46.42	A
ATOM	721	C	PHE	A	88	52.691	24.289	−7.660	1.00	38.83	A
ATOM	722	O	PHE	A	88	51.797	24.474	−8.477	1.00	38.64	A
ATOM	723	N	GLY	A	89	53.881	23.798	−7.985	1.00	37.23	A
ATOM	724	CA	GLY	A	89	54.181	23.459	−9.363	1.00	37.90	A
ATOM	725	C	GLY	A	89	53.471	22.238	−9.922	1.00	38.91	A
ATOM	726	O	GLY	A	89	53.060	22.237	−11.084	1.00	38.66	A
ATOM	727	N	GLY	A	90	53.333	21.195	−9.108	1.00	39.29	A
ATOM	728	CA	GLY	A	90	52.683	19.984	−9.575	1.00	39.04	A
ATOM	729	C	GLY	A	90	51.375	19.628	−8.899	1.00	40.35	A
ATOM	730	O	GLY	A	90	50.404	19.302	−9.569	1.00	39.74	A
ATOM	731	N	PHE	A	91	51.352	19.704	−7.571	1.00	42.03	A
ATOM	732	CA	PHE	A	91	50.151	19.358	−6.788	1.00	42.37	A
ATOM	733	CB	PHE	A	91	50.468	19.367	−5.284	1.00	42.92	A
ATOM	735	CG	PHE	A	91	51.394	18.262	−4.839	1.00	43.42	A
ATOM	735	CD1	PHE	A	91	51.612	18.033	−3.488	1.00	43.83	A
ATOM	736	CD2	PHE	A	91	52.042	17.451	−5.760	1.00	44.58	A
ATOM	737	CE1	PHE	A	91	52.454	17.019	−3.061	1.00	43.20	A
ATOM	738	CE2	PHE	A	91	52.888	16.435	−5.351	1.00	45.02	A
ATOM	739	CZ	PHE	A	91	53.092	16.219	−3.986	1.00	44.77	A
ATOM	740	C	PHE	A	91	48.903	20.206	−7.060	1.00	42.28	A
ATOM	741	O	PHE	A	91	47.777	19.759	−6.826	1.00	41.30	A
ATOM	742	N	THR	A	92	49.102	21.443	−7.502	1.00	41.43	A
ATOM	743	CA	THR	A	92	47.982	22.324	−7.807	1.00	40.22	A
ATOM	744	CB	THR	A	92	48.466	23.783	−8.073	1.00	40.87	A
ATOM	745	OG1	THR	A	92	49.522	23.776	−9.045	1.00	40.52	A
ATOM	746	CG2	THR	A	92	48.968	24.435	−6.796	1.00	40.60	A
ATOM	747	C	THR	A	92	47.297	21.776	−9.060	1.00	40.35	A
ATOM	748	O	THR	A	92	46.074	21.781	−9.176	1.00	38.21	A
ATOM	749	N	THR	A	93	48.118	21.253	−9.969	1.00	41.56	A
ATOM	750	CA	THR	A	93	47.668	20.699	−11.242	1.00	42.13	A
ATOM	751	CB	THR	A	93	48.814	20.782	−12.315	1.00	44.14	A
ATOM	752	OG1	THR	A	93	49.403	22.100	−12.311	1.00	44.71	A
ATOM	753	CG2	THR	A	93	48.276	20.486	−13.707	1.00	41.76	A
ATOM	754	C	THR	A	93	47.159	19.252	−11.100	1.00	42.29	A
ATOM	755	O	THR	A	93	46.405	18.767	−11.949	1.00	41.39	A
ATOM	756	N	THR	A	94	47.570	18.564	−10.030	1.00	42.43	A
ATOM	757	CA	THR	A	94	47.126	17.188	−9.793	1.00	41.22	A
ATOM	758	CB	THR	A	94	48.145	16.374	−8.967	1.00	40.39	A
ATOM	759	OG1	THR	A	94	47.714	15.011	−8.869	1.00	40.43	A
ATOM	760	CG2	THR	A	94	48.284	16.929	−7.598	1.00	41.63	A
ATOM	761	C	THR	A	94	45.763	17.187	−9.105	1.00	41.66	A
ATOM	762	O	THR	A	94	44.996	16.229	−9.239	1.00	41.74	A
ATOM	763	N	LEU	A	95	45.464	18.274	−8.391	1.00	41.76	A
ATOM	764	CA	LEU	A	95	44.185	18.433	−7.702	1.00	40.65	A
ATOM	765	CB	LEU	A	95	44.313	19.389	−6.508	1.00	39.53	A
ATOM	766	CG	LEU	A	95	43.054	19.829	−5.744	1.00	37.83	A
ATOM	767	CD1	LEU	A	95	42.200	18.631	−5.355	1.00	39.55	A
ATOM	768	CD2	LEU	A	95	43.440	20.620	−4.516	1.00	35.85	A
ATOM	769	C	LEU	A	95	43.094	18.917	−8.654	1.00	41.21	A
ATOM	770	O	LEU	A	95	41.961	18.441	−8.567	1.00	41.38	A
ATOM	771	N	TYR	A	96	43.424	19.851	−9.552	1.00	41.59	A
ATOM	772	CA	TYR	A	96	42.439	20.366	−10.517	1.00	43.82	A
ATOM	773	CB	TYR	A	96	43.038	21.514	−11.361	1.00	45.90	A
ATOM	774	CG	TYR	A	96	42.053	22.290	−12.252	1.00	49.44	A
ATOM	775	CD1	TYR	A	96	41.608	23.573	−11.899	1.00	51.05	A
ATOM	776	CE1	TYR	A	96	40.714	24.300	−12.730	1.00	52.83	A
ATOM	777	CD2	TYR	A	96	41.585	21.751	−13.459	1.00	51.30	A
ATOM	778	CE2	TYR	A	96	40.700	22.465	−14.293	1.00	52.69	A
ATOM	779	CZ	TYR	A	96	40.265	23.736	−13.925	1.00	53.45	A
ATOM	780	OH	TYR	A	96	39.376	24.416	−14.744	1.00	53.22	A
ATOM	781	C	TYR	A	96	42.016	19.196	−11.408	1.00	44.11	A
ATOM	782	O	TYR	A	96	40.838	19.036	−11.733	1.00	43.71	A
ATOM	783	N	THR	A	97	42.991	18.357	−11.728	1.00	44.56	A
ATOM	784	CA	THR	A	97	42.800	17.159	−12.561	1.00	44.45	A
ATOM	785	CB	THR	A	97	44.175	16.537	−12.897	1.00	44.67	A
ATOM	786	OG1	THR	A	97	44.880	17.414	−13.784	1.00	43.79	A
ATOM	787	CG2	THR	A	97	44.033	15.163	−13.529	1.00	43.06	A
ATOM	788	C	THR	A	97	41.877	16.107	−11.919	1.00	44.37	A
ATOM	789	O	THR	A	97	40.955	15.612	−12.565	1.00	43.89	A
ATOM	790	N	SER	A	98	42.141	15.764	−10.657	1.00	44.39	A
ATOM	791	CA	SER	A	98	41.330	14.791	−9.928	1.00	42.28	A
ATOM	792	CB	SER	A	98	41.919	14.535	−8.546	1.00	40.92	A
ATOM	793	OG	SER	A	98	43.126	13.809	−8.649	1.00	39.71	A
ATOM	794	C	SER	A	98	39.912	15.312	−9.786	1.00	42.68	A
ATOM	795	O	SER	A	98	38.951	14.550	−9.902	1.00	44.27	A
ATOM	796	N	LEU	A	99	39.792	16.618	−9.550	1.00	41.55	A
ATOM	797	CA	LEU	A	99	38.496	17.269	−9.408	1.00	40.28	A
ATOM	798	CB	LEU	A	99	38.660	18.725	−8.974	1.00	36.43	A
ATOM	799	CG	LEU	A	99	38.740	18.863	−7.460	1.00	33.05	A
ATOM	800	CD1	LEU	A	99	39.120	20.268	−7.076	1.00	31.89	A
ATOM	801	CD2	LEU	A	99	37.412	18.468	−6.859	1.00	29.01	A
ATOM	802	C	LEU	A	99	37.667	17.208	−10.673	1.00	41.12	A
ATOM	803	O	LEU	A	99	36.442	17.147	−10.600	1.00	42.91	A
ATOM	804	N	HIS	A	100	38.333	17.192	−11.824	1.00	41.46	A
ATOM	805	CA	HIS	A	100	37.636	17.142	−13.104	1.00	42.81	A
ATOM	806	CB	HIS	A	100	38.219	18.175	−14.061	1.00	43.12	A
ATOM	807	CG	HIS	A	100	37.953	19.586	−13.644	1.00	44.38	A
ATOM	808	CD2	HIS	A	100	36.985	20.457	−14.017	1.00	45.57	A
ATOM	809	ND1	HIS	A	100	38.716	20.242	−12.704	1.00	44.62	A
ATOM	810	CE1	HIS	A	100	38.230	21.456	−12.515	1.00	46.31	A
ATOM	811	NE2	HIS	A	100	37.180	21.612	−13.300	1.00	46.65	A
ATOM	812	C	HIS	A	100	37.521	15.780	−13.790	1.00	43.64	A
ATOM	813	O	HIS	A	100	36.628	15.594	−14.628	1.00	44.29	A
ATOM	814	N	GLY	A	101	38.418	14.849	−13.446	1.00	44.10	A
ATOM	815	CA	GLY	A	101	38.401	13.506	−14.024	1.00	44.28	A
ATOM	816	C	GLY	A	101	39.430	13.175	−15.101	1.00	44.85	A
ATOM	817	O	GLY	A	101	39.503	12.035	−15.571	1.00	44.25	A
ATOM	818	N	TYR	A	102	40.230	14.168	−15.486	1.00	46.41	A
ATOM	819	CA	TYR	A	102	41.264	14.019	−16.516	1.00	47.26	A
ATOM	820	CB	TYR	A	102	40.616	13.845	−17.900	1.00	50.02	A
ATOM	821	CG	TYR	A	102	39.918	15.093	−18.433	1.00	53.62	A
ATOM	822	CD1	TYR	A	102	38.796	15.631	−17.788	1.00	54.12	A
ATOM	823	CE1	TYR	A	102	38.186	16.795	−18.248	1.00	54.03	A
ATOM	824	CD2	TYR	A	102	40.404	15.756	−19.562	1.00	54.85	A
ATOM	825	CE2	TYR	A	102	39.798	16.921	−20.031	1.00	56.05	A
ATOM	826	CZ	TYR	A	102	38.694	17.435	−19.368	1.00	55.22	A
ATOM	827	OH	TYR	A	102	38.117	18.596	−19.825	1.00	56.48	A
ATOM	828	C	TYR	A	102	42.156	15.268	−16.518	1.00	46.53	A
ATOM	829	O	TYR	A	102	41.977	16.165	−15.695	1.00	46.56	A
ATOM	830	N	PHE	A	103	43.107	15.329	−17.444	1.00	45.77	A
ATOM	831	CA	PHE	A	103	44.004	16.474	−17.541	1.00	46.41	A
ATOM	832	CB	PHE	A	103	45.375	16.036	−18.060	1.00	44.21	A
ATOM	833	CG	PHE	A	103	46.235	15.362	−17.018	1.00	44.01	A
ATOM	835	CD1	PHE	A	103	46.389	13.978	−17.008	1.00	43.52	A
ATOM	835	CD2	PHE	A	103	46.887	16.113	−16.045	1.00	42.31	A
ATOM	836	CE1	PHE	A	103	47.181	13.356	−16.043	1.00	43.72	A
ATOM	837	CE2	PHE	A	103	47.676	15.499	−15.082	1.00	42.38	A
ATOM	838	CZ	PHE	A	103	47.824	14.120	−15.080	1.00	42.24	A
ATOM	839	C	PHE	A	103	43.414	17.580	−18.416	1.00	48.51	A
ATOM	840	O	PHE	A	103	43.589	17.588	−19.631	1.00	49.24	A
ATOM	841	N	VAL	A	104	42.716	18.515	−17.779	1.00	51.21	A
ATOM	842	CA	VAL	A	104	42.071	19.632	−18.471	1.00	53.35	A
ATOM	843	CB	VAL	A	104	41.175	20.478	−17.491	1.00	52.03	A
ATOM	844	CG1	VAL	A	104	40.562	21.681	−18.200	1.00	50.45	A
ATOM	845	CG2	VAL	A	104	40.067	19.611	−16.912	1.00	49.70	A
ATOM	846	C	VAL	A	104	43.071	20.527	−19.207	1.00	56.12	A
ATOM	847	O	VAL	A	104	42.859	20.849	−20.378	1.00	57.69	A
ATOM	848	N	PHE	A	105	44.166	20.904	−18.542	1.00	58.57	A
ATOM	849	CA	PHE	A	105	45.186	21.763	−19.164	1.00	60.74	A
ATOM	850	CB	PHE	A	105	46.106	22.401	−18.113	1.00	63.88	A
ATOM	851	CG	PHE	A	105	45.377	23.218	−17.086	1.00	67.84	A
ATOM	852	CD1	PHE	A	105	44.237	23.949	−17.437	1.00	69.17	A
ATOM	853	CD2	PHE	A	105	45.805	23.230	−15.760	1.00	69.65	A
ATOM	854	CE1	PHE	A	105	43.530	24.677	−16.484	1.00	70.72	A
ATOM	855	CE2	PHE	A	105	45.107	23.955	−14.793	1.00	71.79	A
ATOM	856	CZ	PHE	A	105	43.965	24.680	−15.155	1.00	71.73	A
ATOM	857	C	PHE	A	105	46.018	20.998	−20.186	1.00	60.31	A
ATOM	858	O	PHE	A	105	47.000	21.524	−20.716	1.00	61.32	A
ATOM	859	N	GLY	A	106	45.622	19.752	−20.437	1.00	58.66	A
ATOM	860	CA	GLY	A	106	46.301	18.912	−21.403	1.00	57.21	A
ATOM	861	C	GLY	A	106	47.705	18.469	−21.051	1.00	56.46	A
ATOM	862	O	GLY	A	106	48.035	18.294	−19.881	1.00	55.78	A
ATOM	863	N	PRO	A	107	48.562	18.289	−22.068	1.00	56.71	A
ATOM	864	CD	PRO	A	107	48.217	18.553	−23.475	1.00	57.95	A
ATOM	865	CA	PRO	A	107	49.959	17.861	−21.960	1.00	56.58	A
ATOM	866	CB	PRO	A	107	50.435	17.878	−23.417	1.00	57.59	A
ATOM	867	CG	PRO	A	107	49.553	18.906	−24.063	1.00	58.81	A
ATOM	868	C	PRO	A	107	50.870	18.666	−21.022	1.00	55.43	A
ATOM	869	O	PRO	A	107	51.751	18.077	−20.389	1.00	56.43	A
ATOM	870	N	THR	A	108	50.688	19.989	−20.938	1.00	53.46	A
ATOM	871	CA	THR	A	108	51.511	20.803	−20.027	1.00	51.49	A
ATOM	872	CB	THR	A	108	51.489	22.310	−20.377	1.00	49.95	A
ATOM	873	OG1	THR	A	108	50.154	22.805	−20.276	1.00	50.80	A
ATOM	874	CG2	THR	A	108	52.002	22.545	−21.792	1.00	49.32	A
ATOM	875	C	THR	A	108	51.036	20.572	−18.585	1.00	50.69	A
ATOM	876	O	THR	A	108	51.815	20.688	−17.639	1.00	50.81	A
ATOM	877	N	GLY	A	109	49.757	20.212	−18.440	1.00	49.99	A
ATOM	878	CA	GLY	A	109	49.189	19.899	−17.137	1.00	48.28	A
ATOM	879	C	GLY	A	109	49.767	18.570	−16.668	1.00	47.15	A
ATOM	880	O	GLY	A	109	49.821	18.276	−15.470	1.00	47.93	A
ATOM	881	N	CYS	A	110	50.181	17.760	−17.640	1.00	45.08	A
ATOM	882	CA	CYS	A	110	50.800	16.464	−17.405	1.00	43.45	A
ATOM	883	C	CYS	A	110	52.284	16.697	−17.160	1.00	43.88	A
ATOM	884	O	CYS	A	110	52.908	15.997	−16.365	1.00	44.64	A
ATOM	885	CB	CYS	A	110	50.638	15.569	−18.635	1.00	43.20	A
ATOM	886	SG	CYS	A	110	51.327	13.892	−18.465	1.00	39.51	A
ATOM	887	N	ASN	A	111	52.846	17.684	−17.854	1.00	42.78	A
ATOM	888	CA	ASN	A	111	54.256	18.009	−17.711	1.00	41.71	A
ATOM	889	CB	ASN	A	111	54.730	18.915	−18.861	1.00	42.08	A
ATOM	890	CG	ASN	A	111	54.972	18.148	−20.182	1.00	41.94	A
ATOM	891	OD1	ASN	A	111	55.127	16.923	−20.205	1.00	41.75	A
ATOM	892	ND2	ASN	A	111	55.035	18.890	−21.282	1.00	40.24	A
ATOM	893	C	ASN	A	111	54.563	18.640	−16.350	1.00	41.09	A
ATOM	894	O	ASN	A	111	55.552	18.278	−15.721	1.00	42.02	A
ATOM	895	N	LEU	A	112	53.697	19.536	−15.872	1.00	39.39	A
ATOM	896	CA	LEU	A	112	53.908	20.195	−14.577	1.00	39.01	A
ATOM	897	CB	LEU	A	112	52.983	21.402	−14.414	1.00	38.71	A
ATOM	898	CG	LEU	A	112	53.219	22.658	−15.270	1.00	39.71	A
ATOM	899	CD1	LEU	A	112	51.982	23.547	−15.131	1.00	37.52	A
ATOM	900	CD2	LEU	A	112	54.529	23.407	−14.897	1.00	35.31	A
ATOM	901	C	LEU	A	112	53.676	19.245	−13.421	1.00	39.07	A
ATOM	902	O	LEU	A	112	54.352	19.315	−12.395	1.00	39.21	A
ATOM	903	N	GLU	A	113	52.681	18.383	−13.598	1.00	40.42	A
ATOM	904	CA	GLU	A	113	52.289	17.378	−12.613	1.00	40.49	A
ATOM	905	CB	GLU	A	113	50.971	16.727	−13.054	1.00	39.94	A
ATOM	906	CG	GLU	A	113	50.087	16.224	−11.931	1.00	42.39	A
ATOM	907	CD	GLU	A	113	50.738	15.146	−11.091	1.00	43.87	A
ATOM	908	OE1	GLU	A	113	50.944	15.381	−9.877	1.00	45.43	A
ATOM	909	OE2	GLU	A	113	51.047	14.069	−11.645	1.00	43.84	A
ATOM	910	C	GLU	A	113	53.392	16.319	−12.491	1.00	40.15	A
ATOM	911	O	GLU	A	113	53.760	15.914	−11.384	1.00	39.65	A
ATOM	912	N	GLY	A	114	53.913	15.884	−13.637	1.00	39.92	A
ATOM	913	CA	GLY	A	114	54.973	14.891	−13.658	1.00	39.76	A
ATOM	914	C	GLY	A	114	56.351	15.476	−13.362	1.00	39.98	A
ATOM	915	O	GLY	A	114	57.189	14.800	−12.772	1.00	38.97	A
ATOM	916	N	PHE	A	115	56.547	16.738	−13.745	1.00	39.24	A
ATOM	917	CA	PHE	A	115	57.819	17.407	−13.522	1.00	38.76	A
ATOM	918	CB	PHE	A	115	57.884	18.731	−14.267	1.00	37.99	A
ATOM	919	CG	PHE	A	115	59.235	19.361	−14.230	1.00	38.11	A
ATOM	920	CD1	PHE	A	115	59.457	20.514	−13.496	1.00	38.97	A
ATOM	921	CD2	PHE	A	115	60.301	18.769	−14.888	1.00	38.23	A
ATOM	922	CE1	PHE	A	115	60.729	21.068	−13.412	1.00	39.54	A
ATOM	923	CE2	PHE	A	115	61.579	19.311	−14.813	1.00	37.99	A
ATOM	924	CZ	PHE	A	115	61.794	20.462	−14.074	1.00	39.71	A
ATOM	925	C	PHE	A	115	58.154	17.645	−12.059	1.00	39.22	A
ATOM	926	O	PHE	A	115	59.126	17.096	−11.547	1.00	40.44	A
ATOM	927	N	PHE	A	116	57.358	18.460	−11.388	1.00	39.85	A
ATOM	928	CA	PHE	A	116	57.577	18.786	−9.978	1.00	40.68	A
ATOM	929	CB	PHE	A	116	56.789	20.042	−9.592	1.00	39.22	A
ATOM	930	CG	PHE	A	116	57.143	21.246	−10.404	1.00	37.35	A
ATOM	931	CD1	PHE	A	116	58.335	21.924	−10.179	1.00	37.47	A
ATOM	932	CD2	PHE	A	116	56.285	21.705	−11.397	1.00	37.45	A
ATOM	933	CE1	PHE	A	116	58.668	23.044	−10.930	1.00	36.62	A
ATOM	935	CE2	PHE	A	116	56.606	22.824	−12.155	1.00	36.50	A
ATOM	935	CZ	PHE	A	116	57.801	23.494	−11.920	1.00	36.88	A
ATOM	936	C	PHE	A	116	57.313	17.659	−8.966	1.00	41.90	A
ATOM	937	O	PHE	A	116	57.163	17.925	−7.770	1.00	42.64	A
ATOM	938	N	ALA	A	117	57.187	16.424	−9.451	1.00	41.70	A
ATOM	939	CA	ALA	A	117	56.986	15.263	−8.584	1.00	41.89	A
ATOM	940	CB	ALA	A	117	55.775	14.468	−9.006	1.00	41.09	A
ATOM	941	C	ALA	A	117	58.254	14.452	−8.771	1.00	42.58	A
ATOM	942	O	ALA	A	117	58.754	13.817	−7.843	1.00	42.60	A
ATOM	943	N	THR	A	118	58.775	14.510	−9.993	1.00	44.00	A
ATOM	944	CA	THR	A	118	60.016	13.838	−10.352	1.00	44.87	A
ATOM	945	CB	THR	A	118	60.158	13.685	−11.873	1.00	45.75	A
ATOM	946	OG1	THR	A	118	59.132	12.813	−12.360	1.00	47.91	A
ATOM	947	CG2	THR	A	118	61.521	13.103	−12.231	1.00	47.03	A
ATOM	948	C	THR	A	118	61.155	14.707	−9.841	1.00	43.79	A
ATOM	949	O	THR	A	118	62.169	14.202	−9.377	1.00	43.22	A
ATOM	950	N	LEU	A	119	60.970	16.020	−9.928	1.00	43.55	A
ATOM	951	CA	LEU	A	119	61.970	16.963	−9.460	1.00	43.92	A
ATOM	952	CB	LEU	A	119	61.580	18.398	−9.821	1.00	44.11	A
ATOM	953	CG	LEU	A	119	62.616	19.481	−9.496	1.00	44.08	A
ATOM	954	CD1	LEU	A	119	63.861	19.242	−10.321	1.00	45.02	A
ATOM	955	CD2	LEU	A	119	62.067	20.865	−9.780	1.00	44.39	A
ATOM	956	C	LEU	A	119	62.119	16.840	−7.949	1.00	44.44	A
ATOM	957	O	LEU	A	119	63.222	16.651	−7.456	1.00	45.27	A
ATOM	958	N	GLY	A	120	61.006	16.902	−7.222	1.00	43.91	A
ATOM	959	CA	GLY	A	120	61.058	16.812	−5.770	1.00	43.51	A
ATOM	960	C	GLY	A	120	61.509	15.470	−5.220	1.00	43.14	A
ATOM	961	O	GLY	A	120	62.075	15.400	−4.124	1.00	42.60	A
ATOM	962	N	GLY	A	121	61.220	14.405	−5.963	1.00	42.33	A
ATOM	963	CA	GLY	A	121	61.610	13.072	−5.542	1.00	42.84	A
ATOM	964	C	GLY	A	121	63.094	12.855	−5.733	1.00	42.59	A
ATOM	965	O	GLY	A	121	63.727	12.143	−4.956	1.00	42.51	A
ATOM	966	N	GLU	A	122	63.631	13.471	−6.786	1.00	43.17	A
ATOM	967	CA	GLU	A	122	65.054	13.415	−7.135	1.00	42.89	A
ATOM	968	CB	GLU	A	122	65.231	13.571	−8.649	1.00	43.42	A
ATOM	969	CG	GLU	A	122	64.575	12.480	−9.485	1.00	44.12	A
ATOM	970	CD	GLU	A	122	65.295	11.146	−9.412	1.00	46.25	A
ATOM	971	OE1	GLU	A	122	66.472	11.104	−8.988	1.00	45.99	A
ATOM	972	OE2	GLU	A	122	64.681	10.129	−9.798	1.00	47.00	A
ATOM	973	C	GLU	A	122	65.895	14.481	−6.387	1.00	42.37	A
ATOM	974	O	GLU	A	122	67.080	14.268	−6.138	1.00	42.61	A
ATOM	975	N	ILE	A	123	65.308	15.643	−6.084	1.00	41.53	A
ATOM	976	CA	ILE	A	123	66.013	16.684	−5.324	1.00	39.38	A
ATOM	977	CB	ILE	A	123	65.111	17.928	−5.028	1.00	39.04	A
ATOM	978	CG2	ILE	A	123	65.725	18.788	−3.941	1.00	38.49	A
ATOM	979	CG1	ILE	A	123	64.855	18.769	−6.283	1.00	37.46	A
ATOM	980	CD1	ILE	A	123	66.031	19.537	−6.783	1.00	37.06	A
ATOM	981	C	ILE	A	123	66.303	16.022	−3.980	1.00	40.19	A
ATOM	982	O	ILE	A	123	67.350	16.244	−3.379	1.00	40.05	A
ATOM	983	N	ALA	A	124	65.351	15.201	−3.528	1.00	40.59	A
ATOM	984	CA	ALA	A	124	65.454	14.480	−2.265	1.00	41.56	A
ATOM	985	CB	ALA	A	124	64.094	13.946	−1.857	1.00	41.40	A
ATOM	986	C	ALA	A	124	66.477	13.354	−2.325	1.00	42.51	A
ATOM	987	O	ALA	A	124	67.353	13.253	−1.464	1.00	43.06	A
ATOM	988	N	LEU	A	125	66.377	12.506	−3.358	1.00	42.91	A
ATOM	989	CA	LEU	A	125	67.288	11.365	−3.556	1.00	42.91	A
ATOM	990	CB	LEU	A	125	67.018	10.700	−4.915	1.00	42.56	A
ATOM	991	CG	LEU	A	125	67.337	9.219	−5.183	1.00	42.79	A
ATOM	992	CD1	LEU	A	125	67.796	9.078	−6.629	1.00	43.04	A
ATOM	993	CD2	LEU	A	125	68.381	8.642	−4.228	1.00	41.68	A
ATOM	994	C	LEU	A	125	68.763	11.771	−3.506	1.00	42.92	A
ATOM	995	O	LEU	A	125	69.556	11.177	−2.778	1.00	43.01	A
ATOM	996	N	TRP	A	126	69.121	12.763	−4.315	1.00	43.00	A
ATOM	997	CA	TRP	A	126	70.486	13.250	−4.393	1.00	42.68	A
ATOM	998	CB	TRP	A	126	70.637	14.144	−5.614	1.00	43.60	A
ATOM	999	CG	TRP	A	126	70.566	13.362	−6.879	1.00	45.80	A
ATOM	1000	CD2	TRP	A	126	71.590	12.521	−7.422	1.00	46.59	A
ATOM	1001	CE2	TRP	A	126	71.078	11.951	−8.610	1.00	47.47	A
ATOM	1002	CE3	TRP	A	126	72.890	12.191	−7.020	1.00	47.05	A
ATOM	1003	CD1	TRP	A	126	69.507	13.275	−7.736	1.00	47.93	A
ATOM	1004	NE1	TRP	A	126	69.805	12.428	−8.780	1.00	47.55	A
ATOM	1005	CZ2	TRP	A	126	71.820	11.069	−9.396	1.00	47.93	A
ATOM	1006	CZ3	TRP	A	126	73.626	11.317	−7.800	1.00	48.23	A
ATOM	1007	CH2	TRP	A	126	73.088	10.764	−8.978	1.00	49.28	A
ATOM	1008	C	TRP	A	126	70.938	13.957	−3.128	1.00	42.98	A
ATOM	1009	O	TRP	A	126	72.111	13.891	−2.759	1.00	41.57	A
ATOM	1010	N	SER	A	127	70.003	14.624	−2.457	1.00	43.61	A
ATOM	1011	CA	SER	A	127	70.318	15.307	−1.214	1.00	44.22	A
ATOM	1012	CB	SER	A	127	69.098	16.053	−0.684	1.00	42.67	A
ATOM	1013	OG	SER	A	127	68.883	17.245	−1.417	1.00	41.49	A
ATOM	1014	C	SER	A	127	70.810	14.266	−0.207	1.00	45.89	A
ATOM	1015	O	SER	A	127	71.751	14.519	0.553	1.00	46.53	A
ATOM	1016	N	LEU	A	128	70.197	13.082	−0.245	1.00	46.81	A
ATOM	1017	CA	LEU	A	128	70.574	11.967	0.626	1.00	48.00	A
ATOM	1018	CB	LEU	A	128	69.665	10.767	0.382	1.00	46.81	A
ATOM	1019	CG	LEU	A	128	68.258	10.847	0.950	1.00	46.18	A
ATOM	1020	CD1	LEU	A	128	67.507	9.580	0.597	1.00	46.62	A
ATOM	1021	CD2	LEU	A	128	68.335	11.019	2.454	1.00	46.13	A
ATOM	1022	C	LEU	A	128	72.021	11.533	0.390	1.00	49.70	A
ATOM	1023	O	LEU	A	128	72.674	11.019	1.298	1.00	49.91	A
ATOM	1024	N	VAL	A	129	72.495	11.694	−0.846	1.00	50.97	A
ATOM	1025	CA	VAL	A	129	73.866	11.338	−1.194	1.00	51.62	A
ATOM	1026	CB	VAL	A	129	74.058	11.182	−2.735	1.00	50.44	A
ATOM	1027	CG1	VAL	A	129	75.419	10.594	−3.037	1.00	49.05	A
ATOM	1028	CG2	VAL	A	129	72.978	10.289	−3.322	1.00	49.45	A
ATOM	1029	C	VAL	A	129	74.788	12.433	−0.628	1.00	52.92	A
ATOM	1030	O	VAL	A	129	75.797	12.126	0.016	1.00	55.01	A
ATOM	1031	N	VAL	A	130	74.418	13.701	−0.822	1.00	51.50	A
ATOM	1032	CA	VAL	A	130	75.207	14.817	−0.295	1.00	50.32	A
ATOM	1033	CB	VAL	A	130	74.590	16.175	−0.684	1.00	50.38	A
ATOM	1035	CG1	VAL	A	130	75.255	17.319	0.082	1.00	49.76	A
ATOM	1035	CG2	VAL	A	130	74.725	16.388	−2.173	1.00	50.09	A
ATOM	1036	C	VAL	A	130	75.261	14.706	1.228	1.00	50.42	A
ATOM	1037	O	VAL	A	130	76.241	15.107	1.857	1.00	50.44	A
ATOM	1038	N	LEU	A	131	74.193	14.166	1.810	1.00	49.76	A
ATOM	1039	CA	LEU	A	131	74.121	13.981	3.249	1.00	50.08	A
ATOM	1040	CB	LEU	A	131	72.667	13.949	3.724	1.00	49.85	A
ATOM	1041	CG	LEU	A	131	71.911	15.286	3.779	1.00	48.67	A
ATOM	1042	CD1	LEU	A	131	70.462	15.024	4.144	1.00	47.91	A
ATOM	1043	CD2	LEU	A	131	72.541	16.225	4.796	1.00	47.18	A
ATOM	1044	C	LEU	A	131	74.862	12.711	3.656	1.00	50.12	A
ATOM	1045	O	LEU	A	131	75.578	12.709	4.652	1.00	51.40	A
ATOM	1046	N	ALA	A	132	74.707	11.645	2.876	1.00	49.33	A
ATOM	1047	CA	ALA	A	132	75.400	10.390	3.151	1.00	49.78	A
ATOM	1048	CB	ALA	A	132	75.027	9.335	2.117	1.00	49.70	A
ATOM	1049	C	ALA	A	132	76.904	10.668	3.108	1.00	51.00	A
ATOM	1050	O	ALA	A	132	77.673	10.103	3.891	1.00	51.90	A
ATOM	1051	N	ILE	A	133	77.305	11.550	2.191	1.00	50.84	A
ATOM	1052	CA	ILE	A	133	78.700	11.965	2.038	1.00	50.70	A
ATOM	1053	CB	ILE	A	133	78.876	12.906	0.808	1.00	49.05	A
ATOM	1054	CG2	ILE	A	133	80.209	13.656	0.878	1.00	46.10	A
ATOM	1055	CG1	ILE	A	133	78.752	12.110	−0.492	1.00	48.51	A
ATOM	1056	CD1	ILE	A	133	78.777	12.975	−1.750	1.00	48.56	A
ATOM	1057	C	ILE	A	133	79.095	12.738	3.292	1.00	51.38	A
ATOM	1058	O	ILE	A	133	79.979	12.328	4.043	1.00	49.06	A
ATOM	1059	N	GLU	A	135	78.375	13.830	3.527	1.00	54.22	A
ATOM	1060	CA	GLU	A	135	78.598	14.711	4.662	1.00	57.63	A
ATOM	1061	CB	GLU	A	135	77.478	15.758	4.731	1.00	59.13	A
ATOM	1062	CG	GLU	A	135	77.712	16.912	5.708	1.00	60.64	A
ATOM	1063	CD	GLU	A	135	77.230	16.626	7.127	1.00	61.53	A
ATOM	1064	OE1	GLU	A	135	76.365	15.738	7.308	1.00	60.11	A
ATOM	1065	OE2	GLU	A	135	77.711	17.305	8.063	1.00	62.89	A
ATOM	1066	C	GLU	A	135	78.710	13.935	5.970	1.00	59.04	A
ATOM	1067	O	GLU	A	135	79.322	14.405	6.927	1.00	59.58	A
ATOM	1068	N	ARG	A	135	78.135	12.741	6.014	1.00	60.21	A
ATOM	1069	CA	ARG	A	135	78.235	11.945	7.220	1.00	62.70	A
ATOM	1070	CB	ARG	A	135	77.147	10.870	7.277	1.00	61.49	A
ATOM	1071	CG	ARG	A	135	75.731	11.414	7.305	1.00	59.73	A
ATOM	1072	CD	ARG	A	135	75.633	12.731	8.079	1.00	58.36	A
ATOM	1073	NE	ARG	A	135	75.896	12.583	9.507	1.00	55.30	A
ATOM	1074	CZ	ARG	A	135	76.202	13.586	10.325	1.00	53.79	A
ATOM	1075	NH1	ARG	A	135	76.293	14.829	9.870	1.00	50.17	A
ATOM	1076	NH2	ARG	A	135	76.399	13.354	11.611	1.00	53.57	A
ATOM	1077	C	ARG	A	135	79.615	11.314	7.308	1.00	65.61	A
ATOM	1078	O	ARG	A	135	80.272	11.410	8.339	1.00	66.32	A
ATOM	1079	N	TYR	A	136	80.078	10.729	6.207	1.00	68.73	A
ATOM	1080	CA	TYR	A	136	81.387	10.076	6.177	1.00	72.57	A
ATOM	1081	CB	TYR	A	136	81.673	9.516	4.777	1.00	73.41	A
ATOM	1082	CG	TYR	A	136	82.752	8.450	4.747	1.00	75.00	A
ATOM	1083	CD1	TYR	A	136	82.570	7.237	5.411	1.00	77.20	A
ATOM	1084	CE1	TYR	A	136	83.555	6.244	5.392	1.00	78.60	A
ATOM	1085	CD2	TYR	A	136	83.952	8.649	4.057	1.00	75.08	A
ATOM	1086	CE2	TYR	A	136	84.947	7.660	4.032	1.00	76.27	A
ATOM	1087	CZ	TYR	A	136	84.739	6.458	4.704	1.00	77.65	A
ATOM	1088	OH	TYR	A	136	85.695	5.463	4.700	1.00	77.25	A
ATOM	1089	C	TYR	A	136	82.529	11.003	6.610	1.00	74.52	A
ATOM	1090	O	TYR	A	136	83.316	10.657	7.500	1.00	74.04	A
ATOM	1091	N	VAL	A	137	82.594	12.181	5.989	1.00	77.10	A
ATOM	1092	CA	VAL	A	137	83.635	13.178	6.272	1.00	79.78	A
ATOM	1093	CB	VAL	A	137	83.529	14.399	5.298	1.00	79.12	A
ATOM	1094	CG1	VAL	A	137	84.559	15.471	5.640	1.00	78.80	A
ATOM	1095	CG2	VAL	A	137	83.730	13.941	3.860	1.00	78.73	A
ATOM	1096	C	VAL	A	137	83.623	13.649	7.730	1.00	81.54	A
ATOM	1097	O	VAL	A	137	84.626	14.161	8.239	1.00	82.35	A
ATOM	1098	N	VAL	A	138	82.495	13.456	8.406	1.00	83.08	A
ATOM	1099	CA	VAL	A	138	82.376	13.849	9.802	1.00	84.53	A
ATOM	1100	CB	VAL	A	138	81.020	14.529	10.069	1.00	83.25	A
ATOM	1101	CG1	VAL	A	138	80.888	14.885	11.535	1.00	83.68	A
ATOM	1102	CG2	VAL	A	138	80.896	15.784	9.216	1.00	81.53	A
ATOM	1103	C	VAL	A	138	82.587	12.644	10.731	1.00	86.63	A
ATOM	1104	O	VAL	A	138	83.330	12.727	11.711	1.00	86.47	A
ATOM	1105	N	VAL	A	139	81.968	11.515	10.394	1.00	89.20	A
ATOM	1106	CA	VAL	A	139	82.096	10.296	11.191	1.00	91.64	A
ATOM	1107	CB	VAL	A	139	80.761	9.496	11.217	1.00	91.28	A
ATOM	1108	CG1	VAL	A	139	80.757	8.500	12.368	1.00	91.26	A
ATOM	1109	CG2	VAL	A	139	79.572	10.438	11.338	1.00	91.10	A
ATOM	1110	C	VAL	A	139	83.239	9.423	10.644	1.00	94.09	A
ATOM	1111	O	VAL	A	139	84.199	9.952	10.081	1.00	93.35	A
ATOM	1112	N	CYS	A	140	83.106	8.101	10.805	1.00	97.60	A
ATOM	1113	CA	CYS	A	140	84.073	7.071	10.386	1.00	100.89	A
ATOM	1114	CB	CYS	A	140	83.714	6.465	9.024	1.00	98.92	A
ATOM	1115	SG	CYS	A	140	84.604	4.917	8.676	1.00	95.56	A
ATOM	1116	C	CYS	A	140	85.535	7.501	10.396	1.00	104.29	A
ATOM	1117	O	CYS	A	140	86.335	7.003	11.199	1.00	105.15	A
ATOM	1118	N	LYS	A	141	85.879	8.395	9.471	1.00	107.06	A
ATOM	1119	CA	LYS	A	141	87.228	8.930	9.359	1.00	109.52	A
ATOM	1120	CB	LYS	A	141	88.193	7.842	8.847	1.00	109.22	A
ATOM	1121	CG	LYS	A	141	89.610	7.898	9.432	1.00	108.39	A
ATOM	1122	CD	LYS	A	141	89.648	7.431	10.888	1.00	107.93	A
ATOM	1123	CE	LYS	A	141	91.077	7.400	11.435	1.00	107.77	A
ATOM	1124	NZ	LYS	A	141	91.151	6.961	12.865	1.00	106.81	A
ATOM	1125	C	LYS	A	141	87.172	10.087	8.359	1.00	111.46	A
ATOM	1126	O	LYS	A	141	86.826	9.886	7.181	1.00	111.36	A
ATOM	1127	N	PRO	A	142	87.413	11.327	8.820	1.00	113.63	A
ATOM	1128	CD	PRO	A	142	87.485	11.691	10.247	1.00	113.92	A
ATOM	1129	CA	PRO	A	142	87.403	12.535	7.977	1.00	115.39	A
ATOM	1130	CB	PRO	A	142	87.686	13.652	8.984	1.00	114.68	A
ATOM	1131	CG	PRO	A	142	87.042	13.137	10.231	1.00	114.39	A
ATOM	1132	C	PRO	A	142	88.481	12.483	6.883	1.00	116.90	A
ATOM	1133	O	PRO	A	142	89.328	11.586	6.879	1.00	116.95	A
ATOM	1135	N	MET	A	143	88.451	13.445	5.962	1.00	118.42	A
ATOM	1135	CA	MET	A	143	89.425	13.482	4.874	1.00	119.92	A
ATOM	1136	CB	MET	A	143	89.073	14.586	3.873	1.00	119.73	A
ATOM	1137	CG	MET	A	143	89.795	14.461	2.540	1.00	119.65	A
ATOM	1138	SD	MET	A	143	89.592	15.924	1.522	1.00	120.49	A
ATOM	1139	CE	MET	A	143	87.879	15.761	1.023	1.00	119.00	A
ATOM	1140	C	MET	A	143	90.835	13.691	5.430	1.00	121.20	A
ATOM	1141	O	MET	A	143	91.448	12.750	5.944	1.00	121.07	A
ATOM	1142	N	SER	A	144	91.352	14.913	5.303	1.00	122.66	A
ATOM	1143	CA	SER	A	144	92.681	15.239	5.815	1.00	123.47	A
ATOM	1144	CB	SER	A	144	93.375	16.300	4.939	1.00	123.07	A
ATOM	1145	OG	SER	A	144	92.584	17.466	4.772	1.00	122.96	A
ATOM	1146	C	SER	A	144	92.545	15.710	7.263	1.00	123.81	A
ATOM	1147	O	SER	A	144	93.141	15.120	8.170	1.00	123.93	A
ATOM	1148	N	ASN	A	145	91.709	16.730	7.470	1.00	123.89	A
ATOM	1149	CA	ASN	A	145	91.450	17.304	8.794	1.00	123.78	A
ATOM	1150	CB	ASN	A	145	92.773	17.579	9.524	1.00	123.35	A
ATOM	1151	CG	ASN	A	145	92.608	17.677	11.027	1.00	122.86	A
ATOM	1152	OD1	ASN	A	145	93.166	16.873	11.775	1.00	122.86	A
ATOM	1153	ND2	ASN	A	145	91.850	18.670	11.479	1.00	122.53	A
ATOM	1154	C	ASN	A	145	90.656	18.612	8.656	1.00	123.93	A
ATOM	1155	O	ASN	A	145	91.176	19.691	8.948	1.00	124.33	A
ATOM	1156	N	PHE	A	146	89.396	18.519	8.229	1.00	123.85	A
ATOM	1157	CA	PHE	A	146	88.571	19.718	8.057	1.00	122.90	A
ATOM	1158	CB	PHE	A	146	88.819	20.352	6.665	1.00	123.61	A
ATOM	1159	CG	PHE	A	146	87.927	19.797	5.565	1.00	123.94	A
ATOM	1160	CD1	PHE	A	146	87.124	20.658	4.820	1.00	123.94	A
ATOM	1161	CD2	PHE	A	146	87.881	18.432	5.282	1.00	124.13	A
ATOM	1162	CE1	PHE	A	146	86.291	20.171	3.814	1.00	123.73	A
ATOM	1163	CE2	PHE	A	146	87.049	17.937	4.277	1.00	123.97	A
ATOM	1164	CZ	PHE	A	146	86.253	18.809	3.543	1.00	123.70	A
ATOM	1165	C	PHE	A	146	87.065	19.524	8.277	1.00	121.75	A
ATOM	1166	O	PHE	A	146	86.509	18.454	8.003	1.00	121.89	A
ATOM	1167	N	ARG	A	147	86.424	20.564	8.806	1.00	119.67	A
ATOM	1168	CA	ARG	A	147	84.982	20.551	9.022	1.00	117.46	A
ATOM	1169	CB	ARG	A	147	84.587	21.407	10.231	1.00	119.05	A
ATOM	1170	CG	ARG	A	147	85.185	21.006	11.569	1.00	120.97	A
ATOM	1171	CD	ARG	A	147	84.505	21.802	12.675	1.00	122.99	A
ATOM	1172	NE	ARG	A	147	85.294	21.880	13.903	1.00	125.46	A
ATOM	1173	CZ	ARG	A	147	85.157	22.833	14.825	1.00	126.61	A
ATOM	1174	NH1	ARG	A	147	84.255	23.797	14.666	1.00	126.85	A
ATOM	1175	NH2	ARG	A	147	85.939	22.840	15.899	1.00	127.09	A
ATOM	1176	C	ARG	A	147	84.379	21.176	7.766	1.00	114.90	A
ATOM	1177	O	ARG	A	147	85.062	21.916	7.052	1.00	114.32	A
ATOM	1178	N	PHE	A	148	83.112	20.875	7.488	1.00	112.13	A
ATOM	1179	CA	PHE	A	148	82.436	21.437	6.316	1.00	108.72	A
ATOM	1180	CB	PHE	A	148	81.104	20.722	6.039	1.00	106.72	A
ATOM	1181	CG	PHE	A	148	81.238	19.473	5.215	1.00	104.53	A
ATOM	1182	CD1	PHE	A	148	81.301	19.544	3.832	1.00	103.69	A
ATOM	1183	CD2	PHE	A	148	81.297	18.225	5.821	1.00	104.10	A
ATOM	1184	CE1	PHE	A	148	81.424	18.389	3.064	1.00	103.27	A
ATOM	1185	CE2	PHE	A	148	81.420	17.068	5.058	1.00	103.21	A
ATOM	1186	CZ	PHE	A	148	81.483	17.151	3.679	1.00	102.60	A
ATOM	1187	C	PHE	A	148	82.183	22.931	6.500	1.00	106.83	A
ATOM	1188	O	PHE	A	148	81.760	23.380	7.575	1.00	107.22	A
ATOM	1189	N	GLY	A	149	82.498	23.700	5.464	1.00	103.74	A
ATOM	1190	CA	GLY	A	149	82.281	25.131	5.512	1.00	99.98	A
ATOM	1191	C	GLY	A	149	80.896	25.410	4.977	1.00	97.19	A
ATOM	1192	O	GLY	A	149	80.312	24.565	4.298	1.00	96.60	A
ATOM	1193	N	GLU	A	150	80.363	26.584	5.292	1.00	95.09	A
ATOM	1194	CA	GLU	A	150	79.033	26.973	4.831	1.00	93.26	A
ATOM	1195	CB	GLU	A	150	78.710	28.396	5.320	1.00	93.56	A
ATOM	1196	CG	GLU	A	150	77.245	28.825	5.161	1.00	92.88	A
ATOM	1197	CD	GLU	A	150	76.961	30.236	5.678	1.00	92.63	A
ATOM	1198	OE1	GLU	A	150	75.793	30.686	5.579	1.00	92.03	A
ATOM	1199	OE2	GLU	A	150	77.899	30.897	6.178	1.00	92.40	A
ATOM	1200	C	GLU	A	150	79.005	26.904	3.302	1.00	91.57	A
ATOM	1201	O	GLU	A	150	77.973	26.632	2.692	1.00	91.98	A
ATOM	1202	N	ASN	A	151	80.173	27.097	2.702	1.00	89.63	A
ATOM	1203	CA	ASN	A	151	80.339	27.068	1.255	1.00	87.71	A
ATOM	1204	CB	ASN	A	151	81.735	27.607	0.879	1.00	88.95	A
ATOM	1205	CG	ASN	A	151	82.866	26.993	1.717	1.00	89.12	A
ATOM	1206	OD1	ASN	A	151	83.816	26.433	1.171	1.00	89.31	A
ATOM	1207	ND2	ASN	A	151	82.782	27.131	3.040	1.00	89.04	A
ATOM	1208	C	ASN	A	151	80.112	25.678	0.659	1.00	85.56	A
ATOM	1209	O	ASN	A	151	79.412	25.527	−0.357	1.00	83.88	A
ATOM	1210	N	HIS	A	152	80.690	24.671	1.312	1.00	84.19	A
ATOM	1211	CA	HIS	A	152	80.589	23.272	0.896	1.00	82.65	A
ATOM	1212	CB	HIS	A	152	81.307	22.371	1.909	1.00	84.90	A
ATOM	1213	CG	HIS	A	152	82.739	22.742	2.157	1.00	86.92	A
ATOM	1214	CD2	HIS	A	152	83.893	22.112	1.830	1.00	87.50	A
ATOM	1215	ND1	HIS	A	152	83.106	23.873	2.854	1.00	87.96	A
ATOM	1216	CE1	HIS	A	152	84.424	23.922	2.948	1.00	88.79	A
ATOM	1217	NE2	HIS	A	152	84.925	22.865	2.335	1.00	88.06	A
ATOM	1218	C	HIS	A	152	79.135	22.818	0.779	1.00	80.50	A
ATOM	1219	O	HIS	A	152	78.801	21.980	−0.059	1.00	79.40	A
ATOM	1220	N	ALA	A	153	78.282	23.378	1.636	1.00	77.90	A
ATOM	1221	CA	ALA	A	153	76.862	23.057	1.669	1.00	74.72	A
ATOM	1222	CB	ALA	A	153	76.220	23.683	2.893	1.00	73.68	A
ATOM	1223	C	ALA	A	153	76.115	23.475	0.402	1.00	72.80	A
ATOM	1224	O	ALA	A	153	75.218	22.762	−0.052	1.00	73.35	A
ATOM	1225	N	ILE	A	154	76.498	24.608	−0.182	1.00	69.95	A
ATOM	1226	CA	ILE	A	154	75.839	25.098	−1.393	1.00	68.06	A
ATOM	1227	CB	ILE	A	154	76.064	26.603	−1.580	1.00	67.16	A
ATOM	1228	CG2	ILE	A	154	75.116	27.143	−2.635	1.00	66.16	A
ATOM	1229	CG1	ILE	A	154	75.780	27.321	−0.263	1.00	66.81	A
ATOM	1230	CD1	ILE	A	154	75.932	28.811	−0.325	1.00	67.23	A
ATOM	1231	C	ILE	A	154	76.240	24.335	−2.661	1.00	67.09	A
ATOM	1232	O	ILE	A	154	75.600	24.459	−3.709	1.00	66.43	A
ATOM	1233	N	MET	A	155	77.297	23.541	−2.559	1.00	66.35	A
ATOM	1235	CA	MET	A	155	77.747	22.736	−3.685	1.00	65.89	A
ATOM	1235	CB	MET	A	155	79.163	22.211	−3.444	1.00	69.85	A
ATOM	1236	CG	MET	A	155	80.082	22.358	−4.645	1.00	73.68	A
ATOM	1237	SD	MET	A	155	80.377	24.104	−5.041	1.00	78.00	A
ATOM	1238	CE	MET	A	155	79.062	24.440	−6.283	1.00	78.49	A
ATOM	1239	C	MET	A	155	76.784	21.565	−3.807	1.00	63.00	A
ATOM	1240	O	MET	A	155	76.248	21.295	−4.877	1.00	62.83	A
ATOM	1241	N	GLY	A	156	76.563	20.892	−2.682	1.00	60.05	A
ATOM	1242	CA	GLY	A	156	75.654	19.765	−2.633	1.00	55.80	A
ATOM	1243	C	GLY	A	156	74.246	20.183	−2.992	1.00	53.03	A
ATOM	1244	O	GLY	A	156	73.487	19.376	−3.509	1.00	53.78	A
ATOM	1245	N	VAL	A	157	73.895	21.436	−2.709	1.00	49.41	A
ATOM	1246	CA	VAL	A	157	72.577	21.956	−3.038	1.00	46.20	A
ATOM	1247	CB	VAL	A	157	72.272	23.259	−2.282	1.00	44.97	A
ATOM	1248	CG1	VAL	A	157	71.057	23.953	−2.886	1.00	43.89	A
ATOM	1249	CG2	VAL	A	157	72.019	22.958	−0.821	1.00	43.17	A
ATOM	1250	C	VAL	A	157	72.497	22.211	−4.535	1.00	45.95	A
ATOM	1251	O	VAL	A	157	71.501	21.877	−5.167	1.00	46.38	A
ATOM	1252	N	ALA	A	158	73.541	22.817	−5.092	1.00	46.55	A
ATOM	1253	CA	ALA	A	158	73.586	23.101	−6.528	1.00	47.45	A
ATOM	1254	CB	ALA	A	158	74.813	23.947	−6.863	1.00	47.38	A
ATOM	1255	C	ALA	A	158	73.629	21.775	−7.285	1.00	47.57	A
ATOM	1256	O	ALA	A	158	72.978	21.614	−8.312	1.00	45.76	A
ATOM	1257	N	PHE	A	159	74.382	20.831	−6.723	1.00	49.36	A
ATOM	1258	CA	PHE	A	159	74.563	19.474	−7.242	1.00	49.96	A
ATOM	1259	CB	PHE	A	159	75.517	18.708	−6.309	1.00	50.63	A
ATOM	1260	CG	PHE	A	159	75.595	17.219	−6.565	1.00	51.73	A
ATOM	1261	CD1	PHE	A	159	76.404	16.708	−7.579	1.00	52.40	A
ATOM	1262	CD2	PHE	A	159	74.924	16.321	−5.735	1.00	51.51	A
ATOM	1263	CE1	PHE	A	159	76.551	15.324	−7.756	1.00	51.64	A
ATOM	1264	CE2	PHE	A	159	75.067	14.939	−5.906	1.00	50.81	A
ATOM	1265	CZ	PHE	A	159	75.884	14.441	−6.917	1.00	50.12	A
ATOM	1266	C	PHE	A	159	73.219	18.751	−7.335	1.00	49.29	A
ATOM	1267	O	PHE	A	159	72.845	18.273	−8.403	1.00	50.35	A
ATOM	1268	N	THR	A	160	72.497	18.674	−6.218	1.00	47.51	A
ATOM	1269	CA	THR	A	160	71.199	18.012	−6.209	1.00	45.74	A
ATOM	1270	CB	THR	A	160	70.520	18.068	−4.844	1.00	44.28	A
ATOM	1271	OG1	THR	A	160	70.187	19.426	−4.523	1.00	42.68	A
ATOM	1272	CG2	THR	A	160	71.411	17.459	−3.785	1.00	41.22	A
ATOM	1273	C	THR	A	160	70.255	18.642	−7.219	1.00	46.36	A
ATOM	1274	O	THR	A	160	69.457	17.943	−7.824	1.00	46.97	A
ATOM	1275	N	TRP	A	161	70.330	19.959	−7.385	1.00	46.89	A
ATOM	1276	CA	TRP	A	161	69.476	20.638	−8.350	1.00	47.72	A
ATOM	1277	CB	TRP	A	161	69.479	22.147	−8.132	1.00	49.14	A
ATOM	1278	CG	TRP	A	161	68.239	22.590	−7.472	1.00	51.73	A
ATOM	1279	CD2	TRP	A	161	67.023	23.012	−8.112	1.00	53.47	A
ATOM	1280	CE2	TRP	A	161	66.078	23.254	−7.094	1.00	53.26	A
ATOM	1281	CE3	TRP	A	161	66.642	23.206	−9.448	1.00	55.53	A
ATOM	1282	CD1	TRP	A	161	67.992	22.602	−6.136	1.00	51.81	A
ATOM	1283	NE1	TRP	A	161	66.695	22.996	−5.898	1.00	53.29	A
ATOM	1284	CZ2	TRP	A	161	64.768	23.681	−7.365	1.00	53.82	A
ATOM	1285	CZ3	TRP	A	161	65.332	23.635	−9.720	1.00	55.83	A
ATOM	1286	CH2	TRP	A	161	64.416	23.866	−8.680	1.00	54.71	A
ATOM	1287	C	TRP	A	161	69.862	20.319	−9.783	1.00	47.65	A
ATOM	1288	O	TRP	A	161	69.001	20.227	−10.654	1.00	47.78	A
ATOM	1289	N	VAL	A	162	71.157	20.145	−10.023	1.00	47.02	A
ATOM	1290	CA	VAL	A	162	71.651	19.830	−11.357	1.00	47.22	A
ATOM	1291	CB	VAL	A	162	73.193	20.098	−11.458	1.00	47.42	A
ATOM	1292	CG1	VAL	A	162	73.730	19.737	−12.837	1.00	47.67	A
ATOM	1293	CG2	VAL	A	162	73.486	21.560	−11.177	1.00	47.04	A
ATOM	1294	C	VAL	A	162	71.309	18.368	−11.686	1.00	46.80	A
ATOM	1295	O	VAL	A	162	70.728	18.073	−12.732	1.00	46.36	A
ATOM	1296	N	MET	A	163	71.614	17.474	−10.753	1.00	46.72	A
ATOM	1297	CA	MET	A	163	71.358	16.043	−10.912	1.00	47.40	A
ATOM	1298	CB	MET	A	163	72.091	15.271	−9.820	1.00	49.03	A
ATOM	1299	CG	MET	A	163	73.599	15.272	−9.975	1.00	51.04	A
ATOM	1300	SD	MET	A	163	74.118	14.209	−11.327	1.00	51.92	A
ATOM	1301	CE	MET	A	163	74.167	15.362	−12.709	1.00	52.61	A
ATOM	1302	C	MET	A	163	69.883	15.631	−10.937	1.00	47.21	A
ATOM	1303	O	MET	A	163	69.547	14.576	−11.465	1.00	46.37	A
ATOM	1304	N	ALA	A	164	69.017	16.440	−10.331	1.00	47.66	A
ATOM	1305	CA	ALA	A	164	67.582	16.161	−10.301	1.00	47.42	A
ATOM	1306	CB	ALA	A	164	66.943	16.763	−9.068	1.00	47.89	A
ATOM	1307	C	ALA	A	164	66.941	16.733	−11.548	1.00	47.43	A
ATOM	1308	O	ALA	A	164	65.900	16.259	−11.997	1.00	48.11	A
ATOM	1309	N	LEU	A	165	67.544	17.797	−12.065	1.00	47.64	A
ATOM	1310	CA	LEU	A	165	67.072	18.435	−13.285	1.00	48.45	A
ATOM	1311	CB	LEU	A	165	67.616	19.861	−13.383	1.00	48.08	A
ATOM	1312	CG	LEU	A	165	66.815	20.977	−12.716	1.00	47.09	A
ATOM	1313	CD1	LEU	A	165	67.677	22.215	−12.544	1.00	45.65	A
ATOM	1314	CD2	LEU	A	165	65.589	21.281	−13.562	1.00	46.66	A
ATOM	1315	C	LEU	A	165	67.535	17.603	−14.488	1.00	49.77	A
ATOM	1316	O	LEU	A	165	66.941	17.684	−15.565	1.00	49.98	A
ATOM	1317	N	ALA	A	166	68.597	16.811	−14.296	1.00	50.60	A
ATOM	1318	CA	ALA	A	166	69.147	15.937	−15.351	1.00	50.48	A
ATOM	1319	CB	ALA	A	166	70.588	15.558	−15.004	1.00	48.63	A
ATOM	1320	C	ALA	A	166	68.282	14.672	−15.517	1.00	51.04	A
ATOM	1321	O	ALA	A	166	68.406	13.937	−16.506	1.00	51.57	A
ATOM	1322	N	CYS	A	167	67.392	14.444	−14.553	1.00	50.58	A
ATOM	1323	CA	CYS	A	167	66.486	13.306	−14.565	1.00	49.49	A
ATOM	1324	CB	CYS	A	167	66.518	12.603	−13.209	1.00	50.50	A
ATOM	1325	SG	CYS	A	167	65.361	11.222	−13.027	1.00	52.92	A
ATOM	1326	C	CYS	A	167	65.061	13.757	−14.844	1.00	48.44	A
ATOM	1327	O	CYS	A	167	64.207	12.945	−15.195	1.00	49.64	A
ATOM	1328	N	ALA	A	168	64.798	15.047	−14.677	1.00	45.73	A
ATOM	1329	CA	ALA	A	168	63.457	15.559	−14.885	1.00	44.39	A
ATOM	1330	CB	ALA	A	168	62.997	16.301	−13.651	1.00	43.13	A
ATOM	1331	C	ALA	A	168	63.286	16.431	−16.121	1.00	44.36	A
ATOM	1332	O	ALA	A	168	62.176	16.570	−16.633	1.00	45.08	A
ATOM	1333	N	ALA	A	169	64.379	16.998	−16.618	1.00	43.75	A
ATOM	1335	CA	ALA	A	169	64.314	17.874	−17.788	1.00	42.27	A
ATOM	1335	CB	ALA	A	169	65.498	18.820	−17.800	1.00	42.09	A
ATOM	1336	C	ALA	A	169	64.149	17.196	−19.154	1.00	40.36	A
ATOM	1337	O	ALA	A	169	63.366	17.656	−19.981	1.00	40.15	A
ATOM	1338	N	PRO	A	170	64.882	16.103	−19.407	1.00	38.56	A
ATOM	1339	CD	PRO	A	170	65.912	15.485	−18.550	1.00	37.33	A
ATOM	1350	CA	PRO	A	170	64.778	15.401	−20.689	1.00	38.83	A
ATOM	1351	CB	PRO	A	170	65.564	14.125	−20.431	1.00	38.32	A
ATON	1352	CG	PRO	A	170	66.647	14.602	−19.506	1.00	37.93	A
ATOM	1353	C	PRO	A	170	63.360	15.115	−21.210	1.00	40.49	A
ATOM	1354	O	PRO	A	170	63.087	15.315	−22.388	1.00	40.60	A
ATOM	1355	N	PRO	A	171	62.443	14.630	−20.354	1.00	42.59	A
ATOM	1356	CD	PRO	A	171	62.635	14.120	−18.987	1.00	43.82	A
ATOM	1357	CA	PRO	A	171	61.075	14.353	−20.806	1.00	44.72	A
ATOM	1358	CB	PRO	A	171	60.435	13.722	−19.569	1.00	43.38	A
ATOM	1359	CG	PRO	A	171	61.566	13.072	−18.898	1.00	43.80	A
ATOM	1350	C	PRO	A	171	60.288	15.574	−21.271	1.00	47.48	A
ATOM	1351	O	PRO	A	171	59.106	15.467	−21.635	1.00	48.47	A
ATOM	1352	N	LEU	A	172	60.938	16.738	−21.230	1.00	49.40	A
ATOM	1353	CA	LEU	A	172	60.335	18.009	−21.657	1.00	50.86	A
ATOM	1354	CB	LEU	A	172	60.526	19.086	−20.579	1.00	51.11	A
ATOM	1355	CG	LEU	A	172	59.939	18.892	−19.183	1.00	51.20	A
ATOM	1356	CD1	LEU	A	172	60.412	20.015	−18.288	1.00	51.60	A
ATOM	1357	CD2	LEU	A	172	58.427	18.868	−19.243	1.00	51.26	A
ATOM	1358	C	LEU	A	172	61.017	18.490	−22.944	1.00	51.09	A
ATOM	1359	O	LEU	A	172	60.568	19.450	−23.588	1.00	50.50	A
ATOM	1360	N	VAL	A	173	62.110	17.812	−23.290	1.00	49.84	A
ATOM	1361	CA	VAL	A	173	62.915	18.139	−24.455	1.00	49.16	A
ATOM	1362	CB	VAL	A	173	64.401	18.302	−24.030	1.00	49.37	A
ATOM	1363	CG1	VAL	A	173	65.336	18.369	−25.244	1.00	51.16	A
ATOM	1364	CG2	VAL	A	173	64.544	19.557	−23.193	1.00	48.19	A
ATOM	1365	C	VAL	A	173	62.772	17.138	−25.609	1.00	49.03	A
ATOM	1366	O	VAL	A	173	63.001	17.490	−26.777	1.00	49.26	A
ATOM	1367	N	GLY	A	174	62.381	15.904	−25.291	1.00	47.76	A
ATOM	1368	CA	GLY	A	174	62.215	14.903	−26.329	1.00	45.26	A
ATOM	1369	C	GLY	A	174	62.789	13.551	−25.974	1.00	44.48	A
ATOM	1370	O	GLY	A	174	62.781	12.635	−26.802	1.00	44.57	A
ATOM	1371	N	TRP	A	175	63.360	13.447	−24.777	1.00	42.82	A
ATOM	1372	CA	TRP	A	175	63.916	12.184	−24.321	1.00	42.15	A
ATOM	1373	CB	TRP	A	175	65.268	12.386	−23.631	1.00	40.91	A
ATOM	1374	CG	TRP	A	175	66.054	11.110	−23.537	1.00	40.16	A
ATOM	1375	CD2	TRP	A	175	67.231	10.870	−22.755	1.00	39.77	A
ATOM	1376	CE2	TRP	A	175	67.604	9.527	−22.967	1.00	41.26	A
ATOM	1377	CE3	TRP	A	175	68.005	11.656	−21.896	1.00	39.85	A
ATOM	1378	CD1	TRP	A	175	65.774	9.936	−24.174	1.00	39.62	A
ATOM	1379	NE1	TRP	A	175	66.694	8.982	−23.838	1.00	40.81	A
ATOM	1380	CZ2	TRP	A	175	68.728	8.947	−22.356	1.00	40.79	A
ATOM	1381	CZ3	TRP	A	175	69.122	11.079	−21.280	1.00	40.90	A
ATOM	1382	CH2	TRP	A	175	69.469	9.738	−21.511	1.00	39.10	A
ATOM	1383	C	TRP	A	175	62.871	11.653	−23.352	1.00	42.38	A
ATOM	1384	O	TRP	A	175	62.701	12.203	−22.255	1.00	43.36	A
ATOM	1385	N	SER	A	176	62.177	10.589	−23.772	1.00	40.04	A
ATOM	1386	CA	SER	A	176	61.072	9.985	−23.011	1.00	38.31	A
ATOM	1387	CB	SER	A	176	61.500	9.469	−21.626	1.00	36.67	A
ATOM	1388	OG	SER	A	176	60.457	8.731	−20.994	1.00	32.03	A
ATOM	1389	C	SER	A	176	60.006	11.076	−22.880	1.00	37.83	A
ATOM	1390	O	SER	A	176	60.019	12.056	−23.640	1.00	38.73	A
ATOM	1391	N	ARG	A	177	59.101	10.935	−21.917	1.00	35.55	A
ATOM	1392	CA	ARG	A	177	58.055	11.935	−21.754	1.00	35.08	A
ATOM	1393	CB	ARG	A	177	57.199	12.031	−23.027	1.00	35.10	A
ATOM	1394	CG	ARG	A	177	56.591	10.712	−23.446	1.00	33.29	A
ATOM	1395	CD	ARG	A	177	55.620	10.859	−24.583	1.00	35.72	A
ATOM	1396	NE	ARG	A	177	54.989	9.576	−24.871	1.00	36.74	A
ATOM	1397	CZ	ARG	A	177	54.131	9.357	−25.862	1.00	39.51	A
ATOM	1398	NH1	ARG	A	177	53.779	10.357	−26.683	1.00	39.55	A
ATOM	1399	NH2	ARG	A	177	53.647	8.133	−26.052	1.00	39.43	A
ATOM	1400	C	ARG	A	177	57.158	11.642	−20.576	1.00	32.50	A
ATOM	1401	O	ARG	A	177	57.133	10.525	−20.061	1.00	32.06	A
ATOM	1402	N	TYR	A	178	56.435	12.670	−20.148	1.00	31.30	A
ATOM	1403	CA	TYR	A	178	55.513	12.544	−19.039	1.00	30.90	A
ATOM	1404	CB	TYR	A	178	55.405	13.862	−18.270	1.00	30.96	A
ATOM	1405	CG	TYR	A	178	56.649	14.181	−17.451	1.00	31.46	A
ATOM	1406	CD1	TYR	A	178	57.077	13.321	−16.441	1.00	32.31	A
ATOM	1407	CE1	TYR	A	178	58.240	13.570	−15.720	1.00	32.22	A
ATOM	1408	CD2	TYR	A	178	57.421	15.314	−17.714	1.00	31.39	A
ATOM	1409	CE2	TYR	A	178	58.590	15.573	−16.994	1.00	32.60	A
ATOM	1410	CZ	TYR	A	178	58.992	14.690	−16.000	1.00	32.97	A
ATOM	1411	OH	TYR	A	178	60.153	14.905	−15.294	1.00	32.41	A
ATOM	1412	C	TYR	A	178	54.188	12.101	−19.623	1.00	31.51	A
ATOM	1413	O	TYR	A	178	53.662	12.719	−20.550	1.00	31.31	A
ATOM	1414	N	ILE	A	179	53.692	10.984	−19.104	1.00	32.28	A
ATOM	1415	CA	ILE	A	179	52.455	10.373	−19.567	1.00	31.67	A
ATOM	1416	CB	ILE	A	179	52.805	9.072	−20.354	1.00	31.38	A
ATOM	1417	CG2	ILE	A	179	53.196	7.946	−19.382	1.00	31.92	A
ATOM	1418	CG1	ILE	A	179	51.672	8.659	−21.273	1.00	31.70	A
ATOM	1419	CD1	ILE	A	179	51.977	7.414	−22.075	1.00	31.95	A
ATOM	1420	C	ILE	A	179	51.577	10.083	−18.353	1.00	32.85	A
ATOM	1421	O	ILE	A	179	52.099	9.770	−17.269	1.00	33.92	A
ATOM	1422	N	PRO	A	180	50.238	10.241	−18.468	1.00	35.04	A
ATOM	1423	CD	PRO	A	180	49.488	10.772	−19.620	1.00	35.76	A
ATOM	1424	CA	PRO	A	180	49.318	9.988	−17.351	1.00	33.89	A
ATOM	1425	CB	PRO	A	180	47.956	10.361	−17.941	1.00	33.18	A
ATOM	1426	CG	PRO	A	180	48.288	11.382	−18.954	1.00	33.09	A
ATOM	1427	C	PRO	A	180	49.356	8.533	−16.888	1.00	33.44	A
ATOM	1428	O	PRO	A	180	49.413	7.615	−17.707	1.00	32.18	A
ATOM	1429	N	GLU	A	181	49.270	8.336	−15.573	1.00	32.79	A
ATOM	1430	CA	GLU	A	181	49.309	6.997	−15.000	1.00	32.85	A
ATOM	1431	CB	GLU	A	181	50.595	6.815	−14.185	1.00	31.95	A
ATOM	1432	CG	GLU	A	181	51.889	7.192	−14.883	1.00	31.11	A
ATOM	1433	CD	GLU	A	181	53.085	6.986	−13.985	1.00	31.85	A
ATOM	1435	OE1	GLU	A	181	53.351	7.850	−13.126	1.00	36.43	A
ATOM	1435	OE2	GLU	A	181	53.759	5.952	−14.116	1.00	30.75	A
ATOM	1436	C	GLU	A	181	48.115	6.670	−14.100	1.00	33.13	A
ATOM	1437	O	GLU	A	181	47.499	7.552	−13.500	1.00	32.83	A
ATOM	1438	N	GLY	A	182	47.821	5.382	−13.985	1.00	33.35	A
ATOM	1439	CA	GLY	A	182	46.738	4.945	−13.128	1.00	35.62	A
ATOM	1440	C	GLY	A	182	45.374	5.411	−13.568	1.00	36.98	A
ATOM	1441	O	GLY	A	182	44.971	5.143	−14.697	1.00	37.80	A
ATOM	1442	N	MET	A	183	44.655	6.083	−12.667	1.00	37.89	A
ATOM	1443	CA	MET	A	183	43.320	6.603	−12.971	1.00	38.95	A
ATOM	1444	CB	MET	A	183	42.591	6.994	−11.690	1.00	39.12	A
ATOM	1445	CG	MET	A	183	42.039	5.804	−10.946	1.00	38.93	A
ATOM	1446	SD	MET	A	183	41.432	6.230	−9.352	1.00	37.25	A
ATOM	1447	CE	MET	A	183	39.792	6.715	−9.728	1.00	38.52	A
ATOM	1448	C	MET	A	183	43.389	7.784	−13.923	1.00	39.25	A
ATOM	1449	O	MET	A	183	42.370	8.418	−14.222	1.00	37.95	A
ATOM	1450	N	GLN	A	184	44.615	8.035	−14.393	1.00	40.58	A
ATOM	1451	CA	GLN	A	184	44.992	9.089	−15.339	1.00	41.59	A
ATOM	1452	CB	GLN	A	184	44.141	9.002	−16.626	1.00	41.17	A
ATOM	1453	CG	GLN	A	184	44.049	7.601	−17.271	1.00	41.87	A
ATOM	1454	CD	GLN	A	184	45.392	7.015	−17.702	1.00	42.08	A
ATOM	1455	OE1	GLN	A	184	46.046	7.527	−18.608	1.00	42.56	A
ATOM	1456	NE2	GLN	A	184	45.788	5.918	−17.068	1.00	41.79	A
ATOM	1457	C	GLN	A	184	44.991	10.514	−14.767	1.00	41.75	A
ATOM	1458	O	GLN	A	184	44.767	11.475	−15.496	1.00	43.20	A
ATOM	1459	N	CYS	A	185	45.301	10.649	−13.478	1.00	42.12	A
ATOM	1460	CA	CYS	A	185	45.319	11.955	−12.815	1.00	40.96	A
ATOM	1461	CB	CYS	A	185	44.265	11.984	−11.724	1.00	40.54	A
ATOM	1462	SG	CYS	A	185	42.637	11.796	−12.442	1.00	38.22	A
ATOM	1463	C	CYS	A	185	46.684	12.355	−12.271	1.00	41.30	A
ATOM	1464	O	CYS	A	185	46.853	13.432	−11.682	1.00	40.82	A
ATOM	1465	N	SER	A	186	47.643	11.461	−12.497	1.00	40.66	A
ATOM	1466	CA	SER	A	186	49.039	11.615	−12.121	1.00	39.17	A
ATOM	1467	CB	SER	A	186	49.450	10.531	−11.119	1.00	38.90	A
ATOM	1468	OG	SER	A	186	50.854	10.307	−11.138	1.00	41.77	A
ATOM	1469	C	SER	A	186	49.801	11.426	−13.426	1.00	38.67	A
ATOM	1470	O	SER	A	186	49.301	10.798	−14.353	1.00	37.02	A
ATOM	1471	N	CYS	A	187	51.003	11.976	−13.502	1.00	39.71	A
ATOM	1472	CA	CYS	A	187	51.810	11.850	−14.701	1.00	40.37	A
ATOM	1473	C	CYS	A	187	53.242	11.491	−14.356	1.00	40.53	A
ATOM	1474	O	CYS	A	187	53.859	12.129	−13.512	1.00	42.25	A
ATOM	1475	CB	CYS	A	187	51.760	13.149	−15.517	1.00	41.63	A
ATOM	1476	SG	CYS	A	187	50.432	13.208	−16.775	1.00	44.40	A
ATOM	1477	N	GLY	A	188	53.757	10.452	−15.000	1.00	39.54	A
ATOM	1478	CA	GLY	A	188	55.121	10.037	−14.747	1.00	39.80	A
ATOM	1479	C	GLY	A	188	55.852	9.785	−16.041	1.00	40.57	A
ATOM	1480	O	GLY	A	188	55.376	10.176	−17.100	1.00	40.06	A
ATOM	1481	N	ILE	A	189	57.009	9.136	−15.957	1.00	42.24	A
ATOM	1482	CA	ILE	A	189	57.807	8.831	−17.141	1.00	44.75	A
ATOM	1483	CB	ILE	A	189	59.211	8.336	−16.750	1.00	44.19	A
ATOM	1484	CG2	ILE	A	189	60.023	8.002	−17.996	1.00	45.47	A
ATOM	1485	CG1	ILE	A	189	59.925	9.398	−15.908	1.00	43.12	A
ATOM	1486	CD1	ILE	A	189	60.185	10.692	−16.635	1.00	39.74	A
ATOM	1487	C	ILE	A	189	57.098	7.768	−17.975	1.00	47.04	A
ATOM	1488	O	ILE	A	189	56.319	6.977	−17.446	1.00	49.30	A
ATOM	1489	N	ASP	A	190	57.357	7.748	−19.277	1.00	48.68	A
ATOM	1490	CA	ASP	A	190	56.705	6.780	−20.143	1.00	49.33	A
ATOM	1491	CB	ASP	A	190	56.621	7.313	−21.572	1.00	50.38	A
ATOM	1492	CG	ASP	A	190	55.509	6.657	−22.372	1.00	52.84	A
ATOM	1493	OD1	ASP	A	190	55.077	5.546	−21.990	1.00	55.99	A
ATOM	1494	OD2	ASP	A	190	55.054	7.249	−23.378	1.00	52.41	A
ATOM	1495	C	ASP	A	190	57.369	5.407	−20.133	1.00	49.97	A
ATOM	1496	O	ASP	A	190	58.443	5.222	−20.718	1.00	50.44	A
ATOM	1497	N	TYR	A	191	56.717	4.456	−19.458	1.00	50.22	A
ATOM	1498	CA	TYR	A	191	57.197	3.068	−19.365	1.00	49.75	A
ATOM	1499	CB	TYR	A	191	57.219	2.549	−17.914	1.00	49.03	A
ATOM	1500	CG	TYR	A	191	57.353	3.578	−16.810	1.00	49.66	A
ATOM	1501	CD1	TYR	A	191	58.592	4.007	−16.365	1.00	49.00	A
ATOM	1502	CE1	TYR	A	191	58.710	4.916	−15.312	1.00	48.88	A
ATOM	1503	CD2	TYR	A	191	56.210	4.086	−16.174	1.00	49.91	A
ATOM	1504	CE2	TYR	A	191	56.319	4.992	−15.122	1.00	49.92	A
ATOM	1505	CZ	TYR	A	191	57.571	5.405	−14.695	1.00	49.91	A
ATOM	1506	OH	TYR	A	191	57.685	6.309	−13.660	1.00	50.22	A
ATOM	1507	C	TYR	A	191	56.218	2.180	−20.115	1.00	48.96	A
ATOM	1508	O	TYR	A	191	56.460	0.990	−20.298	1.00	47.51	A
ATOM	1509	N	TYR	A	192	55.108	2.780	−20.528	1.00	49.02	A
ATOM	1510	CA	TYR	A	192	54.027	2.079	−21.202	1.00	50.76	A
ATOM	1511	CB	TYR	A	192	52.717	2.828	−20.946	1.00	50.13	A
ATOM	1512	CG	TYR	A	192	52.457	3.113	−19.485	1.00	48.06	A
ATOM	1513	CD1	TYR	A	192	51.737	2.219	−18.703	1.00	46.82	A
ATOM	1514	CE1	TYR	A	192	51.528	2.454	−17.359	1.00	45.58	A
ATOM	1515	CD2	TYR	A	192	52.960	4.262	−18.878	1.00	47.60	A
ATOM	1516	CE2	TYR	A	192	52.757	4.505	−17.535	1.00	45.89	A
ATOM	1517	CZ	TYR	A	192	52.041	3.595	−16.782	1.00	45.58	A
ATOM	1518	OH	TYR	A	192	51.847	3.814	−15.443	1.00	46.91	A
ATOM	1519	C	TYR	A	192	54.160	1.798	−22.697	1.00	52.85	A
ATOM	1520	O	TYR	A	192	53.724	0.747	−23.176	1.00	53.88	A
ATOM	1521	N	THR	A	193	54.740	2.731	−23.441	1.00	54.04	A
ATOM	1522	CA	THR	A	193	54.865	2.559	−24.878	1.00	55.28	A
ATOM	1523	CB	THR	A	193	54.243	3.756	−25.603	1.00	55.77	A
ATOM	1524	OG1	THR	A	193	54.992	4.939	−25.301	1.00	54.30	A
ATOM	1525	CG2	THR	A	193	52.796	3.958	−25.137	1.00	56.17	A
ATOM	1526	C	THR	A	193	56.297	2.374	−25.353	1.00	57.68	A
ATOM	1527	O	THR	A	193	57.226	2.911	−24.740	1.00	57.04	A
ATOM	1528	N	PRO	A	194	56.495	1.588	−26.418	1.00	60.86	A
ATOM	1529	CD	PRO	A	194	55.466	0.900	−27.221	1.00	62.53	A
ATOM	1530	CA	PRO	A	194	57.836	1.339	−26.961	1.00	63.02	A
ATOM	1531	CB	PRO	A	194	57.576	0.282	−28.039	1.00	63.10	A
ATOM	1532	CG	PRO	A	194	56.195	0.636	−28.527	1.00	63.84	A
ATOM	1533	C	PRO	A	194	58.384	2.633	−27.556	1.00	64.36	A
ATOM	1535	O	PRO	A	194	59.584	2.924	−27.436	1.00	64.26	A
ATOM	1535	N	HIS	A	195	57.462	3.408	−28.142	1.00	65.63	A
ATOM	1536	CA	HIS	A	195	57.707	4.705	−28.782	1.00	66.79	A
ATOM	1537	CB	HIS	A	195	57.053	5.829	−27.966	1.00	67.12	A
ATOM	1538	CG	HIS	A	195	56.642	7.023	−28.780	1.00	67.81	A
ATOM	1539	CD2	HIS	A	195	56.103	7.117	−30.020	1.00	68.35	A
ATOM	1540	ND1	HIS	A	195	56.725	8.315	−28.303	1.00	67.06	A
ATOM	1541	CE1	HIS	A	195	56.252	9.151	−29.211	1.00	66.74	A
ATOM	1542	NE2	HIS	A	195	55.869	8.450	−30.262	1.00	67.55	A
ATOM	1543	C	HIS	A	195	59.178	5.012	−29.017	1.00	67.09	A
ATOM	1544	O	HIS	A	195	59.797	5.784	−28.284	1.00	65.38	A
ATOM	1545	N	GLU	A	196	59.737	4.351	−30.023	1.00	68.86	A
ATOM	1546	CA	GLU	A	196	61.131	4.524	−30.392	1.00	70.93	A
ATOM	1547	CB	GLU	A	196	61.496	3.520	−31.491	1.00	72.72	A
ATOM	1548	CG	GLU	A	196	60.458	3.439	−32.621	1.00	75.55	A
ATOM	1549	CD	GLU	A	196	60.988	2.756	−33.875	1.00	77.32	A
ATOM	1550	OE1	GLU	A	196	61.475	3.467	−35.786	1.00	77.59	A
ATOM	1551	OE2	GLU	A	196	60.913	1.511	−33.953	1.00	78.12	A
ATOM	1552	C	GLU	A	196	61.387	5.949	−30.881	1.00	71.56	A
ATOM	1553	O	GLU	A	196	62.539	6.369	−30.996	1.00	71.65	A
ATOM	1554	N	GLU	A	197	60.304	6.691	−31.125	1.00	73.16	A
ATOM	1555	CA	GLU	A	197	60.363	8.073	−31.630	1.00	73.94	A
ATOM	1556	CB	GLU	A	197	59.054	8.448	−32.364	1.00	77.25	A
ATOM	1557	CG	GLU	A	197	58.404	7.351	−33.269	1.00	81.76	A
ATOM	1558	CD	GLU	A	197	59.180	6.991	−35.565	1.00	84.28	A
ATOM	1559	OE1	GLU	A	197	59.365	7.872	−35.437	1.00	84.37	A
ATOM	1560	OE2	GLU	A	197	59.560	5.807	−35.733	1.00	85.82	A
ATOM	1561	C	GLU	A	197	60.721	9.156	−30.589	1.00	72.18	A
ATOM	1562	O	GLU	A	197	60.971	10.300	−30.963	1.00	70.61	A
ATOM	1563	N	THR	A	198	60.675	8.809	−29.295	1.00	71.95	A
ATOM	1564	CA	THR	A	198	61.046	9.721	−28.186	1.00	70.16	A
ATOM	1565	CB	THR	A	198	59.848	10.135	−27.249	1.00	69.81	A
ATOM	1566	OG1	THR	A	198	59.136	8.977	−26.791	1.00	69.65	A
ATOM	1567	CG2	THR	A	198	58.907	11.086	−27.946	1.00	69.56	A
ATOM	1568	C	THR	A	198	62.124	9.064	−27.305	1.00	69.02	A
ATOM	1569	O	THR	A	198	62.450	9.568	−26.223	1.00	68.29	A
ATOM	1570	N	ASN	A	199	62.648	7.931	−27.784	1.00	67.24	A
ATOM	1571	CA	ASN	A	199	63.691	7.149	−27.116	1.00	65.05	A
ATOM	1572	CB	ASN	A	199	65.008	7.930	−27.074	1.00	66.19	A
ATOM	1573	CG	ASN	A	199	65.475	8.372	−28.454	1.00	66.53	A
ATOM	1574	OD1	ASN	A	199	65.445	7.594	−29.414	1.00	66.10	A
ATOM	1575	ND2	ASN	A	199	65.907	9.630	−28.558	1.00	65.44	A
ATOM	1576	C	ASN	A	199	63.303	6.695	−25.717	1.00	64.00	A
ATOM	1577	O	ASN	A	199	64.085	6.821	−24.770	1.00	63.12	A
ATOM	1578	N	ASN	A	200	62.097	6.140	−25.608	1.00	63.43	A
ATOM	1579	CA	ASN	A	200	61.565	5.654	−24.338	1.00	62.35	A
ATOM	1580	CB	ASN	A	200	60.107	5.188	−24.491	1.00	57.91	A
ATOM	1581	CG	ASN	A	200	59.109	6.331	−24.443	1.00	52.45	A
ATOM	1582	OD1	ASN	A	200	57.938	6.138	−24.722	1.00	48.44	A
ATOM	1583	ND2	ASN	A	200	59.565	7.514	−24.070	1.00	49.94	A
ATOM	1584	C	ASN	A	200	62.394	4.547	−23.684	1.00	63.76	A
ATOM	1585	O	ASN	A	200	62.841	4.714	−22.547	1.00	64.62	A
ATOM	1586	N	GLU	A	201	62.624	3.436	−24.387	1.00	64.15	A
ATOM	1587	CA	GLU	A	201	63.389	2.357	−23.782	1.00	65.48	A
ATOM	1588	CB	GLU	A	201	63.448	1.105	−24.710	1.00	67.62	A
ATOM	1589	CG	GLU	A	201	63.927	−0.205	−23.999	1.00	69.07	A
ATOM	1590	CD	GLU	A	201	63.529	−1.515	−24.705	1.00	70.80	A
ATOM	1591	OE1	GLU	A	201	63.416	−2.557	−24.012	1.00	69.56	A
ATOM	1592	OE2	GLU	A	201	63.350	−1.512	−25.943	1.00	72.96	A
ATOM	1593	C	GLU	A	201	64.786	2.802	−23.306	1.00	65.24	A
ATOM	1594	O	GLU	A	201	65.357	2.220	−22.380	1.00	65.67	A
ATOM	1595	N	SER	A	202	65.279	3.910	−23.859	1.00	63.81	A
ATOM	1596	CA	SER	A	202	66.597	4.432	−23.494	1.00	61.85	A
ATOM	1597	CB	SER	A	202	67.113	5.351	−24.596	1.00	61.44	A
ATOM	1598	OG	SER	A	202	68.398	5.836	−24.265	1.00	62.62	A
ATOM	1599	C	SER	A	202	66.652	5.167	−22.151	1.00	60.45	A
ATOM	1600	O	SER	A	202	67.478	4.850	−21.291	1.00	60.38	A
ATOM	1601	N	PHE	A	203	65.785	6.165	−22.000	1.00	58.93	A
ATOM	1602	CA	PHE	A	203	65.699	6.983	−20.791	1.00	57.14	A
ATOM	1603	CB	PHE	A	203	64.661	8.082	−20.989	1.00	58.46	A
ATOM	1604	CG	PHE	A	203	64.447	8.947	−19.780	1.00	59.16	A
ATOM	1605	CD1	PHE	A	203	63.423	8.668	−18.881	1.00	59.25	A
ATOM	1606	CD2	PHE	A	203	65.249	10.057	−19.553	1.00	59.46	A
ATOM	1607	CE1	PHE	A	203	63.200	9.484	−17.778	1.00	58.29	A
ATOM	1608	CE2	PHE	A	203	65.030	10.878	−18.450	1.00	59.35	A
ATOM	1609	CZ	PHE	A	203	64.002	10.588	−17.563	1.00	58.64	A
ATOM	1610	C	PHE	A	203	65.363	6.206	−19.529	1.00	55.81	A
ATOM	1611	O	PHE	A	203	65.951	6.446	−18.483	1.00	55.22	A
ATOM	1612	N	VAL	A	204	64.372	5.326	−19.617	1.00	54.97	A
ATOM	1613	CA	VAL	A	204	63.958	4.515	−18.476	1.00	54.69	A
ATOM	1614	CB	VAL	A	204	62.863	3.499	−18.869	1.00	54.17	A
ATOM	1615	CG1	VAL	A	204	62.388	2.735	−17.643	1.00	53.41	A
ATOM	1616	CG2	VAL	A	204	61.699	4.203	−19.543	1.00	55.09	A
ATOM	1617	C	VAL	A	204	65.142	3.751	−17.883	1.00	55.32	A
ATOM	1618	O	VAL	A	204	65.281	3.665	−16.665	1.00	55.93	A
ATOM	1619	N	ILE	A	205	65.981	3.185	−18.751	1.00	55.80	A
ATOM	1620	CA	ILE	A	205	67.159	2.437	−18.320	1.00	55.29	A
ATOM	1621	CB	ILE	A	205	67.841	1.703	−19.506	1.00	56.85	A
ATOM	1622	CG2	ILE	A	205	69.145	1.058	−19.051	1.00	57.68	A
ATOM	1623	CG1	ILE	A	205	66.909	0.628	−20.076	1.00	57.39	A
ATOM	1624	CD1	ILE	A	205	67.488	−0.148	−21.250	1.00	56.19	A
ATOM	1625	C	ILE	A	205	68.139	3.428	−17.711	1.00	54.83	A
ATOM	1626	O	ILE	A	205	68.774	3.140	−16.695	1.00	54.58	A
ATOM	1627	N	TYR	A	206	68.247	4.597	−18.350	1.00	54.28	A
ATOM	1628	CA	TYR	A	206	69.123	5.664	−17.864	1.00	54.24	A
ATOM	1629	CB	TYR	A	206	69.098	6.841	−18.866	1.00	56.12	A
ATOM	1630	CG	TYR	A	206	69.473	8.221	−18.315	1.00	58.72	A
ATOM	1631	CD1	TYR	A	206	68.492	9.203	−18.119	1.00	59.81	A
ATOM	1632	CE1	TYR	A	206	68.819	10.482	−17.648	1.00	59.55	A
ATOM	1633	CD2	TYR	A	206	70.802	8.556	−18.023	1.00	59.50	A
ATOM	1635	CE2	TYR	A	206	71.139	9.838	−17.552	1.00	60.11	A
ATOM	1635	CZ	TYR	A	206	70.138	10.791	−17.369	1.00	60.22	A
ATOM	1636	OH	TYR	A	206	70.449	12.050	−16.908	1.00	59.94	A
ATOM	1637	C	TYR	A	206	68.702	6.111	−16.453	1.00	52.77	A
ATOM	1638	O	TYR	A	206	69.497	6.060	−15.516	1.00	53.05	A
ATOM	1639	N	MET	A	207	67.432	6.469	−16.296	1.00	50.16	A
ATOM	1640	CA	MET	A	207	66.913	6.935	−15.019	1.00	47.97	A
ATOM	1641	CB	MET	A	207	65.451	7.321	−15.165	1.00	49.19	A
ATOM	1642	CG	MET	A	207	64.827	7.832	−13.887	1.00	50.67	A
ATOM	1643	SD	MET	A	207	63.054	7.999	−14.070	1.00	55.24	A
ATOM	1644	CE	MET	A	207	62.596	6.274	−14.424	1.00	51.51	A
ATOM	1645	C	MET	A	207	67.065	5.940	−13.880	1.00	46.78	A
ATOM	1646	O	MET	A	207	67.324	6.324	−12.744	1.00	47.05	A
ATOM	1647	N	PHE	A	208	66.874	4.664	−14.172	1.00	45.32	A
ATOM	1648	CA	PHE	A	208	67.001	3.647	−13.145	1.00	44.18	A
ATOM	1649	CB	PHE	A	208	66.328	2.355	−13.590	1.00	44.12	A
ATOM	1650	CG	PHE	A	208	64.900	2.240	−13.156	1.00	43.41	A
ATOM	1651	CD1	PHE	A	208	64.574	1.592	−11.971	1.00	44.18	A
ATOM	1652	CD2	PHE	A	208	63.876	2.767	−13.933	1.00	44.15	A
ATOM	1653	CE1	PHE	A	208	63.252	1.472	−11.571	1.00	43.18	A
ATOM	1654	CE2	PHE	A	208	62.550	2.652	−13.541	1.00	40.59	A
ATOM	1655	CZ	PHE	A	208	62.241	2.006	−12.364	1.00	42.24	A
ATOM	1656	C	PHE	A	208	68.442	3.378	−12.730	1.00	43.64	A
ATOM	1657	O	PHE	A	208	68.694	2.938	−11.614	1.00	43.83	A
ATOM	1658	N	VAL	A	209	69.385	3.631	−13.629	1.00	43.79	A
ATOM	1659	CA	VAL	A	209	70.795	3.415	−13.322	1.00	45.46	A
ATOM	1660	CB	VAL	A	209	71.621	3.100	−14.617	1.00	46.20	A
ATOM	1661	CG1	VAL	A	209	73.103	2.972	−14.282	1.00	47.29	A
ATOM	1662	CG2	VAL	A	209	71.130	1.807	−15.272	1.00	45.39	A
ATOM	1663	C	VAL	A	209	71.373	4.653	−12.622	1.00	45.19	A
ATOM	1664	O	VAL	A	209	71.730	4.618	−11.442	1.00	44.77	A
ATOM	1665	N	VAL	A	210	71.404	5.756	−13.360	1.00	45.47	A
ATOM	1666	CA	VAL	A	210	71.930	7.031	−12.885	1.00	46.19	A
ATOM	1667	CB	VAL	A	210	72.035	8.040	−14.061	1.00	45.88	A
ATOM	1668	CG1	VAL	A	210	72.652	9.358	−13.602	1.00	42.07	A
ATOM	1669	CG2	VAL	A	210	72.823	7.421	−15.215	1.00	44.93	A
ATOM	1670	C	VAL	A	210	71.122	7.689	−11.772	1.00	47.22	A
ATOM	1671	O	VAL	A	210	71.697	8.329	−10.893	1.00	48.22	A
ATOM	1672	N	HIS	A	211	69.802	7.514	−11.793	1.00	47.64	A
ATOM	1673	CA	HIS	A	211	68.932	8.149	−10.803	1.00	48.22	A
ATOM	1674	CB	HIS	A	211	67.981	9.121	−11.509	1.00	49.09	A
ATOM	1675	CG	HIS	A	211	68.680	10.151	−12.338	1.00	48.24	A
ATOM	1676	CD2	HIS	A	211	68.984	10.176	−13.656	1.00	49.84	A
ATOM	1677	ND1	HIS	A	211	69.170	11.325	−11.810	1.00	48.40	A
ATOM	1678	CE1	HIS	A	211	69.749	12.027	−12.766	1.00	50.69	A
ATOM	1679	NE2	HIS	A	211	69.649	11.353	−13.897	1.00	51.54	A
ATOM	1680	C	HIS	A	211	68.137	7.255	−9.851	1.00	48.24	A
ATOM	1681	O	HIS	A	211	67.027	7.612	−9.440	1.00	47.64	A
ATOM	1682	N	PHE	A	212	68.718	6.124	−9.463	1.00	48.14	A
ATOM	1683	CA	PHE	A	212	68.053	5.209	−8.545	1.00	47.62	A
ATOM	1684	CB	PHE	A	212	66.879	4.519	−9.233	1.00	48.00	A
ATOM	1685	CG	PHE	A	212	66.121	3.593	−8.337	1.00	49.71	A
ATOM	1686	CD1	PHE	A	212	65.637	4.036	−7.111	1.00	50.38	A
ATOM	1687	CD2	PHE	A	212	65.881	2.276	−8.720	1.00	51.02	A
ATOM	1688	CE1	PHE	A	212	64.923	3.183	−6.278	1.00	51.84	A
ATOM	1689	CE2	PHE	A	212	65.168	1.409	−7.896	1.00	50.93	A
ATOM	1690	CZ	PHE	A	212	64.688	1.862	−6.673	1.00	51.86	A
ATOM	1691	C	PHE	A	212	69.017	4.172	−7.990	1.00	47.79	A
ATOM	1692	O	PHE	A	212	69.335	4.186	−6.804	1.00	47.09	A
ATOM	1693	N	ILE	A	213	69.472	3.267	−8.850	1.00	48.89	A
ATOM	1694	CA	ILE	A	213	70.411	2.219	−8.453	1.00	49.50	A
ATOM	1695	CB	ILE	A	213	70.735	1.276	−9.641	1.00	50.74	A
ATOM	1696	CG2	ILE	A	213	71.921	0.372	−9.300	1.00	51.20	A
ATOM	1697	CG1	ILE	A	213	69.499	0.449	−10.015	1.00	51.21	A
ATOM	1698	CD1	ILE	A	213	69.690	−0.429	−11.251	1.00	51.53	A
ATOM	1699	C	ILE	A	213	71.715	2.815	−7.923	1.00	48.52	A
ATOM	1700	O	ILE	A	213	72.127	2.517	−6.803	1.00	47.53	A
ATOM	1701	N	ILE	A	214	72.336	3.683	−8.718	1.00	47.85	A
ATOM	1702	CA	ILE	A	214	73.591	4.298	−8.324	1.00	47.37	A
ATOM	1703	CB	ILE	A	214	74.192	5.147	−9.444	1.00	46.77	A
ATOM	1704	CG2	ILE	A	214	75.318	6.005	−8.908	1.00	47.36	A
ATOM	1705	CG1	ILE	A	214	74.735	4.223	−10.532	1.00	47.27	A
ATOM	1706	CD1	ILE	A	214	75.374	4.947	−11.688	1.00	48.53	A
ATOM	1707	C	ILE	A	214	73.525	5.069	−7.015	1.00	47.15	A
ATOM	1708	O	ILE	A	214	74.192	4.690	−6.053	1.00	49.27	A
ATOM	1709	N	PRO	A	215	72.728	6.149	−6.945	1.00	45.44	A
ATOM	1710	CD	PRO	A	215	71.879	6.799	−7.960	1.00	45.26	A
ATOM	1711	CA	PRO	A	215	72.673	6.877	−5.674	1.00	44.93	A
ATOM	1712	CB	PRO	A	215	71.503	7.828	−5.886	1.00	43.60	A
ATOM	1713	CG	PRO	A	215	71.612	8.149	−7.350	1.00	43.62	A
ATOM	1714	C	PRO	A	215	72.447	5.948	−4.473	1.00	45.85	A
ATOM	1715	O	PRO	A	215	73.084	6.109	−3.436	1.00	45.64	A
ATOM	1716	N	LEU	A	216	71.606	4.929	−4.648	1.00	47.60	A
ATOM	1717	CA	LEU	A	216	71.315	3.981	−3.574	1.00	48.84	A
ATOM	1718	CB	LEU	A	216	70.124	3.111	−3.927	1.00	48.33	A
ATOM	1719	CG	LEU	A	216	68.797	3.845	−3.848	1.00	49.44	A
ATOM	1720	CD1	LEU	A	216	67.714	2.890	−4.266	1.00	51.97	A
ATOM	1721	CD2	LEU	A	216	68.551	4.355	−2.442	1.00	49.11	A
ATOM	1722	C	LEU	A	216	72.494	3.101	−3.227	1.00	50.75	A
ATOM	1723	O	LEU	A	216	72.641	2.678	−2.082	1.00	52.08	A
ATOM	1724	N	ILE	A	217	73.301	2.783	−4.231	1.00	52.17	A
ATOM	1725	CA	ILE	A	217	74.497	1.975	−4.028	1.00	53.69	A
ATOM	1726	CB	ILE	A	217	75.163	1.625	−5.407	1.00	55.46	A
ATOM	1727	CG2	ILE	A	217	76.677	1.802	−5.361	1.00	56.63	A
ATOM	1728	CG1	ILE	A	217	74.818	0.192	−5.819	1.00	55.89	A
ATOM	1729	CD1	ILE	A	217	73.338	−0.127	−5.797	1.00	58.18	A
ATOM	1730	C	ILE	A	217	75.446	2.784	−3.127	1.00	53.47	A
ATOM	1731	O	ILE	A	217	75.937	2.277	−2.113	1.00	53.61	A
ATOM	1732	N	VAL	A	218	75.620	4.062	−3.470	1.00	52.29	A
ATOM	1733	CA	VAL	A	218	76.479	4.977	−2.728	1.00	51.83	A
ATOM	1735	CB	VAL	A	218	76.587	6.358	−3.449	1.00	49.95	A
ATOM	1735	CG1	VAL	A	218	77.363	7.359	−2.606	1.00	47.74	A
ATOM	1736	CG2	VAL	A	218	77.273	6.195	−4.786	1.00	48.14	A
ATOM	1737	C	VAL	A	218	75.993	5.176	−1.291	1.00	54.04	A
ATOM	1738	O	VAL	A	218	76.795	5.152	−0.359	1.00	55.49	A
ATOM	1739	N	ILE	A	219	74.687	5.358	−1.103	1.00	55.83	A
ATOM	1740	CA	ILE	A	219	74.142	5.560	0.240	1.00	57.98	A
ATOM	1741	CB	ILE	A	219	72.689	6.074	0.209	1.00	56.82	A
ATOM	1742	CG2	ILE	A	219	72.301	6.579	1.594	1.00	57.01	A
ATOM	1743	CG1	ILE	A	219	72.552	7.228	−0.785	1.00	56.44	A
ATOM	1744	CD1	ILE	A	219	71.131	7.684	−1.015	1.00	54.37	A
ATOM	1745	C	ILE	A	219	74.182	4.266	1.050	1.00	60.44	A
ATOM	1746	O	ILE	A	219	74.228	4.285	2.282	1.00	61.30	A
ATOM	1747	N	PHE	A	220	74.154	3.142	0.350	1.00	62.89	A
ATOM	1748	CA	PHE	A	220	74.196	1.857	1.009	1.00	66.43	A
ATOM	1749	CB	PHE	A	220	73.458	0.814	0.183	1.00	67.98	A
ATOM	1750	CG	PHE	A	220	71.971	0.832	0.390	1.00	69.78	A
ATOM	1751	CD1	PHE	A	220	71.108	0.351	−0.591	1.00	71.00	A
ATOM	1752	CD2	PHE	A	220	71.430	1.311	1.580	1.00	70.17	A
ATOM	1753	CE1	PHE	A	220	69.726	0.355	−0.388	1.00	70.24	A
ATOM	1754	CE2	PHE	A	220	70.055	1.309	1.791	1.00	70.51	A
ATOM	1755	CZ	PHE	A	220	69.203	0.825	0.805	1.00	69.79	A
ATOM	1756	C	PHE	A	220	75.611	1.415	1.330	1.00	68.77	A
ATOM	1757	O	PHE	A	220	75.815	0.525	2.162	1.00	69.58	A
ATOM	1758	N	PHE	A	221	76.588	2.024	0.663	1.00	71.19	A
ATOM	1759	CA	PHE	A	221	77.982	1.702	0.932	1.00	73.13	A
ATOM	1760	CB	PHE	A	221	78.829	1.683	−0.339	1.00	74.82	A
ATOM	1761	CG	PHE	A	221	80.197	1.091	−0.133	1.00	77.85	A
ATOM	1762	CD1	PHE	A	221	80.409	0.129	0.858	1.00	78.13	A
ATOM	1763	CD2	PHE	A	221	81.280	1.514	−0.897	1.00	79.33	A
ATOM	1764	CE1	PHE	A	221	81.675	−0.399	1.088	1.00	79.02	A
ATOM	1765	CE2	PHE	A	221	82.558	0.990	−0.677	1.00	80.04	A
ATOM	1766	CZ	PHE	A	221	82.755	0.032	0.320	1.00	80.20	A
ATOM	1767	C	PHE	A	221	78.558	2.685	1.950	1.00	73.19	A
ATOM	1768	O	PHE	A	221	79.504	2.359	2.659	1.00	74.57	A
ATOM	1769	N	CYS	A	222	78.011	3.896	2.004	1.00	73.37	A
ATOM	1770	CA	CYS	A	222	78.464	4.876	2.985	1.00	73.68	A
ATOM	1771	CB	CYS	A	222	77.871	6.263	2.709	1.00	72.81	A
ATOM	1772	SG	CYS	A	222	77.937	7.404	4.137	1.00	67.01	A
ATOM	1773	C	CYS	A	222	77.974	4.373	4.338	1.00	75.11	A
ATOM	1774	O	CYS	A	222	78.747	4.292	5.288	1.00	75.31	A
ATOM	1775	N	TYR	A	223	76.691	4.009	4.397	1.00	76.47	A
ATOM	1776	CA	TYR	A	223	76.069	3.495	5.613	1.00	77.92	A
ATOM	1777	CB	TYR	A	223	74.553	3.350	5.422	1.00	77.70	A
ATOM	1778	CG	TYR	A	223	73.861	2.629	6.560	1.00	78.10	A
ATOM	1779	CD1	TYR	A	223	74.026	3.046	7.881	1.00	79.19	A
ATOM	1780	CE1	TYR	A	223	73.441	2.354	8.943	1.00	79.08	A
ATOM	1781	CD2	TYR	A	223	73.086	1.496	6.325	1.00	78.26	A
ATOM	1782	CE2	TYR	A	223	72.495	0.787	7.379	1.00	78.09	A
ATOM	1783	CZ	TYR	A	223	72.678	1.215	8.685	1.00	78.27	A
ATOM	1784	OH	TYR	A	223	72.112	0.514	9.732	1.00	77.54	A
ATOM	1785	C	TYR	A	223	76.697	2.161	6.033	1.00	79.81	A
ATOM	1786	O	TYR	A	223	76.542	1.726	7.172	1.00	79.33	A
ATOM	1787	N	GLY	A	224	77.396	1.513	5.105	1.00	82.45	A
ATOM	1788	CA	GLY	A	224	78.065	0.256	5.411	1.00	85.27	A
ATOM	1789	C	GLY	A	224	79.398	0.538	6.084	1.00	87.14	A
ATOM	1790	O	GLY	A	224	79.954	−0.312	6.784	1.00	86.59	A
ATOM	1791	N	GLN	A	225	79.921	1.736	5.830	1.00	89.82	A
ATOM	1792	CA	GLN	A	225	81.177	2.193	6.409	1.00	93.05	A
ATOM	1793	CB	GLN	A	225	81.850	3.228	5.498	1.00	92.45	A
ATOM	1794	CG	GLN	A	225	82.159	2.744	4.084	1.00	91.90	A
ATOM	1795	CD	GLN	A	225	83.095	1.548	4.049	1.00	92.36	A
ATOM	1796	OE1	GLN	A	225	84.277	1.676	3.719	1.00	92.80	A
ATOM	1797	NE2	GLN	A	225	82.565	0.371	4.372	1.00	92.21	A
ATOM	1798	C	GLN	A	225	80.873	2.804	7.780	1.00	95.85	A
ATOM	1799	O	GLN	A	225	81.645	2.635	8.724	1.00	96.09	A
ATOM	1800	N	LEU	A	226	79.757	3.530	7.882	1.00	99.41	A
ATOM	1801	CA	LEU	A	226	79.353	4.128	9.154	1.00	102.99	A
ATOM	1802	CB	LEU	A	226	78.371	5.300	8.967	1.00	102.22	A
ATOM	1803	CG	LEU	A	226	78.910	6.624	8.427	1.00	101.91	A
ATOM	1804	CD1	LEU	A	226	77.984	7.742	8.875	1.00	101.14	A
ATOM	1805	CD2	LEU	A	226	80.312	6.875	8.940	1.00	101.29	A
ATOM	1806	C	LEU	A	226	78.686	3.057	10.011	1.00	105.94	A
ATOM	1807	O	LEU	A	226	77.498	3.135	10.353	1.00	105.92	A
ATOM	1808	N	VAL	A	227	79.469	2.017	10.274	1.00	109.45	A
ATOM	1809	CA	VAL	A	227	79.097	0.871	11.091	1.00	113.40	A
ATOM	1810	CB	VAL	A	227	78.493	−0.293	10.242	1.00	112.97	A
ATOM	1811	CG1	VAL	A	227	78.420	−1.572	11.059	1.00	113.09	A
ATOM	1812	CG2	VAL	A	227	77.089	0.063	9.778	1.00	112.90	A
ATOM	1813	C	VAL	A	227	80.412	0.447	11.750	1.00	116.65	A
ATOM	1814	O	VAL	A	227	80.411	−0.112	12.846	1.00	117.73	A
ATOM	1815	N	PHE	A	228	81.530	0.767	11.089	1.00	120.47	A
ATOM	1816	CA	PHE	A	228	82.878	0.466	11.594	1.00	123.95	A
ATOM	1817	CB	PHE	A	228	83.967	0.993	10.631	1.00	123.54	A
ATOM	1818	CG	PHE	A	228	84.204	0.139	9.398	1.00	123.18	A
ATOM	1819	CD1	PHE	A	228	83.403	−0.965	9.104	1.00	122.93	A
ATOM	1820	CD2	PHE	A	228	85.241	0.464	8.520	1.00	122.50	A
ATOM	1821	CE1	PHE	A	228	83.631	−1.730	7.954	1.00	122.04	A
ATOM	1822	CE2	PHE	A	228	85.476	−0.292	7.374	1.00	122.04	A
ATOM	1823	CZ	PHE	A	228	84.668	−1.391	7.090	1.00	122.05	A
ATOM	1824	C	PHE	A	228	83.067	1.173	12.943	1.00	126.55	A
ATOM	1825	O	PHE	A	228	83.707	0.637	13.858	1.00	126.84	A
ATOM	1826	N	THR	A	229	82.502	2.379	13.048	1.00	129.19	A
ATOM	1827	CA	THR	A	229	82.610	3.196	14.256	1.00	131.49	A
ATOM	1828	CB	THR	A	229	83.612	4.378	14.049	1.00	131.74	A
ATOM	1829	OG1	THR	A	229	83.289	5.086	12.844	1.00	131.60	A
ATOM	1830	CG2	THR	A	229	85.053	3.866	13.965	1.00	131.75	A
ATOM	1831	C	THR	A	229	81.298	3.745	14.850	1.00	132.70	A
ATOM	1832	O	THR	A	229	81.228	3.969	16.060	1.00	133.27	A
ATOM	1833	N	VAL	A	230	80.268	3.957	14.026	1.00	133.77	A
ATOM	1835	CA	VAL	A	230	78.987	4.496	14.518	1.00	135.91	A
ATOM	1835	CB	VAL	A	230	78.898	6.044	14.304	1.00	135.18	A
ATOM	1836	CG1	VAL	A	230	77.464	6.547	14.490	1.00	135.79	A
ATOM	1837	CG2	VAL	A	230	79.814	6.764	15.285	1.00	135.77	A
ATOM	1838	C	VAL	A	230	77.740	3.845	13.913	1.00	135.51	A
ATOM	1839	O	VAL	A	230	77.627	3.714	12.699	1.00	135.69	A
ATOM	1840	N	LYS	A	231	76.783	3.495	14.774	1.00	136.36	A
ATOM	1841	CA	LYS	A	231	75.528	2.868	14.358	1.00	136.93	A
ATOM	1842	CB	LYS	A	231	75.414	1.456	14.944	1.00	135.70	A
ATOM	1843	CG	LYS	A	231	76.509	0.502	14.497	1.00	133.84	A
ATOM	1844	CD	LYS	A	231	76.330	−0.877	15.097	1.00	132.66	A
ATOM	1845	CE	LYS	A	231	77.413	−1.819	14.604	1.00	131.92	A
ATOM	1846	NZ	LYS	A	231	77.248	−3.203	15.117	1.00	131.35	A
ATOM	1847	C	LYS	A	231	74.286	3.713	14.706	1.00	137.88	A
ATOM	1848	O	LYS	A	231	74.311	4.945	14.596	1.00	137.65	A
ATOM	1849	N	GLU	A	232	73.207	3.045	15.123	1.00	138.97	A
ATOM	1850	CA	GLU	A	232	71.949	3.709	15.490	1.00	139.73	A
ATOM	1851	CB	GLU	A	232	70.848	3.384	14.458	1.00	139.01	A
ATOM	1852	CG	GLU	A	232	70.859	1.954	13.874	1.00	137.25	A
ATOM	1853	CD	GLU	A	232	70.426	0.872	14.857	1.00	136.17	A
ATOM	1854	OE1	GLU	A	232	69.454	1.090	15.613	1.00	135.56	A
ATOM	1855	OE2	GLU	A	232	71.051	−0.210	14.854	1.00	135.04	A
ATOM	1856	C	GLU	A	232	71.454	3.410	16.915	1.00	140.55	A
ATOM	1857	O	GLU	A	232	70.247	3.285	17.158	1.00	140.57	A
ATOM	1858	N	ALA	A	233	72.392	3.354	17.859	1.00	141.22	A
ATOM	1859	CA	ALA	A	233	72.072	3.058	19.255	1.00	142.00	A
ATOM	1860	CB	ALA	A	233	73.253	2.354	19.924	1.00	141.46	A
ATOM	1861	C	ALA	A	233	71.660	4.298	20.061	1.00	142.60	A
ATOM	1862	O	ALA	A	233	71.626	4.261	21.294	1.00	142.89	A
ATOM	1863	N	ALA	A	235	71.328	5.384	19.364	1.00	142.94	A
ATOM	1864	CA	ALA	A	235	70.922	6.626	20.021	1.00	143.19	A
ATOM	1865	CB	ALA	A	235	70.953	7.787	19.027	1.00	142.45	A
ATOM	1866	C	ALA	A	235	69.546	6.526	20.691	1.00	143.46	A
ATOM	1867	O	ALA	A	235	68.571	6.065	20.087	1.00	143.62	A
ATOM	1868	N	ALA	A	235	69.492	6.945	21.954	1.00	143.39	A
ATOM	1869	CA	ALA	A	235	68.265	6.932	22.749	1.00	142.70	A
ATOM	1870	CB	ALA	A	235	68.091	5.572	23.432	1.00	142.30	A
ATOM	1871	C	ALA	A	235	68.353	8.048	23.792	1.00	142.15	A
ATOM	1872	O	ALA	A	235	68.669	7.798	24.957	1.00	141.88	A
ATOM	1873	N	GLN	A	236	68.082	9.280	23.359	1.00	141.48	A
ATOM	1874	CA	GLN	A	236	68.145	10.451	24.235	1.00	140.61	A
ATOM	1875	CB	GLN	A	236	69.609	10.876	24.410	1.00	139.84	A
ATOM	1876	CG	GLN	A	236	69.891	11.791	25.597	1.00	138.75	A
ATOM	1877	CD	GLN	A	236	70.273	11.030	26.854	1.00	137.79	A
ATOM	1878	OE1	GLN	A	236	70.888	9.964	26.790	1.00	137.24	A
ATOM	1879	NE2	GLN	A	236	69.929	11.588	28.008	1.00	137.25	A
ATOM	1880	C	GLN	A	236	67.335	11.614	23.643	1.00	140.45	A
ATOM	1881	O	GLN	A	236	67.048	11.632	22.441	1.00	140.64	A
ATOM	1882	N	GLN	A	237	66.960	12.574	24.490	1.00	139.98	A
ATOM	1883	CA	GLN	A	237	66.191	13.744	24.056	1.00	139.46	A
ATOM	1884	CB	GLN	A	237	65.053	14.046	25.054	1.00	138.16	A
ATOM	1885	CG	GLN	A	237	64.406	15.447	24.949	1.00	135.77	A
ATOM	1886	CD	GLN	A	237	63.721	15.741	23.613	1.00	133.96	A
ATOM	1887	OE1	GLN	A	237	63.240	16.853	23.391	1.00	131.78	A
ATOM	1888	NE2	GLN	A	237	63.676	14.751	22.724	1.00	133.56	A
ATOM	1889	C	GLN	A	237	67.044	14.997	23.787	1.00	139.78	A
ATOM	1890	O	GLN	A	237	66.836	15.670	22.772	1.00	139.75	A
ATOM	1891	N	GLN	A	238	67.998	15.306	24.675	1.00	139.89	A
ATOM	1892	CA	GLN	A	238	68.860	16.488	24.498	1.00	139.48	A
ATOM	1893	CB	GLN	A	238	68.931	17.356	25.783	1.00	139.76	A
ATOM	1894	CG	GLN	A	238	69.548	16.711	27.028	1.00	139.50	A
ATOM	1895	CD	GLN	A	238	69.765	17.732	28.141	1.00	139.53	A
ATOM	1896	OE1	GLN	A	238	68.821	18.138	28.822	1.00	139.44	A
ATOM	1897	NE2	GLN	A	238	71.011	18.166	28.314	1.00	139.64	A
ATOM	1898	C	GLN	A	238	70.262	16.261	23.897	1.00	138.86	A
ATOM	1899	O	GLN	A	238	71.222	15.925	24.604	1.00	139.00	A
ATOM	1900	N	GLU	A	239	70.364	16.482	22.583	1.00	137.32	A
ATOM	1901	CA	GLU	A	239	71.607	16.312	21.822	1.00	135.17	A
ATOM	1902	CB	GLU	A	239	71.693	14.876	21.271	1.00	135.82	A
ATOM	1903	CG	GLU	A	239	71.376	13.742	22.253	1.00	136.14	A
ATOM	1904	CD	GLU	A	239	70.791	12.513	21.561	1.00	136.29	A
ATOM	1905	OE1	GLU	A	239	69.549	12.374	21.535	1.00	135.52	A
ATOM	1906	OE2	GLU	A	239	71.567	11.688	21.037	1.00	136.72	A
ATOM	1907	C	GLU	A	239	71.593	17.282	20.627	1.00	133.71	A
ATOM	1908	O	GLU	A	239	71.488	16.844	19.481	1.00	133.71	A
ATOM	1909	N	SER	A	240	71.704	18.586	20.875	1.00	131.85	A
ATOM	1910	CA	SER	A	240	71.673	19.554	19.775	1.00	130.10	A
ATOM	1911	CB	SER	A	240	70.499	20.526	19.943	1.00	129.95	A
ATOM	1912	OG	SER	A	240	70.629	21.325	21.105	1.00	129.22	A
ATOM	1913	C	SER	A	240	72.968	20.328	19.540	1.00	129.21	A
ATOM	1914	O	SER	A	240	73.218	21.356	20.188	1.00	129.33	A
ATOM	1915	N	ALA	A	241	73.767	19.845	18.588	1.00	128.28	A
ATOM	1916	CA	ALA	A	241	75.053	20.443	18.208	1.00	127.54	A
ATOM	1917	CB	ALA	A	241	74.832	21.578	17.202	1.00	127.46	A
ATOM	1918	C	ALA	A	241	75.922	20.919	19.384	1.00	127.07	A
ATOM	1919	O	ALA	A	241	76.643	21.915	19.269	1.00	126.82	A
ATOM	1920	N	THR	A	242	75.866	20.183	20.498	1.00	126.55	A
ATOM	1921	CA	THR	A	242	76.629	20.511	21.710	1.00	125.18	A
ATOM	1922	CB	THR	A	242	75.724	20.551	22.988	1.00	125.22	A
ATOM	1923	OG1	THR	A	242	74.930	19.359	23.072	1.00	125.01	A
ATOM	1924	CG2	THR	A	242	74.821	21.774	22.979	1.00	125.03	A
ATOM	1925	C	THR	A	242	77.876	19.655	22.020	1.00	124.04	A
ATOM	1926	O	THR	A	242	78.994	20.179	22.002	1.00	124.73	A
ATOM	1927	N	THR	A	243	77.693	18.355	22.289	1.00	121.68	A
ATOM	1928	CA	THR	A	243	78.812	17.462	22.646	1.00	118.32	A
ATOM	1929	CB	THR	A	243	78.538	16.751	24.003	1.00	117.71	A
ATOM	1930	OG1	THR	A	243	77.576	17.500	24.755	1.00	117.57	A
ATOM	1931	CG2	THR	A	243	79.816	16.655	24.824	1.00	117.04	A
ATOM	1932	C	THR	A	243	79.272	16.408	21.610	1.00	116.36	A
ATOM	1933	O	THR	A	243	79.520	16.726	20.442	1.00	115.64	A
ATOM	1935	N	GLN	A	244	79.426	15.164	22.072	1.00	114.26	A
ATOM	1935	CA	GLN	A	244	79.882	14.031	21.250	1.00	111.63	A
ATOM	1936	CB	GLN	A	244	80.613	13.006	22.139	1.00	111.67	A
ATOM	1937	CG	GLN	A	244	81.260	13.562	23.421	1.00	110.44	A
ATOM	1938	CD	GLN	A	244	82.484	14.422	23.154	1.00	110.49	A
ATOM	1939	OE1	GLN	A	244	83.530	13.924	22.739	1.00	109.65	A
ATOM	1940	NE2	GLN	A	244	82.361	15.720	23.405	1.00	110.27	A
ATOM	1941	C	GLN	A	244	78.730	13.314	20.522	1.00	109.26	A
ATOM	1942	O	GLN	A	244	78.843	12.954	19.352	1.00	107.40	A
ATOM	1943	N	LYS	A	245	77.649	13.076	21.269	1.00	106.78	A
ATOM	1944	CA	LYS	A	245	76.446	12.405	20.779	1.00	103.39	A
ATOM	1945	CB	LYS	A	245	75.718	11.722	21.949	1.00	104.18	A
ATOM	1946	CG	LYS	A	245	74.728	10.622	21.544	1.00	105.57	A
ATOM	1947	CD	LYS	A	245	74.004	10.021	22.754	1.00	105.85	A
ATOM	1948	CE	LYS	A	245	73.052	8.892	22.350	1.00	105.71	A
ATOM	1949	NZ	LYS	A	245	72.298	8.331	23.514	1.00	105.03	A
ATOM	1950	C	LYS	A	245	75.514	13.403	20.084	1.00	100.53	A
ATOM	1951	O	LYS	A	245	74.309	13.176	19.973	1.00	99.89	A
ATOM	1952	N	ALA	A	246	76.078	14.522	19.646	1.00	97.35	A
ATOM	1953	CA	ALA	A	246	75.314	15.546	18.948	1.00	94.04	A
ATOM	1954	CB	ALA	A	246	75.971	16.899	19.116	1.00	94.87	A
ATOM	1955	C	ALA	A	246	75.254	15.169	17.477	1.00	91.59	A
ATOM	1956	O	ALA	A	246	74.184	15.156	16.878	1.00	91.12	A
ATOM	1957	N	GLU	A	247	76.413	14.862	16.902	1.00	89.19	A
ATOM	1958	CA	GLU	A	247	76.494	14.465	15.502	1.00	87.21	A
ATOM	1959	CB	GLU	A	247	77.938	14.559	14.993	1.00	86.46	A
ATOM	1960	CG	GLU	A	247	78.430	15.983	14.732	1.00	86.54	A
ATOM	1961	CD	GLU	A	247	77.632	16.703	13.655	1.00	86.92	A
ATOM	1962	OE1	GLU	A	247	77.454	16.121	12.564	1.00	86.55	A
ATOM	1963	OE2	GLU	A	247	77.187	17.851	13.896	1.00	87.90	A
ATOM	1964	C	GLU	A	247	75.946	13.048	15.309	1.00	86.07	A
ATOM	1965	O	GLU	A	247	75.816	12.567	14.178	1.00	87.23	A
ATOM	1966	N	LYS	A	248	75.602	12.397	16.418	1.00	83.11	A
ATOM	1967	CA	LYS	A	248	75.056	11.044	16.391	1.00	80.27	A
ATOM	1968	CB	LYS	A	248	75.527	10.279	17.633	1.00	81.81	A
ATOM	1969	CG	LYS	A	248	75.405	8.757	17.561	1.00	83.89	A
ATOM	1970	CD	LYS	A	248	76.243	8.086	18.657	1.00	84.52	A
ATOM	1971	CE	LYS	A	248	77.736	8.390	18.481	1.00	85.16	A
ATOM	1972	NZ	LYS	A	248	78.575	7.895	19.609	1.00	84.44	A
ATOM	1973	C	LYS	A	248	73.521	11.072	16.297	1.00	77.87	A
ATOM	1974	O	LYS	A	248	72.894	10.048	16.035	1.00	77.74	A
ATOM	1975	N	GLU	A	249	72.931	12.248	16.527	1.00	75.36	A
ATOM	1976	CA	GLU	A	249	71.477	12.454	16.443	1.00	71.41	A
ATOM	1977	CB	GLU	A	249	71.038	13.584	17.383	1.00	72.05	A
ATOM	1978	CG	GLU	A	249	69.552	13.928	17.326	1.00	73.55	A
ATOM	1979	CD	GLU	A	249	69.259	15.353	17.787	1.00	74.44	A
ATOM	1980	OE1	GLU	A	249	69.826	16.302	17.201	1.00	74.49	A
ATOM	1981	OE2	GLU	A	249	68.451	15.531	18.725	1.00	74.97	A
ATOM	1982	C	GLU	A	249	71.135	12.823	14.996	1.00	68.27	A
ATOM	1983	O	GLU	A	249	70.009	12.611	14.538	1.00	67.49	A
ATOM	1984	N	VAL	A	250	72.117	13.412	14.308	1.00	64.63	A
ATOM	1985	CA	VAL	A	250	71.999	13.804	12.907	1.00	61.06	A
ATOM	1986	CB	VAL	A	250	73.066	14.856	12.498	1.00	59.72	A
ATOM	1987	CG1	VAL	A	250	73.089	15.033	10.989	1.00	57.65	A
ATOM	1988	CG2	VAL	A	250	72.775	16.191	13.158	1.00	59.55	A
ATOM	1989	C	VAL	A	250	72.218	12.554	12.075	1.00	59.98	A
ATOM	1990	O	VAL	A	250	71.480	12.298	11.131	1.00	59.52	A
ATOM	1991	N	THR	A	251	73.235	11.775	12.437	1.00	59.13	A
ATOM	1992	CA	THR	A	251	73.539	10.544	11.720	1.00	58.16	A
ATOM	1993	CB	THR	A	251	74.818	9.856	12.250	1.00	58.64	A
ATOM	1994	OG1	THR	A	251	75.941	10.741	12.110	1.00	56.90	A
ATOM	1995	CG2	THR	A	251	75.087	8.572	11.470	1.00	57.75	A
ATOM	1996	C	THR	A	251	72.359	9.582	11.797	1.00	57.48	A
ATOM	1997	O	THR	A	251	71.983	9.000	10.790	1.00	57.56	A
ATOM	1998	N	ARG	A	252	71.769	9.428	12.981	1.00	57.31	A
ATOM	1999	CA	ARG	A	252	70.612	8.548	13.135	1.00	57.64	A
ATOM	2000	CB	ARG	A	252	70.183	8.390	14.612	1.00	62.22	A
ATOM	2001	CG	ARG	A	252	68.918	7.499	14.821	1.00	67.65	A
ATOM	2002	CD	ARG	A	252	68.565	7.178	16.311	1.00	73.56	A
ATOM	2003	NE	ARG	A	252	67.751	8.192	17.014	1.00	77.86	A
ATOM	2004	CZ	ARG	A	252	66.804	7.922	17.924	1.00	78.42	A
ATOM	2005	NH1	ARG	A	252	66.523	6.664	18.263	1.00	77.83	A
ATOM	2006	NH2	ARG	A	252	66.132	8.913	18.505	1.00	77.51	A
ATOM	2007	C	ARG	A	252	69.472	9.145	12.328	1.00	55.25	A
ATOM	2008	O	ARG	A	252	68.638	8.422	11.808	1.00	55.54	A
ATOM	2009	N	MET	A	253	69.451	10.467	12.203	1.00	53.09	A
ATOM	2010	CA	MET	A	253	68.397	11.125	11.444	1.00	52.02	A
ATOM	2011	CB	MET	A	253	68.372	12.625	11.731	1.00	52.23	A
ATOM	2012	CG	MET	A	253	67.287	13.365	10.956	1.00	53.70	A
ATOM	2013	SD	MET	A	253	67.037	15.084	11.449	1.00	53.84	A
ATOM	2014	CE	MET	A	253	67.877	15.971	10.145	1.00	53.74	A
ATOM	2015	C	MET	A	253	68.551	10.888	9.946	1.00	51.09	A
ATOM	2016	O	MET	A	253	67.591	10.539	9.260	1.00	50.86	A
ATOM	2017	N	VAL	A	254	69.767	11.081	9.448	1.00	49.96	A
ATOM	2018	CA	VAL	A	254	70.064	10.890	8.036	1.00	48.21	A
ATOM	2019	CB	VAL	A	254	71.521	11.309	7.727	1.00	47.73	A
ATOM	2020	CG1	VAL	A	254	71.863	11.050	6.260	1.00	48.55	A
ATOM	2021	CG2	VAL	A	254	71.706	12.787	8.057	1.00	46.97	A
ATOM	2022	C	VAL	A	254	69.798	9.445	7.603	1.00	47.41	A
ATOM	2023	O	VAL	A	254	69.466	9.189	6.444	1.00	46.63	A
ATOM	2024	N	ILE	A	255	69.891	8.519	8.557	1.00	46.77	A
ATOM	2025	CA	ILE	A	255	69.655	7.092	8.304	1.00	46.06	A
ATOM	2026	CB	ILE	A	255	70.402	6.198	9.365	1.00	46.75	A
ATOM	2027	CG2	ILE	A	255	70.213	4.721	9.066	1.00	46.22	A
ATOM	2028	CG1	ILE	A	255	71.905	6.541	9.422	1.00	47.02	A
ATOM	2029	CD1	ILE	A	255	72.638	6.603	8.072	1.00	48.93	A
ATOM	2030	C	ILE	A	255	68.144	6.758	8.262	1.00	44.05	A
ATOM	2031	O	ILE	A	255	67.737	5.717	7.745	1.00	42.96	A
ATOM	2032	N	ILE	A	256	67.323	7.664	8.787	1.00	43.37	A
ATOM	2033	CA	ILE	A	256	65.868	7.496	8.800	1.00	43.41	A
ATOM	2035	CB	ILE	A	256	65.209	8.243	10.000	1.00	44.47	A
ATOM	2035	CG2	ILE	A	256	63.694	8.360	9.801	1.00	44.70	A
ATOM	2036	CG1	ILE	A	256	65.530	7.535	11.323	1.00	43.60	A
ATOM	2037	CD1	ILE	A	256	64.911	6.159	11.469	1.00	41.35	A
ATOM	2038	C	ILE	A	256	65.285	8.036	7.499	1.00	42.61	A
ATOM	2039	O	ILE	A	256	64.437	7.404	6.877	1.00	42.07	A
ATOM	2040	N	MET	A	257	65.754	9.211	7.096	1.00	42.41	A
ATOM	2041	CA	MET	A	257	65.300	9.842	5.866	1.00	43.10	A
ATOM	2042	CB	MET	A	257	66.080	11.131	5.622	1.00	43.22	A
ATOM	2043	CG	MET	A	257	66.141	12.077	6.798	1.00	42.93	A
ATOM	2044	SD	MET	A	257	67.177	13.503	6.422	1.00	41.97	A
ATOM	2045	CE	MET	A	257	66.006	14.822	6.425	1.00	40.96	A
ATOM	2046	C	MET	A	257	65.520	8.896	4.679	1.00	44.35	A
ATOM	2047	O	MET	A	257	64.909	9.056	3.620	1.00	44.44	A
ATOM	2048	N	VAL	A	258	66.431	7.941	4.850	1.00	44.88	A
ATOM	2049	CA	VAL	A	258	66.723	6.967	3.811	1.00	45.11	A
ATOM	2050	CB	VAL	A	258	68.081	6.265	4.055	1.00	46.14	A
ATOM	2051	CG1	VAL	A	258	68.295	5.141	3.046	1.00	45.87	A
ATOM	2052	CG2	VAL	A	258	69.215	7.283	3.936	1.00	46.82	A
ATOM	2053	C	VAL	A	258	65.591	5.949	3.787	1.00	44.97	A
ATOM	2054	O	VAL	A	258	65.033	5.655	2.726	1.00	46.08	A
ATOM	2055	N	ILE	A	259	65.226	5.441	4.960	1.00	42.72	A
ATOM	2056	CA	ILE	A	259	64.144	4.473	5.043	1.00	42.09	A
ATOM	2057	CB	ILE	A	259	63.944	3.976	6.470	1.00	43.29	A
ATOM	2058	CG2	ILE	A	259	62.825	2.952	6.513	1.00	42.70	A
ATOM	2059	CG1	ILE	A	259	65.244	3.367	6.998	1.00	45.47	A
ATOM	2060	CD1	ILE	A	259	65.214	3.075	8.485	1.00	45.00	A
ATOM	2061	C	ILE	A	259	62.863	5.142	4.583	1.00	41.75	A
ATOM	2062	O	ILE	A	259	62.176	4.635	3.700	1.00	43.89	A
ATOM	2063	N	ALA	A	260	62.570	6.308	5.153	1.00	39.70	A
ATOM	2064	CA	ALA	A	260	61.374	7.057	4.799	1.00	37.88	A
ATOM	2065	CB	ALA	A	260	61.382	8.400	5.477	1.00	36.09	A
ATOM	2066	C	ALA	A	260	61.289	7.223	3.288	1.00	37.55	A
ATOM	2067	O	ALA	A	260	60.200	7.193	2.713	1.00	40.62	A
ATOM	2068	N	PHE	A	261	62.445	7.355	2.646	1.00	35.91	A
ATOM	2069	CA	PHE	A	261	62.511	7.494	1.198	1.00	35.03	A
ATOM	2070	CB	PHE	A	261	63.944	7.827	0.765	1.00	33.51	A
ATOM	2071	CG	PHE	A	261	64.139	7.878	−0.730	1.00	32.58	A
ATOM	2072	CD1	PHE	A	261	64.042	9.084	−1.414	1.00	30.86	A
ATOM	2073	CD2	PHE	A	261	64.421	6.717	−1.451	1.00	31.18	A
ATOM	2074	CE1	PHE	A	261	64.221	9.131	−2.787	1.00	31.54	A
ATOM	2075	CE2	PHE	A	261	64.600	6.758	−2.823	1.00	29.70	A
ATOM	2076	CZ	PHE	A	261	64.500	7.964	−3.494	1.00	30.18	A
ATOM	2077	C	PHE	A	261	62.054	6.214	0.512	1.00	36.10	A
ATOM	2078	O	PHE	A	261	61.200	6.239	−0.376	1.00	35.59	A
ATOM	2079	N	LEU	A	262	62.656	5.102	0.925	1.00	37.17	A
ATOM	2080	CA	LEU	A	262	62.350	3.787	0.376	1.00	36.67	A
ATOM	2081	CB	LEU	A	262	63.166	2.714	1.093	1.00	35.55	A
ATOM	2082	CG	LEU	A	262	64.682	2.867	1.119	1.00	31.36	A
ATOM	2083	CD1	LEU	A	262	65.250	1.713	1.925	1.00	30.40	A
ATOM	2084	CD2	LEU	A	262	65.255	2.907	−0.286	1.00	27.84	A
ATOM	2085	C	LEU	A	262	60.866	3.448	0.476	1.00	37.31	A
ATOM	2086	O	LEU	A	262	60.228	3.177	−0.544	1.00	38.41	A
ATOM	2087	N	ILE	A	263	60.322	3.470	1.695	1.00	36.21	A
ATOM	2088	CA	ILE	A	263	58.905	3.165	1.918	1.00	35.23	A
ATOM	2089	CB	ILE	A	263	58.456	3.528	3.363	1.00	33.58	A
ATOM	2090	CG2	ILE	A	263	56.977	3.199	3.567	1.00	32.44	A
ATOM	2091	CG1	ILE	A	263	59.304	2.796	4.399	1.00	31.09	A
ATOM	2092	CD1	ILE	A	263	58.886	3.070	5.828	1.00	27.29	A
ATOM	2093	C	ILE	A	263	58.045	3.989	0.963	1.00	36.17	A
ATOM	2094	O	ILE	A	263	57.038	3.510	0.442	1.00	37.15	A
ATOM	2095	N	CYS	A	264	58.513	5.203	0.688	1.00	36.76	A
ATOM	2096	CA	CYS	A	264	57.817	6.164	−0.158	1.00	36.18	A
ATOM	2097	CB	CYS	A	264	58.241	7.579	0.245	1.00	35.16	A
ATOM	2098	SG	CYS	A	264	57.040	8.835	−0.115	1.00	33.33	A
ATOM	2099	C	CYS	A	264	57.988	5.990	−1.657	1.00	35.31	A
ATOM	2100	O	CYS	A	264	57.005	5.932	−2.393	1.00	36.82	A
ATOM	2101	N	TRP	A	265	59.235	5.918	−2.106	1.00	33.91	A
ATOM	2102	CA	TRP	A	265	59.525	5.793	−3.526	1.00	33.08	A
ATOM	2103	CB	TRP	A	265	60.704	6.681	−3.888	1.00	32.58	A
ATOM	2104	CG	TRP	A	265	60.351	8.109	−3.855	1.00	33.77	A
ATOM	2105	CD2	TRP	A	265	59.481	8.792	−4.780	1.00	35.96	A
ATOM	2106	CE2	TRP	A	265	59.451	10.152	−4.394	1.00	35.73	A
ATOM	2107	CE3	TRP	A	265	58.735	8.387	−5.904	1.00	36.21	A
ATOM	2108	CD1	TRP	A	265	60.775	9.046	−2.967	1.00	32.57	A
ATOM	2109	NE1	TRP	A	265	60.249	10.278	−3.285	1.00	35.18	A
ATOM	2110	CZ2	TRP	A	265	58.707	11.114	−5.092	1.00	33.80	A
ATOM	2111	CZ3	TRP	A	265	57.997	9.353	−6.598	1.00	35.57	A
ATOM	2112	CH2	TRP	A	265	57.990	10.693	−6.187	1.00	35.16	A
ATOM	2113	C	TRP	A	265	59.723	4.404	−4.112	1.00	32.53	A
ATOM	2114	O	TRP	A	265	59.693	4.243	−5.332	1.00	33.01	A
ATOM	2115	N	LEU	A	266	59.929	3.405	−3.260	1.00	31.86	A
ATOM	2116	CA	LEU	A	266	60.122	2.038	−3.745	1.00	31.40	A
ATOM	2117	CB	LEU	A	266	60.707	1.127	−2.658	1.00	32.38	A
ATOM	2118	CG	LEU	A	266	62.124	0.608	−2.932	1.00	32.35	A
ATOM	2119	CD1	LEU	A	266	63.060	1.777	−3.253	1.00	32.05	A
ATOM	2120	CD2	LEU	A	266	62.621	−0.168	−1.727	1.00	30.76	A
ATOM	2121	C	LEU	A	266	58.862	1.419	−4.356	1.00	29.79	A
ATOM	2122	O	LEU	A	266	58.924	0.854	−5.440	1.00	29.51	A
ATOM	2123	N	PRO	A	267	57.706	1.513	−3.648	1.00	26.85	A
ATOM	2124	CD	PRO	A	267	57.422	2.107	−2.333	1.00	24.35	A
ATOM	2125	CA	PRO	A	267	56.484	0.936	−4.201	1.00	25.82	A
ATOM	2126	CB	PRO	A	267	55.423	1.432	−3.235	1.00	23.65	A
ATOM	2127	CG	PRO	A	267	56.147	1.442	−1.966	1.00	22.24	A
ATOM	2128	C	PRO	A	267	56.261	1.464	−5.614	1.00	27.30	A
ATOM	2129	O	PRO	A	267	55.949	0.694	−6.525	1.00	27.01	A
ATOM	2130	N	TYR	A	268	56.483	2.765	−5.799	1.00	27.85	A
ATOM	2131	CA	TYR	A	268	56.326	3.384	−7.114	1.00	28.65	A
ATOM	2132	CB	TYR	A	268	56.427	4.911	−7.025	1.00	26.86	A
ATOM	2133	CG	TYR	A	268	56.251	5.612	−8.357	1.00	23.42	A
ATOM	2135	CD1	TYR	A	268	54.997	6.030	−8.779	1.00	23.50	A
ATOM	2135	CE1	TYR	A	268	54.822	6.666	−10.005	1.00	23.96	A
ATOM	2136	CD2	TYR	A	268	57.338	5.844	−9.197	1.00	21.90	A
ATOM	2137	CE2	TYR	A	268	57.180	6.471	−10.424	1.00	21.42	A
ATOM	2138	CZ	TYR	A	268	55.916	6.886	−10.823	1.00	23.32	A
ATOM	2139	OH	TYR	A	268	55.749	7.550	−12.017	1.00	19.42	A
ATOM	2140	C	TYR	A	268	57.404	2.868	−8.056	1.00	30.33	A
ATOM	2141	O	TYR	A	268	57.112	2.474	−9.177	1.00	29.92	A
ATOM	2142	N	ALA	A	269	58.653	2.895	−7.594	1.00	33.21	A
ATOM	2143	CA	ALA	A	269	59.790	2.439	−8.384	1.00	33.85	A
ATOM	2144	CB	ALA	A	269	61.066	2.578	−7.582	1.00	33.68	A
ATOM	2145	C	ALA	A	269	59.581	0.996	−8.796	1.00	35.54	A
ATOM	2146	O	ALA	A	269	59.842	0.620	−9.940	1.00	33.94	A
ATOM	2147	N	GLY	A	270	59.076	0.200	−7.859	1.00	38.24	A
ATOM	2148	CA	GLY	A	270	58.813	−1.202	−8.123	1.00	42.31	A
ATOM	2149	C	GLY	A	270	57.745	−1.403	−9.185	1.00	45.09	A
ATOM	2150	O	GLY	A	270	58.004	−2.006	−10.226	1.00	46.85	A
ATOM	2151	N	VAL	A	271	56.557	−0.852	−8.950	1.00	46.68	A
ATOM	2152	CA	VAL	A	271	55.448	−0.982	−9.894	1.00	48.20	A
ATOM	2153	CB	VAL	A	271	54.110	−0.606	−9.213	1.00	47.47	A
ATOM	2154	CG1	VAL	A	271	54.053	0.875	−8.920	1.00	49.70	A
ATOM	2155	CG2	VAL	A	271	52.954	−1.035	−10.055	1.00	46.58	A
ATOM	2156	C	VAL	A	271	55.638	−0.213	−11.219	1.00	48.96	A
ATOM	2157	O	VAL	A	271	54.820	−0.338	−12.127	1.00	49.07	A
ATOM	2158	N	ALA	A	272	56.713	0.575	−11.319	1.00	50.43	A
ATOM	2159	CA	ALA	A	272	57.036	1.351	−12.529	1.00	50.41	A
ATOM	2160	CB	ALA	A	272	57.600	2.700	−12.176	1.00	48.29	A
ATOM	2161	C	ALA	A	272	58.042	0.553	−13.360	1.00	51.66	A
ATOM	2162	O	ALA	A	272	58.082	0.680	−14.582	1.00	52.48	A
ATOM	2163	N	PHE	A	273	58.882	−0.235	−12.692	1.00	53.08	A
ATOM	2164	CA	PHE	A	273	59.853	−1.065	−13.400	1.00	55.36	A
ATOM	2165	CB	PHE	A	273	61.021	−1.463	−12.493	1.00	54.53	A
ATOM	2166	CG	PHE	A	273	62.130	−2.183	−13.216	1.00	53.59	A
ATOM	2167	CD1	PHE	A	273	62.958	−1.502	−14.104	1.00	53.46	A
ATOM	2168	CD2	PHE	A	273	62.359	−3.541	−13.009	1.00	53.41	A
ATOM	2169	CE1	PHE	A	273	63.990	−2.161	−14.775	1.00	52.07	A
ATOM	2170	CE2	PHE	A	273	63.377	−4.206	−13.674	1.00	52.45	A
ATOM	2171	CZ	PHE	A	273	64.198	−3.514	−14.558	1.00	52.25	A
ATOM	2172	C	PHE	A	273	59.122	−2.317	−13.898	1.00	57.31	A
ATOM	2173	O	PHE	A	273	59.519	−2.923	−14.898	1.00	58.22	A
ATOM	2174	N	TYR	A	274	58.071	−2.709	−13.172	1.00	57.98	A
ATOM	2175	CA	TYR	A	274	57.244	−3.859	−13.536	1.00	57.73	A
ATOM	2176	CB	TYR	A	274	56.099	−4.035	−12.523	1.00	58.49	A
ATOM	2177	CG	TYR	A	274	55.041	−5.037	−12.951	1.00	60.77	A
ATOM	2178	CD1	TYR	A	274	55.059	−6.358	−12.480	1.00	61.81	A
ATOM	2179	CE1	TYR	A	274	54.120	−7.288	−12.923	1.00	63.12	A
ATOM	2180	CD2	TYR	A	274	54.049	−4.685	−13.871	1.00	61.71	A
ATOM	2181	CE2	TYR	A	274	53.110	−5.611	−14.319	1.00	62.50	A
ATOM	2182	CZ	TYR	A	274	53.151	−6.910	−13.846	1.00	63.26	A
ATOM	2183	OH	TYR	A	274	52.236	−7.827	−14.314	1.00	63.28	A
ATOM	2184	C	TYR	A	274	56.667	−3.558	−14.918	1.00	57.73	A
ATOM	2185	O	TYR	A	274	56.841	−4.322	−15.867	1.00	58.39	A
ATOM	2186	N	ILE	A	275	55.997	−2.415	−15.004	1.00	56.83	A
ATOM	2187	CA	ILE	A	275	55.375	−1.930	−16.223	1.00	56.05	A
ATOM	2188	CB	ILE	A	275	54.779	−0.523	−15.972	1.00	54.80	A
ATOM	2189	CG2	ILE	A	275	54.358	0.131	−17.271	1.00	53.84	A
ATOM	2190	CG1	ILE	A	275	53.611	−0.635	−14.991	1.00	54.03	A
ATOM	2191	CD1	ILE	A	275	53.116	0.684	−14.454	1.00	55.23	A
ATOM	2192	C	ILE	A	275	56.361	−1.900	−17.395	1.00	57.21	A
ATOM	2193	O	ILE	A	275	56.117	−2.524	−18.429	1.00	56.89	A
ATOM	2194	N	PHE	A	276	57.497	−1.230	−17.206	1.00	58.42	A
ATOM	2195	CA	PHE	A	276	58.509	−1.112	−18.258	1.00	59.12	A
ATOM	2196	CB	PHE	A	276	59.788	−0.455	−17.724	1.00	59.21	A
ATOM	2197	CG	PHE	A	276	60.880	−0.336	−18.757	1.00	59.54	A
ATOM	2198	CD1	PHE	A	276	60.662	0.368	−19.942	1.00	58.88	A
ATOM	2199	CD2	PHE	A	276	62.117	−0.952	−18.559	1.00	58.95	A
ATOM	2200	CE1	PHE	A	276	61.656	0.454	−20.911	1.00	58.84	A
ATOM	2201	CE2	PHE	A	276	63.118	−0.871	−19.523	1.00	57.76	A
ATOM	2202	CZ	PHE	A	276	62.888	−0.168	−20.699	1.00	58.30	A
ATOM	2203	C	PHE	A	276	58.847	−2.450	−18.903	1.00	59.10	A
ATOM	2204	O	PHE	A	276	59.073	−2.527	−20.114	1.00	59.36	A
ATOM	2205	N	THR	A	277	58.900	−3.497	−18.087	1.00	59.31	A
ATOM	2206	CA	THR	A	277	59.203	−4.823	−18.599	1.00	59.55	A
ATOM	2207	CB	THR	A	277	59.822	−5.741	−17.509	1.00	59.00	A
ATOM	2208	OG1	THR	A	277	58.936	−5.844	−16.390	1.00	58.43	A
ATOM	2209	CG2	THR	A	277	61.150	−5.174	−17.041	1.00	57.71	A
ATOM	2210	C	THR	A	277	57.937	−5.436	−19.194	1.00	59.28	A
ATOM	2211	O	THR	A	277	57.881	−5.718	−20.397	1.00	61.80	A
ATOM	2212	N	HIS	A	278	56.900	−5.565	−18.373	1.00	56.62	A
ATOM	2213	CA	HIS	A	278	55.639	−6.131	−18.830	1.00	54.45	A
ATOM	2214	CB	HIS	A	278	54.870	−6.747	−17.655	1.00	54.79	A
ATOM	2215	CG	HIS	A	278	55.635	−7.795	−16.904	1.00	57.46	A
ATOM	2216	CD2	HIS	A	278	55.226	−8.721	−16.002	1.00	58.18	A
ATOM	2217	ND1	HIS	A	278	57.000	−7.954	−17.019	1.00	58.58	A
ATOM	2218	CE1	HIS	A	278	57.398	−8.929	−16.220	1.00	58.89	A
ATOM	2219	NE2	HIS	A	278	56.351	−9.411	−15.591	1.00	58.08	A
ATOM	2220	C	HIS	A	278	54.764	−5.080	−19.525	1.00	52.89	A
ATOM	2221	O	HIS	A	278	53.670	−4.779	−19.047	1.00	53.05	A
ATOM	2222	N	GLN	A	279	55.255	−4.506	−20.627	1.00	50.29	A
ATOM	2223	CA	GLN	A	279	54.497	−3.505	−21.392	1.00	48.60	A
ATOM	2224	CB	GLN	A	279	55.419	−2.730	−22.339	1.00	47.61	A
ATOM	2225	CG	GLN	A	279	56.485	−1.911	−21.656	1.00	47.39	A
ATOM	2226	CD	GLN	A	279	57.573	−1.441	−22.608	1.00	47.41	A
ATOM	2227	OE1	GLN	A	279	57.623	−0.267	−22.982	1.00	45.83	A
ATOM	2228	NE2	GLN	A	279	58.470	−2.354	−22.980	1.00	47.00	A
ATOM	2229	C	GLN	A	279	53.410	−4.199	−22.222	1.00	48.17	A
ATOM	2230	O	GLN	A	279	53.588	−5.337	−22.652	1.00	48.61	A
ATOM	2231	N	GLY	A	280	52.294	−3.514	−22.458	1.00	47.46	A
ATOM	2232	CA	GLY	A	280	51.217	−4.105	−23.241	1.00	46.73	A
ATOM	2233	C	GLY	A	280	50.454	−5.149	−22.456	1.00	45.87	A
ATOM	2235	O	GLY	A	280	49.437	−5.676	−22.906	1.00	43.90	A
ATOM	2235	N	SER	A	281	50.976	−5.441	−21.270	1.00	47.33	A
ATOM	2236	CA	SER	A	281	50.396	−6.398	−20.350	1.00	49.09	A
ATOM	2237	CB	SER	A	281	51.376	−6.660	−19.195	1.00	49.85	A
ATOM	2238	OG	SER	A	281	50.852	−7.590	−18.268	1.00	54.43	A
ATOM	2239	C	SER	A	281	49.091	−5.840	−19.782	1.00	49.40	A
ATOM	2240	O	SER	A	281	48.747	−4.676	−20.018	1.00	49.09	A
ATOM	2241	N	ASP	A	282	48.386	−6.659	−19.007	1.00	50.61	A
ATOM	2242	CA	ASP	A	282	47.107	−6.245	−18.446	1.00	50.96	A
ATOM	2243	CB	ASP	A	282	46.073	−7.367	−18.595	1.00	54.91	A
ATOM	2244	CG	ASP	A	282	44.635	−6.865	−18.473	1.00	59.55	A
ATOM	2245	OD1	ASP	A	282	44.427	−5.640	−18.262	1.00	62.64	A
ATOM	2246	OD2	ASP	A	282	43.709	−7.703	−18.603	1.00	60.36	A
ATOM	2247	C	ASP	A	282	47.148	−5.769	−17.003	1.00	48.73	A
ATOM	2248	O	ASP	A	282	47.286	−6.564	−16.073	1.00	49.41	A
ATOM	2249	N	PHE	A	283	47.031	−4.459	−16.835	1.00	45.70	A
ATOM	2250	CA	PHE	A	283	47.006	−3.848	−15.514	1.00	44.46	A
ATOM	2251	CB	PHE	A	283	48.359	−3.193	−15.124	1.00	44.55	A
ATOM	2252	CG	PHE	A	283	49.094	−2.546	−16.267	1.00	43.56	A
ATOM	2253	CD1	PHE	A	283	48.907	−1.198	−16.568	1.00	43.66	A
ATOM	2254	CD2	PHE	A	283	50.001	−3.279	−17.024	1.00	41.48	A
ATOM	2255	CE1	PHE	A	283	49.612	−0.595	−17.603	1.00	42.01	A
ATOM	2256	CE2	PHE	A	283	50.706	−2.684	−18.057	1.00	40.78	A
ATOM	2257	CZ	PHE	A	283	50.512	−1.351	−18.358	1.00	41.31	A
ATOM	2258	CP	ILE	A	283	45.847	−2.864	−15.461	1.00	43.97	A
ATOM	2259	O	PHE	A	283	45.322	−2.460	−16.507	1.00	44.68	A
ATOM	2260	N	GLY	A	284	45.387	−2.563	−14.247	1.00	41.85	A
ATOM	2261	CA	GLY	A	284	44.268	−1.660	−14.094	1.00	38.42	A
ATOM	2262	C	GLY	A	284	44.720	−0.274	−13.738	1.00	38.04	A
ATOM	2263	O	GLY	A	284	45.916	−0.028	−13.543	1.00	39.00	A
ATOM	2264	N	PRO	A	285	43.783	0.682	−13.716	1.00	37.28	A
ATOM	2265	CD	PRO	A	285	42.395	0.535	−14.182	1.00	35.40	A
ATOM	2266	CA	PRO	A	285	44.083	2.080	−13.376	1.00	35.62	A
ATOM	2267	CB	PRO	A	285	42.728	2.765	−13.542	1.00	33.73	A
ATOM	2268	CG	PRO	A	285	42.066	1.945	−14.591	1.00	35.90	A
ATOM	2269	C	PRO	A	285	44.552	2.144	−11.926	1.00	35.06	A
ATOM	2270	O	PRO	A	285	45.542	2.785	−11.607	1.00	33.73	A
ATOM	2271	N	ILE	A	286	43.851	1.411	−11.069	1.00	36.06	A
ATOM	2272	CA	ILE	A	286	44.151	1.358	−9.651	1.00	37.31	A
ATOM	2273	CB	ILE	A	286	43.287	0.270	−8.942	1.00	39.02	A
ATOM	2274	CG2	ILE	A	286	43.304	0.494	−7.437	1.00	39.47	A
ATOM	2275	CG1	ILE	A	286	41.837	0.298	−9.453	1.00	41.72	A
ATOM	2276	CD1	ILE	A	286	41.506	−0.773	−10.527	1.00	42.91	A
ATOM	2277	C	ILE	A	286	45.627	1.005	−9.441	1.00	37.84	A
ATOM	2278	O	ILE	A	286	46.333	1.699	−8.704	1.00	37.37	A
ATOM	2279	N	PHE	A	287	46.086	−0.037	−10.135	1.00	37.55	A
ATOM	2280	CA	PHE	A	287	47.470	−0.526	−10.059	1.00	37.12	A
ATOM	2281	CB	PHE	A	287	47.866	−1.195	−11.386	1.00	35.42	A
ATOM	2282	CG	PHE	A	287	49.133	−2.013	−11.314	1.00	32.85	A
ATOM	2283	CD1	PHE	A	287	49.373	−2.869	−10.244	1.00	31.42	A
ATOM	2284	CD2	PHE	A	287	50.067	−1.964	−12.350	1.00	33.77	A
ATOM	2285	CE1	PHE	A	287	50.522	−3.673	−10.202	1.00	31.08	A
ATOM	2286	CE2	PHE	A	287	51.219	−2.764	−12.320	1.00	32.37	A
ATOM	2287	CZ	PHE	A	287	51.444	−3.621	−11.239	1.00	31.41	A
ATOM	2288	C	PHE	A	287	48.514	0.535	−9.685	1.00	37.14	A
ATOM	2289	O	PHE	A	287	49.095	0.477	−8.593	1.00	37.20	A
ATOM	2290	N	MET	A	288	48.712	1.509	−10.576	1.00	37.23	A
ATOM	2291	CA	MET	A	288	49.692	2.586	−10.374	1.00	35.99	A
ATOM	2292	CB	MET	A	288	50.290	3.017	−11.718	1.00	35.12	A
ATOM	2293	CG	MET	A	288	51.420	4.018	−11.599	1.00	35.52	A
ATOM	2294	SD	MET	A	288	52.783	3.446	−10.557	1.00	41.44	A
ATOM	2295	CE	MET	A	288	54.071	3.254	−11.755	1.00	39.91	A
ATOM	2296	C	MET	A	288	49.196	3.821	−9.606	1.00	35.08	A
ATOM	2297	O	MET	A	288	50.005	4.548	−9.028	1.00	35.29	A
ATOM	2298	N	THR	A	289	47.882	4.041	−9.570	1.00	33.54	A
ATOM	2299	CA	THR	A	289	47.355	5.202	−8.876	1.00	33.29	A
ATOM	2300	CB	THR	A	289	45.793	5.205	−8.813	1.00	31.59	A
ATOM	2301	OG1	THR	A	289	45.249	4.986	−10.117	1.00	32.39	A
ATOM	2302	CG2	THR	A	289	45.294	6.547	−8.331	1.00	28.33	A
ATOM	2303	C	THR	A	289	47.883	5.255	−7.455	1.00	35.26	A
ATOM	2304	O	THR	A	289	48.506	6.248	−7.059	1.00	37.52	A
ATOM	2305	N	ILE	A	290	47.722	4.151	−6.728	1.00	35.25	A
ATOM	2306	CA	ILE	A	290	48.150	4.058	−5.335	1.00	33.46	A
ATOM	2307	CB	ILE	A	290	47.692	2.710	−4.724	1.00	32.86	A
ATOM	2308	CG2	ILE	A	290	48.066	2.629	−3.248	1.00	35.18	A
ATOM	2309	CG1	ILE	A	290	46.174	2.581	−4.851	1.00	30.60	A
ATOM	2310	CD1	ILE	A	290	45.601	1.418	−4.100	1.00	26.49	A
ATOM	2311	C	ILE	A	290	49.629	4.399	−4.982	1.00	33.58	A
ATOM	2312	O	ILE	A	290	49.875	5.242	−4.105	1.00	33.59	A
ATOM	2313	N	PRO	A	291	50.620	3.773	−5.655	1.00	31.46	A
ATOM	2314	CD	PRO	A	291	50.546	2.704	−6.659	1.00	31.92	A
ATOM	2315	CA	PRO	A	291	52.022	4.078	−5.352	1.00	31.65	A
ATOM	2316	CB	PRO	A	291	52.797	3.122	−6.248	1.00	31.69	A
ATOM	2317	CG	PRO	A	291	51.861	2.003	−6.455	1.00	33.20	A
ATOM	2318	C	PRO	A	291	52.355	5.511	−5.709	1.00	31.27	A
ATOM	2319	O	PRO	A	291	52.990	6.228	−4.955	1.00	31.95	A
ATOM	2320	N	ALA	A	292	51.886	5.915	−6.885	1.00	31.58	A
ATOM	2321	CA	ALA	A	292	52.112	7.260	−7.381	1.00	33.06	A
ATOM	2322	CB	ALA	A	292	51.373	7.459	−8.714	1.00	31.25	A
ATOM	2323	C	ALA	A	292	51.651	8.285	−6.358	1.00	35.35	A
ATOM	2324	O	ALA	A	292	52.442	9.118	−5.892	1.00	35.03	A
ATOM	2325	N	PHE	A	293	50.392	8.167	−5.932	1.00	35.51	A
ATOM	2326	CA	PHE	A	293	49.811	9.081	−4.953	1.00	36.82	A
ATOM	2327	CB	PHE	A	293	48.287	8.938	−4.899	1.00	39.63	A
ATOM	2328	CG	PHE	A	293	47.571	9.785	−5.915	1.00	42.47	A
ATOM	2329	CD1	PHE	A	293	46.737	10.817	−5.513	1.00	43.75	A
ATOM	2330	CD2	PHE	A	293	47.754	9.571	−7.277	1.00	43.67	A
ATOM	2331	CE1	PHE	A	293	46.097	11.628	−6.454	1.00	45.19	A
ATOM	2332	CE2	PHE	A	293	47.117	10.378	−8.224	1.00	44.16	A
ATOM	2333	CZ	PHE	A	293	46.290	11.407	−7.813	1.00	42.98	A
ATOM	2335	C	PHE	A	293	50.415	8.989	−3.560	1.00	35.19	A
ATOM	2335	O	PHE	A	293	50.696	10.009	−2.933	1.00	36.47	A
ATOM	2336	N	PHE	A	294	50.625	7.775	−3.075	1.00	32.15	A
ATOM	2337	CA	PHE	A	294	51.220	7.616	−1.764	1.00	29.30	A
ATOM	2338	CB	PHE	A	294	51.427	6.138	−1.466	1.00	29.77	A
ATOM	2339	CG	PHE	A	294	52.338	5.887	−0.313	1.00	28.91	A
ATOM	2350	CD1	PHE	A	294	52.090	6.473	0.923	1.00	27.15	A
ATOM	2351	CD2	PHE	A	294	53.437	5.056	−0.459	1.00	29.06	A
ATOM	2352	CE1	PHE	A	294	52.918	6.235	2.005	1.00	28.12	A
ATOM	2353	CE2	PHE	A	294	54.272	4.810	0.617	1.00	31.35	A
ATOM	2354	CZ	PHE	A	294	54.011	5.401	1.858	1.00	29.82	A
ATOM	2355	C	PHE	A	294	52.567	8.322	−1.769	1.00	27.31	A
ATOM	2356	O	PHE	A	294	52.877	9.097	−0.869	1.00	24.65	A
ATOM	2357	N	ALA	A	295	53.355	8.035	−2.813	1.00	26.84	A
ATOM	2358	CA	ALA	A	295	54.671	8.594	−3.025	1.00	25.76	A
ATOM	2359	CB	ALA	A	295	55.230	8.097	−4.356	1.00	24.47	A
ATOM	2350	C	ALA	A	295	54.625	10.116	−3.009	1.00	27.29	A
ATOM	2351	O	ALA	A	295	55.645	10.777	−2.770	1.00	26.82	A
ATOM	2352	N	RET	A	296	53.436	10.669	−3.247	1.00	26.76	A
ATOM	2353	CA	RET	A	296	53.257	12.110	−3.242	1.00	26.52	A
ATOM	2354	C	RET	A	296	53.391	12.727	−1.855	1.00	27.41	A
ATOM	2355	O	RET	A	296	53.444	13.951	−1.727	1.00	28.93	A
ATOM	2356	CB	RET	A	296	51.926	12.489	−3.851	1.00	25.35	A
ATOM	2357	CG	RET	A	296	51.924	12.144	−5.310	1.00	24.94	A
ATOM	2358	CD	RET	A	296	50.750	12.863	−5.939	1.00	27.60	A
ATOM	2359	CE	RET	A	296	50.378	12.496	−7.370	1.00	26.89	A
ATOM	2360	NZ	RET	A	296	51.396	12.427	−8.416	1.00	26.08	A
ATOM	2361	C1	RET	A	296	62.366	6.604	−9.481	1.00	29.92	A
ATOM	2362	C2	RET	A	296	63.468	6.151	−8.555	1.00	31.18	A
ATOM	2363	C3	RET	A	296	63.157	6.427	−7.112	1.00	31.98	A
ATOM	2364	C4	RET	A	296	62.951	7.955	−6.853	1.00	33.20	A
ATOM	2365	C5	RET	A	296	62.157	8.646	−7.962	1.00	32.58	A
ATOM	2366	C6	RET	A	296	61.904	8.021	−9.146	1.00	31.44	A
ATOM	2367	C7	RET	A	296	61.137	8.661	−10.235	1.00	31.85	A
ATOM	2368	C8	RET	A	296	59.880	9.096	−9.988	1.00	29.18	A
ATOM	2369	C9	RET	A	296	58.946	9.759	−10.914	1.00	29.35	A
ATOM	2370	C10	RET	A	296	57.716	10.151	−10.568	1.00	29.07	A
ATOM	2371	C11	RET	A	296	56.723	10.823	−11.410	1.00	26.77	A
ATOM	2372	C12	RET	A	296	55.469	11.191	−11.050	1.00	24.11	A
ATOM	2373	C13	RET	A	296	54.638	11.077	−9.809	1.00	21.23	A
ATOM	2374	C14	RET	A	296	53.493	11.758	−9.672	1.00	19.10	A
ATOM	2375	C15	RET	A	296	52.635	11.658	−8.478	1.00	23.86	A
ATOM	2376	C16	RET	A	296	62.887	6.561	−10.879	1.00	28.97	A
ATOM	2377	C17	RET	A	296	61.189	5.619	−9.408	1.00	30.51	A
ATOM	2378	C18	RET	A	296	61.687	10.060	−7.597	1.00	31.58	A
ATOM	2379	C19	RET	A	296	59.509	9.945	−12.282	1.00	28.33	A
ATOM	2380	C20	RET	A	296	55.139	10.138	−8.741	1.00	15.13	A
ATOM	2381	N	THR	A	297	53.435	11.893	−0.815	1.00	27.21	A
ATOM	2382	CA	THR	A	297	53.611	12.403	0.540	1.00	26.06	A
ATOM	2383	CB	THR	A	297	53.250	11.363	1.637	1.00	24.39	A
ATOM	2384	OG1	THR	A	297	54.106	10.210	1.546	1.00	22.52	A
ATOM	2385	CG2	THR	A	297	51.803	10.965	1.515	1.00	18.35	A
ATOM	2386	C	THR	A	297	55.070	12.839	0.689	1.00	28.48	A
ATOM	2387	O	THR	A	297	55.487	13.284	1.752	1.00	30.19	A
ATOM	2388	N	SER	A	298	55.835	12.705	−0.393	1.00	29.14	A
ATOM	2389	CA	SER	A	298	57.242	13.100	−0.439	1.00	30.79	A
ATOM	2390	CB	SER	A	298	57.841	12.720	−1.790	1.00	32.38	A
ATOM	2391	OG	SER	A	298	57.047	13.218	−2.857	1.00	35.08	A
ATOM	2392	C	SER	A	298	57.414	14.603	−0.214	1.00	31.42	A
ATOM	2393	O	SER	A	298	58.480	15.062	0.232	1.00	31.99	A
ATOM	2394	N	ALA	A	299	56.364	15.361	−0.541	1.00	31.20	A
ATOM	2395	CA	ALA	A	299	56.357	16.814	−0.371	1.00	31.98	A
ATOM	2396	CB	ALA	A	299	55.321	17.453	−1.290	1.00	30.76	A
ATOM	2397	C	ALA	A	299	56.055	17.187	1.071	1.00	32.13	A
ATOM	2398	O	ALA	A	299	56.126	18.359	1.442	1.00	30.56	A
ATOM	2399	N	VAL	A	300	55.789	16.170	1.889	1.00	32.91	A
ATOM	2400	CA	VAL	A	300	55.424	16.370	3.286	1.00	33.83	A
ATOM	2401	CB	VAL	A	300	53.965	15.870	3.528	1.00	35.58	A
ATOM	2402	CG1	VAL	A	300	53.660	15.753	5.035	1.00	35.20	A
ATOM	2403	CG2	VAL	A	300	52.969	16.809	2.849	1.00	35.28	A
ATOM	2404	C	VAL	A	300	56.306	15.776	4.383	1.00	33.13	A
ATOM	2405	O	VAL	A	300	56.658	16.474	5.337	1.00	33.86	A
ATOM	2406	N	TYR	A	301	56.660	14.502	4.258	1.00	31.36	A
ATOM	2407	CA	TYR	A	301	57.418	13.835	5.306	1.00	31.19	A
ATOM	2408	CB	TYR	A	301	57.418	12.330	5.096	1.00	29.62	A
ATOM	2409	CG	TYR	A	301	58.416	11.879	4.081	1.00	28.60	A
ATOM	2410	CD1	TYR	A	301	58.102	11.871	2.720	1.00	29.02	A
ATOM	2411	CE1	TYR	A	301	59.035	11.448	1.766	1.00	29.21	A
ATOM	2412	CD2	TYR	A	301	59.681	11.457	4.474	1.00	28.45	A
ATOM	2413	CE2	TYR	A	301	60.623	11.032	3.533	1.00	29.77	A
ATOM	2414	CZ	TYR	A	301	60.298	11.030	2.180	1.00	28.64	A
ATOM	2415	OH	TYR	A	301	61.239	10.637	1.254	1.00	25.84	A
ATOM	2416	C	TYR	A	301	58.806	14.297	5.721	1.00	31.16	A
ATOM	2417	O	TYR	A	301	59.202	14.027	6.847	1.00	31.86	A
ATOM	2418	N	ASN	A	302	59.544	14.991	4.859	1.00	33.00	A
ATOM	2419	CA	ASN	A	302	60.894	15.435	5.245	1.00	33.17	A
ATOM	2420	CB	ASN	A	302	61.684	15.981	4.067	1.00	35.62	A
ATOM	2421	CG	ASN	A	302	62.491	14.924	3.388	1.00	33.91	A
ATOM	2422	OD1	ASN	A	302	63.536	14.522	3.882	1.00	32.47	A
ATOM	2423	ND2	ASN	A	302	62.007	14.455	2.246	1.00	36.38	A
ATOM	2424	C	ASN	A	302	60.973	16.406	6.405	1.00	33.25	A
ATOM	2425	O	ASN	A	302	61.763	16.192	7.316	1.00	33.35	A
ATOM	2426	N	PRO	A	303	60.245	17.539	6.352	1.00	35.12	A
ATOM	2427	CD	PRO	A	303	59.565	18.175	5.199	1.00	35.64	A
ATOM	2428	CA	PRO	A	303	60.320	18.466	7.479	1.00	35.54	A
ATOM	2429	CB	PRO	A	303	59.607	19.717	6.952	1.00	33.95	A
ATOM	2430	CG	PRO	A	303	58.713	19.198	5.873	1.00	35.15	A
ATOM	2431	C	PRO	A	303	59.665	17.884	8.750	1.00	35.46	A
ATOM	2432	O	PRO	A	303	59.948	18.315	9.871	1.00	32.89	A
ATOM	2433	N	VAL	A	304	58.845	16.855	8.565	1.00	35.02	A
ATOM	2435	CA	VAL	A	304	58.173	16.205	9.674	1.00	35.69	A
ATOM	2435	CB	VAL	A	304	57.054	15.272	9.162	1.00	35.55	A
ATOM	2436	CG1	VAL	A	304	56.943	14.002	9.998	1.00	35.37	A
ATOM	2437	CG2	VAL	A	304	55.741	16.027	9.189	1.00	35.47	A
ATOM	2438	C	VAL	A	304	59.183	15.473	10.540	1.00	35.91	A
ATOM	2439	O	VAL	A	304	59.095	15.513	11.766	1.00	37.73	A
ATOM	2440	N	ILE	A	305	60.155	14.828	9.898	1.00	37.24	A
ATOM	2441	CA	ILE	A	305	61.221	14.096	10.596	1.00	37.44	A
ATOM	2442	CB	ILE	A	305	62.002	13.190	9.599	1.00	35.65	A
ATOM	2443	CG2	ILE	A	305	63.115	12.447	10.305	1.00	36.59	A
ATOM	2444	CG1	ILE	A	305	61.055	12.169	8.971	1.00	35.71	A
ATOM	2445	CD1	ILE	A	305	61.657	11.393	7.820	1.00	35.98	A
ATOM	2446	C	ILE	A	305	62.171	15.121	11.253	1.00	38.05	A
ATOM	2447	O	ILE	A	305	62.472	15.043	12.447	1.00	38.75	A
ATOM	2448	N	TYR	A	306	62.584	16.106	10.459	1.00	37.80	A
ATOM	2449	CA	TYR	A	306	63.457	17.201	10.866	1.00	36.59	A
ATOM	2450	CB	TYR	A	306	63.408	18.265	9.766	1.00	37.57	A
ATOM	2451	CG	TYR	A	306	64.467	19.339	9.838	1.00	40.05	A
ATOM	2452	CD1	TYR	A	306	65.664	19.124	10.516	1.00	41.13	A
ATOM	2453	CE1	TYR	A	306	66.686	20.076	10.504	1.00	41.99	A
ATOM	2454	CD2	TYR	A	306	64.308	20.543	9.154	1.00	40.52	A
ATOM	2455	CE2	TYR	A	306	65.323	21.502	9.135	1.00	41.90	A
ATOM	2456	CZ	TYR	A	306	66.514	21.257	9.809	1.00	42.01	A
ATOM	2457	OH	TYR	A	306	67.549	22.170	9.753	1.00	44.09	A
ATOM	2458	C	TYR	A	306	63.006	17.840	12.182	1.00	36.04	A
ATOM	2459	O	TYR	A	306	63.757	17.888	13.152	1.00	35.12	A
ATOM	2460	N	ILE	A	307	61.771	18.352	12.180	1.00	36.69	A
ATOM	2461	CA	ILE	A	307	61.146	19.018	13.322	1.00	37.98	A
ATOM	2462	CB	ILE	A	307	59.911	19.835	12.820	1.00	37.07	A
ATOM	2463	CG2	ILE	A	307	59.415	20.787	13.891	1.00	35.40	A
ATOM	2464	CG1	ILE	A	307	60.287	20.635	11.569	1.00	36.49	A
ATOM	2465	CD1	ILE	A	307	59.106	21.191	10.798	1.00	36.94	A
ATOM	2466	C	ILE	A	307	60.696	18.020	14.410	1.00	40.01	A
ATOM	2467	O	ILE	A	307	59.788	18.304	15.204	1.00	40.89	A
ATOM	2468	N	MET	A	308	61.380	16.878	14.477	1.00	40.63	A
ATOM	2469	CA	MET	A	308	61.040	15.816	15.420	1.00	40.61	A
ATOM	2470	CB	MET	A	308	60.196	14.762	14.689	1.00	38.72	A
ATOM	2471	CG	MET	A	308	58.828	14.458	15.292	1.00	37.70	A
ATOM	2472	SD	MET	A	308	57.594	15.732	15.031	1.00	36.84	A
ATOM	2473	CE	MET	A	308	57.452	16.387	16.627	1.00	36.99	A
ATOM	2474	C	MET	A	308	62.293	15.141	15.984	1.00	42.16	A
ATOM	2475	O	MET	A	308	62.295	14.640	17.116	1.00	42.35	A
ATOM	2476	N	MET	A	309	63.358	15.121	15.173	1.00	43.48	A
ATOM	2477	CA	MET	A	309	64.610	14.490	15.540	1.00	43.93	A
ATOM	2478	CB	MET	A	309	64.993	13.429	14.502	1.00	43.90	A
ATOM	2479	CG	MET	A	309	64.016	12.276	14.356	1.00	43.56	A
ATOM	2480	SD	MET	A	309	64.735	10.975	13.319	1.00	43.66	A
ATOM	2481	CE	MET	A	309	65.505	9.951	14.561	1.00	42.13	A
ATOM	2482	C	MET	A	309	65.775	15.460	15.680	1.00	44.03	A
ATOM	2483	O	MET	A	309	66.902	15.033	15.936	1.00	45.37	A
ATOM	2484	N	ASN	A	310	65.533	16.746	15.449	1.00	43.52	A
ATOM	2485	CA	ASN	A	310	66.604	17.735	15.566	1.00	43.78	A
ATOM	2486	CB	ASN	A	310	66.866	18.446	14.236	1.00	44.61	A
ATOM	2487	CG	ASN	A	310	68.269	19.035	14.157	1.00	45.88	A
ATOM	2488	OD1	ASN	A	310	68.458	20.251	14.261	1.00	47.18	A
ATOM	2489	ND2	ASN	A	310	69.264	18.164	13.979	1.00	45.89	A
ATOM	2490	C	ASN	A	310	66.224	18.752	16.614	1.00	43.64	A
ATOM	2491	O	ASN	A	310	65.623	19.780	16.294	1.00	44.46	A
ATOM	2492	N	LYS	A	311	66.609	18.464	17.857	1.00	43.09	A
ATOM	2493	CA	LYS	A	311	66.314	19.310	19.010	1.00	42.17	A
ATOM	2494	CB	LYS	A	311	67.046	18.780	20.247	1.00	43.92	A
ATOM	2495	CG	LYS	A	311	66.562	19.377	21.554	1.00	45.89	A
ATOM	2496	CD	LYS	A	311	67.191	18.674	22.732	1.00	46.69	A
ATOM	2497	CE	LYS	A	311	66.308	18.766	23.971	1.00	48.85	A
ATOM	2498	NZ	LYS	A	311	66.144	20.159	24.447	1.00	49.39	A
ATOM	2499	C	LYS	A	311	66.644	20.783	18.783	1.00	41.32	A
ATOM	2500	O	LYS	A	311	65.940	21.668	19.284	1.00	40.00	A
ATOM	2501	N	GLN	A	312	67.705	21.041	18.018	1.00	40.16	A
ATOM	2502	CA	GLN	A	312	68.100	22.406	17.722	1.00	39.31	A
ATOM	2503	CB	GLN	A	312	69.449	22.451	17.008	1.00	41.92	A
ATOM	2504	CG	GLN	A	312	70.084	23.849	16.947	1.00	44.73	A
ATOM	2505	CD	GLN	A	312	71.357	23.894	16.099	1.00	47.96	A
ATOM	2506	OE1	GLN	A	312	72.466	23.987	16.636	1.00	49.48	A
ATOM	2507	NE2	GLN	A	312	71.201	23.829	14.767	1.00	47.92	A
ATOM	2508	C	GLN	A	312	67.035	23.064	16.861	1.00	37.93	A
ATOM	2509	O	GLN	A	312	66.544	24.127	17.205	1.00	37.66	A
ATOM	2510	N	PHE	A	313	66.623	22.405	15.784	1.00	37.01	A
ATOM	2511	CA	PHE	A	313	65.619	22.991	14.905	1.00	37.62	A
ATOM	2512	CB	PHE	A	313	65.527	22.238	13.578	1.00	38.44	A
ATOM	2513	CG	PHE	A	313	64.726	22.974	12.530	1.00	38.61	A
ATOM	2514	CD1	PHE	A	313	63.387	22.659	12.303	1.00	38.35	A
ATOM	2515	CD2	PHE	A	313	65.299	24.020	11.805	1.00	37.11	A
ATOM	2516	CE1	PHE	A	313	62.633	23.377	11.376	1.00	37.13	A
ATOM	2517	CE2	PHE	A	313	64.554	24.738	10.880	1.00	36.33	A
ATOM	2518	CZ	PHE	A	313	63.218	24.416	10.667	1.00	37.08	A
ATOM	2519	C	PHE	A	313	64.220	23.135	15.494	1.00	38.19	A
ATOM	2520	O	PHE	A	313	63.550	24.148	15.282	1.00	35.66	A
ATOM	2521	N	ARG	A	314	63.759	22.106	16.194	1.00	40.70	A
ATOM	2522	CA	ARG	A	314	62.426	22.147	16.782	1.00	43.32	A
ATOM	2523	CB	ARG	A	314	62.109	20.840	17.517	1.00	42.19	A
ATOM	2524	CG	ARG	A	314	60.786	20.853	18.262	1.00	41.53	A
ATOM	2525	CD	ARG	A	314	60.446	19.488	18.823	1.00	42.32	A
ATOM	2526	NE	ARG	A	314	61.443	18.944	19.750	1.00	41.37	A
ATOM	2527	CZ	ARG	A	314	62.358	18.032	19.421	1.00	40.72	A
ATOM	2528	NH1	ARG	A	314	62.426	17.564	18.182	1.00	40.64	A
ATOM	2529	NH2	ARG	A	314	63.158	17.529	20.358	1.00	41.92	A
ATOM	2530	C	ARG	A	314	62.264	23.357	17.711	1.00	45.16	A
ATOM	2531	O	ARG	A	314	61.387	24.180	17.500	1.00	44.33	A
ATOM	2532	N	ASN	A	315	63.141	23.462	18.704	1.00	47.23	A
ATOM	2533	CA	ASN	A	315	63.057	24.574	19.639	1.00	48.50	A
ATOM	2535	CB	ASN	A	315	64.145	24.479	20.714	1.00	48.67	A
ATOM	2535	CG	ASN	A	315	64.030	23.213	21.547	1.00	50.52	A
ATOM	2536	OD1	ASN	A	315	65.029	22.536	21.798	1.00	51.63	A
ATOM	2537	ND2	ASN	A	315	62.806	22.876	21.962	1.00	50.43	A
ATOM	2538	C	ASN	A	315	63.154	25.879	18.874	1.00	49.08	A
ATOM	2539	O	ASN	A	315	62.617	26.891	19.309	1.00	50.41	A
ATOM	2540	N	CYS	A	316	63.783	25.832	17.699	1.00	50.36	A
ATOM	2541	CA	CYS	A	316	63.932	27.017	16.857	1.00	50.62	A
ATOM	2542	CB	CYS	A	316	65.042	26.843	15.810	1.00	51.43	A
ATOM	2543	SG	CYS	A	316	66.663	27.579	16.272	1.00	52.48	A
ATOM	2544	C	CYS	A	316	62.631	27.423	16.190	1.00	50.70	A
ATOM	2545	O	CYS	A	316	62.412	28.605	15.984	1.00	51.42	A
ATOM	2546	N	MET	A	317	61.776	26.462	15.836	1.00	51.87	A
ATOM	2547	CA	MET	A	317	60.484	26.802	15.225	1.00	52.21	A
ATOM	2548	CB	MET	A	317	59.891	25.638	14.412	1.00	51.62	A
ATOM	2549	CG	MET	A	317	59.533	24.402	15.223	1.00	50.77	A
ATOM	2550	SD	MET	A	317	58.078	23.525	14.622	1.00	49.39	A
ATOM	2551	CE	MET	A	317	57.464	22.810	16.157	1.00	47.19	A
ATOM	2552	C	MET	A	317	59.510	27.235	16.328	1.00	52.69	A
ATOM	2553	O	MET	A	317	58.577	27.995	16.079	1.00	53.23	A
ATOM	2554	N	VAL	A	318	59.738	26.737	17.544	1.00	52.72	A
ATOM	2555	CA	VAL	A	318	58.911	27.081	18.696	1.00	52.59	A
ATOM	2556	CB	VAL	A	318	59.088	26.055	19.857	1.00	52.16	A
ATOM	2557	CG1	VAL	A	318	58.276	26.465	21.072	1.00	52.18	A
ATOM	2558	CG2	VAL	A	318	58.639	24.673	19.404	1.00	52.36	A
ATOM	2559	C	VAL	A	318	59.313	28.492	19.131	1.00	52.84	A
ATOM	2560	O	VAL	A	318	58.512	29.226	19.709	1.00	53.74	A
ATOM	2561	N	THR	A	319	60.556	28.866	18.831	1.00	52.88	A
ATOM	2562	CA	THR	A	319	61.068	30.199	19.145	1.00	53.14	A
ATOM	2563	CB	THR	A	319	62.636	30.259	19.109	1.00	51.52	A
ATOM	2564	OG1	THR	A	319	63.178	29.654	20.289	1.00	49.93	A
ATOM	2565	CG2	THR	A	319	63.133	31.690	19.038	1.00	49.25	A
ATOM	2566	C	THR	A	319	60.490	31.175	18.121	1.00	54.40	A
ATOM	2567	O	THR	A	319	60.211	32.329	18.442	1.00	55.98	A
ATOM	2568	N	THR	A	320	60.304	30.703	16.891	1.00	55.33	A
ATOM	2569	CA	THR	A	320	59.751	31.533	15.830	1.00	56.69	A
ATOM	2570	CB	THR	A	320	60.015	30.933	14.426	1.00	57.18	A
ATOM	2571	OG1	THR	A	320	61.409	31.037	14.116	1.00	58.92	A
ATOM	2572	CG2	THR	A	320	59.217	31.669	13.350	1.00	58.23	A
ATOM	2573	C	THR	A	320	58.259	31.707	16.043	1.00	58.00	A
ATOM	2574	O	THR	A	320	57.772	32.835	16.072	1.00	58.61	A
ATOM	2575	N	LEU	A	321	57.548	30.594	16.230	1.00	59.38	A
ATOM	2576	CA	LEU	A	321	56.098	30.618	16.439	1.00	60.65	A
ATOM	2577	CB	LEU	A	321	55.515	29.195	16.424	1.00	58.90	A
ATOM	2578	CG	LEU	A	321	55.594	28.362	15.141	1.00	56.53	A
ATOM	2579	CD1	LEU	A	321	55.014	26.981	15.393	1.00	57.01	A
ATOM	2580	CD2	LEU	A	321	54.853	29.044	14.020	1.00	55.19	A
ATOM	2581	C	LEU	A	321	55.681	31.352	17.724	1.00	62.50	A
ATOM	2582	O	LEU	A	321	54.568	31.867	17.802	1.00	62.64	A
ATOM	2583	N	CYS	A	322	56.563	31.360	18.727	1.00	64.96	A
ATOM	2584	CA	CYS	A	322	56.269	32.033	19.994	1.00	67.26	A
ATOM	2585	CB	CYS	A	322	56.788	31.223	21.195	1.00	66.18	A
ATOM	2586	SG	CYS	A	322	55.649	29.910	21.776	1.00	64.95	A
ATOM	2587	C	CYS	A	322	56.755	33.489	20.033	1.00	69.71	A
ATOM	2588	O	CYS	A	322	56.938	35.068	21.109	1.00	71.51	A
ATOM	2589	N	CYS	A	323	56.948	35.062	18.839	1.00	71.03	A
ATOM	2590	CA	CYS	A	323	57.364	35.458	18.615	1.00	71.18	A
ATOM	2591	CB	CYS	A	323	56.293	36.416	19.148	1.00	69.51	A
ATOM	2592	SG	CYS	A	323	54.657	36.152	18.429	1.00	65.90	A
ATOM	2593	C	CYS	A	323	58.760	35.937	19.039	1.00	72.67	A
ATOM	2594	O	CYS	A	323	59.030	37.146	19.032	1.00	73.38	A
ATOM	2595	N	GLY	A	324	59.649	35.005	19.375	1.00	73.68	A
ATOM	2596	CA	GLY	A	324	60.993	35.387	19.774	1.00	75.65	A
ATOM	2597	C	GLY	A	324	61.462	35.902	21.135	1.00	77.45	A
ATOM	2598	O	GLY	A	324	62.632	35.071	21.481	1.00	78.20	A
ATOM	2599	N	LYS	A	325	60.552	35.335	21.924	1.00	78.51	A
ATOM	2600	CA	LYS	A	325	60.888	33.823	23.251	1.00	80.08	A
ATOM	2601	CB	LYS	A	325	60.303	35.738	24.353	1.00	79.40	A
ATOM	2602	CG	LYS	A	325	61.067	36.075	24.555	1.00	79.38	A
ATOM	2603	CD	LYS	A	325	60.705	37.191	23.550	1.00	78.35	A
ATOM	2604	CE	LYS	A	325	61.701	38.363	23.621	1.00	77.80	A
ATOM	2605	NZ	LYS	A	325	61.356	39.539	22.764	1.00	76.46	A
ATOM	2606	C	LYS	A	325	60.405	32.365	23.385	1.00	81.61	A
ATOM	2607	O	LYS	A	325	59.621	31.895	22.559	1.00	82.41	A
ATOM	2608	N	ASN	A	326	60.872	31.650	24.410	1.00	83.47	A
ATOM	2609	CA	ASN	A	326	60.495	30.244	24.584	1.00	84.83	A
ATOM	2610	CB	ASN	A	326	61.368	29.385	23.652	1.00	84.66	A
ATOM	2611	CG	ASN	A	326	61.096	27.889	23.782	1.00	85.12	A
ATOM	2612	OD1	ASN	A	326	59.946	27.457	23.914	1.00	86.02	A
ATOM	2613	ND2	ASN	A	326	62.160	27.090	23.720	1.00	83.92	A
ATOM	2614	C	ASN	A	326	60.599	29.712	26.021	1.00	86.51	A
ATOM	2615	O	ASN	A	326	61.703	29.550	26.548	1.00	87.06	A
ATOM	2616	N	PRO	A	327	59.449	29.481	26.688	1.00	88.01	A
ATOM	2617	CD	PRO	A	327	58.187	30.156	26.330	1.00	87.56	A
ATOM	2618	CA	PRO	A	327	59.380	28.960	28.069	1.00	89.39	A
ATOM	2619	CB	PRO	A	327	57.945	29.297	28.486	1.00	88.77	A
ATOM	2620	CG	PRO	A	327	57.648	30.543	27.683	1.00	87.91	A
ATOM	2621	C	PRO	A	327	59.704	27.446	28.242	1.00	91.03	A
ATOM	2622	O	PRO	A	327	58.804	26.609	28.410	1.00	89.48	A
ATOM	2623	N	LEU	A	328	61.006	27.138	28.200	1.00	93.88	A
ATOM	2624	CA	LEU	A	328	61.614	25.792	28.351	1.00	96.36	A
ATOM	2625	CB	LEU	A	328	61.360	24.888	27.106	1.00	96.00	A
ATOM	2626	CG	LEU	A	328	60.091	24.048	26.798	1.00	95.31	A
ATOM	2627	CD1	LEU	A	328	60.096	23.602	25.325	1.00	91.86	A
ATOM	2628	CD2	LEU	A	328	59.973	22.829	27.721	1.00	93.47	A
ATOM	2629	C	LEU	A	328	63.147	26.024	28.521	1.00	98.08	A
ATOM	2630	O	LEU	A	328	63.635	27.141	28.301	1.00	98.35	A
ATOM	2631	N	GLY	A	329	63.893	24.991	28.928	1.00	99.90	A
ATOM	2632	CA	GLY	A	329	65.353	25.111	29.097	1.00	101.45	A
ATOM	2633	C	GLY	A	329	66.054	23.974	28.374	1.00	102.65	A
ATOM	2635	O	GLY	A	329	65.960	22.827	28.821	1.00	103.01	A
ATOM	2635	N	ASP	A	330	66.805	24.284	27.306	1.00	103.57	A
ATOM	2636	CA	ASP	A	330	67.481	23.252	26.490	1.00	104.00	A
ATOM	2637	CB	ASP	A	330	66.780	23.154	25.120	1.00	105.06	A
ATOM	2638	CG	ASP	A	330	65.260	23.003	25.237	1.00	106.12	A
ATOM	2639	OD1	ASP	A	330	64.787	22.050	25.897	1.00	107.06	A
ATOM	2640	OD2	ASP	A	330	64.535	23.843	24.661	1.00	107.22	A
ATOM	2641	C	ASP	A	330	69.029	23.260	26.293	1.00	103.13	A
ATOM	2642	O	ASP	A	330	69.786	23.197	27.272	1.00	103.16	A
ATOM	2643	N	ASP	A	331	69.480	23.293	25.026	1.00	101.48	A
ATOM	2644	CA	ASP	A	331	70.914	23.258	24.664	1.00	98.70	A
ATOM	2645	CB	ASP	A	331	71.198	22.037	23.780	1.00	98.64	A
ATOM	2646	CG	ASP	A	331	71.276	20.744	24.569	1.00	98.66	A
ATOM	2647	OD1	ASP	A	331	70.336	20.451	25.353	1.00	99.00	A
ATOM	2648	OD2	ASP	A	331	72.281	20.018	24.410	1.00	98.02	A
ATOM	2649	C	ASP	A	331	71.587	24.499	24.040	1.00	96.32	A
ATOM	2650	O	ASP	A	331	71.392	25.621	24.517	1.00	95.80	A
ATOM	2651	N	GLU	A	332	72.409	24.276	23.005	1.00	93.22	A
ATOM	2652	CA	GLU	A	332	73.152	25.350	22.331	1.00	90.42	A
ATOM	2653	CB	GLU	A	332	74.310	24.802	21.486	1.00	90.52	A
ATOM	2654	CG	GLU	A	332	75.274	25.912	21.027	1.00	91.65	A
ATOM	2655	CD	GLU	A	332	76.031	25.615	19.728	1.00	92.83	A
ATOM	2656	OE1	GLU	A	332	75.625	24.706	18.964	1.00	91.90	A
ATOM	2657	OE2	GLU	A	332	77.031	26.327	19.459	1.00	93.14	A
ATOM	2658	C	GLU	A	332	72.328	26.287	21.459	1.00	88.35	A
ATOM	2659	O	GLU	A	332	71.661	25.855	20.515	1.00	87.20	A
ATOM	2660	N	ALA	A	333	72.455	27.583	21.748	1.00	86.14	A
ATOM	2661	CA	ALA	A	333	71.755	28.640	21.025	1.00	83.87	A
ATOM	2662	CB	ALA	A	333	71.894	29.950	21.767	1.00	82.93	A
ATOM	2663	C	ALA	A	333	72.296	28.777	19.607	1.00	83.07	A
ATOM	2664	O	ALA	A	333	73.512	28.802	19.395	1.00	83.41	A
ATOM	2665	N	SER	A	335	71.380	28.892	18.646	1.00	81.91	A
ATOM	2666	CA	SER	A	335	71.726	29.010	17.226	1.00	80.68	A
ATOM	2667	CB	SER	A	335	71.761	27.620	16.587	1.00	81.82	A
ATOM	2668	OG	SER	A	335	72.541	26.724	17.365	1.00	84.81	A
ATOM	2669	C	SER	A	335	70.758	29.915	16.449	1.00	78.72	A
ATOM	2670	O	SER	A	335	71.136	30.546	15.465	1.00	78.28	A
ATOM	2671	N	THR	A	335	69.497	29.929	16.862	1.00	77.24	A
ATOM	2672	CA	THR	A	335	68.491	30.766	16.235	1.00	75.70	A
ATOM	2673	CB	THR	A	335	67.132	30.593	16.887	1.00	73.35	A
ATOM	2674	OG1	THR	A	335	66.403	31.814	16.753	1.00	70.56	A
ATOM	2675	CG2	THR	A	335	67.271	30.271	18.367	1.00	72.63	A
ATOM	2676	C	THR	A	335	68.875	32.182	16.529	1.00	77.98	A
ATOM	2677	O	THR	A	335	68.987	32.528	17.693	1.00	78.98	A
ATOM	2678	N	THR	A	336	69.040	33.017	15.511	1.00	81.56	A
ATOM	2679	CA	THR	A	336	69.402	35.403	15.781	1.00	85.77	A
ATOM	2680	CB	THR	A	336	69.960	35.136	14.560	1.00	86.05	A
ATOM	2681	OG1	THR	A	336	69.084	35.961	13.441	1.00	86.25	A
ATOM	2682	CG2	THR	A	336	71.351	35.623	14.243	1.00	86.82	A
ATOM	2683	C	THR	A	336	68.232	35.164	16.386	1.00	88.98	A
ATOM	2684	O	THR	A	336	67.800	36.213	15.883	1.00	89.59	A
ATOM	2685	N	VAL	A	337	67.714	35.570	17.461	1.00	92.09	A
ATOM	2686	CA	VAL	A	337	66.618	35.091	18.263	1.00	94.70	A
ATOM	2687	CB	VAL	A	337	65.273	35.425	17.913	1.00	95.24	A
ATOM	2688	CG1	VAL	A	337	64.172	35.013	18.774	1.00	95.76	A
ATOM	2689	CG2	VAL	A	337	64.942	35.642	16.441	1.00	96.48	A
ATOM	2690	C	VAL	A	337	66.965	35.818	19.735	1.00	95.46	A
ATOM	2691	O	VAL	A	337	66.960	35.748	20.557	1.00	96.74	A
ATOM	2692	N	SER	A	338	67.282	33.557	20.056	1.00	95.41	A
ATOM	2693	CA	SER	A	338	67.660	33.175	21.426	1.00	95.50	A
ATOM	2694	CB	SER	A	338	67.808	31.650	21.566	1.00	94.05	A
ATOM	2695	OG	SER	A	338	68.098	31.278	22.909	1.00	91.56	A
ATOM	2696	C	SER	A	338	68.983	33.873	21.758	1.00	96.27	A
ATOM	2697	O	SER	A	338	69.099	35.535	22.797	1.00	97.75	A
ATOM	2698	N	LYS	A	339	69.965	33.721	20.865	1.00	95.29	A
ATOM	2699	CA	LYS	A	339	71.271	35.356	21.007	1.00	93.97	A
ATOM	2700	CB	LYS	A	339	72.312	33.424	21.619	1.00	92.90	A
ATOM	2701	CG	LYS	A	339	72.822	33.882	22.991	1.00	91.78	A
ATOM	2702	CD	LYS	A	339	73.166	35.374	23.051	1.00	90.29	A
ATOM	2703	CE	LYS	A	339	74.007	35.827	21.865	1.00	91.04	A
ATOM	2704	NZ	LYS	A	339	75.095	35.863	21.544	1.00	91.11	A
ATOM	2705	C	LYS	A	339	71.752	35.854	19.656	1.00	94.33	A
ATOM	2706	O	LYS	A	339	72.322	35.105	18.859	1.00	93.20	A
ATOM	2707	N	THR	A	350	71.547	36.153	19.453	1.00	95.82	A
ATOM	2708	CA	TNR	A	350	71.893	36.870	18.232	1.00	96.50	A
ATOM	2709	CB	THR	A	350	71.988	38.395	18.493	1.00	95.39	A
ATOM	2710	OG1	THR	A	350	72.738	38.630	19.694	1.00	94.13	A
ATOM	2711	CG2	THR	A	350	70.589	39.011	18.617	1.00	94.00	A
ATOM	2712	C	THR	A	350	73.117	36.425	17.432	1.00	97.56	A
ATOM	2713	O	THR	A	350	72.989	36.156	16.232	1.00	98.37	A
ATOM	2714	N	GLU	A	351	74.281	36.283	18.070	1.00	97.50	A
ATOM	2715	CA	GLU	A	351	75.453	35.919	17.284	1.00	98.02	A
ATOM	2716	CB	GLU	A	351	76.095	37.185	16.727	1.00	100.37	A
ATOM	2717	CG	GLU	A	351	75.388	37.745	15.500	1.00	102.69	A
ATOM	2718	CD	GLU	A	351	75.537	39.245	15.386	1.00	104.03	A
ATOM	2719	OE1	GLU	A	351	76.655	39.702	15.044	1.00	104.65	A
ATOM	2720	OE2	GLU	A	351	74.536	39.959	15.648	1.00	103.84	A
ATOM	2721	C	GLU	A	351	76.541	35.964	17.755	1.00	97.29	A
ATOM	2722	O	GLU	A	351	76.552	35.496	18.887	1.00	97.04	A
ATOM	2723	N	THR	A	352	77.467	35.737	16.822	1.00	97.15	A
ATOM	2724	CA	THR	A	352	78.627	33.846	16.898	1.00	97.07	A
ATOM	2725	CB	THR	A	352	79.606	35.150	15.737	1.00	96.63	A
ATOM	2726	OG1	THR	A	352	80.816	33.397	15.893	1.00	96.58	A
ATOM	2727	CG2	THR	A	352	79.923	35.616	15.693	1.00	95.40	A
ATOM	2728	C	THR	A	352	79.435	33.620	18.170	1.00	97.91	A
ATOM	2729	O	THR	A	352	79.968	35.549	18.778	1.00	96.66	A
ATOM	2730	N	SER	A	353	79.599	32.335	18.473	1.00	99.97	A
ATOM	2731	CA	SER	A	353	80.355	31.841	19.626	1.00	102.48	A
ATOM	2732	CB	SER	A	353	79.402	31.082	20.576	1.00	101.74	A
ATOM	2733	OG	SER	A	353	78.764	29.985	19.933	1.00	101.04	A
ATOM	2735	C	SER	A	353	81.427	30.894	19.102	1.00	104.70	A
ATOM	2735	O	SER	A	353	81.966	30.067	19.842	1.00	105.05	A
ATOM	2736	N	GLN	A	354	81.751	31.050	17.820	1.00	107.65	A
ATOM	2737	CA	GLN	A	354	82.736	30.215	17.136	1.00	110.87	A
ATOM	2738	CB	GLN	A	354	82.649	30.448	15.622	1.00	111.40	A
ATOM	2739	CG	GLN	A	354	83.596	29.578	14.800	1.00	112.29	A
ATOM	2740	CD	GLN	A	354	83.544	29.882	13.317	1.00	112.55	A
ATOM	2741	OE1	GLN	A	354	82.598	30.508	12.831	1.00	112.76	A
ATOM	2742	NE2	GLN	A	354	84.563	29.431	12.584	1.00	112.24	A
ATOM	2743	C	GLN	A	354	84.187	30.372	17.582	1.00	112.38	A
ATOM	2744	O	GLN	A	354	84.638	31.472	17.909	1.00	112.63	A
ATOM	2745	N	VAL	A	355	84.910	29.252	17.571	1.00	114.55	A
ATOM	2746	CA	VAL	A	355	86.329	29.216	17.925	1.00	116.38	A
ATOM	2747	CB	VAL	A	355	86.843	27.744	18.066	1.00	116.15	A
ATOM	2748	CG1	VAL	A	355	88.360	27.712	18.256	1.00	115.78	A
ATOM	2749	CG2	VAL	A	355	86.160	27.055	19.240	1.00	115.57	A
ATOM	2750	C	VAL	A	355	87.102	29.924	16.804	1.00	117.70	A
ATOM	2751	O	VAL	A	355	87.017	29.526	15.635	1.00	117.56	A
ATOM	2752	N	ALA	A	356	87.828	30.982	17.172	1.00	118.99	A
ATOM	2753	CA	ALA	A	356	88.626	31.780	16.235	1.00	120.61	A
ATOM	2754	CB	ALA	A	356	89.536	32.750	17.012	1.00	119.21	A
ATOM	2755	C	ALA	A	356	89.456	30.919	15.264	1.00	121.61	A
ATOM	2756	O	ALA	A	356	89.856	29.797	15.597	1.00	121.84	A
ATOM	2757	N	PRO	A	357	89.711	31.435	14.044	1.00	122.73	A
ATOM	2758	CD	PRO	A	357	89.215	32.740	13.565	1.00	122.99	A
ATOM	2759	CA	PRO	A	357	90.479	30.759	12.986	1.00	123.78	A
ATOM	2760	CB	PRO	A	357	90.598	31.841	11.912	1.00	124.02	A
ATOM	2761	CG	PRO	A	357	89.312	32.587	12.066	1.00	123.26	A
ATOM	2762	C	PRO	A	357	91.855	30.213	13.392	1.00	124.05	A
ATOM	2763	O	PRO	A	357	92.381	30.546	14.459	1.00	125.55	A
ATOM	2764	N	ALA	A	358	92.413	29.363	12.526	1.00	124.08	A
ATOM	2765	CA	ALA	A	358	93.721	28.728	12.729	1.00	123.47	A
ATOM	2766	CB	ALA	A	358	94.858	29.722	12.424	1.00	123.92	A
ATOM	2767	C	ALA	A	358	93.883	28.122	14.127	1.00	123.50	A
ATOM	2768	O	ALA	A	358	92.980	27.361	14.545	1.00	124.39	A
ATOM	2769	OT	ALA	A	358	94.899	28.421	14.793	1.00	122.85	A
ATOM	2770	CA	ACE	B	0	52.528	−9.795	41.796	1.00	56.62	B
ATOM	2771	C	ACE	B	0	51.609	−8.901	40.990	1.00	56.17	B
ATOM	2772	O	ACE	B	0	50.788	−9.378	40.201	1.00	54.42	B
ATOM	2773	N	MET	B	1	51.771	−7.593	41.176	1.00	56.29	B
ATOM	2774	CA	MET	B	1	50.965	−6.595	40.485	1.00	56.64	B
ATOM	2775	CB	MET	B	1	51.127	−5.241	41.172	1.00	57.66	B
ATOM	2776	CG	MET	B	1	50.729	−5.255	42.636	1.00	57.54	B
ATOM	2777	SD	MET	B	1	49.127	−6.054	42.881	1.00	57.08	B
ATOM	2778	CE	MET	B	1	47.987	−4.658	42.691	1.00	56.81	B
ATOM	2779	C	MET	B	1	51.277	−6.469	38.989	1.00	56.84	B
ATOM	2780	O	MET	B	1	52.426	−6.239	38.600	1.00	56.03	B
ATOM	2781	N	ASN	B	2	50.233	−6.595	38.166	1.00	56.36	B
ATOM	2782	CA	ASN	B	2	50.356	−6.509	36.710	1.00	54.69	B
ATOM	2783	CB	ASN	B	2	49.064	−6.993	36.038	1.00	55.70	B
ATOM	2784	CG	ASN	B	2	48.735	−8.419	36.372	1.00	57.32	B
ATOM	2785	OD1	ASN	B	2	49.569	−9.309	36.235	1.00	57.17	B
ATOM	2786	ND2	ASN	B	2	47.498	−8.628	36.811	1.00	62.05	B
ATOM	2787	C	ASN	B	2	50.619	−5.097	36.232	1.00	53.06	B
ATOM	2788	O	ASN	B	2	50.915	−4.883	35.057	1.00	54.59	B
ATOM	2789	N	GLY	B	3	50.464	−4.132	37.127	1.00	49.84	B
ATOM	2790	CA	GLY	B	3	50.705	−2.754	36.760	1.00	47.67	B
ATOM	2791	C	GLY	B	3	51.379	−2.053	37.905	1.00	46.92	B
ATOM	2792	O	GLY	B	3	51.728	−2.683	38.900	1.00	46.96	B
ATOM	2793	N	THR	B	4	51.593	−0.753	37.763	1.00	46.69	B
ATOM	2794	CA	THR	B	4	52.218	0.015	38.827	1.00	47.21	B
ATOM	2795	CB	THR	B	4	53.689	0.330	38.504	1.00	44.95	B
ATOM	2796	OG1	THR	B	4	54.367	−0.885	38.170	1.00	44.68	B
ATOM	2797	CG2	THR	B	4	54.379	0.935	39.704	1.00	44.31	B
ATOM	2798	C	THR	B	4	51.420	1.295	39.117	1.00	49.22	B
ATOM	2799	O	THR	B	4	51.407	2.235	38.319	1.00	50.55	B
ATOM	2800	N	GLU	B	5	50.706	1.291	40.242	1.00	49.95	B
ATOM	2801	CA	GLU	B	5	49.899	2.433	40.656	1.00	50.04	B
ATOM	2802	CB	GLU	B	5	48.656	1.966	41.433	1.00	52.37	B
ATOM	2803	CG	GLU	B	5	47.690	3.097	41.851	1.00	56.21	B
ATOM	2804	CD	GLU	B	5	46.372	2.608	42.482	1.00	58.67	B
ATOM	2805	OE1	GLU	B	5	46.172	1.376	42.633	1.00	58.88	B
ATOM	2806	OE2	GLU	B	5	45.526	3.474	42.820	1.00	60.22	B
ATOM	2807	C	GLU	B	5	50.689	3.454	41.481	1.00	48.61	B
ATOM	2808	O	GLU	B	5	51.524	3.116	42.323	1.00	47.10	B
ATOM	2809	N	GLY	B	6	50.471	4.715	41.159	1.00	47.47	B
ATOM	2810	CA	GLY	B	6	51.116	5.777	41.886	1.00	47.49	B
ATOM	2811	C	GLY	B	6	49.991	6.556	42.522	1.00	47.93	B
ATOM	2812	O	GLY	B	6	48.811	6.249	42.302	1.00	48.43	B
ATOM	2813	N	PRO	B	7	50.313	7.560	43.337	1.00	47.40	B
ATOM	2814	CD	PRO	B	7	51.641	7.998	43.789	1.00	47.05	B
ATOM	2815	CA	PRO	B	7	49.248	8.338	43.969	1.00	48.37	B
ATOM	2816	CB	PRO	B	7	50.020	9.246	44.926	1.00	47.93	B
ATOM	2817	CG	PRO	B	7	51.364	9.384	44.266	1.00	48.00	B
ATOM	2818	C	PRO	B	7	48.418	9.125	42.946	1.00	48.85	B
ATOM	2819	O	PRO	B	7	47.276	9.499	43.223	1.00	49.90	B
ATOM	2820	N	ASN	B	8	48.971	9.293	41.743	1.00	48.30	B
ATOM	2821	CA	ASN	B	8	48.312	10.037	40.670	1.00	46.71	B
ATOM	2822	CB	ASN	B	8	48.753	11.516	40.708	1.00	46.51	B
ATOM	2823	CG	ASN	B	8	50.251	11.711	40.441	1.00	47.21	B
ATOM	2824	OD1	ASN	B	8	50.653	12.714	39.853	1.00	47.27	B
ATOM	2825	ND2	ASN	B	8	51.076	10.767	40.889	1.00	48.76	B
ATOM	2826	C	ASN	B	8	48.474	9.452	39.248	1.00	45.89	B
ATOM	2827	O	ASN	B	8	48.033	10.057	38.266	1.00	45.00	B
ATOM	2828	N	PHE	B	9	49.066	8.265	39.140	1.00	44.76	B
ATOM	2829	CA	PHE	B	9	49.263	7.627	37.841	1.00	42.84	B
ATOM	2830	CB	PHE	B	9	50.691	7.874	37.331	1.00	41.93	B
ATOM	2831	CG	PHE	B	9	51.772	7.295	38.207	1.00	41.23	B
ATOM	2832	CD1	PHE	B	9	52.190	5.975	38.045	1.00	41.40	B
ATOM	2833	CD2	PHE	B	9	52.375	8.068	39.194	1.00	41.08	B
ATOM	2835	CE1	PHE	B	9	53.191	5.435	38.857	1.00	42.03	B
ATOM	2835	CE2	PHE	B	9	53.377	7.535	40.011	1.00	40.42	B
ATOM	2836	CZ	PHE	B	9	53.785	6.218	39.845	1.00	40.11	B
ATOM	2837	C	PHE	B	9	48.991	6.133	37.909	1.00	42.97	B
ATOM	2838	O	PHE	B	9	48.629	5.619	38.960	1.00	44.24	B
ATOM	2839	N	TYR	B	10	49.133	5.452	36.773	1.00	43.02	B
ATOM	2840	CA	TYR	B	10	48.950	4.005	36.694	1.00	42.81	B
ATOM	2841	CB	TYR	B	10	47.472	3.635	36.747	1.00	42.77	B
ATOM	2842	CG	TYR	B	10	47.237	2.148	36.883	1.00	46.21	B
ATOM	2843	CD1	TYR	B	10	46.962	1.571	38.123	1.00	48.04	B
ATOM	2844	CE1	TYR	B	10	46.752	0.196	38.253	1.00	49.11	B
ATOM	2845	CD2	TYR	B	10	47.297	1.312	35.774	1.00	48.04	B
ATOM	2846	CE2	TYR	B	10	47.092	−0.061	35.891	1.00	49.88	B
ATOM	2847	CZ	TYR	B	10	46.822	−0.613	37.128	1.00	50.02	B
ATOM	2848	OH	TYR	B	10	46.637	−1.975	37.222	1.00	50.51	B
ATOM	2849	C	TYR	B	10	49.592	3.464	35.415	1.00	43.15	B
ATOM	2850	O	TYR	B	10	48.971	3.483	35.356	1.00	43.52	B
ATOM	2851	N	VAL	B	11	50.838	2.997	35.524	1.00	42.85	B
ATOM	2852	CA	VAL	B	11	51.597	2.450	35.387	1.00	44.43	B
ATOM	2853	CB	VAL	B	11	53.155	2.599	35.614	1.00	43.59	B
ATOM	2854	CG1	VAL	B	11	53.937	2.153	33.389	1.00	41.18	B
ATOM	2855	CG2	VAL	B	11	53.518	4.031	35.957	1.00	42.85	B
ATOM	2856	C	VAL	B	11	51.259	0.961	35.131	1.00	45.66	B
ATOM	2857	O	VAL	B	11	51.386	0.128	35.033	1.00	46.74	B
ATOM	2858	N	PRO	B	12	50.829	0.613	32.893	1.00	46.01	B
ATOM	2859	CD	PRO	B	12	50.611	1.536	31.767	1.00	46.47	B
ATOM	2860	CA	PRO	B	12	50.472	−0.757	32.493	1.00	44.73	B
ATOM	2861	CB	PRO	B	12	49.850	−0.561	31.109	1.00	44.56	B
ATOM	2862	CG	PRO	B	12	49.476	0.879	31.063	1.00	46.00	B
ATOM	2863	C	PRO	B	12	51.731	−1.600	32.369	1.00	44.72	B
ATOM	2864	O	PRO	B	12	52.005	−2.163	31.310	1.00	45.60	B
ATOM	2865	N	PHE	B	13	52.506	−1.666	33.443	1.00	44.06	B
ATOM	2866	CA	PHE	B	13	53.751	−2.414	33.431	1.00	44.50	B
ATOM	2867	CB	PHE	B	13	54.861	−1.552	32.808	1.00	43.88	B
ATOM	2868	CG	PHE	B	13	55.895	−2.329	32.022	1.00	41.83	B
ATOM	2869	CD1	PHE	B	13	57.173	−2.536	32.539	1.00	41.60	B
ATOM	2870	CD2	PHE	B	13	55.606	−2.807	30.747	1.00	40.40	B
ATOM	2871	CE1	PHE	B	13	58.149	−3.205	31.795	1.00	41.21	B
ATOM	2872	CE2	PHE	B	13	56.575	−3.476	29.996	1.00	40.71	B
ATOM	2873	CZ	PHE	B	13	57.849	−3.674	30.523	1.00	39.93	B
ATOM	2874	C	PHE	B	13	54.100	−2.743	35.870	1.00	45.08	B
ATOM	2875	O	PHE	B	13	54.031	−1.881	35.745	1.00	44.21	B
ATOM	2876	N	SER	B	14	54.457	−4.001	35.105	1.00	46.27	B
ATOM	2877	CA	SER	B	14	54.823	−4.462	36.432	1.00	47.36	B
ATOM	2878	CB	SER	B	14	54.866	−5.982	36.477	1.00	48.14	B
ATOM	2879	OG	SER	B	14	55.322	−6.425	37.742	1.00	50.05	B
ATOM	2880	C	SER	B	14	56.167	−3.919	36.862	1.00	48.44	B
ATOM	2881	O	SER	B	14	57.145	−3.957	36.111	1.00	47.74	B
ATOM	2882	N	ASN	B	15	56.213	−3.444	38.096	1.00	50.73	B
ATOM	2883	CA	ASN	B	15	57.438	−2.904	38.635	1.00	53.70	B
ATOM	2884	CB	ASN	B	15	57.141	−1.751	39.564	1.00	53.94	B
ATOM	2885	CG	ASN	B	15	58.350	−0.922	39.798	1.00	56.30	B
ATOM	2886	OD1	ASN	B	15	59.354	−1.068	39.109	1.00	55.48	B
ATOM	2887	ND2	ASN	B	15	58.278	−0.052	40.781	1.00	61.35	B
ATOM	2888	C	ASN	B	15	58.253	−3.974	39.357	1.00	55.76	B
ATOM	2889	O	ASN	B	15	58.927	−3.702	40.360	1.00	56.06	B
ATOM	2890	N	LYS	B	16	58.181	−5.190	38.815	1.00	57.67	B
ATOM	2891	CA	LYS	B	16	58.882	−6.367	39.330	1.00	58.60	B
ATOM	2892	CB	LYS	B	16	58.385	−7.608	38.584	1.00	59.76	B
ATOM	2893	CG	LYS	B	16	58.948	−8.937	39.062	1.00	62.07	B
ATOM	2894	CD	LYS	B	16	59.570	−9.727	37.904	1.00	65.24	B
ATOM	2895	CE	LYS	B	16	58.690	−9.726	36.639	1.00	66.08	B
ATOM	2896	NZ	LYS	B	16	57.356	−10.356	36.837	1.00	66.16	B
ATOM	2897	C	LYS	B	16	60.377	−6.206	39.100	1.00	57.83	B
ATOM	2898	O	LYS	B	16	61.200	−6.799	39.795	1.00	58.83	B
ATOM	2899	N	THR	B	17	60.705	−5.373	38.123	1.00	56.97	B
ATOM	2900	CA	THR	B	17	62.074	−5.096	37.735	1.00	57.19	B
ATOM	2901	CB	THR	B	17	62.162	−5.069	36.211	1.00	58.29	B
ATOM	2902	OG1	THR	B	17	60.932	−4.552	35.675	1.00	59.73	B
ATOM	2903	CG2	THR	B	17	62.382	−6.468	35.680	1.00	59.13	B
ATOM	2904	C	THR	B	17	62.642	−3.794	38.305	1.00	57.36	B
ATOM	2905	O	THR	B	17	63.814	−3.469	38.068	1.00	56.18	B
ATOM	2906	N	GLY	B	18	61.808	−3.059	39.049	1.00	57.45	B
ATOM	2907	CA	GLY	B	18	62.215	−1.793	39.648	1.00	55.33	B
ATOM	2908	C	GLY	B	18	62.690	−0.808	38.603	1.00	53.99	B
ATOM	2909	O	GLY	B	18	63.593	−0.011	38.852	1.00	54.42	B
ATOM	2910	N	VAL	B	19	62.064	−0.873	37.431	1.00	52.46	B
ATOM	2911	CA	VAL	B	19	62.411	−0.030	36.296	1.00	50.97	B
ATOM	2912	CB	VAL	B	19	62.702	−0.903	35.063	1.00	50.14	B
ATOM	2913	CG1	VAL	B	19	61.453	−1.675	35.664	1.00	51.27	B
ATOM	2914	CG2	VAL	B	19	63.190	−0.059	33.914	1.00	51.15	B
ATOM	2915	C	VAL	B	19	61.296	0.959	35.962	1.00	50.47	B
ATOM	2916	O	VAL	B	19	61.519	1.944	35.248	1.00	51.39	B
ATOM	2917	N	VAL	B	20	60.096	0.687	36.472	1.00	48.86	B
ATOM	2918	CA	VAL	B	20	58.941	1.553	36.232	1.00	46.66	B
ATOM	2919	CB	VAL	B	20	57.616	0.881	36.665	1.00	46.82	B
ATOM	2920	CG1	VAL	B	20	56.449	1.855	36.524	1.00	44.47	B
ATOM	2921	CG2	VAL	B	20	57.371	−0.375	35.836	1.00	46.66	B
ATOM	2922	C	VAL	B	20	59.078	2.876	36.964	1.00	45.36	B
ATOM	2923	O	VAL	B	20	59.219	2.906	38.184	1.00	44.95	B
ATOM	2924	N	ARG	B	21	59.049	3.961	36.196	1.00	44.38	B
ATOM	2925	CA	ARG	B	21	59.156	5.317	36.726	1.00	43.70	B
ATOM	2926	CB	ARG	B	21	60.395	6.011	36.133	1.00	45.42	B
ATOM	2927	CG	ARG	B	21	61.480	6.396	37.159	1.00	48.26	B
ATOM	2928	CD	ARG	B	21	62.522	5.303	37.378	1.00	50.22	B
ATOM	2929	NE	ARG	B	21	61.932	4.037	37.809	1.00	51.58	B
ATOM	2930	CZ	ARG	B	21	62.459	3.230	38.726	1.00	51.28	B
ATOM	2931	NH1	ARG	B	21	63.600	3.556	39.325	1.00	50.75	B
ATOM	2932	NH2	ARG	B	21	61.852	2.086	39.026	1.00	50.33	B
ATOM	2933	C	ARG	B	21	57.872	6.111	36.404	1.00	42.26	B
ATOM	2935	O	ARG	B	21	57.160	5.783	35.449	1.00	40.96	B
ATOM	2935	N	SER	B	22	57.578	7.137	37.208	1.00	40.62	B
ATOM	2936	CA	SER	B	22	56.382	7.974	37.029	1.00	41.61	B
ATOM	2937	CB	SER	B	22	56.277	8.994	38.169	1.00	41.89	B
ATOM	2938	OG	SER	B	22	55.163	9.868	38.014	1.00	40.44	B
ATOM	2939	C	SER	B	22	56.315	8.714	35.689	1.00	43.45	B
ATOM	2940	O	SER	B	22	57.330	9.230	35.213	1.00	43.99	B
ATOM	2941	N	PRO	B	23	55.106	8.797	35.075	1.00	44.21	B
ATOM	2942	CD	PRO	B	23	53.844	8.207	35.551	1.00	43.55	B
ATOM	2943	CA	PRO	B	23	54.885	9.477	33.791	1.00	44.13	B
ATOM	2944	CB	PRO	B	23	53.411	9.189	33.495	1.00	42.97	B
ATOM	2945	CG	PRO	B	23	53.117	7.966	35.267	1.00	42.67	B
ATOM	2946	C	PRO	B	23	55.081	10.978	33.955	1.00	45.22	B
ATOM	2947	O	PRO	B	23	55.017	11.727	32.983	1.00	45.47	B
ATOM	2948	N	PHE	B	24	55.306	11.401	35.199	1.00	45.50	B
ATOM	2949	CA	PHE	B	24	55.490	12.801	35.537	1.00	46.93	B
ATOM	2950	CB	PHE	B	24	54.558	13.159	36.692	1.00	44.61	B
ATOM	2951	CG	PHE	B	24	53.094	13.010	36.362	1.00	44.39	B
ATOM	2952	CD1	PHE	B	24	52.508	13.779	35.358	1.00	43.60	B
ATOM	2953	CD2	PHE	B	24	52.298	12.096	37.045	1.00	43.97	B
ATOM	2954	CE1	PHE	B	24	51.149	13.638	35.039	1.00	41.94	B
ATOM	2955	CE2	PHE	B	24	50.938	11.951	36.729	1.00	42.77	B
ATOM	2956	CZ	PHE	B	24	50.368	12.724	35.724	1.00	41.56	B
ATOM	2957	C	PHE	B	24	56.929	13.198	35.882	1.00	50.05	B
ATOM	2958	O	PHE	B	24	57.294	14.375	35.775	1.00	49.62	B
ATOM	2959	N	GLN	B	25	57.751	12.217	36.261	1.00	53.32	B
ATOM	2960	CA	GLN	B	25	59.149	12.467	36.646	1.00	55.67	B
ATOM	2961	CB	GLN	B	25	59.462	11.798	37.996	1.00	58.60	B
ATOM	2962	CG	GLN	B	25	58.972	12.555	39.229	1.00	61.68	B
ATOM	2963	CD	GLN	B	25	57.958	11.769	40.043	1.00	64.32	B
ATOM	2964	OE1	GLN	B	25	56.941	12.317	40.482	1.00	65.08	B
ATOM	2965	NE2	GLN	B	25	58.233	10.477	40.257	1.00	65.77	B
ATOM	2966	C	GLN	B	25	60.231	12.062	35.643	1.00	55.07	B
ATOM	2967	O	GLN	B	25	61.258	12.739	35.514	1.00	55.13	B
ATOM	2968	N	ALA	B	26	60.023	10.938	35.969	1.00	53.95	B
ATOM	2969	CA	ALA	B	26	61.003	10.454	35.013	1.00	53.46	B
ATOM	2970	CB	ALA	B	26	61.935	9.456	35.691	1.00	53.87	B
ATOM	2971	C	ALA	B	26	60.351	9.813	32.808	1.00	52.28	B
ATOM	2972	O	ALA	B	26	59.217	9.324	32.896	1.00	52.55	B
ATOM	2973	N	PRO	B	27	61.019	9.845	31.650	1.00	51.44	B
ATOM	2974	CD	PRO	B	27	62.250	10.589	31.338	1.00	51.28	B
ATOM	2975	CA	PRO	B	27	60.457	9.244	30.440	1.00	50.95	B
ATOM	2976	CB	PRO	B	27	61.546	9.499	29.382	1.00	51.43	B
ATOM	2977	CG	PRO	B	27	62.784	9.817	30.173	1.00	52.04	B
ATOM	2978	C	PRO	B	27	60.096	7.762	30.583	1.00	49.53	B
ATOM	2979	O	PRO	B	27	60.773	7.008	31.285	1.00	48.39	B
ATOM	2980	N	GLN	B	28	58.978	7.389	29.958	1.00	48.35	B
ATOM	2981	CA	GLN	B	28	58.462	6.025	29.972	1.00	47.77	B
ATOM	2982	CB	GLN	B	28	56.935	6.038	29.905	1.00	44.02	B
ATOM	2983	CG	GLN	B	28	56.268	6.722	31.065	1.00	40.76	B
ATOM	2984	CD	GLN	B	28	56.652	6.109	32.383	1.00	40.11	B
ATOM	2985	OE1	GLN	B	28	57.779	6.256	32.837	1.00	40.38	B
ATOM	2986	NE2	GLN	B	28	55.718	5.416	33.009	1.00	41.93	B
ATOM	2987	C	GLN	B	28	59.005	5.218	28.804	1.00	48.87	B
ATOM	2988	O	GLN	B	28	58.287	4.401	28.224	1.00	48.93	B
ATOM	2989	N	TYR	B	29	60.278	5.426	28.482	1.00	50.89	B
ATOM	2990	CA	TYR	B	29	60.915	4.727	27.369	1.00	53.12	B
ATOM	2991	CB	TYR	B	29	62.254	5.385	26.998	1.00	55.23	B
ATOM	2992	CG	TYR	B	29	62.126	6.747	26.335	1.00	57.61	B
ATOM	2993	CD1	TYR	B	29	61.132	6.998	25.390	1.00	59.10	B
ATOM	2994	CE1	TYR	B	29	61.002	8.254	24.778	1.00	61.35	B
ATOM	2995	CD2	TYR	B	29	62.996	7.787	26.658	1.00	59.95	B
ATOM	2996	CE2	TYR	B	29	62.875	9.052	26.051	1.00	62.31	B
ATOM	2997	CZ	TYR	B	29	61.876	9.275	25.112	1.00	62.09	B
ATOM	2998	OH	TYR	B	29	61.755	10.505	24.499	1.00	62.36	B
ATOM	2999	C	TYR	B	29	61.108	3.236	27.623	1.00	54.08	B
ATOM	3000	O	TYR	B	29	61.603	2.520	26.748	1.00	54.62	B
ATOM	3001	N	TYR	B	30	60.705	2.773	28.809	1.00	54.30	B
ATOM	3002	CA	TYR	B	30	60.818	1.357	29.178	1.00	54.04	B
ATOM	3003	CB	TYR	B	30	61.160	1.221	30.670	1.00	52.99	B
ATOM	3004	CG	TYR	B	30	60.078	1.738	31.578	1.00	50.95	B
ATOM	3005	CD1	TYR	B	30	58.980	0.939	31.902	1.00	50.37	B
ATOM	3006	CE1	TYR	B	30	57.941	1.431	32.666	1.00	50.74	B
ATOM	3007	CD2	TYR	B	30	60.111	3.044	32.054	1.00	49.32	B
ATOM	3008	CE2	TYR	B	30	59.075	3.545	32.822	1.00	49.99	B
ATOM	3009	CZ	TYR	B	30	57.991	2.735	33.122	1.00	50.78	B
ATOM	3010	OH	TYR	B	30	56.943	3.223	33.865	1.00	52.47	B
ATOM	3011	C	TYR	B	30	59.550	0.543	28.843	1.00	54.25	B
ATOM	3012	O	TYR	B	30	59.496	−0.662	29.096	1.00	53.09	B
ATOM	3013	N	LEU	B	31	58.525	1.222	28.320	1.00	55.52	B
ATOM	3014	CA	LEU	B	31	57.262	0.586	27.931	1.00	56.72	B
ATOM	3015	CB	LEU	B	31	56.102	1.586	28.035	1.00	54.35	B
ATOM	3016	CG	LEU	B	31	55.758	2.183	29.399	1.00	52.39	B
ATOM	3017	CD1	LEU	B	31	54.478	2.974	29.314	1.00	50.81	B
ATOM	3018	CD2	LEU	B	31	55.586	1.080	30.398	1.00	52.70	B
ATOM	3019	C	LEU	B	31	57.367	0.077	26.489	1.00	58.94	B
ATOM	3020	O	LEU	B	31	56.976	−1.053	26.182	1.00	58.91	B
ATOM	3021	N	ALA	B	32	57.914	0.939	25.628	1.00	61.55	B
ATOM	3022	CA	ALA	B	32	58.131	0.679	24.201	1.00	63.06	B
ATOM	3023	CB	ALA	B	32	56.906	1.087	23.415	1.00	63.21	B
ATOM	3024	C	ALA	B	32	59.361	1.480	23.721	1.00	64.31	B
ATOM	3025	O	ALA	B	32	59.738	2.472	24.352	1.00	64.84	B
ATOM	3026	N	GLU	B	33	59.973	1.068	22.606	1.00	64.73	B
ATOM	3027	CA	GLU	B	33	61.168	1.749	22.072	1.00	65.17	B
ATOM	3028	CB	GLU	B	33	61.681	1.048	20.801	1.00	67.02	B
ATOM	3029	CG	GLU	B	33	62.494	−0.233	21.023	1.00	69.78	B
ATOM	3030	CD	GLU	B	33	61.641	−1.496	21.031	1.00	72.86	B
ATOM	3031	OE1	GLU	B	33	61.459	−2.082	22.122	1.00	73.06	B
ATOM	3032	OE2	GLU	B	33	61.166	−1.911	19.943	1.00	74.78	B
ATOM	3033	C	GLU	B	33	60.979	3.251	21.790	1.00	63.68	B
ATOM	3035	O	GLU	B	33	59.850	3.735	21.714	1.00	64.86	B
ATOM	3035	N	PRO	B	35	62.086	4.017	21.693	1.00	61.73	B
ATOM	3036	CD	PRO	B	35	63.442	3.664	22.150	1.00	60.81	B
ATOM	3037	CA	PRO	B	35	62.001	5.460	21.422	1.00	60.44	B
ATOM	3038	CB	PRO	B	35	63.446	5.933	21.625	1.00	60.44	B
ATOM	3039	CG	PRO	B	35	63.961	4.991	22.659	1.00	59.98	B
ATOM	3040	C	PRO	B	35	61.474	5.839	20.028	1.00	58.64	B
ATOM	3041	O	PRO	B	35	61.189	7.016	19.778	1.00	58.02	B
ATOM	3042	N	TRP	B	35	61.367	4.860	19.124	1.00	56.22	B
ATOM	3043	CA	TRP	B	35	60.860	5.132	17.775	1.00	55.17	B
ATOM	3044	CB	TRP	B	35	61.328	4.076	16.737	1.00	54.01	B
ATOM	3045	CG	TRP	B	35	60.612	2.726	16.753	1.00	53.08	B
ATOM	3046	CD2	TRP	B	35	59.380	2.380	16.086	1.00	52.89	B
ATOM	3047	CE2	TRP	B	35	59.089	1.039	16.417	1.00	52.45	B
ATOM	3048	CE3	TRP	B	35	58.494	3.077	15.248	1.00	53.64	B
ATOM	3049	CD1	TRP	B	35	61.002	1.606	17.423	1.00	52.53	B
ATOM	3050	NE1	TRP	B	35	60.094	0.592	17.232	1.00	52.19	B
ATOM	3051	CZ2	TRP	B	35	57.945	0.375	15.943	1.00	52.90	B
ATOM	3052	CZ3	TRP	B	35	57.354	2.415	14.775	1.00	53.17	B
ATOM	3053	CH2	TRP	B	35	57.095	1.078	15.126	1.00	53.05	B
ATOM	3054	C	TRP	B	35	59.336	5.250	17.782	1.00	54.39	B
ATOM	3055	O	TRP	B	35	58.756	6.006	16.996	1.00	55.11	B
ATOM	3056	N	GLN	B	36	58.698	4.526	18.698	1.00	52.03	B
ATOM	3057	CA	GLN	B	36	57.247	4.529	18.818	1.00	50.05	B
ATOM	3058	CB	GLN	B	36	56.790	3.330	19.664	1.00	51.17	B
ATOM	3059	CG	GLN	B	36	57.586	2.055	19.354	1.00	52.08	B
ATOM	3060	CD	GLN	B	36	56.811	0.769	19.560	1.00	53.58	B
ATOM	3061	OE1	GLN	B	36	57.045	0.039	20.522	1.00	54.93	B
ATOM	3062	NE2	GLN	B	36	55.919	0.457	18.625	1.00	54.05	B
ATOM	3063	C	GLN	B	36	56.748	5.861	19.385	1.00	48.52	B
ATOM	3064	O	GLN	B	36	55.633	6.281	19.093	1.00	47.47	B
ATOM	3065	N	PHE	B	37	57.599	6.532	20.161	1.00	48.07	B
ATOM	3066	CA	PHE	B	37	57.286	7.839	20.761	1.00	47.14	B
ATOM	3067	CB	PHE	B	37	58.189	8.126	21.963	1.00	45.09	B
ATOM	3068	CG	PHE	B	37	57.759	7.435	23.208	1.00	42.17	B
ATOM	3069	CD1	PHE	B	37	56.976	8.092	24.140	1.00	42.47	B
ATOM	3070	CD2	PHE	B	37	58.122	6.123	23.445	1.00	41.83	B
ATOM	3071	CE1	PHE	B	37	56.561	7.457	25.294	1.00	42.78	B
ATOM	3072	CE2	PHE	B	37	57.712	5.475	24.598	1.00	42.89	B
ATOM	3073	CZ	PHE	B	37	56.929	6.145	25.527	1.00	42.86	B
ATOM	3074	C	PHE	B	37	57.438	8.968	19.753	1.00	46.95	B
ATOM	3075	O	PHE	B	37	56.563	9.831	19.635	1.00	47.86	B
ATOM	3076	N	SER	B	38	58.576	8.987	19.066	1.00	46.08	B
ATOM	3077	CA	SER	B	38	58.820	10.002	18.057	1.00	45.36	B
ATOM	3078	CB	SER	B	38	60.263	9.926	17.555	1.00	45.66	B
ATOM	3079	OG	SER	B	38	61.139	10.589	18.453	1.00	46.91	B
ATOM	3080	C	SER	B	38	57.821	9.805	16.922	1.00	44.05	B
ATOM	3081	O	SER	B	38	57.476	10.745	16.215	1.00	43.74	B
ATOM	3082	N	MET	B	39	57.317	8.583	16.796	1.00	43.22	B
ATOM	3083	CA	MET	B	39	56.339	8.252	15.769	1.00	44.60	B
ATOM	3084	CB	MET	B	39	56.304	6.728	15.581	1.00	46.93	B
ATOM	3085	CG	MET	B	39	55.816	6.241	14.226	1.00	50.25	B
ATOM	3086	SD	MET	B	39	56.823	6.850	12.855	1.00	53.99	B
ATOM	3087	CE	MET	B	39	55.502	7.271	11.628	1.00	53.21	B
ATOM	3088	C	MET	B	39	54.947	8.811	16.166	1.00	43.67	B
ATOM	3089	O	MET	B	39	54.100	9.074	15.304	1.00	42.24	B
ATOM	3090	N	LEU	B	40	54.720	8.957	17.475	1.00	42.15	B
ATOM	3091	CA	LEU	B	40	53.476	9.506	18.016	1.00	39.42	B
ATOM	3092	CB	LEU	B	40	53.296	9.119	19.486	1.00	37.40	B
ATOM	3093	CG	LEU	B	40	53.068	7.669	19.906	1.00	35.78	B
ATOM	3094	CD1	LEU	B	40	52.869	7.623	21.413	1.00	35.54	B
ATOM	3095	CD2	LEU	B	40	51.857	7.087	19.200	1.00	35.18	B
ATOM	3096	C	LEU	B	40	53.585	11.025	17.926	1.00	39.67	B
ATOM	3097	O	LEU	B	40	52.616	11.716	17.611	1.00	38.83	B
ATOM	3098	N	ALA	B	41	54.776	11.535	18.231	1.00	39.27	B
ATOM	3099	CA	ALA	B	41	55.046	12.960	18.167	1.00	39.60	B
ATOM	3100	CB	ALA	B	41	56.433	13.243	18.718	1.00	38.44	B
ATOM	3101	C	ALA	B	41	54.923	13.453	16.713	1.00	40.46	B
ATOM	3102	O	ALA	B	41	54.617	14.627	16.478	1.00	41.22	B
ATOM	3103	N	ALA	B	42	55.152	12.545	15.753	1.00	39.53	B
ATOM	3104	CA	ALA	B	42	55.066	12.837	14.315	1.00	37.70	B
ATOM	3105	CB	ALA	B	42	55.744	11.736	13.510	1.00	35.72	B
ATOM	3106	C	ALA	B	42	53.605	12.939	13.912	1.00	38.00	B
ATOM	3107	O	ALA	B	42	53.208	13.835	13.168	1.00	37.79	B
ATOM	3108	N	TYR	B	43	52.820	11.988	14.408	1.00	38.90	B
ATOM	3109	CA	TYR	B	43	51.383	11.912	14.164	1.00	39.12	B
ATOM	3110	CB	TYR	B	43	50.821	10.682	14.900	1.00	37.93	B
ATOM	3111	CG	TYR	B	43	49.312	10.472	14.881	1.00	37.01	B
ATOM	3112	CD1	TYR	B	43	48.618	10.236	16.066	1.00	36.07	B
ATOM	3113	CE1	TYR	B	43	47.258	9.963	16.070	1.00	36.64	B
ATOM	3114	CD2	TYR	B	43	48.592	10.438	13.684	1.00	37.92	B
ATOM	3115	CE2	TYR	B	43	47.216	10.163	13.678	1.00	38.14	B
ATOM	3116	CZ	TYR	B	43	46.561	9.925	14.880	1.00	38.00	B
ATOM	3117	OH	TYR	B	43	45.211	9.645	14.899	1.00	38.37	B
ATOM	3118	C	TYR	B	43	50.745	13.195	14.682	1.00	39.72	B
ATOM	3119	O	TYR	B	43	50.052	13.901	13.943	1.00	38.83	B
ATOM	3120	N	MET	B	44	51.038	13.524	15.938	1.00	40.88	B
ATOM	3121	CA	MET	B	44	50.483	14.721	16.552	1.00	42.90	B
ATOM	3122	CB	MET	B	44	50.847	14.802	18.031	1.00	42.31	B
ATOM	3123	CG	MET	B	44	50.163	13.740	18.894	1.00	41.95	B
ATOM	3124	SD	MET	B	44	48.393	13.488	18.578	1.00	41.47	B
ATOM	3125	CE	MET	B	44	47.685	14.957	19.163	1.00	39.26	B
ATOM	3126	C	MET	B	44	50.884	15.996	15.828	1.00	43.78	B
ATOM	3127	O	MET	B	44	50.150	16.979	15.845	1.00	43.29	B
ATOM	3128	N	PHE	B	45	52.038	15.971	15.171	1.00	45.28	B
ATOM	3129	CA	PHE	B	45	52.492	17.135	14.428	1.00	45.81	B
ATOM	3130	CB	PHE	B	45	53.967	17.000	14.042	1.00	46.23	B
ATOM	3131	CG	PHE	B	45	54.516	18.214	13.361	1.00	45.63	B
ATOM	3132	CD1	PHE	B	45	54.541	18.295	11.974	1.00	45.05	B
ATOM	3133	CD2	PHE	B	45	54.953	19.298	14.104	1.00	46.24	B
ATOM	3135	CE1	PHE	B	45	54.985	19.438	11.339	1.00	45.91	B
ATOM	3135	CE2	PHE	B	45	55.402	20.452	13.475	1.00	48.36	B
ATOM	3136	CZ	PHE	B	45	55.417	20.522	12.087	1.00	47.45	B
ATOM	3137	C	PHE	B	45	51.612	17.294	13.184	1.00	46.20	B
ATOM	3138	O	PHE	B	45	51.279	18.420	12.787	1.00	47.47	B
ATOM	3139	N	LEU	B	46	51.239	16.163	12.582	1.00	45.25	B
ATOM	3140	CA	LEU	B	46	50.372	16.154	11.404	1.00	44.05	B
ATOM	3141	CB	LEU	B	46	50.307	14.752	10.792	1.00	43.08	B
ATOM	3142	CG	LEU	B	46	51.638	14.282	10.221	1.00	41.43	B
ATOM	3143	CD1	LEU	B	46	51.489	12.926	9.576	1.00	40.47	B
ATOM	3144	CD2	LEU	B	46	52.113	15.303	9.219	1.00	40.35	B
ATOM	3145	C	LEU	B	46	48.967	16.620	11.785	1.00	43.60	B
ATOM	3146	O	LEU	B	46	48.358	17.427	11.074	1.00	43.76	B
ATOM	3147	N	LEU	B	47	48.469	16.132	12.923	1.00	42.05	B
ATOM	3148	CA	LEU	B	47	47.144	16.510	13.398	1.00	39.55	B
ATOM	3149	CB	LEU	B	47	46.740	15.669	14.603	1.00	36.17	B
ATOM	3150	CG	LEU	B	47	46.297	14.251	14.244	1.00	35.72	B
ATOM	3151	CD1	LEU	B	47	45.799	13.532	15.476	1.00	35.52	B
ATOM	3152	CD2	LEU	B	47	45.204	14.311	13.198	1.00	35.00	B
ATOM	3153	C	LEU	B	47	47.079	17.990	13.728	1.00	39.58	B
ATOM	3154	O	LEU	B	47	46.041	18.621	13.570	1.00	38.78	B
ATOM	3155	N	ILE	B	48	48.208	18.542	14.159	1.00	41.00	B
ATOM	3156	CA	ILE	B	48	48.293	19.958	14.496	1.00	42.13	B
ATOM	3157	CB	ILE	B	48	49.504	20.276	15.421	1.00	43.41	B
ATOM	3158	CG2	ILE	B	48	49.729	21.796	15.519	1.00	43.99	B
ATOM	3159	CG1	ILE	B	48	49.272	19.699	16.824	1.00	42.88	B
ATOM	3160	CD1	ILE	B	48	50.448	19.881	17.778	1.00	40.74	B
ATOM	3161	C	ILE	B	48	48.407	20.796	13.239	1.00	42.20	B
ATOM	3162	O	ILE	B	48	47.735	21.816	13.113	1.00	43.54	B
ATOM	3163	N	MET	B	49	49.245	20.365	12.304	1.00	42.04	B
ATOM	3164	CA	MET	B	49	49.427	21.119	11.073	1.00	42.55	B
ATOM	3165	CB	MET	B	49	50.792	20.808	10.475	1.00	43.09	B
ATOM	3166	CG	MET	B	49	51.965	21.326	11.330	1.00	44.02	B
ATOM	3167	SD	MET	B	49	52.289	23.128	11.199	1.00	43.54	B
ATOM	3168	CE	MET	B	49	51.507	23.740	12.693	1.00	43.50	B
ATOM	3169	C	MET	B	49	48.287	20.987	10.050	1.00	43.25	B
ATOM	3170	O	MET	B	49	48.294	21.654	9.009	1.00	43.37	B
ATOM	3171	N	LEU	B	50	47.289	20.161	10.374	1.00	43.51	B
ATOM	3172	CA	LEU	B	50	46.110	19.980	9.516	1.00	43.62	B
ATOM	3173	CB	LEU	B	50	45.916	18.508	9.123	1.00	40.80	B
ATOM	3174	CG	LEU	B	50	45.360	18.176	7.725	1.00	37.18	B
ATOM	3175	CD1	LEU	B	50	44.935	16.728	7.689	1.00	35.08	B
ATOM	3176	CD2	LEU	B	50	44.199	19.067	7.332	1.00	35.57	B
ATOM	3177	C	LEU	B	50	44.864	20.461	10.281	1.00	44.86	B
ATOM	3178	O	LEU	B	50	44.070	21.258	9.768	1.00	44.74	B
ATOM	3179	N	GLY	B	51	44.711	19.972	11.512	1.00	44.90	B
ATOM	3180	CA	GLY	B	51	43.577	20.356	12.350	1.00	43.55	B
ATOM	3181	C	GLY	B	51	43.424	21.843	12.494	1.00	42.29	B
ATOM	3182	O	GLY	B	51	42.322	22.339	12.707	1.00	41.07	B
ATOM	3183	N	PHE	B	52	44.532	22.567	12.380	1.00	41.81	B
ATOM	3184	CA	PHE	B	52	44.490	24.018	12.494	1.00	41.83	B
ATOM	3185	CB	PHE	B	52	45.857	24.589	12.899	1.00	42.44	B
ATOM	3186	CG	PHE	B	52	45.964	26.074	12.723	1.00	43.44	B
ATOM	3187	CD1	PHE	B	52	47.035	26.624	12.046	1.00	44.68	B
ATOM	3188	CD2	PHE	B	52	44.968	26.922	13.207	1.00	45.28	B
ATOM	3189	CE1	PHE	B	52	47.111	27.994	11.852	1.00	46.38	B
ATOM	3190	CE2	PHE	B	52	45.035	28.291	13.021	1.00	45.02	B
ATOM	3191	CZ	PHE	B	52	46.104	28.830	12.353	1.00	45.78	B
ATOM	3192	C	PHE	B	52	43.983	24.706	11.225	1.00	40.74	B
ATOM	3193	O	PHE	B	52	42.901	25.304	11.235	1.00	41.11	B
ATOM	3194	N	PRO	B	53	44.730	24.591	10.109	1.00	39.25	B
ATOM	3195	CD	PRO	B	53	45.954	23.810	9.846	1.00	37.51	B
ATOM	3196	CA	PRO	B	53	44.269	25.250	8.885	1.00	37.86	B
ATOM	3197	CB	PRO	B	53	45.308	24.814	7.849	1.00	37.65	B
ATOM	3198	CG	PRO	B	53	46.538	24.533	8.674	1.00	38.31	B
ATOM	3199	C	PRO	B	53	42.859	24.858	8.468	1.00	37.26	B
ATOM	3200	O	PRO	B	53	42.074	25.714	8.080	1.00	36.92	B
ATOM	3201	N	ILE	B	54	42.524	23.582	8.630	1.00	38.07	B
ATOM	3202	CA	ILE	B	54	41.216	23.067	8.232	1.00	40.73	B
ATOM	3203	CB	ILE	B	54	41.235	21.535	8.071	1.00	41.18	B
ATOM	3204	CG2	ILE	B	54	41.127	20.854	9.430	1.00	42.67	B
ATOM	3205	CG1	ILE	B	54	40.078	21.084	7.175	1.00	41.30	B
ATOM	3206	CD1	ILE	B	54	40.167	19.629	6.738	1.00	40.59	B
ATOM	3207	C	ILE	B	54	40.035	23.451	9.115	1.00	41.79	B
ATOM	3208	O	ILE	B	54	38.912	23.549	8.625	1.00	42.70	B
ATOM	3209	N	ASN	B	55	40.268	23.601	10.417	1.00	42.68	B
ATOM	3210	CA	ASN	B	55	39.197	23.981	11.329	1.00	41.66	B
ATOM	3211	CB	ASN	B	55	39.484	23.484	12.749	1.00	40.62	B
ATOM	3212	CG	ASN	B	55	39.189	21.996	12.921	1.00	39.17	B
ATOM	3213	OD1	ASN	B	55	38.061	21.546	12.742	1.00	38.79	B
ATOM	3214	ND2	ASN	B	55	40.197	21.239	13.308	1.00	38.41	B
ATOM	3215	C	ASN	B	55	39.040	25.492	11.290	1.00	41.58	B
ATOM	3216	O	ASN	B	55	37.924	26.016	11.301	1.00	40.80	B
ATOM	3217	N	PHE	B	56	40.169	26.185	11.197	1.00	42.04	B
ATOM	3218	CA	PHE	B	56	40.150	27.635	11.126	1.00	43.31	B
ATOM	3219	CB	PHE	B	56	41.532	28.219	11.361	1.00	43.87	B
ATOM	3220	CG	PHE	B	56	41.549	29.711	11.335	1.00	44.28	B
ATOM	3221	CD1	PHE	B	56	41.844	30.395	10.163	1.00	44.19	B
ATOM	3222	CD2	PHE	B	56	41.251	30.438	12.482	1.00	44.80	B
ATOM	3223	CE1	PHE	B	56	41.843	31.782	10.135	1.00	43.99	B
ATOM	3224	CE2	PHE	B	56	41.248	31.824	12.464	1.00	43.88	B
ATOM	3225	CZ	PHE	B	56	41.544	32.498	11.288	1.00	43.49	B
ATOM	3226	C	PHE	B	56	39.624	28.109	9.778	1.00	43.47	B
ATOM	3227	O	PHE	B	56	38.994	29.161	9.696	1.00	44.96	B
ATOM	3228	N	LEU	B	57	39.941	27.375	8.714	1.00	42.27	B
ATOM	3229	CA	LEU	B	57	39.442	27.720	7.388	1.00	41.52	B
ATOM	3230	CB	LEU	B	57	39.902	26.690	6.355	1.00	39.96	B
ATOM	3231	CG	LEU	B	57	39.352	26.797	4.929	1.00	38.23	B
ATOM	3232	CD1	LEU	B	57	39.567	28.197	4.382	1.00	39.02	B
ATOM	3233	CD2	LEU	B	57	40.016	25.756	4.037	1.00	37.04	B
ATOM	3235	C	LEU	B	57	37.917	27.713	7.482	1.00	42.18	B
ATOM	3235	O	LEU	B	57	37.263	28.666	7.070	1.00	42.00	B
ATOM	3236	N	THR	B	58	37.373	26.646	8.072	1.00	43.26	B
ATOM	3237	CA	THR	B	58	35.930	26.475	8.271	1.00	43.04	B
ATOM	3238	CB	THR	B	58	35.621	25.182	9.091	1.00	42.28	B
ATOM	3239	OG1	THR	B	58	36.217	24.051	8.453	1.00	41.87	B
ATOM	3240	CG2	THR	B	58	35.125	24.937	9.197	1.00	39.06	B
ATOM	3241	C	THR	B	58	35.400	27.680	9.052	1.00	44.38	B
ATOM	3242	O	THR	B	58	35.413	28.307	8.654	1.00	43.04	B
ATOM	3243	N	LEU	B	59	36.076	28.005	10.154	1.00	45.70	B
ATOM	3244	CA	LEU	B	59	35.689	29.135	10.988	1.00	46.53	B
ATOM	3245	CB	LEU	B	59	36.628	29.258	12.198	1.00	44.18	B
ATOM	3246	CG	LEU	B	59	36.442	30.443	13.158	1.00	43.38	B
ATOM	3247	CD1	LEU	B	59	36.651	29.981	14.582	1.00	44.81	B
ATOM	3248	CD2	LEU	B	59	37.415	31.579	12.828	1.00	43.40	B
ATOM	3249	C	LEU	B	59	35.662	30.432	10.175	1.00	47.73	B
ATOM	3250	O	LEU	B	59	35.690	31.173	10.213	1.00	47.64	B
ATOM	3251	N	TYR	B	60	36.691	30.662	9.374	1.00	49.50	B
ATOM	3252	CA	TYR	B	60	36.761	31.881	8.582	1.00	52.48	B
ATOM	3253	CB	TYR	B	60	38.186	32.083	8.076	1.00	53.02	B
ATOM	3254	CG	TYR	B	60	38.419	33.361	7.312	1.00	53.59	B
ATOM	3255	CD1	TYR	B	60	38.377	33.375	5.920	1.00	55.22	B
ATOM	3256	CE1	TYR	B	60	38.672	35.528	5.197	1.00	56.80	B
ATOM	3257	CD2	TYR	B	60	38.755	35.540	7.973	1.00	54.41	B
ATOM	3258	CE2	TYR	B	60	39.054	35.703	7.262	1.00	56.19	B
ATOM	3259	CZ	TYR	B	60	39.014	35.691	5.869	1.00	57.00	B
ATOM	3260	OH	TYR	B	60	39.335	36.825	5.143	1.00	56.41	B
ATOM	3261	C	TYR	B	60	35.765	31.937	7.426	1.00	53.99	B
ATOM	3262	O	TYR	B	60	35.383	33.018	6.993	1.00	53.88	B
ATOM	3263	N	VAL	B	61	35.359	30.780	6.927	1.00	56.00	B
ATOM	3264	CA	VAL	B	61	35.401	30.735	5.818	1.00	58.22	B
ATOM	3265	CB	VAL	B	61	35.555	29.432	4.997	1.00	57.55	B
ATOM	3266	CG1	VAL	B	61	33.450	29.311	3.958	1.00	56.49	B
ATOM	3267	CG2	VAL	B	61	35.916	29.421	4.313	1.00	56.91	B
ATOM	3268	C	VAL	B	61	32.949	30.939	6.266	1.00	60.81	B
ATOM	3269	O	VAL	B	61	32.246	31.758	5.674	1.00	61.97	B
ATOM	3270	N	THR	B	62	32.504	30.213	7.301	1.00	62.00	B
ATOM	3271	CA	THR	B	62	31.131	30.360	7.818	1.00	61.97	B
ATOM	3272	CB	THR	B	62	30.773	29.303	8.919	1.00	60.52	B
ATOM	3273	OG1	THR	B	62	31.877	29.135	9.809	1.00	61.43	B
ATOM	3274	CG2	THR	B	62	30.413	27.956	8.310	1.00	58.78	B
ATOM	3275	C	THR	B	62	30.940	31.771	8.384	1.00	63.24	B
ATOM	3276	O	THR	B	62	29.884	32.385	8.220	1.00	64.75	B
ATOM	3277	N	VAL	B	63	31.972	32.285	9.044	1.00	64.63	B
ATOM	3278	CA	VAL	B	63	31.926	33.628	9.599	1.00	66.86	B
ATOM	3279	CB	VAL	B	63	33.138	33.890	10.547	1.00	66.16	B
ATOM	3280	CG1	VAL	B	63	33.493	35.365	10.599	1.00	65.76	B
ATOM	3281	CG2	VAL	B	63	32.814	33.407	11.950	1.00	64.33	B
ATOM	3282	C	VAL	B	63	31.907	35.625	8.440	1.00	70.13	B
ATOM	3283	O	VAL	B	63	31.082	35.541	8.428	1.00	70.35	B
ATOM	3284	N	GLN	B	64	32.762	35.392	7.440	1.00	73.56	B
ATOM	3285	CA	GLN	B	64	32.864	35.264	6.264	1.00	76.86	B
ATOM	3286	CB	GLN	B	64	35.053	35.868	5.384	1.00	77.18	B
ATOM	3287	CG	GLN	B	64	35.280	35.797	4.188	1.00	77.73	B
ATOM	3288	CD	GLN	B	64	35.848	35.075	2.969	1.00	78.53	B
ATOM	3289	OE1	GLN	B	64	35.193	35.205	2.383	1.00	77.80	B
ATOM	3290	NE2	GLN	B	64	36.066	35.444	2.575	1.00	78.56	B
ATOM	3291	C	GLN	B	64	31.614	35.311	5.386	1.00	78.58	B
ATOM	3292	O	GLN	B	64	31.166	36.395	5.002	1.00	79.72	B
ATOM	3293	N	HIS	B	65	31.084	35.146	5.021	1.00	80.03	B
ATOM	3294	CA	HIS	B	65	29.898	35.103	4.172	1.00	81.92	B
ATOM	3295	CB	HIS	B	65	29.785	32.767	3.436	1.00	81.80	B
ATOM	3296	CG	HIS	B	65	30.172	32.849	1.993	1.00	81.41	B
ATOM	3297	CD2	HIS	B	65	31.385	32.926	1.399	1.00	80.70	B
ATOM	3298	ND1	HIS	B	65	29.243	32.910	0.976	1.00	82.27	B
ATOM	3299	CE1	HIS	B	65	29.866	33.024	−0.183	1.00	81.77	B
ATOM	3300	NE2	HIS	B	65	31.167	33.037	0.047	1.00	82.15	B
ATOM	3301	C	HIS	B	65	28.597	35.468	4.876	1.00	83.27	B
ATOM	3302	O	HIS	B	65	28.139	33.780	5.791	1.00	83.81	B
ATOM	3303	N	LYS	B	66	28.025	35.579	4.420	1.00	85.13	B
ATOM	3304	CA	LYS	B	66	26.785	36.156	4.935	1.00	86.35	B
ATOM	3305	CB	LYS	B	66	26.504	37.490	4.214	1.00	86.15	B
ATOM	3306	CG	LYS	B	66	26.328	37.383	2.680	1.00	85.39	B
ATOM	3307	CD	LYS	B	66	27.605	36.955	1.958	1.00	83.02	B
ATOM	3308	CE	LYS	B	66	27.316	36.469	0.554	1.00	81.72	B
ATOM	3309	NZ	LYS	B	66	28.566	36.009	−0.093	1.00	80.76	B
ATOM	3310	C	LYS	B	66	25.561	35.240	4.842	1.00	87.16	B
ATOM	3311	O	LYS	B	66	24.678	35.292	5.704	1.00	87.08	B
ATOM	3312	N	LYS	B	67	25.514	35.411	3.800	1.00	88.07	B
ATOM	3313	CA	LYS	B	67	24.391	33.495	3.587	1.00	88.76	B
ATOM	3314	CB	LYS	B	67	24.050	33.415	2.090	1.00	90.46	B
ATOM	3315	CG	LYS	B	67	23.482	35.727	1.522	1.00	92.79	B
ATOM	3316	CD	LYS	B	67	23.174	35.643	0.031	1.00	94.47	B
ATOM	3317	CE	LYS	B	67	22.702	35.989	−0.514	1.00	95.14	B
ATOM	3318	NZ	LYS	B	67	22.522	35.973	−1.996	1.00	95.36	B
ATOM	3319	C	LYS	B	67	24.600	32.099	4.185	1.00	87.91	B
ATOM	3320	O	LYS	B	67	23.756	31.214	4.025	1.00	86.53	B
ATOM	3321	N	LEU	B	68	25.708	31.932	4.910	1.00	87.76	B
ATOM	3322	CA	LEU	B	68	26.064	30.663	5.558	1.00	87.06	B
ATOM	3323	CB	LEU	B	68	27.549	30.354	5.311	1.00	85.82	B
ATOM	3324	CG	LEU	B	68	27.973	29.138	4.474	1.00	84.62	B
ATOM	3325	CD1	LEU	B	68	27.158	29.006	3.194	1.00	83.95	B
ATOM	3326	CD2	LEU	B	68	29.451	29.258	4.154	1.00	83.53	B
ATOM	3327	C	LEU	B	68	25.762	30.702	7.068	1.00	87.14	B
ATOM	3328	O	LEU	B	68	26.671	30.754	7.906	1.00	86.28	B
ATOM	3329	N	ARG	B	69	24.473	30.676	7.401	1.00	87.03	B
ATOM	3330	CA	ARG	B	69	24.026	30.715	8.791	1.00	86.91	B
ATOM	3331	CB	ARG	B	69	23.561	32.139	9.172	1.00	86.74	B
ATOM	3332	CG	ARG	B	69	24.524	33.304	8.848	1.00	86.72	B
ATOM	3333	CD	ARG	B	69	25.694	33.446	9.831	1.00	87.85	B
ATOM	3335	NE	ARG	B	69	26.365	35.748	9.711	1.00	88.87	B
ATOM	3335	CZ	ARG	B	69	25.969	35.873	10.318	1.00	89.51	B
ATOM	3336	NH1	ARG	B	69	24.898	35.884	11.108	1.00	88.97	B
ATOM	3337	NH2	ARG	B	69	26.633	37.007	10.118	1.00	88.89	B
ATOM	3338	C	ARG	B	69	22.889	29.696	9.039	1.00	86.82	B
ATOM	3339	O	ARG	B	69	21.909	30.000	9.720	1.00	86.89	B
ATOM	3350	N	THR	B	70	23.023	28.498	8.463	1.00	86.95	B
ATOM	3351	CA	THR	B	70	22.046	27.401	8.618	1.00	87.04	B
ATOM	3352	CB	THR	B	70	22.248	26.323	7.488	1.00	86.57	B
ATOM	3353	OG1	THR	B	70	22.616	26.967	6.263	1.00	87.13	B
ATOM	3354	CG2	THR	B	70	20.978	25.522	7.228	1.00	86.00	B
ATOM	3355	C	THR	B	70	22.339	26.748	9.990	1.00	87.47	B
ATOM	3356	O	THR	B	70	23.394	27.011	10.582	1.00	88.35	B
ATOM	3357	N	PRO	B	71	21.396	25.953	10.551	1.00	87.07	B
ATOM	3358	CD	PRO	B	71	19.986	25.701	10.192	1.00	86.75	B
ATOM	3359	CA	PRO	B	71	21.710	25.339	11.852	1.00	85.74	B
ATOM	3350	CB	PRO	B	71	20.491	24.452	12.109	1.00	85.81	B
ATOM	3351	CG	PRO	B	71	19.389	25.240	11.507	1.00	86.12	B
ATOM	3352	C	PRO	B	71	22.991	24.505	11.749	1.00	84.08	B
ATOM	3353	O	PRO	B	71	23.868	24.581	12.617	1.00	84.74	B
ATOM	3354	N	LEU	B	72	23.099	23.768	10.642	1.00	81.07	B
ATOM	3355	CA	LEU	B	72	24.245	22.916	10.352	1.00	77.83	B
ATOM	3356	CB	LEU	B	72	24.081	22.321	8.941	1.00	77.81	B
ATOM	3357	CG	LEU	B	72	24.849	21.057	8.548	1.00	77.32	B
ATOM	3358	CD1	LEU	B	72	24.131	19.828	9.088	1.00	78.03	B
ATOM	3359	CD2	LEU	B	72	24.935	20.970	7.038	1.00	76.55	B
ATOM	3360	C	LEU	B	72	25.527	23.746	10.399	1.00	75.67	B
ATOM	3361	O	LEU	B	72	26.525	23.318	10.975	1.00	76.00	B
ATOM	3362	N	ASN	B	73	25.468	24.953	9.840	1.00	72.68	B
ATOM	3363	CA	ASN	B	73	26.607	25.870	9.808	1.00	69.98	B
ATOM	3364	CB	ASN	B	73	26.265	27.142	9.025	1.00	71.09	B
ATOM	3365	CG	ASN	B	73	25.747	26.858	7.621	1.00	72.01	B
ATOM	3366	OD1	ASN	B	73	25.628	27.767	6.800	1.00	71.65	B
ATOM	3367	ND2	ASN	B	73	25.409	25.602	7.359	1.00	72.97	B
ATOM	3368	C	ASN	B	73	27.025	26.269	11.209	1.00	67.98	B
ATOM	3369	O	ASN	B	73	28.215	26.373	11.499	1.00	68.72	B
ATOM	3370	N	TYR	B	74	26.041	26.524	12.066	1.00	65.42	B
ATOM	3371	CA	TYR	B	74	26.313	26.912	13.441	1.00	63.38	B
ATOM	3372	CB	TYR	B	74	25.025	27.296	14.157	1.00	63.75	B
ATOM	3373	CG	TYR	B	74	24.668	28.750	13.976	1.00	65.64	B
ATOM	3374	CD1	TYR	B	74	25.237	29.733	14.789	1.00	65.10	B
ATOM	3375	CE1	TYR	B	74	24.929	31.084	14.609	1.00	65.09	B
ATOM	3376	CD2	TYR	B	74	23.778	29.153	12.977	1.00	66.04	B
ATOM	3377	CE2	TYR	B	74	23.465	30.504	12.790	1.00	65.30	B
ATOM	3378	CZ	TYR	B	74	24.044	31.460	13.608	1.00	64.62	B
ATOM	3379	OH	TYR	B	74	23.736	32.786	13.422	1.00	64.45	B
ATOM	3380	C	TYR	B	74	27.005	25.794	14.188	1.00	61.41	B
ATOM	3381	O	TYR	B	74	27.963	26.019	14.928	1.00	62.22	B
ATOM	3382	N	ILE	B	75	26.524	24.579	13.975	1.00	57.72	B
ATOM	3383	CA	ILE	B	75	27.103	23.432	14.628	1.00	54.65	B
ATOM	3384	CB	ILE	B	75	26.154	22.228	14.547	1.00	55.46	B
ATOM	3385	CG2	ILE	B	75	26.926	20.913	14.556	1.00	56.19	B
ATOM	3386	CG1	ILE	B	75	25.172	22.319	15.718	1.00	56.55	B
ATOM	3387	CD1	ILE	B	75	24.104	21.288	15.714	1.00	57.78	B
ATOM	3388	C	ILE	B	75	28.478	23.135	14.066	1.00	51.79	B
ATOM	3389	O	ILE	B	75	29.416	22.878	14.814	1.00	51.27	B
ATOM	3390	N	LEU	B	76	28.613	23.231	12.751	1.00	48.94	B
ATOM	3391	CA	LEU	B	76	29.896	22.976	12.124	1.00	46.79	B
ATOM	3392	CB	LEU	B	76	29.747	22.798	10.616	1.00	45.52	B
ATOM	3393	CG	LEU	B	76	29.599	21.352	10.112	1.00	44.53	B
ATOM	3394	CD1	LEU	B	76	30.867	20.576	10.413	1.00	44.00	B
ATOM	3395	CD2	LEU	B	76	28.385	20.659	10.718	1.00	43.41	B
ATOM	3396	C	LEU	B	76	30.910	24.060	12.464	1.00	45.93	B
ATOM	3397	O	LEU	B	76	32.116	23.820	12.435	1.00	46.22	B
ATOM	3398	N	LEU	B	77	30.429	25.257	12.779	1.00	45.06	B
ATOM	3399	CA	LEU	B	77	31.336	26.322	13.167	1.00	44.52	B
ATOM	3400	CB	LEU	B	77	30.625	27.672	13.221	1.00	43.71	B
ATOM	3401	CG	LEU	B	77	31.444	28.766	13.920	1.00	44.62	B
ATOM	3402	CD1	LEU	B	77	32.735	29.027	13.172	1.00	41.87	B
ATOM	3403	CD2	LEU	B	77	30.633	30.039	14.050	1.00	45.59	B
ATOM	3404	C	LEU	B	77	31.801	25.941	14.561	1.00	45.84	B
ATOM	3405	O	LEU	B	77	32.986	26.041	14.876	1.00	47.84	B
ATOM	3406	N	ASN	B	78	30.856	25.458	15.370	1.00	45.27	B
ATOM	3407	CA	ASN	B	78	31.104	25.038	16.747	1.00	42.99	B
ATOM	3408	CB	ASN	B	78	29.831	24.414	17.326	1.00	41.67	B
ATOM	3409	CG	ASN	B	78	29.792	24.451	18.836	1.00	41.58	B
ATOM	3410	OD1	ASN	B	78	30.427	25.296	19.463	1.00	39.86	B
ATOM	3411	ND2	ASN	B	78	29.025	23.541	19.432	1.00	41.05	B
ATOM	3412	C	ASM	B	78	32.243	24.024	16.770	1.00	42.61	B
ATOM	3413	O	ASN	B	78	33.264	24.241	17.417	1.00	41.64	B
ATOM	3414	N	LEU	B	79	32.071	22.943	16.017	1.00	42.92	B
ATOM	3415	CA	LEU	B	79	33.065	21.878	15.911	1.00	43.77	B
ATOM	3416	CB	LEU	B	79	32.584	20.820	14.920	1.00	44.31	B
ATOM	3417	CG	LEU	B	79	31.327	20.103	15.412	1.00	46.33	B
ATOM	3418	CD1	LEU	B	79	30.706	19.248	14.314	1.00	46.81	B
ATOM	3419	CD2	LEU	B	79	31.682	19.263	16.641	1.00	47.27	B
ATOM	3420	C	LEU	B	79	35.432	22.411	15.490	1.00	43.75	B
ATOM	3521	O	LEU	B	79	35.461	21.954	15.987	1.00	44.55	B
ATOM	3422	N	ALA	B	80	35.431	23.379	14.575	1.00	41.97	B
ATOM	3423	CA	ALA	B	80	35.660	24.003	14.106	1.00	39.52	B
ATOM	3424	CB	ALA	B	80	35.355	25.003	12.999	1.00	38.49	B
ATOM	3425	C	ALA	B	80	36.312	24.714	15.285	1.00	39.01	B
ATOM	3426	O	ALA	B	80	37.535	24.715	15.420	1.00	39.68	B
ATOM	3427	N	VAL	B	81	35.484	25.282	16.159	1.00	38.43	B
ATOM	3428	CA	VAL	B	81	35.973	26.002	17.330	1.00	37.96	B
ATOM	3429	CB	VAL	B	81	35.908	26.958	17.894	1.00	37.26	B
ATOM	3430	CG1	VAL	B	81	35.529	27.883	18.925	1.00	38.55	B
ATOM	3431	CG2	VAL	B	81	35.287	27.770	16.785	1.00	36.06	B
ATOM	3432	C	VAL	B	81	36.442	25.055	18.430	1.00	37.99	B
ATOM	3433	O	VAL	B	81	37.423	25.353	19.113	1.00	41.24	B
ATOM	3435	N	ALA	B	82	35.735	23.941	18.609	1.00	36.78	B
ATOM	3435	CA	ALA	B	82	36.094	22.941	19.615	1.00	35.82	B
ATOM	3436	CB	ALA	B	82	35.963	21.956	19.804	1.00	33.65	B
ATOM	3437	C	ALA	B	82	37.354	22.212	19.154	1.00	36.60	B
ATOM	3438	O	ALA	B	82	38.198	21.815	19.976	1.00	35.42	B
ATOM	3439	N	ASP	B	83	37.448	22.028	17.832	1.00	37.15	B
ATOM	3440	CA	ASP	B	83	38.585	21.373	17.187	1.00	38.25	B
ATOM	3441	CB	ASP	B	83	38.284	21.076	15.712	1.00	38.37	B
ATOM	3442	CG	ASP	B	83	37.458	19.800	15.504	1.00	42.19	B
ATOM	3443	OD1	ASP	B	83	36.956	19.225	16.496	1.00	43.24	B
ATOM	3444	OD2	ASP	B	83	37.307	19.364	14.335	1.00	41.93	B
ATOM	3445	C	ASP	B	83	39.832	22.257	17.296	1.00	38.97	B
ATOM	3446	O	ASP	B	83	40.953	21.751	17.398	1.00	39.62	B
ATOM	3447	N	LEU	B	84	39.645	23.575	17.251	1.00	37.82	B
ATOM	3448	CA	LEU	B	84	40.774	24.481	17.385	1.00	36.67	B
ATOM	3449	CB	LEU	B	84	40.399	25.913	16.997	1.00	35.69	B
ATOM	3450	CG	LEU	B	84	40.415	26.120	15.477	1.00	33.30	B
ATOM	3451	CD1	LEU	B	84	39.897	27.492	15.096	1.00	31.12	B
ATOM	3452	CD2	LEU	B	84	41.824	25.911	14.949	1.00	30.99	B
ATOM	3453	C	LEU	B	84	41.262	24.392	18.821	1.00	37.98	B
ATOM	3454	O	LEU	B	84	42.460	24.278	19.061	1.00	38.48	B
ATOM	3455	N	PHE	B	85	40.329	24.388	19.771	1.00	38.14	B
ATOM	3456	CA	PHE	B	85	40.678	24.264	21.186	1.00	38.83	B
ATOM	3457	CB	PHE	B	85	39.429	24.318	22.052	1.00	39.38	B
ATOM	3458	CG	PHE	B	85	39.059	25.693	22.472	1.00	41.28	B
ATOM	3459	CD1	PHE	B	85	37.759	26.152	22.319	1.00	41.19	B
ATOM	3460	CD2	PHE	B	85	40.014	26.533	23.039	1.00	41.59	B
ATOM	3461	CE1	PHE	B	85	37.412	27.429	22.727	1.00	42.28	B
ATOM	3462	CE2	PHE	B	85	39.680	27.811	23.451	1.00	42.23	B
ATOM	3463	CZ	PHE	B	85	38.374	28.263	23.297	1.00	42.17	B
ATOM	3464	C	PHE	B	85	41.387	22.941	21.438	1.00	38.84	B
ATOM	3465	O	PHE	B	85	42.433	22.888	22.090	1.00	39.09	B
ATOM	3466	N	MET	B	86	40.789	21.874	20.917	1.00	37.28	B
ATOM	3467	CA	MET	B	86	41.319	20.528	21.035	1.00	33.45	B
ATOM	3468	CB	MET	B	86	40.480	19.614	20.160	1.00	33.21	B
ATOM	3469	CG	MET	B	86	40.600	18.147	20.454	1.00	33.98	B
ATOM	3470	SD	MET	B	86	39.404	17.221	19.478	1.00	31.86	B
ATOM	3471	CE	MET	B	86	38.114	18.431	19.364	1.00	35.60	B
ATOM	3472	C	MET	B	86	42.769	20.517	20.565	1.00	31.96	B
ATOM	3473	O	MET	B	86	43.649	20.018	21.254	1.00	30.77	B
ATOM	3474	N	VAL	B	87	43.012	21.124	19.409	1.00	31.41	B
ATOM	3475	CA	VAL	B	87	44.352	21.202	18.826	1.00	33.20	B
ATOM	3476	CB	VAL	B	87	44.268	21.594	17.310	1.00	33.61	B
ATOM	3477	CG1	VAL	B	87	45.634	21.980	16.769	1.00	33.21	B
ATOM	3478	CG2	VAL	B	87	43.690	20.444	16.492	1.00	32.78	B
ATOM	3479	C	VAL	B	87	45.351	22.128	19.573	1.00	34.64	B
ATOM	3480	O	VAL	B	87	46.518	21.765	19.764	1.00	33.67	B
ATOM	3481	N	PHE	B	88	44.903	23.317	19.987	1.00	35.55	B
ATOM	3482	CA	PHE	B	88	45.774	24.269	20.693	1.00	34.44	B
ATOM	3483	CB	PHE	B	88	45.318	25.704	20.448	1.00	33.91	B
ATOM	3484	CG	PHE	B	88	45.674	26.206	19.093	1.00	33.91	B
ATOM	3485	CD1	PHE	B	88	44.719	26.282	18.095	1.00	32.65	B
ATOM	3486	CD2	PHE	B	88	46.999	26.525	18.787	1.00	33.89	B
ATOM	3487	CE1	PHE	B	88	45.081	26.658	16.814	1.00	33.49	B
ATOM	3488	CE2	PHE	B	88	47.370	26.901	17.506	1.00	29.84	B
ATOM	3489	CZ	PHE	B	88	46.418	26.967	16.520	1.00	31.73	B
ATOM	3490	C	PHE	B	88	45.922	24.029	22.179	1.00	34.62	B
ATOM	3491	O	PHE	B	88	46.995	24.239	22.747	1.00	32.98	B
ATOM	3492	N	GLY	B	89	44.830	23.616	22.806	1.00	34.86	B
ATOM	3493	CA	GLY	B	89	44.862	23.353	24.224	1.00	38.01	B
ATOM	3494	C	GLY	B	89	45.395	21.966	24.500	1.00	39.85	B
ATOM	3495	O	GLY	B	89	46.324	21.800	25.296	1.00	39.88	B
ATOM	3496	N	GLY	B	90	44.841	20.985	23.790	1.00	41.36	B
ATOM	3497	CA	GLY	B	90	45.233	19.595	23.973	1.00	42.56	B
ATOM	3498	C	GLY	B	90	46.430	19.081	23.192	1.00	43.20	B
ATOM	3499	O	GLY	B	90	47.421	18.667	23.798	1.00	43.09	B
ATOM	3500	N	PHE	B	91	46.347	19.111	21.860	1.00	43.31	B
ATOM	3501	CA	PHE	B	91	47.424	18.619	20.986	1.00	42.80	B
ATOM	3502	CB	PHE	B	91	47.016	18.695	19.512	1.00	41.13	B
ATOM	3503	CG	PHE	B	91	45.850	17.822	19.150	1.00	39.60	B
ATOM	3504	CD1	PHE	B	91	45.486	17.662	17.821	1.00	39.83	B
ATOM	3505	CD2	PHE	B	91	45.099	17.186	20.128	1.00	38.80	B
ATOM	3506	CE1	PHE	B	91	44.390	16.884	17.473	1.00	40.71	B
ATOM	3507	CE2	PHE	B	91	44.004	16.409	19.790	1.00	39.94	B
ATOM	3508	CZ	PHE	B	91	43.647	16.256	18.461	1.00	40.14	B
ATOM	3509	C	PHE	B	91	48.802	19.266	21.170	1.00	43.97	B
ATOM	3510	O	PHE	B	91	49.815	18.709	20.753	1.00	44.06	B
ATOM	3511	N	THR	B	92	48.837	20.452	21.765	1.00	45.57	B
ATOM	3512	CA	THR	B	92	50.093	21.149	22.014	1.00	46.56	B
ATOM	3513	CB	THR	B	92	49.819	22.575	22.576	1.00	48.44	B
ATOM	3514	OG1	THR	B	92	49.016	23.312	21.645	1.00	49.91	B
ATOM	3515	CG2	THR	B	92	51.120	23.330	22.818	1.00	50.68	B
ATOM	3516	C	THR	B	92	50.894	20.330	23.040	1.00	46.47	B
ATOM	3517	O	THR	B	92	52.087	20.066	22.849	1.00	46.48	B
ATOM	3518	N	THR	B	93	50.199	19.902	24.098	1.00	45.57	B
ATOM	3519	CA	THR	B	93	50.767	19.115	25.192	1.00	43.57	B
ATOM	3520	CB	THR	B	93	49.779	19.033	26.369	1.00	43.67	B
ATOM	3521	OG1	THR	B	93	49.467	20.356	26.823	1.00	43.26	B
ATOM	3522	CG2	THR	B	93	50.363	18.218	27.514	1.00	42.99	B
ATOM	3523	C	THR	B	93	51.125	17.697	24.769	1.00	43.06	B
ATOM	3524	O	THR	B	93	52.250	17.247	24.980	1.00	41.71	B
ATOM	3525	N	THR	B	94	50.163	16.995	24.178	1.00	42.85	B
ATOM	3526	CA	THR	B	94	50.387	15.623	23.729	1.00	44.60	B
ATOM	3527	CB	THR	B	94	49.069	14.947	23.210	1.00	43.94	B
ATOM	3528	OG1	THR	B	94	49.371	13.826	22.371	1.00	43.33	B
ATOM	3529	CG2	THR	B	94	48.216	15.916	22.467	1.00	44.68	B
ATOM	3530	C	THR	B	94	51.549	15.497	22.735	1.00	45.24	B
ATOM	3531	O	THR	B	94	52.242	14.478	22.713	1.00	46.70	B
ATOM	3532	N	LEU	B	95	51.797	16.552	21.961	1.00	45.71	B
ATOM	3533	CA	LEU	B	95	52.907	16.566	21.005	1.00	44.84	B
ATOM	3534	CB	LEU	B	95	52.877	17.834	20.146	1.00	44.93	B
ATOM	3535	CG	LEU	B	95	54.191	18.167	19.428	1.00	43.41	B
ATOM	3536	CD1	LEU	B	95	54.520	17.085	18.407	1.00	44.93	B
ATOM	3537	CD2	LEU	B	95	54.094	19.522	18.772	1.00	41.59	B
ATOM	3538	C	LEU	B	95	54.221	16.542	21.766	1.00	44.83	B
ATOM	3539	O	LEU	B	95	55.080	15.703	21.501	1.00	44.42	B
ATOM	3540	N	TYR	B	96	54.360	17.481	22.704	1.00	45.66	B
ATOM	3541	CA	TYR	B	96	55.563	17.615	23.512	1.00	45.79	B
ATOM	3542	CB	TYR	B	96	55.646	19.015	24.138	1.00	47.61	B
ATOM	3543	CG	TYR	B	96	56.550	19.964	23.360	1.00	51.64	B
ATOM	3544	CD1	TYR	B	96	57.584	20.661	24.001	1.00	54.86	B
ATOM	3545	CE1	TYR	B	96	58.468	21.481	23.275	1.00	56.97	B
ATOM	3546	CD2	TYR	B	96	56.414	20.117	21.973	1.00	51.89	B
ATOM	3547	CE2	TYR	B	96	57.288	20.930	21.238	1.00	53.88	B
ATOM	3548	CZ	TYR	B	96	58.313	21.605	21.893	1.00	57.06	B
ATOM	3549	OH	TYR	B	96	59.201	22.374	21.172	1.00	58.82	B
ATOM	3550	C	TYR	B	96	55.767	16.513	24.548	1.00	44.75	B
ATOM	3551	O	TYR	B	96	56.903	16.225	24.933	1.00	45.37	B
ATOM	3552	N	THR	B	97	54.680	15.866	24.961	1.00	42.84	B
ATOM	3553	CA	THR	B	97	54.757	14.774	25.933	1.00	41.44	B
ATOM	3554	CB	THR	B	97	53.346	14.371	26.403	1.00	41.57	B
ATOM	3555	OG1	THR	B	97	52.791	15.428	27.194	1.00	40.43	B
ATOM	3556	CG2	THR	B	97	53.380	13.093	27.218	1.00	41.81	B
ATOM	3557	C	THR	B	97	55.466	13.569	25.299	1.00	41.35	B
ATOM	3558	O	THR	B	97	56.361	12.965	25.905	1.00	39.85	B
ATOM	3559	N	SER	B	98	55.060	13.256	24.066	1.00	41.41	B
ATOM	3560	CA	SER	B	98	55.614	12.158	23.275	1.00	40.89	B
ATOM	3561	CB	SER	B	98	54.837	12.008	21.954	1.00	40.98	B
ATOM	3562	OG	SER	B	98	53.510	11.545	22.159	1.00	38.11	B
ATOM	3563	C	SER	B	98	57.086	12.433	22.964	1.00	41.28	B
ATOM	3564	O	SER	B	98	57.923	11.516	22.958	1.00	41.36	B
ATOM	3565	N	LEU	B	99	57.395	13.704	22.703	1.00	40.38	B
ATOM	3566	CA	LEU	B	99	58.761	14.105	22.397	1.00	39.33	B
ATOM	3567	CB	LEU	B	99	58.819	15.567	21.922	1.00	35.08	B
ATOM	3568	CG	LEU	B	99	58.410	15.830	20.462	1.00	32.17	B
ATOM	3569	CD1	LEU	B	99	58.381	17.308	20.191	1.00	29.93	B
ATOM	3570	CD2	LEU	B	99	59.360	15.149	19.493	1.00	30.63	B
ATOM	3571	C	LEU	B	99	59.706	13.855	23.573	1.00	40.07	B
ATOM	3572	O	LEU	B	99	60.883	13.555	23.368	1.00	40.86	B
ATOM	3573	N	HIS	B	100	59.175	13.916	24.794	1.00	41.40	B
ATOM	3574	CA	HIS	B	100	59.980	13.686	25.991	1.00	41.65	B
ATOM	3575	CB	HIS	B	100	59.728	14.772	27.033	1.00	44.08	B
ATOM	3576	CG	HIS	B	100	60.236	16.121	26.626	1.00	47.99	B
ATOM	3577	CD2	HIS	B	100	59.630	17.146	25.980	1.00	48.90	B
ATOM	3578	ND1	HIS	B	100	61.534	16.526	26.856	1.00	51.04	B
ATOM	3579	CE1	HIS	B	100	61.706	17.743	26.366	1.00	52.64	B
ATOM	3580	NE2	HIS	B	100	60.566	18.141	25.829	1.00	51.72	B
ATOM	3581	C	HIS	B	100	59.750	12.311	26.585	1.00	40.40	B
ATOM	3582	O	HIS	B	100	60.469	11.900	27.493	1.00	40.79	B
ATOM	3583	N	GLY	B	101	58.761	11.601	26.049	1.00	39.01	B
ATOM	3584	CA	GLY	B	101	58.448	10.264	26.518	1.00	38.24	B
ATOM	3585	C	GLY	B	101	57.658	10.187	27.811	1.00	38.92	B
ATOM	3586	O	GLY	B	101	57.487	9.102	28.366	1.00	38.35	B
ATOM	3587	N	TYR	B	102	57.176	11.332	28.292	1.00	39.45	B
ATOM	3588	CA	TYR	B	102	56.400	11.403	29.530	1.00	39.23	B
ATOM	3589	CB	TYR	B	102	57.279	11.072	30.742	1.00	40.66	B
ATOM	3590	CG	TYR	B	102	58.223	12.187	31.158	1.00	43.33	B
ATOM	3591	CD1	TYR	B	102	59.399	12.447	30.446	1.00	43.99	B
ATOM	3592	CE1	TYR	B	102	60.270	13.476	30.832	1.00	44.34	B
ATOM	3593	CD2	TYR	B	102	57.937	12.988	32.266	1.00	44.67	B
ATOM	3594	CE2	TYR	B	102	58.795	14.020	32.657	1.00	45.20	B
ATOM	3595	CZ	TYR	B	102	59.958	14.257	31.940	1.00	44.63	B
ATOM	3596	OH	TYR	B	102	60.801	15.268	32.338	1.00	44.32	B
ATOM	3597	C	TYR	B	102	55.865	12.819	29.684	1.00	39.26	B
ATOM	3598	O	TYR	B	102	56.196	13.698	28.888	1.00	38.43	B
ATOM	3599	N	PHE	B	103	55.077	13.039	30.735	1.00	39.45	B
ATOM	3600	CA	PHE	B	103	54.502	14.346	31.014	1.00	40.04	B
ATOM	3601	CB	PHE	B	103	53.212	14.215	31.817	1.00	36.19	B
ATOM	3602	CG	PHE	B	103	51.997	14.048	30.963	1.00	36.86	B
ATOM	3603	CD1	PHE	B	103	51.498	12.786	30.674	1.00	35.01	B
ATOM	3604	CD2	PHE	B	103	51.381	15.160	30.383	1.00	37.62	B
ATOM	3605	CE1	PHE	B	103	50.411	12.633	29.817	1.00	35.13	B
ATOM	3606	CE2	PHE	B	103	50.287	15.014	29.518	1.00	35.82	B
ATOM	3607	CZ	PHE	B	103	49.805	13.753	29.235	1.00	33.98	B
ATOM	3608	C	PHE	B	103	55.459	15.306	31.701	1.00	43.64	B
ATOM	3609	O	PHE	B	103	55.536	15.356	32.929	1.00	44.28	B
ATOM	3610	N	VAL	B	104	56.200	16.057	30.887	1.00	47.92	B
ATOM	3611	CA	VAL	B	104	57.157	17.054	31.372	1.00	50.24	B
ATOM	3612	CB	VAL	B	104	58.077	17.594	30.238	1.00	48.67	B
ATOM	3613	CG1	VAL	B	104	59.050	16.539	29.807	1.00	48.46	B
ATOM	3614	CG2	VAL	B	104	57.252	18.068	29.041	1.00	46.06	B
ATOM	3615	C	VAL	B	104	56.427	18.249	31.969	1.00	52.88	B
ATOM	3616	O	VAL	B	104	56.982	18.960	32.809	1.00	54.89	B
ATOM	3617	N	PHE	B	105	55.192	18.475	31.515	1.00	54.60	B
ATOM	3618	CA	PHE	B	105	54.382	19.597	31.987	1.00	56.79	B
ATOM	3619	CB	PHE	B	105	53.404	20.068	30.887	1.00	60.01	B
ATOM	3620	CG	PHE	B	105	54.079	20.574	29.613	1.00	62.03	B
ATOM	3621	CD1	PHE	B	105	53.650	20.126	28.357	1.00	61.61	B
ATOM	3622	CD2	PHE	B	105	55.136	21.490	29.667	1.00	62.54	B
ATOM	3623	CE1	PHE	B	105	54.265	20.580	27.175	1.00	62.11	B
ATOM	3624	CE2	PHE	B	105	55.759	21.949	28.486	1.00	63.12	B
ATOM	3625	CZ	PHE	B	105	55.320	21.490	27.241	1.00	62.44	B
ATOM	3626	C	PHE	B	105	53.624	19.250	33.271	1.00	56.35	B
ATOM	3627	O	PHE	B	105	52.946	20.104	33.850	1.00	55.85	B
ATOM	3628	N	GLY	B	106	53.759	17.997	33.710	1.00	56.19	B
ATOM	3629	CA	GLY	B	106	53.104	17.527	34.925	1.00	55.85	B
ATOM	3630	C	GLY	B	106	51.593	17.367	34.824	1.00	55.01	B
ATOM	3631	O	GLY	B	106	51.070	17.163	33.723	1.00	56.20	B
ATOM	3632	N	PRO	B	107	50.869	17.374	35.962	1.00	53.70	B
ATOM	3633	CD	PRO	B	107	51.378	17.262	37.339	1.00	53.68	B
ATOM	3634	CA	PRO	B	107	49.412	17.234	35.956	1.00	52.75	B
ATOM	3635	CB	PRO	B	107	49.071	17.221	37.442	1.00	52.61	B
ATOM	3636	CG	PRO	B	107	50.245	16.549	38.036	1.00	51.47	B
ATOM	3637	C	PRO	B	107	48.728	18.385	35.208	1.00	52.32	B
ATOM	3638	O	PRO	B	107	47.710	18.169	34.561	1.00	52.99	B
ATOM	3639	N	THR	B	108	49.295	19.594	35.284	1.00	51.70	B
ATOM	3640	CA	THR	B	108	48.755	20.761	34.572	1.00	50.34	B
ATOM	3641	CB	THR	B	108	49.678	22.001	34.738	1.00	49.79	B
ATOM	3642	OG1	THR	B	108	49.704	22.400	36.111	1.00	49.11	B
ATOM	3643	CG2	THR	B	108	49.200	23.172	33.886	1.00	49.40	B
ATOM	3644	C	THR	B	108	48.677	20.395	33.085	1.00	50.20	B
ATOM	3645	O	THR	B	108	47.711	20.731	32.398	1.00	50.87	B
ATOM	3646	N	GLY	B	109	49.691	19.666	32.622	1.00	50.13	B
ATOM	3647	CA	GLY	B	109	49.763	19.225	31.239	1.00	49.64	B
ATOM	3648	C	GLY	B	109	48.820	18.075	30.949	1.00	49.44	B
ATOM	3649	O	GLY	B	109	48.169	18.058	29.903	1.00	50.17	B
ATOM	3650	N	CYS	B	110	48.758	17.104	31.859	1.00	48.34	B
ATOM	3651	CA	CYS	B	110	47.870	15.954	31.695	1.00	47.98	B
ATOM	3652	C	CYS	B	110	46.404	16.392	31.701	1.00	48.94	B
ATOM	3653	O	CYS	B	110	45.553	15.771	31.050	1.00	49.22	B
ATOM	3654	CB	CYS	B	110	48.113	14.919	32.793	1.00	46.09	B
ATOM	3655	SG	CYS	B	110	46.765	13.711	33.007	1.00	44.69	B
ATOM	3656	N	ASN	B	111	46.118	17.454	32.454	1.00	48.31	B
ATOM	3657	CA	ASN	B	111	44.771	18.008	32.543	1.00	46.74	B
ATOM	3658	CB	ASN	B	111	44.682	19.037	33.674	1.00	48.98	B
ATOM	3659	CG	ASN	B	111	44.689	18.399	35.053	1.00	49.71	B
ATOM	3660	OD1	ASN	B	111	44.142	17.311	35.252	1.00	52.62	B
ATOM	3661	ND2	ASN	B	111	45.298	19.082	36.015	1.00	48.23	B
ATOM	3662	C	ASN	B	111	44.444	18.674	31.216	1.00	45.36	B
ATOM	3663	O	ASN	B	111	43.389	18.422	30.632	1.00	45.49	B
ATOM	3664	N	LEU	B	112	45.362	19.518	30.744	1.00	42.47	B
ATOM	3665	CA	LEU	B	112	45.198	20.210	29.475	1.00	39.90	B
ATOM	3666	CB	LEU	B	112	46.467	21.008	29.148	1.00	36.99	B
ATOM	3667	CG	LEU	B	112	46.816	22.245	29.972	1.00	33.75	B
ATOM	3668	CD1	LEU	B	112	48.194	22.754	29.595	1.00	33.80	B
ATOM	3669	CD2	LEU	B	112	45.790	23.316	29.736	1.00	33.98	B
ATOM	3670	C	LEU	B	112	44.904	19.193	28.358	1.00	39.79	B
ATOM	3671	O	LEU	B	112	43.955	19.358	27.586	1.00	39.52	B
ATOM	3672	N	GLU	B	113	45.682	18.111	28.349	1.00	39.85	B
ATOM	3673	CA	GLU	B	113	45.585	17.025	27.370	1.00	40.08	B
ATOM	3674	CB	GLU	B	113	46.679	15.988	27.672	1.00	38.45	B
ATOM	3675	CG	GLU	B	113	47.347	15.354	26.463	1.00	37.81	B
ATOM	3676	CD	GLU	B	113	46.370	14.660	25.553	1.00	38.73	B
ATOM	3677	OE1	GLU	B	113	46.172	15.127	24.411	1.00	38.16	B
ATOM	3678	OE2	GLU	B	113	45.776	13.658	25.992	1.00	40.50	B
ATOM	3679	C	GLU	B	113	44.215	16.325	27.292	1.00	41.34	B
ATOM	3680	O	GLU	B	113	43.651	16.175	26.205	1.00	41.79	B
ATOM	3681	N	GLY	B	114	43.703	15.884	28.442	1.00	43.30	B
ATOM	3682	CA	GLY	B	114	42.426	15.182	28.496	1.00	44.82	B
ATOM	3683	C	GLY	B	114	41.180	16.045	28.423	1.00	46.18	B
ATOM	3684	O	GLY	B	114	40.206	15.676	27.758	1.00	47.23	B
ATOM	3685	N	PHE	B	115	41.200	17.183	29.115	1.00	45.79	B
ATOM	3686	CA	PHE	B	115	40.070	18.109	29.127	1.00	45.41	B
ATOM	3687	CB	PHE	B	115	40.404	19.353	29.961	1.00	45.36	B
ATOM	3688	CG	PHE	B	115	39.330	20.411	29.947	1.00	46.49	B
ATOM	3689	CD1	PHE	B	115	39.623	21.710	29.532	1.00	48.45	B
ATOM	3690	CD2	PHE	B	115	38.032	20.115	30.339	1.00	46.60	B
ATOM	3691	CE1	PHE	B	115	38.641	22.693	29.506	1.00	48.23	B
ATOM	3692	CE2	PHE	B	115	37.043	21.091	30.317	1.00	46.86	B
ATOM	3693	CZ	PHE	B	115	37.347	22.381	29.899	1.00	48.14	B
ATOM	3694	C	PHE	B	115	39.655	18.521	27.722	1.00	45.17	B
ATOM	3695	O	PHE	B	115	38.512	18.309	27.322	1.00	46.00	B
ATOM	3696	N	PHE	B	116	40.592	19.080	26.964	1.00	44.38	B
ATOM	3697	CA	PHE	B	116	40.294	19.526	25.613	1.00	44.00	B
ATOM	3698	CB	PHE	B	116	41.439	20.372	25.080	1.00	42.64	B
ATOM	3699	CG	PHE	B	116	41.514	21.725	25.709	1.00	42.99	B
ATOM	3700	CD1	PHE	B	116	40.697	22.758	25.259	1.00	43.18	B
ATOM	3701	CD2	PHE	B	116	42.368	21.965	26.773	1.00	42.55	B
ATOM	3702	CE1	PHE	B	116	40.729	24.009	25.863	1.00	42.57	B
ATOM	3703	CE2	PHE	B	116	42.406	23.216	27.383	1.00	43.12	B
ATOM	3704	CZ	PHE	B	116	41.583	24.239	26.926	1.00	42.69	B
ATOM	3705	C	PHE	B	116	39.929	18.414	24.640	1.00	44.52	B
ATOM	3706	O	PHE	B	116	39.290	18.672	23.614	1.00	45.35	B
ATOM	3707	N	ALA	B	117	40.302	17.181	24.986	1.00	43.79	B
ATOM	3708	CA	ALA	B	117	40.021	16.008	24.159	1.00	43.32	B
ATOM	3709	CB	ALA	B	117	41.077	14.940	24.386	1.00	43.27	B
ATOM	3710	C	ALA	B	117	38.641	15.455	24.475	1.00	43.50	B
ATOM	3711	O	ALA	B	117	37.953	14.934	23.596	1.00	43.60	B
ATOM	3712	N	THR	B	118	38.262	15.545	25.747	1.00	43.31	B
ATOM	3713	CA	THR	B	118	36.960	15.078	26.212	1.00	42.88	B
ATOM	3714	CB	THR	B	118	36.969	14.832	27.734	1.00	41.92	B
ATOM	3715	OG1	THR	B	118	38.063	13.971	28.064	1.00	41.86	B
ATOM	3716	CG2	THR	B	118	35.667	14.178	28.182	1.00	40.79	B
ATOM	3717	C	THR	B	118	35.937	16.158	25.876	1.00	42.86	B
ATOM	3718	O	THR	B	118	34.790	15.860	25.528	1.00	42.47	B
ATOM	3719	N	LEU	B	119	36.364	17.413	26.006	1.00	41.98	B
ATOM	3720	CA	LEU	B	119	35.522	18.555	25.686	1.00	41.28	B
ATOM	3721	CB	LEU	B	119	36.217	19.868	26.077	1.00	39.09	B
ATOM	3722	CG	LEU	B	119	35.446	21.192	25.944	1.00	37.37	B
ATOM	3723	CD1	LEU	B	119	34.283	21.235	26.909	1.00	35.07	B
ATOM	3724	CD2	LEU	B	119	36.379	22.364	26.207	1.00	36.70	B
ATOM	3725	C	LEU	B	119	35.331	18.498	24.174	1.00	42.38	B
ATOM	3726	O	LEU	B	119	34.265	18.821	23.659	1.00	43.88	B
ATOM	3727	N	GLY	B	120	36.359	18.033	23.473	1.00	42.14	B
ATOM	3728	CA	GLY	B	120	36.280	17.940	22.032	1.00	42.32	B
ATOM	3729	C	GLY	B	120	35.334	16.858	21.564	1.00	42.80	B
ATOM	3730	O	GLY	B	120	34.487	17.098	20.705	1.00	42.95	B
ATOM	3731	N	GLY	B	121	35.485	15.663	22.127	1.00	44.01	B
ATOM	3732	CA	GLY	B	121	34.636	14.544	21.753	1.00	45.43	B
ATOM	3733	C	GLY	B	121	33.194	14.675	22.209	1.00	45.94	B
ATOM	3734	O	GLY	B	121	32.286	14.129	21.573	1.00	44.97	B
ATOM	3735	N	GLU	B	122	32.986	15.365	23.328	1.00	46.14	B
ATOM	3736	CA	GLU	B	122	31.642	15.566	23.853	1.00	47.59	B
ATOM	3737	CB	GLU	B	122	31.667	15.827	25.361	1.00	47.31	B
ATOM	3738	CG	GLU	B	122	31.875	14.565	26.192	1.00	47.02	B
ATOM	3739	CD	GLU	B	122	30.825	13.492	25.912	1.00	46.61	B
ATOM	3740	OE1	GLU	B	122	29.621	13.771	26.069	1.00	48.82	B
ATOM	3741	OE2	GLU	B	122	31.199	12.364	25.537	1.00	47.01	B
ATOM	3742	C	GLU	B	122	30.884	16.663	23.106	1.00	48.47	B
ATOM	3743	O	GLU	B	122	29.675	16.557	22.913	1.00	49.08	B
ATOM	3744	N	ILE	B	123	31.587	17.708	22.675	1.00	48.34	B
ATOM	3745	CA	ILE	B	123	30.944	18.771	21.909	1.00	47.51	B
ATOM	3746	CB	ILE	B	123	31.904	19.962	21.641	1.00	46.65	B
ATOM	3747	CG2	ILE	B	123	31.362	20.843	20.519	1.00	47.07	B
ATOM	3748	CG1	ILE	B	123	32.087	20.781	22.924	1.00	44.79	B
ATOM	3749	CD1	ILE	B	123	32.978	21.992	22.781	1.00	43.99	B
ATOM	3750	C	ILE	B	123	30.492	18.137	20.594	1.00	47.83	B
ATOM	3751	O	ILE	B	123	29.450	18.490	20.054	1.00	48.33	B
ATOM	3752	N	ALA	B	124	31.259	17.146	20.140	1.00	48.25	B
ATOM	3753	CA	ALA	B	124	30.982	16.398	18.914	1.00	48.76	B
ATOM	3754	CB	ALA	B	124	32.205	15.564	18.525	1.00	48.96	B
ATOM	3755	C	ALA	B	124	29.759	15.491	19.073	1.00	48.88	B
ATOM	3756	O	ALA	B	124	28.902	15.431	18.190	1.00	47.71	B
ATOM	3757	N	LEU	B	125	29.711	14.760	20.186	1.00	50.22	B
ATOM	3758	CA	LEU	B	125	28.593	13.865	20.489	1.00	51.05	B
ATOM	3759	CB	LEU	B	125	28.900	13.018	21.728	1.00	50.63	B
ATOM	3760	CG	LEU	B	125	28.271	11.630	21.916	1.00	49.87	B
ATOM	3761	CD1	LEU	B	125	28.113	11.364	23.401	1.00	48.75	B
ATOM	3762	CD2	LEU	B	125	26.929	11.510	21.229	1.00	50.11	B
ATOM	3763	C	LEU	B	125	27.354	14.721	20.762	1.00	52.16	B
ATOM	3764	O	LEU	B	125	26.252	14.362	20.347	1.00	51.60	B
ATOM	3765	N	TRP	B	126	27.541	15.848	21.455	1.00	53.09	B
ATOM	3766	CA	TRP	B	126	26.432	16.752	21.769	1.00	54.49	B
ATOM	3767	CB	TRP	B	126	26.758	17.659	22.968	1.00	55.97	B
ATOM	3768	CG	TRP	B	126	26.806	16.897	24.286	1.00	58.33	B
ATOM	3769	CD2	TRP	B	126	25.766	16.087	24.848	1.00	58.57	B
ATOM	3770	CE2	TRP	B	126	26.276	15.506	26.028	1.00	58.63	B
ATOM	3771	CE3	TRP	B	126	24.450	15.793	24.465	1.00	59.26	B
ATOM	3772	CD1	TRP	B	126	27.872	16.786	25.140	1.00	59.36	B
ATOM	3773	NE1	TRP	B	126	27.562	15.949	26.185	1.00	58.29	B
ATOM	3774	CZ2	TRP	B	126	25.519	14.649	26.823	1.00	60.10	B
ATOM	3775	CZ3	TRP	B	126	23.698	14.940	25.259	1.00	59.04	B
ATOM	3776	CH2	TRP	B	126	24.234	14.379	26.424	1.00	59.35	B
ATOM	3777	C	TRP	B	126	25.961	17.551	20.555	1.00	54.14	B
ATOM	3778	O	TRP	B	126	24.792	17.921	20.463	1.00	53.26	B
ATOM	3779	N	SER	B	127	26.863	17.801	19.615	1.00	54.40	B
ATOM	3780	CA	SER	B	127	26.477	18.505	18.402	1.00	55.30	B
ATOM	3781	CB	SER	B	127	27.688	19.112	17.689	1.00	55.22	B
ATOM	3782	OG	SER	B	127	28.169	20.247	18.393	1.00	56.21	B
ATOM	3783	C	SER	B	127	25.753	17.514	17.496	1.00	55.23	B
ATOM	3784	O	SER	B	127	24.914	17.901	16.693	1.00	55.29	B
ATOM	3785	N	LEU	B	128	26.078	16.231	17.629	1.00	56.20	B
ATOM	3786	CA	LEU	B	128	25.413	15.203	16.837	1.00	57.61	B
ATOM	3787	CB	LEU	B	128	26.094	13.844	16.985	1.00	57.29	B
ATOM	3788	CG	LEU	B	128	27.477	13.607	16.392	1.00	56.44	B
ATOM	3789	CD1	LEU	B	128	27.681	12.109	16.264	1.00	55.64	B
ATOM	3790	CD2	LEU	B	128	27.593	14.267	15.036	1.00	56.71	B
ATOM	3791	C	LEU	B	128	23.972	15.083	17.305	1.00	59.21	B
ATOM	3792	O	LEU	B	128	23.125	14.544	16.593	1.00	58.61	B
ATOM	3793	N	VAL	B	129	23.710	15.550	18.527	1.00	61.62	B
ATOM	3794	CA	VAL	B	129	22.359	15.518	19.090	1.00	63.83	B
ATOM	3795	CB	VAL	B	129	22.336	15.597	20.636	1.00	63.76	B
ATOM	3796	CG1	VAL	B	129	21.162	14.798	21.177	1.00	63.03	B
ATOM	3797	CG2	VAL	B	129	23.628	15.117	21.227	1.00	64.25	B
ATOM	3798	C	VAL	B	129	21.585	16.725	18.566	1.00	64.71	B
ATOM	3799	O	VAL	B	129	20.517	16.571	17.968	1.00	65.71	B
ATOM	3800	N	VAL	B	130	22.129	17.922	18.798	1.00	64.55	B
ATOM	3801	CA	VAL	B	130	21.506	19.161	18.340	1.00	63.77	B
ATOM	3802	CB	VAL	B	130	22.418	20.380	18.629	1.00	62.58	B
ATOM	3803	CG1	VAL	B	130	21.797	21.649	18.110	1.00	62.49	B
ATOM	3804	CG2	VAL	B	130	22.639	20.511	20.121	1.00	62.69	B
ATOM	3805	C	VAL	B	130	21.164	19.050	16.847	1.00	64.50	B
ATOM	3806	O	VAL	B	130	20.160	19.600	16.404	1.00	64.32	B
ATOM	3807	N	LEU	B	131	21.968	18.282	16.103	1.00	66.15	B
ATOM	3808	CA	LEU	B	131	21.755	18.043	14.666	1.00	67.53	B
ATOM	3809	CB	LEU	B	131	23.065	17.628	13.968	1.00	66.53	B
ATOM	3810	CG	LEU	B	131	24.114	18.691	13.606	1.00	65.91	B
ATOM	3811	CD1	LEU	B	131	25.360	18.028	13.064	1.00	64.91	B
ATOM	3812	CD2	LEU	B	131	23.557	19.682	12.591	1.00	65.41	B
ATOM	3813	C	LEU	B	131	20.700	16.954	14.439	1.00	68.71	B
ATOM	3814	O	LEU	B	131	19.860	17.066	13.550	1.00	67.98	B
ATOM	3815	N	ALA	B	132	20.757	15.904	15.253	1.00	70.91	B
ATOM	3816	CA	ALA	B	132	19.822	14.785	15.159	1.00	73.30	B
ATOM	3817	CB	ALA	B	132	20.163	13.727	16.210	1.00	74.56	B
ATOM	3818	C	ALA	B	132	18.370	15.223	15.314	1.00	74.21	B
ATOM	3819	O	ALA	B	132	17.495	14.759	14.584	1.00	73.79	B
ATOM	3820	N	ILE	B	133	18.127	16.105	16.280	1.00	75.90	B
ATOM	3821	CA	ILE	B	133	16.789	16.629	16.556	1.00	77.86	B
ATOM	3822	CB	ILE	B	133	16.768	17.453	17.871	1.00	78.06	B
ATOM	3823	CG2	ILE	B	133	15.447	18.210	18.014	1.00	77.94	B
ATOM	3824	CG1	ILE	B	133	17.002	16.528	19.069	1.00	77.27	B
ATOM	3825	CD1	ILE	B	133	17.120	17.251	20.394	1.00	76.25	B
ATOM	3826	C	ILE	B	133	16.268	17.490	15.406	1.00	78.62	B
ATOM	3827	O	ILE	B	133	15.084	17.423	15.068	1.00	77.69	B
ATOM	3828	N	GLU	B	134	17.151	18.298	14.814	1.00	79.88	B
ATOM	3829	CA	GLU	B	134	16.763	19.154	13.695	1.00	80.97	B
ATOM	3830	CB	GLU	B	134	17.942	19.993	13.174	1.00	80.17	B
ATOM	3831	CG	GLU	B	134	17.540	20.984	12.063	1.00	79.68	B
ATOM	3832	CD	GLU	B	134	18.674	21.362	11.109	1.00	79.87	B
ATOM	3833	OE1	GLU	B	134	18.461	22.267	10.272	1.00	79.09	B
ATOM	3834	OE2	GLU	B	134	19.764	20.752	11.169	1.00	80.71	B
ATOM	3835	C	GLU	B	134	16.239	18.281	12.563	1.00	82.00	B
ATOM	3836	O	GLU	B	134	15.226	18.599	11.949	1.00	83.60	B
ATOM	3837	N	ARG	B	135	16.900	17.155	12.325	1.00	82.35	B
ATOM	3838	CA	ARG	B	135	16.485	16.266	11.252	1.00	83.46	B
ATOM	3839	CB	ARG	B	135	17.637	15.344	10.843	1.00	81.55	B
ATOM	3840	CG	ARG	B	135	18.986	16.053	10.705	1.00	79.05	B
ATOM	3841	CD	ARG	B	135	18.885	17.464	10.097	1.00	77.21	B
ATOM	3842	NE	ARG	B	135	18.503	17.473	8.685	1.00	74.76	B
ATOM	3843	CZ	ARG	B	135	18.590	18.535	7.887	1.00	72.21	B
ATOM	3844	NH1	ARG	B	135	19.046	19.691	8.353	1.00	70.55	B
ATOM	3845	NH2	ARG	B	135	18.220	18.438	6.618	1.00	70.99	B
ATOM	3846	C	ARG	B	135	15.206	15.480	11.567	1.00	85.85	B
ATOM	3847	O	ARG	B	135	14.739	14.685	10.752	1.00	86.58	B
ATOM	3848	N	TYR	B	136	14.659	15.686	12.761	1.00	88.26	B
ATOM	3849	CA	TYR	B	136	13.411	15.043	13.164	1.00	90.79	B
ATOM	3850	CB	TYR	B	136	13.509	14.519	14.610	1.00	92.30	B
ATOM	3851	CG	TYR	B	136	12.193	14.076	15.245	1.00	93.95	B
ATOM	3852	CD1	TYR	B	136	11.568	12.882	14.866	1.00	94.13	B
ATOM	3853	CE1	TYR	B	136	10.361	12.480	15.458	1.00	95.20	B
ATOM	3854	CD2	TYR	B	136	11.578	14.857	16.234	1.00	94.05	B
ATOM	3855	CE2	TYR	B	136	10.379	14.465	16.830	1.00	94.61	B
ATOM	3856	CZ	TYR	B	136	9.774	13.278	16.440	1.00	95.52	B
ATOM	3857	OH	TYR	B	136	8.592	12.894	17.039	1.00	95.57	B
ATOM	3858	C	TYR	B	136	12.346	16.131	13.047	1.00	91.94	B
ATOM	3859	O	TYR	B	136	11.165	15.891	13.276	1.00	92.42	B
ATOM	3860	N	VAL	B	137	12.786	17.331	12.675	1.00	93.53	B
ATOM	3861	CA	VAL	B	137	11.902	18.482	12.518	1.00	95.78	B
ATOM	3862	CB	VAL	B	137	12.339	19.647	13.443	1.00	95.49	B
ATOM	3863	CG1	VAL	B	137	11.438	20.860	13.249	1.00	95.53	B
ATOM	3864	CG2	VAL	B	137	12.309	19.194	14.897	1.00	95.34	B
ATOM	3865	C	VAL	B	137	11.833	18.956	11.060	1.00	97.47	B
ATOM	3866	O	VAL	B	137	10.744	19.144	10.521	1.00	97.89	B
ATOM	3867	N	VAL	B	138	12.986	19.148	10.423	1.00	99.41	B
ATOM	3868	CA	VAL	B	138	13.014	19.585	9.030	1.00	101.72	B
ATOM	3869	CB	VAL	B	138	14.315	20.354	8.684	1.00	100.87	B
ATOM	3870	CG1	VAL	B	138	14.385	21.657	9.463	1.00	100.20	B
ATOM	3871	CG2	VAL	B	138	15.526	19.507	8.979	1.00	100.97	B
ATOM	3872	C	VAL	B	138	12.804	18.414	8.061	1.00	104.51	B
ATOM	3873	O	VAL	B	138	12.824	18.593	6.843	1.00	105.14	B
ATOM	3874	N	VAL	B	139	12.616	17.217	8.615	1.00	108.02	B
ATOM	3875	CA	VAL	B	139	12.366	16.003	7.833	1.00	111.89	B
ATOM	3876	CB	VAL	B	139	13.483	14.944	8.014	1.00	112.38	B
ATOM	3877	CG1	VAL	B	139	13.145	13.674	7.234	1.00	112.79	B
ATOM	3878	CG2	VAL	B	139	14.822	15.504	7.544	1.00	112.54	B
ATOM	3879	C	VAL	B	139	11.018	15.437	8.286	1.00	114.39	B
ATOM	3880	O	VAL	B	139	10.225	14.979	7.467	1.00	113.91	B
ATOM	3881	N	CYS	B	140	10.791	15.423	9.599	1.00	118.58	B
ATOM	3882	CA	CYS	B	140	9.513	14.983	10.157	1.00	123.05	B
ATOM	3883	CB	CYS	B	140	9.702	14.224	11.474	1.00	123.02	B
ATOM	3884	SG	CYS	B	140	10.525	12.627	11.304	1.00	124.41	B
ATOM	3885	C	CYS	B	140	8.748	16.297	10.364	1.00	125.73	B
ATOM	3886	O	CYS	B	140	8.627	17.067	9.412	1.00	126.45	B
ATOM	3887	N	LYS	B	141	8.280	16.590	11.579	1.00	128.80	B
ATOM	3888	CA	LYS	B	141	7.554	17.848	11.827	1.00	131.99	B
ATOM	3889	CB	LYS	B	141	6.251	17.889	11.016	1.00	133.36	B
ATOM	3890	CG	LYS	B	141	6.338	18.774	9.772	1.00	135.18	B
ATOM	3891	CD	LYS	B	141	5.181	18.535	8.817	1.00	136.68	B
ATOM	3892	CE	LYS	B	141	5.349	19.341	7.536	1.00	137.18	B
ATOM	3893	NZ	LYS	B	141	4.262	19.060	6.555	1.00	137.49	B
ATOM	3894	C	LYS	B	141	7.267	18.188	13.295	1.00	133.51	B
ATOM	3895	O	LYS	B	141	7.181	17.292	14.141	1.00	133.68	B
ATOM	3896	N	PRO	B	142	7.119	19.498	13.611	1.00	134.82	B
ATOM	3897	CD	PRO	B	142	7.290	20.627	12.673	1.00	135.03	B
ATOM	3898	CA	PRO	B	142	6.841	20.002	14.966	1.00	135.59	B
ATOM	3899	CB	PRO	B	142	6.624	21.501	14.734	1.00	135.60	B
ATOM	3900	CG	PRO	B	142	7.545	21.796	13.604	1.00	135.30	B
ATOM	3901	C	PRO	B	142	5.615	19.364	15.620	1.00	136.09	B
ATOM	3902	O	PRO	B	142	4.561	19.229	14.996	1.00	136.49	B
ATOM	3903	N	GLY	B	149	16.541	29.203	13.561	1.00	127.68	B
ATOM	3904	CA	GLY	B	149	17.040	30.543	13.308	1.00	128.21	B
ATOM	3905	C	GLY	B	149	18.379	30.788	13.975	1.00	128.39	B
ATOM	3906	O	GLY	B	149	18.932	29.871	14.587	1.00	128.64	B
ATOM	3907	N	GLU	B	150	18.895	32.017	13.866	1.00	128.57	B
ATOM	3908	CA	GLU	B	150	20.182	32.397	14.469	1.00	128.11	B
ATOM	3909	CB	GLU	B	150	20.574	33.851	14.106	1.00	126.77	B
ATOM	3910	CG	GLU	B	150	21.117	34.074	12.679	1.00	123.79	B
ATOM	3911	CD	GLU	B	150	21.715	35.470	12.469	1.00	122.23	B
ATOM	3912	OE1	GLU	B	150	22.694	35.824	13.161	1.00	120.84	B
ATOM	3913	OE2	GLU	B	150	21.212	36.213	11.600	1.00	121.02	B
ATOM	3914	C	GLU	B	150	20.194	32.218	16.000	1.00	128.37	B
ATOM	3915	O	GLU	B	150	21.223	32.443	16.647	1.00	129.08	B
ATOM	3916	N	ASN	B	151	19.057	31.802	16.565	1.00	127.64	B
ATOM	3917	CA	ASN	B	151	18.923	31.585	18.008	1.00	126.44	B
ATOM	3918	CB	ASN	B	151	17.637	32.231	18.533	1.00	127.74	B
ATOM	3919	CG	ASN	B	151	17.762	33.731	18.694	1.00	128.73	B
ATOM	3920	OD1	ASN	B	151	17.802	34.245	19.814	1.00	129.41	B
ATOM	3921	ND2	ASN	B	151	17.827	34.444	17.573	1.00	129.30	B
ATOM	3922	C	ASN	B	151	18.951	30.115	18.424	1.00	124.70	B
ATOM	3923	O	ASN	B	151	19.809	29.700	19.206	1.00	125.42	B
ATOM	3924	N	HIS	B	152	18.000	29.340	17.906	1.00	121.62	B
ATOM	3925	CA	HIS	B	152	17.878	27.915	18.215	1.00	118.40	B
ATOM	3926	CB	HIS	B	152	16.754	27.303	17.378	1.00	119.05	B
ATOM	3927	CG	HIS	B	152	15.471	28.076	17.428	1.00	119.29	B
ATOM	3928	CD2	HIS	B	152	14.206	27.724	17.100	1.00	119.25	B
ATOM	3929	ND1	HIS	B	152	15.407	29.389	17.846	1.00	119.47	B
ATOM	3930	CE1	HIS	B	152	14.157	29.811	17.773	1.00	119.54	B
ATOM	3931	NE2	HIS	B	152	13.408	28.820	17.323	1.00	119.51	B
ATOM	3932	C	HIS	B	152	19.188	27.168	17.966	1.00	115.80	B
ATOM	3933	O	HIS	B	152	19.518	26.211	18.670	1.00	115.47	B
ATOM	3934	N	ALA	B	153	19.927	27.621	16.960	1.00	112.43	B
ATOM	3935	CA	ALA	B	153	21.207	27.035	16.613	1.00	109.07	B
ATOM	3936	CB	ALA	B	153	21.639	27.507	15.247	1.00	109.45	B
ATOM	3937	C	ALA	B	153	22.239	27.425	17.664	1.00	106.85	B
ATOM	3938	O	ALA	B	153	23.136	26.643	17.970	1.00	107.45	B
ATOM	3939	N	ILE	B	154	22.112	28.635	18.209	1.00	103.57	B
ATOM	3940	CA	ILE	B	154	23.029	29.108	19.244	1.00	101.42	B
ATOM	3941	CB	ILE	B	154	23.091	30.660	19.309	1.00	100.90	B
ATOM	3942	CG2	ILE	B	154	23.486	31.147	20.711	1.00	100.24	B
ATOM	3943	CG1	ILE	B	154	24.079	31.165	18.250	1.00	100.98	B
ATOM	3944	CD1	ILE	B	154	24.528	32.609	18.426	1.00	101.03	B
ATOM	3945	C	ILE	B	154	22.724	28.493	20.612	1.00	100.15	B
ATOM	3946	O	ILE	B	154	23.614	28.370	21.457	1.00	100.70	B
ATOM	3947	N	MET	B	155	21.471	28.101	20.826	1.00	98.04	B
ATOM	3948	CA	MET	B	155	21.084	27.461	22.081	1.00	95.74	B
ATOM	3949	CB	MET	B	155	19.571	27.470	22.260	1.00	97.60	B
ATOM	3950	CG	MET	B	155	19.035	28.781	22.787	1.00	99.64	B
ATOM	3951	SD	MET	B	155	17.258	28.705	23.005	1.00	102.63	B
ATOM	3952	CE	MET	B	155	16.705	29.956	21.823	1.00	102.27	B
ATOM	3953	C	MET	B	155	21.596	26.030	22.051	1.00	92.96	B
ATOM	3954	O	MET	B	155	22.054	25.505	23.064	1.00	92.82	B
ATOM	3955	N	GLY	B	156	21.500	25.407	20.878	1.00	89.63	B
ATOM	3956	CA	GLY	B	156	21.993	24.054	20.701	1.00	85.10	B
ATOM	3957	C	GLY	B	156	23.509	24.094	20.786	1.00	81.64	B
ATOM	3958	O	GLY	B	156	24.136	23.149	21.262	1.00	82.85	B
ATOM	3959	N	VAL	B	157	24.089	25.201	20.321	1.00	76.82	B
ATOM	3960	CA	VAL	B	157	25.529	25.426	20.357	1.00	71.27	B
ATOM	3961	CB	VAL	B	157	25.924	26.610	19.433	1.00	69.95	B
ATOM	3962	CG1	VAL	B	157	27.123	27.375	19.978	1.00	68.93	B
ATOM	3963	CG2	VAL	B	157	26.222	26.087	18.039	1.00	68.69	B
ATOM	3964	C	VAL	B	157	25.939	25.690	21.804	1.00	69.06	B
ATOM	3965	O	VAL	B	157	26.979	25.218	22.256	1.00	69.32	B
ATOM	3966	N	ALA	B	158	25.097	26.412	22.538	1.00	65.63	B
ATOM	3967	CA	ALA	B	158	25.373	26.713	23.937	1.00	63.38	B
ATOM	3968	CB	ALA	B	158	24.526	27.878	24.405	1.00	63.05	B
ATOM	3969	C	ALA	B	158	25.088	25.482	24.788	1.00	61.54	B
ATOM	3970	O	ALA	B	158	25.665	25.308	25.860	1.00	61.64	B
ATOM	3971	N	PHE	B	159	24.191	24.636	24.297	1.00	58.78	B
ATOM	3972	CA	PHE	B	159	23.809	23.409	24.981	1.00	56.72	B
ATOM	3973	CB	PHE	B	159	22.503	22.880	24.388	1.00	57.14	B
ATOM	3974	CG	PHE	B	159	22.168	21.483	24.802	1.00	57.52	B
ATOM	3975	CD1	PHE	B	159	21.568	21.233	26.030	1.00	58.26	B
ATOM	3976	CD2	PHE	B	159	22.439	20.414	23.955	1.00	56.66	B
ATOM	3977	CE1	PHE	B	159	21.242	19.934	26.406	1.00	58.36	B
ATOM	3978	CE2	PHE	B	159	22.118	19.118	24.322	1.00	56.20	B
ATOM	3979	CZ	PHE	B	159	21.519	18.874	25.547	1.00	56.88	B
ATOM	3980	C	PHE	B	159	24.909	22.360	24.874	1.00	55.46	B
ATOM	3981	O	PHE	B	159	25.089	21.560	25.790	1.00	54.64	B
ATOM	3982	N	THR	B	160	25.618	22.350	23.743	1.00	54.66	B
ATOM	3983	CA	THR	B	160	26.713	21.405	23.522	1.00	53.60	B
ATOM	3984	CB	THR	B	160	27.272	21.456	22.082	1.00	52.79	B
ATOM	3985	OG1	THR	B	160	27.810	22.755	21.816	1.00	51.94	B
ATOM	3986	CG2	THR	B	160	26.197	21.116	21.071	1.00	50.01	B
ATOM	3987	C	THR	B	160	27.845	21.723	24.482	1.00	54.09	B
ATOM	3988	O	THR	B	160	28.510	20.823	24.978	1.00	53.56	B
ATOM	3989	N	TRP	B	161	28.072	23.013	24.718	1.00	55.27	B
ATOM	3990	CA	TRP	B	161	29.105	23.462	25.643	1.00	56.72	B
ATOM	3991	CB	TRP	B	161	29.354	24.952	25.479	1.00	57.70	B
ATOM	3992	CG	TRP	B	161	30.131	25.218	24.283	1.00	60.02	B
ATOM	3993	CD2	TRP	B	161	31.540	25.434	24.219	1.00	61.91	B
ATOM	3994	CE2	TRP	B	161	31.879	25.559	22.859	1.00	62.64	B
ATOM	3995	CE3	TRP	B	161	32.553	25.532	25.181	1.00	63.01	B
ATOM	3996	CD1	TRP	B	161	29.679	25.229	23.004	1.00	60.79	B
ATOM	3997	NE1	TRP	B	161	30.721	25.429	22.137	1.00	62.55	B
ATOM	3998	CZ2	TRP	B	161	33.193	25.776	22.432	1.00	63.03	B
ATOM	3999	CZ3	TRP	B	161	33.860	25.750	24.757	1.00	62.82	B
ATOM	4000	CH2	TRP	B	161	34.166	25.868	23.393	1.00	62.68	B
ATOM	4001	C	TRP	B	161	28.694	23.173	27.069	1.00	57.31	B
ATOM	4002	O	TRP	B	161	29.521	22.811	27.895	1.00	56.86	B
ATOM	4003	N	VAL	B	162	27.407	23.354	27.351	1.00	58.66	B
ATOM	4004	CA	VAL	B	162	26.854	23.097	28.676	1.00	59.63	B
ATOM	4005	CB	VAL	B	162	25.346	23.409	28.719	1.00	59.58	B
ATOM	4006	CG1	VAL	B	162	24.727	22.838	29.982	1.00	60.11	B
ATOM	4007	CG2	VAL	B	162	25.125	24.912	28.660	1.00	59.16	B
ATOM	4008	C	VAL	B	162	27.062	21.633	29.022	1.00	59.85	B
ATOM	4009	O	VAL	B	162	27.735	21.309	30.000	1.00	59.86	B
ATOM	4010	N	MET	B	163	26.494	20.762	28.192	1.00	60.26	B
ATOM	4011	CA	MET	B	163	26.602	19.318	28.363	1.00	60.61	B
ATOM	4012	CB	MET	B	163	25.777	18.607	27.297	1.00	59.43	B
ATOM	4013	CG	MET	B	163	24.340	19.008	27.320	1.00	58.01	B
ATOM	4014	SD	MET	B	163	23.717	18.842	28.979	1.00	58.03	B
ATOM	4015	CE	MET	B	163	22.838	17.275	28.847	1.00	56.41	B
ATOM	4016	C	MET	B	163	28.050	18.828	28.312	1.00	61.41	B
ATOM	4017	O	MET	B	163	28.517	18.193	29.252	1.00	62.39	B
ATOM	4018	N	ALA	B	164	28.763	19.135	27.228	1.00	61.09	B
ATOM	4019	CA	ALA	B	164	30.158	18.717	27.092	1.00	59.69	B
ATOM	4020	CB	ALA	B	164	30.778	19.322	25.843	1.00	58.83	B
ATOM	4021	C	ALA	B	164	30.965	19.102	28.330	1.00	58.60	B
ATOM	4022	O	ALA	B	164	31.760	18.304	28.819	1.00	57.87	B
ATOM	4023	N	LEU	B	165	30.729	20.308	28.850	1.00	58.24	B
ATOM	4024	CA	LEU	B	165	31.427	20.781	30.047	1.00	58.33	B
ATOM	4025	CB	LEU	B	165	31.195	22.276	30.295	1.00	57.25	B
ATOM	4026	CG	LEU	B	165	32.096	23.257	29.537	1.00	56.84	B
ATOM	4027	CD1	LEU	B	165	31.539	24.664	29.651	1.00	57.38	B
ATOM	4028	CD2	LEU	B	165	33.518	23.199	30.064	1.00	55.20	B
ATOM	4029	C	LEU	B	165	31.018	19.996	31.280	1.00	58.61	B
ATOM	4030	O	LEU	B	165	31.788	19.901	32.230	1.00	58.81	B
ATOM	4031	N	ALA	B	166	29.812	19.431	31.258	1.00	58.81	B
ATOM	4032	CA	ALA	B	166	29.307	18.630	32.380	1.00	59.28	B
ATOM	4033	CB	ALA	B	166	27.793	18.433	32.254	1.00	58.78	B
ATOM	4034	C	ALA	B	166	30.012	17.268	32.466	1.00	59.29	B
ATOM	4035	O	ALA	B	166	29.825	16.516	33.431	1.00	59.22	B
ATOM	4036	N	CYS	B	167	30.822	16.963	31.450	1.00	58.64	B
ATOM	4037	CA	CYS	B	167	31.562	15.706	31.383	1.00	55.37	B
ATOM	4038	CB	CYS	B	167	31.273	14.982	30.074	1.00	55.43	B
ATOM	4039	SG	CYS	B	167	31.838	13.283	30.097	1.00	56.58	B
ATOM	4040	C	CYS	B	167	33.058	15.926	31.482	1.00	52.70	B
ATOM	4041	O	CYS	B	167	33.748	15.205	32.189	1.00	52.52	B
ATOM	4042	N	ALA	B	168	33.551	16.924	30.761	1.00	50.34	B
ATOM	4043	CA	ALA	B	168	34.971	17.233	30.749	1.00	48.72	B
ATOM	4044	CB	ALA	B	168	35.322	17.980	29.470	1.00	48.38	B
ATOM	4045	C	ALA	B	168	35.466	18.008	31.963	1.00	47.33	B
ATOM	4046	O	ALA	B	168	36.611	17.847	32.374	1.00	46.02	B
ATOM	4047	N	ALA	B	169	34.591	18.807	32.564	1.00	47.60	B
ATOM	4048	CA	ALA	B	169	34.972	19.643	33.709	1.00	48.37	B
ATOM	4049	CB	ALA	B	169	34.081	20.887	33.764	1.00	47.42	B
ATOM	4050	C	ALA	B	169	35.152	19.043	35.124	1.00	48.27	B
ATOM	4051	O	ALA	B	169	36.001	19.520	35.889	1.00	47.85	B
ATOM	4052	N	PRO	B	170	34.342	18.032	35.509	1.00	47.76	B
ATOM	4053	CD	PRO	B	170	33.096	17.575	34.863	1.00	47.21	B
ATOM	4054	CA	PRO	B	170	34.475	17.428	36.843	1.00	46.74	B
ATOM	4055	CB	PRO	B	170	33.372	16.373	36.842	1.00	46.38	B
ATOM	4056	CG	PRO	B	170	32.308	17.026	36.031	1.00	45.54	B
ATOM	4057	C	PRO	B	170	35.843	16.853	37.269	1.00	46.63	B
ATOM	4058	O	PRO	B	170	36.271	17.080	38.397	1.00	45.37	B
ATOM	4059	N	PRO	B	171	36.537	16.097	36.391	1.00	47.67	B
ATOM	4060	CD	PRO	B	171	36.104	15.603	35.071	1.00	48.29	B
ATOM	4061	CA	PRO	B	171	37.848	15.521	36.740	1.00	48.14	B
ATOM	4062	CB	PRO	B	171	38.245	14.788	35.464	1.00	47.84	B
ATOM	4063	CG	PRO	B	171	36.931	14.349	34.914	1.00	48.53	B
ATOM	4064	C	PRO	B	171	38.900	16.552	37.109	1.00	49.12	B
ATOM	4065	O	PRO	B	171	39.948	16.214	37.660	1.00	49.58	B
ATOM	4066	N	LEU	B	172	38.609	17.804	36.772	1.00	51.01	B
ATOM	4067	CA	LEU	B	172	39.491	18.939	37.032	1.00	53.26	B
ATOM	4068	CB	LEU	B	172	39.300	20.002	35.942	1.00	52.30	B
ATOM	4069	CG	LEU	B	172	39.620	19.648	34.487	1.00	51.06	B
ATOM	4070	CD1	LEU	B	172	39.010	20.684	33.563	1.00	50.52	B
ATOM	4071	CD2	LEU	B	172	41.122	19.558	34.293	1.00	49.55	B
ATOM	4072	C	LEU	B	172	39.190	19.570	38.388	1.00	54.85	B
ATOM	4073	O	LEU	B	172	39.913	20.456	38.846	1.00	55.44	B
ATOM	4074	N	VAL	B	173	38.102	19.126	39.010	1.00	57.06	B
ATOM	4075	CA	VAL	B	173	37.682	19.657	40.302	1.00	57.94	B
ATOM	4076	CB	VAL	B	173	36.258	20.273	40.215	1.00	56.97	B
ATOM	4077	CG1	VAL	B	173	35.769	20.691	41.587	1.00	58.52	B
ATOM	4078	CG2	VAL	B	173	36.271	21.476	39.285	1.00	56.63	B
ATOM	4079	C	VAL	B	173	37.758	18.620	41.424	1.00	58.50	B
ATOM	4080	O	VAL	B	173	38.498	18.817	42.390	1.00	60.34	B
ATOM	4081	N	GLY	B	174	37.022	17.517	41.295	1.00	57.60	B
ATOM	4082	CA	GLY	B	174	37.048	16.503	42.334	1.00	56.64	B
ATOM	4083	C	GLY	B	174	36.351	15.197	42.007	1.00	56.60	B
ATOM	4084	O	GLY	B	174	36.396	14.248	42.792	1.00	56.67	B
ATOM	4085	N	TRP	B	175	35.683	15.144	40.862	1.00	56.31	B
ATOM	4086	CA	TRP	B	175	34.992	13.930	40.459	1.00	56.36	B
ATOM	4087	CB	TRP	B	175	33.563	14.265	40.016	1.00	57.56	B
ATOM	4088	CG	TRP	B	175	32.620	13.113	40.132	1.00	59.30	B
ATOM	4089	CD2	TRP	B	175	31.319	13.011	39.547	1.00	60.10	B
ATOM	4090	CE2	TRP	B	175	30.813	11.732	39.876	1.00	60.83	B
ATOM	4091	CE3	TRP	B	175	30.534	13.872	38.770	1.00	59.77	B
ATOM	4092	CD1	TRP	B	175	32.843	11.929	40.783	1.00	59.81	B
ATOM	4093	NE1	TRP	B	175	31.764	11.094	40.630	1.00	61.38	B
ATOM	4094	CZ2	TRP	B	175	29.553	11.293	39.454	1.00	60.54	B
ATOM	4095	CZ3	TRP	B	175	29.287	13.435	38.349	1.00	60.67	B
ATOM	4096	CH2	TRP	B	175	28.808	12.155	38.694	1.00	60.78	B
ATOM	4097	C	TRP	B	175	35.814	13.279	39.341	1.00	55.38	B
ATOM	4098	O	TRP	B	175	35.861	13.778	38.220	1.00	57.12	B
ATOM	4099	N	SER	B	176	36.470	12.168	39.668	1.00	53.14	B
ATOM	4100	CA	SER	B	176	37.350	11.450	38.747	1.00	50.42	B
ATOM	4101	CB	SER	B	176	36.680	11.140	37.408	1.00	50.16	B
ATOM	4102	OG	SER	B	176	37.527	10.344	36.594	1.00	49.09	B
ATOM	4103	C	SER	B	176	38.594	12.295	38.520	1.00	49.46	B
ATOM	4104	O	SER	B	176	38.694	13.425	39.004	1.00	48.70	B
ATOM	4105	N	ARG	B	177	39.551	11.742	37.790	1.00	49.22	B
ATOM	4106	CA	ARG	B	177	40.798	12.448	37.521	1.00	48.37	B
ATOM	4107	CB	ARG	B	177	41.814	12.164	38.642	1.00	46.91	B
ATOM	4108	CG	ARG	B	177	42.065	10.684	38.926	1.00	46.91	B
ATOM	4109	CD	ARG	B	177	43.022	10.487	40.092	1.00	47.67	B
ATOM	4110	NE	ARG	B	177	43.436	9.090	40.236	1.00	48.53	B
ATOM	4111	CZ	ARG	B	177	44.368	8.666	41.086	1.00	49.45	B
ATOM	4112	NH1	ARG	B	177	44.994	9.527	41.876	1.00	50.40	B
ATOM	4113	NH2	ARG	B	177	44.663	7.377	41.164	1.00	50.73	B
ATOM	4114	C	ARG	B	177	41.370	12.038	36.174	1.00	47.50	B
ATOM	4115	O	ARG	B	177	41.135	10.919	35.711	1.00	48.13	B
ATOM	4116	N	TYR	B	178	42.027	12.975	35.499	1.00	46.23	B
ATOM	4117	CA	TYR	B	178	42.652	12.659	34.223	1.00	45.94	B
ATOM	4118	CB	TYR	B	178	42.860	13.912	33.374	1.00	44.57	B
ATOM	4119	CG	TYR	B	178	41.573	14.465	32.793	1.00	44.05	B
ATOM	4120	CD1	TYR	B	178	40.736	13.667	32.016	1.00	42.98	B
ATOM	4121	CE1	TYR	B	178	39.555	14.170	31.488	1.00	42.81	B
ATOM	4122	CD2	TYR	B	178	41.187	15.788	33.024	1.00	44.15	B
ATOM	4123	CE2	TYR	B	178	40.003	16.296	32.499	1.00	41.93	B
ATOM	4124	CZ	TYR	B	178	39.199	15.481	31.737	1.00	42.50	B
ATOM	4125	OH	TYR	B	178	38.030	15.972	31.228	1.00	44.24	B
ATOM	4126	C	TYR	B	178	43.967	11.995	34.615	1.00	46.85	B
ATOM	4127	O	TYR	B	178	44.707	12.491	35.477	1.00	47.37	B
ATOM	4128	N	ILE	B	179	44.211	10.830	34.028	1.00	46.80	B
ATOM	4129	CA	ILE	B	179	45.382	10.026	34.348	1.00	44.70	B
ATOM	4130	CB	ILE	B	179	44.928	8.889	35.321	1.00	42.92	B
ATOM	4131	CG2	ILE	B	179	43.920	7.971	34.639	1.00	42.83	B
ATOM	4132	CG1	ILE	B	179	46.111	8.139	35.918	1.00	41.23	B
ATOM	4133	CD1	ILE	B	179	45.713	7.295	37.102	1.00	39.79	B
ATOM	4134	C	ILE	B	179	45.992	9.495	33.045	1.00	44.54	B
ATOM	4135	O	ILE	B	179	45.264	9.049	32.155	1.00	43.77	B
ATOM	4136	N	PRO	B	180	47.333	9.583	32.898	1.00	44.43	B
ATOM	4137	CD	PRO	B	180	48.308	10.041	33.903	1.00	45.33	B
ATOM	4138	CA	PRO	B	180	48.031	9.117	31.695	1.00	43.02	B
ATOM	4139	CB	PRO	B	180	49.507	9.230	32.087	1.00	44.26	B
ATOM	4140	CG	PRO	B	180	49.494	9.184	33.588	1.00	44.53	B
ATOM	4141	C	PRO	B	180	47.634	7.716	31.258	1.00	42.16	B
ATOM	4142	O	PRO	B	180	47.543	6.802	32.085	1.00	40.86	B
ATOM	4143	N	GLU	B	181	47.344	7.589	29.959	1.00	41.21	B
ATOM	4144	CA	GLU	B	181	46.911	6.334	29.347	1.00	40.51	B
ATOM	4145	CB	GLU	B	181	45.583	6.535	28.591	1.00	40.40	B
ATOM	4146	CG	GLU	B	181	44.364	6.877	29.465	1.00	41.68	B
ATOM	4147	CD	GLU	B	181	43.017	6.546	28.797	1.00	43.21	B
ATOM	4148	OE1	GLU	B	181	42.499	7.370	28.000	1.00	41.17	B
ATOM	4149	OE2	GLU	B	181	42.474	5.450	29.077	1.00	43.24	B
ATOM	4150	C	GLU	B	181	47.937	5.703	28.398	1.00	39.87	B
ATOM	4151	O	GLU	B	181	48.829	6.389	27.883	1.00	37.55	B
ATOM	4152	N	GLY	B	182	47.788	4.390	28.190	1.00	39.24	B
ATOM	4153	CA	GLY	B	182	48.653	3.632	27.298	1.00	38.68	B
ATOM	4154	C	GLY	B	182	50.139	3.768	27.552	1.00	39.01	B
ATOM	4155	O	GLY	B	182	50.660	3.242	28.532	1.00	39.43	B
ATOM	4156	N	MET	B	183	50.830	4.434	26.632	1.00	39.97	B
ATOM	4157	CA	MET	B	183	52.266	4.666	26.758	1.00	40.34	B
ATOM	4158	CB	MET	B	183	52.900	4.825	25.380	1.00	39.84	B
ATOM	4159	CG	MET	B	183	52.923	3.555	24.551	1.00	39.88	B
ATOM	4160	SD	MET	B	183	53.539	3.897	22.885	1.00	40.41	B
ATOM	4161	CE	MET	B	183	53.383	2.258	22.102	1.00	40.66	B
ATOM	4162	C	MET	B	183	52.558	5.910	27.609	1.00	40.79	B
ATOM	4163	O	MET	B	183	53.648	6.474	27.538	1.00	39.75	B
ATOM	4164	N	GLN	B	184	51.566	6.319	28.405	1.00	41.35	B
ATOM	4165	CA	GLN	B	184	51.645	7.481	29.297	1.00	40.52	B
ATOM	4166	CB	GLN	B	184	52.667	7.231	30.409	1.00	39.42	B
ATOM	4167	CG	GLN	B	184	52.609	5.842	31.019	1.00	38.43	B
ATOM	4168	CD	GLN	B	184	51.247	5.491	31.569	1.00	38.46	B
ATOM	4169	OE1	GLN	B	184	50.838	5.993	32.616	1.00	40.67	B
ATOM	4170	NE2	GLN	B	184	50.542	4.607	30.878	1.00	37.04	B
ATOM	4171	C	GLN	B	184	51.982	8.770	28.557	1.00	40.33	B
ATOM	4172	O	GLN	B	184	52.861	9.518	28.973	1.00	40.26	B
ATOM	4173	N	CYS	B	185	51.260	9.022	27.469	1.00	42.60	B
ATOM	4174	CA	CYS	B	185	51.457	10.206	26.626	1.00	44.30	B
ATOM	4175	CB	CYS	B	185	52.122	9.816	25.307	1.00	45.15	B
ATOM	4176	SG	CYS	B	185	53.907	9.820	25.365	1.00	50.28	B
ATOM	4177	C	CYS	B	185	50.181	10.997	26.323	1.00	44.47	B
ATOM	4178	O	CYS	B	185	50.252	12.085	25.747	1.00	44.04	B
ATOM	4179	N	SER	B	186	49.028	10.413	26.657	1.00	44.87	B
ATOM	4180	CA	SER	B	186	47.705	11.028	26.472	1.00	44.16	B
ATOM	4181	CB	SER	B	186	46.956	10.398	25.285	1.00	41.83	B
ATOM	4182	OG	SER	B	186	46.726	9.007	25.461	1.00	39.43	B
ATOM	4183	C	SER	B	186	46.924	10.789	27.769	1.00	45.42	B
ATOM	4184	O	SER	B	186	47.147	9.773	28.437	1.00	46.77	B
ATOM	4185	N	CYS	B	187	46.049	11.726	28.148	1.00	45.09	B
ATOM	4186	CA	CYS	B	187	45.260	11.577	29.379	1.00	44.35	B
ATOM	4187	C	CYS	B	187	43.774	11.352	29.157	1.00	44.12	B
ATOM	4188	O	CYS	B	187	43.229	11.744	28.121	1.00	44.48	B
ATOM	4189	CB	CYS	B	187	45.493	12.747	30.352	1.00	43.77	B
ATOM	4190	SG	CYS	B	187	46.945	12.465	31.418	1.00	45.34	B
ATOM	4191	N	GLY	B	188	43.151	10.682	30.134	1.00	43.53	B
ATOM	4192	CA	GLY	B	188	41.728	10.372	30.098	1.00	42.46	B
ATOM	4193	C	GLY	B	188	41.175	9.996	31.466	1.00	42.57	B
ATOM	4194	O	GLY	B	188	41.933	9.856	32.424	1.00	42.76	B
ATOM	4195	N	ILE	B	189	39.854	9.820	31.554	1.00	43.21	B
ATOM	4196	CA	ILE	B	189	39.175	9.463	32.804	1.00	41.80	B
ATOM	4197	CB	ILE	B	189	37.639	9.287	32.592	1.00	41.60	B
ATOM	4198	CG2	ILE	B	189	37.013	8.474	33.722	1.00	40.87	B
ATOM	4199	CG1	ILE	B	189	36.954	10.658	32.538	1.00	40.52	B
ATOM	4200	CD1	ILE	B	189	37.284	11.493	31.334	1.00	39.03	B
ATOM	4201	C	ILE	B	189	39.781	8.230	33.462	1.00	42.24	B
ATOM	4202	O	ILE	B	189	40.234	7.303	32.789	1.00	40.73	B
ATOM	4203	N	ASP	B	190	39.788	8.241	34.790	1.00	44.04	B
ATOM	4204	CA	ASP	B	190	40.370	7.162	35.574	1.00	46.15	B
ATOM	4205	CB	ASP	B	190	40.672	7.661	36.985	1.00	44.43	B
ATOM	4206	CG	ASP	B	190	41.630	6.766	37.719	1.00	45.23	B
ATOM	4207	OD1	ASP	B	190	41.688	6.871	38.954	1.00	48.80	B
ATOM	4208	OD2	ASP	B	190	42.331	5.958	37.076	1.00	45.03	B
ATOM	4209	C	ASP	B	190	39.566	5.861	35.616	1.00	47.95	B
ATOM	4210	O	ASP	B	190	38.871	5.563	36.598	1.00	49.71	B
ATOM	4211	N	TYR	B	191	39.680	5.082	34.543	1.00	48.65	B
ATOM	4212	CA	TYR	B	191	38.987	3.802	34.436	1.00	48.64	B
ATOM	4213	CB	TYR	B	191	38.917	3.330	32.967	1.00	46.89	B
ATOM	4214	CG	TYR	B	191	38.662	4.404	31.923	1.00	45.79	B
ATOM	4215	CD1	TYR	B	191	37.435	5.046	31.839	1.00	46.76	B
ATOM	4216	CE1	TYR	B	191	37.191	6.027	30.871	1.00	47.03	B
ATOM	4217	CD2	TYR	B	191	39.648	4.766	31.008	1.00	45.22	B
ATOM	4218	CE2	TYR	B	191	39.414	5.744	30.036	1.00	45.26	B
ATOM	4219	CZ	TYR	B	191	38.182	6.371	29.974	1.00	45.44	B
ATOM	4220	OH	TYR	B	191	37.929	7.346	29.031	1.00	43.89	B
ATOM	4221	C	TYR	B	191	39.816	2.787	35.217	1.00	50.06	B
ATOM	4222	O	TYR	B	191	39.291	1.810	35.753	1.00	50.55	B
ATOM	4223	N	TYR	B	192	41.111	3.080	35.309	1.00	51.23	B
ATOM	4224	CA	TYR	B	192	42.123	2.235	35.945	1.00	53.52	B
ATOM	4225	CB	TYR	B	192	43.508	2.812	35.617	1.00	52.90	B
ATOM	4226	CG	TYR	B	192	43.713	3.051	34.127	1.00	52.17	B
ATOM	4227	CD1	TYR	B	192	44.092	2.006	33.272	1.00	50.77	B
ATOM	4228	CE1	TYR	B	192	44.240	2.210	31.896	1.00	49.16	B
ATOM	4229	CD2	TYR	B	192	43.491	4.309	33.566	1.00	51.18	B
ATOM	4230	CE2	TYR	B	192	43.635	4.521	32.193	1.00	50.26	B
ATOM	4231	CZ	TYR	B	192	44.007	3.469	31.365	1.00	49.81	B
ATOM	4232	OH	TYR	B	192	44.139	3.681	30.010	1.00	47.02	B
ATOM	4233	C	TYR	B	192	42.029	1.873	37.436	1.00	55.19	B
ATOM	4234	O	TYR	B	192	42.268	0.712	37.811	1.00	55.26	B
ATOM	4235	N	THR	B	193	41.717	2.854	38.284	1.00	56.39	B
ATOM	4236	CA	THR	B	193	41.616	2.613	39.723	1.00	56.95	B
ATOM	4237	CB	THR	B	193	42.753	3.304	40.489	1.00	53.89	B
ATOM	4238	OG1	THR	B	193	42.602	4.723	40.396	1.00	49.79	B
ATOM	4239	CG2	THR	B	193	44.090	2.901	39.917	1.00	52.25	B
ATOM	4240	C	THR	B	193	40.287	3.050	40.342	1.00	60.85	B
ATOM	4241	O	THR	B	193	39.572	3.895	39.790	1.00	61.01	B
ATOM	4242	N	PRO	B	194	39.915	2.429	41.480	1.00	64.06	B
ATOM	4243	CD	PRO	B	194	40.555	1.251	42.100	1.00	65.86	B
ATOM	4244	CA	PRO	B	194	38.668	2.760	42.176	1.00	64.52	B
ATOM	4245	CB	PRO	B	194	38.528	1.623	43.202	1.00	65.79	B
ATOM	4246	CG	PRO	B	194	39.367	0.502	42.643	1.00	66.14	B
ATOM	4247	C	PRO	B	194	38.822	4.091	42.899	1.00	64.24	B
ATOM	4248	O	PRO	B	194	37.832	4.793	43.116	1.00	64.07	B
ATOM	4249	N	HIS	B	195	40.074	4.410	43.254	1.00	63.80	B
ATOM	4250	CA	HIS	B	195	40.468	5.619	43.990	1.00	63.97	B
ATOM	4251	CB	HIS	B	195	40.964	6.726	43.046	1.00	60.74	B
ATOM	4252	CG	HIS	B	195	41.792	7.780	43.726	1.00	57.89	B
ATOM	4253	CD2	HIS	B	195	42.959	7.695	44.409	1.00	57.54	B
ATOM	4254	ND1	HIS	B	195	41.438	9.112	43.746	1.00	56.68	B
ATOM	4255	CE1	HIS	B	195	42.347	9.801	44.413	1.00	54.90	B
ATOM	4256	NE2	HIS	B	195	43.281	8.965	44.826	1.00	55.47	B
ATOM	4257	C	HIS	B	195	39.341	6.126	44.878	1.00	65.97	B
ATOM	4258	O	HIS	B	195	38.519	6.936	44.445	1.00	66.06	B
ATOM	4259	N	GLU	B	196	39.278	5.587	46.096	1.00	68.45	B
ATOM	4260	CA	GLU	B	196	38.252	5.947	47.082	1.00	69.90	B
ATOM	4261	CB	GLU	B	196	38.657	5.445	48.487	1.00	71.96	B
ATOM	4262	CG	GLU	B	196	38.857	3.927	48.643	1.00	73.01	B
ATOM	4263	CD	GLU	B	196	37.624	3.206	49.168	1.00	73.64	B
ATOM	4264	OE1	GLU	B	196	37.008	3.699	50.142	1.00	73.54	B
ATOM	4265	OE2	GLU	B	196	37.284	2.134	48.617	1.00	74.06	B
ATOM	4266	C	GLU	B	196	38.007	7.462	47.144	1.00	69.54	B
ATOM	4267	O	GLU	B	196	36.871	7.917	47.016	1.00	68.88	B
ATOM	4268	N	GLU	B	197	39.097	8.224	47.270	1.00	69.83	B
ATOM	4269	CA	GLU	B	197	39.087	9.690	47.386	1.00	69.78	B
ATOM	4270	CB	GLU	B	197	40.530	10.213	47.481	1.00	70.97	B
ATOM	4271	CG	GLU	B	197	41.253	9.826	48.777	1.00	73.85	B
ATOM	4272	CD	GLU	B	197	42.538	9.037	48.545	1.00	76.18	B
ATOM	4273	OE1	GLU	B	197	43.625	9.596	48.810	1.00	77.41	B
ATOM	4274	OE2	GLU	B	197	42.465	7.860	48.115	1.00	76.60	B
ATOM	4275	C	GLU	B	197	38.282	10.539	46.385	1.00	69.42	B
ATOM	4276	O	GLU	B	197	37.903	11.666	46.704	1.00	68.51	B
ATOM	4277	N	THR	B	198	38.025	10.017	45.187	1.00	69.76	B
ATOM	4278	CA	THR	B	198	37.262	10.752	44.169	1.00	68.94	B
ATOM	4279	CB	THR	B	198	38.176	11.191	42.967	1.00	67.00	B
ATOM	4280	OG1	THR	B	198	38.737	10.040	42.320	1.00	66.04	B
ATOM	4281	CG2	THR	B	198	39.314	12.074	43.443	1.00	64.47	B
ATOM	4282	C	THR	B	198	36.078	9.917	43.643	1.00	70.10	B
ATOM	4283	O	THR	B	198	35.038	10.456	43.253	1.00	70.11	B
ATOM	4284	N	ASN	B	199	36.232	8.598	43.729	1.00	70.89	B
ATOM	4285	CA	ASN	B	199	35.263	7.605	43.259	1.00	72.04	B
ATOM	4286	CB	ASN	B	199	33.934	7.606	44.050	1.00	72.71	B
ATOM	4287	CG	ASN	B	199	33.252	6.211	44.072	1.00	72.67	B
ATOM	4288	OD1	ASM	B	199	32.023	6.098	44.129	1.00	71.02	B
ATOM	4289	ND2	ASN	B	199	34.063	5.153	44.030	1.00	72.35	B
ATOM	4290	C	ASN	B	199	35.031	7.689	41.753	1.00	71.85	B
ATOM	4291	O	ASN	B	199	34.133	8.381	41.257	1.00	70.00	B
ATOM	4292	N	ASN	B	200	35.933	7.026	41.038	1.00	72.67	B
ATOM	4293	CA	ASN	B	200	35.883	6.937	39.590	1.00	73.08	B
ATOM	4294	CB	ASN	B	200	37.252	6.501	39.038	1.00	70.97	B
ATOM	4295	CG	ASN	B	200	38.426	7.112	39.810	1.00	67.38	B
ATOM	4296	OD1	ASN	B	200	39.381	6.422	40.135	1.00	65.29	B
ATOM	4297	ND2	ASN	B	200	38.345	8.400	40.112	1.00	64.62	B
ATOM	4298	C	ASN	B	200	34.817	5.867	39.317	1.00	73.80	B
ATOM	4299	O	ASN	B	200	34.139	5.902	38.291	1.00	74.18	B
ATOM	4300	N	GLU	B	201	34.654	4.951	40.280	1.00	73.80	B
ATOM	4301	CA	GLU	B	201	33.667	3.874	40.214	1.00	73.19	B
ATOM	4302	CB	GLU	B	201	33.728	3.001	41.479	1.00	74.84	B
ATOM	4303	CG	GLU	B	201	34.719	1.825	41.469	1.00	76.21	B
ATOM	4304	CD	GLU	B	201	34.651	0.971	42.756	1.00	77.63	B
ATOM	4305	OE1	GLU	B	201	33.708	1.147	43.561	1.00	77.96	B
ATOM	4306	OE2	GLU	B	201	35.542	0.118	42.970	1.00	77.13	B
ATOM	4307	C	GLU	B	201	32.257	4.458	40.088	1.00	72.15	B
ATOM	4308	O	GLU	B	201	31.298	3.726	39.851	1.00	72.61	B
ATOM	4309	N	SER	B	202	32.131	5.768	40.287	1.00	70.83	B
ATOM	4310	CA	SER	B	202	30.839	6.440	40.187	1.00	69.39	B
ATOM	4311	CB	SER	B	202	30.520	7.219	41.461	1.00	70.07	B
ATOM	4312	OG	SER	B	202	31.289	8.407	41.530	1.00	70.02	B
ATOM	4313	C	SER	B	202	30.798	7.392	39.005	1.00	67.83	B
ATOM	4314	O	SER	B	202	29.732	7.611	38.431	1.00	69.25	B
ATOM	4315	N	PHE	B	203	31.938	7.997	38.671	1.00	65.32	B
ATOM	4316	CA	PHE	B	203	31.993	8.923	37.536	1.00	62.82	B
ATOM	4317	CB	PHE	B	203	33.238	9.807	37.585	1.00	60.78	B
ATOM	4318	CG	PHE	B	203	33.341	10.756	36.419	1.00	58.42	B
ATOM	4319	CD1	PHE	B	203	33.909	10.350	35.220	1.00	57.15	B
ATOM	4320	CD2	PHE	B	203	32.827	12.039	36.507	1.00	56.92	B
ATOM	4321	CE1	PHE	B	203	33.954	11.203	34.137	1.00	56.13	B
ATOM	4322	CE2	PHE	B	203	32.871	12.895	35.425	1.00	55.40	B
ATOM	4323	CZ	PHE	B	203	33.433	12.476	34.240	1.00	55.37	B
ATOM	4324	C	PHE	B	203	31.959	8.199	36.195	1.00	62.08	B
ATOM	4325	O	PHE	B	203	31.323	8.657	35.249	1.00	61.06	B
ATOM	4326	N	VAL	B	204	32.701	7.101	36.108	1.00	61.78	B
ATOM	4327	CA	VAL	B	204	32.764	6.305	34.890	1.00	61.46	B
ATOM	4328	CB	VAL	B	204	33.863	5.221	35.000	1.00	59.71	B
ATOM	4329	CG1	VAL	B	204	34.076	4.547	33.663	1.00	59.13	B
ATOM	4330	CG2	VAL	B	204	35.162	5.840	35.500	1.00	57.48	B
ATOM	4331	C	VAL	B	204	31.396	5.675	34.578	1.00	62.44	B
ATOM	4332	O	VAL	B	204	31.104	5.333	33.431	1.00	62.70	B
ATOM	4333	N	ILE	B	205	30.557	5.530	35.600	1.00	63.14	B
ATOM	4334	CA	ILE	B	205	29.222	4.976	35.404	1.00	64.37	B
ATOM	4335	CB	ILE	B	205	28.697	4.278	36.679	1.00	64.39	B
ATOM	4336	CG2	ILE	B	205	27.216	3.926	36.526	1.00	64.34	B
ATOM	4337	CG1	ILE	B	205	29.531	3.019	36.949	1.00	65.00	B
ATOM	4338	CD1	ILE	B	205	29.058	2.172	38.119	1.00	65.93	B
ATOM	4339	C	ILE	B	205	28.278	6.097	34.974	1.00	65.49	B
ATOM	4340	O	ILE	B	205	27.338	5.869	34.217	1.00	66.16	B
ATOM	4341	N	TYR	B	206	28.560	7.312	35.441	1.00	66.08	B
ATOM	4342	CA	TYR	B	206	27.766	8.495	35.110	1.00	66.83	B
ATOM	4343	CB	TYR	B	206	27.994	9.589	36.165	1.00	66.69	B
ATOM	4344	CG	TYR	B	206	27.996	10.996	35.607	1.00	66.80	B
ATOM	4345	CD1	TYR	B	206	29.184	11.601	35.197	1.00	66.93	B
ATOM	4346	CE1	TYR	B	206	29.192	12.876	34.645	1.00	67.38	B
ATOM	4347	CD2	TYR	B	206	26.811	11.708	35.455	1.00	67.66	B
ATOM	4348	CE2	TYR	B	206	26.807	12.987	34.904	1.00	67.93	B
ATOM	4349	CZ	TYR	B	206	28.001	13.564	34.500	1.00	67.51	B
ATOM	4350	OH	TYR	B	206	27.999	14.823	33.944	1.00	66.55	B
ATOM	4351	C	TYR	B	206	28.089	9.036	33.709	1.00	67.37	B
ATOM	4352	O	TYR	B	206	27.204	9.526	33.004	1.00	67.33	B
ATOM	4353	N	MET	B	207	29.368	8.999	33.343	1.00	67.98	B
ATOM	4354	CA	MET	B	207	29.821	9.484	32.042	1.00	67.79	B
ATOM	4355	CB	MET	B	207	31.349	9.602	32.013	1.00	68.72	B
ATOM	4356	CG	MET	B	207	31.910	10.142	30.704	1.00	69.21	B
ATOM	4357	SD	MET	B	207	33.713	10.198	30.648	1.00	69.17	B
ATOM	4358	CE	MET	B	207	34.094	8.447	30.351	1.00	68.41	B
ATOM	4359	C	MET	B	207	29.348	8.553	30.934	1.00	67.24	B
ATOM	4360	O	MET	B	207	28.945	9.006	29.866	1.00	67.29	B
ATOM	4361	N	PHE	B	208	29.399	7.251	31.189	1.00	66.80	B
ATOM	4362	CA	PHE	B	208	28.953	6.283	30.203	1.00	67.07	B
ATOM	4363	CB	PHE	B	208	29.483	4.890	30.529	1.00	67.24	B
ATOM	4364	CG	PHE	B	208	30.848	4.627	29.971	1.00	68.87	B
ATOM	4365	CD1	PHE	B	208	31.039	3.651	28.997	1.00	69.66	B
ATOM	4366	CD2	PHE	B	208	31.944	5.378	30.390	1.00	69.70	B
ATOM	4367	CE1	PHE	B	208	32.298	3.427	28.448	1.00	68.53	B
ATOM	4368	CE2	PHE	B	208	33.208	5.160	29.846	1.00	68.94	B
ATOM	4369	CZ	PHE	B	208	33.382	4.184	28.875	1.00	68.87	B
ATOM	4370	C	PHE	B	208	27.437	6.264	30.045	1.00	67.34	B
ATOM	4371	O	PHE	B	208	26.916	5.614	29.144	1.00	66.92	B
ATOM	4372	N	VAL	B	209	26.731	6.979	30.921	1.00	67.20	B
ATOM	4373	CA	VAL	B	209	25.276	7.044	30.838	1.00	66.20	B
ATOM	4374	CB	VAL	B	209	24.574	6.616	32.161	1.00	67.12	B
ATOM	4375	CG1	VAL	B	209	24.915	5.167	32.500	1.00	66.84	B
ATOM	4376	CG2	VAL	B	209	24.947	7.538	33.307	1.00	66.98	B
ATOM	4377	C	VAL	B	209	24.786	8.422	30.401	1.00	65.18	B
ATOM	4378	O	VAL	B	209	24.033	8.529	29.439	1.00	64.88	B
ATOM	4379	N	VAL	B	210	25.254	9.480	31.058	1.00	64.35	B
ATOM	4380	CA	VAL	B	210	24.817	10.829	30.702	1.00	64.49	B
ATOM	4381	CB	VAL	B	210	24.819	11.780	31.925	1.00	64.11	B
ATOM	4382	CG1	VAL	B	210	24.151	13.104	31.569	1.00	64.03	B
ATOM	4383	CG2	VAL	B	210	24.085	11.142	33.087	1.00	64.99	B
ATOM	4384	C	VAL	B	210	25.609	11.470	29.560	1.00	63.87	B
ATOM	4385	O	VAL	B	210	25.180	12.475	28.993	1.00	64.51	B
ATOM	4386	N	HIS	B	211	26.741	10.878	29.194	1.00	62.79	B
ATOM	4387	CA	HIS	B	211	27.558	11.441	28.121	1.00	61.21	B
ATOM	4388	CB	HIS	B	211	28.770	12.167	28.712	1.00	59.84	B
ATOM	4389	CG	HIS	B	211	28.422	13.438	29.422	1.00	57.51	B
ATOM	4390	CD2	HIS	B	211	28.250	13.706	30.738	1.00	56.91	B
ATOM	4391	ND1	HIS	B	211	28.194	14.622	28.755	1.00	56.23	B
ATOM	4392	CE1	HIS	B	211	27.892	15.563	29.631	1.00	56.04	B
ATOM	4393	NE2	HIS	B	211	27.921	15.035	30.841	1.00	54.69	B
ATOM	4394	C	HIS	B	211	28.005	10.446	27.054	1.00	60.42	B
ATOM	4395	O	HIS	B	211	28.984	10.693	26.344	1.00	59.14	B
ATOM	4396	N	PHE	B	212	27.270	9.343	26.924	1.00	59.96	B
ATOM	4397	CA	PHE	B	212	27.595	8.323	25.932	1.00	60.62	B
ATOM	4398	CB	PHE	B	212	28.672	7.363	26.468	1.00	58.17	B
ATOM	4399	CG	PHE	B	212	29.078	6.293	25.484	1.00	55.88	B
ATOM	4400	CD1	PHE	B	212	29.390	6.617	24.168	1.00	55.24	B
ATOM	4401	CD2	PHE	B	212	29.115	4.957	25.867	1.00	55.65	B
ATOM	4402	CE1	PHE	B	212	29.730	5.628	23.245	1.00	55.07	B
ATOM	4403	CE2	PHE	B	212	29.454	3.959	24.951	1.00	55.06	B
ATOM	4404	CZ	PHE	B	212	29.761	4.298	23.637	1.00	54.41	B
ATOM	4405	C	PHE	B	212	26.381	7.528	25.450	1.00	61.88	B
ATOM	4406	O	PHE	B	212	25.938	7.679	24.307	1.00	60.63	B
ATOM	4407	N	ILE	B	213	25.864	6.674	26.327	1.00	64.65	B
ATOM	4408	CA	ILE	B	213	24.723	5.822	26.013	1.00	67.89	B
ATOM	4409	CB	ILE	B	213	24.411	4.859	27.190	1.00	69.62	B
ATOM	4410	CG2	ILE	B	213	23.101	4.128	26.944	1.00	70.30	B
ATOM	4411	CG1	ILE	B	213	25.550	3.842	27.351	1.00	71.80	B
ATOM	4412	CD1	ILE	B	213	25.462	2.972	28.613	1.00	73.77	B
ATOM	4413	C	ILE	B	213	23.469	6.598	25.616	1.00	68.84	B
ATOM	4414	O	ILE	B	213	22.976	6.441	24.499	1.00	69.55	B
ATOM	4415	N	ILE	B	214	22.966	7.437	26.522	1.00	69.74	B
ATOM	4416	CA	ILE	B	214	21.766	8.232	26.261	1.00	70.08	B
ATOM	4417	CB	ILE	B	214	21.402	9.158	27.453	1.00	71.06	B
ATOM	4418	CG2	ILE	B	214	20.205	10.046	27.096	1.00	70.96	B
ATOM	4419	CG1	ILE	B	214	21.090	8.324	28.696	1.00	71.62	B
ATOM	4420	CD1	ILE	B	214	20.840	9.154	29.943	1.00	72.73	B
ATOM	4421	C	ILE	B	214	21.886	9.065	24.988	1.00	69.85	B
ATOM	4422	O	ILE	B	214	21.049	8.944	24.100	1.00	70.12	B
ATOM	4423	N	PRO	B	215	22.930	9.913	24.878	1.00	69.94	B
ATOM	4424	CD	PRO	B	215	24.029	10.187	25.823	1.00	70.48	B
ATOM	4425	CA	PRO	B	215	23.082	10.728	23.672	1.00	70.21	B
ATOM	4426	CB	PRO	B	215	24.488	11.301	23.828	1.00	69.96	B
ATOM	4427	CG	PRO	B	215	24.602	11.472	25.288	1.00	70.00	B
ATOM	4428	C	PRO	B	215	22.962	9.889	22.404	1.00	70.39	B
ATOM	4429	O	PRO	B	215	22.239	10.257	21.479	1.00	71.18	B
ATOM	4430	N	LEU	B	216	23.614	8.730	22.394	1.00	69.89	B
ATOM	4431	CA	LEU	B	216	23.570	7.855	21.232	1.00	69.96	B
ATOM	4432	CB	lEU	B	216	24.607	6.746	21.353	1.00	69.42	B
ATOM	4433	CG	LEU	B	216	26.039	7.226	21.139	1.00	68.49	B
ATOM	4434	CD1	LEU	B	216	26.957	6.067	21.394	1.00	68.72	B
ATOM	4435	CD2	LEU	B	216	26.228	7.767	19.724	1.00	67.13	B
ATOM	4436	C	LEU	B	216	22.195	7.277	20.911	1.00	70.30	B
ATOM	4437	O	LEU	B	216	21.849	7.130	19.743	1.00	71.51	B
ATOM	4438	N	ILE	B	217	21.402	6.964	21.930	1.00	70.58	B
ATOM	4439	CA	ILE	B	217	20.068	6.423	21.684	1.00	70.87	B
ATOM	4440	CB	ILE	B	217	19.420	5.863	22.973	1.00	70.86	B
ATOM	4441	CG2	ILE	B	217	18.092	5.190	22.641	1.00	70.67	B
ATOM	4442	CG1	ILE	B	217	20.348	4.830	23.625	1.00	70.97	B
ATOM	4443	CD1	ILE	B	217	19.835	4.273	24.941	1.00	68.75	B
ATOM	4444	C	ILE	B	217	19.170	7.499	21.062	1.00	71.48	B
ATOM	4445	O	ILE	B	217	18.358	7.199	20.193	1.00	71.18	B
ATOM	4446	N	VAL	B	218	19.344	8.749	21.496	1.00	72.73	B
ATOM	4447	CA	VAL	B	218	18.577	9.888	20.978	1.00	73.59	B
ATOM	4448	CB	VAL	B	218	18.894	11.185	21.760	1.00	72.18	B
ATOM	4449	CG1	VAL	B	218	18.126	12.348	21.180	1.00	71.58	B
ATOM	4450	CG2	VAL	B	218	18.554	11.019	23.229	1.00	70.55	B
ATOM	4451	C	VAL	B	218	18.930	10.091	19.500	1.00	75.95	B
ATOM	4452	O	VAL	B	218	18.125	10.600	18.715	1.00	75.94	B
ATOM	4453	N	ILE	B	219	20.160	9.721	19.149	1.00	78.76	B
ATOM	4454	CA	ILE	B	219	20.648	9.798	17.775	1.00	81.61	B
ATOM	4455	CB	ILE	B	219	22.209	9.757	17.718	1.00	80.62	B
ATOM	4456	CG2	ILE	B	219	22.705	9.294	16.355	1.00	79.82	B
ATOM	4457	CG1	ILE	B	219	22.789	11.135	18.011	1.00	80.49	B
ATOM	4458	CD1	ILE	B	219	24.302	11.155	18.027	1.00	80.71	B
ATOM	4459	C	ILE	B	219	20.086	8.593	17.020	1.00	84.09	B
ATOM	4460	O	ILE	B	219	19.982	8.614	15.796	1.00	85.12	B
ATOM	4461	N	PHE	B	220	19.706	7.556	17.763	1.00	86.68	B
ATOM	4462	CA	PHE	B	220	19.165	6.336	17.175	1.00	90.16	B
ATOM	4463	CB	PHE	B	220	19.569	5.122	18.014	1.00	91.50	B
ATOM	4464	CG	PHE	B	220	21.040	4.801	17.962	1.00	92.44	B
ATOM	4465	CD1	PHE	B	220	21.672	4.208	19.057	1.00	92.69	B
ATOM	4466	CD2	PHE	B	220	21.791	5.079	16.821	1.00	92.52	B
ATOM	4467	CE1	PHE	B	220	23.030	3.896	19.017	1.00	93.15	B
ATOM	4468	CE2	PHE	B	220	23.149	4.772	16.768	1.00	93.21	B
ATOM	4469	CZ	PHE	B	220	23.772	4.179	17.869	1.00	93.66	B
ATOM	4470	C	PHE	B	220	17.653	6.315	16.932	1.00	92.20	B
ATOM	4471	O	PHE	B	220	17.213	5.894	15.863	1.00	92.11	B
ATOM	4472	N	PHE	B	221	16.859	6.734	17.920	1.00	94.69	B
ATOM	4473	CA	PHE	B	221	15.398	6.737	17.774	1.00	96.69	B
ATOM	4474	CB	PHE	B	221	14.697	6.878	19.139	1.00	99.21	B
ATOM	4475	CG	PHE	B	221	13.569	5.884	19.356	1.00	102.34	B
ATOM	4476	CD1	PHE	B	221	13.762	4.517	19.119	1.00	102.92	B
ATOM	4477	CD2	PHE	B	221	12.313	6.314	19.794	1.00	103.55	B
ATOM	4478	CE1	PHE	B	221	12.718	3.591	19.315	1.00	103.51	B
ATOM	4479	CE2	PHE	B	221	11.262	5.396	19.993	1.00	104.06	B
ATOM	4480	CZ	PHE	B	221	11.468	4.033	19.753	1.00	103.90	B
ATOM	4481	C	PHE	B	221	14.944	7.826	16.803	1.00	96.41	B
ATOM	4482	O	PHE	B	221	13.997	7.633	16.042	1.00	96.77	B
ATOM	4483	N	CYS	B	222	15.628	8.965	16.829	1.00	95.98	B
ATOM	4484	CA	CYS	B	222	15.319	10.063	15.924	1.00	96.48	B
ATOM	4485	CB	CYS	B	222	16.182	11.276	16.269	1.00	95.74	B
ATOM	4486	SG	CYS	B	222	16.443	12.420	14.897	1.00	93.40	B
ATOM	4487	C	CYS	B	222	15.632	9.590	14.508	1.00	97.75	B
ATOM	4488	O	CYS	B	222	15.020	10.025	13.536	1.00	97.51	B
ATOM	4489	N	TYR	B	223	16.579	8.663	14.429	1.00	100.22	B
ATOM	4490	CA	TYR	B	223	17.051	8.071	13.183	1.00	103.15	B
ATOM	4491	CB	TYR	B	223	18.450	7.484	13.426	1.00	104.94	B
ATOM	4492	CG	TYR	B	223	19.210	6.977	12.217	1.00	106.85	B
ATOM	4493	CD1	TYR	B	223	20.503	7.432	11.947	1.00	107.64	B
ATOM	4494	CE1	TYR	B	223	21.233	6.925	10.878	1.00	108.95	B
ATOM	4495	CD2	TYR	B	223	18.666	6.004	11.377	1.00	107.25	B
ATOM	4496	CE2	TYR	B	223	19.384	5.493	10.307	1.00	108.27	B
ATOM	4497	CZ	TYR	B	223	20.664	5.954	10.063	1.00	109.52	B
ATOM	4498	OH	TYR	B	223	21.369	5.433	9.004	1.00	111.54	B
ATOM	4499	C	TYR	B	223	16.092	6.976	12.724	1.00	104.22	B
ATOM	4500	O	TYR	B	223	15.729	6.913	11.549	1.00	104.39	B
ATOM	4501	N	GLY	B	224	15.713	6.101	13.653	1.00	105.81	B
ATOM	4502	CA	GLY	B	224	14.802	5.010	13.341	1.00	107.61	B
ATOM	4503	C	GLY	B	224	13.440	5.507	12.898	1.00	108.64	B
ATOM	4504	O	GLY	B	224	12.804	4.909	12.021	1.00	108.96	B
ATOM	4505	N	GLN	B	225	12.988	6.595	13.524	1.00	108.97	B
ATOM	4506	CA	GLN	B	225	11.711	7.213	13.194	1.00	108.74	B
ATOM	4507	CB	GLN	B	225	11.149	7.978	14.403	1.00	109.09	B
ATOM	4508	CG	GLN	B	225	10.664	7.076	15.540	1.00	109.96	B
ATOM	4509	CD	GLN	B	225	10.049	7.852	16.695	1.00	110.13	B
ATOM	4510	OE1	GLN	B	225	10.453	7.692	17.848	1.00	109.55	B
ATOM	4511	NE2	GLN	B	225	9.060	8.689	16.391	1.00	110.13	B
ATOM	4512	C	GLN	B	225	11.900	8.147	11.996	1.00	108.39	B
ATOM	4513	O	GLN	B	225	11.876	9.372	12.139	1.00	108.54	B
ATOM	4514	N	LEU	B	226	12.141	7.541	10.832	1.00	107.96	B
ATOM	4515	CA	LEU	B	226	12.342	8.243	9.560	1.00	107.21	B
ATOM	4516	CB	LEU	B	226	13.767	8.810	9.448	1.00	106.23	B
ATOM	4517	CG	LEU	B	226	14.205	9.987	10.327	1.00	105.05	B
ATOM	4518	CD1	LEU	B	226	15.650	10.320	10.025	1.00	105.81	B
ATOM	4519	CD2	LEU	B	226	13.327	11.199	10.089	1.00	104.20	B
ATOM	4520	C	LEU	B	226	12.086	7.285	8.392	1.00	107.27	B
ATOM	4521	O	LEU	B	226	12.807	6.299	8.203	1.00	107.08	B
ATOM	4522	N	GLN	B	244	14.004	22.695	−0.662	1.00	107.22	B
ATOM	4523	CA	GLN	B	244	12.922	21.827	−0.213	1.00	106.85	B
ATOM	4524	CB	GLN	B	244	11.647	22.093	−1.027	1.00	108.05	B
ATOM	4525	CG	GLN	B	244	10.483	21.152	−0.691	1.00	108.58	B
ATOM	4526	CD	GLN	B	244	9.281	21.335	−1.599	1.00	107.84	B
ATOM	4527	OE1	GLN	B	244	9.307	20.948	−2.768	1.00	107.03	B
ATOM	4528	NE2	GLN	B	244	8.213	21.914	−1.059	1.00	107.50	B
ATOM	4529	C	GLN	B	244	13.292	20.348	−0.314	1.00	106.00	B
ATOM	4530	O	GLN	B	244	13.492	19.674	0.696	1.00	106.12	B
ATOM	4531	N	LYS	B	245	13.365	19.849	−1.542	1.00	104.79	B
ATOM	4532	CA	LYS	B	245	13.691	18.454	−1.788	1.00	103.81	B
ATOM	4533	CB	LYS	B	245	13.462	18.124	−3.269	1.00	104.20	B
ATOM	4534	CG	LYS	B	245	12.173	18.681	−3.886	1.00	103.65	B
ATOM	4535	CD	LYS	B	245	10.925	17.945	−3.411	1.00	103.47	B
ATOM	4536	CE	LYS	B	245	9.692	18.417	−4.173	1.00	102.09	B
ATOM	4537	NZ	LYS	B	245	8.448	17.703	−3.776	1.00	101.09	B
ATOM	4538	C	LYS	B	245	15.146	18.146	−1.418	1.00	103.22	B
ATOM	4539	O	LYS	B	245	15.459	17.031	−1.002	1.00	103.31	B
ATOM	4540	N	ALA	B	246	16.014	19.154	−1.537	1.00	102.18	B
ATOM	4541	CA	ALA	B	246	17.455	19.028	−1.267	1.00	100.38	B
ATOM	4542	CB	ALA	B	246	18.203	20.188	−1.914	1.00	100.82	B
ATOM	4543	C	ALA	B	246	17.925	18.859	0.180	1.00	99.04	B
ATOM	4544	O	ALA	B	246	19.133	18.828	0.435	1.00	97.64	B
ATOM	4545	N	GLU	B	247	16.989	18.772	1.124	1.00	98.22	B
ATOM	4546	CA	GLU	B	247	17.342	18.593	2.535	1.00	97.42	B
ATOM	4547	CB	GLU	B	247	16.198	19.039	3.460	1.00	97.39	B
ATOM	4548	CG	GLU	B	247	16.049	20.563	3.627	1.00	99.00	B
ATOM	4549	CD	GLU	B	247	17.065	21.188	4.591	1.00	99.28	B
ATOM	4550	OE1	GLU	B	247	16.996	20.886	5.801	1.00	99.27	B
ATOM	4551	OE2	GLU	B	247	17.911	22.003	4.148	1.00	99.06	B
ATOM	4552	C	GLU	B	247	17.729	17.146	2.840	1.00	96.61	B
ATOM	4553	O	GLU	B	247	17.981	16.799	3.993	1.00	96.67	B
ATOM	4554	N	LYS	B	248	17.769	16.310	1.802	1.00	95.75	B
ATOM	4555	CA	LYS	B	248	18.136	14.899	1.941	1.00	94.90	B
ATOM	4556	CB	LYS	B	248	17.579	14.075	0.768	1.00	95.46	B
ATOM	4557	CG	LYS	B	248	17.933	12.570	0.783	1.00	95.73	B
ATOM	4558	CD	LYS	B	248	17.272	11.817	1.942	1.00	95.88	B
ATOM	4559	CE	LYS	B	248	17.537	10.318	1.872	1.00	94.99	B
ATOM	4560	NZ	LYS	B	248	16.849	9.585	2.975	1.00	94.98	B
ATOM	4561	C	LYS	B	248	19.657	14.736	2.016	1.00	93.98	B
ATOM	4562	O	LYS	B	248	20.153	13.771	2.608	1.00	94.04	B
ATOM	4563	N	GLU	B	249	20.390	15.663	1.397	1.00	92.29	B
ATOM	4564	CA	GLU	B	249	21.851	15.611	1.409	1.00	89.52	B
ATOM	4565	CB	GLU	B	249	22.451	16.245	0.150	1.00	90.95	B
ATOM	4566	CG	GLU	B	249	22.416	15.323	−1.080	1.00	92.62	B
ATOM	4567	CD	GLU	B	249	23.131	13.983	−0.856	1.00	94.07	B
ATOM	4568	OE1	GLU	B	249	24.321	13.990	−0.460	1.00	94.34	B
ATOM	4569	OE2	GLU	B	249	22.501	12.922	−1.082	1.00	94.16	B
ATOM	4570	C	GLU	B	249	22.444	16.216	2.670	1.00	86.32	B
ATOM	4571	O	GLU	B	249	23.555	15.873	3.059	1.00	86.14	B
ATOM	4572	N	VAL	B	250	21.709	17.125	3.300	1.00	82.86	B
ATOM	4573	CA	VAL	B	250	22.167	17.716	4.548	1.00	80.28	B
ATOM	4574	CB	VAL	B	250	21.381	18.997	4.886	1.00	80.04	B
ATOM	4575	CG1	VAL	B	250	21.902	19.620	6.167	1.00	79.05	B
ATOM	4576	CG2	VAL	B	250	21.483	19.989	3.737	1.00	80.30	B
ATOM	4577	C	VAL	B	250	21.935	16.635	5.613	1.00	79.17	B
ATOM	4578	O	VAL	B	250	22.550	16.649	6.683	1.00	78.77	B
ATOM	4579	N	THR	B	251	21.057	15.685	5.281	1.00	77.86	B
ATOM	4580	CA	THR	B	251	20.718	14.547	6.143	1.00	75.71	B
ATOM	4581	CB	THR	B	251	19.321	13.934	5.788	1.00	76.54	B
ATOM	4582	OG1	THR	B	251	18.294	14.920	5.967	1.00	76.86	B
ATOM	4583	CG2	THR	B	251	19.011	12.721	6.671	1.00	75.53	B
ATOM	4584	C	THR	B	251	21.788	13.477	5.945	1.00	73.36	B
ATOM	4585	O	THR	B	251	22.411	13.032	6.908	1.00	73.52	B
ATOM	4586	N	ARG	B	252	22.012	13.095	4.685	1.00	70.86	B
ATOM	4587	CA	ARG	B	252	23.015	12.092	4.328	1.00	68.07	B
ATOM	4588	CB	ARG	B	252	23.072	11.887	2.808	1.00	69.51	B
ATOM	4589	CG	ARG	B	252	22.420	10.587	2.333	1.00	71.95	B
ATOM	4590	CD	ARG	B	252	22.733	10.267	0.866	1.00	72.64	B
ATOM	4591	NE	ARG	B	252	22.496	8.852	0.568	1.00	74.53	B
ATOM	4592	CZ	ARG	B	252	23.454	7.933	0.419	1.00	75.25	B
ATOM	4593	NH1	ARG	B	252	24.741	8.259	0.525	1.00	74.61	B
ATOM	4594	NH2	ARG	B	252	23.120	6.667	0.200	1.00	75.05	B
ATOM	4595	C	ARG	B	252	24.393	12.479	4.856	1.00	65.51	B
ATOM	4596	O	ARG	B	252	25.345	11.711	4.761	1.00	65.17	B
ATOM	4597	N	MET	B	253	24.497	13.693	5.384	1.00	62.65	B
ATOM	4598	CA	MET	B	253	25.741	14.162	5.952	1.00	60.05	B
ATOM	4599	CB	MET	B	253	25.880	15.667	5.796	1.00	58.69	B
ATOM	4600	CG	MET	B	253	27.253	16.158	6.172	1.00	57.31	B
ATOM	4601	SD	MET	B	253	27.435	17.899	5.897	1.00	55.71	B
ATOM	4602	CE	MET	B	253	28.121	18.412	7.479	1.00	57.39	B
ATOM	4603	C	MET	B	253	25.675	13.811	7.419	1.00	59.38	B
ATOM	4604	O	MET	B	253	26.531	13.090	7.931	1.00	59.65	B
ATOM	4605	N	VAL	B	254	24.629	14.301	8.082	1.00	57.66	B
ATOM	4606	CA	VAL	B	254	24.419	14.034	9.497	1.00	56.92	B
ATOM	4607	CB	VAL	B	254	23.023	14.505	9.948	1.00	56.63	B
ATOM	4608	CG1	VAL	B	254	22.557	13.738	11.190	1.00	57.09	B
ATOM	4609	CG2	VAL	B	254	23.070	15.995	10.246	1.00	57.03	B
ATOM	4610	C	VAL	B	254	24.603	12.551	9.786	1.00	56.69	B
ATOM	4611	O	VAL	B	254	25.242	12.182	10.769	1.00	56.79	B
ATOM	4612	N	ILE	B	255	24.084	11.710	8.897	1.00	55.90	B
ATOM	4613	CA	ILE	B	255	24.214	10.267	9.044	1.00	55.43	B
ATOM	4614	CB	ILE	B	255	23.556	9.523	7.873	1.00	55.14	B
ATOM	4615	CG2	ILE	B	255	23.749	8.026	8.017	1.00	53.10	B
ATOM	4616	CG1	ILE	B	255	22.072	9.891	7.784	1.00	57.11	B
ATOM	4617	CD1	ILE	B	255	21.282	9.699	9.072	1.00	58.84	B
ATOM	4618	C	ILE	B	255	25.691	9.914	9.068	1.00	55.84	B
ATOM	4619	O	ILE	B	255	26.169	9.250	9.987	1.00	56.88	B
ATOM	4620	N	ILE	B	256	26.413	10.417	8.076	1.00	55.46	B
ATOM	4621	CA	ILE	B	256	27.838	10.169	7.950	1.00	55.70	B
ATOM	4622	CB	ILE	B	256	28.369	10.759	6.618	1.00	56.49	B
ATOM	4623	CG2	ILE	B	256	29.812	11.210	6.751	1.00	56.80	B
ATOM	4624	CG1	ILE	B	256	28.253	9.716	5.503	1.00	56.60	B
ATOM	4625	CD1	ILE	B	256	26.848	9.219	5.234	1.00	57.63	B
ATOM	4626	C	ILE	B	256	28.641	10.676	9.149	1.00	55.55	B
ATOM	4627	O	ILE	B	256	29.548	9.992	9.624	1.00	55.44	B
ATOM	4628	N	MET	B	257	28.296	11.858	9.648	1.00	55.41	B
ATOM	4629	CA	MET	B	257	28.994	12.436	10.797	1.00	56.51	B
ATOM	4630	CB	MET	B	257	28.450	13.829	11.106	1.00	58.66	B
ATOM	4631	CG	MET	B	257	28.512	14.797	9.947	1.00	61.03	B
ATOM	4632	SD	MET	B	257	27.872	16.407	10.404	1.00	62.63	B
ATOM	4633	CE	MET	B	257	29.270	17.047	11.335	1.00	63.44	B
ATOM	4634	C	MET	B	257	28.828	11.552	12.029	1.00	56.15	B
ATOM	4635	O	MET	B	257	29.763	11.368	12.811	1.00	55.65	B
ATOM	4636	N	VAL	B	258	27.616	11.032	12.205	1.00	55.72	B
ATOM	4637	CA	VAL	B	258	27.310	10.160	13.327	1.00	55.06	B
ATOM	4638	CB	VAL	B	258	25.811	9.805	13.374	1.00	54.66	B
ATOM	4639	CG1	VAL	B	258	25.556	8.745	14.416	1.00	54.60	B
ATOM	4640	CG2	VAL	B	258	25.002	11.038	13.706	1.00	56.19	B
ATOM	4641	C	VAL	B	258	28.131	8.890	13.200	1.00	54.58	B
ATOM	4642	O	VAL	B	258	28.770	8.468	14.161	1.00	54.84	B
ATOM	4643	N	ILE	B	259	28.146	8.318	11.998	1.00	53.84	B
ATOM	4644	CA	ILE	B	259	28.887	7.088	11.718	1.00	53.39	B
ATOM	4645	CB	ILE	B	259	28.643	6.620	10.270	1.00	52.45	B
ATOM	4646	CG2	ILE	B	259	29.398	5.334	9.994	1.00	51.47	B
ATOM	4647	CG1	ILE	B	259	27.151	6.406	10.031	1.00	50.87	B
ATOM	4648	CD1	ILE	B	259	26.802	6.279	8.571	1.00	51.36	B
ATOM	4649	C	ILE	B	259	30.397	7.240	11.952	1.00	54.21	B
ATOM	4650	O	ILE	B	259	31.027	6.375	12.569	1.00	54.54	B
ATOM	4651	N	ALA	B	260	30.967	8.346	11.470	1.00	54.03	B
ATOM	4652	CA	ALA	B	260	32.398	8.622	11.618	1.00	52.48	B
ATOM	4653	CB	ALA	B	260	32.773	9.824	10.792	1.00	51.29	B
ATOM	4654	C	ALA	B	260	32.818	8.824	13.076	1.00	52.34	B
ATOM	4655	O	ALA	B	260	33.961	8.546	13.443	1.00	52.14	B
ATOM	4656	N	PHE	B	261	31.885	9.325	13.887	1.00	52.14	B
ATOM	4657	CA	PHE	B	261	32.094	9.563	15.315	1.00	51.14	B
ATOM	4658	CB	PHE	B	261	30.897	10.335	15.883	1.00	52.58	B
ATOM	4659	CG	PHE	B	261	30.985	10.607	17.365	1.00	54.80	B
ATOM	4660	CD1	PHE	B	261	31.524	11.806	17.837	1.00	56.01	B
ATOM	4661	CD2	PHE	B	261	30.505	9.681	18.288	1.00	55.37	B
ATOM	4662	CE1	PHE	B	261	31.584	12.084	19.208	1.00	56.04	B
ATOM	4663	CE2	PHE	B	261	30.561	9.946	19.661	1.00	56.73	B
ATOM	4664	CZ	PHE	B	261	31.102	11.153	20.119	1.00	56.46	B
ATOM	4665	C	PHE	B	261	32.221	8.229	16.037	1.00	49.83	B
ATOM	4666	O	PHE	B	261	33.066	8.058	16.913	1.00	47.49	B
ATOM	4667	N	LEU	B	262	31.343	7.302	15.665	1.00	50.42	B
ATOM	4668	CA	LEU	B	262	31.298	5.960	16.238	1.00	51.04	B
ATOM	4669	CB	LEU	B	262	30.044	5.216	15.750	1.00	50.80	B
ATOM	4670	CG	LEU	B	262	28.681	5.742	16.240	1.00	51.69	B
ATOM	4671	CD1	LEU	B	262	27.550	5.198	15.388	1.00	50.52	B
ATOM	4672	CD2	LEU	B	262	28.458	5.400	17.711	1.00	51.14	B
ATOM	4673	C	LEU	B	262	32.548	5.171	15.878	1.00	51.43	B
ATOM	4674	O	LEU	B	262	32.811	4.115	16.450	1.00	52.83	B
ATOM	4675	N	ILE	B	263	33.320	5.697	14.932	1.00	50.52	B
ATOM	4676	CA	ILE	B	263	34.546	5.052	14.491	1.00	48.36	B
ATOM	4677	CB	ILE	B	263	34.735	5.238	12.982	1.00	48.54	B
ATOM	4678	CG2	ILE	B	263	36.080	4.674	12.531	1.00	48.64	B
ATOM	4679	CG1	ILE	B	263	33.576	4.548	12.253	1.00	48.46	B
ATOM	4680	CD1	ILE	B	263	33.481	4.847	10.775	1.00	47.43	B
ATOM	4681	C	ILE	B	263	35.756	5.559	15.266	1.00	47.89	B
ATOM	4682	O	ILE	B	263	36.720	4.820	15.461	1.00	47.32	B
ATOM	4683	N	CYS	B	264	35.687	6.804	15.736	1.00	48.09	B
ATOM	4684	CA	CYS	B	264	36.774	7.409	16.518	1.00	47.63	B
ATOM	4685	CB	CYS	B	264	36.722	8.953	16.437	1.00	47.18	B
ATOM	4686	SG	CYS	B	264	37.430	9.749	14.944	1.00	49.56	B
ATOM	4687	C	CYS	B	264	36.711	6.993	17.992	1.00	46.97	B
ATOM	4688	O	CYS	B	264	37.716	6.588	18.588	1.00	46.20	B
ATOM	4689	N	TRP	B	265	35.503	7.042	18.548	1.00	46.59	B
ATOM	4690	CA	TRP	B	265	35.290	6.746	19.951	1.00	45.62	B
ATOM	4691	CB	TRP	B	265	34.353	7.793	20.551	1.00	46.49	B
ATOM	4692	CG	TRP	B	265	34.846	9.184	20.314	1.00	46.82	B
ATOM	4693	CD2	TRP	B	265	35.969	9.823	20.944	1.00	48.60	B
ATOM	4694	CE2	TRP	B	265	36.094	11.108	20.370	1.00	47.79	B
ATOM	4695	CE3	TRP	B	265	36.887	9.432	21.934	1.00	50.04	B
ATOM	4696	CD1	TRP	B	265	34.352	10.079	19.420	1.00	46.45	B
ATOM	4697	NE1	TRP	B	265	35.093	11.238	19.444	1.00	47.86	B
ATOM	4698	CZ2	TRP	B	265	37.100	12.009	20.750	1.00	47.37	B
ATOM	4699	CZ3	TRP	B	265	37.893	10.332	22.313	1.00	48.88	B
ATOM	4700	CH2	TRP	B	265	37.987	11.604	21.718	1.00	47.88	B
ATOM	4701	C	TRP	B	265	34.867	5.351	20.374	1.00	44.86	B
ATOM	4702	O	TRP	B	265	34.968	5.032	21.550	1.00	46.27	B
ATOM	4703	N	LEU	B	266	34.371	4.519	19.468	1.00	43.54	B
ATOM	4704	CA	LEU	B	266	33.997	3.175	19.905	1.00	43.80	B
ATOM	4705	CB	LEU	B	266	33.050	2.480	18.927	1.00	44.03	B
ATOM	4706	CG	LEU	B	266	31.573	2.568	19.341	1.00	43.63	B
ATOM	4707	CD1	LEU	B	266	31.189	4.006	19.715	1.00	43.73	B
ATOM	4708	CD2	LEU	B	266	30.690	2.044	18.221	1.00	42.27	B
ATOM	4709	C	LEU	B	266	35.216	2.318	20.240	1.00	43.56	B
ATOM	4710	O	LEU	B	266	35.174	1.537	21.190	1.00	43.08	B
ATOM	4711	N	PRO	B	267	36.302	2.412	19.439	1.00	42.97	B
ATOM	4712	CD	PRO	B	267	36.458	2.985	18.091	1.00	42.09	B
ATOM	4713	CA	PRO	B	267	37.474	1.603	19.781	1.00	42.83	B
ATOM	4714	CB	PRO	B	267	38.451	1.944	18.661	1.00	41.74	B
ATOM	4715	CG	PRO	B	267	37.560	2.141	17.507	1.00	40.98	B
ATOM	4716	C	PRO	B	267	37.987	2.092	21.136	1.00	43.77	B
ATOM	4717	O	PRO	B	267	38.384	1.297	21.984	1.00	44.27	B
ATOM	4718	N	TYR	B	268	37.919	3.406	21.348	1.00	43.65	B
ATOM	4719	CA	TYR	B	268	38.362	4.009	22.595	1.00	43.70	B
ATOM	4720	CB	TYR	B	268	38.374	5.529	22.490	1.00	44.78	B
ATOM	4721	CG	TYR	B	268	38.793	6.201	23.777	1.00	46.75	B
ATOM	4722	CD1	TYR	B	268	40.085	6.026	24.288	1.00	47.60	B
ATOM	4723	CE1	TYR	B	268	40.473	6.613	25.494	1.00	47.29	B
ATOM	4724	CD2	TYR	B	268	37.894	6.986	24.506	1.00	46.71	B
ATOM	4725	CE2	TYR	B	268	38.270	7.576	25.713	1.00	46.41	B
ATOM	4726	CZ	TYR	B	268	39.561	7.385	26.199	1.00	47.05	B
ATOM	4727	OH	TYR	B	268	39.948	7.967	27.380	1.00	45.81	B
ATOM	4728	C	TYR	B	268	37.468	3.606	23.750	1.00	44.35	B
ATOM	4729	O	TYR	B	268	37.929	2.996	24.705	1.00	45.00	B
ATOM	4730	N	ALA	B	269	36.195	3.983	23.664	1.00	45.88	B
ATOM	4731	CA	ALA	B	269	35.198	3.673	24.692	1.00	46.78	B
ATOM	4732	CB	ALA	B	269	33.824	4.190	24.273	1.00	45.30	B
ATOM	4733	C	ALA	B	269	35.131	2.177	24.973	1.00	48.16	B
ATOM	4734	O	ALA	B	269	34.894	1.768	26.110	1.00	48.24	B
ATOM	4735	N	GLY	B	270	35.343	1.369	23.935	1.00	49.48	B
ATOM	4736	CA	GLY	B	270	35.322	−0.076	24.095	1.00	50.85	B
ATOM	4737	C	GLY	B	270	36.455	−0.529	25.001	1.00	51.42	B
ATOM	4738	O	GLY	B	270	36.253	−1.356	25.898	1.00	51.44	B
ATOM	4739	N	VAL	B	271	37.643	0.028	24.768	1.00	50.30	B
ATOM	4740	CA	VAL	B	271	38.827	−0.284	25.561	1.00	50.31	B
ATOM	4741	CB	VAL	B	271	40.105	0.265	24.899	1.00	51.26	B
ATOM	4742	CG1	VAL	B	271	41.274	0.166	25.857	1.00	51.46	B
ATOM	4743	CG2	VAL	B	271	40.414	−0.505	23.621	1.00	52.05	B
ATOM	4744	C	VAL	B	271	38.690	0.349	26.936	1.00	50.14	B
ATOM	4745	O	VAL	B	271	39.106	−0.227	27.939	1.00	49.36	B
ATOM	4746	N	ALA	B	272	38.106	1.542	26.963	1.00	50.37	B
ATOM	4747	CA	ALA	B	272	37.889	2.281	28.200	1.00	51.65	B
ATOM	4748	CB	ALA	B	272	37.309	3.650	27.893	1.00	50.79	B
ATOM	4749	C	ALA	B	272	36.970	1.520	29.160	1.00	52.22	B
ATOM	4750	O	ALA	B	272	37.214	1.475	30.370	1.00	53.09	B
ATOM	4751	N	PHE	B	273	35.930	0.899	28.617	1.00	51.65	B
ATOM	4752	CA	PHE	B	273	35.001	0.162	29.451	1.00	51.42	B
ATOM	4753	CB	PHE	B	273	33.678	−0.050	28.737	1.00	52.75	B
ATOM	4754	CG	PHE	B	273	32.566	−0.410	29.657	1.00	54.23	B
ATOM	4755	CD1	PHE	B	273	32.089	0.522	30.574	1.00	55.34	B
ATOM	4756	CD2	PHE	B	273	32.008	−1.682	29.631	1.00	55.12	B
ATOM	4757	CE1	PHE	B	273	31.069	0.196	31.456	1.00	57.07	B
ATOM	4758	CE2	PHE	B	273	30.986	−2.027	30.505	1.00	56.44	B
ATOM	4759	CZ	PHE	B	273	30.512	−1.086	31.423	1.00	58.11	B
ATOM	4760	C	PHE	B	273	35.559	−1.172	29.906	1.00	50.85	B
ATOM	4761	O	PHE	B	273	35.280	−1.611	31.019	1.00	50.86	B
ATOM	4762	N	TYR	B	274	36.313	−1.831	29.031	1.00	50.42	B
ATOM	4763	CA	TYR	B	274	36.919	−3.114	29.366	1.00	49.91	B
ATOM	4764	CB	TYR	B	274	37.756	−3.652	28.196	1.00	51.66	B
ATOM	4765	CG	TYR	B	274	38.635	−4.858	28.525	1.00	53.90	B
ATOM	4766	CD1	TYR	B	274	38.206	−6.162	28.257	1.00	54.80	B
ATOM	4767	CE1	TYR	B	274	39.030	−7.274	28.534	1.00	55.82	B
ATOM	4768	CD2	TYR	B	274	39.909	−4.691	29.085	1.00	56.28	B
ATOM	4769	CE2	TYR	B	274	40.737	−5.795	29.370	1.00	56.94	B
ATOM	4770	CZ	TYR	B	274	40.291	−7.079	29.089	1.00	56.53	B
ATOM	4771	OH	TYR	B	274	41.113	−8.153	29.348	1.00	56.33	B
ATOM	4772	C	TYR	B	274	37.807	−2.908	30.582	1.00	49.02	B
ATOM	4773	O	TYR	B	274	37.817	−3.732	31.495	1.00	50.29	B
ATOM	4774	N	ILE	B	275	38.537	−1.797	30.603	1.00	46.15	B
ATOM	4775	CA	ILE	B	275	39.421	−1.515	31.720	1.00	43.11	B
ATOM	4776	CB	ILE	B	275	40.395	−0.387	31.395	1.00	40.55	B
ATOM	4777	CG2	ILE	B	275	41.226	−0.052	32.609	1.00	39.48	B
ATOM	4778	CG1	ILE	B	275	41.305	−0.821	30.251	1.00	39.49	B
ATOM	4779	CD1	ILE	B	275	42.262	0.242	29.794	1.00	38.31	B
ATOM	4780	C	ILE	B	275	38.671	−1.203	33.007	1.00	43.45	B
ATOM	4781	O	ILE	B	275	39.030	−1.715	34.055	1.00	43.33	B
ATOM	4782	N	PHE	B	276	37.614	−0.402	32.935	1.00	44.12	B
ATOM	4783	CA	PHE	B	276	36.865	−0.064	34.139	1.00	45.20	B
ATOM	4784	CB	PHE	B	276	35.715	0.895	33.824	1.00	44.26	B
ATOM	4785	CG	PHE	B	276	34.901	1.281	35.032	1.00	43.72	B
ATOM	4786	CD1	PHE	B	276	35.519	1.549	36.250	1.00	42.43	B
ATOM	4787	CD2	PHE	B	276	33.513	1.353	34.956	1.00	45.15	B
ATOM	4788	CE1	PHE	B	276	34.773	1.877	37.372	1.00	43.75	B
ATOM	4789	CE2	PHE	B	276	32.753	1.682	36.077	1.00	44.68	B
ATOM	4790	CZ	PHE	B	276	33.385	1.943	37.287	1.00	44.38	B
ATOM	4791	C	PHE	B	276	36.337	−1.297	34.874	1.00	47.18	B
ATOM	4792	O	PHE	B	276	36.498	−1.412	36.096	1.00	48.44	B
ATOM	4793	N	THR	B	277	35.714	−2.213	34.132	1.00	48.44	B
ATOM	4794	CA	THR	B	277	35.165	−3.440	34.715	1.00	49.38	B
ATOM	4795	CB	THR	B	277	34.302	−4.206	33.686	1.00	47.25	B
ATOM	4796	OG1	THR	B	277	35.029	−4.343	32.466	1.00	45.90	B
ATOM	4797	CG2	THR	B	277	33.016	−3.457	33.401	1.00	44.96	B
ATOM	4798	C	TUR	B	277	36.271	−4.351	35.283	1.00	51.81	B
ATOM	4799	O	THR	B	277	36.121	−4.921	36.377	1.00	52.70	B
ATOM	4800	N	HIS	B	278	37.393	−4.439	34.560	1.00	53.17	B
ATOM	4801	CA	HIS	B	278	38.554	−5.250	34.967	1.00	53.25	B
ATOM	4802	CG	HIS	B	278	39.083	−6.091	33.797	1.00	51.92	B
ATOM	4803	CG	HIS	B	278	38.026	−6.642	32.894	1.00	51.18	B
ATOM	4804	CD2	HIS	B	278	38.115	−7.172	31.653	1.00	49.67	B
ATOM	4805	ND1	HIS	B	278	36.689	−6.669	33.228	1.00	51.49	B
ATOM	4806	CE1	HIS	B	278	36.001	−7.191	32.228	1.00	51.51	B
ATOM	4807	NE2	HIS	B	278	36.843	−7.504	31.260	1.00	49.22	B
ATOM	4808	C	HIS	B	278	39.723	−4.374	35.469	1.00	53.89	B
ATOM	4809	O	HIS	B	278	40.783	−4.321	34.831	1.00	52.31	B
ATOM	4810	N	GLN	B	279	39.537	−3.692	36.598	1.00	54.92	B
ATOM	4811	CA	GLN	B	279	40.588	−2.842	37.151	1.00	56.15	B
ATOM	4812	CB	GLN	B	279	40.006	−1.846	38.158	1.00	56.19	B
ATOM	4813	CG	GLN	B	279	39.038	−0.854	37.552	1.00	56.00	B
ATOM	4814	CD	GLN	B	279	38.567	0.183	38.541	1.00	57.20	B
ATOM	4815	OE1	GLN	B	279	38.346	1.340	38.187	1.00	58.74	B
ATOM	4816	NE2	GLN	B	279	38.405	−0.224	39.790	1.00	58.47	B
ATOM	4817	C	GLN	B	279	41.683	−3.684	37.803	1.00	57.53	B
ATOM	4818	O	GLN	B	279	41.709	−3.853	39.033	1.00	59.37	B
ATOM	4819	N	GLY	B	280	42.564	−4.230	36.965	1.00	57.13	B
ATOM	4820	CA	GLY	B	280	43.663	−5.054	37.452	1.00	56.74	B
ATOM	4821	C	GLY	B	280	44.337	−5.974	36.437	1.00	56.78	B
ATOM	4822	O	GLY	B	280	45.433	−6.477	36.706	1.00	55.43	B
ATOM	4823	N	SER	B	281	43.713	−6.144	35.264	1.00	57.49	B
ATOM	4824	CA	SER	B	281	44.192	−7.015	34.169	1.00	57.29	B
ATOM	4825	CB	SER	B	281	43.311	−6.839	32.924	1.00	57.42	B
ATOM	4826	OG	SER	B	281	41.969	−6.539	33.263	1.00	56.93	B
ATOM	4827	C	SER	B	281	45.662	−6.866	33.751	1.00	57.69	B
ATOM	4828	O	SER	B	281	46.372	−5.962	34.213	1.00	57.70	B
ATOM	4829	N	ASP	B	282	46.095	−7.739	32.839	1.00	57.55	B
ATOM	4830	CA	ASP	B	282	47.475	−7.733	32.355	1.00	57.97	B
ATOM	4831	CB	ASP	B	282	48.063	−9.157	32.422	1.00	60.97	B
ATOM	4832	CG	ASP	B	282	49.604	−9.179	32.405	1.00	63.90	B
ATOM	4833	OD1	ASP	B	282	50.180	−10.286	32.534	1.00	64.30	B
ATOM	4834	OD2	ASP	B	282	50.242	−8.105	32.272	1.00	65.04	B
ATOM	4835	C	ASP	B	282	47.605	−7.167	30.939	1.00	56.61	B
ATOM	4836	O	ASP	B	282	48.381	−7.673	30.128	1.00	56.83	B
ATOM	4837	N	PHE	B	283	46.855	−6.111	30.649	1.00	54.52	B
ATOM	4838	CA	PHE	B	283	46.905	−5.476	29.337	1.00	5345	B
ATOM	4839	CB	PHE	B	283	45.661	−4.611	29.127	1.00	53.76	B
ATOM	4840	CG	PHE	B	283	45.369	−3.674	30.274	1.00	52.72	B
ATOM	4841	CD1	PHE	B	283	45.833	−2.367	30.261	1.00	52.65	B
ATOM	4842	CD2	PHE	B	283	44.634	−4.104	31.367	1.00	52.36	B
ATOM	4843	CE1	PHE	B	283	45.566	−1.507	31.322	1.00	52.09	B
ATOM	4844	CE2	PHE	B	283	44.363	−3.247	32.432	1.00	50.64	B
ATOM	4845	CZ	PHE	B	283	44.828	−1.954	32.409	1.00	50.80	B
ATOM	4846	C	PHE	B	283	48.169	−4.627	29.243	1.00	52.65	B
ATOM	4847	O	PHE	B	283	48.690	−4.191	30.270	1.00	51.91	B
ATOM	4848	N	GLY	B	284	48.658	−4.398	28.023	1.00	51.82	B
ATOM	4849	CA	CLY	B	284	49.865	−3.603	27.836	1.00	50.78	B
ATOM	4850	C	GLY	B	284	49.629	−2.123	27.584	1.00	50.42	B
ATOM	4851	O	GLY	B	284	48.509	−1.637	27.730	1.00	50.37	B
ATOM	4852	N	PRO	B	285	50.688	−1.354	27.298	1.00	50.23	B
ATOM	4853	CD	PRO	B	285	52.089	−1.668	27.607	1.00	50.55	B
ATOM	4854	CA	PRO	B	285	50.544	0.080	27.034	1.00	50.35	B
ATOM	4855	CB	PRO	B	285	51.978	0.591	27.163	1.00	49.82	B
ATOM	4856	CG	PRO	B	285	52.573	−0.344	28.142	1.00	50.72	B
ATOM	4857	C	PRO	B	285	49.981	0.344	25.632	1.00	51.07	B
ATOM	4858	O	PRO	B	285	49.117	1.203	25.453	1.00	52.78	B
ATOM	4859	N	ILE	B	286	50.458	−0.417	24.649	1.00	50.07	B
ATOM	4860	CA	ILE	B	286	50.017	−0.286	23.258	1.00	47.15	B
ATOM	4861	CB	ILE	B	286	50.786	−1.279	22.357	1.00	47.01	B
ATOM	4862	CG2	ILE	B	286	50.477	−1.022	20.901	1.00	45.93	B
ATOM	4863	CG1	ILE	B	286	52.291	−1.135	22.597	1.00	48.91	B
ATOM	4864	CD1	ILE	B	286	53.153	−2.176	21.887	1.00	51.46	B
ATOM	4865	C	ILE	B	286	48.515	−0.559	23.137	1.00	46.30	B
ATOM	4866	O	ILE	B	286	47.875	−0.172	22.160	1.00	45.72	B
ATOM	4867	N	PHE	B	287	47.962	−1.209	24.154	1.00	45.59	B
ATOM	4868	CA	PHE	B	287	46.548	−1.563	24.196	1.00	44.72	B
ATOM	4869	CB	PHE	B	287	46.238	−2.315	25.508	1.00	45.12	B
ATOM	4870	CG	PHE	B	287	44.822	−2.829	25.612	1.00	44.43	B
ATOM	4871	CD1	PHE	B	287	44.305	−3.703	24.657	1.00	45.49	B
ATOM	4872	CD2	PHE	B	287	44.004	−2.437	26.671	1.00	43.84	B
ATOM	4873	CE1	PHE	B	287	42.989	−4.176	24.756	1.00	44.75	B
ATOM	4874	CE2	PHE	B	287	42.691	−2.903	26.779	1.00	43.63	B
ATOM	4875	CZ	PHE	B	287	42.184	−3.772	25.821	1.00	43.59	B
ATOM	4876	C	PHE	B	287	45.619	−0.357	24.013	1.00	43.27	B
ATOM	4877	O	PHE	B	287	44.864	−0.301	23.041	1.00	44.29	B
ATOM	4878	N	MET	B	288	45.684	0.608	24.927	1.00	40.94	B
ATOM	4879	CA	MET	B	288	44.822	1.785	24.843	1.00	39.65	B
ATOM	4880	CB	MET	B	288	44.498	2.299	26.246	1.00	37.14	B
ATOM	4881	CG	MET	B	288	43.752	3.628	26.300	1.00	36.40	B
ATOM	4882	SD	MET	B	288	42.179	3.685	25.438	1.00	36.77	B
ATOM	4883	CE	MET	B	288	41.072	3.530	26.786	1.00	36.34	B
ATOM	4884	C	MET	B	288	45.386	2.914	23.976	1.00	40.67	B
ATOM	4885	O	MET	B	288	44.637	3.801	23.547	1.00	41.58	B
ATOM	4886	N	THR	B	289	46.689	2.853	23.687	1.00	39.39	B
ATOM	4887	CA	THR	B	289	47.377	3.867	22.881	1.00	37.66	B
ATOM	4888	CB	THR	B	289	48.924	3.640	22.898	1.00	39.02	B
ATOM	4889	OG1	THR	B	289	49.479	4.230	24.086	1.00	40.69	B
ATOM	4890	CG2	THR	B	289	49.605	4.240	21.671	1.00	37.11	B
ATOM	4891	C	THR	B	289	46.855	4.021	21.452	1.00	36.25	B
ATOM	4892	O	THR	B	289	46.904	5.112	20.891	1.00	34.96	B
ATOM	4893	N	ILE	B	290	46.323	2.944	20.885	1.00	36.69	B
ATOM	4894	CA	ILE	B	290	45.787	2.975	19.526	1.00	36.15	B
ATOM	4895	CB	ILE	B	290	45.676	1.572	18.906	1.00	37.75	B
ATOM	4896	CG2	ILE	B	290	45.562	1.697	17.391	1.00	37.64	B
ATOM	4897	CG1	ILE	B	290	46.860	0.697	19.333	1.00	38.40	B
ATOM	4898	CD1	ILE	B	290	48.222	1.280	18.976	1.00	40.52	B
ATOM	4899	C	ILE	B	290	44.407	3.617	19.469	1.00	35.26	B
ATOM	4900	O	ILE	B	290	44.217	4.580	18.734	1.00	34.65	B
ATOM	4901	N	PRO	B	291	43.427	3.093	20.245	1.00	34.78	B
ATOM	4902	CD	PRO	B	291	43.516	1.958	21.179	1.00	34.72	B
ATOM	4903	CA	PRO	B	291	42.065	3.636	20.262	1.00	34.91	B
ATOM	4904	CB	PRO	B	291	41.356	2.743	21.284	1.00	34.38	B
ATOM	4905	CG	PRO	B	291	42.099	1.476	21.220	1.00	35.02	B
ATOM	4906	C	PRO	B	291	42.046	5.078	20.739	1.00	35.38	B
ATOM	4907	O	PRO	B	291	41.185	5.872	20.336	1.00	35.33	B
ATOM	4908	N	ALA	B	292	43.005	5.400	21.605	1.00	35.46	B
ATOM	4909	CA	ALA	B	292	43.114	6.728	22.183	1.00	34.93	B
ATOM	4910	CB	ALA	B	292	43.828	6.673	23.514	1.00	32.87	B
ATOM	4911	C	ALA	B	292	43.775	7.734	21.270	1.00	34.76	B
ATOM	4912	O	ALA	B	292	43.408	8.898	21.293	1.00	37.53	B
ATOM	4913	N	PHE	B	293	44.743	7.304	20.470	1.00	34.33	B
ATOM	4914	CA	PHE	B	293	45.418	8.234	19.569	1.00	34.12	B
ATOM	4915	CB	PHE	B	293	46.888	7.851	19.364	1.00	33.89	B
ATOM	4916	CG	PHE	B	293	47.829	8.604	20.270	1.00	37.89	B
ATOM	4917	CD1	PHE	B	293	48.631	9.635	19.771	1.00	39.71	B
ATOM	4918	CD2	PHE	B	293	47.865	8.342	21.643	1.00	38.32	B
ATOM	4919	CE1	PHE	B	293	49.452	10.404	20.635	1.00	38.53	B
ATOM	4920	CE2	PHE	B	293	48.680	9.103	22.509	1.00	37.06	B
ATOM	4921	CZ	PHE	B	293	49.471	10.133	22.004	1.00	35.54	B
ATOM	4922	C	PHE	B	293	44.688	8.363	18.250	1.00	34.65	B
ATOM	4923	O	PHE	B	293	44.676	9.427	17.622	1.00	33.35	B
ATOM	4924	N	PHE	B	294	44.068	7.266	17.836	1.00	34.98	B
ATOM	4925	CA	PHE	B	294	43.307	7.250	16.606	1.00	34.72	B
ATOM	4926	CB	PHE	B	294	42.740	5.850	16.367	1.00	33.46	B
ATOM	4927	CG	PHE	B	294	41.692	5.798	15.307	1.00	33.13	B
ATOM	4928	CD1	PHE	B	294	41.986	6.166	13.996	1.00	33.95	B
ATOM	4929	CD2	PHE	B	294	40.405	5.392	15.614	1.00	33.03	B
ATOM	4930	CE1	PHE	B	294	41.009	6.130	13.000	1.00	33.82	B
ATOM	4931	CE2	PHE	B	294	39.421	5.354	14.627	1.00	34.88	B
ATOM	4932	CZ	PHE	B	294	39.725	5.724	13.314	1.00	34.30	B
ATOM	4933	C	PHE	B	294	42.181	8.266	16.762	1.00	35.55	B
ATOM	4934	O	PHE	B	294	41.957	9.092	15.879	1.00	37.03	B
ATOM	4935	N	ALA	B	295	41.538	8.240	17.930	1.00	35.53	B
ATOM	4936	CA	ALA	B	295	40.425	9.124	18.265	1.00	34.37	B
ATOM	4937	CB	ALA	B	295	39.930	8.821	19.671	1.00	33.02	B
ATOM	4938	C	ALA	B	295	40.725	10.619	18.114	1.00	34.91	B
ATOM	4939	O	ALA	B	295	39.803	11.426	17.939	1.00	36.92	B
ATOM	4940	N	RET	B	296	42.001	10.993	18.175	1.00	33.13	B
ATOM	4941	CA	RET	B	296	42.382	12.394	18.030	1.00	32.32	B
ATOM	4942	C	RET	B	296	42.115	12.946	16.625	1.00	33.09	B
ATOM	4943	O	RET	B	296	42.268	14.146	16.403	1.00	34.02	B
ATOM	4944	CB	RET	B	296	43.846	12.603	18.416	1.00	31.65	B
ATOM	4945	CG	RET	B	296	43.997	12.746	19.926	1.00	29.35	B
ATOM	4946	CD	RET	B	296	45.275	12.019	20.350	1.00	29.04	B
ATOM	4947	CE	RET	B	296	45.810	12.238	21.768	1.00	27.26	B
ATOM	4948	NZ	RET	B	296	44.923	12.219	22.932	1.00	27.67	B
ATOM	4949	C1	RET	B	296	33.232	8.627	25.654	1.00	37.79	B
ATOM	4950	C2	RET	B	296	31.971	8.464	24.824	1.00	38.11	B
ATOM	4951	C3	RET	B	296	32.212	8.731	23.365	1.00	37.14	B
ATOM	4952	C4	RET	B	296	32.732	10.181	23.125	1.00	37.19	B
ATOM	4953	C5	RET	B	296	33.753	10.633	24.167	1.00	37.13	B
ATOM	4954	C6	RET	B	296	33.968	9.922	25.308	1.00	37.31	B
ATOM	4955	C7	RET	B	296	34.958	10.330	26.330	1.00	35.96	B
ATOM	4956	C8	RET	B	296	36.234	10.482	25.906	1.00	34.78	B
ATOM	4957	C9	RET	B	296	37.457	10.860	26.638	1.00	34.56	B
ATOM	4958	C10	RET	B	296	38.679	10.972	26.050	1.00	33.42	B
ATOM	4959	C11	RET	B	296	39.948	11.346	26.699	1.00	31.77	B
ATOM	4960	C12	RET	B	296	41.196	11.450	26.156	1.00	28.71	B
ATOM	4961	C13	RET	B	296	41.813	11.248	24.811	1.00	27.08	B
ATOM	4962	C14	RET	B	296	42.994	11.781	24.481	1.00	25.44	B
ATOM	4963	C15	RET	B	296	43.630	11.590	23.165	1.00	24.74	B
ATOM	4964	C16	RET	B	296	32.836	8.633	27.112	1.00	37.07	B
ATOM	4965	C17	RET	B	296	34.161	7.424	25.437	1.00	37.93	B
ATOM	4966	C18	RET	B	296	34.487	11.915	23.784	1.00	35.57	B
ATOM	4967	C19	RET	B	296	37.211	11.099	28.087	1.00	31.84	B
ATOM	4968	C20	RET	B	296	41.052	10.395	23.847	1.00	28.77	B
ATOM	4969	N	THR	B	297	41.736	12.081	15.677	1.00	33.05	B
ATOM	4970	CA	THR	B	297	41.418	12.536	14.316	1.00	33.12	B
ATOM	4971	CB	THR	B	297	41.347	11.374	13.258	1.00	31.86	B
ATOM	4972	OG1	THR	B	297	40.251	10.493	13.549	1.00	29.77	B
ATOM	4973	CG2	THR	B	297	42.651	10.590	13.213	1.00	28.34	B
ATOM	4974	C	THR	B	297	40.059	13.248	14.368	1.00	35.30	B
ATOM	4975	O	THR	B	297	39.620	13.857	13.387	1.00	34.43	B
ATOM	4976	N	SER	B	298	39.398	13.156	15.522	1.00	35.98	B
ATOM	4977	CA	SER	B	298	38.110	13.792	15.725	1.00	37.81	B
ATOM	4978	CB	SER	B	298	37.567	13.468	17.124	1.00	38.78	B
ATOM	4979	OG	SER	B	298	36.143	13.564	17.173	1.00	40.95	B
ATOM	4980	C	SER	B	298	38.322	15.294	15.562	1.00	39.39	B
ATOM	4981	O	SER	B	298	37.406	16.037	15.177	1.00	42.60	B
ATOM	4982	N	ALA	B	299	39.557	15.722	15.806	1.00	38.93	B
ATOM	4983	CA	ALA	B	299	39.927	17.123	15.696	1.00	38.71	B
ATOM	4984	CB	ALA	B	299	41.219	17.388	16.441	1.00	37.76	B
ATOM	4985	C	ALA	B	299	40.083	17.543	14.252	1.00	39.61	B
ATOM	4986	O	ALA	B	299	40.271	18.724	13.973	1.00	41.81	B
ATOM	4987	N	VAL	B	300	39.993	16.590	13.328	1.00	39.77	B
ATOM	4988	CA	VAL	B	300	40.168	16.915	11.918	1.00	38.43	B
ATOM	4989	CB	VAL	B	300	41.570	16.468	11.405	1.00	36.46	B
ATOM	4990	CG1	VAL	B	300	41.853	17.085	10.066	1.00	37.40	B
ATOM	4991	CG2	VAL	B	300	42.658	16.860	12.377	1.00	34.76	B
ATOM	4992	C	VAL	B	300	39.102	16.357	10.981	1.00	39.08	B
ATOM	4993	O	VAL	B	300	38.724	17.029	10.023	1.00	38.52	B
ATOM	4994	N	TYR	B	301	38.599	15.156	11.265	1.00	40.35	B
ATOM	4995	CA	TYR	B	301	37.598	14.504	10.403	1.00	41.51	B
ATOM	4996	CB	TYR	B	301	37.294	13.078	10.890	1.00	39.56	B
ATOM	4997	CG	TYR	B	301	36.110	12.959	11.832	1.00	37.52	B
ATOM	4998	CD1	TYR	B	301	36.282	13.025	13.211	1.00	37.65	B
ATOM	4999	CE1	TYR	B	301	35.200	12.917	14.078	1.00	35.05	B
ATOM	5000	CD2	TYR	B	301	34.819	12.782	11.343	1.00	35.63	B
ATOM	5001	CE2	TYR	B	301	33.738	12.677	12.203	1.00	34.61	B
ATOM	5002	CZ	TYR	B	301	33.938	12.744	13.565	1.00	33.47	B
ATOM	5003	OH	TYR	B	301	32.875	12.628	14.415	1.00	34.10	B
ATOM	5004	C	TYR	B	301	36.280	15.243	10.128	1.00	43.59	B
ATOM	5005	O	TYR	B	301	35.698	15.072	9.058	1.00	42.93	B
ATOM	5006	N	ASN	B	302	35.787	16.012	11.100	1.00	46.84	B
ATOM	5007	CA	ASN	B	302	34.534	16.756	10.934	1.00	48.26	B
ATOM	5008	CB	ASN	B	302	34.198	17.544	12.196	1.00	49.62	B
ATOM	5009	CG	ASN	B	302	33.383	16.749	13.160	1.00	50.79	B
ATOM	5010	OD1	ASN	B	302	32.248	16.371	12.856	1.00	49.97	B
ATOM	5011	ND2	ASN	B	302	33.953	16.476	14.339	1.00	52.10	B
ATOM	5012	C	ASN	B	302	34.540	17.685	9.725	1.00	49.34	B
ATOM	5013	O	ASN	B	302	33.685	17.557	8.844	1.00	47.57	B
ATOM	5014	N	PRO	B	303	35.494	18.642	9.670	1.00	50.64	B
ATOM	5015	CD	PRO	B	303	36.487	19.046	10.685	1.00	50.43	B
ATOM	5016	CA	PRO	B	303	35.540	19.553	8.522	1.00	51.60	B
ATOM	5017	CB	PRO	B	303	36.600	20.580	8.941	1.00	50.73	B
ATOM	5018	CG	PRO	B	303	37.477	19.822	9.867	1.00	50.78	B
ATOM	5019	C	PRO	B	303	35.838	18.904	7.149	1.00	52.83	B
ATOM	5020	O	PRO	B	303	35.651	19.546	6.117	1.00	53.44	B
ATOM	5021	N	VAL	B	304	36.279	17.644	7.126	1.00	54.30	B
ATOM	5022	CA	VAL	B	304	36.561	16.957	5.856	1.00	54.36	B
ATOM	5023	CB	VAL	B	304	37.618	15.830	6.008	1.00	51.93	B
ATOM	5024	CG1	VAL	B	304	38.025	15.310	4.645	1.00	49.40	B
ATOM	5025	CG2	VAL	B	304	38.837	16.343	6.742	1.00	50.06	B
ATOM	5026	C	VAL	B	304	35.265	16.388	5.255	1.00	56.15	B
ATOM	5027	O	VAL	B	304	35.105	16.332	4.034	1.00	55.72	B
ATOM	5028	N	ILE	B	305	34.343	15.970	6.117	1.00	58.53	B
ATOM	5029	CA	ILE	B	305	33.055	15.440	5.671	1.00	61.73	B
ATOM	5030	CG	ILE	B	305	32.229	14.866	6.861	1.00	61.90	B
ATOM	5031	CG2	ILE	B	305	30.805	14.538	6.419	1.00	62.23	B
ATOM	5032	CG1	ILE	B	305	32.904	13.619	7.436	1.00	61.89	B
ATOM	5033	CD1	ILE	B	305	32.251	13.111	8.699	1.00	61.73	B
ATOM	5034	C	ILE	B	305	32.275	16.605	5.072	1.00	63.37	B
ATOM	5035	O	ILE	B	305	31.558	16.458	4.086	1.00	63.64	B
ATOM	5036	N	TYR	B	306	32.456	17.767	5.686	1.00	65.69	B
ATOM	5037	CA	TYR	B	306	31.797	19.005	5.295	1.00	68.12	B
ATOM	5038	CB	TYR	B	306	32.254	20.111	6.260	1.00	69.83	B
ATOM	5039	CG	TYR	B	306	31.297	21.269	6.501	1.00	71.53	B
ATOM	5040	CD1	TYR	B	306	29.961	21.224	6.091	1.00	71.63	B
ATOM	5041	CE1	TYR	B	306	29.110	22.320	6.292	1.00	72.21	B
ATOM	5042	CD2	TYR	B	306	31.752	22.435	7.124	1.00	72.15	B
ATOM	5043	CE2	TYR	B	306	30.916	23.525	7.327	1.00	72.24	B
ATOM	5044	CZ	TYR	B	306	29.604	23.468	6.910	1.00	72.37	B
ATOM	5045	OH	TYR	B	306	28.809	24.572	7.106	1.00	73.36	B
ATOM	5046	C	TYR	B	306	32.067	19.374	3.822	1.00	68.58	B
ATOM	5047	O	TYR	B	306	31.137	19.404	3.013	1.00	69.09	B
ATOM	5048	N	ILE	B	307	33.329	19.616	3.470	1.00	68.85	B
ATOM	5049	CA	ILE	B	307	33.706	19.972	2.094	1.00	69.45	B
ATOM	5050	CB	ILE	B	307	35.244	20.126	1.958	1.00	68.98	B
ATOM	5051	CG2	ILE	B	307	35.634	20.416	0.519	1.00	68.67	B
ATOM	5052	CG1	ILE	B	307	35.746	21.243	2.867	1.00	68.35	B
ATOM	5053	CD1	ILE	B	307	37.243	21.297	2.975	1.00	68.78	B
ATOM	5054	C	ILE	B	307	33.242	18.894	1.115	1.00	70.48	B
ATOM	5055	O	ILE	B	307	32.710	19.193	0.045	1.00	70.11	B
ATOM	5056	N	MET	B	308	33.417	17.642	1.528	1.00	71.82	B
ATOM	5057	CA	MET	B	308	33.054	16.474	0.742	1.00	72.59	B
ATOM	5058	CB	MET	B	308	33.459	15.216	1.503	1.00	71.96	B
ATOM	5059	CG	MET	B	308	34.216	14.206	0.680	1.00	73.14	B
ATOM	5060	SD	MET	B	308	35.853	14.785	0.281	1.00	73.49	B
ATOM	5061	CE	MET	B	308	35.605	15.396	−1.387	1.00	74.45	B
ATOM	5062	C	MET	B	308	31.571	16.384	0.355	1.00	74.35	B
ATOM	5063	O	MET	B	308	31.246	16.260	−0.828	1.00	76.03	B
ATOM	5064	N	MET	B	309	30.673	16.451	1.338	1.00	75.68	B
ATOM	5065	CA	MET	B	309	29.242	16.344	1.050	1.00	76.73	B
ATOM	5066	CB	MET	B	309	28.700	14.996	1.549	1.00	76.51	B
ATOM	5067	CG	MET	B	309	28.871	14.736	3.034	1.00	75.75	B
ATOM	5068	SD	MET	B	309	28.720	12.987	3.411	1.00	76.52	B
ATOM	5069	CE	MET	B	309	27.279	12.529	2.417	1.00	77.23	B
ATOM	5070	C	MET	B	309	28.318	17.504	1.458	1.00	77.66	B
ATOM	5071	O	MET	B	309	27.458	17.369	2.335	1.00	77.83	B
ATOM	5072	N	ASN	B	310	28.507	18.639	0.788	1.00	78.49	B
ATOM	5073	CA	ASN	B	310	27.702	19.846	0.977	1.00	78.75	B
ATOM	5074	CB	ASN	B	310	27.799	20.401	2.398	1.00	76.72	B
ATOM	5075	CG	ASN	B	310	26.851	21.564	2.621	1.00	74.96	B
ATOM	5076	OD1	ASN	B	310	27.281	22.676	2.901	1.00	73.40	B
ATOM	5077	ND2	ASN	B	310	25.553	21.317	2.457	1.00	74.47	B
ATOM	5078	C	ASN	B	310	28.098	20.921	−0.037	1.00	79.70	B
ATOM	5079	O	ASN	B	310	29.009	21.721	0.202	1.00	77.64	B
ATOM	5080	N	LYS	B	311	27.392	20.918	−1.169	1.00	81.71	B
ATOM	5081	CA	LYS	B	311	27.620	21.858	−2.266	1.00	83.03	B
ATOM	5082	CB	LYS	B	311	26.539	21.685	−3.346	1.00	83.63	B
ATOM	5083	CG	LYS	B	311	26.971	20.890	−4.582	1.00	85.01	B
ATOM	5084	CD	LYS	B	311	25.933	20.987	−5.706	1.00	85.72	B
ATOM	5085	CE	LYS	B	311	26.497	20.515	−7.045	1.00	85.94	B
ATOM	5086	NZ	LYS	B	311	27.592	21.398	−7.554	1.00	85.03	B
ATOM	5087	C	LYS	B	311	27.655	23.313	−1.808	1.00	83.94	B
ATOM	5088	O	LYS	B	311	28.477	24.094	−2.284	1.00	83.79	B
ATOM	5089	N	GLN	B	312	26.773	23.655	−0.870	1.00	85.38	B
ATOM	5090	CA	GLN	B	312	26.650	25.011	−0.325	1.00	86.88	B
ATOM	5091	CB	GLN	B	312	25.580	25.031	0.788	1.00	89.83	B
ATOM	5092	CG	GLN	B	312	24.223	24.405	0.404	1.00	93.26	B
ATOM	5093	CD	GLN	B	312	23.296	24.160	1.604	1.00	95.18	B
ATOM	5094	OE1	GLN	B	312	23.184	24.995	2.510	1.00	95.86	B
ATOM	5095	NE2	GLN	B	312	22.622	23.008	1.603	1.00	95.28	B
ATOM	5096	C	GLN	B	312	27.969	25.581	0.225	1.00	86.09	B
ATOM	5097	O	GLN	B	312	28.277	26.758	0.023	1.00	85.90	B
ATOM	5098	N	PHE	B	313	28.746	24.723	0.885	1.00	85.16	B
ATOM	5099	CA	PHE	B	313	30.017	25.094	1.512	1.00	83.26	B
ATOM	5100	CB	PHE	B	313	30.235	24.216	2.746	1.00	82.11	B
ATOM	5101	CG	PHE	B	313	31.363	24.662	3.620	1.00	80.91	B
ATOM	5102	CD1	PHE	B	313	32.577	23.986	3.610	1.00	80.11	B
ATOM	5103	CD2	PHE	B	313	31.211	25.757	4.462	1.00	80.84	B
ATOM	5104	CE1	PHE	B	313	33.625	24.394	4.424	1.00	80.12	B
ATOM	5105	CE2	PHE	B	313	32.252	26.175	5.282	1.00	80.56	B
ATOM	5106	CZ	PHE	B	313	33.463	25.492	5.264	1.00	80.63	B
ATOM	5107	C	PHE	B	313	31.253	25.033	0.609	1.00	83.10	B
ATOM	5108	O	PHE	B	313	32.064	25.958	0.616	1.00	82.08	B
ATOM	5109	N	ARG	B	314	31.405	23.928	−0.128	1.00	83.78	B
ATOM	5110	CA	ARG	B	314	32.540	23.708	−1.042	1.00	83.58	B
ATOM	5111	CB	ARG	B	314	32.363	22.364	−1.797	1.00	85.54	B
ATOM	5112	CG	ARG	B	314	33.656	21.699	−2.335	1.00	87.80	B
ATOM	5113	CD	ARG	B	314	33.423	20.268	−2.933	1.00	90.32	B
ATOM	5114	NE	ARG	B	314	34.682	19.507	−3.096	1.00	93.13	B
ATOM	5115	CZ	ARG	B	314	34.794	18.261	−3.578	1.00	92.42	B
ATOM	5116	NH1	ARG	B	314	33.725	17.577	−3.975	1.00	92.23	B
ATOM	5117	NH2	ARG	B	314	35.989	17.678	−3.633	1.00	90.83	B
ATOM	5118	C	ARG	B	314	32.673	24.888	−2.021	1.00	82.63	B
ATOM	5119	O	ARG	B	314	33.783	25.331	−2.313	1.00	82.49	B
ATOM	5120	N	ASN	B	315	31.533	25.406	−2.491	1.00	81.19	B
ATOM	5121	CA	ASN	B	315	31.488	26.547	−3.416	1.00	78.77	B
ATOM	5122	CB	ASN	B	315	30.071	26.754	−3.979	1.00	79.64	B
ATOM	5123	CG	ASN	B	315	29.701	25.752	−5.062	1.00	79.78	B
ATOM	5124	OD1	ASN	B	315	30.535	24.972	−5.522	1.00	79.80	B
ATOM	5125	ND2	ASN	B	315	28.438	25.782	−5.485	1.00	79.84	B
ATOM	5126	C	ASN	B	315	31.874	27.808	−2.666	1.00	76.34	B
ATOM	5127	O	ASN	B	315	32.644	28.625	−3.161	1.00	76.19	B
ATOM	5128	N	CYS	B	316	31.307	27.958	−1.473	1.00	73.90	B
ATOM	5129	CA	CYS	B	316	31.556	29.116	−0.629	1.00	71.70	B
ATOM	5130	CB	CYS	B	316	30.441	29.252	0.419	1.00	71.82	B
ATOM	5131	SG	CYS	B	316	28.779	29.594	−0.309	1.00	67.40	B
ATOM	5132	C	CYS	B	316	32.952	29.131	0.001	1.00	70.45	B
ATOM	5133	O	CYS	B	316	33.441	30.181	0.412	1.00	70.02	B
ATOM	5134	N	MET	B	317	33.594	27.970	0.065	1.00	69.49	B
ATOM	5135	CA	MET	B	317	34.946	27.881	0.594	1.00	69.28	B
ATOM	5136	CB	MET	B	317	35.290	26.443	0.982	1.00	68.48	B
ATOM	5137	CG	MET	B	317	36.775	26.205	1.275	1.00	66.61	B
ATOM	5138	SD	MET	B	317	37.248	24.453	1.328	1.00	65.00	B
ATOM	5139	CE	MET	B	317	37.840	24.183	−0.345	1.00	63.53	B
ATOM	5140	C	MET	B	317	35.863	28.324	−0.534	1.00	71.27	B
ATOM	5141	O	MET	B	317	36.776	29.119	−0.326	1.00	71.91	B
ATOM	5142	N	VAL	B	318	35.595	27.812	−1.735	1.00	73.65	B
ATOM	5143	CA	VAL	B	318	36.379	28.130	−2.930	1.00	75.99	B
ATOM	5144	CB	VAL	B	318	35.853	27.346	−4.174	1.00	75.39	B
ATOM	5145	CG1	VAL	B	318	36.488	27.862	−5.455	1.00	75.23	B
ATOM	5146	CG2	VAL	B	318	36.165	25.866	−4.026	1.00	75.75	B
ATOM	5147	C	VAL	B	318	36.399	29.635	−3.216	1.00	78.29	B
ATOM	5148	O	VAL	B	318	37.426	30.180	−3.632	1.00	78.85	B
ATOM	5149	N	THR	B	319	35.275	30.302	−2.954	1.00	80.48	B
ATOM	5150	CA	THR	B	319	35.150	31.745	−3.171	1.00	82.50	B
ATOM	5151	CB	THR	B	319	33.668	32.200	−3.072	1.00	82.78	B
ATOM	5152	OG1	THR	B	319	32.860	31.403	−3.949	1.00	83.02	B
ATOM	5153	CG2	THR	B	319	33.526	33.663	−3.476	1.00	83.31	B
ATOM	5154	C	THR	B	319	36.009	32.543	−2.177	1.00	83.66	B
ATOM	5155	O	THR	B	319	36.381	33.691	−2.445	1.00	84.48	B
ATOM	5156	N	THR	B	320	36.325	31.921	−1.041	1.00	84.41	B
ATOM	5157	CA	THR	B	320	37.148	32.536	0.002	1.00	85.04	B
ATOM	5158	CB	THR	B	320	36.924	31.832	1.364	1.00	84.74	B
ATOM	5159	OG1	THR	B	320	35.544	31.938	1.734	1.00	84.79	B
ATOM	5160	CG2	THR	B	320	37.789	32.451	2.454	1.00	84.08	B
ATOM	5161	C	THR	B	320	38.633	32.447	−0.363	1.00	85.83	B
ATOM	5162	O	THR	B	320	39.427	33.327	−0.016	1.00	85.51	B
ATOM	5163	N	LEU	B	321	38.989	31.381	−1.076	1.00	86.96	B
ATOM	5164	CA	LEU	B	321	40.366	31.136	−1.493	1.00	88.25	B
ATOM	5165	CB	LEU	B	321	40.619	29.622	−1.594	1.00	85.33	B
ATOM	5166	CG	LEU	B	321	40.345	28.738	−0.369	1.00	82.12	B
ATOM	5167	CD1	LEU	B	321	40.487	27.288	−0.754	1.00	81.32	B
ATOM	5168	CD2	LEU	B	321	41.284	29.066	0.771	1.00	80.53	B
ATOM	5169	C	LEU	B	321	40.775	31.838	−2.803	1.00	90.63	B
ATOM	5170	O	LEU	B	321	41.848	32.444	−2.872	1.00	90.99	B
ATOM	5171	N	CYS	B	322	39.925	31.767	−3.829	1.00	92.98	B
ATOM	5172	CA	CYS	B	322	40.227	32.386	−5.121	1.00	95.39	B
ATOM	5173	CB	CYS	B	322	39.528	31.645	−6.252	1.00	93.92	B
ATOM	5174	SG	CYS	B	322	40.449	30.197	−6.772	1.00	93.30	B
ATOM	5175	C	CYS	B	322	39.963	33.878	−5.232	1.00	98.18	B
ATOM	5176	O	CYS	B	322	40.239	34.485	−6.271	1.00	98.25	B
ATOM	5177	N	CYS	B	323	39.425	34.459	−4.162	1.00	101.67	B
ATOM	5178	CA	CYS	B	323	39.130	35.891	−4.091	1.00	105.54	B
ATOM	5179	CB	CYS	B	323	40.441	36.687	−4.031	1.00	106.50	B
ATOM	5180	SG	CYS	B	323	41.611	36.129	−2.753	1.00	107.31	B
ATOM	5181	C	CYS	B	323	38.242	36.408	−5.232	1.00	107.70	B
ATOM	5182	O	CYS	B	323	38.528	37.453	−5.836	1.00	107.52	B
ATOM	5183	N	GLY	B	324	37.175	35.665	−5.528	1.00	110.15	B
ATOM	5184	CA	GLY	B	324	36.257	36.062	−6.585	1.00	112.37	B
ATOM	5185	C	GLY	B	324	35.942	35.006	−7.635	1.00	113.39	B
ATOM	5186	O	GLY	B	324	34.772	34.685	−7.863	1.00	113.56	B
ATOM	5187	N	LYS	B	325	36.981	34.487	−8.290	1.00	114.16	B
ATOM	5188	CA	LYS	B	325	36.832	33.472	−9.335	1.00	114.70	B
ATOM	5189	CB	LYS	B	325	38.206	33.096	−9.917	1.00	114.20	B
ATOM	5190	CG	LYS	B	325	38.920	34.213	−10.685	1.00	113.67	B
ATOM	5191	CD	LYS	B	325	39.283	35.404	−9.795	1.00	113.81	B
ATOM	5192	CE	LYS	B	325	39.872	36.556	−10.601	1.00	114.17	B
ATOM	5193	NZ	LYS	B	325	40.069	37.778	−9.772	1.00	113.16	B
ATOM	5194	C	LYS	B	325	36.109	32.227	−8.809	1.00	115.27	B
ATOM	5195	O	LYS	B	325	36.720	31.348	−8.196	1.00	115.29	B
ATOM	5196	N	ASN	B	326	34.800	32.172	−9.053	1.00	115.86	B
ATOM	5197	CA	ASN	B	326	33.951	31.065	−8.607	1.00	115.98	B
ATOM	5198	CB	ASN	B	326	32.481	31.517	−8.574	1.00	115.47	B
ATOM	5199	CG	ASN	B	326	31.624	30.678	−7.636	1.00	114.92	B
ATOM	5200	OD1	ASN	B	326	32.059	29.642	−7.123	1.00	114.01	B
ATOM	5201	ND2	ASN	B	326	30.399	31.134	−7.398	1.00	114.75	B
ATOM	5202	C	ASN	B	326	34.110	29.819	−9.486	1.00	115.97	B
ATOM	5203	O	ASN	B	326	34.637	28.810	−8.970	1.00	115.78	B
ATOM	5204	OT	ASN	B	326	33.705	29.860	−10.671	1.00	116.11	B
ATOM	5205	OH2	WAT		953	53.913	9.916	−31.259	1.00	41.73
ATOM	5206	OH2	WAT		956	57.696	−2.053	43.265	1.00	41.22
ATOM	5207	OH2	WAT		957	48.693	4.852	−18.060	1.00	24.01
ATOM	5208	OH2	WAT		960	33.888	27.069	−11.307	1.00	32.67
ATOM	5209	OH2	WAT		961	63.709	16.988	43.214	1.00	36.42
ATOM	5210	OH2	WAT		962	27.271	2.233	41.823	1.00	36.67
ATOM	5211	OH2	WAT		964	15.610	6.952	2.044	1.00	37.53
ATOM	5212	OH2	WAT		965	45.976	8.381	−11.066	1.00	14.67
ATOM	5213	OH2	WAT		966	56.871	−11.644	−13.182	1.00	35.46
ATOM	5214	OH2	WAT		967	30.304	2.564	43.209	1.00	18.38
ATOM	5215	OH2	WAT		969	63.220	4.609	−36.622	1.00	30.11
ATOM	5216	OH2	WAT		970	61.784	21.128	26.096	1.00	35.05
ATOM	5217	OH2	WAT		971	89.670	5.459	7.567	1.00	31.75
ATOM	5218	OH2	WAT		972	59.969	−6.175	−22.347	1.00	37.13
ATOM	5219	OH2	WAT		974	45.137	20.260	−15.703	1.00	29.76
ATOM	5220	OH2	WAT		975	55.915	−17.781	−20.267	1.00	29.16
ATOM	5221	OH2	WAT		976	41.975	−2.817	−17.030	1.00	25.63
ATOM	5222	OH2	WAT		980	4.811	32.025	11.115	1.00	35.45
ATOM	5223	OH2	WAT		982	45.771	−10.820	−26.055	1.00	28.68
ATOM	5224	OH2	WAT		986	25.963	26.533	−7.731	1.00	12.74
ATOM	5225	OH2	WAT		987	65.137	3.207	−27.249	1.00	22.76
ATOM	5226	OH2	WAT		988	66.257	7.500	39.600	1.00	44.93
ATOM	5227	OH2	WAT		989	41.842	37.561	−7.728	1.00	37.92
ATOM	5228	OH2	WAT		992	52.765	−0.772	−21.390	1.00	25.73
ATOM	5229	OH2	WAT		993	45.447	−12.557	−30.728	1.00	12.66
ATOM	5230	OH2	WAT		997	56.459	2.341	−32.514	1.00	42.07
ATOM	5231	OH2	WAT		998	52.227	11.940	−32.300	1.00	31.62
ATOM	5232	OH2	WAT		999	62.677	0.656	−28.418	1.00	32.09
ATOM	5233	OH2	WAT		1000	48.299	7.644	−20.117	1.00	16.54
ATOM	5234	OH2	WAT		1001	55.271	4.766	−3.712	1.00	20.72
ATOM	5235	OH2	WAT		1002	53.890	−6.325	−8.895	1.00	17.25
ATOM	5236	OH2	WAT		1003	39.361	6.475	−1.390	1.00	41.40
ATOM	5237	OH2	WAT		1004	45.211	7.251	−2.669	1.00	11.67
ATOM	5238	OH2	WAT		1005	38.939	−2.110	−7.622	1.00	23.05
ATOM	5239	OH2	WAT		1006	51.790	−8.851	−10.509	1.00	11.04
ATOM	5240	OH2	WAT		1007	48.972	−6.522	−11.350	1.00	23.14
ATOM	5241	OH2	WAT		1011	65.749	−1.044	−33.726	1.00	26.43
ATOM	5242	OH2	WAT		1013	48.494	3.326	−15.517	1.00	36.74
ATOM	5243	OH2	WAT		1016	24.891	4.670	−0.996	1.00	35.61
ATOM	5244	OH2	WAT		1017	37.931	19.049	−2.376	1.00	16.88
ATOM	5245	OH2	WAT		1018	38.360	11.376	6.697	1.00	31.52
ATOM	5246	OH2	WAT		1019	33.617	8.373	7.513	1.00	8.59
ATOM	5247	OH2	WAT		1020	23.737	5.532	11.924	1.00	24.20
ATOM	5248	OH2	WAT		1024	40.934	12.629	7.938	1.00	8.85
ATOM	5249	OH2	WAT		1025	40.053	11.850	2.670	1.00	23.45
ATOM	5250	OH2	WAT		1026	46.429	13.194	4.378	1.00	23.75
ATOM	5251	OH2	WAT		1027	53.020	12.008	5.967	1.00	18.30
ATOM	5252	OH2	WAT		1028	51.838	1.707	−1.574	1.00	23.60
ATOM	5253	OH2	WAT		1029	53.174	−0.673	17.026	1.00	29.69
ATOM	5254	OH2	WAT		1030	60.075	−2.752	16.285	1.00	18.53
ATOM	5255	OH2	WAT		1031	57.140	−3.814	15.835	1.00	19.18
ATOM	5256	OH2	WAT		1032	58.304	0.394	11.516	1.00	38.89
ATOM	5257	OH2	WAT		1033	61.312	3.285	10.939	1.00	32.15
ATOM	5258	OH2	WAT		1035	63.136	15.447	29.402	1.00	34.06
ATOM	5259	OH2	WAT		1036	82.241	5.815	17.976	1.00	25.42
ATOM	5260	OH2	WAT		1038	79.465	32.501	13.073	1.00	11.23
ATOM	5261	OH2	WAT		1039	79.216	27.939	13.962	1.00	20.32
ATOM	5262	OH2	WAT		1040	83.625	34.117	4.154	1.00	27.91
ATOM	5263	OH2	WAT		1041	72.943	34.850	5.629	1.00	32.55
ATOM	5264	OH2	WAT		1042	70.005	32.721	3.931	1.00	33.09
ATOM	5265	OH2	WAT		1043	75.035	36.861	5.711	1.00	26.45
ATOM	5266	OH2	WAT		1044	72.133	38.485	8.094	1.00	41.84
ATOM	5267	OH2	WAT		1045	77.254	22.274	14.258	1.00	31.98
ATOM	5268	OH2	WAT		1046	70.808	37.464	23.933	1.00	38.59
ATOM	5269	OH2	WAT		1050	49.710	26.774	23.090	1.00	12.15
ATOM	5270	OH2	WAT		1051	54.596	23.922	21.214	1.00	32.99
ATOM	5271	OH2	WAT		1052	53.984	22.762	16.617	1.00	24.07
ATOM	5272	OH2	WAT		1053	51.272	26.798	12.270	1.00	26.72
ATOM	5273	OH2	WAT		1054	43.278	22.320	32.646	1.00	10.89
ATOM	5274	OH2	WAT		1055	37.413	26.489	27.956	1.00	28.32
ATOM	5275	OH2	WAT		1057	31.077	14.193	13.681	1.00	18.38
ATOM	5276	OH2	WAT		1058	23.204	12.489	20.424	1.00	44.02
ATOM	5277	OH2	WAT		1059	47.668	3.781	32.197	1.00	30.06
ATOM	5278	OH2	WAT		1060	50.939	−4.121	24.751	1.00	9.34
ATOM	5279	OH2	WAT		1061	47.779	5.603	16.212	1.00	17.20
ATOM	5280	OH2	WAT		1062	43.163	−1.845	20.479	1.00	23.74
ATOM	5281	OH2	WAT		1063	41.909	1.748	16.597	1.00	45.68
ATOM	5282	OH2	WAT		1070	42.975	3.359	44.850	1.00	30.99
ATOM	5283	OH2	WAT		1073	67.697	13.092	−10.446	1.00	54.00
ATOM	5284	OH2	WAT		1074	71.480	14.327	−20.030	1.00	22.44
ATOM	5285	OH2	WAT		1075	77.293	−2.434	0.752	1.00	31.26
ATOM	5286	OH2	WAT		1076	79.159	−2.050	2.806	1.00	43.11
ATOM	5287	OH2	WAT		1078	61.524	25.307	−11.731	1.00	31.57
ATOM	5288	OH2	WAT		1079	79.455	18.433	−5.909	1.00	31.52
ATOM	5289	OH2	WAT		1080	67.684	38.913	17.286	1.00	35.93
ATOM	5290	OH2	WAT		1081	43.486	34.420	−5.591	1.00	39.96
ATOM	5291	OH2	WAT		1082	64.553	23.788	32.156	1.00	27.64
ATOM	5292	OH2	WAT		1083	30.762	13.635	−3.241	1.00	31.60
ATOM	5293	OH2	WAT		1084	39.782	19.522	−26.715	1.00	42.36
ATOM	5294	OH2	WAT		1085	37.920	21.630	−29.215	1.00	28.98
ATOM	5295	OH2	WAT		1086	43.431	−2.928	−11.223	1.00	6.22
ATOM	5296	OH2	WAT		1087	32.514	11.440	−2.914	1.00	37.54
ATOM	5297	OH2	WAT		1089	77.691	22.271	−9.133	1.00	49.70
ATOM	5298	OH2	WAT		1090	74.297	13.373	−15.590	1.00	20.65
ATOM	5299	OH2	WAT		1091	75.613	19.439	−17.439	1.00	50.06
ATOM	5300	OH2	WAT		1092	67.967	15.630	−24.059	1.00	11.64
ATOM	5301	OH2	WAT		1093	56.494	22.470	−18.207	1.00	29.66
ATOM	5302	OH2	WAT		1094	50.974	−6.630	−30.593	1.00	50.58
ATOM	5303	OH2	WAT		1095	55.246	−3.921	−26.698	1.00	48.06
ATOM	5304	OH2	WAT		1096	52.411	−5.738	−27.300	1.00	37.70
ATOM	5305	OH2	WAT		1099	54.349	0.788	2.241	1.00	31.86
ATOM	5306	OH2	WAT		1101	61.950	−1.675	−7.346	1.00	20.67
ATOM	5307	OH2	WAT		1102	50.741	−1.708	−5.388	1.00	30.66
ATOM	5308	OH2	WAT		1103	47.627	6.817	−0.692	1.00	30.79
ATOM	5309	OH2	WAT		1104	61.714	11.915	−1.183	1.00	49.70
ATOM	5310	OH2	WAT		1105	59.768	9.614	12.849	1.00	16.74
ATOM	5311	OH2	WAT		1106	65.159	12.105	18.290	1.00	17.95
ATOM	5312	OH2	WAT		1107	63.693	7.802	16.545	1.00	21.10
ATOM	5313	OH2	WAT		1109	62.963	20.214	28.973	1.00	37.91
ATOM	5314	OH2	WAT		1113	73.949	25.515	26.500	1.00	38.67
ATOM	5315	OH2	WAT		1114	48.747	−1.771	41.770	1.00	20.02
ATOM	5316	OH2	WAT		1116	47.201	12.467	43.915	1.00	26.66
ATOM	5317	OH2	WAT		1117	56.207	10.614	9.300	1.00	20.84
ATOM	5318	OH2	WAT		1118	46.498	13.040	9.645	1.00	16.94
ATOM	5319	OH2	WAT		1119	41.677	31.007	5.484	1.00	34.21
ATOM	5320	OH2	WAT		1120	33.082	33.712	15.589	1.00	31.25
ATOM	5321	OH2	WAT		1125	53.578	17.029	29.102	1.00	54.39
ATOM	5322	OH2	WAT		1126	40.126	23.609	43.572	1.00	42.59
ATOM	5323	OH2	WAT		1127	43.903	22.002	43.326	1.00	37.80
ATOM	5324	OH2	WAT		1128	34.165	23.338	43.252	1.00	60.20
ATOM	5325	OH2	WAT		1129	42.955	25.744	40.297	1.00	43.55
ATOM	5326	OH2	WAT		1130	40.234	27.438	42.317	1.00	49.39
ATOM	5327	OH2	WAT		1132	34.831	25.934	45.691	1.00	34.67
ATOM	5328	OH2	WAT		1133	32.002	27.666	44.841	1.00	48.38
ATOM	5329	OH2	WAT		1134	33.848	23.686	47.690	1.00	29.08
ATOM	5330	OH2	WAT		1135	28.991	26.854	48.167	1.00	15.30
ATOM	5331	OH2	WAT		1136	32.130	16.400	44.102	1.00	35.55
ATOM	5332	OH2	WAT		1137	30.283	13.820	43.194	1.00	9.98
ATOM	5333	OH2	WAT		1138	48.321	27.265	38.177	1.00	48.00
ATOM	5334	OH2	WAT		1139	51.449	25.575	37.454	1.00	26.46
ATOM	5335	OH2	WAT		1140	44.074	22.628	35.709	1.00	38.15
ATOM	5336	OH2	WAT		1141	37.862	30.118	40.823	1.00	46.99
ATOM	5337	OH2	WAT		1143	43.601	36.250	32.951	1.00	50.69
ATOM	5338	OH2	WAT		1144	48.131	27.139	33.409	1.00	45.07
ATOM	5339	OH2	WAT		1145	49.374	27.310	30.343	1.00	40.90
ATOM	5340	OH2	WAT		1146	51.656	23.495	30.980	1.00	34.63
ATOM	5341	OH2	WAT		1148	40.259	31.824	33.951	1.00	32.25
ATOM	5342	OH2	WAT		1149	43.303	29.383	40.123	1.00	53.84
ATOM	5343	OH2	WAT		1150	43.595	32.246	38.437	1.00	57.69
ATOM	5344	OH2	WAT		1151	46.556	30.993	39.694	1.00	40.86
ATOM	5345	OH2	WAT		1152	46.624	31.005	42.503	1.00	27.58
ATOM	5346	OH2	WAT		1153	51.937	33.587	36.279	1.00	72.22
ATOM	5347	OH2	WAT		1154	43.315	38.652	27.775	1.00	51.33
ATOM	5348	OH2	WAT		1155	44.255	38.349	30.528	1.00	64.73
ATOM	5349	OH2	WAT		1156	46.784	40.192	32.331	1.00	42.28
ATOM	5350	OH2	WAT		1157	52.483	35.355	31.663	1.00	46.93
ATOM	5351	OH2	WAT		1158	40.813	42.731	28.896	1.00	49.57
ATOM	5352	OH2	WAT		1160	14.320	32.912	7.669	1.00	41.93
ATOM	5353	OH2	WAT		1162	10.204	25.817	4.927	1.00	50.26
ATOM	5354	OH2	WAT		1163	13.519	26.496	4.953	1.00	37.28
ATOM	5355	OH2	WAT		1164	30.958	−1.556	37.591	1.00	47.66
ATOM	5356	OH2	WAT		1165	26.512	−3.662	42.716	1.00	37.02
ATOM	5357	OH2	WAT		1166	26.382	9.048	45.911	1.00	52.79
ATOM	5358	OH2	WAT		1169	9.761	17.242	−6.985	1.00	90.24
ATOM	5359	OH2	WAT		1171	21.804	21.889	−2.245	1.00	51.81
ATOM	5360	OH2	WAT		1172	31.612	6.434	6.178	1.00	41.00
ATOM	5361	OH2	WAT		1173	31.787	3.027	4.544	1.00	36.50
ATOM	5362	OH2	WAT		1174	30.409	11.976	−1.079	1.00	25.70
ATOM	5363	OH2	WAT		1175	37.985	−4.085	22.286	1.00	22.60
ATOM	5364	OH2	WAT		1176	38.657	−2.558	15.728	1.00	39.58
ATOM	5365	OH2	WAT		1177	40.343	−1.549	18.515	1.00	55.07
ATOM	5366	OH2	WAT		1178	37.655	−0.152	13.597	1.00	25.18
ATOM	5367	OH2	WAT		1179	43.735	−8.994	26.965	1.00	21.79
ATOM	5368	OH2	WAT		1180	45.247	−6.720	26.195	1.00	19.01
ATOM	5369	OH2	WAT		1181	40.893	−7.988	25.357	1.00	31.63
ATOM	5370	OH2	WAT		1183	48.295	−5.377	25.111	1.00	21.86
ATOM	5371	OH2	WAT		1184	39.196	−11.269	22.201	1.00	27.65
ATOM	5372	OH2	WAT		1185	45.834	−3.108	21.000	1.00	27.28
ATOM	5373	OH2	WAT		1187	47.336	−10.925	19.269	1.00	32.21
ATOM	5374	OH2	WAT		1189	49.721	−11.350	21.806	1.00	27.73
ATOM	5375	OH2	WAT		1190	45.751	−14.313	20.212	1.00	32.70
ATOM	5376	OH2	WAT		1191	47.280	−5.311	22.044	1.00	21.49
ATOM	5377	OH2	WAT		1192	53.003	−8.918	11.321	1.00	28.61
ATOM	5378	OH2	WAT		1196	50.381	−17.972	20.320	1.00	27.49
ATOM	5379	OH2	WAT		1197	41.828	−16.171	23.949	1.00	36.78
ATOM	5380	OH2	WAT		1198	44.472	−14.097	16.153	1.00	29.45
ATOM	5381	OH2	WAT		1199	43.487	−19.987	16.077	1.00	39.54
ATOM	5382	OH2	WAT		1200	44.561	−11.587	14.584	1.00	41.08
ATOM	5383	OH2	WAT		1201	51.404	−15.017	11.938	1.00	44.86
ATOM	5384	OH2	WAT		1202	47.565	−6.231	13.570	1.00	35.05
ATOM	5385	OH2	WAT		1203	42.589	−8.089	21.774	1.00	45.49
ATOM	5386	OH2	WAT		1204	43.716	−5.476	21.813	1.00	49.36
ATOM	5387	OH2	WAT		1205	31.001	15.176	−7.654	1.00	41.72
ATOM	5388	OH2	WAT		1206	31.965	15.881	−5.171	1.00	23.88
ATOM	5389	OH2	WAT		1208	54.348	−23.974	−20.322	1.00	40.38
ATOM	5390	OH2	WAT		1209	52.470	−22.910	−17.579	1.00	35.13
ATOM	5391	OH2	WAT		1210	52.411	−22.520	−14.464	1.00	45.37
ATOM	5392	OH2	WAT		1212	55.169	−20.963	−15.174	1.00	34.24
ATOM	5393	OH2	WAT		1213	28.327	4.770	1.846	1.00	42.59
ATOM	5394	OH2	WAT		1214	70.425	−0.584	−4.634	1.00	49.45
ATOM	5395	OH2	WAT		1215	69.680	2.181	5.942	1.00	12.32
ATOM	5396	C1	NAG		504	35.535	7.769	−31.651	1.00	74.79
ATOM	5397	C2	NAG		504	34.175	8.440	−31.887	1.00	76.39
ATOM	5398	N2	NAG		504	33.271	7.529	−32.561	1.00	75.75
ATOM	5399	C7	NAG		504	32.003	7.449	−32.170	1.00	76.55
ATOM	5400	O7	NAG		504	31.558	6.473	−31.570	1.00	77.62
ATOM	5401	C8	NAG		504	31.079	8.619	−32.500	1.00	75.40
ATOM	5402	C3	NAG		504	34.310	9.721	−32.718	1.00	78.14
ATOM	5403	O3	NAG		504	33.070	10.422	−32.718	1.00	79.57
ATOM	5404	C4	NAG		504	35.406	10.633	−32.163	1.00	78.58
ATOM	5405	O4	NAG		504	35.661	11.688	−33.086	1.00	77.72
ATOM	5406	C5	NAG		504	36.696	9.846	−31.919	1.00	78.64
ATOM	5407	O5	NAG		504	36.436	8.712	−31.065	1.00	77.15
ATOM	5408	C6	NAG		504	37.758	10.691	−31.223	1.00	79.38
ATOM	5409	O6	NAG		504	38.747	11.147	−32.139	1.00	80.08
ATOM	5410	C1	NAG		505	37.738	3.977	−28.738	1.00	64.36
ATOM	5411	C2	NAG		505	38.503	5.203	−29.193	1.00	65.62
ATOM	5412	N2	NAG		505	39.287	5.707	−28.082	1.00	64.80
ATOM	5413	C7	NAG		505	40.584	5.941	−28.239	1.00	65.21
ATOM	5414	O7	NAG		505	41.386	5.060	−28.544	1.00	65.51
ATOM	5415	C8	NAG		505	41.057	7.376	−28.078	1.00	65.00
ATOM	5416	C3	NAG		505	37.555	6.299	−29.688	1.00	67.19
ATOM	5417	O3	NAG		505	38.324	7.256	−30.400	1.00	65.07
ATOM	5418	C4	NAG		505	36.444	5.751	−30.612	1.00	69.54
ATOM	5419	O4	NAG		505	35.379	6.725	−30.744	1.00	71.66
ATOM	5420	C5	NAG		505	35.848	4.448	−30.057	1.00	69.13
ATOM	5421	O5	NAG		505	36.892	3.507	−29.775	1.00	67.16
ATOM	5422	C6	NAG		505	34.873	3.762	−31.000	1.00	70.64
ATOM	5423	O6	NAG		505	34.978	4.265	−32.327	1.00	73.21
ATOM	5424	C1	MAN		603	64.984	8.473	43.789	1.00	99.72
ATOM	5425	C2	MAN		603	64.881	9.795	44.551	1.00	101.44
ATOM	5426	O2	MAN		603	65.242	9.606	45.914	1.00	100.71
ATOM	5427	C3	MAN		603	65.802	10.830	43.901	1.00	103.30
ATOM	5428	O3	MAN		603	65.797	12.028	44.668	1.00	103.63
ATOM	5429	C4	MAN		603	67.235	10.276	43.784	1.00	104.23
ATOM	5430	O4	MAN		603	68.042	11.175	43.028	1.00	105.21
ATOM	5431	C5	MAN		603	67.228	8.901	43.100	1.00	104.13
ATOM	5432	O5	MAN		603	66.338	8.001	43.794	1.00	102.02
ATOM	5433	C6	MAN		603	68.601	8.249	43.072	1.00	105.06
ATOM	5434	O6	MAN		603	69.293	8.554	41.867	1.00	106.02
ATOM	5435	C1	NAG		604	62.911	3.631	43.526	1.00	83.09
ATOM	5436	C2	NAG		604	64.385	3.786	43.908	1.00	85.55
ATOM	5437	N2	NAG		604	64.785	2.756	44.847	1.00	86.66
ATOM	5438	C7	NAG		604	64.558	1.474	44.588	1.00	87.52
ATOM	5439	O7	NAG		604	65.288	0.795	43.863	1.00	87.25
ATOM	5440	C8	NAG		604	63.317	0.859	45.220	1.00	89.12
ATOM	5441	C3	NAG		604	64.637	5.144	44.545	1.00	87.70
ATOM	5442	O3	NAG		604	66.036	5.333	44.704	1.00	87.82
ATOM	5443	C4	NAG		604	64.068	6.261	43.681	1.00	90.00
ATOM	5444	O4	NAG		604	64.178	7.514	44.384	1.00	95.14
ATOM	5445	C5	NAG		604	62.605	5.970	43.354	1.00	88.29
ATOM	5446	O5	NAG		604	62.516	4.709	42.686	1.00	84.77
ATOM	5447	C6	NAG		604	61.966	7.004	42.438	1.00	89.08
ATOM	5448	O6	NAG		604	60.886	6.453	41.691	1.00	90.03
ATOM	5449	C1	NAG		605	59.488	0.645	41.117	1.00	66.12
ATOM	5450	C2	NAG		605	59.183	2.025	41.622	1.00	68.77
ATOM	5451	N2	NAG		605	58.407	2.727	40.620	1.00	67.98
ATOM	5452	C7	NAG		605	57.276	3.331	40.960	1.00	66.31
ATOM	5453	O7	NAG		605	56.309	2.728	41.419	1.00	65.03
ATOM	5454	C8	NAG		605	57.232	4.840	40.801	1.00	66.75
ATOM	5455	C3	NAG		605	60.497	2.750	41.887	1.00	71.55
ATOM	5456	O3	NAG		605	60.217	3.984	42.528	1.00	73.03
ATOM	5457	C4	NAG		605	61.420	1.900	42.776	1.00	73.19
ATOM	5458	O4	NAG		605	62.740	2.471	42.796	1.00	78.34
ATOM	5459	C5	NAG		605	61.522	0.482	42.237	1.00	70.64
ATOM	5460	O5	NAG		605	60.222	−0.071	42.085	1.00	69.34
ATOM	5461	C6	NAG		605	62.294	−0.451	43.127	1.00	70.23
ATOM	5462	O6	NAG		605	63.445	−0.932	42.457	1.00	69.84
ATOM	5463	C1	NAG		704	50.576	−12.496	−21.236	1.00	82.96
ATOM	5464	C2	NAG		704	49.968	−13.245	−20.006	1.00	85.21
ATOM	5465	N2	NAG		704	49.668	−12.280	−18.950	1.00	85.80
ATOM	5466	C7	NAG		704	50.335	−12.262	−17.791	1.00	84.71
ATOM	5467	O7	NAG		704	49.866	−12.715	−16.740	1.00	83.06
ATOM	5468	C8	NAG		704	51.697	−11.577	−17.774	1.00	83.45
ATOM	5469	C3	NAG		704	50.810	−14.391	−19.402	1.00	86.77
ATOM	5470	O3	NAG		704	49.930	−15.352	−18.834	1.00	87.19
ATOM	5471	C4	NAG		704	51.703	−15.079	−20.427	1.00	87.23
ATOM	5472	O4	NAG		704	52.640	−15.933	−19.774	1.00	88.80
ATOM	5473	C5	NAG		704	52.424	−14.000	−21.202	1.00	86.25
ATOM	5474	O5	NAG		704	51.464	−13.315	−22.012	1.00	84.41
ATOM	5475	C6	NAG		704	53.517	−14.530	−22.110	1.00	86.40
ATOM	5476	O6	NAG		704	54.578	−15.105	−21.354	1.00	85.61
ATOM	5477	C1	NAG		705	47.363	−8.699	−23.082	1.00	67.64
ATOM	5478	C2	NAG		705	48.703	−8.838	−23.811	1.00	70.78
ATOM	5479	N2	NAG		705	48.539	−8.506	−25.219	1.00	70.41
ATOM	5480	C7	NAG		705	49.031	−7.366	−25.701	1.00	71.09
ATOM	5481	O7	NAG		705	48.570	−6.257	−25.412	1.00	71.04
ATOM	5482	C8	NAG		705	50.229	−7.464	−26.630	1.00	72.03
ATOM	5483	C3	NAG		705	49.224	−10.276	−23.653	1.00	72.74
ATOM	5484	O3	NAG		705	50.539	−10.377	−24.187	1.00	74.09
ATOM	5485	C4	NAG		705	49.241	−10.694	−22.176	1.00	73.43
ATOM	5486	O4	NAG		705	49.543	−12.105	−22.083	1.00	77.77
ATOM	5487	C5	NAG		705	47.879	−10.411	−21.527	1.00	70.78
ATOM	5488	O5	NAG		705	47.518	−9.034	−21.709	1.00	68.19
ATOM	5489	C6	NAG		705	47.849	−10.676	−20.032	1.00	70.46
ATOM	5490	O6	NAG		705	48.257	−9.535	−19.286	1.00	68.86
ATOM	5491	C1	NAG		804	42.494	−12.858	36.191	1.00	85.90
ATOM	5492	C2	NAG		804	42.005	−14.295	36.051	1.00	88.19
ATOM	5493	N2	NAG		804	42.604	−14.945	34.900	1.00	87.63
ATOM	5494	C7	NAG		804	43.894	−15.265	34.929	1.00	86.68
ATOM	5495	O7	NAG		804	44.659	−15.041	33.994	1.00	85.64
ATOM	5496	C8	NAG		804	44.417	−15.920	36.201	1.00	86.59
ATOM	5497	C3	NAG		804	40.479	−14.268	35.963	1.00	90.26
ATOM	5498	O3	NAG		804	39.963	−15.582	35.768	1.00	90.69
ATOM	5499	C4	NAG		804	39.950	−13.664	37.272	1.00	91.23
ATOM	5500	O4	NAG		804	38.531	−13.572	37.227	1.00	92.33
ATOM	5501	C5	NAG		804	40.560	−12.265	37.503	1.00	91.44
ATOM	5502	O5	NAG		804	42.008	−12.311	37.428	1.00	89.95
ATOM	5503	C6	NAG		804	40.197	−11.674	38.868	1.00	92.91
ATOM	5504	O6	NAG		804	41.167	−11.984	39.868	1.00	93.63
ATOM	5505	C1	NAG		805	46.862	−9.930	36.703	1.00	66.90
ATOM	5506	C2	NAG		805	45.830	−10.052	37.819	1.00	68.78
ATOM	5507	N2	NAG		805	46.466	−9.913	39.112	1.00	69.64
ATOM	5508	C7	NAG		805	46.032	−8.994	39.966	1.00	70.44
ATOM	5509	O7	NAG		805	45.083	−9.187	40.724	1.00	72.88
ATOM	5510	C8	NAG		805	46.750	−7.653	39.972	1.00	71.03
ATOM	5511	C3	NAG		805	45.109	−11.383	37.740	1.00	70.92
ATOM	5512	O3	NAG		805	44.101	−11.426	38.743	1.00	69.58
ATOM	5513	C4	NAG		805	44.488	−11.534	36.349	1.00	73.05
ATOM	5514	O4	NAG		805	43.881	−12.831	36.219	1.00	78.67
ATOM	5515	C5	NAG		805	45.562	−11.363	35.276	1.00	71.05
ATOM	5516	O5	NAG		805	46.218	−10.081	35.424	1.00	69.47
ATOM	5517	C6	NAG		805	45.007	−11.458	33.851	1.00	70.54
ATOM	5518	O6	NAG		805	44.701	−10.186	33.294	1.00	68.65
ATOM	5519	HG + 2	HG2		901	56.595	8.520	2.461	1.00	70.48
ATOM	5520	HG + 2	HG2		902	37.255	9.013	12.962	0.98	74.03
ATOM	5521	HG + 2	HG2		903	76.320	7.361	5.541	0.92	88.92
ATOM	5522	HG + 2	HG2		904	17.925	11.864	12.861	0.93	103.54
ATOM	5523	HG + 2	HG2		905	67.379	27.091	18.402	0.95	116.55
ATOM	5524	HG + 2	HG2		906	28.136	31.133	−1.762	0.73	200.00
ATOM	5525	ZN + 2	ZN2		951	60.258	−0.973	−24.343	1.00	109.89
ATOM	5526	ZN + 2	ZN2		952	35.103	−0.702	39.316	0.89	124.85
ATOM	5527	ZN + 2	ZN2		954	45.879	9.602	45.758	0.54	75.33
ATOM	5528	ZN + 2	ZN2		955	62.511	19.877	23.367	0.96	60.06
END

[0059] The data shown in Table 1 are expressed based on the Protein Data Bank (PDB) format: The PDB format is a format containing coordinates (X, Y, Z,), etc. of individual atoms constituting a protein, and is one of the standard formats in handling coordinates of biopolymers. In Table 1, the “ATOM” appearing in the utmost left column (1st column)denotes each atom of the atomic coordinates. The numbers (1, 2, 3, . . . 5528) appearing in the next column (2nd column) are serial numbers of individual atoms. Subsequently, in the left to right direction in this Table, there are denoted the type of each atom and its position in the amino acid to which it belongs (e.g., “CB”, “CG”, “SD”) (in the 3rd column); the amino acid residue to which each atom belongs (three-letter abbreviations for amino acids, e.g. “MET”, “ASN”) (in the 4th column); the protein chain identifier (expressed by “A” “B”) (in the 5th column); the sequence number of the residue counted from the N-terminal (in the 6th column); X-coordinate (in angstrom unit) (in the 7th column); Y-coordinate (in angstrom unit) (in the 8th column); Z-coordinate (in angstrom unit)(in the 9th column); occupancy ratio (e.g., “1.00”) (in the 10th column); isotropic thermal factor (e.g., 58.37 for atom No. 1 and 58.09 for atom No. 2) (in the 11th column); and the protein chain identifier (expressed by “A” or “B”) (in the 12th column). In bovine rhodopsin, two molecules are present in a non-crystallographic unit. In order to discriminate these two molecules, the protein chain identifiers “A” and “B” are used. “A” denotes one molecule in the non-crystallographic unit and “B” the other.

[0060] It should be noted that the entry “ACE” in the 4th column for atom No. 1 to atom No. 3 represents an acetyl group. For atom serial No. 5205 and thereafter, the entries “WAT”, “NAG”, “MAN”, “HG2” and “ZN2” in the 4th column represent water, N-acetyl-D-glucosamine, α-D-mannose, divalent mercury ion, and divalent zinc ion, respectively; and the numbers in the 6th column (e.g., 956, 957) represent numbers given to those atoms without a protein chain identifier since they do not belong to any protein chain, in order to discriminate the constituent units of the molecules contained in the crystal.

[0061] In addition to the above-described atomic coordinates, the present invention also includes derivatives therefrom, i.e., derivatives from the above-mentioned atomic coordinates (related receptors, etc.) obtained by techniques such as homology modeling on computer. The term “derivatives” means proteins of the GPCR family that have 15% or more, preferably 30% or more, homology to native bovine rhodopsin in the amino acid sequence; or atomic coordinates (derived coordinates) in which a part of the amino acid sequence of native bovine rhodopsin (preferably one or several (e.g., one to ten) amino acids) is deleted, substituted or added and which exhibit a three-dimensional structure of a protein having activity functionally equivalent to native bovine rhodopsin (i.e., the signal transduction activity of GPCRs). Further, in the case of a GPCR family protein that is too low in homology to make an alignment of amino acid sequences with bovine rhodopsin in all regions, modeling may be performed on the seven helix sites alone that can be determined using hydrophobicity or the like as an indicator. In the present invention, whether or not atomic coordinates (derived coordinates) of a GPCR constituting a three-dimensional structure of a mutated amino acid sequence are included in the derivatives of the atomic coordinates constituting the three-dimensional structure of native bovine rhodopsin can be analyzed by comparing the three-dimensional structures of the GPCR in question and native bovine rhodopsin and using as a parameter the discrepancies between the positions of α carbon atoms of specific amino acid residues.

[0062] Specifically, an image of the three-dimensional structure composed of the atomic coordinates of native bovine rhodopsin (designated “three-dimensional structure I”) and an image of the three-dimensional structure composed of the derived coordinates in question (designated “three-dimensional structure II”) are created on computer based on the two sets of atomic coordinates. Subsequently, one image is superposed on the other image on a computer display. The image of three-dimensional structure I contains seven helix sites of bovine rhodopsin. These regions are superposed on the regions of the corresponding helix sites in the image of three-dimensional structure II, or vice versa. This superposing may be processed automatically based on a computer program, or may be carried out manually on a computer display in a manner similar to the one employed in comparing fingerprints.

[0063] The seven helix sites (regions) of bovine rhodopsin include the first helix (expressed as “H-I (36-64)”) consisting of an amino acid sequence from position 36 to position 64 (SEQ ID NO: 2) of the amino acid sequence as shown in SEQ ID NO: 1 (hereinafter, all the position numbers mentioned in this paragraph refer to position numbers in SEQ ID NO: 1), the second helix (expressed as “H-II (71-100)”) consisting of an amino acid sequence from position 71 to position 100 (SEQ ID NO: 3), the third helix (expressed as “H-III (107-139)”) consisting of an amino acid sequence from position 107 to position 139 (SEQ ID NO: 4), the fourth helix (expressed as “H-IV (151-173)”) consisting of an amino acid sequence from position 151 to position 173 (SEQ ID NO: 5), the fifth helix (expressed as “H-V (200-225)”) consisting of an amino acid sequence from position 200 to position 225 (SEQ ID NO: 6), the sixth helix (expressed as “H-VI (247-277)”) consisting of an amino acid sequence from position 247 to position 277 (SEQ ID NO: 7), and the seventh helix (expressed as “H-VII (286-306)”) consisting of an amino acid sequence from position 286 to position 306 (SEQ ID NO: 8). Then, these helix regions are superposed on the corresponding helix regions of the three-dimensional structure II or vice versa, to calculate the discrepancies between the positions of the α carbon atoms in the amino acid residues of those helices in the three-dimensional structure I and the positions of the corresponding α carbon atoms in the amino acid residues of the corresponding helices in the three-dimensional structure II. When the mean residual of the discrepancies is 1.5 Å or less, the three-dimensional structure II is regarded as a derivative of the atomic coordinates as shown in Table 1 (derived coordinates). Discrepancies between the positions of corresponding α carbon atoms can be calculated by the so-called least squares method. Generally, such discrepancies can be calculated using a computer software (e.g., LSQKAB, Quanta). The mean residual is calculated as follows. Briefly, individual distances between two corresponding α carbon atoms are squared; the mean value of these squares is calculated; and then the square root of the mean value is calculated to obtain the mean residual.

[0064] An active site or protein-binding site is formed by at least one helix selected from the above-described seven helices. Accordingly, a G protein-coupled receptor that has a three-dimensional structure of that active site or protein-binding site is also included in the G protein-coupled receptor of the invention. Preferably, the at least one helix consists of H-III, H-V, H-VI and H-VII.

[0065] In addition to the GPCR (bovine rhodopsin) having the three-dimensional structure consisting of the atomic coordinates as shown in Table 1, the present invention also includes a three-dimensional structure consisting of such derived coordinates as the GPCRs of the invention.

[0066] In Table 1, atomic coordinates for the amino acid residues of individual helices corresponds to amino acid residues 36-64 for H-I, 71-100 for H-II, 107-139 for H-III, 151-173 for H-IV, 200-225 for H-V, 247-277 for H-VI and 286-306 for H-VII (residue numbers are entered in the 6th column).

[0067] 4. Method of Virtual Screening for Drugs

[0068] In the present invention, it is possible to carry out virtual screening for drugs using the above-described atomic coordinates or derived coordinates therefrom.

[0069] Briefly, the atomic coordinates of the three-dimensional structure elucidated by the invention are input into a computer so that images of the structure and various parameters are shown on the display. All the information contained in Table 1 may be input, or atomic coordinates corresponding to at least one helix of the seven helices may be input. For example, atomic coordinates corresponding to H-I (107-139), H-V (200-225), H-VI (247-277) and H-VII (286-306) may be input.

[0070] Then, the resultant data are input into a virtual compound library. Since a virtual compound library is contained in a virtual screening software such as DOCK-4 (Kuntz, UCSF), the above-described data may be input into such a software. Candidate drugs may be searched for using a three-dimensional structure database for drug candidate compounds, such as MDDR (Prous Science, Spain).

[0071] 5. Method of Drug Design

[0072] In the present invention, it is possible to construct epoch-making and yet highly reliable drug design models by applying the atomic coordinates of rhodopsin as shown in Table 1 to computer drug discovery. As described in the virtual screening method, all the information (atomic coordinates) contained in Table 1 may be used or atomic coordinates corresponding to the seven helices may be appropriately selected and used in this method of drug design. For example, atomic coordinates corresponding to H-III, H-V, H-VI and H-VII may be selected.

[0073] When the atomic coordinates as shown in Table 1 or derived coordinates therefrom have been input into a computer graphic program, the structure of rhodopsin can be seen three-dimensionally. Using this information on the three-dimensional structure, various modeling or drug designs can be performed.

[0074] Specific examples of computer programs for modeling include “FRODO” or “O” (Program O) for crystallographic analysis, and molecular modeling programs “QUANTA” and “Insight” (MSI, San Diego, USA) for use in creative drug design.

[0075] This method will be described below taking as an example angiotensin II receptor (AG22_HUMAN) which is one of the target GPCRs in pharmaceutical development. Briefly, an alignment of the amino acid sequence of angiotensin II receptor with the amino acid sequence of bovine rhodopsin is prepared as shown in FIG. 4 by conventional methods. Then, the atomic coordinates of bovine rhodopsin are input into a molecular design program such as QUANTA. While showing the total image of bovine rhodopsin by computer graphic, the features of the amino acid sequence of angiotensin II (AT-II) receptor are compared with those of rhodopsin to thereby construct a new three-dimensional structure (FIG. 8).

[0076] When drugs that act on a target GPCR have been already known as in the case of opioid hormone receptor or angiotensin II receptor, sites of specific interaction can be estimated by superposing the three-dimensional structures of such drugs on the model created as described above on graphics; thus, novel and still improved drugs can be designed (Pogozheva, I.D. et al., Biophys. J. 75, 612-634 (1998)).

[0077] 6. Method of Screening for Substances that Influence the Effect of GPCR

[0078] In the present invention, it is possible to screen for target substances that influence the effect of GPCR by comparing the three-dimensional structure defined by the atomic coordinates as shown in Table 1 with three-dimensional structures of test substances that may influence the effect of GPCR. As described in the virtual screening method and drug design method, all the information (atomic coordinates) contained in Table 1 may be used or atomic coordinates corresponding to the seven helices may be appropriately selected and used in this method of screening. For example, atomic coordinates corresponding to H-I, H-V, H-VI and H-VII may be selected.

[0079] The expression “influence the effect of GPCR” means that a test substance and GPCR perform specific, chemical interactions to thereby promote or inhibit the function of the GPCR itself to receive molecules and transmit signals. Candidate substances that may influence in such a manner include naturally occurring compounds, artificially synthesized compounds, and synthetic peptides of ten or less amino acid residues. A therapeutic for asthma that is targeted at histamine receptor involved in asthma may also be exemplified. But, candidate substances are not limited to these substances.

[0080] Three-dimensional structures may be compared using as a parameter the discrepancies between the positions of α carbon atoms in the above-defined seven helices, or may be compared visually using as a parameter the images of structures displayed by computer graphic. If stereochemical energy conditions (e.g., hydrogen bond distance, Vander Waals contact, electrostatic interaction) between the test substance and the GPCR of the invention are suitable for them to interact with each other, the test substance is selected as a candidate for useful drug. This selection can be made appropriately using a computer software commonly used for this purpose, such as QUANTA, CHARMm, Insight I, or DISCOVER (MSI, USA).

[0081] 7. Peptide Fragments or Proteins Having G protein-Coupled Receptor Activity

[0082] (1) Peptide Fragments or Salts thereof

[0083] In the present invention, it is possible to specify active sites of G protein-coupled receptors from the above-described structural analysis of bovine rhodopsin and to prepare peptide fragments that constitute the specified active sites. The peptide fragment consists of an amino acid sequence of positions 36-64 (SEQ ID NO: 2), positions 71-100 (SEQ ID NO: 3), positions 107-139 (SEQ ID NO: 4), positions 151-173 (SEQ ID NO: 5), positions 200-225 (SEQ ID NO: 6positions 247-277 (SEQ ID NO: 7) or positions 286-306 (SEQ ID NO: 8) of the amino acid sequence as shown in SEQ ID NO: 1. All or part of these peptide fragments can be included in the present invention. These peptide fragments may be synthesized, for example, by conventional peptide synthesis. The peptides of the invention also include their salts.

[0084] When the peptides of the invention are synthesized by chemical synthesis, they may be synthesized by conventional means. For example, the azide method, the acid chloride method, the acid anhydride method, the mixed acid anhydride method, the DCC method, the active ester method, the carboimidazole method, the oxidation-reduction method, or the like may be used. Either solid phase synthesis or liquid phase synthesis may be applied.

[0085] Briefly, amino acids that may constitute the peptide of the invention are condensed with each other and, if the resultant product has a protective group, the protective group is removed. Thus, a peptide of interest is synthesized. The condensation and the removal of protective groups may be carried out by any known techniques (see, e.g., Bodanszky, M. and M. A. Ondetti, Peptide Synthesis, Interscience Publishers, New York (1966); Schroeder and Leubke, The Peptide, Academic Press, New York (1965); N. Izumiya et al., Basics and Experiments in Peptide Synthesis, Maruzen Co., Tokyo (1975)). After the reaction, the peptide of the invention may be purified by a combination of conventional purification techniques such as solvent extraction, distillation, column chromatography, liquid chromatography, and recrystallization. Alternatively, the peptide of the invention may be synthesized using a commercial, automated peptide synthesizer (e.g., model PSSM-8 manufactured by Shimadzu Corp. for simultaneous, solid phase synthesis of multiple peptides).

[0086] Salts of the peptide of the invention are, preferably, physiologically acceptable acid-added salts or basic salts. Examples of acid-added salts include salts formed by the peptide and an inorganic acid such as hydrochloric acid, phosphoric acid, hydrobromic acid, or sulfuric acid; or salts formed by the peptide and an organic acid such as acetic acid, formic acid, propionic acid, fumaric acid, maleic acid, succinic acid, tartaric acid, citric acid, malic acid, oxalic acid, benzoic acid, methanesulfonic acid, or benzenesulfonic acid. Examples of basic salts include salts formed by the peptide and an inorganic base such as sodium hydroxide, potassium hydroxide, ammonium hydroxide, or magnesium hydroxide; or salts formed by the peptide and an organic base such as caffeine, piperidine, trimethylamine, or pyridine. Salts may be prepared using an appropriate acid such as hydrochloric acid or an appropriate base such as sodium hydroxide.

[0087] Although the C-terminal of the peptide of the invention is usually a carboxyl group (—COOH) or carboxylate (—COO−), its C-terminal may be an amide (—CONH2) or ester (—COOR). The R in the ester may be, for example, C1-12alkyl,C3-10cycloalkyl,C6-12aryl,or C7-12aralkyl.

[0088] The peptide of the invention further include those peptides whose amino group of the alanine residue at the N-terminal is protected with a protective group, or conjugated peptides such as glycopeptides with sugar chains linked thereto.

[0089] The biochemical and physicochemical properties of the peptide of the invention can be analyzed by mass spectrometry, nuclear magnetic resonance, electrophoresis, high performance liquid chromatography, and the like.

[0090] (2) Proteins Having G protein-Coupled Receptor Activity

[0091] The G protein-coupled receptor of the invention has the seven helix sites (regions) of H-I (36-64), H-II (71-100), H-III (107-139), H-IV (151-173), H-V (200-225), H-VII (286-306). Activity of the G protein-coupled receptor arises from these helix sites. In particular, H-III (107-139), H-V (200-225) and H-VI (247-277) form an active core. Therefore, a protein consisting of an amino acid sequence spanning from H-I (36-64) to H-VII (286-306) (positions 36-306) of the amino acid sequence as shown in SEQ ID NO: 1 is included in the protein of the invention having G protein-coupled receptor activity. Also, a protein comprising a region containing H-I (107-139), H-V (200-225) and H-VI (247-277) that form an active core, more specifically, a protein consisting of a part of an amino acid sequence of positions 36-306 of the amino acid sequence as shown in SEQ ID NO: 1, the part comprising at least a region from H-III (107-139) to H-VI (247-277) (positions 107-277), is included in the protein of the invention having G protein-coupled receptor activity.

[0092] Further, the above-described protein having G protein-coupled receptor activity may have a mutation(s) such as deletion(s), substitution(s) or addition(s) of one or more amino acids, as long as it retains G protein-coupled receptor activity. Such a protein is also included in the protein of the invention.

[0093] Hereinbelow, the present invention will be described more specifically with reference to the following Examples. However, the present invention is not limited to these Examples.

EXAMPLE 1

Isolation, Purification and Crystallization of Rhodopsin

[0094] Bovine retinas (purchased from Schenk Packing Co., Inc., Stanwood Wash., USA) were solubilized with nonyl glycoside (NG), heptane-1,2,3-triol (HPTO) and zinc acetate to prepare a rhodopsin solution with a sufficient purity for crystallization (Okada, T. et al., Photochem. Photobiol. 67,495-499 (1998)).

[0095] Briefly, a rhodopsin solution was concentrated by centrifugation to give a concentration of 10 mg/ml or more. The concentrated solution contained 30-50 mM MES buffer (pH 6.3-6.4), 90-120 mM zinc acetate, 0.5-0.65% (v/v) HPTO, and NG about 2.2 times the amount of rhodopsin molecules in molar ratio.

[0096] This rhodopsin solution was mixed with a reservoir solution [3.0-3.4 M ammonium sulfate, 0.1 M MES buffer (pH 6.0-6.1)] at approximately 3:1 to give final concentrations of 30 mM MES, 5-7 mM β-mercaptoethanol, 65-90 mM zinc acetate, 0.55-0.75% (v/v) HPTO, and 0.45-0.55% (w/v) NG, 0.84-0.86 M ammonium sulfate, to thereby prepare a crystallization solution. Then, crystallization was carried out by hanging drop vapor diffusion.

[0097] Crystals were obtained after leaving the solution stationary for 45 days to half a year in darkness.

[0098] All of the operations, including crystal data measurement, were carried out under dim red light (Fuji Film SC66 or SC68).

EXAMPLE 2

X-Ray Analysis of Bovine Rhodopsin

[0099] Rhodopsin crystals obtained in Example 1 were transferred in succession to a mother liquor containing 1-5 mM mercury acetate and soaked for 2.5 months to half a year to prepare a mercury derivative.

[0100] To this mother liquor of mercury derivative, 10 μl of cryoprotectant solution containing 15% (w/v) sucrose, 0.4% (v/v) HPTO, and 3.4 M ammonium sulfate was added directly. Then, crystals were dipped up with a small nylon loop according to a conventional method. The crystals were immediately placed under a nitrogen gas flow of 100 K (−173° C.) in a liquid nitrogen cooling device to perform flash freezing.

[0101] Thus, crystals were frozen in succession. Photos of their X-ray diffraction images were taken and good crystals were searched for. Selected crystals were transferred with CryoTong™ (Hampton Research, USA) or the like into a liquid nitrogen container and stored until use in experiments.

[0102] (1) Data Collection

[0103] First, in order to estimate X-ray wavelengths to be used in MAD method, the XANES spectrum was measured for experimentally determining the absorption edge wavelength of the mercury atom contained in the crystal.

[0104] The selected and stored mercury derivatives of crystals were mounted on the head of a goniometer in an X-ray diffraction device under a nitrogen gas flow of 100 K according to conventional methods. Their images were photographed, and the qualities of these crystals were examined again. For high quality crystals, three wavelength diffraction image data (MAD data) were collected using RIKEN Beamline I (BL45XU) at SPring-8 optimized for MAD measurement (M. Yamamoto, T. Kumasaka, T. Fujisawa and T. Ueki, J. Synchrotron Rad. 5, 222 (1998)).

[0105] From the collected MAD data, diffraction intensity data were obtained using ENZO and Scalepack (Z. Otwinowski & W. Minor, Methods Enzymol. 276, 307 (1997)) (programs for calculating diffraction intensities from diffraction image data), and twin ratios were estimated using an integrated crystallographic analysis program CNS (Brunger, A. T. et al., Acta Crystallogr. D54, 905-921 (1998)). Twinned crystals are crystals that have a plurality of segments of different azimuths. They may reduce the anomalous diffraction effect expected in MAD method. A crystal whose twin ratio had been estimated 11% was selected for use in data collection since this ratio was lower than those of other crystals. In order to improve accuracy, MAD data measurement was repeated, and six data sets for MAD phase calculation were collected to 3.3 Å from that crystal. Statistics for crystal parameters and measured data are shown in Table 2.

[0106] In addition to the above-mentioned measurement data, diffraction data were collected to 2.8 Å in a similar manner at APS (synchrotron radiation facility), the Argonne National Laboratory (Chicago, USA). In these measurements, the twin ratio was estimated about 30%.

[0107] (2) Structural Determination and Refinement

[0108] For structural determination, the positions of mercury atoms were determined from the diffraction intensity data measured at the beginning, using SOLVE (T. C. Terwilliger and J. Berendzen, Acta Crystallogr. Sect. D 55, 849 (1999) according to conventional methods. The refinement of mercury sites in the crystal lattice, occupancy ratios and thermal factors, as well as the calculation of phases were performed with SHARP (E. de la Fortelle & G. Bricogne, Methods Enzymol. 276, 472 (1997)). In order to improve this experimental phase, the averaging of electron densities by non-crystallographic symmetry utilizing the fact that two identical rhodopsin molecules are present in a non-crystallographic unit, the smoothing of solution regions, and the histogram matching of electron densities were carried out. For these purposes, DM/CCP4 (K. Cowtan, Joint CCP4 and ESF-FACBM Newsletter on Protein Crystallography 31, 34 (1994)) was used. The thus obtained electron density map was input into the program O (T. A. Jones, S. Cowan, J. Y. Zou & M. Kjeltgaard, Acta Crystallogr. Sect. A 47, 110 (1991)). At that time, most of the models for the crystal structure could be constructed. Refinement of models was performed further with CNS, and re-construction of models was repeated with the program O. The R value by the refinement using this 3.3 Å diffraction intensity data set was 23.9% (free R=28%) as a result of calculation using all of the diffraction data measured to 3.3 Å resolution.

[0109] Using the thus obtained structure, model molecules were newly placed in a crystal lattice by the molecular replacement method using a different, 2.8 Å data set in which the length of the crystal lattice is changed. Based on the results, re-construction and refinement of models were performed with the above-mentioned programs CNS and O to obtain the final crystal structure of bovine rhodopsin. During this process, correction of the twin ratio was carried out repeatedly. The results are shown in Table 2.

[0110] (3) Results

[0111] The atomic coordinates as shown in Table 1 were obtained. Statistics for data collection, phasing and refinement are shown in Table 2.

TABLE 2
Statistics for data collection, phasing and refinement.
Data Collection and Phasing
Space group	P41
Unit cell	a = 96.73,						a = 97.25,
	c = 149.63Å						c = 149.54Å
Resolution(Å)	3.3(MAD)						2.8(Refine)
Data set	Remote 1	Edge 1	Peak 1	Remote 2	Edge 2	Peak 2	High resolution
Wavelength(Å)	0.96000	1.00876	1.00800	1.04000	1.00866	1.00700	1.00000
Observed reflections	66,421	66,589	66,651	75,521	74,715	73,603	111,245
Unique reflections	20,499	20,529	20,541	20,636	20,613	20,624	33,221
Completeness*	99.0(99.5)	99.2(99.7)	99.1(99.4)	99.4(99.8)	99.3(99.7)	99.3(99.8)	97.1(80.7)
I/sigma	12.6	11.9	10.6	11.1	11.7	11.6	7.8
Rmerge*#	8.5(39.3)	9.2(43.6)	10.0(55.3)	10.6(54.6)	10.3(51.3)	10.4(53.5)	12.1(69.3)
Phasing power&	0.0/1.1/--	0.6/1.0/0.4	0.9/1.0/0.7	1.6/1.0/1.1	1.5/1.1/1.1	1.4/1.2/1.0
Figure of merit	0.37/0.31
Twin fraction							0.25
	Refinement statistics		Model statistics
	Resolution range(Å)	−2.8	Rmsd from ideality
	Rcryst∥(%)	19.98	bond length(Å)	0.0112
	Rfree(%)	25.55	bond angle(degree)	1.49
	Reflections (Completeness)		Ramachandran plot
	Working set	29,987(87.7%)	Favored(%)	82.9
	Test set	1,465(4.3%)	Allowed(%)	14.0
	Number of atoms	5,105	Generous(%)	2.1
	Average B Values(Å)	67.8	Disallowed(%)	0.9
	*Values in parentheses indicate the highest resolution shell. #Rmerge = ΣhklΣi | Ii(hkl) − <I(hkl)> | /ΣhklΣiI1(hkl).
	&Phasing power = FH(calc)/E where E is phase-integrated lack-of-closure. The three values for each wavelength are for acentric isomorphous/acentric anomalous/centric contrubution.
	∥Rcryst = Σhkl | Fobs(hkl) − Fcalc(hkl) | /ΣhklFobs(hkl).

[0112] The data obtained by the determination of atomic coordinates (Table 1) were input into the computer graphic program O to create graphic images of the three-dimensional structure from various viewpoints. Hereinbelow, the results will be described based on the images obtained.

[0113] (4-1) Structural Determination: Overall Fold and Molecular Contacts

[0114] To obtain structural information for rhodopsin in the ground state, diffraction data for bovine rhodopsin crystallized from mixed micelles were collected. Phasing information was obtained using multiwavelength anomalous diffraction (MAD) methods. Rhodopsin molecules are packed in the crystal lattice as shown in FIG. 1A. The two molecules in the asymmetric unit marked with “A” and “B”, respectively, are related by a non-crystallographic twofold axis between the two H-I helices. In FIG. 1A, a unit cell in the crystal lattice is shown by a box (“0” denotes the origin of the crystal unit cell; “b” and “c” denotes the crystal axes). These H-I helices run almost antiparallel to each other and are within van der Waals contact distance. Thus, the two rhodopsin molecules are packed in almost opposite directions in this crystal.

[0115] This packing allows the electrostatic potentials of the monomers to compensate for each other (FIG. 1B). In FIG. 1B, light gray indicates regions with negative potential and dark gray regions with positive potential.

[0116] Due to these electrostatic properties, rhodopsin molecules in native membranes are arranged in the same orientation and present in a monomeric form. Points of contact between protein molecules between non-crystallographic symmetric units are present mainly at the N-terminal regions including the sites where oligosaccharides are attached (the two saccharide regions shown in the stick model in FIG. 1C). On the other hand, the cytoplasmic moiety of rhodopsin appears not to be involved in any specific interactions between molecules in the crystal packing. The direction of the dipole moment of the retinylidene chromophore in the dimer is almost perpendicular to the z-axis of the crystal lattice, which is consistent with the observation that rhodopsin crystals do not exhibit any color upon exposure to light polarized in z-direction (T. Okada, et al., J. Struct. Biol. 130, 73 (2000)).

[0117] The current model of bovine rhodopsin includes all of the residues that make up seven transmembrane helices; they are 36 to 64 for H-I, 71 to 100 for H-II, 107 to 139 for H-III, 151 to 173 for H-IV, 200 to 225 for H-V, 247 to 277 for H-VI, and 286 to 306 for H-VII in the amino acid sequence of bovine rhodopsin as shown in SEQ ID NO: 1. Ribbon drawings of bovine rhodopsin including models of these helices are shown in FIG. 2. In FIG. 2, Panel A shows the structural model viewed parallel to the plane of the membrane. The upper most part of this drawing corresponds to the outer surface of the disc of rod outer segment. Panel B shows the same model rotated by 90° C. around the vertical axis. Panel C and Panel D show the same model viewed from the intradiscal side and the extradiscal side, respectively.

[0118] A total of 191 amino acids are present in the transmembrane region, and they amount to 54.9% of the total amino acids (348) in the whole molecule. Further, the intradiscal moiety composed of the N-terminal tail and three inter-helical regions (E-I, E-II and E-III) contains the following residues. 1 to 34 for NH2-terminal tail, 101 to 106 for E-I, 174 to 199 for E-II, and 278 to 285 for E-III; 74 residues in the total.

[0119] The structural model of rhodopsin of the invention includes approximately 60% of the amino acid residues in the cytoplasmic moiety of rhodopsin (C-I, C-II, C-III and C-terminal tail): 65 to 70 for C-I, 140 to 150 for C-II, 226 to 235 and 240 to 246 for C-III, and 307 to 327 and 334 to 348 for the C-terminal region including helix H-VIII.

[0120] From the above results, it has been found that a total of 338 amino acids in the current model correspond to 97.1% of the whole rhodopsin molecule. In addition, the 11-cis-retinal chromophore connected to Lys296, a part of two oligosaccharides at Asn2 and Asn15 (M.. N. Fukuda et al., J. Biol. Chem. 254, 8201 (1979)), one Zn ion and three Hg ions are also included in the current structural model.

[0121] It should be noted that the number appearing after each of the amino acids expressed in three-letter abbreviations herein indicates the position of the relevant amino acid in the amino acid sequence of bovine rhodopsin (SEQ ID NO: 1).

[0122] The shape of rhodopsin appears to be very different depending on the viewpoint (FIG. 2A-B). On the plane of the membrane, rhodopsin appears to assume an elliptical shape (FIG. 2C-D). The extracellular domain is folded compactly. Most of the mass of this region comes from the N-terminal and E-II region corresponding to 27 and 35 residues, respectively. The extracellular domain and the transmembrane domain are tightly associated, and a part of E-II appears to be inside the transmembrane domain.

[0123] The transmembrane helices are grouped into long helices (H-I, H-II, H-III, H-V and H-VI) and short helices (H-IV and H-VII), with a maximum of 33 residues for H-III and a minimum of 21 residues for H-VII.

[0124] The key residues involved in interhelical hydrogen bonds are presented in FIG. 3A. The position numbers of the residues in the amino acid primary sequence are indicated in this Figure. The cytoplasmic region forms a flat structure with characteristic ruggedness, and most of the C-II loop and the C-terminal region just follows the H-VII helix extending along the expected surface of the membrane.

[0125] The 4th loop (C-IV) in this region includes a short helical structure (H-VIII) connected perpendicularly to H-VII. C-III, the largest interhelical loop in the cytoplasmic region, does not seem to be folded over the helix region, but seems to extend the flat surface defined by the edge of the rod of rhodopsin.

[0126] In contrast to the compactly folded structure of the extracellular domain, most of the cytoplasmic regions exhibit high thermal factors, and the electron densities of some residues could not be specified (FIG. 3B). In FIG. 3B, light gray indicates high thermal factors. The four regions (C-I to III and C-terminal) do not interact with each other closely. The retinal chromophore is attached to the middle of molecule, is U-shaped in appearance, and is covalently bound to the side chain of Lys296. The electron density is consistent with the 11-cis-conformation for the retinal. The dimensions of rhodopsin molecule are approximately 35 Å×25 Å×55 Å, making the total volume ˜48,000Å3.

[0127] (4-2) Comparison to Other Receptors

[0128] The structural model of rhodopsin of the invention offers a structural template for other GPCRs, including the assignment of secondary structural elements and the location of highly conserved amino acids.

[0129] The molecular size of bovine rhodopsin, 348 amino acids, is intermediate among the members of the family and thus can feature most of the essential parts of functional importance in G-protein activation. The lengths of the seven transmembrane helices and of the three extracellular loops are expected to be nearly the same for most of the family members, as can be seen in the sequence of β-adrenergic receptor (FIG. 4A). Variation in other regions probably reflects the specificity of each receptor for either its ligand or its G protein. Because most of the vertebrate visual pigments share very similar size distributions for all of the domains, structure-function relationships deduced from the structural model of the invention are directly applicable to the members of this subfamily. The structure of bovine rhodopsin, represented schematically in FIG. 4B, exhibits those features found in most GPCRs, and at the same time demonstrates differences between GPCRs and bacterial retinal-binding proteins (M. Kolbe et al., Science 288, 1390 (2000; H. Luecke et al., J. Mol. Biol. 291, 899 (1999); H. Belrhali et al., Structure 7, 909 (1999)).

[0130] In FIG. 4A, abbreviations denote the following:

[0131] rRho: bovine rhodopsin (P02699)

[0132] hRho: human rhodopsin (P08100)

[0133] red: human red cone pigment (P04000)

[0134] green: human green cone pigment (P04001)

[0135] blue: human blue cone pigment (P03999)

[0136] bAR: human β-adrenergic receptor (P07550)

[0137] The sequences of the above substances were obtained from the GenBank. Identical amino acids in all receptors are shown in white letters on black background. Conservative replacement residues (T=S, E=D=Q=N, M=L=I=V,R=K, and Y=F=W) are shown in white letters on black background. Conservative replacement residues between rhodopsins and cone pigments are shaded in gray. Transmembrane helices (H-I to H-VII) are shown as thick black bars, and encompass residues Gln36-Gln64 for H-I, Pro71-His100 for H-II, Pro107-Val139 for H-III, Asn151-Val173 for H-IV, Asn200-Gln225 for H-V, Glu247-Thr277 for H-VI and Ile286-Tyr306 for H-VII. Post-translational modifications are N-terminal acetylation, glycosylation (Asn2 and Asn15, numbers 1 and 2), Cys-Cys bridge (residues 3 and 4), Lys296 that forms the Schiff base with the chromophore (number 5) and two palmitoylation sites (6, 7).

[0138] (4-3) Extracelular (Intradiscal) Regions

[0139] Regions in the extracellular domain of rhodopsin (N-terminal and interhelical loops E-I, E-II, and E-III) associate to form a compact structure (FIG. 2 and FIG. 5A). FIG. 5 presents stereoviews of the C α-traces showing the flow of the polypeptide chain, with some key residues, on the inside of the extracellular domain of the transmembrane helices (Panel A) and on the cytoplasmic side of the molecule (Panel B). The N-terminal tail of rhodopsin contains five distorted β-strand-like structures, forming a substantial domain by itself. The N-terminus is located just below loop E-III, with the side chain of Asp282 close to that of Asn2.

[0140] The first two antiparallel strands, Gly3 to Pro12, form a typical β-sheet fold (designated S1 and S2) running almost parallel to the expected plane of the membrane.

[0141] The subsequent three strands form a right triangle from Phe13 to Pro34, with the third strand running just below E-III, almost parallel to the long axis of rhodopsin viewed from the extracellular direction. S4 connects Ser14-Asn15 in the N-terminal region of the molecule with Pro23, located close to E-I. S5 from Pro27 to Pro34 runs along the surface of the membrane covering the extracellular (intradiscal) space between H-I and H-II. Oligosaccharides at Asn2 and Asn15 extend from the domain and are not involved in any interactions with any parts of the polypeptide.

[0142] Mutations of Pro23 or Gln28 cause the eye disease retinitis pigmentosa (T. P. Dryja et al., Nature 343, 364-366 (1990); P. Humphries et al., Science 256, 804 (1992); A. Rattner et al., Annu. Rev. Genet. 33, 89 (1999)). In the model of the present invention, these side chains are located close together in a space between the 4th and 5th distorted β-strands, and are also close to the side chain of Tyr102 on E-I loop (His100-Pro107).

[0143] These findings indicate that the above-mentioned residues maintain the proper orientation between the E-I loop and the N-terminal domain. The N-terminal domain may also contact the E-III loop around Pro12.

[0144] While both the E-I and E-III loops run along the periphery of the molecule, a part of E-II folds deeply into the center of rhodopsin. Just after the extracellular end of H-IV, a long strand fromGly174 to Met183 crosses the molecule along the membrane surface. The side chain of Met183 extends toward a hydrophobic pocket around H-I, and the side chain of Gln184 is surrounded by hydrophilic groups containing bound water. Residues in the middle of this strand, Arg177 to Glu181(designated β3), form a typical antiparallel β-sheet with the next region (residues Ser186 to Asp190, designated β4), which is deeper inside the molecule than β3. β4 is just below the 11-cis-retinal and is a part of the chromophore-binding pocket. The side chain of Cys187 points to that of Cys110 the extracellular end of H-III, forming a disulfide bridge. This disulfide bridge is conserved in most GPCRs (FIG. 4A and FIG. 6A). Residues Tyr191 to Asn200 from E-II loop form another loop region at the periphery of the molecule, like E-I and E-III. The side-chain amide of GIn279, which is at the beginning of E-III, and the peptide carboxyl of Tyr191 in E-II are close to each other, while Asn199 is near to Trp175, which is one of the initial residues of E-II thus in proximity to the extracellular end of H-IV. This arrangement places E-II in extensive contact with the extracellular regions and also with retinal.

[0145] The above-described findings not only well explain the results of many experiments carried out to date, but also prove that the structure of bovine rhodopsin currently determined is correct. Further, it was confirmed this time that important amino acid residues expected by mutation experiments, etc. are forming a hydrogen bond or salt bridge in a hydrophobic environment. Thus, it has become clear that these amino acid residues are key residues in the maintenance of the structure. In particular, the S-S bridge, which is most conserved in GPCRs, forms the lower part of the extracellular domain on the N-terminal side along the cis-retinal in charge of photo absorption of rhodopsin. It is suggested that his site plays an important role in the binding of ligand to GPCRs. In fact, in a homology model of angiotensin-II receptor, a site corresponding to the retinal-binding site of rhodopsin has an amino acid side chain supplementing the site, and a specific space is provided on the opposite side of this extended chain. This space runs toward the N-terminal, forming a channel-like shape. This strongly suggests that a ligand (such as hormone)-binding site of GPCRs exists in that space.

[0146] This also means that the mechanism of molecular switch (i.e., as retinal changes into all-trans-configuration upon absorption of light, this change causes structural change in the protein, switching the receptor to active conformation called metarhodopsin II) is almost directly applicable to GPCRs in general. Thus, various structures of GPCRs can be created by techniques such as homology modeling based on the three-dimensional structure of bovine rhodopsin elucidated by the invention. Further, the structural model of the invention opens up a possibility to create new ligands when applied to drug creation using homology models.

[0147] (4-4) Transmembrane Helices

[0148] From a cryo-EM study, the helical bundle of rhodopsin appears to have differently extending faces on the two ends, suggesting that it could be asymmetric along the axis perpendicular to the membrane surface (V. M. Unger et al., Nature 389, 203 (1997)). However, examination of the cross section of the bundle at the two surfaces indicates that these are nearly equal in area irrespective of the difference in shape.

[0149] The cytoplasmic ends of H-II and H-IV are near each other, but they diverge in the region of Trp161, one of the residues that are highly conserved among GPCRs. This residue is near the point where H-III penetrates toward H-V between H-II and H-IV. Although H-III has in its central part two consecutive Gly residues (Gly120 and Gly121) that are believed apt to disturb the two-dimensional structure, these residues do not distort H-III. On the other hand, the region of the three residues Glu134-Arg135-Tyr136 that are believed important for activity in H-III does exhibit a slight deviation from typical helical structure.

[0150] The cytoplasmic terminal region of H-III is surrounded mostly by hydrophobic residues forming the binding site for a G protein. H-IV and H-V exhibit a deviation from regular helicity in the cytoplasmic region and at His211, respectively. The regular helicity of H-V is interfered by the side chain of Tyr136 at Cys222. Near this region, the phenolic ring of Tyr223, which is also highly conserved among GPCRs, partially covers the interhelical region between H-V and H-VI near the lipid interface. The cytoplasmic end of H-VI extends past the putative membrane surface to Thr243. This terminal region is slightly distorted. Three basic residues, Lys245, Lys248, and Arg252, located near the cytoplasmic end of H-VI project from the helical bundle, making this region of C-III highly basic.

[0151] In H-VII, two phenyl rings of Phe293 and Phe294 interact with Leu40 of H-I and Cys264 of H-VI, respectively. This interaction with H-VI is particularly important because the region in H-VI is where the direction of helix significantly changes. H-VII is distorted in the region from Ala295 to Tyr301. This region includes Ala299, whose peptide carbonyl can hydrogen bond with the side chain NH of Asn55 in H-I. A highly conserved NPXXY motif in GPCRs follows this region in a regular helical structure.

[0152] The results of structural analysis described so far revealed that bovine rhodopsin has a transmembrane helical structure greatly different from that of bacteriorhodopsin whose structure has already been elucidated though its function is completely different, and that this helical structure of bovine rhodopsin is the first structure ever obtained that can be used as a general model for GPCRs.

[0153] (4-5) 11-cis-Retinal Chromophore

[0154] From the experimental electron density, the conformation of the retinal chromophore in the Schiff base linkage with Lys296 is 6s-cis, 11-cis, 12s-trans, anti C=N (FIG. 7). FIG. 7A shows an experimental electron density of the retinal chromophore (2Fo-Fc map (1σ)); and FIG. 7B shows an electron density of the retinal chromophore after structural refinement (2Fo-Fc map (1σ)). The electron density indicated by a double basket near the retinal molecule shows an omit map (5 σ). FIG. 7C-D presents schematics showing the side chains surrounding the 11-cis-retinylidene group.

[0155] The electron density for the β-ionone ring exhibits a larger bulge indicating the positions of the two methyl groups connected to C1 and a smaller bulge for the single methyl at C5 (FIG. 7B).

[0156] Two small bulges along the polyene chain indicate the positions of the C9- and C13-methyl groups. The refined structure of the retinylidene group is consistent with resonance Raman spectroscopy (R. H. Callender et al., Biochemistry 15, 1621 (1976)), nuclear magnetic resonance (NMR), (P. O. Smith et al., Biochemistry 26, 1606 (1987)) and chemical analysis (P. K. Brown & G. Bald, J. Biol. Chem. 222, 865 (1956)). The electron density of the polyene chain merges with that of the side chain of Lys296, indicating the presence of a Schiff base linkage. The retinylidene group is located closer to the extracellular side in the putative lipid bilayer, as suggested previously (D. D. Thomas & L. Stryer, J. Mol. Biol. 154, 145 (1982)).

[0157] The position of the β-ionone ring is mainly covered from the cytoplasmic side by the residues in H-III and H-VI, Glu122, Phe261, and Trp265 (FIG. 7C). The indole ring of Trp265 points down to the retinylidene group near the β-ionone ring, and also comes close to its C13-methyl group with a distance of 3.8 Å. Because deletion of the C13-methyl group induces partial expression of rhodopsin activity in the dark (T. Ebrey et al., FEBS Lett. 116, 217 (1980)), loss of the interaction between Trp265 and C13-methyl group may be a possible mechanism of the activation of rhodopsin. From the β-ionone ring to C11, the retinylidene group runs almost parallel to H-III. On H-III, there are amino acid residues that provide many side chains constituting the binding pocket surrounding the polyene chain. These amino acid residues are Glu113, Gly114, Ala117, Thr118, Gly120, and Gly121, mainly around the polyene chain of Thr118, in addition to Tyr268 and Ile189 from the extracellular side, appears to determine the position of the C9-methyl of the retinylidene group. Side chains mostly from H-V and H-VI (Met207, Phe208, His211, Phe212, Tyr268, and Ala269) also surround the β-ionone ring. The proximity of Phe261 and Ala269 to the retinylidene group is consistent with information showing that these amino acid residues located near the retinal are responsible for the absorption difference between red and green pigments in humans (M. Neitz et al., Science 252, 971 (1991)).

[0158] Arrangement of the four residues from H-VI (Phe261, Trp265, Tyr268 and Ala269) appears to be determined by a significant bend around Pro267. From H-IV, only Cys167 participates covering a part of this pocket. Residues from H-I, H-II, and H-VII (Tyr43, Met44, Leu47, Thr94, and Phe293) are part of the region surrounding the Schiff base.

[0159] Finally, the extracellular side of the polyene chain is covered by a part of the E-II loop, β-sheet S4 from Ser186 to Ile189. The side chain of Glu181 belonging to S3 of the E-II loop extends toward the retinylidene group. This supports the previous results demonstrating that the corresponding amino acid in red/green pigments may be the binding site for chloride ion, which is responsible for the red shift in their absorption compared with rhodopsin (Z. Wang et al., Biochemistry 32, 2125 (1993)). Another amino acid from the E-II loop participating in the retinylidene group binding site is Tyr191, whose OH group is also close to that of Tyr286 in H-VI. Since mutation of this residue does not affect the absorption but reduces the ability to activate transducin (T. Doi et al., Proc. Natl. Acad. Sci. USA 87, 4991 (1990)), Tyr191 may participate in the transition to the active form of rhodopsinthrough interaction with Tyr268.

[0160] The arrangement around the Schiff base is of particular interest in terms of understanding the mechanism of the primary process in photoactivation of rhodopsin. The direction of the side chain of Lys296, almost along the long axis of rhodopsin, is supported by two hydrophobic side chains in H-I, Met44 and Leu47, and by a nearby peptide bond between Phe293 and Phe294. This region is stabilized through the two phenyl rings interacting with other helices. Since it is difficult to determine exactly from the current structure how the protonated Schiff base linkage is stabilized in the protein environment, the current model is unable to discriminate whether water molecules participate in the formation of a coordinated counterion or not.

[0161] Since the distances between the oxygen atoms of the side chain carboxyl group of Glu113 and the Schiff base nitrogen are 3.3 Å and 3.5 Å, a salt bridge is formed directly. Also, the OH group of Thr94 comes close to one of the oxygen atoms of Glu113 with a distance of 3.4 Å. Any other residues, including the nearby Thr92 and Thr93, are too far from the Schiff base region to contribute to stabilization of its protonated state.

[0162] From the above-described results of structural analysis, the environment surrounding retinal has been clearly shown, and the structural basis for discussing photoactivation has been established. As described previously, the β-strand from Ser186 to Ile189 includes the disulfide bridge between Cys187 and Cys110, which is conserved in most GPCRs. This structural site has been found important for the mechanism of activation switch that is turned on by the binding of a ligand.

[0163] (4-6) Cytoplasmic Surface (Extradiscal Region)

[0164] The structure around the C-I loop exhibits a rigid organization (FIG. 5B). Of the three basic side chains in this region, Lys67 extends toward the solvent, whereas Lys66 and Arg69 point toward a lipid-facing region. The peptide carbonyl group of Lys67 appears to easily hydrogen-bond with the side chain of Asn73 in H-II. This constraint may be important for maintaining an arrangement of the two exposed basic residues and His65 forming a line of positive charges over H-I. These make up one of the most conserved amino acid clusters among GPCRs in the rhodopsin subfamily.

[0165] The present inventors assign the region from Cys140 to Glu150 as the C-II loop. This loop exhibits an L-shaped structure, when viewed parallel to membraneplane, with a barrel (Met143 to Phe146) almost along the main axis of rhodopsin. Four polar side chains in this loop (Lys141, Ser144, Asn145, and Arg147) form a distinct cytoplasmic border from the transmembrane region. The height of these side chains is roughly comparable to that of the cytoplasmic border of C-III loop.

[0166] The carboxyl-terminal half of the loop C-II, Asn145 to Gly149, stretches to the outside of the molecule, probably along the expected membrane surface. In the C-II loop, the position of Cys140 is mainly along the membrane surface, forming an external flat domain on the cytoplasmic side of rhodopsin. In contrast to C-I in which basic side chains are exposed to the solvent region, two phenyl rings of Phe146 and Phe148 form a part of a cytoplasmic border of rhodopsin. In fact, a continuous curved line of such a border, which is distinct from the rest of the molecule, is formed by the side chains from HiS65 to Phe146, covering both the C-I and C-II loops (FIG. 5B). This line merges with a part formed by the side chains of C-IV, Arg314, Asn315 and Thr319, although its spatial separation from the transmembrane region becomes obscure around this region.

[0167] Thus, the model of the invention can assign a border corresponding to the major cytoplasmic part of rhodopsin.

[0168] Several amino acid residues on the cytoplasmic side following H-VI have a helical structure comparable to standard β-helix structure. In contrast, the cytoplasmic extension from H-V exhibits an S-shaped flat loop structure almost along the surface of membrane. The C-III loop connecting from H-V to H-VI reaches close to the lipid-facing side of H-VI at Ala235, without covering the cytoplasmic surface of the helical bundle of rhodopsin.

[0169] The model of the invention shows that this region is of highly flexible nature. Although the four amino acid residues from Gln236 to Glu239 are not included in the current model, it is evident that the C-III loop is not folded over the helical region of rhodopsin.

[0170] It should also be noted that the C-III loop is known to vary considerably among related GPCRs, so the flexibility and variability of this region may be critical for functionality and specificity in G-protein activation. In particular, the C-terminal part of the C-III loop is drawing a large arc as if covering a part of the cytoplasmic region that has been experimentally demonstrated to interact with G proteins. This relation between the C-terminal part and the site of interaction with G proteins is important when considering structural changes after the activation switch has been turned on. The amphiphilic helical structure of the H-VIII is of particular interest in the cytoplasmic region, considering previous studies of a variety of synthetic peptides and their effects on the activation of G proteins. Direct evidence for interaction of the amphiphilic helical structure region of H-VIII with the G-protein transducin has been provided using a synthetic peptide from Asn310 to Leu321 of bovine rhodopsin (B. Konig et al., Proc Natl. Acad. Sci. USA 86, 6878 (1989); E. P. Marin et al., J. Biol. Chem. 275, 1930 (2000)). The short amphiphilic helix of H-VIII is clearly distinct from H-VII and, via the tripeptide Met309 to Lys311, lies nearly perpendicular to H-VII. It is also the region that follows the NPXXY motif as a part of a conserved block of residues up to Cys322. The presence of a short helix structure in this region was demonstrated for a corresponding peptide of turkey β-adrenergic receptor by solution NMR spectroscopy in a nonpolar solvent (H. Jung et al., Biochemistry 35, 6399 (1996)).

[0171] It has also been supposed that a group of peptides called mastoparans, which assume an amphiphilic helical structure and have activity on G proteins, mimic the structure of receptors in this region (K. Wakamatsu et al., Biochemistry 31, 5654 (1992)). From the rhodopsin structure, it appears that this short stretch of amino acids is located in a hydrophobic environment, which could induce α-helical structure. Further, the distribution of side chains along this helix also exhibits an amphiphilic pattern; the charged/polar groups cluster on one side while hydrophobic ones are on the other. This suggests that Phe313, Met317 and Leu321 are buried in hydrophobic core of the receptor (FIG. 6B).

[0172] In FIG. 6, Panel A shows the E-II loop near the disulfide bridge between Cys110 and Cys187, viewed from the extracellular side. Panel B shows the C-IV cytoplasmic loop from Lys311 to Leu321 forming a short amphiphillic helix (H-VI). Panel C shows interhelical hydrogen bonds mediated by a highly conserved Asn55, connecting H-H, H-II and H-VII, and by a highly conserved Asn78, connecting H-II, H-III and H-IV. Panel D shows the tripeptide region, Glu134-Arg135-Tyr136 known as (D/E)R(Y/W) motif, located near the cytoplasmic end of H-III.

[0173] Phe313 and Arg314 are the most conserved residues in this region. Thus, Arg314, along with Asn315 and Thr319, participates in the continuous cytoplasmic border of rhodopsin, suggesting that this short helix in rhodopsin may be functionally important for fixing H-VII to the membrane as an anchor.

[0174] Although the model of the invention does not include any lipid-like structure, the side chains of Cys322 and Cys323 to which attachment of palmitic acid has been reported (Y. A. Ovchinnikov et al., FEBS Lett. 230, 1 (1988)) project to the outside of rhodopsin, causing no collision between atoms on the model. Thus, the current model is consistent with the above report.

[0175] The helical structure appears to be terminated by Gly324 and the following C-terminal tail changes the direction (FIG. 6B). The region from Lys325 to Leu328 runs as an elongated structure almost antiparallel to the above-described helix, forming one of the most exposed borders of rhodopsin.

[0176] (4-7) Intramolecular Interactions and Activation

[0177] The transmembrane region of rhodopsin is stabilized by a number of interhelical hydrogen bonds and hydrophobic interactions, and most of them are mediated by highly conserved residues in GPCRs (FIG. 4A). One of the residues that exhibit the highest conservation is Asn55 in H-I. Its side chain is responsible for two interhelical hydrogen bonds to Asp83 in H-II and to the peptide carbonyl of Ala299 in H-VII (FIG. 6C). Another region that mediates constraints for three helices includes Asn78 of H-II, which is hydrogen-bonded to OH groups of Ser127 of H-III and Thr160 of H-IV.

[0178] The tripeptide Glu134-Arg135-Tyr136 is part of a highly conserved (D/E)R(Y/W) motif found in GPCRs (FIG. 4A and FIG. 6D). These residues participate in several hydrogen bonds with surrounding residues. The carboxyl group of Glu134 forms a salt bridge with the guanidinium group of neighboring Arg135. Arg135 is also linked to Glu247 and Thr251 in H-IV. Also, H-III is close to H-V at the side chain of Tyr136, whose OH group can form a hydrogen bond with the side chain of Gln225. The three Val residues from Val137 to Val139 are also close enough to partly cover the cytoplasmic side of Glu134 and Arg135. These hydrophobic residues could be one of the critical constraints keeping rhodopsin in the inactive conformation.

[0179] H-VII of most of the GPCRs in the rhodopsin subfamily contains an NPXXY sequence near the cytoplasmic end, but the functional importance of this motif remains unclear. The side chains of the two polar residues in this region, Asn302 and Tyr306 in bovine rhodopsin, project inside the molecule. The OH group of Tyr306 is at 3.2 Å distance from Asn73, which is also highly conserved among GPCRs, suggesting the presence of additional interhelical hydrogen-bonding constraints between H-VII and H-III. Asn73 is also hydrogen-bonded with the peptide carbonyl of Lys67 in the C-I loop. Although the distance between Asn302 and Asp83 is too long to form a hydrogen bond, water molecules near Asp83 might possibly interact with the side chain of Asn302. In this case, the water molecules mediate the interhelical contact among H-II, H-III and H-VII.

[0180] The energy of light is utilized for photoisomerization of the 11-cis-retinal chromophore to an all-trans-configuration. This change in conformation would cause multiple effects, including movement of β-ionone toward H-III and/or displacement of Schiff base/C9/C13-methyl regions, ultimately switching the receptor to active conformation, metarhodopsin II (R. G. Matthews et al., J. Gen. Physiol. 47, 215 (1963); C. J. Weitz & J. Nathans, Neuron 8, 465 (1992); J. Kibelbek et al., Biochemistry 30, 6761 (1991); Tachibanaki et al., Biochemistry 36, 14173 (1997); I. Szundi et al., Biochemistry 37, 14237 (1998); S. Dickopf et al., Biochemistry 37, 16888 (1998)).

[0181] The model of bovine rhodopsin of the invention confirms that these effects can change the environment of the salt-bridge between the Schiff base and Glu113, resulting in its neutralization (K. Fahmy et al., Proc. Natl. Acad. Sci. USA 90, 10206 (1993); F. Jager et al., Biochemistry 33, 10878 (1994)). Displacement of H-III will result in environmental changes in the ERY motif and cause its reorientation. The rhodopsin model of the invention also suggests that interaction between β-ionone ring and H-III occurs at Glu122, which is one of the residues that determine the rate of metarhodopsin II decay (H. Imai et al., Proc. Natl. Acad. Sci. USA 94, 2322 (1997)). Because Glu122 interacts with His211 in rhodopsin, the proposed movement of H-III caused by the β-ionone ring can affect the interaction between these residues in the transition to metarhodopsin II. In addition, the change around the Schiff base region can affect the interaction between the C13-methyl group of retinal and Trp265. The photoactivation may also cause breakage of some of the three interhelical constraints mediated by Ala299, Asn302, and Tyr306, and hydrophobic constraints via Phe294 to the highly kinked region in H-VI. As a result, rearrangement of the helical bundle may be triggered, and finally lead to the movements of H-III and/or H-VI (D. L. Farrens et al., Science 274, 768 (1996); S. P. Sheikh et al., Nature 383, 347 (1996)).

[0182] (5) Summary

[0183] The GPCR family is one of the largest, most diverse and most interesting groups of proteins encoded by 2 to 5% of the genes present in human genome. They are involved in many physiological processes and are attractive targets for pharmacological intervention to improve these processes in normal and pathological states. The determination of crystal structure of rhodopsin has revealed a comprehensive molecular model and a highly organized heptahelical transmembrane bundle with 11-cis-retinal as a key cofactor involved in maintaining rhodopsin in the ground state. Numerous papers have reported many features of rhodopsin found in the structural model of the invention.

[0184] A set of residues that interacts with the 11-cis-retinal chromophore produce the specific environment that results in an absorption shift of the chromophore to a longer wavelength. However, long distance interactions and electrochemical properties of the chromophore-binding site, as a whole, are responsible for this characteristic maximum absorption. The structure of the invention provides insight into the spectral tuning of related receptors, cone pigments.

[0185] Another major issue is what is the molecular mechanism for GPCR activation. The positions of a conserved set of residues on the cytoplasmic surface, where G-protein activation occurs, suggest a possible conformational change upon photoactivation of the chromophore that leads to rhodopsin activation and signal transduction. Therefore, the crystal structure of bovine rhodopsin discloses many fascinating structural features commonly found in GPCRs that will be useful to elucidate the principles that govern receptor activation and spectral tuning. The structure will also lead to molecular explanation of structural changes that occur in mutated receptors as well as several human pathologies as a result of such structural changes. More importantly, the structure of the invention will reveal the nature of the membrane protein bovine rhodopsin in detail.

[0186] All the publications, patents and patent applications cited in the present specification are incorporated herein by reference in their entireties.

EFFECT OF THE INVENTION

[0187] According to the present invention, a three-dimensional structure of bovine rhodopsin provided with the basic structure of GPCRs is disclosed. The structural data of the invention provide GPCR-targeting drug design with a structure as an extremely realistic model molecule. Further, the basic structure of bovine rhodopsin of the invention is useful for computer-utilizing development of various drugs targeting GPCR family receptors.

Claims

1. A peptide fragment consisting of an amino acid sequence of positions 36-64, positions 71-100, positions 107-139, positions 151-173, positions 200-225, positions 247-277 or positions 286-306 of the amino acid sequence as shown in SEQ ID NO: 1, or a salt of said peptide fragment.

2. A protein selected from the group consisting of the following (a), (b) and (c): (a) an isolated protein consisting of an amino acid sequence of positions 36-306 of the amino acid sequence as shown in SEQ ID NO: 1; (b) an isolated protein which consists of a part of an amino acid sequence of positions 36-306 of the amino acid sequence as shown in SEQ ID NO: 1, said part comprising at least positions 107-277, and which has G protein-coupled receptor activity; (c) an isolated protein which consists of an amino acid sequence of positions 36-306 or 107-277 of the amino acid sequence as shown in SEQ ID NO: 1 having a deletion(s), substitution(s) or addition(s) of one or more amino acids, and which has G protein-coupled receptor activity.

3. A G protein-coupled receptor selected from the group consisting of the following (a) and (b): (a) a G protein-coupled receptor having three-dimensional structure I defined by the atomic coordinates as shown in Table 1; (b) a G protein-coupled receptor having three-dimensional structure II defined by derived coordinates from the atomic coordinates as shown in Table 1, wherein the mean residual of the discrepancies between the positions of the α carbon atoms in the amino acid residues of seven helix sites H-I (36-64), H-II (71-100), H-III (107-139), H-IV (151-173), H-V (200-225), H-VI (247-277) and H-VII (286-306) in the amino acid sequence as shown in SEQ ID NO: 1 of the three-dimensional structure I and the positions of the corresponding α carbon atoms in the amino acid residues of the corresponding seven helix sites of the three-dimensional structure II is 1.5 Å or less when an image of the three-dimensional structure I obtained by computer-processing the atomic coordinates of Table 1 and an image of the three-dimensional structure II obtained by computer-processing said derived coordinates are superposed.

4. The receptor according to claim 3, wherein the G protein-coupled receptor is bovine rhodopsin.

5. The receptor according to claim 4, wherein the bovine rhodopsin is a metal derivative of its crystal.

6. The receptor according to claim 5, wherein the metal is a mercury compound.

7. A method of virtual screening for drugs, comprising computer-processing the following atomic coordinates (a) or (b), or derived coordinates therefrom, inputting the resultant computer-processed data into a virtual compound library and searching for useful drugs through said library: (a) a part of the atomic coordinates as shown in Table 1, said part corresponding to the amino acid residues of at least the three helix sites of H-III (107-139), H-V (200-225) and H-VI (247-277) selected from seven helix sites H-I (36-64), H-II (71-100), H-III (107-139), H-IV (151-173), H-V (200-225), H-VI (247-277) and H-VII (286-306) in the amino acid sequence as shown in SEQ ID NO: 1; (b) the atomic coordinates as shown in Table 1.

8. The method according to claim 7, wherein said derived coordinates are generated by homology modeling based on the atomic coordinates as shown in Table 1, the mean residual of the discrepancies between the positions of the α carbon atoms in the amino acid residues of the three helix sites H-III (107-139), H-V (200-225) and H-VI (247-277) in the amino acid sequence as shown in SEQ ID NO: 1 and the positions of the corresponding α carbon atoms in the amino acid residues of the corresponding three helix sites in said derived coordinates being 1.5 Å or less.

9. A method of drug design, comprising imaging three-dimensional structures of G protein-coupled receptors using the following atomic coordinates (a) or (b), or derived coordinates therefrom, analyzing the resultant images by computer graphics and designing structures of useful drugs based on the resultant analysis data: (a) a part of the atomic coordinates as shown in Table 1, said part corresponding to the amino acid residues of at least the three helix sites of H-III (107-139), H-V (200-225) and H-VI (247-277) selected from seven helix sites H-I (36-64), H-II (71-100), H-III (107-139), H-IV (151-173), H-V (200-225), H-VI (247-277) and H-VII (286-306) in the amino acid sequence as shown in SEQ ID NO: 1; (b) the atomic coordinates as shown in Table 1.

10. The method according to claim 9, wherein the derived coordinates are generated by homology modeling based on the atomic coordinates as shown in Table 1, the mean residual of the discrepancies between the positions of the α carbon atoms in the amino acid residues of the three helix sites H-III (107-139), H-V (200-225) and H-VI (247-277) in the amino acid sequence as shown in SEQ ID NO: 1 and the positions of the corresponding α carbon atoms in the amino acid residues of the corresponding three helix sites in said derived coordinates being 1.5 Å or less.

11. A method of screening for target substances that influence the effect of the G protein-coupled receptor according to any one of claims 3 to 6, comprising comparing the three-dimensional structure of the receptor with three-dimensional structures of test substances.