| Literature DB >> 12421562 |
Gail J Bartlett1, Craig T Porter, Neera Borkakoti, Janet M Thornton.
Abstract
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.Mesh:
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Year: 2002 PMID: 12421562 DOI: 10.1016/s0022-2836(02)01036-7
Source DB: PubMed Journal: J Mol Biol ISSN: 0022-2836 Impact factor: 5.469