Understanding nature's catalytic toolkit

被引:150
作者
Gutteridge, A [1 ]
Thornton, JM [1 ]
机构
[1] EBI, Cambridge CB10 1SD, England
关键词
D O I
10.1016/j.tibs.2005.09.006
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
Enzymes catalyse numerous reactions in nature, often causing spectacular accelerations in the catalysis rate. One aspect of understanding how enzymes achieve these feats is to explore how they use the limited set of residue side chains that form their 'catalytic toolkit'. Combinations of different residues form 'catalytic units' that are found repeatedly in different unrelated enzymes. Most catalytic units facilitate rapid catalysis in the enzyme active site either by providing charged groups to polarize substrates and to stabilize transition states, or by modifying the pK(a) values of other residues to provide more effective acids and bases. Given recent efforts to design novel enzymes, the rise of structural genomics and subsequent efforts to predict the function of enzymes from their structure, these units provide a simple framework to describe how nature uses the tools at her disposal, and might help to improve techniques for designing and predicting enzyme function.
引用
收藏
页码:622 / 629
页数:8
相关论文
共 41 条
[1]   Analysis of catalytic residues in enzyme active sites [J].
Bartlett, GJ ;
Porter, CT ;
Borkakoti, N ;
Thornton, JM .
JOURNAL OF MOLECULAR BIOLOGY, 2002, 324 (01) :105-121
[2]   The Protein Data Bank [J].
Berman, HM ;
Westbrook, J ;
Feng, Z ;
Gilliland, G ;
Bhat, TN ;
Weissig, H ;
Shindyalov, IN ;
Bourne, PE .
NUCLEIC ACIDS RESEARCH, 2000, 28 (01) :235-242
[3]  
Berry MB, 1998, PROTEINS, V32, P276, DOI 10.1002/(SICI)1097-0134(19980815)32:3<276::AID-PROT3>3.0.CO
[4]  
2-G
[5]   So do we understand how enzymes work? [J].
Blow, D .
STRUCTURE WITH FOLDING & DESIGN, 2000, 8 (04) :R77-R81
[6]   RETRACTED: Computational design of a biologically active enzyme (Retracted article. See vol 319, pg 569, 2008) [J].
Dwyer, MA ;
Looger, LL ;
Hellinga, HW .
SCIENCE, 2004, 304 (5679) :1967-1971
[7]   Structural and catalytic diversity in the two family 11 aldo-keto reductases [J].
Ehrensberger, AH ;
Wilson, DK .
JOURNAL OF MOLECULAR BIOLOGY, 2004, 337 (03) :661-673
[8]   Crystal structure of cardosin A, a glycosylated and Arg-Gly-Asp-containing aspartic proteinase from the flowers of Cynara cardunculus L. [J].
Frazao, C ;
Bento, I ;
Costa, J ;
Soares, CM ;
Veríssimo, P ;
Faro, C ;
Pires, E ;
Cooper, J ;
Carrondo, MA .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (39) :27694-27701
[9]   Divergent evolution of enzymatic function: Mechanistically diverse superfamilies and functionally distinct suprafamilies [J].
Gerlt, JA ;
Babbitt, PC .
ANNUAL REVIEW OF BIOCHEMISTRY, 2001, 70 :209-246
[10]   Conformational changes observed in enzyme crystal structures upon substrate binding [J].
Gutteridge, A ;
Thornton, J .
JOURNAL OF MOLECULAR BIOLOGY, 2005, 346 (01) :21-28