Protein-protein docking benchmark 2.0: An update

被引:226
|
作者
Mintseris, J
Wiehe, K
Pierce, B
Anderson, R
Chen, R
Janin, J
Weng, ZP
机构
[1] Boston Univ, Dept Biomed Engn, Boston, MA 02215 USA
[2] Boston Univ, Bioinformat Program, Boston, MA 02215 USA
[3] Lab Enzymol & Biochim Struct, Gif Sur Yvette, France
关键词
protein-protein docking; protein complexes; protein-protein interactions; complex structure;
D O I
10.1002/prot.20560
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 present a new version of the Protein-Protein Docking Benchmark, reconstructed from the bottom up to include more complexes, particularly focusing on more unbound-unbound test cases. SCOP (Structural Classification of Proteins) Was used to assess redundancy between the complexes in this version. The new benchmark consists of 72 unbound-unbound cases, with 52 rigid-body cases, 13 medium-difficulty cases, and 7 high-difficulty cases with substantial conformational change. In addition, we retained 12 antibody-antigen test cases with the antibody structure in the bound form. The new benchmark provides a platform for evaluating the progress of docking methods on a wide variety of targets. The new version of the benchmark is available to the public at http://zlab.bu.edu/benchmark2. (c) 2005 Wiley-Liss,Inc.
引用
收藏
页码:214 / 216
页数:3
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