A new test set for validating predictions of protein-ligand interaction

被引:371
作者
Nissink, JWM
Murray, C
Hartshorn, M
Verdonk, ML
Cole, JC
Taylor, R
机构
[1] Cambridge Crystallog Data Ctr, Cambridge CB2 1EZ, England
[2] Astex Technol Ltd, Cambridge, England
关键词
docking test set; ligand docking; validation; drug design; flexible docking; protein-ligand data set; GOLD; SuperStar;
D O I
10.1002/prot.10232
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 large test set of protein-ligand complexes for the purpose of validating algorithms that rely on the prediction of protein-ligand interactions. The set consists of 305 complexes with protonation states assigned by manual inspection. The following checks have been carried out to identify unsuitable entries in this set: (1) assessing the involvement of crystallographically related protein units in ligand binding; (2) identification of bad clashes between protein side chains and ligand; and (3) assessment of structural errors, and/or inconsistency of ligand placement with crystal structure electron density. In addition, the set has been pruned to assure diversity in terms of protein-ligand structures, and subsets are supplied for different protein-structure resolution ranges. A classification of the set by protein type is available. As an illustration, validation results are shown for GOLD and SuperStar. GOLD is a program that performs flexible protein-ligand docking, and SuperStar is used for the prediction of favorable interaction sites in proteins. The new CCDC/Astex test set is freely available to the scientific community (http:// www.ecdc.cam.ac.uk). (C) 2002 Wiley-Liss, Inc.
引用
收藏
页码:457 / 471
页数:15
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