Substrate specificity in thiamin diphosphate-dependent decarboxylases

被引:32
作者
Andrews, Forest H. [1 ]
McLeish, Michael J. [1 ]
机构
[1] Indiana Univ Purdue Univ, Dept Chem & Chem Biol, Indianapolis, IN 46202 USA
关键词
Thiamin-diphosphate; Pyruvate; Benzoylformate; Mutagenesis; Carboligation; YEAST PYRUVATE DECARBOXYLASE; SITE-DIRECTED MUTAGENESIS; OXALYL-COA DECARBOXYLASE; KETO ACID DECARBOXYLASE; C BOND FORMATION; BENZOYLFORMATE DECARBOXYLASE; ZYMOMONAS-MOBILIS; PSEUDOMONAS-PUTIDA; CRYSTAL-STRUCTURE; PHENYLPYRUVATE DECARBOXYLASE;
D O I
10.1016/j.bioorg.2011.12.001
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Thiamin diphosphate (ThDP) is the biologically active form of vitamin B-1, and ThDP-dependent enzymes are found in all forms of life. The catalytic mechanism of this family requires the formation of a common intermediate, the 2 alpha-carbanion-enamine, regardless of whether the enzyme is involved in C-C bond formation or breakdown, or even formation of C-N, C-O and C-S bonds. This demands that the enzymes must screen substrates prior to, and/or after, formation of the common intermediate. This review is focused on the group for which the second step is the protonation of the 2 alpha-carbanion, i.e., the ThDP-dependent decarboxylases. Based on kinetic data, sequence/structure alignments and mutagenesis studies the factors involved in substrate specificity have been identified. (C) 2011 Elsevier Inc. All rights reserved.
引用
收藏
页码:26 / 36
页数:11
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