Literature DB >> 17876821

Prediction and scoring of docking poses with pyDock.

Solène Grosdidier1, Carles Pons, Albert Solernou, Juan Fernández-Recio.   

Abstract

The two previous CAPRI experiments showed the success of our rigid-body and refinement approach. For this third edition of CAPRI, we have used a new faster protocol called pyDock, which uses electrostatics and desolvation energy to score docking poses generated with FFT-based algorithms. In target T24 (unbound/model), our best prediction had the highest value of fraction of native contacts (40%) among all participants, although it was not considered as acceptable by the CAPRI criteria. In target T25 (unbound/bound), we submitted a model with medium quality. In target T26 (unbound/unbound), we did not submit any acceptable model (but we would have submitted acceptable predictions if we had included available mutational information about the binding site). For targets T27 (unbound/unbound) and T28 (homo-dimer using model), nobody (including us) submitted any acceptable model. Intriguingly, the crystal structure of target T27 shows an alternative interface that correlates with available biological data (we would have submitted acceptable predictions if we had included this). We also participated in all targets of the SCORERS experiment, with at least acceptable accuracy in all valid cases. We submitted two medium and four acceptable scoring models of T25. Using additional distance restraints (from mutational data), we had two medium and two acceptable scoring models of T26. For target T27, we submitted two acceptable scoring models of the alternative interface in the crystal structure. In summary, CAPRI showed the excellent capabilities of pyDock in identifying near-native docking poses. (c) 2007 Wiley-Liss, Inc.

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Year:  2007        PMID: 17876821     DOI: 10.1002/prot.21796

Source DB:  PubMed          Journal:  Proteins        ISSN: 0887-3585


  12 in total

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2.  pyDockSAXS: protein-protein complex structure by SAXS and computational docking.

Authors:  Brian Jiménez-García; Carles Pons; Dmitri I Svergun; Pau Bernadó; Juan Fernández-Recio
Journal:  Nucleic Acids Res       Date:  2015-04-20       Impact factor: 16.971

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Journal:  Cell Chem Biol       Date:  2017-03-16       Impact factor: 8.116

4.  IGF2BP1: a novel binding protein of p38 MAPK.

Authors:  Jacob Rini; Moorthy Anbalagan
Journal:  Mol Cell Biochem       Date:  2017-05-11       Impact factor: 3.396

5.  Protein docking by Rotation-Based Uniform Sampling (RotBUS) with fast computing of intermolecular contact distance and residue desolvation.

Authors:  Albert Solernou; Juan Fernandez-Recio
Journal:  BMC Bioinformatics       Date:  2010-06-28       Impact factor: 3.169

6.  Building macromolecular assemblies by information-driven docking: introducing the HADDOCK multibody docking server.

Authors:  Ezgi Karaca; Adrien S J Melquiond; Sjoerd J de Vries; Panagiotis L Kastritis; Alexandre M J J Bonvin
Journal:  Mol Cell Proteomics       Date:  2010-03-19       Impact factor: 5.911

7.  Prediction of protein-binding areas by small-world residue networks and application to docking.

Authors:  Carles Pons; Fabian Glaser; Juan Fernandez-Recio
Journal:  BMC Bioinformatics       Date:  2011-09-26       Impact factor: 3.169

8.  Scoring function based on weighted residue network.

Authors:  Xiong Jiao; Shan Chang
Journal:  Int J Mol Sci       Date:  2011-12-02       Impact factor: 5.923

9.  Pushing structural information into the yeast interactome by high-throughput protein docking experiments.

Authors:  Roberto Mosca; Carles Pons; Juan Fernández-Recio; Patrick Aloy
Journal:  PLoS Comput Biol       Date:  2009-08-28       Impact factor: 4.475

10.  Structural assembly of two-domain proteins by rigid-body docking.

Authors:  Tammy M K Cheng; Tom L Blundell; Juan Fernandez-Recio
Journal:  BMC Bioinformatics       Date:  2008-10-16       Impact factor: 3.169

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