Crystal structure of biotin synthase, an S-adenosylmethionine-dependent radical enzyme

被引:338
作者
Berkovitch, F
Nicolet, Y
Wan, JT
Jarrett, JT
Drennan, CL [1 ]
机构
[1] MIT, Dept Chem, Cambridge, MA 02139 USA
[2] Univ Penn, Dept Biochem & Biophys, Philadelphia, PA 19104 USA
[3] Univ Penn, Johnson Res Fdn, Philadelphia, PA 19104 USA
关键词
D O I
10.1126/science.1088493
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The crystal structure of biotin synthase from Escherichia coli in complex with S-adenosyl-L-methionine and dethiobiotin has been determined to 3.4 angstrom resolution. This structure addresses how "AdoMet radical" or "radical SAM" enzymes use Fe4S4 clusters and S-adenosyl-L-methionine to generate organic radicals. Biotin synthase catalyzes the radical-mediated insertion of sulfur into dethiobiotin to form biotin. The structure places the substrates between the Fe4S4 cluster, essential for radical generation, and the Fe2S2 cluster, postulated to be the source of sulfur, with both clusters in unprecedented coordination environments.
引用
收藏
页码:76 / 79
页数:4
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