Literature DB >> 2005961

Enzyme catalysis: not different, just better.

J R Knowles1.   

Abstract

Where are we in our understanding of enzyme catalysis? The gloomier view is that protein structure and enzyme function are the finely balanced end-products of many weak interactions that can be summed only by massive computing power, and more precise parameterization than we enjoy at present. The cheerier position is that proteins are built on definable principles, and that enzymes use recognizable catalytic devices that will allow us to understand how existing enzymes work and to design new ones. To assess which interpretation is the more realistic, the simple reaction catalysed by triosephosphate isomerase is considered here. This examination illustrates some of the catalytic features of enzymes that are understood, and exposes a few that are not. But overall, the question turns out to have an optimistic answer.

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Year:  1991        PMID: 2005961     DOI: 10.1038/350121a0

Source DB:  PubMed          Journal:  Nature        ISSN: 0028-0836            Impact factor:   49.962


  123 in total

1.  The maximal affinity of ligands.

Authors:  I D Kuntz; K Chen; K A Sharp; P A Kollman
Journal:  Proc Natl Acad Sci U S A       Date:  1999-08-31       Impact factor: 11.205

2.  Role of constraint in catalysis and high-affinity binding by proteins.

Authors:  Donald G Vanselow
Journal:  Biophys J       Date:  2002-05       Impact factor: 4.033

3.  High resolution crystal structures of triosephosphate isomerase complexed with its suicide inhibitors: the conformational flexibility of the catalytic glutamate in its closed, liganded active site.

Authors:  Rajaram Venkatesan; Markus Alahuhta; Petri M Pihko; Rik K Wierenga
Journal:  Protein Sci       Date:  2011-07-07       Impact factor: 6.725

4.  Mechanism for activation of triosephosphate isomerase by phosphite dianion: the role of a ligand-driven conformational change.

Authors:  M Merced Malabanan; Tina L Amyes; John P Richard
Journal:  J Am Chem Soc       Date:  2011-09-28       Impact factor: 15.419

5.  A paradigm for enzyme-catalyzed proton transfer at carbon: triosephosphate isomerase.

Authors:  John P Richard
Journal:  Biochemistry       Date:  2012-03-20       Impact factor: 3.162

6.  Optimal alignment for enzymatic proton transfer: structure of the Michaelis complex of triosephosphate isomerase at 1.2-A resolution.

Authors:  Gerwald Jogl; Sharon Rozovsky; Ann E McDermott; Liang Tong
Journal:  Proc Natl Acad Sci U S A       Date:  2002-12-30       Impact factor: 11.205

7.  Taking Ockham's razor to enzyme dynamics and catalysis.

Authors:  David R Glowacki; Jeremy N Harvey; Adrian J Mulholland
Journal:  Nat Chem       Date:  2012-01-29       Impact factor: 24.427

8.  Dynamic covalent chemistry: Catalysing dynamic libraries.

Authors:  Benjamin L Miller
Journal:  Nat Chem       Date:  2010-05-16       Impact factor: 24.427

9.  Reflections on the catalytic power of a TIM-barrel.

Authors:  John P Richard; Xiang Zhai; M Merced Malabanan
Journal:  Bioorg Chem       Date:  2014-07-11       Impact factor: 5.275

Review 10.  Specificity in transition state binding: the Pauling model revisited.

Authors:  Tina L Amyes; John P Richard
Journal:  Biochemistry       Date:  2013-02-04       Impact factor: 3.162

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