Coenzyme-B12-dependent glutamate mutase

被引:56
作者
Marsh, ENG [1 ]
机构
[1] Univ Michigan, Dept Chem, Ann Arbor, MI 48109 USA
基金
美国国家卫生研究院;
关键词
D O I
10.1006/bioo.2000.1168
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Adenosylcobalamin (coenzyme B-12)-dependent glutamate mutase catalyzes a most unusual carbon skeleton rearrangement involving the isomerization of L-glutamate to L-threomethylaspartate, a reaction that is without precedent in organic chemistry. This reaction proceeds through a mechanism involving free radical intermediates that are initiated by homolysis of the cobalt-carbon bond of the coenzyme. The enzyme serves as a paradigm for adenosylcobalamin-dependent catalysis and, more generally, provides insights into how enzymes generate and control reactive free radical species, This review describes how recent studies on the mechanism and structure of glutamate mutase have contributed to our understanding of adenosylcobalamin-mediated catalysis. (C) 2000 Academic Press.
引用
收藏
页码:176 / 189
页数:14
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