| Literature DB >> 7854413 |
A Volbeda1, M H Charon, C Piras, E C Hatchikian, M Frey, J C Fontecilla-Camps.
Abstract
The X-ray structure of the heterodimeric Ni-Fe hydrogenase from Desulfovibrio gigas, the enzyme responsible for the metabolism of molecular hydrogen, has been solved at 2.85 A resolution. The active site, which appears to contain, besides nickel, a second metal ion, is buried in the 60K subunit. The 28K subunit, which coordinates one [3Fe-4S] and two [4Fe-4S] clusters, contains an amino-terminal domain with similarities to the redox protein flavodoxin. The structure suggests plausible electron and proton transfer pathways.Entities:
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Year: 1995 PMID: 7854413 DOI: 10.1038/373580a0
Source DB: PubMed Journal: Nature ISSN: 0028-0836 Impact factor: 49.962