Title of article
OMP decarboxylase—An enigma persists
Author/Authors
Callahan، نويسنده , , Brian P. and Miller، نويسنده , , Brian G.، نويسنده ,
Issue Information
روزنامه با شماره پیاپی سال 2007
Pages
5
From page
465
To page
469
Abstract
In 1995, Radzicka and Wolfenden reported that the rate enhancement produced by orotidine 5′-phosphate decarboxylase (ODCase) approaches 1017, making this enzyme the most effective pure protein catalyst known in Nature [A. Radzicka, R. Wolfenden, Science 267 (1995) 90–93]. Over the last 12 years, there have been many hypotheses put forward to explain that impressive effect. In this perspective, we provide a summary of the reaction pathways under consideration for ODCase, highlight the supporting and refuting data, and suggest experiments designed to further test each of the candidate pathways.
Keywords
Mechanism , Decarboxylase , Carbanion , Ylide , Electrostatic stress , Orotidine , OMP , Carbene , Decarboxylation , transition state
Journal title
Bioorganic Chemistry: an International Journal
Serial Year
2007
Journal title
Bioorganic Chemistry: an International Journal
Record number
1385963
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