Literature DB >> 12909013

Catalysing new reactions during evolution: economy of residues and mechanism.

Gail J Bartlett1, Neera Borkakoti, Janet M Thornton.   

Abstract

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.

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Year:  2003        PMID: 12909013     DOI: 10.1016/s0022-2836(03)00734-4

Source DB:  PubMed          Journal:  J Mol Biol        ISSN: 0022-2836            Impact factor:   5.469


  35 in total

1.  Automated prediction of protein function and detection of functional sites from structure.

Authors:  Florencio Pazos; Michael J E Sternberg
Journal:  Proc Natl Acad Sci U S A       Date:  2004-09-29       Impact factor: 11.205

2.  A novel function for the N-terminal nucleophile hydrolase fold demonstrated by the structure of an archaeal inosine monophosphate cyclohydrolase.

Authors:  You-Na Kang; Anh Tran; Robert H White; Steven E Ealick
Journal:  Biochemistry       Date:  2007-04-04       Impact factor: 3.162

3.  Control of stereoselectivity in an enzymatic reaction by backdoor access.

Authors:  Richard Wombacher; Sonja Keiper; Sandra Suhm; Alexander Serganov; Dinshaw J Patel; Andres Jäschke
Journal:  Angew Chem Int Ed Engl       Date:  2006-04-03       Impact factor: 15.336

4.  Correspondences between low-energy modes in enzymes: dynamics-based alignment of enzymatic functional families.

Authors:  Andrea Zen; Vincenzo Carnevale; Arthur M Lesk; Cristian Micheletti
Journal:  Protein Sci       Date:  2008-03-27       Impact factor: 6.725

Review 5.  Toward mechanistic classification of enzyme functions.

Authors:  Daniel E Almonacid; Patricia C Babbitt
Journal:  Curr Opin Chem Biol       Date:  2011-04-12       Impact factor: 8.822

6.  Molecular modeling and dynamics studies with explicit inclusion of electronic polarizability. Theory and applications.

Authors:  Pedro E M Lopes; Benoit Roux; Alexander D Mackerell
Journal:  Theor Chem Acc       Date:  2009-09       Impact factor: 1.702

7.  Quantitative comparison of catalytic mechanisms and overall reactions in convergently evolved enzymes: implications for classification of enzyme function.

Authors:  Daniel E Almonacid; Emmanuel R Yera; John B O Mitchell; Patricia C Babbitt
Journal:  PLoS Comput Biol       Date:  2010-03-12       Impact factor: 4.475

8.  FACT: functional annotation transfer between proteins with similar feature architectures.

Authors:  Tina Koestler; Arndt von Haeseler; Ingo Ebersberger
Journal:  BMC Bioinformatics       Date:  2010-08-09       Impact factor: 3.169

9.  Hydration number, topological control, and ion selectivity.

Authors:  Haibo Yu; Sergei Yu Noskov; Benoît Roux
Journal:  J Phys Chem B       Date:  2009-06-25       Impact factor: 2.991

10.  Classification of nonenzymatic homologues of protein kinases.

Authors:  K Anamika; K R Abhinandan; K Deshmukh; N Srinivasan
Journal:  Comp Funct Genomics       Date:  2009-09-28
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