Catalysing new reactions during evolution: Economy of residues and mechanism

被引:73
作者
Bartlett, GJ
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
[4] Brikberk Coll, Dept Crystallog, London WC1E 7HX, England
关键词
active site; catalytic mechanism; enzyme evolution; enzyme reaction;
D O I
10.1016/S0022-2836(03)00734-4
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
The diversity of function in some enzyme superfamilies shows that during evolution, enzymes have evolved to catalyse different reactions on the same structure scaffold. In this analysis, we examine in detail how enzymes can modify their chemistry, through a comparison of the catalytic residues and mechanisms in 27 pairs of homologous enzymes of totally different functions. We find that evolution is very economical. Enzymes retain structurally conserved residues to aid catalysis, including residues that bind catalytic metal ions and modulate cofactor chemistry. We examine the conservation of residue type and residue function in these structurally conserved residue pairs. Additionally, enzymes often retain common mechanistic steps catalyzed by structurally conserved residues. We have examined these steps in the context of their overall reactions. (C) 2003 Elsevier Ltd. All rights reserved.
引用
收藏
页码:829 / 860
页数:32
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