4.8 Article

ModBase, a database of annotated comparative protein structure models and associated resources

期刊

NUCLEIC ACIDS RESEARCH
卷 42, 期 D1, 页码 D336-D346

出版社

OXFORD UNIV PRESS
DOI: 10.1093/nar/gkt1144

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资金

  1. National Institutes of Health [U54 GM094662, U54 GM094625, U54 GM093342, MINOS R01GM105404]
  2. Sandler Family Supporting Foundation
  3. Department of Energy Lawrence Berkeley National Lab IDAT program
  4. European Union [FP7-IDEAS-ERC 294809]
  5. NIGMS [P41-GM103311]
  6. NIH
  7. NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCES [U54GM094625, P41GM103311, U54GM094662, R01GM105404, U54GM093342] Funding Source: NIH RePORTER

向作者/读者索取更多资源

ModBase (http://salilab.org/modbase) is a database of annotated comparative protein structure models. The models are calculated by ModPipe, an automated modeling pipeline that relies primarily on Modeller for fold assignment, sequence-structure alignment, model building and model assessment (http://salilab.org/modeller/). ModBase currently contains almost 30 million reliable models for domains in 4.7 million unique protein sequences. ModBase allows users to compute or update comparative models on demand, through an interface to the ModWeb modeling server (http://salilab.org/modweb). ModBase models are also available through the Protein Model Portal (http://www.proteinmodelportal.org/). Recently developed associated resources include the AllosMod server for modeling ligand-induced protein dynamics (http://salilab.org/allosmod), the AllosMod-FoXS server for predicting a structural ensemble that fits an SAXS profile (http://salilab.org/allosmod-foxs), the FoXSDock server for protein-protein docking filtered by an SAXS profile (http://salilab.org/foxsdock), the SAXS Merge server for automatic merging of SAXS profiles (http://salilab.org/saxsmerge) and the Pose & Rank server for scoring protein-ligand complexes (http://salilab.org/poseandrank). In this update, we also highlight two applications of ModBase: a PSI: Biology initiative to maximize the structural coverage of the human alpha-helical transmembrane proteome and a determination of structural determinants of human immunodeficiency virus-1 protease specificity.

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