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S-Adenosylmethionine radical enzymes
被引:47
|作者:
Marsh, ENG
[1
]
Patwardhan, A
[1
]
Huhta, MS
[1
]
机构:
[1] Univ Michigan, Dept Chem, Ann Arbor, MI 48109 USA
关键词:
S-Adenosylmethionine;
D O I:
10.1016/j.bioorg.2004.06.001
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:
The role of S-adenosylmethionine (SAM) as a precursor to organic radicals, generated by one-electron reduction of SAM and subsequent fission to form 5'-deoxyadenosyl radical and methionine, has been known for some time. Only recently, however, has it become apparent how widespread such enzymes are, and what a wide range of chemical reactions they catalyze. In the last few years several new SAM radical enzymes have been identified. Spectroscopic and kinetic investigations have begun to uncover the mechanism by which an iron sulfur cluster unique to these enzymes reduces SAM to generate adenosyl radical. Most recently, the first Xray structures of SAM radical enzymes, coproporphyrinogen-Ill oxidase, and biotin synthase have been solved, providing a structural framework within which to interpret mechanistic studies. (C) 2004 Elsevier Inc. All rights reserved.
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页码:326 / 340
页数:15
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