Integrated Resource for Nucleic Acid Structures

Information

  • Research Project
  • 10268964
  • ApplicationId
    10268964
  • Core Project Number
    R01GM085328
  • Full Project Number
    5R01GM085328-10
  • Serial Number
    085328
  • FOA Number
    PA-19-056
  • Sub Project Id
  • Project Start Date
    8/10/2010 - 15 years ago
  • Project End Date
    8/31/2024 - a year ago
  • Program Officer Name
    SAKALIAN, MICHAEL
  • Budget Start Date
    9/1/2021 - 4 years ago
  • Budget End Date
    8/31/2022 - 3 years ago
  • Fiscal Year
    2021
  • Support Year
    10
  • Suffix
  • Award Notice Date
    8/23/2021 - 4 years ago

Integrated Resource for Nucleic Acid Structures

SUMMARY We are analyzing, annotating, organizing, and integrating nucleic acid 3D structural data with sequence and functional data and delivering it to biomedical researchers. The significance of the proposal lies in the prominent roles of nucleic acids in a host of cellular and physiological processes, mediated by interaction with specific DNA- and RNA-binding proteins. DNA encodes genetic information and takes part in replication, recombination, transcription, and repair. RNA transmits genetic information and takes part in all aspects of gene regulation. RNA is also the key component of the ribosome, the universal protein-making nano-machine and an important target for drug design. RNA/DNA hybrids occur in many biological contexts, including transcription complexes, origins of replication, and the widely heralded CRISPR-CAS systems for precision editing of genes (Wright 2016). They form unique structures different from double helical RNA or DNA. High throughput methods have catalogued many new non-coding RNAs (ncRNAs) and RNA-binding proteins lacking previously known RNA-binding domains. The Specific Aims of this proposal are: 1) Create more complete annotations for all nucleic acid 3D structures, 2) create new annotations for nucleic acid-protein complexes, and 3) create a Nucleic Acid Knowledge Base (NAKB) that allows for both deep and wide searching of information about nucleic acid sequences and structures. Under these aims, we will analyze and annotate all types of nucleic acid 3D structures, including DNA, RNA, and DNA/RNA hybrids, and improve our ability to predict 3D structures from sequence. The NAKB resource will provide new search capabilities, enhanced reports, and link-outs to external data, features and tools. The proposed enhancements will greatly improve our abilities to search and visualize existing data on nucleic acid sequence and structural features and will further enrich the user experience and enable data discovery. The innovation of the proposal is the creation of a unified resource for all nucleic acid 3D structures.

IC Name
NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCES
  • Activity
    R01
  • Administering IC
    GM
  • Application Type
    5
  • Direct Cost Amount
    320582
  • Indirect Cost Amount
    51199
  • Total Cost
    371781
  • Sub Project Total Cost
  • ARRA Funded
    False
  • CFDA Code
    859
  • Ed Inst. Type
    SCHOOLS OF ARTS AND SCIENCES
  • Funding ICs
    NIGMS:371781\
  • Funding Mechanism
    Non-SBIR/STTR RPGs
  • Study Section
    MSFD
  • Study Section Name
    Macromolecular Structure and Function D Study Section
  • Organization Name
    BOWLING GREEN STATE UNIVERSITY
  • Organization Department
    CHEMISTRY
  • Organization DUNS
    617407325
  • Organization City
    BOWLING GREEN
  • Organization State
    OH
  • Organization Country
    UNITED STATES
  • Organization Zip Code
    434030230
  • Organization District
    UNITED STATES