Analysis of catalytic residues in enzyme active sites

被引:486
作者
Bartlett, GJ
Porter, CT
Borkakoti, N
Thornton, JM
机构
[1] UCL, Dept Biochem & Mol Biol, London WC1E 6BT, England
[2] European Bioinformat Inst, European Mol Biol Lab, Cambridge CB10 1SD, England
[3] Roche Discovery Welwyn, Welwyn Garden City AL7 3AY, Herts, England
基金
英国生物技术与生命科学研究理事会;
关键词
enzyme active site; catalysis; amino acid residue; enzyme function;
D O I
10.1016/S0022-2836(02)01036-7
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 an analysis of the residues directly involved in catalysis in 178 enzyme active sites. Specific criteria were derived to define a catalytic residue, and used to create a catalytic residue dataset, which was then analysed in terms of properties including secondary structure, solvent accessibility, flexibility, conservation, quaternary structure and function. The results indicate the dominance of a small set of amino acid residues in catalysis and give a picture of a general active site environment. It is hoped that this information will provide a better understanding of the molecular mechanisms involved in catalysis and a heuristic basis for predicting catalytic residues in enzymes of unknown function. (C) 2002 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:105 / 121
页数:17
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