cDNA sequence of Dengue virus serotype 1 (Singapore strain)

The present invention relates to Dengue Virus Type 1. Dengue virus infection may lead to dengue fever (DF) or its more severe dengue haemorrhagic fever (DHF) and dengue shock syndrome (DSS). DHF is an important virus disease of global significance, especially in Southeast Asia. There are four serotypes of Dengue virus (DEN1, DEN2, DEN3 and DEN4) belonging to the family Flaviviradae.
The complete genomic sequence of DEN2 (Jamaica) has been published by Deubel et al; Virology 165, 234-244 (1988). The complete genomic sequence of DEN3 (HS87) has been published by Osatomi and Sumiyoshi; Virology 176, 643-647 (1990). The complete genomic sequence of DEN4 has been published by Zhao et al; Virology 155, 77-88. To date, only a partial sequence of any variant of DEN1, DEN1 (Nauru Island), has been determined; Mason et al, Virology 161, 262-267 (1987).
We have now identified a previously unknown strain of DEN1 and established its complete nucleotide sequence. The new strain, DEN1-S275/90, was deposited at the European Collection of Animal Cell Cultures (ECACC) Porton Down, GB under Budapest Treaty conditions on (Apr. 21, 1992) and given accession number V92042111. DEN1-S275/90 differs significantly from DEN2, DEN3 and DEN4 in terms of sequence homology. There are also a number of significant differences between DEN1-S275/90 and DEN1 (Nauru Island).
The present invention thus provides DEN1-S275/90 (ECACC V92042111). The invention further provides DEN1-S275/90 (ECACC V92042111) for use as a diagnostic reagent. The invention also provides DEN1-S275/90 in inactivated form for use as a diagnostic reagent or a vaccine.
The invention also provides the nucleic acid sequence of Seq. ID No. 1 and DNA sequences substantially corresponding to SEQ ID No. 1, e.g. degenerate variants thereof having one or more nucleotide changes but nevertheless capable of being translated to give the same protein sequence. The invention further provides fragments of such DNA polynucleotides, in particular the fragments encoding the C, C', PreM, M, E, NS1, NS2A, NS2B, NS3, NS4A, NS4B and NS5 genes of the genome of the virus. The start and end points of these preferred fragments in the nucleic acid sequence of Seq I.D. No. 1 are shown below in Table 1. Table 1 also shows the start and end points of the proteins encoded by these genes, using the numbering of Seq. ID Nos. 1 and 2.
TABLE 1______________________________________Start and end points of the nucleic acid (n) numbers encoding the genes of S275/90. The table also shows the start and end points of the corresponding proteins (p) within the polyprotein encoded by S275/90. Gene Start(n) End(n) Start(p) End(p)______________________________________C 81 422 1 114 C' 123 422 15 114 PreM 423 695 115 205 M 696 920 206 280 E 921 2402 281 774 NS1 2403 3464 775 1128 NS2A 3465 4112 1129 1344 NS2B 4113 4499 1345 1474 NS3 4500 6359 1475 2093 NS4A 6360 6809 2094 2242 NS4B 6810 7556 2243 2492 NS5 7557 10268 2493 3396______________________________________
The nucleic acid sequences of the invention may be used as probes in an assay to determine the presence or absence of DEN1-S275/90, or they may be incorporated into a vector, eg. an expression vector.
Nucleic acid fragments according to the invention may be made by known methods of chemical synthesis or cloned from the virus itself using known recombinant techniques. Fragments according to the invention may also be produced by replication of DNA or RNA, by transcription from DNA to form RNA fragments or reverse transcription from RNA fragments to form DNA fragments. Such transcription may be in a cell free system or may be effected in cells for instance by cloning. Cell free systems include an appropriate replicase, transcriptase or reverse transcriptase, suitable nucleotide precursors and a nucleic acid template or appropriate sequence, together with buffers and any necessary or desirable cofactors.
The present invention also provides a polyprotein as set forth in Seq. ID No. 1 and Seq. ID No. 2 and fragments thereof, eg. the C, C', PreM, M, E, NS1, NS2A, NS2B, NS3, NS4A, NS4B and NS5 proteins as identified above in Table 1. The invention thus provides a polypeptide having an amino acid sequence substantially corresponding to the sequence shown in SEQ ID No. 2 or a fragment thereof. Fusion proteins which incorporate these peptides are also provided.
The polyprotein and proteins according to the invention may be produced by synthetic peptide chemistry or by expressing vectors carrying DNA encoding the proteins in a suitable cell in order to produce expression of the DNA, followed by recovery of the expressed protein. Methods of expressing and recovering recombinant proteins, including fusion proteins, are well known in the art.
For example, for expression of a polypeptide of the invention, an expression vector may be constructed. An expression vector is prepared which comprises a DNA sequence encoding a polypeptide of the invention and which is capable of expressing the polypeptide when provided with a suitable host, eucaryotic or procaryotic. Appropriate transcriptional and translational control elements are provided, including a promoter for the DNA sequence, a transcriptional termination site, and translational start and stop codons. The DNA sequence is provided in the correct frame such as to enable expression of the polypeptide to occur in a host compatible with the vector. The expression vector may be selected to be suitable to express the nucleic acid sequences of the invention in, for example, a bacterial e.g. E. coli, yeast, insect or mammalian cell. A baculovirus expression system may be used. The nucleic acid may be expressed in order that a protein or peptide encoded by the fragment alone is produced or alternatively it may be expressed to provide a fusion protein in which DEN1-S275/90 or a protein thereof, e.g. E, NS1, NS2, NS3 or NS5 as identified in Table 1 above is fused to a second amino acid sequence, e.g. a C-terminal sequence derived from glutathione S-transferase or maltose binding protein or a C-terminal or N-terminal signal sequence. Such a sequence may for example cause the fusion protein to be exported from the cell. The expression vector is then provided with an appropriate host. Cells harbouring the vector are grown so as to enable expression to occur. The vector may be a plasmid or a viral vector.
Recovery and where desirable, further purification of the protein produced by an expression vector in a host cell may be by means known in the art. Such means are designed to separate the protein of the invention from the other proteins of the host cell. Suitable means include chromatographic separation of the recovered protein.
The polyprotein and peptides of the invention may be used as immunogens for a vaccine against DEN1-S275/90 and other DEN1 viruses. Suitably, the proteins and peptides of the invention will be combined with a pharmaceutically acceptable carrier or diluent in order to prepare a sterile vaccine composition. The vaccine composition may then be used in a method of immunizing a human against DEN1 infections.
Advantageously, a vaccine composition against DEN1 may comprise a mixture of two or more peptides. For example, it may comprise one non-structural (NS) peptide, eg. NS1 or NS3, together with a capsid (C), M or E peptide. A mixture of two or more NS peptides could also be used.
The proteins and peptides of the invention may also be used as antigens in an immunoassay to detect the presence or absence of DEN1, and especially DEN1-S275/90. The proteins and peptides are optionally labelled with a detectable label, eg a radioisotope, biotin or a fluorophore. The immunoassay may be conducted by bringing a known quantity of labelled protein (antigen) into contact with a sample suspected of containing antibody against DEN1 and detecting the presence or absence of antibody-antigen complex containing the labelled antigen.
The invention also provides antibodies against the above-mentioned proteins and peptides of the invention. The antibodies may be monoclonal or polyconal. Monoclonal antibodies may be produced by hybridoma techniques known in the art or by recombinant means to provide hybrid antibodies such as humanized antibodies.
The antibodies of the invention may be used in a method of treatment, eg passive immunisation, of DEN1 infections. The antibodies may also be used in a method of diagnosis, eg by immunoassay, to detect the presence or absence of DEN1 in a sample. The antibodies may be labelled as described above for the proteins and peptides of the invention. They may also be labelled with a toxin or isotope selected to kill virus-infected cells. Antibodies against NS1 are particularly favoured since NS1 is expressed on the surface of Dengue virus-infected cells.
The antibodies of the invention may also be used in a method to detect the presence or absence of DEN1 protein in a sample. The method may comprise bringing the antibody into contact with a sample suspected to contain DEN1 proteins (antigens) and detecting the amount of antibody-antigen complex formed. Immunoassays according to the invention may be, for example, competitive (eg radioimmune assays--RIA) or non-competitive (eg enzyme linked immunosorbent assays--ELISA).

The following Examples illustrate the invention. In the accompanying drawings:
FIG. 1 is a diagrammatic representation of the cDNA of Dengue virus Type 1 (Singapore strain S275/90) and fragments of said DNA in expression vectors;
FIG. 2 shows gel results confirming serologic responses in mice after immunisations with fusion proteins prepared as in Examples 2-5 with or without complete Freund's adjuvant (CFA).
Gel Lanes: Lane 1: M, Lane 2: anti E, Lane 3: anti-E+ CFA, Lane 4: anti-NS1, Lane 5: anti-NS2, Lane 6: anti-NS2+ CFA, Lane 7: anti-NS3, Lane 8: anti-NS3+ CFA, Lane 9: anti-NS5, Lane 10: anti-NS5+ CFA, Lane 11: positive rabbit sera, Lane 12: negative rabbit sera, Lane 13: M;
FIG. 3 shows gel results confirming serologic response in rabbits after immunisations with fusion proteins prepared as in Examples 2 to 5. (-), serum before immunisation; (+) serum after immunisation.
Gel Lanes: Lane 1: (-), Lane 2: (+) anti-E, Lane 3: (-), Lane 4: (+) anti-NS1, Lane 5: (-), Lane 6: (+) anti-NS2, Lane 7: (-), Lane 8: (+) anti-NS3, Lane 9: (-), Lane 10: (+) anti-NS5, Lane 11: positive Dengue, Lane 12: patient sera;
FIG. 4 shows fluorescence microscopy of C6/36 cells infected with Dengue Type 1 DI-275 and probed with antibodies against recombinant fusion proteins. A, control antiserum; B, anti-E; C, anti-NS1; D, anti-NS2; E, anti-NS3; F anti-NS5.

EXAMPLE 1
DEN1 virus, strain S275/90, was isolated in 1990 from the serum of a DHF patient in Singapore by 3 passages in AP61 (Aedes psuedoscutellaris) cells followed by 3 passages in C6/36 (Aedes albopictus) cells, and identified by immunofluorescence using type-specific monoclonal antibodies. After a further 8 to 13 passages in C6/36 cells, the virus-infected culture fluid was partially purified by precipitation with polyethylene glycol and ultracentrifugation on a 30% sucrose cushion (6). The viral RNA was extracted from the purified virus by treatment with phenol in the presence of sodium dodecyl sulphate. Following cDNA synthesis (cDNA Synthesis System Plus, Amersham) using random primers, the assorted cDNAs were cloned into EcoRI sites of pUC18 vector via EcoRI adaptors (Promega). The Esherichia coli transformants containing Dengue-specific sequences were screened by colony hybridisation with .sup.32 P-labelled cDNA probes prepared by reverse transcription of strain S275/90 RNA. The cloning procedure yielded overlapping cDNA clones containing inserts ranging in size from 0.5 kb to 2.7 kb. The ends of these primary clones and their subclones obtained by nested deletional analysis (Erase-a-Base System, Promega) were subjected to double-strand sequencing (Sequenase Version 2.0, United States Biochemical). The sequence data generated covers about 90% of the genomic sequence of S275/90.
Potential secondary structures have been postulated for the 5' and 3' ends of flaviviruses (4, 7, 8), posing a problem in obtaining clones with intact ends. A different stragegy for sequencing the 5' and 3' noncoding regions was used to increase the chances of obtaining clones which contain these sequences as well as the terminal end sequences of the genome. cDNAs of strain S275/90 were obtained by random priming and oligo(dT) priming (after poly(A) tailing of the virus RNA]; these were amplified by polymerase chain reaction (PCR) in the presence of specific primers, 796 and 10090/B, respectively. The cDNAs of interest were then religated into pUC18 vector. The nucleotide sequences of the primers are as follows: primer 796, 5' CCG TGA ATC CTG GGT GTC 3' (SEQ ID NO: 13); primer 10090/B, 5' GGG AAT TCC AGT GGT GTG GATC 3' (SEQ ID NO:14) with a BamHI site at its 5' end. The sequences of the primers were selected from that of the initial clones of strain S275/90. To obtain the sequences at the 5' noncoding region, random cDNA clones were first generated as described above, followed by ligation to EcoRI adaptors before insertion into the EcoRI sites of the pUC18 vector. These ligated products of assorted cDNA inserts were flanked by the reverse and forward sequencing primers of M13 in the pUC18 vector. The forward sequencing primer was thus used as one of the primers for PCR. The ligated cDNA clones were used as templates for PCR in the presence of primer 796 (which binds to the plus strand of the template at nucleotide position 808 to 825 of strain S275/90) and the commercial M13 single-strand primer (5'GTA AAA CGA CGG CCAGT 3' (SEQ ID NO: 15), Pharmacia). The amplified cDNAs thus contained the polylinker from the pUC18 vector at one end and an XbaI site (at nucleotide position 728) at the other end. For the 3' noncoding region, an additional step was included before cDNA synthesis. After extraction, the purified Dengue viral RNA was tailed by poly A polymerase (Bethesda Research Laboratories) with ATP. This was followed by cDNA synthesis using oligo(dT) as primer for the first strand cDNA synthesis. The same procedures of EcoRI adaptors ligation and insertion into EcoRI sites of the pUC18 vector were repeated. The ligated products were again subjected to PCR amplification using the primer 10090/B (which binds to the minus strand of the template at nucleotide positions 10,086 to 10,099 of strain S275/90) and the commercial M13 single-strand primer.
All samples were amplified by 30 cycles of PCR with melting, annealing and polymerisation conditions of 1 minute at 94.degree. C., 2 minutes at 55.degree. C. and 3 minutes at 72.degree. C., respectively. The amplified DNA was purified by electroelution in agarose gel followed by appropriate restriction enzyme digestions. The PCR amplified cDNAs at the 5' noncoding region were double digested with XbaI and EcoRI, while those at the 3' noncoding region were digested with BamHI and EcoIR before cloning into the appropriate sites of the pUC18 vector. The clones were screened and subjected to double-strand sequencing as described above.
The sequence data obtained from the overlapping cDNA clones was ordered by homology alignment with the published sequences of the four Dengue serotypes DEN1, DEN2, DEN3 and DEN4 using the computer program of Wilbur and Lipman (9). Seq ID No. 1 shows the complete nucleotide sequence of strain S275/90, which is 10,718 nucleotides in length, and its deduced amino acid sequence. The reading frame begins with the first AUG start codon, corresponding to nucleotides 81 to 83, and contains an open reading frame of 10,188 nucleotides encoding a polyprotein of 3396 amino acids; there are 80 nucleotides in the 5' noncoding region and 450 nucleotides in the 3' noncoding region. The sequence in the 5' noncoding region preceding the first AUG codon of the open reading frame appears to be conserved for all Dengue virus types (1-4). The length of the 3' noncoding region of strain S275/90 is longer than that of DEN2 (412 nucleotides), DEN3 (433 nucleotides) and DEN4 (384 nucleotides).
The nucleotide composition of strain S275/90 is 31.9% A, 25.9% G, 21.5% T and 20.7% C. As reported for the other flaviviruses, the same purine-rich composition was observed, and there is an absence of poly(A) tract at the 3' end.
The individual protein coding segments are based on comparison with protein sequence data for all the proteins determined from the four Dengue serotypes. These cleavage sites may reveal the involvement of viral or cellular proteases involved in protein processing. The C, preM, M, E, NS1, NS2A, NS2B, NS3, NS4A, NS4B and NS5 proteins are cleaved at the sites M/MNQRKK, A/FXL, RXKR/SV, X/MRCXG, VQA/DXGCV, VXA/GXG, X/SWPLN, KXQR/XG, GRX/S, VXA/NE (SEQ ID NO:s 16-25, respectively) and R/G, respectively, where X refers to any residue. The cleavage sites of NS2A, NS3 and NS4B conform to the reported consensus sequences (4, 5), which were originally established by Rice et al (10).
The nucleotide sequences of the structural and nonstructural regions (5' noncoding end to NS1, about 2400 nucleotides in length) of Nauru Island strain of DEN1 (isolated in 1974) and strain S275/90 were compared. Nucleotide variation shows that transitions are about 85.0% [transitions/(transitions+transversions).times.100%] in the structural region and 92.1% in the NS1 region; 15% of these base changes are transversions in the structural region and 7.9% in the NS1 region. The overall 236 nucleotide differences have given rise to 27 amino acid substitutions. As shown in Table 2, the nucleotide homology is 93.1% and when translated, the amino acid homology is 97.6%. Although both strains were isolated from different geographic regions with an interval of 16 years, a higher homology was still observed between the two strains. It can also be seen in Table 2 that strain S275/90 shows a higher homology with DEN3 then with DEN2 and DEN4. The nucleotide divergence of each gene is less than the translated amino acid divergence. The greatest nucleotide and amino acid changes, and hence the greatest evolution, lie in the nonstructural gene NS2A in all the four Dengue serotypes. A high homology is found in NS3 and NS5, which contain conserved sequences.
Chu et al (11) compared three topotypes of DEN1 strains (Thailand, Philippines and Caribbean) genetically at the envelope region. They found nucleotide changes to be less than 5% but translational differences of 2% at the amino acid level. Our strain S275/90 shows nucleotide changes of 7.7% and amino acid changes of 2.6% in the envelope region. Rico-Hesse (6) compared nucleotide sequences within a chosen E/NS1 region to estimate evolutionary relationships among 40 DEN1 strains of different geographic range and time period.
TABLE 2______________________________________HOMOLOGY (%) COMPARISON OF ALIGNED NUCLEOTIDE SEQUENCES OF THE FOUR DENGUE SEROTYPES WITH STRAIN S275/90 (AMINO ACID ALIGNMENT WITHIN BRACKETS). S275/90 DEN1 DEN2 DEN3 DEN4______________________________________Full 93.1 (97.6) 67.1 (70.9) 70.4 (75.5) 65.1 (67.6) length 5' non- 100 81.7 93.8 87.7 coding C 97.4 (98.2) 70.5 (67.5) 80.5 (80.7) 68.1 (67.9) PrM 91.6 (95.6) 71.1 (75.8) 75.8 (78.0) 68.0 (68.1) M 93.3 (98.7) 64.0 (70.7) 70.3 (78.7) 60.7 (60.3) E 92.3 (97.4) 65.4 (67.7) 69.0 (76.4) 64.8 (61.8) NS1 92.6 (98.0) 70.1 (73.6) 74.5 (78.7) 70.1 (68.8) NS2A -- 55.1 (39.0) 57.0 (46.8) 51.7 (37.9) NS2B -- 66.0 (60.8) 69.4 (69.2) 63.1 (60.8) NS3 -- 72.0 (79.3) 74.0 (84.5) 69.9 (75.4) NS4A -- 63.0 (61.4) 69.6 (68.7) 62.8 (58.7) NS4B -- 69.7 (76.7) 74.9 (82.3) 71.1 (75.9) NS5 -- 71.7 (78.7) 73.8 (81.0) 69.9 (72.9) 3' non- -- 83.8 87.4 79.5 coding______________________________________
REFERENCES
1. WESTAWAY, E. G., BRINTON, M. A., GAIDAMOVICH, S. Ya, HORZINEK, M. C., IGARASHI, A., KAARIAINEN, L., LVOV, D. K., PORTERFIELD, J. S., RUSSEL, P. K., and TRENT, D. W., Intervirology 24, 183-192 (1985).
2. ROSEN, L., Supplement to S. Afr. J. Med. 11, 40-42 (1986).
3. HALSTEAD, S., Science 239, 476-481 (1988).
4. DEUBEL, V., KINNEY, R. M., and TRENT, D. W., Virology 165, 234-244 (1988).
5. OSATOMI, K. and SUMIYOSHI, H., Virology 176, 643-647 (1990).
6. RICO-HESSE, R., PALLANSCH, M. A., NOTTAY, B. K., AND KEW, O. M., Virology 174, 479-493 (1990)
7. BRINTON, M. A., and DISPOTO, J. H., Virology 162, 290-299 (1988).
8. IRIE, K., MOHAN, P. M., SASAGURI, Y., PUTNAK, R. and PADMANABHAN, R., Gene 75, 197-211 (1989).
9. WILBUR, W. J., and LIPMAN, D. J., Proc. Natl. Acad. Sci. USA 80, 726-730 (1983).
10. RICE, C. M., LENCHES, E. M., EDDY, S. R., SHIN, S. J., SHEETS, R. L., and STRAUSS, J. H., Science 229, 726-733 (1985).
11. CHU, M. C., O'ROURKE, E. J. and TRENT, D. W., J. Gen. Virol. 70, 1701-1712 (1989).
EXAMPLE 2
Construction of Expression Plasmids
Standard recombinant DNA techniques were used for construction of the expression plasmids described below and summarised in FIG. 1 (Sambrook et al., Molecular Cloning: a laboratory manual. Cold Spring Harbor Laboratory Press, N.Y.).
For construction of plasmids, the cDNA regions for E, NS1, NS2, NS3 and NS5 of clone DI-275, a DEN1 cDNA clone derived from DEN1 virus Singapore Strain S275/90 as in Example 1, were amplified by the polymerase chain reaction (PCR) and digested with restriction enzymes. The restriction enzyme sites were built into the oligonucleotide primers used in the PCR as set out in Table 3 and Seq ID Nos. 3-12.
Fragments of E, NS3 and NS5 cDNA digested with restriction enzymes were ligated to the pGEX-KG vector (Guan and Dixon, Anal. Biochem. 192, 262-267, 1991). Fragments of NS1 and NS2 cDNA were ligated to pMAL-c and pMAL-cRI vectors (New England Biolabs), respectively (Ford et al., Prot. Exp. Pur. 2, 96-107, 1991; Maina et al., Gene 74, 365-373, 1988; di Guan et al., Gene, 67, 21-30, 1991). The construction of NS5 cDNA was done in two stages. The 5'-region, the cDNA fragment from nucleotide 7544-8365 of NS5, was made by PCR, digested with SalI and ClaI; and the 3'-region, the fragment from nucleotide 8275 (ClaI) to the 3'-end of NS5, was isolated directly from the cDNA of clone DI-275 (D-275 cDNA) by ClaI and SacI double digestion. The two parts of NS5 were ligated together, then ligated into the pGEX-KG vector. Recombinant plasmids were transformed into E. coli DH5.alpha. or c600 HF1 strains. All plasmids encoded Dengue virus proteins fused to the C-terminus of glutathione S-transferase or Maltose Binding Protein (MBP).
EXAMPLE 3
Purification of E, Ns3 And Ns5 Proteins from Recombinant E. Coli
E. coli, harbouring E, NS3 and NS5 genes (separately) were grown in LB medium A.sub.600 of 0.5 at 37.degree. C., then induced with IPTG at 0.2 mM for 2 h at 30.degree. C. The bacteria were harvested and resuspended on ice in MTPBS buffer (0.15 M NaCl, 0.016 M Na.sub.2 HPO.sub.4, 0.005 M NaH.sub.2 PO.sub.4) with 0.1 mg/ml lysozyme, 1% triton X-100, 0.5 .mu.g/ml aprotinin, 0.05 .mu.g/ml Leupeptin, 0.25 .mu.g/ml pepstatin, 5 mM DTT and 0.175 .mu.g/ml PMSF, and kept on ice for 10 min. The cells were sonicated at maximum power for 3.times.1 min while chilled. The lysate was centrifuged at 12,000.times. g. The supernatant was added to 1 ml Glutathione-Sepharose 4B beads (Pharmacia), and incubated at 4.degree. C. on a rotator for 1 h to absorb the fusion proteins. Then the beads were centrifuged and washed with PBS buffer (by centrifugation) at least 6 times, or until the wash solution read zero at A.sub.280 in a spectrophotometer. The beads were resuspended in thrombin cleavage buffer, and the Dengue virus proteins were cleaved off the beads with thrombin at 4.degree. C. for 1 hr. The supernatant, containing Dengue virus proteins, was recovered by centrifugation, and the proteins were stored at -80.degree. C.
EXAMPLE 4
Solubilisation and Purification of a Fusion Protein of NS1 from Inclusion Bodies
E. coli containing the NS1 fusion protein was grown as above, except the tac promoters were induced with 0.3 mM IPTG for 16 h. The bacteria were harvested, 1 gram wet weight of E. coli was resuspended in 5 ml lysis buffer with lysozyme at 1.6 mg/ml and was sonicated for 2.times.15 sec. After centrifugation at 1000.times. g the supernatant was again centrifuged (25,000.times. g). The pellet was resuspended in 2 ml H.sub.2 O, adding a final concentration of 0.5% Triton X-100, 10 mM EDTA, and 100 mM NaCl, then centrifuged at 20,000.times. g twice. The pellet was washed with 1 ml 2 M urea twice and dissolved in 8 M urea in 0.1 M Tris-HCl pH 8.8, 0.14 M 2-mercaptoethanol. The urea concentration was reduced to 1 M by adding H.sub.2 O, and amylose resin (New England Biolabs) was added to adsorb the solubilised fusion protein at 22.degree. C. for 1 h. The amylose resin was washed with buffer (New England Biolabs) five times until the A.sub.280 of the clarified supernatant was near zero. A final concentration of 50 mM maltose was then added to elute the fusion protein, which was recovered by removing the beads by centrifugation.
EXAMPLE 5
Purification of a Soluble Fusion Protein of NS2
After growth of E. Coli transformed with pMAL-cRI/NS2-1, lysis and sonication as in Example 3 above, the clarified extract containing the soluble NS2 fusion protein was adsorbed onto amylose resin, followed by washing and elution of the NS2 fusion protein as in Example 4 above.
EXAMPLE 6
Immunisation of Rabbits and Mice
The soluble fusion proteins of E, NS2, NS3 and NS5 purified from recombinant E. coli, as in Examples 3 and 5 above, and inclusion bodies containing the NS1 fusion protein which had been purified up to the 2M urea wash stage as in Example 4, were placed directly in SDS loading buffer for preparative SDS-PAGE in 10% SDS-polyacrylamide gels. The proteins were visualised by staining with 0.05% Coomassie Blue for 10 min. The gel segments were cut and homogenized in sterile PBS, mixed with Freund's adjuvant and injected directly into white rabbits intramuscularly and subcutaneously on the first, sixth and twenty first days with about 200-500 .mu.g of fusion protein per injected dose. The rabbits were bled 14 days after the last booster dose. For immunisation of mice, 12-day old female Swiss mice were immunised with the soluble proteins of E, NS1, NS2, NS3 and NS5 fusion proteins with or without Freund's adjuvant. The injections were intraperitoneal or subcutaneous on the first, fourth, and fourteenth day, using about 20 .mu.g fusion protein per dose. The mice were bled 14 days after the last dose. The sera of rabbits and mice were used for IFA and immunoprecipitation assays.
EXAMPLE 7
Radioimmunoprecipitations
Radioimmunoprecipitations were done with rabbit and mouse antibodies against the structural and non-structural Dengue virus recombinant fusion proteins of D-275. At 36-40 h post-infection of C6/36 cells with Dengue virus S275/90 strain, cell culture medium was replaced with methionine-free medium containing 3 .mu.g/ml actinomycin D for 3 h, followed by the addition of fresh medium with [.sup.35 S] methionine at 20 .mu.Ci/ml and 3 .mu.g/ml actinomycin D for a further 3 h. The cells were washed with cold PBS, dissolved in RIPA buffer [100 mM Tris-HCl pH7.5, 150 mM NaCl, 10 mM EDTA, 0.1% SDS, 0.1% NP 40, 1% sodium dexoycholate, 100 .mu.g/ml PMSF] on ice for 1 h, then clarified at 1000.times. g for 10 min. The lysates were precleared with normal serum and protein A Sepharose. For immunoprecipitation, rabbit and mouse sera that had been preabsorbed with normal, uninfected C6/36 cell extract fixed by cold acetone were incubated with labeled antigen overnight at 4.degree. C. The virus protein-antibody complexes were precipitated with protein A-Sepharose and were washed with immunoprecipitation buffer [10 mM Tris-HCl, pH7.4, 0.05% aprotinin, 1% NP40, 2 mM EDTA, 0.15 M NaCl], 6 times then 2.times. SDS-PAGE buffer was added, boiled for 2 min, and the supernatant was loaded on a 12% SDS-polyacrylamide gel. After fixing enhancing and drying, the gel was exposed to X-ray film. The results confirmed that antibodies to recombinant E, NS1, NS2, NS3 and NS5 had been generated in mice (FIG. 2) and in rabbits (FIG. 3). These antibodies reacted with the native E, NS1, NS2, NS3 and NS5 proteins synthesised in infected C6/36 cells.
EXAMPLE 8
Indirect Immunofluorescence Assay
The C6/36 cells infected with Dengue virus S275/90 for 2 days were fixed on glass plates with cold acetone for immunofluorescence. 2-fold dilutions of the sera of rabbits or mice were incubated with the fixed cells for 1 h at 37.degree. C., then washed with PBS. Secondary antibodies were linked to fluorescein and incubated for 1 h, followed by washing with PBS for observation using fluorescence microscopy. FIG. 4 shows the antisera to E, NS1, NS2, NS3 and NS5 reacted specifically with the Dengue virus S275/90 infected cells, but control antiserum did no react. Quantitation of the result (as set out in Table 4) showed that an immune response to all recombinant Dengue virus proteins (E, NS1, NS2, NS3 and NS5) occurred in both mice and rabbits.
TABLE 3______________________________________Oligonucleotides used to prepare cDNA fragments corresponding to Dengue virus proteins (by PCR)______________________________________ #STR1## - - #STR2## - - #STR3## - - #STR4## - - ##STR5##______________________________________
TABLE 4______________________________________IMMUNE RESPONSES OF MICE AND RABBITS: INDIRECT IMMUNOFLUORESCENCE ASSAYS______________________________________Dengue virus type 1 recombinant .SIGMA. Titrations of proteins No. of mice IFA______________________________________ E 11 14.91 E + CFA 10 39.62 NS1 10 14.89 NS2 10 12.05 NS2 + CFA 10 12.07 NS3 11 10.94 NS3 + CFA 10 42.56 NS5 10 7.94 NS5 + CFA 10 10.47 E + NS1 17 16.66 NS3 + NS1 18 10.87 NS2 + NS3 14 9.23 NS5 + NS3 10 32.14 MBP 4 <4 GST 4 <4 PBS 2 <4______________________________________ Dengue virus type 1 recombinant .SIGMA. Titrations of proteins No. of rabbits IFA______________________________________ E 1 160 NS1 1 160 NS2 (67) 1 2560 NS2 (68) 1 640 NS3 1 2560 NS5 1 160______________________________________
__________________________________________________________________________# SEQUENCE LISTING - - - - (1) GENERAL INFORMATION: - - (iii) NUMBER OF SEQUENCES: 25 - - - - (2) INFORMATION FOR SEQ ID NO:1: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 10718 base - #pairs (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: CDNA sequence corresp - #onding to the genom - #ic RNA of DEN1-S275/90 - - (iii) HYPOTHETICAL: NO - - (iv) ANTI-SENSE: NO - - (vi) ORIGINAL SOURCE: (A) ORGANISM: Dengue Fe - #ver Virus Type 1 (B) STRAIN: S275/90 - - (ix) FEATURE: (A) NAME/KEY: CDS (B) LOCATION: 81..10268 - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:1: - - GTGGACCGCA AAGAACAGTT TCGAATCGGA AGCTTGCTTA ACGTAGTTCT AA -#CAGTTTTT 60 - - TATTAGAGAG CAGATCTCTG ATG AAC AAC CAA CGA AAA AA - #G ACG GCT CGA 110 - # Met Asn Asn Gln Arg Lys Lys Thr - #Ala Arg - # 1 - # 5 - # 10 - - CCG TCT TTC AAT ATG CTG AAA CGC GCG AGA AA - #C CGC GTG TCA ACT GGT 158 Pro Ser Phe Asn Met Leu Lys Arg Ala Arg As - #n Arg Val Ser Thr Gly 15 - # 20 - # 25 - - TCA CAG TTG GCG AAG AGA TTC TCA AAA GGA TT - #G CTT TCA GGC CAA GGA 206 Ser Gln Leu Ala Lys Arg Phe Ser Lys Gly Le - #u Leu Ser Gly Gln Gly 30 - # 35 - # 40 - - CCC ATG AAA TTG GTG ATG GCT TTC ATA GCA TT - #C CTA AGA TTT CTA GCC 254 Pro Met Lys Leu Val Met Ala Phe Ile Ala Ph - #e Leu Arg Phe Leu Ala 45 - # 50 - # 55 - - ATA CCC CCA ACA GCA GGA ATT TTG GCT AGA TG - #G GGC TCA TTC AAG AAG 302 Ile Pro Pro Thr Ala Gly Ile Leu Ala Arg Tr - #p Gly Ser Phe Lys Lys 60 - # 65 - # 70 - - AAT GGA GCG ATC AAA GTG CTA CGG GGT TTC AA - #G AAA GAA ATC TCA AAC 350 Asn Gly Ala Ile Lys Val Leu Arg Gly Phe Ly - #s Lys Glu Ile Ser Asn 75 - # 80 - # 85 - # 90 - - ATG TTG AAC ATA ATG AAT AGA AGG AAA AGA TC - #T GTG ACC ATG CTC CTC 398 Met Leu Asn Ile Met Asn Arg Arg Lys Arg Se - #r Val Thr Met Leu Leu 95 - # 100 - # 105 - - ATG CTG CTG CCC ACA GCC TTG GCG TTC CAT TT - #G ACT ACA CGA GGG GGA 446 Met Leu Leu Pro Thr Ala Leu Ala Phe His Le - #u Thr Thr Arg Gly Gly 110 - # 115 - # 120 - - GAG CCA CAC ATG ATA GTT AGC AAG CAG GAA AG - #A GAA AAG TCA CTC TTG 494 Glu Pro His Met Ile Val Ser Lys Gln Glu Ar - #g Glu Lys Ser Leu Leu 125 - # 130 - # 135 - - TTT AAG ACC TCT GTA GGT GTC AAC ATG TGC AC - #C CTT ATA GCG ATG GAT 542 Phe Lys Thr Ser Val Gly Val Asn Met Cys Th - #r Leu Ile Ala Met Asp 140 - # 145 - # 150 - - TTG GGA GAG TTA TGT GAG GAC ACA ATG ACT TA - #C AAA TGC CCT CGA ATT 590 Leu Gly Glu Leu Cys Glu Asp Thr Met Thr Ty - #r Lys Cys Pro Arg Ile 155 1 - #60 1 - #65 1 -#70 - - ACT GAG GCG GAA CCA GAT GAC GTT GAT TGT TG - #G TGC AAT GCT ACAGAC 638 Thr Glu Ala Glu Pro Asp Asp Val Asp Cys Tr - #p Cys Asn Ala Thr Asp 175 - # 180 - # 185 - - ACA TGG GTG ACC TAT GGA ACA TGT TCC CAA AC - #T GGC GAG CAC CGA CGG 686 Thr Trp Val Thr Tyr Gly Thr Cys Ser Gln Th - #r Gly Glu His Arg Arg 190 - # 195 - # 200 - - GAC AAA CGT TCC GTC GCA CTG GCC CCA CAC GT - #G GGA CTT GGT CTA GAA 734 Asp Lys Arg Ser Val Ala Leu Ala Pro His Va - #l Gly Leu Gly Leu Glu 205 - # 210 - # 215 - - ACA AGA ACC GAA ACG TGG ATG TCC TCT GAA GG - #C GCT TGG AAA CAA ATA 782 Thr Arg Thr Glu Thr Trp Met Ser Ser Glu Gl - #y Ala Trp Lys Gln Ile 220 - # 225 - # 230 - - CAA AGA GTG GAG ACT TGG GCT TTG CGA CAC CC - #A GGA TTC ACG GTG ATA 830 Gln Arg Val Glu Thr Trp Ala Leu Arg His Pr - #o Gly Phe Thr Val Ile 235 2 - #40 2 - #45 2 -#50 - - GCC CTT TTT CTT GCA CAT GCC ATA GGA ACA TC - #C ATC ACT CAG AAAGGG 878 Ala Leu Phe Leu Ala His Ala Ile Gly Thr Se - #r Ile Thr Gln Lys Gly 255 - # 260 - # 265 - - ATT ATT TTC ATT TTG TTA ATG CTA GTA ACA CC - #A TCC ATG GCC ATG CGA 926 Ile Ile Phe Ile Leu Leu Met Leu Val Thr Pr - #o Ser Met Ala Met Arg 270 - # 275 - # 280 - - TGC GTG GGA ATA GGC AGC AGG GAC TTC GTG GA - #A GGA CTA TCA GGA GCA 974 Cys Val Gly Ile Gly Ser Arg Asp Phe Val Gl - #u Gly Leu Ser Gly Ala 285 - # 290 - # 295 - - ACT TGG GTA GAC GTG GTA CTG GAA CAT GGA AG - #T TGC GTC ACC ACC ATG 1022 Thr Trp Val Asp Val Val Leu Glu His Gly Se - #r Cys Val Thr Thr Met 300 - # 305 - # 310 - - GCA AAA GAC AAA CCA ACA TTG GAC ATT GAA CT - #C CTG AAA ACG GAG GTC 1070 Ala Lys Asp Lys Pro Thr Leu Asp Ile Glu Le - #u Leu Lys Thr Glu Val 315 3 - #20 3 - #25 3 -#30 - - ACG AAC CCT GCC GTC CTG CGC AAA CTG TGC AT - #T GAA GCT AAA ATATCA 1118 Thr Asn Pro Ala Val Leu Arg Lys Leu Cys Il - #e Glu Ala Lys Ile Ser 335 - # 340 - # 345 - - AAC ACC ACC ACC GAT TCA AGA TGT CCA ACA CA - #A GGA GAA GCT ACA CTG 1166 Asn Thr Thr Thr Asp Ser Arg Cys Pro Thr Gl - #n Gly Glu Ala Thr Leu 350 - # 355 - # 360 - - GTG GAA GAA CAA GAC GCG AAC TTT GTG TGT CG - #A CGA ACG TTC GTG GAC 1214 Val Glu Glu Gln Asp Ala Asn Phe Val Cys Ar - #g Arg Thr Phe Val Asp 365 - # 370 - # 375 - - AGA GGC TGG GGT AAT GGC TGC GGA CTA TTT GG - #A AAA GGA AGC CTA CTG 1262 Arg Gly Trp Gly Asn Gly Cys Gly Leu Phe Gl - #y Lys Gly Ser Leu Leu 380 - # 385 - # 390 - - ACG TGT GCT AAG TTC AAG TGT GTG ACA AAA CT - #A GAA GGA AAG ATA GTT 1310 Thr Cys Ala Lys Phe Lys Cys Val Thr Lys Le - #u Glu Gly Lys Ile Val 395 4 - #00 4 - #05 4 -#10 - - CAA TAT GAA AAC TTA AAA TAT TCA GTG ATA GT - #C ACT GTC CAC ACTGGG 1358 Gln Tyr Glu Asn Leu Lys Tyr Ser Val Ile Va - #l Thr Val His Thr Gly 415 - # 420 - # 425 - - GAC CAG CAC CAG GTG GGA AAC GAG ACT ACA GA - #A CAT GGA ACA ATT GCA 1406 Asp Gln His Gln Val Gly Asn Glu Thr Thr Gl - #u His Gly Thr Ile Ala 430 - # 435 - # 440 - - ACC ATA ACA CCT CAA GCT CCT ACG TCG GAA AT - #A CAG CTG ACC GAC TAC 1454 Thr Ile Thr Pro Gln Ala Pro Thr Ser Glu Il - #e Gln Leu Thr Asp Tyr 445 - # 450 - # 455 - - GGA GCC CTC ACA TTG GAC TGC TCA CCT AGA AC - #T GGG CTG GAC TTT AAT 1502 Gly Ala Leu Thr Leu Asp Cys Ser Pro Arg Th - #r Gly Leu Asp Phe Asn 460 - # 465 - # 470 - - GAG ATG GTG CTA TTG ACA ATG AAA GAA AAA TC - #A TGG CTT GTT CAC AAA 1550 Glu Met Val Leu Leu Thr Met Lys Glu Lys Se - #r Trp Leu Val His Lys 475 4 - #80 4 - #85 4 -#90 - - CAA TGG TTT CTA GAC TTA CCA CTG CCT TGG AC - #T TCG GGG GCT TCAACA 1598 Gln Trp Phe Leu Asp Leu Pro Leu Pro Trp Th - #r Ser Gly Ala Ser Thr 495 - # 500 - # 505 - - TCC CAA GAG ACT TGG AAC AGA CAA GAT TTG CT - #G GTC ACA TTC AAG ACA 1646 Ser Gln Glu Thr Trp Asn Arg Gln Asp Leu Le - #u Val Thr Phe Lys Thr 510 - # 515 - # 520 - - GCT CAT GCA AAG AAG CAG GAA GTA GTC GTA CT - #G GGA TCA CAG GAA GGA 1694 Ala His Ala Lys Lys Gln Glu Val Val Val Le - #u Gly Ser Gln Glu Gly 525 - # 530 - # 535 - - GCA ATG CAC ACT GCG TTG ACT GGG GCG ACA GA - #A ATC CAA ACG TCT GGA 1742 Ala Met His Thr Ala Leu Thr Gly Ala Thr Gl - #u Ile Gln Thr Ser Gly 540 - # 545 - # 550 - - ACG ACA ACA ATT TTT GCA GGA CAC CTG AAA TG - #T AGA CTA AAA ATG GAC 1790 Thr Thr Thr Ile Phe Ala Gly His Leu Lys Cy - #s Arg Leu Lys Met Asp 555 5 - #60 5 - #65 5 -#70 - - AAA CTG ACT CTA AAA GGG ATG TCA TAT GTG AT - #G TGC ACA GGC TCATTT 1838 Lys Leu Thr Leu Lys Gly Met Ser Tyr Val Me - #t Cys Thr Gly Ser Phe 575 - # 580 - # 585 - - AAG CTA GAG AAG GAA GTG GCT GAG ACC CAG CA - #T GGA ACT GTT TTA GTG 1886 Lys Leu Glu Lys Glu Val Ala Glu Thr Gln Hi - #s Gly Thr Val Leu Val 590 - # 595 - # 600 - - CAG GTT AAA TAC GAA GGA ACA GAT GCA CCA TG - #C AAG ATC CCC TTT TCG 1934 Gln Val Lys Tyr Glu Gly Thr Asp Ala Pro Cy - #s Lys Ile Pro Phe Ser 605 - # 610 - # 615 - - ACC CAA GAT GAG AAA GGA GTG ACC CAG AAT AG - #A TTG ATA ACA GCC AAT 1982 Thr Gln Asp Glu Lys Gly Val Thr Gln Asn Ar - #g Leu Ile Thr Ala Asn 620 - # 625 - # 630 - - CCT ATA GTT ACT GAC AAA GAA AAA CCA GTC AA - #C ATT GAG ACA GAA CCA 2030 Pro Ile Val Thr Asp Lys Glu Lys Pro Val As - #n Ile Glu Thr Glu Pro 635 6 - #40 6 - #45 6 -#50 - - CCT TTT GGT GAG AGC TAC ATC GTG GTA GGG GC - #A GGT GAA AAA GCTTTG 2078 Pro Phe Gly Glu Ser Tyr Ile Val Val Gly Al - #a Gly Glu Lys Ala Leu 655 - # 660 - # 665 - - AAA CAA TGC TGG TTC AAG AAA GGA AGC AGC AT - #A GGG AAA ATG TTC GAA 2126 Lys Gln Cys Trp Phe Lys Lys Gly Ser Ser Il - #e Gly Lys Met Phe Glu 670 - # 675 - # 680 - - GCA ACC GCC CGA GGA GCA CGA AGG ATG GCT AT - #C CTG GGA GAC ACC GCA 2174 Ala Thr Ala Arg Gly Ala Arg Arg Met Ala Il - #e Leu Gly Asp Thr Ala 685 - # 690 - # 695 - - TGG GAC TTC GGT TCT ATA GGA GGA GTG TTC AC - #G TCT GTG GGA AAA TTA 2222 Trp Asp Phe Gly Ser Ile Gly Gly Val Phe Th - #r Ser Val Gly Lys Leu 700 - # 705 - # 710 - - GTG CAT CAG GTT TTT GGA ACC GCA TAT GGG GT - #T CTG TTC AGC GGT GTT 2270 Val His Gln Val Phe Gly Thr Ala Tyr Gly Va - #l Leu Phe Ser Gly Val 715 7 - #20 7 - #25 7 -#30 - - TCT TGG ACC ATG AAA ATA GGA ATA GGG ATT CT - #G CTG ACA TGG TTGGGA 2318 Ser Trp Thr Met Lys Ile Gly Ile Gly Ile Le - #u Leu Thr Trp Leu Gly 735 - # 740 - # 745 - - TTA AAT TCA AGG AGC ACG TCA CTT TCG ATG AC - #G TGC ATT GCA GTT GGC 2366 Leu Asn Ser Arg Ser Thr Ser Leu Ser Met Th - #r Cys Ile Ala Val Gly 750 - # 755 - # 760 - - ATG GTC ACA CTG TAC CTA GGA GTC ATG GTT CA - #A GCG GAC TCG GGA TGT 2414 Met Val Thr Leu Tyr Leu Gly Val Met Val Gl - #n Ala Asp Ser Gly Cys 765 - # 770 - # 775 - - GTA ATC AAC TGG AAG GGC AGA GAA CTC AAA TG - #T GGA AGT GGC ATT TTT 2462 Val Ile Asn Trp Lys Gly Arg Glu Leu Lys Cy - #s Gly Ser Gly Ile Phe 780 - # 785 - # 790 - - GTC ACT AAT GAA GTC CAC ACT TGG ACA GAG CA - #A TAC AAA TTT CAA GCT 2510 Val Thr Asn Glu Val His Thr Trp Thr Glu Gl - #n Tyr Lys Phe Gln Ala 795 8 - #00 8 - #05 8 -#10 - - GAC TCC CCA AAA AGA CTA TCA GCA GCC ATC GG - #A AAG GCA TGG GAGGAG 2558 Asp Ser Pro Lys Arg Leu Ser Ala Ala Ile Gl - #y Lys Ala Trp Glu Glu 815 - # 820 - # 825 - - GGT GTG TGT GGA ATT CGA TCA GCC ACT CGT CT - #C GAG AAC ATC ATG TGG 2606 Gly Val Cys Gly Ile Arg Ser Ala Thr Arg Le - #u Glu Asn Ile Met Trp 830 - # 835 - # 840 - - AAG CAA ATA TCA AAT GAA CTG AAC CAC ATC TT - #A CTT GAA AAT GAC ATG 2654 Lys Gln Ile Ser Asn Glu Leu Asn His Ile Le - #u Leu Glu Asn Asp Met 845 - # 850 - # 855 - - AAA TTC ACA GTG GTT GTA GGA GAT GTT GTT GG - #G ATC TTG GCC CAA GGG 2702 Lys Phe Thr Val Val Val Gly Asp Val Val Gl - #y Ile Leu Ala Gln Gly 860 - # 865 - # 870 - - AAA AAA ATG ATT AGA CCA CAA CCC ATG GAA CA - #C AAA TAC TCA TGG AAA 2750 Lys Lys Met Ile Arg Pro Gln Pro Met Glu Hi - #s Lys Tyr Ser Trp Lys 875 8 - #80 8 - #85 8 -#90 - - AGC TGG GGA AAA GCC AAA ATC ATA GGA GCA GA - #C ATA CAG AAC ACCACC 2798 Ser Trp Gly Lys Ala Lys Ile Ile Gly Ala As - #p Ile Gln Asn Thr Thr 895 - # 900 - # 905 - - TTC ATC ATT GAC GGC CCA GAT ACT CCA GAA TG - #T CCT GAT GAC CAA AGA 2846 Phe Ile Ile Asp Gly Pro Asp Thr Pro Glu Cy - #s Pro Asp Asp Gln Arg 910 - # 915 - # 920 - - GCA TGG AAC ATT TGG GAA GTT GAG GAC TAT GG - #G TTC GGA ATT TTC ACG 2894 Ala Trp Asn Ile Trp Glu Val Glu Asp Tyr Gl - #y Phe Gly Ile Phe Thr 925 - # 930 - # 935 - - ACA AAC ATA TGG TTG AAA TTG CGT GAC TCC TA - #C ACC CAA ATG TGT GAC 2942 Thr Asn Ile Trp Leu Lys Leu Arg Asp Ser Ty - #r Thr Gln Met Cys Asp 940 - # 945 - # 950 - - CAC CGG CTA ATG TCA GCT GCC ATC AAG GAC AG - #C AAG GCA GTC CAT GCT 2990 His Arg Leu Met Ser Ala Ala Ile Lys Asp Se - #r Lys Ala Val His Ala 955 9 - #60 9 - #65 9 -#70 - - GAT ATG GGG TAC TGG ATA GAA AGT GAA AAG AA - #C GAG ACC TGG AAGCTG 3038 Asp Met Gly Tyr Trp Ile Glu Ser Glu Lys As - #n Glu Thr Trp Lys Leu 975 - # 980 - # 985 - - GCA AGA GCC TCT TTC ATA GAA GTT AAA ACA TG - #T GTC TGG CCA AAA TCC 3086 Ala Arg Ala Ser Phe Ile Glu Val Lys Thr Cy - #s Val Trp Pro Lys Ser 990 - # 995 - # 1000 - - CAC ACT CTA TGG AGC AAT GGA GTT CTG GAA AG - #T GAA ATG ATA ATT CCA 3134 His Thr Leu Trp Ser Asn Gly Val Leu Glu Se - #r Glu Met Ile Ile Pro 1005 - # 1010 - # 1015 - - AAG ATC TAT GGA GGA CCA ATA TCT CAG CAC AA - #C TAC AGA CCA GGA TAT 3182 Lys Ile Tyr Gly Gly Pro Ile Ser Gln His As - #n Tyr Arg Pro Gly Tyr 1020 - # 1025 - # 1030 - - TTC ACA CAA ACG GCA GGG CCA TGG CAC CTA GG - #C AAG TTG GAA CTG GAT 3230 Phe Thr Gln Thr Ala Gly Pro Trp His Leu Gl - #y Lys Leu Glu Leu Asp 1035 1040 - # 1045 - # 1050 - - TTT GAT TTG TGT GAG GGT ACC ACA GTT GTT GT - #G GAT GAA CAT TGT GGA 3278 Phe Asp Leu Cys Glu Gly Thr Thr Val Val Va - #l Asp Glu His Cys Gly 1055 - # 1060 - # 1065 - - AAT CGA GGT CCA TCT CTT AGA ACC ACA ACA GT - #C ACA GGA AAG ATA ATT 3326 Asn Arg Gly Pro Ser Leu Arg Thr Thr Thr Va - #l Thr Gly Lys Ile Ile 1070 - # 1075 - # 1080 - - CAT GAA TGG TGT TGC AGA TCT TGT ACG CTA CC - #A CCC TTA CGT TTC AAA 3374 His Glu Trp Cys Cys Arg Ser Cys Thr Leu Pr - #o Pro Leu Arg Phe Lys 1085 - # 1090 - # 1095 - - GGA GAA GAT GGA TGT TGG TAC GGT ATG GAA AT - #C AGA CCA GTC AAG GAA 3422 Gly Glu Asp Gly Cys Trp Tyr Gly Met Glu Il - #e Arg Pro Val Lys Glu 1100 - # 1105 - # 1110 - - AAG GAA GAG AAT CTA GTC AAA TCA ATG GTC TC - #T GCA GGG TCA GGG GAA 3470 Lys Glu Glu Asn Leu Val Lys Ser Met Val Se - #r Ala Gly Ser Gly Glu 1115 1120 - # 1125 - # 1130 - - GTG GAC AGC TTT TCA CTA GGA CTG CTA TGC AT - #A TCA ATA ATG ATC GAA 3518 Val Asp Ser Phe Ser Leu Gly Leu Leu Cys Il - #e Ser Ile Met Ile Glu 1135 - # 1140 - # 1145 - - GAG GTG ATG AGA TCC AGA TGG AGC AGA AAA AT - #G CTG ATG ACT GGA ACA 3566 Glu Val Met Arg Ser Arg Trp Ser Arg Lys Me - #t Leu Met Thr Gly Thr 1150 - # 1155 - # 1160 - - CTG GCT GTG TTC CTC CTT CTC ATA ATG GGA CA - #A TTG ACA TGG AAT GAT 3614 Leu Ala Val Phe Leu Leu Leu Ile Met Gly Gl - #n Leu Thr Trp Asn Asp 1165 - # 1170 - # 1175 - - CTG ATC AGG TTA TGC ATC ATG GTT GGA GCC AA - #T GCT TCA GAC AGG ATG 3662 Leu Ile Arg Leu Cys Ile Met Val Gly Ala As - #n Ala Ser Asp Arg Met 1180 - # 1185 - # 1190 - - GGG ATG GGA ACA ACG TAC CTA GCT CTG ATG GC - #C ACT TTT AAA ATG AGA 3710 Gly Met Gly Thr Thr Tyr Leu Ala Leu Met Al - #a Thr Phe Lys Met Arg 1195 1200 - # 1205 - # 1210 - - CCA ATG TTT GCT GTC GGG CTG TTG TTC CGC AG - #A CTA ACA TCT AGA GAA 3758 Pro Met Phe Ala Val Gly Leu Leu Phe Arg Ar - #g Leu Thr Ser Arg Glu 1215 - # 1220 - # 1225 - - GTT CTT CTT CTT ACA ATT GGA TTG AGT CTA GT - #G GCA TCT GTG GAG TTA 3806 Val Leu Leu Leu Thr Ile Gly Leu Ser Leu Va - #l Ala Ser Val Glu Leu 1230 - # 1235 - # 1240 - - CCA AAT TCC CTG GAG GAG CTG GGG GAT GGA CT - #T GCA ATG GGC ATT ATG 3854 Pro Asn Ser Leu Glu Glu Leu Gly Asp Gly Le - #u Ala Met Gly Ile Met 1245 - # 1250 - # 1255 - - ATT TTA AAA TTA TTG ACT GAC TTT CAG TCA CA - #T CAG CTG TGG GCT ACC 3902 Ile Leu Lys Leu Leu Thr Asp Phe Gln Ser Hi - #s Gln Leu Trp Ala Thr 1260 - # 1265 - # 1270 - - TTG CTG TCC TTG ACA TTT GTC AAA ACA ACG TT - #T TCC TTG CAC TAT GCA 3950 Leu Leu Ser Leu Thr Phe Val Lys Thr Thr Ph - #e Ser Leu His Tyr Ala 1275 1280 - # 1285 - # 1290 - - TGG AAG ACA ATG GCT ATG GTA CTG TCA ATT GT - #A TCT CTC TTC CCC TTA 3998 Trp Lys Thr Met Ala Met Val Leu Ser Ile Va - #l Ser Leu Phe Pro Leu 1295 - # 1300 - # 1305 - - TGC CTG TCC ACG ACC TCC CAA AAA ACA ACA TG - #G CTT CCG GTG CTA TTG 4046 Cys Leu Ser Thr Thr Ser Gln Lys Thr Thr Tr - #p Leu Pro Val Leu Leu 1310 - # 1315 - # 1320 - - GGA TCT CTT GGA TGC AAA CCA CTA ACC ATG TT - #T CTC ATA GCA GAA AAC 4094 Gly Ser Leu Gly Cys Lys Pro Leu Thr Met Ph - #e Leu Ile Ala Glu Asn 1325 - # 1330 - # 1335 - - AAA ATC TGG GGA AGG AAA AGT TGG CCC CTC AA - #T GAA GGA ATC ATG GCT 4142 Lys Ile Trp Gly Arg Lys Ser Trp Pro Leu As - #n Glu Gly Ile Met Ala 1340 - # 1345 - # 1350 - - GTT GGA ATA GTC AGC ATC CTA CTA AGT TCA CT - #C CTC AAA AAT GAT GTG 4190 Val Gly Ile Val Ser Ile Leu Leu Ser Ser Le - #u Leu Lys Asn Asp Val 1355 1360 - # 1365 - # 1370 - - CCG CTA GCT GGG CCA CTA ATA GCT GGA GGC AT - #G CTA ATA GCA TGT TAC 4238 Pro Leu Ala Gly Pro Leu Ile Ala Gly Gly Me - #t Leu Ile Ala Cys Tyr 1375 - # 1380 - # 1385 - - GTT ATA TCT GGA AGC TCA GCC GAC TTA TCA CT - #A GAG AAA GCG GCT GAG 4286 Val Ile Ser Gly Ser Ser Ala Asp Leu Ser Le - #u Glu Lys Ala Ala Glu 1390 - # 1395 - # 1400 - - GTC TCC TGG GAA GAA GAA GCA GAA CAC TCT GG - #T GCC TCA CAC AAT ATA 4334 Val Ser Trp Glu Glu Glu Ala Glu His Ser Gl - #y Ala Ser His Asn Ile 1405 - # 1410 - # 1415 - - TTA GTG GAG GTC CAA GAT GAT GGA ACC ATG AA - #G ATA AAA GAT GAA GAG 4382 Leu Val Glu Val Gln Asp Asp Gly Thr Met Ly - #s Ile Lys Asp Glu Glu 1420 - # 1425 - # 1430 - - AGA GAT GAC ACG CTA ACC ATT CTC CTT AAA GC - #A ACC CTG CTA GCA GTT 4430 Arg Asp Asp Thr Leu Thr Ile Leu Leu Lys Al - #a Thr Leu Leu Ala Val 1435 1440 - # 1445 - # 1450 - - TCA GGG GTG TAC CCA TTA TCA ATA CCA GCA AC - #C CTT TTT GTG TGG TAC 4478 Ser Gly Val Tyr Pro Leu Ser Ile Pro Ala Th - #r Leu Phe Val Trp Tyr 1455 - # 1460 - # 1465 - - TTT TGG CAG AAA AAG AAA CAA AGA TCT GGA GT - #G TTA TGG GAC ACA CCT 4526 Phe Trp Gln Lys Lys Lys Gln Arg Ser Gly Va - #l Leu Trp Asp Thr Pro 1470 - # 1475 - # 1480 - - AGC CCT CCA GAA GTG GAA AGA GCA GTC CTT GA - #T GAT GGT ATC TAT AGA 4574 Ser Pro Pro Glu Val Glu Arg Ala Val Leu As - #p Asp Gly Ile Tyr Arg 1485 - # 1490 - # 1495 - - ATT ATG CAG AGA GGA CTG TTG GGC AGG TCC CA - #A GTA GGA GTG GGA GTT 4622 Ile Met Gln Arg Gly Leu Leu Gly Arg Ser Gl - #n Val Gly Val Gly Val 1500 - # 1505 - # 1510 - - TTC CAA GAC GGC GTG TTC CAC ACA ATG TGG CA - #C GTC ACC AGG GGA GCT 4670 Phe Gln Asp Gly Val Phe His Thr Met Trp Hi - #s Val Thr Arg Gly Ala 1515 1520 - # 1525 - # 1530 - - GTC CTT ATG TAC CAA GGG AAG AGG CTG GAA CC - #A AGC TGG GCC AGT GTC 4718 Val Leu Met Tyr Gln Gly Lys Arg Leu Glu Pr - #o Ser Trp Ala Ser Val 1535 - # 1540 - # 1545 - - AAA AAA GAC TTG ATC TCA TAT GGA GGA GGT TG - #G AGG TTT CAA GGA TCC 4766 Lys Lys Asp Leu Ile Ser Tyr Gly Gly Gly Tr - #p Arg Phe Gln Gly Ser 1550 - # 1555 - # 1560 - - TGG AAC ACG GGA GAA GAA GTG CAG GTG ATT GC - #T GTT GAA CCA GGA AAA 4814 Trp Asn Thr Gly Glu Glu Val Gln Val Ile Al - #a Val Glu Pro Gly Lys 1565 - # 1570 - # 1575 - - AAC CCC AAA AAT GTA CAG ACA GCG CCG GGT AC - #C TTC AAG ACC CCT GAA 4862 Asn Pro Lys Asn Val Gln Thr Ala Pro Gly Th - #r Phe Lys Thr Pro Glu 1580 - # 1585 - # 1590 - - GGT GAA GTT GGA GCT ATT GCC CTA GAT TTT AA - #A CCC GGC ACA TCT GGA 4910 Gly Glu Val Gly Ala Ile Ala Leu Asp Phe Ly - #s Pro Gly Thr Ser Gly 1595 1600 - # 1605 - # 1610 - - TCT CCC ATC GTG AAC AGA GAA GGA AAA ATA GT - #A GGT CTT TAT GGA AAT 4958 Ser Pro Ile Val Asn Arg Glu Gly Lys Ile Va - #l Gly Leu Tyr Gly Asn 1615 - # 1620 - # 1625 - - GGA GTA GTG ACA ACA AGT GGA ACC TAC GTC AG - #T GCC ATA GCC CAA GCC 5006 Gly Val Val Thr Thr Ser Gly Thr Tyr Val Se - #r Ala Ile Ala Gln Ala 1630 - # 1635 - # 1640 - - AAA GCA TCA CAA GAA GGG CCC CTA CCA GAG AT - #T GAG GAC GAG GTG TTT 5054 Lys Ala Ser Gln Glu Gly Pro Leu Pro Glu Il - #e Glu Asp Glu Val Phe 1645 - # 1650 - # 1655 - - AGG AAA AGA AAC TTA ACA ATA ATG GAC CTA CA - #T CCA GGA TCG GGG AAA 5102 Arg Lys Arg Asn Leu Thr Ile Met Asp Leu Hi - #s Pro Gly Ser Gly Lys 1660 - # 1665 - # 1670 - - ACA AGA AGA TAT CTT CCA GCC ATA GTC CGT GA - #G GCC ATA AGA AGG AAC 5150 Thr Arg Arg Tyr Leu Pro Ala Ile Val Arg Gl - #u Ala Ile Arg Arg Asn 1675 1680 - # 1685 - # 1690 - - GTG CGC ACA CTA ATT TTG GCT CCC ACA AGG GT - #T GTC GCT TCC GAA ATG 5198 Val Arg Thr Leu Ile Leu Ala Pro Thr Arg Va - #l Val Ala Ser Glu Met 1695 - # 1700 - # 1705 - - GCA GAG GCG CTC AAG GGA ATG CCA ATA AGG TA - #C CAA ACA ACA GCA GTG 5246 Ala Glu Ala Leu Lys Gly Met Pro Ile Arg Ty - #r Gln Thr Thr Ala Val 1710 - # 1715 - # 1720 - - AAG AGT GAA CAC ACA GGA AAA GAG ATA GTT GA - #C CTC ATG TGT CAC GCC 5294 Lys Ser Glu His Thr Gly Lys Glu Ile Val As - #p Leu Met Cys His Ala 1725 - # 1730 - # 1735 - - ACT TTC ACC ATG CGT CTC CTG TCT CCC GTG AG - #A GTT CCC AAT TAC AAC 5342 Thr Phe Thr Met Arg Leu Leu Ser Pro Val Ar - #g Val Pro Asn Tyr Asn 1740 - # 1745 - # 1750 - - ATG ATT ATC ATG GAT GAA GCA CAT TTT ACC GA - #T CCA GCC AGC ATA GCG 5390 Met Ile Ile Met Asp Glu Ala His Phe Thr As - #p Pro Ala Ser Ile Ala 1755 1760 - # 1765 - # 1770 - - CGC AGA GGG TAC ATC TCA ACC CGA GTG GGC AT - #G GGT GAA GCA GCT GCG 5438 Arg Arg Gly Tyr Ile Ser Thr Arg Val Gly Me - #t Gly Glu Ala Ala Ala 1775 - # 1780 - # 1785 - - ATC TTC ATG ACA GCC ACT CCC CCA GGA TCG GT - #G GAG GCC TTT CCA CAG 5486 Ile Phe Met Thr Ala Thr Pro Pro Gly Ser Va - #l Glu Ala Phe Pro Gln 1790 - # 1795 - # 1800 - - AGC AAT GCA GTT ATC CAA GAT GAG GAA AGA GA - #C ATT CCT GAG AGA TCA 5534 Ser Asn Ala Val Ile Gln Asp Glu Glu Arg As - #p Ile Pro Glu Arg Ser 1805 - # 1810 - # 1815 - - TGG AAC TCA GGC TAT GAG TGG ATC ACT GAC TT - #C CCA GGT AAA ACA GTC 5582 Trp Asn Ser Gly Tyr Glu Trp Ile Thr Asp Ph - #e Pro Gly Lys Thr Val 1820 - # 1825 - # 1830 - - TGG TTT GTT CCA AGC ATC AAA TCA GGA AAT GA - #C ATT GCC AAC TGC TTA 5630 Trp Phe Val Pro Ser Ile Lys Ser Gly Asn As - #p Ile Ala Asn Cys Leu 1835 1840 - # 1845 - # 1850 - - AGA AAG AAT GGG AAA CGG GTG ATT CAA TTG AG - #C AGG AAA ACC TTT GAT 5678 Arg Lys Asn Gly Lys Arg Val Ile Gln Leu Se - #r Arg Lys Thr Phe Asp 1855 - # 1860 - # 1865 - - ACA GAG TAC CAA AAA ACA AAA AAC AAC GAC TG - #G GAC TAT GTC GTC ACA 5726 Thr Glu Tyr Gln Lys Thr Lys Asn Asn Asp Tr - #p Asp Tyr Val Val Thr 1870 - # 1875 - # 1880 - - ACA GAT ATC TCC GAA ATG GGA GCA AAC TTC CG - #A GCC GAC AGG GTG ATA 5774 Thr Asp Ile Ser Glu Met Gly Ala Asn Phe Ar - #g Ala Asp Arg Val Ile 1885 - # 1890 - # 1895 - - GAC CCA AGA CGG TGT CTG AAA CCG GTA ATA CT - #A AAA GAT GGT CCA GAG 5822 Asp Pro Arg Arg Cys Leu Lys Pro Val Ile Le - #u Lys Asp Gly Pro Glu 1900 - # 1905 - # 1910 - - CGC GTC ATT CTA GCC GGA CCG ATG CCA GTG AC - #T GTG GCC AGT GCT GCC 5870 Arg Val Ile Leu Ala Gly Pro Met Pro Val Th - #r Val Ala Ser Ala Ala 1915 1920 - # 1925 - # 1930 - - CAG AGG AGA GGA AGA ATT GGA AGG AAC CAA AA - #C AAA GAA GGT GAT CAG 5918 Gln Arg Arg Gly Arg Ile Gly Arg Asn Gln As - #n Lys Glu Gly Asp Gln 1935 - # 1940 - # 1945 - - TAC GTT TAC ATG GGA CAG CCT TTA AAT AAT GA - #T GAG GAT CAC GCT CAT 5966 Tyr Val Tyr Met Gly Gln Pro Leu Asn Asn As - #p Glu Asp His Ala His 1950 - # 1955 - # 1960 - - TGG ACA GAA GCA AAA ATG CTC CTT GAC AAT AT - #A AAC ACA CCA GAA GGG 6014 Trp Thr Glu Ala Lys Met Leu Leu Asp Asn Il - #e Asn Thr Pro Glu Gly 1965 - # 1970 - # 1975 - - ATC ATC CCA GCC CTC TTT GAG CCA GAG AGA GA - #A AAG AGT GCA GCA ATA 6062 Ile Ile Pro Ala Leu Phe Glu Pro Glu Arg Gl - #u Lys Ser Ala Ala Ile 1980 - # 1985 - # 1990 - - GAC GGG GAG TAC AGA CTG CGG GGA GAA GCA AG - #A AAA ACG TTT GTG GAG 6110 Asp Gly Glu Tyr Arg Leu Arg Gly Glu Ala Ar - #g Lys Thr Phe Val Glu 1995 2000 - # 2005 - # 2010 - - CTC ATG AGA AGA GGA GAT CTA CCT GTC TGG CT - #A TCC TAC AAA GTT GCC 6158 Leu Met Arg Arg Gly Asp Leu Pro Val Trp Le - #u Ser Tyr Lys Val Ala 2015 - # 2020 - # 2025 - - TCA GAA GGC TTC CAG TAC TCT GAC AGA AGA TG - #G TGC TTT GAC GGG GAA 6206 Ser Glu Gly Phe Gln Tyr Ser Asp Arg Arg Tr - #p Cys Phe Asp Gly Glu 2030 - # 2035 - # 2040 - - AGG AAC AAC CAG GTG TTG GAG GAG AAC ATG GA - #C GTG GAG ATG TGG ACA 6254 Arg Asn Asn Gln Val Leu Glu Glu Asn Met As - #p Val Glu Met Trp Thr 2045 - # 2050 - # 2055 - - AAA GAA GGA GAA CGA AAG AAA CTA CGA CCC CG - #C TGG CTG GAT GCC AGA 6302 Lys Glu Gly Glu Arg Lys Lys Leu Arg Pro Ar - #g Trp Leu Asp Ala Arg 2060 - # 2065 - # 2070 - - ACA TAC TCA GAC CCA CTG GCC CTG CGC GAG TT - #T AAA GAG TTT GCA GCA 6350 Thr Tyr Ser Asp Pro Leu Ala Leu Arg Glu Ph - #e Lys Glu Phe Ala Ala 2075 2080 - # 2085 - # 2090 - - GGA AGA AGA AGT GTC TCA GGT GAT CTA ATA TT - #A GAA ATA GGG AAA CTT 6398 Gly Arg Arg Ser Val Ser Gly Asp Leu Ile Le - #u Glu Ile Gly Lys Leu 2095 - # 2100 - # 2105 - - CCA CAA CAC TTG ACG CAA AGG GCC CAG AAT GC - #C TTG GAC AAC CTG GTT 6446 Pro Gln His Leu Thr Gln Arg Ala Gln Asn Al - #a Leu Asp Asn Leu Val 2110 - # 2115 - # 2120 - - ATG TTG CAC AAC TCC GAA CAA GGA GGA AGA GC - #C TAC AGA CAT GCA ATG 6494 Met Leu His Asn Ser Glu Gln Gly Gly Arg Al - #a Tyr Arg His Ala Met 2125 - # 2130 - # 2135 - - GAA GAA CTT CCA GAC ACC ATA GAA ACG TTG AT - #G CTC CTA GCT TTG ATA 6542 Glu Glu Leu Pro Asp Thr Ile Glu Thr Leu Me - #t Leu Leu Ala Leu Ile 2140 - # 2145 - # 2150 - - GCT GTG TTA ACT GGT GGA GTG ACG CTG TTC TT - #C CTA TCA GGA AAG GGC 6590 Ala Val Leu Thr Gly Gly Val Thr Leu Phe Ph - #e Leu Ser Gly Lys Gly 2155 2160 - # 2165 - # 2170 - - CTA GGG AAA ACA TCT ATT GGC CTA CTC TGC GT - #G ATG GCT TCA AGC GTA 6638 Leu Gly Lys Thr Ser Ile Gly Leu Leu Cys Va - #l Met Ala Ser Ser Val 2175 - # 2180 - # 2185 - - CTG CTA TGG ATG GCC AGC GTG GAG CCT CAT TG - #G ATA GCG GCC TCC ATC 6686 Leu Leu Trp Met Ala Ser Val Glu Pro His Tr - #p Ile Ala Ala Ser Ile 2190 - # 2195 - # 2200 - - ATA CTA GAG TTT TTC CTG ATG GTG CTG CTT AT - #T CCA GAG CCA GAC AGA 6734 Ile Leu Glu Phe Phe Leu Met Val Leu Leu Il - #e Pro Glu Pro Asp Arg 2205 - # 2210 - # 2215 - - CAG CGC ACT CCA CAG GAC AAC CAG TTA GCA TA - #T GTG GTG ATA GGT TTG 6782 Gln Arg Thr Pro Gln Asp Asn Gln Leu Ala Ty - #r Val Val Ile Gly Leu 2220 - # 2225 - # 2230 - - TTA TTC ATG ATA CTC ACA GTG GCA GCC AAT GA - #G ATG GGA TTA TTG GAA 6830 Leu Phe Met Ile Leu Thr Val Ala Ala Asn Gl - #u Met Gly Leu Leu Glu 2235 2240 - # 2245 - # 2250 - - ACC ACA AAG AAA GAC TTA GGG ATT GGC CAT GT - #A GCC GCC GAA AAC CAC 6878 Thr Thr Lys Lys Asp Leu Gly Ile Gly His Va - #l Ala Ala Glu Asn His 2255 - # 2260 - # 2265 - - CAC CAT GCT ACA ATG CTG GAC GTA GAC CTA CG - #T CCA GCT TCA GCC TGG 6926 His His Ala Thr Met Leu Asp Val Asp Leu Ar - #g Pro Ala Ser Ala Trp 2270 - # 2275 - # 2280 - - ACC CTC TAT GCA GTA GCC ACA ACA GTT ATC AC - #C CCC ATG ATG AGA CAC 6974 Thr Leu Tyr Ala Val Ala Thr Thr Val Ile Th - #r Pro Met Met Arg His 2285 - # 2290 - # 2295 - - ACA ATT GAA AAT ACA ACG GCA AAT ATT TCC CT - #G ACA GCC ATT GCA AAC 7022 Thr Ile Glu Asn Thr Thr Ala Asn Ile Ser Le - #u Thr Ala Ile Ala Asn 2300 - # 2305 - # 2310 - - CAG GCA GCT ATA TTG ATG GGA CTT GAT AAA GG - #A TGG CCA ATA TCG AAG 7070 Gln Ala Ala Ile Leu Met Gly Leu Asp Lys Gl - #y Trp Pro Ile Ser Lys 2315 2320 - # 2325 - # 2330 - - ATG GAC ATA GGA GTT CCA CTT CTC GCC TTG GG - #G TGC TAT TCC CAG GTG 7118 Met Asp Ile Gly Val Pro Leu Leu Ala Leu Gl - #y Cys Tyr Ser Gln Val 2335 - # 2340 - # 2345 - - AAT CCA CTG ACG CTG ACA GCG GCG GTA TTG AT - #G CTA GTG GCT CAT TAC 7166 Asn Pro Leu Thr Leu Thr Ala Ala Val Leu Me - #t Leu Val Ala His Tyr 2350 - # 2355 - # 2360 - - GCC ATA ATT GGA CCT GGA CTG CAA GCA AAA GC - #G ACT AGA GAA GCT CAA 7214 Ala Ile Ile Gly Pro Gly Leu Gln Ala Lys Al - #a Thr Arg Glu Ala Gln 2365 - # 2370 - # 2375 - - AAA AGG ACA GCG GCC GGA ATA ATG AAA AAT CC - #A ACC GTT GAT GGA ATT 7262 Lys Arg Thr Ala Ala Gly Ile Met Lys Asn Pr - #o Thr Val Asp Gly Ile 2380 - # 2385 - # 2390 - - GTT GCA ATA GAT TTG GAC CCT GTG GTT TAT GA - #T GCA AAA TTT GAG AAA 7310 Val Ala Ile Asp Leu Asp Pro Val Val Tyr As - #p Ala Lys Phe Glu Lys 2395 2400 - # 2405 - # 2410 - - CAA CTA GGC CAA ATA ATG TTG TTG ATA CTA TG - #C ACA TCA CAG ATC CTC 7358 Gln Leu Gly Gln Ile Met Leu Leu Ile Leu Cy - #s Thr Ser Gln Ile Leu 2415 - # 2420 - # 2425 - - TTG ATG CGG ACT ACA TGG GCC TTG TGT GAA TC - #C ATC ACA CTG GCC ACT 7406 Leu Met Arg Thr Thr Trp Ala Leu Cys Glu Se - #r Ile Thr Leu Ala Thr 2430 - # 2435 - # 2440 - - GGA CCT CTG ACC ACG CTT TGG GAG GGA TCT CC - #A GGA AAA TTT TGG AAC 7454 Gly Pro Leu Thr Thr Leu Trp Glu Gly Ser Pr - #o Gly Lys Phe Trp Asn 2445 - # 2450 - # 2455 - - ACC ACG ATA GCG GTT TCC ATG GCA AAC ATT TT - #C AGG GGA AGT TAT CTA 7502 Thr Thr Ile Ala Val Ser Met Ala Asn Ile Ph - #e Arg Gly Ser Tyr Leu 2460 - # 2465 - # 2470 - - GCA GGA GCA GGC CTG GCC TTC TCA TTA ATG AA - #A TCT CTA GGA GGA GGT 7550 Ala Gly Ala Gly Leu Ala Phe Ser Leu Met Ly - #s Ser Leu Gly Gly Gly 2475 2480 - # 2485 - # 2490 - - AGG AGA GGT ACG GGA GCC AAG GGG AAA CAC TG - #G GAG AGA AAT GGA AAA 7598 Arg Arg Gly Thr Gly Ala Lys Gly Lys His Tr - #p Glu Arg Asn Gly Lys 2495 - # 2500 - # 2505 - - GAC AGA CTG AAC CAA CTG AGC AAG TCA GAA TT - #C AAC ACT TAC AAA AGG 7646 Asp Arg Leu Asn Gln Leu Ser Lys Ser Glu Ph - #e Asn Thr Tyr Lys Arg 2510 - # 2515 - # 2520 - - AGT GGG ATT ATG GAA GTG GAC AGA TCC GAA GC - #C AAA GAG GGA CTG AAA 7694 Ser Gly Ile Met Glu Val Asp Arg Ser Glu Al - #a Lys Glu Gly Leu Lys 2525 - # 2530 - # 2535 - - AGA GGA GAA ACA ACC AAA CAT GCA GTG TCG AG - #A GGA ACC GCC AAA TTG 7742 Arg Gly Glu Thr Thr Lys His Ala Val Ser Ar - #g Gly Thr Ala Lys Leu 2540 - # 2545 - # 2550 - - AGG TGG TTC GTG GAG AGG AAC CTT GTG AAA CC - #A GAA GGG AAA GTC ATA 7790 Arg Trp Phe Val Glu Arg Asn Leu Val Lys Pr - #o Glu Gly Lys Val Ile 2555 2560 - # 2565 - # 2570 - - GAC CTC GGT TGT GGA AGA GGT GGC TGG TCA TA - #C TAT TGC GCT GGG CTG 7838 Asp Leu Gly Cys Gly Arg Gly Gly Trp Ser Ty - #r Tyr Cys Ala Gly Leu 2575 - # 2580 - # 2585 - - AAG AAA GTC ACA GAA GTG AAG GGA TAC ACA AA - #A GGA GGA CCT GGA CAT 7886 Lys Lys Val Thr Glu Val Lys Gly Tyr Thr Ly - #s Gly Gly Pro Gly His 2590 - # 2595 - # 2600 - - GAG GAA CCA ATC CCA ATG GCG ACC TAT GGA TG - #G AAC CTA GTA AAG CTA 7934 Glu Glu Pro Ile Pro Met Ala Thr Tyr Gly Tr - #p Asn Leu Val Lys Leu 2605 - # 2610 - # 2615 - - TAC TCC GGG AAA GAC GTA TTC TTT ACA CCA CC - #T GAG AAG TGT GAC ACC 7982 Tyr Ser Gly Lys Asp Val Phe Phe Thr Pro Pr - #o Glu Lys Cys Asp Thr 2620 - # 2625 - # 2630 - - CTT TTG TGT GAT ATT GGT GAG TCC TCT CCA AA - #C CCA ACT ATA GAA GAA 8030 Leu Leu Cys Asp Ile Gly Glu Ser Ser Pro As - #n Pro Thr Ile Glu Glu 2635 2640 - # 2645 - # 2650 - - GGA AGA ACG TTA CGC GTC CTA AAG ATG GTG GA - #A CCA TGG CTC AGA GGG 8078 Gly Arg Thr Leu Arg Val Leu Lys Met Val Gl - #u Pro Trp Leu Arg Gly 2655 - # 2660 - # 2665 - - AAC CAA TTT TGC ATA AAA ATT CTA AAT CCC TA - #C ATG CCA AGT GTG GTG 8126 Asn Gln Phe Cys Ile Lys Ile Leu Asn Pro Ty - #r Met Pro Ser Val Val 2670 - # 2675 - # 2680 - - GAA ACT CTG GAG CAA ATG CAA AGA AAA CAT GG - #A GGA ATG CTA GTG CGG 8174 Glu Thr Leu Glu Gln Met Gln Arg Lys His Gl - #y Gly Met Leu Val Arg 2685 - # 2690 - # 2695 - - AAT CCA CTT TCA AGA AAT TCT ACT CAT GAA AT - #G TAT TGG GTT TCA TGT 8222 Asn Pro Leu Ser Arg Asn Ser Thr His Glu Me - #t Tyr Trp Val Ser Cys 2700 - # 2705 - # 2710 - - GGA ACA GGA AAC ATT GTG TCA GCA GTA AAC AT - #G ACA TCT AGA ATG TTG 8270 Gly Thr Gly Asn Ile Val Ser Ala Val Asn Me - #t Thr Ser Arg Met Leu 2715 2720 - # 2725 - # 2730 - - CTA AAT CGA TTC ACA ATG GCT CAC AGG AAA CC - #A ACA TAT GAA AGA GAC 8318 Leu Asn Arg Phe Thr Met Ala His Arg Lys Pr - #o Thr Tyr Glu Arg Asp 2735 - # 2740 - # 2745 - - GTG GAC TTA GGC GCT GGA ACA AGA CAT GTG GC - #A GTG GAA CCA GAG GTA 8366 Val Asp Leu Gly Ala Gly Thr Arg His Val Al - #a Val Glu Pro Glu Val 2750 - # 2755 - # 2760 - - GCC AAC CTA GAT ATC ATT GGC CAG AGG ATA GA - #G AAC ATA AAA CAT GAA 8414 Ala Asn Leu Asp Ile Ile Gly Gln Arg Ile Gl - #u Asn Ile Lys His Glu 2765 - # 2770 - # 2775 - - CAT AAG TCA ACA TGG CAT TAT GAT GAG GAC AA - #T CCA TAT AAA ACA TGG 8462 His Lys Ser Thr Trp His Tyr Asp Glu Asp As - #n Pro Tyr Lys Thr Trp 2780 - # 2785 - # 2790 - - GCC TAT CAT GGA TCA TAT GAG GTC AAG CCA TC - #A GGA TCA GCC TCA TCC 8510 Ala Tyr His Gly Ser Tyr Glu Val Lys Pro Se - #r Gly Ser Ala Ser Ser 2795 2800 - # 2805 - # 2810 - - ATG GTC AAT GGC GTG GTG AAA CTG CTC ACC AA - #A CCA TGG GAT GCC ATC 8558 Met Val Asn Gly Val Val Lys Leu Leu Thr Ly - #s Pro Trp Asp Ala Ile 2815 - # 2820 - # 2825 - - CCC ATG GTC ACA CAA ATA GCC ATG ACT GAC AC - #C ACA CCC TTT GGA CAA 8606 Pro Met Val Thr Gln Ile Ala Met Thr Asp Th - #r Thr Pro Phe Gly Gln 2830 - # 2835 - # 2840 - - CAG AGG GTG TTT AAA GAG AAA GTT GAC ACG CG - #C ACA CCA AAA GCA AAA 8654 Gln Arg Val Phe Lys Glu Lys Val Asp Thr Ar - #g Thr Pro Lys Ala Lys 2845 - # 2850 - # 2855 - - CGA GGC ACA GCA CAA ATC ATG GAG GTG ACA GC - #C AGG TGG TTA TGG GGT 8702 Arg Gly Thr Ala Gln Ile Met Glu Val Thr Al - #a Arg Trp Leu Trp Gly 2860 - # 2865 - # 2870 - - TTT CTC TCT AGA AAC AAA AAA CCA AGA ATT TG - #T ACA AGA GAG GAG TTC 8750 Phe Leu Ser Arg Asn Lys Lys Pro Arg Ile Cy - #s Thr Arg Glu Glu Phe 2875 2880 - # 2885 - # 2890 - - ACA AGA AAA GTT AGG TCA AAC GCA GCC ATT GG - #A GCA GTG TTC GTT GAT 8798 Thr Arg Lys Val Arg Ser Asn Ala Ala Ile Gl - #y Ala Val Phe Val Asp 2895 - # 2900 - # 2905 - - GAA AAT CAA TGG AAC TCA GCA AAA GAA GCA GT - #G GAA GAT GAG CGG TTC 8846 Glu Asn Gln Trp Asn Ser Ala Lys Glu Ala Va - #l Glu Asp Glu Arg Phe 2910 - # 2915 - # 2920 - - TGG GAC CTT GTG CAC AGA GAG AGG GAG CTT CA - #C AAA CAG GGA AAA TGT 8894 Trp Asp Leu Val His Arg Glu Arg Glu Leu Hi - #s Lys Gln Gly Lys Cys 2925 - # 2930 - # 2935 - - GCC ACG TGT GTT TAC AAC ATG ATG GGG AAG AG - #A GAG AAA AAA CTA GGA 8942 Ala Thr Cys Val Tyr Asn Met Met Gly Lys Ar - #g Glu Lys Lys Leu Gly 2940 - # 2945 - # 2950 - - GAG TTC GGA AAG GCA AAA GGA AGT CGT GCA AT - #A TGG TAC ATG TGG TTG 8990 Glu Phe Gly Lys Ala Lys Gly Ser Arg Ala Il - #e Trp Tyr Met Trp Leu 2955 2960 - # 2965 - # 2970 - - GGA GCA CGC TTT CTA GAG TTC GAA GCT CTT GG - #T TTC ATG AAC GAA GAT 9038 Gly Ala Arg Phe Leu Glu Phe Glu Ala Leu Gl - #y Phe Met Asn Glu Asp 2975 - # 2980 - # 2985 - - CAC TGG TTC AGT AGA GAG AAT TCA CTC AGT GG - #A GTG GAA GGA GAA GGA 9086 His Trp Phe Ser Arg Glu Asn Ser Leu Ser Gl - #y Val Glu Gly Glu Gly 2990 - # 2995 - # 3000 - - CTC CAC AAA CTC GGA TAT ATA CTC AGA GAC AT - #A TCA AAG ATT CCA GGG 9134 Leu His Lys Leu Gly Tyr Ile Leu Arg Asp Il - #e Ser Lys Ile Pro Gly 3005 - # 3010 - # 3015 - - GGA AAT ATG TAT GCA GAT GAC ACA GCC GGA TG - #G GAT ACA AGG ATA ACA 9182 Gly Asn Met Tyr Ala Asp Asp Thr Ala Gly Tr - #p Asp Thr Arg Ile Thr 3020 - # 3025 - # 3030 - - GAG GAT GAT CTT CAG AAT GAG GCC AAA ATT AC - #T GAC ATC ATG GAG CCC 9230 Glu Asp Asp Leu Gln Asn Glu Ala Lys Ile Th - #r Asp Ile Met Glu Pro 3035 3040 - # 3045 - # 3050 - - GAA CAT GCC CTA CTG GCT ACG TCA ATC TTC AA - #G CTG ACC TAC CAA AAT 9278 Glu His Ala Leu Leu Ala Thr Ser Ile Phe Ly - #s Leu Thr Tyr Gln Asn 3055 - # 3060 - # 3065 - - AAG GTG GTA AGG GTA CAG AGA CCA GCG AAA AA - #T GGA ACC GTG ATG GAT 9326 Lys Val Val Arg Val Gln Arg Pro Ala Lys As - #n Gly Thr Val Met Asp 3070 - # 3075 - # 3080 - - GTC ATA TCC AGA CGT GAC CAG AGA GGA AGT GG - #C CAG GTC GGA ACT TAT 9374 Val Ile Ser Arg Arg Asp Gln Arg Gly Ser Gl - #y Gln Val Gly Thr Tyr 3085 - # 3090 - # 3095 - - GGC TTA AAC ACT TTC ACT AAC ATG GAA GCC CA - #G CTA ATA AGA CAA ATG 9422 Gly Leu Asn Thr Phe Thr Asn Met Glu Ala Gl - #n Leu Ile Arg Gln Met 3100 - # 3105 - # 3110 - - GAG TCT GAG GGA ATC TTT TCA CCC AGC GAA TT - #G GAG ACC CCA AAT TTA 9470 Glu Ser Glu Gly Ile Phe Ser Pro Ser Glu Le - #u Glu Thr Pro Asn Leu 3115 3120 - # 3125 - # 3130 - - GCC GAG AGA GTT CTC GAC TGG CTG GAA AAA TA - #T GGC GTC GAA AGG CTG 9518 Ala Glu Arg Val Leu Asp Trp Leu Glu Lys Ty - #r Gly Val Glu Arg Leu 3135 - # 3140 - # 3145 - - AAA AGA ATG GCA ATC AGC GGA GAT GAC TGC GT - #G GTG AAA CCA ATT GAT 9566 Lys Arg Met Ala Ile Ser Gly Asp Asp Cys Va - #l Val Lys Pro Ile Asp 3150 - # 3155 - # 3160 - - GAC AGG TTC GCA ACA GCC TTA ACA GCT CTG AA - #T GAT ATG GGA AAA GTA 9614 Asp Arg Phe Ala Thr Ala Leu Thr Ala Leu As - #n Asp Met Gly Lys Val 3165 - # 3170 - # 3175 - - AGA AAA GAT ATA CCA CAA TGG GAA CCC TCA AA - #A GGA TGG AAT GAT TGG 9662 Arg Lys Asp Ile Pro Gln Trp Glu Pro Ser Ly - #s Gly Trp Asn Asp Trp 3180 - # 3185 - # 3190 - - CAA CAG GTG CCT TTT TGT TCA CAC CAT TTC CA - #C CAG CTG ATT ATG AAG 9710 Gln Gln Val Pro Phe Cys Ser His His Phe Hi - #s Gln Leu Ile Met Lys 3195 3200 - # 3205 - # 3210 - - GAT GGG AGG GAA ATA GTG GTG CCA TGC CGC AA - #C CAA GAT GAA CTT GTG 9758 Asp Gly Arg Glu Ile Val Val Pro Cys Arg As - #n Gln Asp Glu Leu Val 3215 - # 3220 - # 3225 - - GGT AGG GCT AGA GTA TCA CAA GGT GCT GGA TG - #G AGC CTG AGA GAA ACT 9806 Gly Arg Ala Arg Val Ser Gln Gly Ala Gly Tr - #p Ser Leu Arg Glu Thr 3230 - # 3235 - # 3240 - - GCA TGC CTA GGC AAG TCA TAT GCA CAA ATG TG - #G CAG CTG ATG TAC TTC 9854 Ala Cys Leu Gly Lys Ser Tyr Ala Gln Met Tr - #p Gln Leu Met Tyr Phe 3245 - # 3250 - # 3255 - - CAC AGG AGA GAC CTG AGA CTA GCT GCT AAT GC - #T ATC TGT TCA GCC GTT 9902 His Arg Arg Asp Leu Arg Leu Ala Ala Asn Al - #a Ile Cys Ser Ala Val 3260 - # 3265 - # 3270 - - CCA GTT GAT TGG GTC CCA ACC AGC CGC ACC AC - #T TGG TCG ATC CAT GCC 9950 Pro Val Asp Trp Val Pro Thr Ser Arg Thr Th - #r Trp Ser Ile His Ala 3275 3280 - # 3285 - # 3290 - - CAT CAC CAA TGG ATG ACA ACA GAA GAC ATG TT - #G TCA GTG TGG AAT AGG 9998 His His Gln Trp Met Thr Thr Glu Asp Met Le - #u Ser Val Trp Asn Arg 3295 - # 3300 - # 3305 - - GTT TGG ATA GAG GAA AAC CCA TGG ATG GAG GA - #C AAA ACC CAT GTA TCC 10046 Val Trp Ile Glu Glu Asn Pro Trp Met Glu As - #p Lys Thr His Val Ser 3310 - # 3315 - # 3320 - - AGT TGG GAA GAT GTT CCA TAT TTA GGA AAA AG - #G GAA GAT CAG TGG TGT 10094 Ser Trp Glu Asp Val Pro Tyr Leu Gly Lys Ar - #g Glu Asp Gln Trp Cys 3325 - # 3330 - # 3335 - - GGA TCC CTG ATA GGC TTA ACA GCA AGG GCT AC - #C TGG GCC ACC AAC ATA 10142 Gly Ser Leu Ile Gly Leu Thr Ala Arg Ala Th - #r Trp Ala Thr Asn Ile 3340 - # 3345 - # 3350 - - CAA GTG GCC ATA AAC CAA GTG AGA AGA CTA AT - #C GGG AAT GAG AAT TAT 10190 Gln Val Ala Ile Asn Gln Val Arg Arg Leu Il - #e Gly Asn Glu Asn Tyr 3355 3360 - # 3365 - # 3370 - - CTA GAT TAC ATG ACA TCA ATG AAG AGA TTC AA - #G AAC GAG AGT GAT CCG 10238 Leu Asp Tyr Met Thr Ser Met Lys Arg Phe Ly - #s Asn Glu Ser Asp Pro 3375 - # 3380 - # 3385 - - AAG GGG CAC TCT GGT GAG TCA ACA CAC TTA TG - #AAAATAAA GGAAAATAAG 10288 Lys Gly His Ser Gly Glu Ser Thr His Leu 3390 - # 3395 - - AAATCAAACA AGGCAAGAAG TCAGGCCGGA TTAAGCCATA GTACGGTAAG AG -#CTATGCTG 10348 - - CCTGTGAGCC CCGTCCAAGG ACGTAAAATG AAGTCAGGCC GAAAGCCACG GT -#TTGAGCAA 10408 - - ACCGTGCTGC CTGTAGCTTC ATCGTGGGGA TGTAAAAACC TGGGAGGCTG CA -#ACCCATGG 10468 - - AAGCTGTACG CATGGGGTAG CAGACTAGTG GTTAGAGGAG ACCCCTCCCA AA -#ACATAACG 10528 - - CAGCAGCGGG GCCCAACACC AGGGGAAGCT GTATCCTGGT GGTAAGGACT AG -#AGGTTAGA 10588 - - GGAGACCCCC GGCATAACAA TAAACAGCAT ATTGACGCTG GGAGAGACCA GA -#GATCCTGC 10648 - - TGTCTCTACA GCATCATTCC AGGCACAGAA CGCCAGAAAA TGGAATGGTG CT -#GTTGAATC 10708 - - AACAGGTTCT - # - # - # 10718 - - - - (2) INFORMATION FOR SEQ ID NO:2: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 3396 amino - #acids (B) TYPE: amino acid (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: protein - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:2: - - Met Asn Asn Gln Arg Lys Lys Thr Ala Arg Pr - #o Ser Phe Asn Met Leu 1 5 - # 10 - # 15 - - Lys Arg Ala Arg Asn Arg Val Ser Thr Gly Se - #r Gln Leu Ala Lys Arg 20 - # 25 - # 30 - - Phe Ser Lys Gly Leu Leu Ser Gly Gln Gly Pr - #o Met Lys Leu Val Met 35 - # 40 - # 45 - - Ala Phe Ile Ala Phe Leu Arg Phe Leu Ala Il - #e Pro Pro Thr Ala Gly 50 - # 55 - # 60 - - Ile Leu Ala Arg Trp Gly Ser Phe Lys Lys As - #n Gly Ala Ile Lys Val 65 - # 70 - # 75 - # 80 - - Leu Arg Gly Phe Lys Lys Glu Ile Ser Asn Me - #t Leu Asn Ile Met Asn 85 - # 90 - # 95 - - Arg Arg Lys Arg Ser Val Thr Met Leu Leu Me - #t Leu Leu Pro Thr Ala 100 - # 105 - # 110 - - Leu Ala Phe His Leu Thr Thr Arg Gly Gly Gl - #u Pro His Met Ile Val 115 - # 120 - # 125 - - Ser Lys Gln Glu Arg Glu Lys Ser Leu Leu Ph - #e Lys Thr Ser Val Gly 130 - # 135 - # 140 - - Val Asn Met Cys Thr Leu Ile Ala Met Asp Le - #u Gly Glu Leu Cys Glu 145 1 - #50 1 - #55 1 -#60 - - Asp Thr Met Thr Tyr Lys Cys Pro Arg Ile Th - #r Glu Ala Glu ProAsp 165 - # 170 - # 175 - - Asp Val Asp Cys Trp Cys Asn Ala Thr Asp Th - #r Trp Val Thr Tyr Gly 180 - # 185 - # 190 - - Thr Cys Ser Gln Thr Gly Glu His Arg Arg As - #p Lys Arg Ser Val Ala 195 - # 200 - # 205 - - Leu Ala Pro His Val Gly Leu Gly Leu Glu Th - #r Arg Thr Glu Thr Trp 210 - # 215 - # 220 - - Met Ser Ser Glu Gly Ala Trp Lys Gln Ile Gl - #n Arg Val Glu Thr Trp 225 2 - #30 2 - #35 2 -#40 - - Ala Leu Arg His Pro Gly Phe Thr Val Ile Al - #a Leu Phe Leu AlaHis 245 - # 250 - # 255 - - Ala Ile Gly Thr Ser Ile Thr Gln Lys Gly Il - #e Ile Phe Ile Leu Leu 260 - # 265 - # 270 - - Met Leu Val Thr Pro Ser Met Ala Met Arg Cy - #s Val Gly Ile Gly Ser 275 - # 280 - # 285 - - Arg Asp Phe Val Glu Gly Leu Ser Gly Ala Th - #r Trp Val Asp Val Val 290 - # 295 - # 300 - - Leu Glu His Gly Ser Cys Val Thr Thr Met Al - #a Lys Asp Lys Pro Thr 305 3 - #10 3 - #15 3 -#20 - - Leu Asp Ile Glu Leu Leu Lys Thr Glu Val Th - #r Asn Pro Ala ValLeu 325 - # 330 - # 335 - - Arg Lys Leu Cys Ile Glu Ala Lys Ile Ser As - #n Thr Thr Thr Asp Ser 340 - # 345 - # 350 - - Arg Cys Pro Thr Gln Gly Glu Ala Thr Leu Va - #l Glu Glu Gln Asp Ala 355 - # 360 - # 365 - - Asn Phe Val Cys Arg Arg Thr Phe Val Asp Ar - #g Gly Trp Gly Asn Gly 370 - # 375 - # 380 - - Cys Gly Leu Phe Gly Lys Gly Ser Leu Leu Th - #r Cys Ala Lys Phe Lys 385 3 - #90 3 - #95 4 -#00 - - Cys Val Thr Lys Leu Glu Gly Lys Ile Val Gl - #n Tyr Glu Asn LeuLys 405 - # 410 - # 415 - - Tyr Ser Val Ile Val Thr Val His Thr Gly As - #p Gln His Gln Val Gly 420 - # 425 - # 430 - - Asn Glu Thr Thr Glu His Gly Thr Ile Ala Th - #r Ile Thr Pro Gln Ala 435 - # 440 - # 445 - - Pro Thr Ser Glu Ile Gln Leu Thr Asp Tyr Gl - #y Ala Leu Thr Leu Asp 450 - # 455 - # 460 - - Cys Ser Pro Arg Thr Gly Leu Asp Phe Asn Gl - #u Met Val Leu Leu Thr 465 4 - #70 4 - #75 4 -#80 - - Met Lys Glu Lys Ser Trp Leu Val His Lys Gl - #n Trp Phe Leu AspLeu 485 - # 490 - # 495 - - Pro Leu Pro Trp Thr Ser Gly Ala Ser Thr Se - #r Gln Glu Thr Trp Asn 500 - # 505 - # 510 - - Arg Gln Asp Leu Leu Val Thr Phe Lys Thr Al - #a His Ala Lys Lys Gln 515 - # 520 - # 525 - - Glu Val Val Val Leu Gly Ser Gln Glu Gly Al - #a Met His Thr Ala Leu 530 - # 535 - # 540 - - Thr Gly Ala Thr Glu Ile Gln Thr Ser Gly Th - #r Thr Thr Ile Phe Ala 545 5 - #50 5 - #55 5 -#60 - - Gly His Leu Lys Cys Arg Leu Lys Met Asp Ly - #s Leu Thr Leu LysGly 565 - # 570 - # 575 - - Met Ser Tyr Val Met Cys Thr Gly Ser Phe Ly - #s Leu Glu Lys Glu Val 580 - # 585 - # 590 - - Ala Glu Thr Gln His Gly Thr Val Leu Val Gl - #n Val Lys Tyr Glu Gly 595 - # 600 - # 605 - - Thr Asp Ala Pro Cys Lys Ile Pro Phe Ser Th - #r Gln Asp Glu Lys Gly 610 - # 615 - # 620 - - Val Thr Gln Asn Arg Leu Ile Thr Ala Asn Pr - #o Ile Val Thr Asp Lys 625 6 - #30 6 - #35 6 -#40 - - Glu Lys Pro Val Asn Ile Glu Thr Glu Pro Pr - #o Phe Gly Glu SerTyr 645 - # 650 - # 655 - - Ile Val Val Gly Ala Gly Glu Lys Ala Leu Ly - #s Gln Cys Trp Phe Lys 660 - # 665 - # 670 - - Lys Gly Ser Ser Ile Gly Lys Met Phe Glu Al - #a Thr Ala Arg Gly Ala 675 - # 680 - # 685 - - Arg Arg Met Ala Ile Leu Gly Asp Thr Ala Tr - #p Asp Phe Gly Ser Ile 690 - # 695 - # 700 - - Gly Gly Val Phe Thr Ser Val Gly Lys Leu Va - #l His Gln Val Phe Gly 705 7 - #10 7 - #15 7 -#20 - - Thr Ala Tyr Gly Val Leu Phe Ser Gly Val Se - #r Trp Thr Met LysIle 725 - # 730 - # 735 - - Gly Ile Gly Ile Leu Leu Thr Trp Leu Gly Le - #u Asn Ser Arg Ser Thr 740 - # 745 - # 750 - - Ser Leu Ser Met Thr Cys Ile Ala Val Gly Me - #t Val Thr Leu Tyr Leu 755 - # 760 - # 765 - - Gly Val Met Val Gln Ala Asp Ser Gly Cys Va - #l Ile Asn Trp Lys Gly 770 - # 775 - # 780 - - Arg Glu Leu Lys Cys Gly Ser Gly Ile Phe Va - #l Thr Asn Glu Val His 785 7 - #90 7 - #95 8 -#00 - - Thr Trp Thr Glu Gln Tyr Lys Phe Gln Ala As - #p Ser Pro Lys ArgLeu 805 - # 810 - # 815 - - Ser Ala Ala Ile Gly Lys Ala Trp Glu Glu Gl - #y Val Cys Gly Ile Arg 820 - # 825 - # 830 - - Ser Ala Thr Arg Leu Glu Asn Ile Met Trp Ly - #s Gln Ile Ser Asn Glu 835 - # 840 - # 845 - - Leu Asn His Ile Leu Leu Glu Asn Asp Met Ly - #s Phe Thr Val Val Val 850 - # 855 - # 860 - - Gly Asp Val Val Gly Ile Leu Ala Gln Gly Ly - #s Lys Met Ile Arg Pro 865 8 - #70 8 - #75 8 -#80 - - Gln Pro Met Glu His Lys Tyr Ser Trp Lys Se - #r Trp Gly Lys AlaLys 885 - # 890 - # 895 - - Ile Ile Gly Ala Asp Ile Gln Asn Thr Thr Ph - #e Ile Ile Asp Gly Pro 900 - # 905 - # 910 - - Asp Thr Pro Glu Cys Pro Asp Asp Gln Arg Al - #a Trp Asn Ile Trp Glu 915 - # 920 - # 925 - - Val Glu Asp Tyr Gly Phe Gly Ile Phe Thr Th - #r Asn Ile Trp Leu Lys 930 - # 935 - # 940 - - Leu Arg Asp Ser Tyr Thr Gln Met Cys Asp Hi - #s Arg Leu Met Ser Ala 945 9 - #50 9 - #55 9 -#60 - - Ala Ile Lys Asp Ser Lys Ala Val His Ala As - #p Met Gly Tyr TrpIle 965 - # 970 - # 975 - - Glu Ser Glu Lys Asn Glu Thr Trp Lys Leu Al - #a Arg Ala Ser Phe Ile 980 - # 985 - # 990 - - Glu Val Lys Thr Cys Val Trp Pro Lys Ser Hi - #s Thr Leu Trp Ser Asn 995 - # 1000 - # 1005 - - Gly Val Leu Glu Ser Glu Met Ile Ile Pro Ly - #s Ile Tyr Gly Gly Pro 1010 - # 1015 - # 1020 - - Ile Ser Gln His Asn Tyr Arg Pro Gly Tyr Ph - #e Thr Gln Thr Ala Gly 1025 1030 - # 1035 - # 1040 - - Pro Trp His Leu Gly Lys Leu Glu Leu Asp Ph - #e Asp Leu Cys Glu Gly 1045 - # 1050 - # 1055 - - Thr Thr Val Val Val Asp Glu His Cys Gly As - #n Arg Gly Pro Ser Leu 1060 - # 1065 - # 1070 - - Arg Thr Thr Thr Val Thr Gly Lys Ile Ile Hi - #s Glu Trp Cys Cys Arg 1075 - # 1080 - # 1085 - - Ser Cys Thr Leu Pro Pro Leu Arg Phe Lys Gl - #y Glu Asp Gly Cys Trp 1090 - # 1095 - # 1100 - - Tyr Gly Met Glu Ile Arg Pro Val Lys Glu Ly - #s Glu Glu Asn Leu Val 1105 1110 - # 1115 - # 1120 - - Lys Ser Met Val Ser Ala Gly Ser Gly Glu Va - #l Asp Ser Phe Ser Leu 1125 - # 1130 - # 1135 - - Gly Leu Leu Cys Ile Ser Ile Met Ile Glu Gl - #u Val Met Arg Ser Arg 1140 - # 1145 - # 1150 - - Trp Ser Arg Lys Met Leu Met Thr Gly Thr Le - #u Ala Val Phe Leu Leu 1155 - # 1160 - # 1165 - - Leu Ile Met Gly Gln Leu Thr Trp Asn Asp Le - #u Ile Arg Leu Cys Ile 1170 - # 1175 - # 1180 - - Met Val Gly Ala Asn Ala Ser Asp Arg Met Gl - #y Met Gly Thr Thr Tyr 1185 1190 - # 1195 - # 1200 - - Leu Ala Leu Met Ala Thr Phe Lys Met Arg Pr - #o Met Phe Ala Val Gly 1205 - # 1210 - # 1215 - - Leu Leu Phe Arg Arg Leu Thr Ser Arg Glu Va - #l Leu Leu Leu Thr Ile 1220 - # 1225 - # 1230 - - Gly Leu Ser Leu Val Ala Ser Val Glu Leu Pr - #o Asn Ser Leu Glu Glu 1235 - # 1240 - # 1245 - - Leu Gly Asp Gly Leu Ala Met Gly Ile Met Il - #e Leu Lys Leu Leu Thr 1250 - # 1255 - # 1260 - - Asp Phe Gln Ser His Gln Leu Trp Ala Thr Le - #u Leu Ser Leu Thr Phe 1265 1270 - # 1275 - # 1280 - - Val Lys Thr Thr Phe Ser Leu His Tyr Ala Tr - #p Lys Thr Met Ala Met 1285 - # 1290 - # 1295 - - Val Leu Ser Ile Val Ser Leu Phe Pro Leu Cy - #s Leu Ser Thr Thr Ser 1300 - # 1305 - # 1310 - - Gln Lys Thr Thr Trp Leu Pro Val Leu Leu Gl - #y Ser Leu Gly Cys Lys 1315 - # 1320 - # 1325 - - Pro Leu Thr Met Phe Leu Ile Ala Glu Asn Ly - #s Ile Trp Gly Arg Lys 1330 - # 1335 - # 1340 - - Ser Trp Pro Leu Asn Glu Gly Ile Met Ala Va - #l Gly Ile Val Ser Ile 1345 1350 - # 1355 - # 1360 - - Leu Leu Ser Ser Leu Leu Lys Asn Asp Val Pr - #o Leu Ala Gly Pro Leu 1365 - # 1370 - # 1375 - - Ile Ala Gly Gly Met Leu Ile Ala Cys Tyr Va - #l Ile Ser Gly Ser Ser 1380 - # 1385 - # 1390 - - Ala Asp Leu Ser Leu Glu Lys Ala Ala Glu Va - #l Ser Trp Glu Glu Glu 1395 - # 1400 - # 1405 - - Ala Glu His Ser Gly Ala Ser His Asn Ile Le - #u Val Glu Val Gln Asp 1410 - # 1415 - # 1420 - - Asp Gly Thr Met Lys Ile Lys Asp Glu Glu Ar - #g Asp Asp Thr Leu Thr 1425 1430 - # 1435 - # 1440 - - Ile Leu Leu Lys Ala Thr Leu Leu Ala Val Se - #r Gly Val Tyr Pro Leu 1445 - # 1450 - # 1455 - - Ser Ile Pro Ala Thr Leu Phe Val Trp Tyr Ph - #e Trp Gln Lys Lys Lys 1460 - # 1465 - # 1470 - - Gln Arg Ser Gly Val Leu Trp Asp Thr Pro Se - #r Pro Pro Glu Val Glu 1475 - # 1480 - # 1485 - - Arg Ala Val Leu Asp Asp Gly Ile Tyr Arg Il - #e Met Gln Arg Gly Leu 1490 - # 1495 - # 1500 - - Leu Gly Arg Ser Gln Val Gly Val Gly Val Ph - #e Gln Asp Gly Val Phe 1505 1510 - # 1515 - # 1520 - - His Thr Met Trp His Val Thr Arg Gly Ala Va - #l Leu Met Tyr Gln Gly 1525 - # 1530 - # 1535 - - Lys Arg Leu Glu Pro Ser Trp Ala Ser Val Ly - #s Lys Asp Leu Ile Ser 1540 - # 1545 - # 1550 - - Tyr Gly Gly Gly Trp Arg Phe Gln Gly Ser Tr - #p Asn Thr Gly Glu Glu 1555 - # 1560 - # 1565 - - Val Gln Val Ile Ala Val Glu Pro Gly Lys As - #n Pro Lys Asn Val Gln 1570 - # 1575 - # 1580 - - Thr Ala Pro Gly Thr Phe Lys Thr Pro Glu Gl - #y Glu Val Gly Ala Ile 1585 1590 - # 1595 - # 1600 - - Ala Leu Asp Phe Lys Pro Gly Thr Ser Gly Se - #r Pro Ile Val Asn Arg 1605 - # 1610 - # 1615 - - Glu Gly Lys Ile Val Gly Leu Tyr Gly Asn Gl - #y Val Val Thr Thr Ser 1620 - # 1625 - # 1630 - - Gly Thr Tyr Val Ser Ala Ile Ala Gln Ala Ly - #s Ala Ser Gln Glu Gly 1635 - # 1640 - # 1645 - - Pro Leu Pro Glu Ile Glu Asp Glu Val Phe Ar - #g Lys Arg Asn Leu Thr 1650 - # 1655 - # 1660 - - Ile Met Asp Leu His Pro Gly Ser Gly Lys Th - #r Arg Arg Tyr Leu Pro 1665 1670 - # 1675 - # 1680 - - Ala Ile Val Arg Glu Ala Ile Arg Arg Asn Va - #l Arg Thr Leu Ile Leu 1685 - # 1690 - # 1695 - - Ala Pro Thr Arg Val Val Ala Ser Glu Met Al - #a Glu Ala Leu Lys Gly 1700 - # 1705 - # 1710 - - Met Pro Ile Arg Tyr Gln Thr Thr Ala Val Ly - #s Ser Glu His Thr Gly 1715 - # 1720 - # 1725 - - Lys Glu Ile Val Asp Leu Met Cys His Ala Th - #r Phe Thr Met Arg Leu 1730 - # 1735 - # 1740 - - Leu Ser Pro Val Arg Val Pro Asn Tyr Asn Me - #t Ile Ile Met Asp Glu 1745 1750 - # 1755 - # 1760 - - Ala His Phe Thr Asp Pro Ala Ser Ile Ala Ar - #g Arg Gly Tyr Ile Ser 1765 - # 1770 - # 1775 - - Thr Arg Val Gly Met Gly Glu Ala Ala Ala Il - #e Phe Met Thr Ala Thr 1780 - # 1785 - # 1790 - - Pro Pro Gly Ser Val Glu Ala Phe Pro Gln Se - #r Asn Ala Val Ile Gln 1795 - # 1800 - # 1805 - - Asp Glu Glu Arg Asp Ile Pro Glu Arg Ser Tr - #p Asn Ser Gly Tyr Glu 1810 - # 1815 - # 1820 - - Trp Ile Thr Asp Phe Pro Gly Lys Thr Val Tr - #p Phe Val Pro Ser Ile 1825 1830 - # 1835 - # 1840 - - Lys Ser Gly Asn Asp Ile Ala Asn Cys Leu Ar - #g Lys Asn Gly Lys Arg 1845 - # 1850 - # 1855 - - Val Ile Gln Leu Ser Arg Lys Thr Phe Asp Th - #r Glu Tyr Gln Lys Thr 1860 - # 1865 - # 1870 - - Lys Asn Asn Asp Trp Asp Tyr Val Val Thr Th - #r Asp Ile Ser Glu Met 1875 - # 1880 - # 1885 - - Gly Ala Asn Phe Arg Ala Asp Arg Val Ile As - #p Pro Arg Arg Cys Leu 1890 - # 1895 - # 1900 - - Lys Pro Val Ile Leu Lys Asp Gly Pro Glu Ar - #g Val Ile Leu Ala Gly 1905 1910 - # 1915 - # 1920 - - Pro Met Pro Val Thr Val Ala Ser Ala Ala Gl - #n Arg Arg Gly Arg Ile 1925 - # 1930 - # 1935 - - Gly Arg Asn Gln Asn Lys Glu Gly Asp Gln Ty - #r Val Tyr Met Gly Gln 1940 - # 1945 - # 1950 - - Pro Leu Asn Asn Asp Glu Asp His Ala His Tr - #p Thr Glu Ala Lys Met 1955 - # 1960 - # 1965 - - Leu Leu Asp Asn Ile Asn Thr Pro Glu Gly Il - #e Ile Pro Ala Leu Phe 1970 - # 1975 - # 1980 - - Glu Pro Glu Arg Glu Lys Ser Ala Ala Ile As - #p Gly Glu Tyr Arg Leu 1985 1990 - # 1995 - # 2000 - - Arg Gly Glu Ala Arg Lys Thr Phe Val Glu Le - #u Met Arg Arg Gly Asp 2005 - # 2010 - # 2015 - - Leu Pro Val Trp Leu Ser Tyr Lys Val Ala Se - #r Glu Gly Phe Gln Tyr 2020 - # 2025 - # 2030 - - Ser Asp Arg Arg Trp Cys Phe Asp Gly Glu Ar - #g Asn Asn Gln Val Leu 2035 - # 2040 - # 2045 - - Glu Glu Asn Met Asp Val Glu Met Trp Thr Ly - #s Glu Gly Glu Arg Lys 2050 - # 2055 - # 2060 - - Lys Leu Arg Pro Arg Trp Leu Asp Ala Arg Th - #r Tyr Ser Asp Pro Leu 2065 2070 - # 2075 - # 2080 - - Ala Leu Arg Glu Phe Lys Glu Phe Ala Ala Gl - #y Arg Arg Ser Val Ser 2085 - # 2090 - # 2095 - - Gly Asp Leu Ile Leu Glu Ile Gly Lys Leu Pr - #o Gln His Leu Thr Gln 2100 - # 2105 - # 2110 - - Arg Ala Gln Asn Ala Leu Asp Asn Leu Val Me - #t Leu His Asn Ser Glu 2115 - # 2120 - # 2125 - - Gln Gly Gly Arg Ala Tyr Arg His Ala Met Gl - #u Glu Leu Pro Asp Thr 2130 - # 2135 - # 2140 - - Ile Glu Thr Leu Met Leu Leu Ala Leu Ile Al - #a Val Leu Thr Gly Gly 2145 2150 - # 2155 - # 2160 - - Val Thr Leu Phe Phe Leu Ser Gly Lys Gly Le - #u Gly Lys Thr Ser Ile 2165 - # 2170 - # 2175 - - Gly Leu Leu Cys Val Met Ala Ser Ser Val Le - #u Leu Trp Met Ala Ser 2180 - # 2185 - # 2190 - - Val Glu Pro His Trp Ile Ala Ala Ser Ile Il - #e Leu Glu Phe Phe Leu 2195 - # 2200 - # 2205 - - Met Val Leu Leu Ile Pro Glu Pro Asp Arg Gl - #n Arg Thr Pro Gln Asp 2210 - # 2215 - # 2220 - - Asn Gln Leu Ala Tyr Val Val Ile Gly Leu Le - #u Phe Met Ile Leu Thr 2225 2230 - # 2235 - # 2240 - - Val Ala Ala Asn Glu Met Gly Leu Leu Glu Th - #r Thr Lys Lys Asp Leu 2245 - # 2250 - # 2255 - - Gly Ile Gly His Val Ala Ala Glu Asn His Hi - #s His Ala Thr Met Leu 2260 - # 2265 - # 2270 - - Asp Val Asp Leu Arg Pro Ala Ser Ala Trp Th - #r Leu Tyr Ala Val Ala 2275 - # 2280 - # 2285 - - Thr Thr Val Ile Thr Pro Met Met Arg His Th - #r Ile Glu Asn Thr Thr 2290 - # 2295 - # 2300 - - Ala Asn Ile Ser Leu Thr Ala Ile Ala Asn Gl - #n Ala Ala Ile Leu Met 2305 2310 - # 2315 - # 2320 - - Gly Leu Asp Lys Gly Trp Pro Ile Ser Lys Me - #t Asp Ile Gly Val Pro 2325 - # 2330 - # 2335 - - Leu Leu Ala Leu Gly Cys Tyr Ser Gln Val As - #n Pro Leu Thr Leu Thr 2340 - # 2345 - # 2350 - - Ala Ala Val Leu Met Leu Val Ala His Tyr Al - #a Ile Ile Gly Pro Gly 2355 - # 2360 - # 2365 - - Leu Gln Ala Lys Ala Thr Arg Glu Ala Gln Ly - #s Arg Thr Ala Ala Gly 2370 - # 2375 - # 2380 - - Ile Met Lys Asn Pro Thr Val Asp Gly Ile Va - #l Ala Ile Asp Leu Asp 2385 2390 - # 2395 - # 2400 - - Pro Val Val Tyr Asp Ala Lys Phe Glu Lys Gl - #n Leu Gly Gln Ile Met 2405 - # 2410 - # 2415 - - Leu Leu Ile Leu Cys Thr Ser Gln Ile Leu Le - #u Met Arg Thr Thr Trp 2420 - # 2425 - # 2430 - - Ala Leu Cys Glu Ser Ile Thr Leu Ala Thr Gl - #y Pro Leu Thr Thr Leu 2435 - # 2440 - # 2445 - - Trp Glu Gly Ser Pro Gly Lys Phe Trp Asn Th - #r Thr Ile Ala Val Ser 2450 - # 2455 - # 2460 - - Met Ala Asn Ile Phe Arg Gly Ser Tyr Leu Al - #a Gly Ala Gly Leu Ala 2465 2470 - # 2475 - # 2480 - - Phe Ser Leu Met Lys Ser Leu Gly Gly Gly Ar - #g Arg Gly Thr Gly Ala 2485 - # 2490 - # 2495 - - Lys Gly Lys His Trp Glu Arg Asn Gly Lys As - #p Arg Leu Asn Gln Leu 2500 - # 2505 - # 2510 - - Ser Lys Ser Glu Phe Asn Thr Tyr Lys Arg Se - #r Gly Ile Met Glu Val 2515 - # 2520 - # 2525 - - Asp Arg Ser Glu Ala Lys Glu Gly Leu Lys Ar - #g Gly Glu Thr Thr Lys 2530 - # 2535 - # 2540 - - His Ala Val Ser Arg Gly Thr Ala Lys Leu Ar - #g Trp Phe Val Glu Arg 2545 2550 - # 2555 - # 2560 - - Asn Leu Val Lys Pro Glu Gly Lys Val Ile As - #p Leu Gly Cys Gly Arg 2565 - # 2570 - # 2575 - - Gly Gly Trp Ser Tyr Tyr Cys Ala Gly Leu Ly - #s Lys Val Thr Glu Val 2580 - # 2585 - # 2590 - - Lys Gly Tyr Thr Lys Gly Gly Pro Gly His Gl - #u Glu Pro Ile Pro Met 2595 - # 2600 - # 2605 - - Ala Thr Tyr Gly Trp Asn Leu Val Lys Leu Ty - #r Ser Gly Lys Asp Val 2610 - # 2615 - # 2620 - - Phe Phe Thr Pro Pro Glu Lys Cys Asp Thr Le - #u Leu Cys Asp Ile Gly 2625 2630 - # 2635 - # 2640 - - Glu Ser Ser Pro Asn Pro Thr Ile Glu Glu Gl - #y Arg Thr Leu Arg Val 2645 - # 2650 - # 2655 - - Leu Lys Met Val Glu Pro Trp Leu Arg Gly As - #n Gln Phe Cys Ile Lys 2660 - # 2665 - # 2670 - - Ile Leu Asn Pro Tyr Met Pro Ser Val Val Gl - #u Thr Leu Glu Gln Met 2675 - # 2680 - # 2685 - - Gln Arg Lys His Gly Gly Met Leu Val Arg As - #n Pro Leu Ser Arg Asn 2690 - # 2695 - # 2700 - - Ser Thr His Glu Met Tyr Trp Val Ser Cys Gl - #y Thr Gly Asn Ile Val 2705 2710 - # 2715 - # 2720 - - Ser Ala Val Asn Met Thr Ser Arg Met Leu Le - #u Asn Arg Phe Thr Met 2725 - # 2730 - # 2735 - - Ala His Arg Lys Pro Thr Tyr Glu Arg Asp Va - #l Asp Leu Gly Ala Gly 2740 - # 2745 - # 2750 - - Thr Arg His Val Ala Val Glu Pro Glu Val Al - #a Asn Leu Asp Ile Ile 2755 - # 2760 - # 2765 - - Gly Gln Arg Ile Glu Asn Ile Lys His Glu Hi - #s Lys Ser Thr Trp His 2770 - # 2775 - # 2780 - - Tyr Asp Glu Asp Asn Pro Tyr Lys Thr Trp Al - #a Tyr His Gly Ser Tyr 2785 2790 - # 2795 - # 2800 - - Glu Val Lys Pro Ser Gly Ser Ala Ser Ser Me - #t Val Asn Gly Val Val 2805 - # 2810 - # 2815 - - Lys Leu Leu Thr Lys Pro Trp Asp Ala Ile Pr - #o Met Val Thr Gln Ile 2820 - # 2825 - # 2830 - - Ala Met Thr Asp Thr Thr Pro Phe Gly Gln Gl - #n Arg Val Phe Lys Glu 2835 - # 2840 - # 2845 - - Lys Val Asp Thr Arg Thr Pro Lys Ala Lys Ar - #g Gly Thr Ala Gln Ile 2850 - # 2855 - # 2860 - - Met Glu Val Thr Ala Arg Trp Leu Trp Gly Ph - #e Leu Ser Arg Asn Lys 2865 2870 - # 2875 - # 2880 - - Lys Pro Arg Ile Cys Thr Arg Glu Glu Phe Th - #r Arg Lys Val Arg Ser 2885 - # 2890 - # 2895 - - Asn Ala Ala Ile Gly Ala Val Phe Val Asp Gl - #u Asn Gln Trp Asn Ser 2900 - # 2905 - # 2910 - - Ala Lys Glu Ala Val Glu Asp Glu Arg Phe Tr - #p Asp Leu Val His Arg 2915 - # 2920 - # 2925 - - Glu Arg Glu Leu His Lys Gln Gly Lys Cys Al - #a Thr Cys Val Tyr Asn 2930 - # 2935 - # 2940 - - Met Met Gly Lys Arg Glu Lys Lys Leu Gly Gl - #u Phe Gly Lys Ala Lys 2945 2950 - # 2955 - # 2960 - - Gly Ser Arg Ala Ile Trp Tyr Met Trp Leu Gl - #y Ala Arg Phe Leu Glu 2965 - # 2970 - # 2975 - - Phe Glu Ala Leu Gly Phe Met Asn Glu Asp Hi - #s Trp Phe Ser Arg Glu 2980 - # 2985 - # 2990 - - Asn Ser Leu Ser Gly Val Glu Gly Glu Gly Le - #u His Lys Leu Gly Tyr 2995 - # 3000 - # 3005 - - Ile Leu Arg Asp Ile Ser Lys Ile Pro Gly Gl - #y Asn Met Tyr Ala Asp 3010 - # 3015 - # 3020 - - Asp Thr Ala Gly Trp Asp Thr Arg Ile Thr Gl - #u Asp Asp Leu Gln Asn 3025 3030 - # 3035 - # 3040 - - Glu Ala Lys Ile Thr Asp Ile Met Glu Pro Gl - #u His Ala Leu Leu Ala 3045 - # 3050 - # 3055 - - Thr Ser Ile Phe Lys Leu Thr Tyr Gln Asn Ly - #s Val Val Arg Val Gln 3060 - # 3065 - # 3070 - - Arg Pro Ala Lys Asn Gly Thr Val Met Asp Va - #l Ile Ser Arg Arg Asp 3075 - # 3080 - # 3085 - - Gln Arg Gly Ser Gly Gln Val Gly Thr Tyr Gl - #y Leu Asn Thr Phe Thr 3090 - # 3095 - # 3100 - - Asn Met Glu Ala Gln Leu Ile Arg Gln Met Gl - #u Ser Glu Gly Ile Phe 3105 3110 - # 3115 - # 3120 - - Ser Pro Ser Glu Leu Glu Thr Pro Asn Leu Al - #a Glu Arg Val Leu Asp 3125 - # 3130 - # 3135 - - Trp Leu Glu Lys Tyr Gly Val Glu Arg Leu Ly - #s Arg Met Ala Ile Ser 3140 - # 3145 - # 3150 - - Gly Asp Asp Cys Val Val Lys Pro Ile Asp As - #p Arg Phe Ala Thr Ala 3155 - # 3160 - # 3165 - - Leu Thr Ala Leu Asn Asp Met Gly Lys Val Ar - #g Lys Asp Ile Pro Gln 3170 - # 3175 - # 3180 - - Trp Glu Pro Ser Lys Gly Trp Asn Asp Trp Gl - #n Gln Val Pro Phe Cys 3185 3190 - # 3195 - # 3200 - - Ser His His Phe His Gln Leu Ile Met Lys As - #p Gly Arg Glu Ile Val 3205 - # 3210 - # 3215 - - Val Pro Cys Arg Asn Gln Asp Glu Leu Val Gl - #y Arg Ala Arg Val Ser 3220 - # 3225 - # 3230 - - Gln Gly Ala Gly Trp Ser Leu Arg Glu Thr Al - #a Cys Leu Gly Lys Ser 3235 - # 3240 - # 3245 - - Tyr Ala Gln Met Trp Gln Leu Met Tyr Phe Hi - #s Arg Arg Asp Leu Arg 3250 - # 3255 - # 3260 - - Leu Ala Ala Asn Ala Ile Cys Ser Ala Val Pr - #o Val Asp Trp Val Pro 3265 3270 - # 3275 - # 3280 - - Thr Ser Arg Thr Thr Trp Ser Ile His Ala Hi - #s His Gln Trp Met Thr 3285 - # 3290 - # 3295 - - Thr Glu Asp Met Leu Ser Val Trp Asn Arg Va - #l Trp Ile Glu Glu Asn 3300 - # 3305 - # 3310 - - Pro Trp Met Glu Asp Lys Thr His Val Ser Se - #r Trp Glu Asp Val Pro 3315 - # 3320 - # 3325 - - Tyr Leu Gly Lys Arg Glu Asp Gln Trp Cys Gl - #y Ser Leu Ile Gly Leu 3330 - # 3335 - # 3340 - - Thr Ala Arg Ala Thr Trp Ala Thr Asn Ile Gl - #n Val Ala Ile Asn Gln 3345 3350 - # 3355 - # 3360 - - Val Arg Arg Leu Ile Gly Asn Glu Asn Tyr Le - #u Asp Tyr Met Thr Ser 3365 - # 3370 - # 3375 - - Met Lys Arg Phe Lys Asn Glu Ser Asp Pro Ly - #s Gly His Ser Gly Glu 3380 - # 3385 - # 3390 - - Ser Thr His Leu 3395 - - - - (2) INFORMATION FOR SEQ ID NO:3: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 27 base - #pairs (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: DNA (genomic) - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:3: - - CCATGAATTC CCATGCGATG CGTGGGA - # - # 27 - - - - (2) INFORMATION FOR SEQ ID NO:4: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 27 base - #pairs (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: DNA (genomic) - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:4: - - CACATCTCGA GTCCGCTTGA ACCATGA - # - # 27 - - - - (2) INFORMATION FOR SEQ ID NO:5: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 26 base - #pairs (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: DNA (genomic) - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:5: - - TGGTTCCCGG GGACTCGGGA TGTGTA - # - # 26 - - - - (2) INFORMATION FOR SEQ ID NO:6: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 29 base - #pairs (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: DNA (genomic) - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:6: - - ACTAAGCTTG ATCATGCAGA GACCATTGA - # - # 29 - - - - (2) INFORMATION FOR SEQ ID NO:7: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 29 base - #pairs (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: DNA (genomic) - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:7: - - AATCAGAATT CTCTGCAGGG TCAGGGGAA - # - # 29 - - - - (2) INFORMATION FOR SEQ ID NO:8: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 30 base - #pairs (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: DNA (genomic) - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:8: - - ATAACAAAGC TTATCTTTGT TTCTTTTTCT - # - # 30 - - - - (2) INFORMATION FOR SEQ ID NO:9: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 31 base - #pairs (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: DNA (genomic) - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:9: - - GAAAGGATCC TCTGGAGTGT TATGGGACAC A - # - # 31 - - - - (2) INFORMATION FOR SEQ ID NO:10: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 27 base - #pairs (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: DNA (genomic) - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:10: - - ACCCAAGCTT CATCTTCTTC CTGCTGC - # - # 27 - - - - (2) INFORMATION FOR SEQ ID NO:11: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 25 base - #pairs (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: DNA (genomic) - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:11: - - AGGAGGTCGA CGAGGTACGG GAGCC - # - # 25 - - - - (2) INFORMATION FOR SEQ ID NO:12: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 20 base - #pairs (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: DNA (genomic) - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:12: - - CAATGATATC TAGGTTGGCT - # - # - # 20 - - - - (2) INFORMATION FOR SEQ ID NO:13: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 18 base - #pairs (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: cDNA - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:13: - - CCGTGAATCC TGGGTGTC - # - # - # 18 - - - - (2) INFORMATION FOR SEQ ID NO:14: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 22 base - #pairs (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: cDNA - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:14: - - GGGAATTCCA GTGGTGTGGA TC - # - # 22 - - - - (2) INFORMATION FOR SEQ ID NO:15: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 17 base - #pairs (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: cDNA - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:15: - - GTAAAACGAC GGCCAGT - # - # - # 17 - - - - (2) INFORMATION FOR SEQ ID NO:16: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 7 amino - #acids (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: peptide - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:16: - - Met Met Asn Gln Arg Lys Lys 1 5 - - - - (2) INFORMATION FOR SEQ ID NO:17: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 4 amino - #acids (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: peptide - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:17: - - Ala Phe Xaa Leu 1 - - - - (2) INFORMATION FOR SEQ ID NO:18: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 6 amino - #acids (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: peptide - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:18: - - Arg Xaa Lys Arg Ser Val 1 5 - - - - (2) INFORMATION FOR SEQ ID NO:19: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 6 amino - #acids (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: peptide - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:19: - - Xaa Met Arg Cys Xaa Gly 1 5 - - - - (2) INFORMATION FOR SEQ ID NO:20: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 8 amino - #acids (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: peptide - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:20: - - Val Gln Ala Asp Xaa Gly Cys Val 1 5 - - - - (2) INFORMATION FOR SEQ ID NO:21: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 6 amino - #acids (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: peptide - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:21: - - Val Xaa Ala Gly Xaa Gly 1 5 - - - - (2) INFORMATION FOR SEQ ID NO:22: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 6 amino - #acids (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: peptide - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:22: - - Xaa Ser Trp Pro Leu Asn 1 5 - - - - (2) INFORMATION FOR SEQ ID NO:23: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 6 amino - #acids (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: peptide - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:23: - - Lys Xaa Gln Arg Xaa Gly 1 5 - - - - (2) INFORMATION FOR SEQ ID NO:24: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 4 amino - #acids (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: peptide - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:24: - - Gly Arg Xaa Ser 1 - - - - (2) INFORMATION FOR SEQ ID NO:25: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 5 amino - #acids (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: peptide - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:25: - - Val Xaa Ala Asn Glu 1 5__________________________________________________________________________

cDNA sequence of Dengue virus serotype 1 (Singapore strain)

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Non-Patent Literature Citations (24)

Entry
Fu et al, "Full-Length cDNA Sequence of Dengue Type 1 Virus (Singapore Strain S275/90)", Virology 188:953-958 (1992).
Rico-Hesse, "Molecular Evolution and Distribution of Dengue Viruses Type 1 and 2 in Nature", Virology 174:479-493 (1990).
Lal et al, "Cloning Full-Length DNA Sequences of the Dneue Virus Genome for Use in Elucidating Pathogenesis and Development of Immunoprophylaxis", Vaccines, pp. 393-399 (1988).
Deubel et al, "Nucleotide Sequence and Deduced Amino Acid Sequence of the Nonstructural Proteins of Dengue Type 2 Virus, Jamaica Genotype: Comparative Analysis of the Full-Length Genome", Virology 165:234-244 (1988).
Osatomi et al, "Complete Nucleotide Sequence of Dengue Type 3 Virus Genome RNA", Virology 176:643-647 (1990).
Zhao et al, "Cloning Full-Length Dengue Type 4 Viral DNA Sequences: Analysis of Genes Coding for Structural Proteins", Virology 155:77-88 (1986).
Mason et al, "Sequence of the Dengue-1 Virus Genome in the REgion Encoding the Three Structural Proteins and the Major Nonstructural Protein NS1", Virology 161:262-267 (1987).
Westaway et al, "Flaviviridae", Intervirology 24:183-192 (1985).
Rosen, "The Pathogenesis of denuge haemorrhagic fever", Supplement to S. Afr. J. Med. 11:40-42 (1986).
Halstead, "Pathogenesis of Dengue: Challenges to Molecular Biology", Science 239:476-481 (1988).
Brinton and Dispoto, "Sequence and Secondary Structure Analysis of the 5'-Terminal Region of Flavivirus Genome RNA", Virology 162:290-299 (1988).
Irie et al, "Sequence analysis of cloned dengue virus type 2 genome (New Guinea-C strain)", Gene 75:197-211 (1989).
Wilbur and Lipman, "Rapid similarity searches of nucleic acid and protein data banks", Proc. Natl. Acad. Sci. USA 80:726-730 (1983).
Rice et al, "Nucleotide Sequence of Yellow Fever Virus: Implications for Flavivirus Gene Expression and Evolution", Science 229:726-733 (1985).
Chu et al, "Genetic Relatedness among Structural Protein Genes of Dengue 1 Virus Strains", J. Gen. Virol. 70:1701-1712 (1989).
Guan and Dixon, "Eukaryotic Proteins Expressed in Escherichia coli: An Improved Thrombin Cleavaged and Purification Procedure of Fusion Proteins with Glutathione S-Transferase", Anal. Biochem. 192:262-267 (1991).
Ford et al, "Fusion Tails for the Recovery and Purification of Recombinant Protiens", Prot. Exp. Pur. 2:96-107 (1991).
Maina et al, "An Escherichia coli vector to express and purify foreign proteins by fusion to and separation from maltose-binding protein", Gene 74:365-373 (1988).
di Guan et al, "Vectors that facilitate the expression and purification of foreign peptides in Escherichia coli by fusion to maltose-binding protein", Gene 67:21-30 (1991).
Zhang et al., Journal of Virology 62:3027-3031 "Immunization of mice with dengue structural proteins and nonstructural protein NS1 expressed by baculovirus recombinant induces resistance to dengue virus encephalitis", 1988.
Henchal et al., Journal of General Virology 69:2101-2107 "Synergistic interactions of anti-NS1 monoclonal antibodies protect passively immunized mice from lethal challenge with dengue 2 virus", 1988.
Hayes et al., Pediatric Infectious Disease Journal 11:311-317, "Dengue and dengue hemorrhagic fever", (Abstract Only), 1992.
Suggs et al. "Use of Synthetic oligonucleotides as hybridization probes: Isolation of cloned cDNA for human beta-2 microglobulin". PNAS. vol. 87, No. 11, pp. 6613-6617, Nov. 1981.
Doraisingham, S. "Dengue Virus Infection". Singapore Medical Journal. No. 30:523-524, 1989.