Center for Critical Assessment of Structure Prediction

NIH RePORTER · NIH · R01 · $638,701 · view on reporter.nih.gov ↗

Abstract

 DESCRIPTION (provided by applicant): This project provides the enabling infrastructure for the Critical Assessment of Structure Prediction (CASP) program, dedicated to the objective evaluation of protein structure modeling methods. Knowledge of protein structure significantly aids in the investigation of macromolecular function, interactions, and biochemical pathways. It also has a major impact on the understanding of human disease, and on the development of therapeutics. Experimental determination of structure is inherently time-consuming, costly, and often meets with insurmountable obstacles. Computational modeling offers an alternative approach but modeling methods vary in their effectiveness and typically do not directly provide measures of accuracy. CASP aims at answering these concerns by objective evaluation of methods, so driving progress. CASP is a community-wide program, with over 100 research groups world-wide submitting over 60,000 predictions in the last round (2014). The Center is the primary infrastructure resource for CASP, and handles processing of predictions, develops evaluation software, performs model assessment, develops analysis and display tools, and facilitates access to models and evaluation data. The current proposal includes two major new initiatives, extending the impact of CASP to important new areas of structural biology. First, we will collaborate with appropriate experimental groups to develop modeling methods that maximally leverage sparse and low resolution data. Preliminary results with NMR and crosslinking demonstrate the potential in this area. Second, in partnership with the CAPRI initiative (Critical Assessment of Protein Interactions), we will include modeling of biological assemblies. We will also continue the successful CASP strategy of focusing on overcoming specific bottleneck problems, such as model refinement, estimation of model accuracy, and prediction of three dimensional contacts; adding modeling of non-template regions in homology models. In addition, we will place special emphasis on evaluating the usefulness of models in specific life science applications. Finally, we will interact with teachers and researchers, with te goal of disseminating the insights on modeling and the wealth of data gained through CASP.

Key facts

NIH application ID
9936397
Project number
5R01GM100482-09
Recipient
UNIVERSITY OF CALIFORNIA AT DAVIS
Principal Investigator
KRZYSZTOF A FIDELIS
Activity code
R01
Funding institute
NIH
Fiscal year
2020
Award amount
$638,701
Award type
5
Project period
2012-06-15 → 2021-05-31