Bayesian Statistics and Algorithms for Homology Modeling

Information

  • Research Project
  • 7461332
  • ApplicationId
    7461332
  • Core Project Number
    R01GM084453
  • Full Project Number
    9R01GM084453-06
  • Serial Number
    84453
  • FOA Number
    PA-07-70
  • Sub Project Id
  • Project Start Date
    5/15/2008 - 17 years ago
  • Project End Date
    3/31/2012 - 14 years ago
  • Program Officer Name
    REMINGTON, KARIN A
  • Budget Start Date
    5/15/2008 - 17 years ago
  • Budget End Date
    3/31/2009 - 17 years ago
  • Fiscal Year
    2008
  • Support Year
    6
  • Suffix
  • Award Notice Date
    5/15/2008 - 17 years ago

Bayesian Statistics and Algorithms for Homology Modeling

[unreadable] DESCRIPTION (provided by applicant): Our main goal is to improve protein structure prediction methods in order to develop models of proteins in biologically relevant states. Such states may include the target protein as a homo-oligomer; complexed with other proteins, nucleic acids, and ligands; covalently modified through phosphorylation and glycosylation; and in alternate physiologically relevant conformations. Information on the structure of these states for any one target may come from a number of different templates; this information can be assembled into a composite model from which biological inferences can be made. The next generation of the backbone-dependent rotamer library will be developed using classical and Bayesian non-parametric statistics, and it will be extended to include protein modifications, such as phosphorylated and glycosylated amino acids. Electron density analysis will be used to exclude residues with uncertain or dynamic conformations. The resulting libraries will be incorporated into the next generation of our widely used side-chain prediction program SCWRL. A very general structural bioinformatics platform will be constructed to enable statistical and conformational analysis of protein structures on a routine basis. We propose to develop interactive methods and software for producing biologically meaningful models of proteins and protein complexes, based on multiple structure alignments, hidden Markov models, and combined information from diverse structures - ligand-bound and unbound structures, monomers and homo-oligomers, and protein complexes. Project narrative Knowledge of protein structures and their complexes is vital to understanding function and mechanism. We will develop algorithms, databases, and software for predicting structure in biologically relevant states, including homo-oligomers, post-translational modifications, and protein complexes. These methods will be used to improve human health through the prediction of proteins involved in disease. [unreadable] [unreadable] [unreadable]

IC Name
NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCES
  • Activity
    R01
  • Administering IC
    GM
  • Application Type
    9
  • Direct Cost Amount
  • Indirect Cost Amount
  • Total Cost
    311175
  • Sub Project Total Cost
  • ARRA Funded
  • CFDA Code
    859
  • Ed Inst. Type
  • Funding ICs
    NIGMS:311175\
  • Funding Mechanism
  • Study Section
    MSFD
  • Study Section Name
    Macromolecular Structure and Function D Study Section
  • Organization Name
    INSTITUTE FOR CANCER RESEARCH
  • Organization Department
  • Organization DUNS
    872612445
  • Organization City
    Philadelphia
  • Organization State
    PA
  • Organization Country
    UNITED STATES
  • Organization Zip Code
    191112434
  • Organization District
    UNITED STATES