Protein-protein docking benchmark version 4.0

被引:349
|
作者
Hwang, Howook [1 ]
Vreven, Thom [1 ]
Janin, Joel [2 ]
Weng, Zhiping [1 ]
机构
[1] Univ Massachusetts, Sch Med, Program Bioinformat & Integrat Biol, Worcester, MA 01605 USA
[2] IBBMC Univ Paris Sud, CNRS, UMR 8619, F-91405 Orsay, France
关键词
protein-protein docking; protein complexes; protein-protein interactions; complex structure;
D O I
10.1002/prot.22830
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We updated our protein protein docking benchmark to include complexes that became available since our previous release. As before, we only considered high-resolution complex structures that are nonredundant at the family family pair level, for which the X-ray or NMR unbound structures of the constituent proteins are also available. Benchmark 4.0 adds 52 new complexes to the 124 cases of Benchmark 3.0, representing an increase of 42%. Thus, benchmark 4.0 provides 176 unbound unbound cases that can be used for protein protein docking method development and assessment. Seventeen of the newly added cases are enzyme-inhibitor complexes, and we found no new antigen-antibody complexes. Classifying the new cases according to expected difficulty for protein protein docking algorithms gives 33 rigid body cases, 11 cases of medium difficulty, and 8 cases that are difficult. Benchmark 4.0 listings and processed structure files are publicly accessible at http://zlab.umassmed.edu/benchmark/Proteins 2010; 78:3111-3114. (C) 2010 Wiley-Liss, Inc.
引用
收藏
页码:3111 / 3114
页数:4
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