Structural variability of the active site of Fe-only hydrogenase and its hydrogenated forms

被引：24

作者：

Dance, I ^{[1
]}

机构：

[1] Univ New S Wales, Sch Chem, Sydney, NSW 2052, Australia

来源：

CHEMICAL COMMUNICATIONS | 1999年 / 17期

关键词：

D O I：

10.1039/a903803e

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

Density functional calculations show that the (cys-S)- (CO)(CN)FeS2(mu-CO)Fe(CO)(CN) active site of the Fe-only hydrogenase from Clostridium pasteurianum is redox ambivalent and stereochemically flexible at the CO and S bridges, and at the Fe atoms, and with bound hydrogen: the fundamentals of probable mechanisms are revealed.

引用

页码：1655 / 1656

页数：2

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