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PMID: 7854413 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Crystal structure of the nickel-iron hydrogenase from Desulfovibrio gigas.

Nature ·Vol. 373 ·No. 6515 ·1995-02-16 ·Pages 580-7

Volbeda A, Charon MH, Piras C, Hatchikian EC, Frey M, Fontecilla-Camps JC

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.

MeSH Terms
Amino Acid Sequence Binding Sites Computer Graphics Crystallography, X-Ray Desulfovibrio/enzymology Electron Transport Hydrogenase/chemistry,metabolism Iron/chemistry Iron-Sulfur Proteins/chemistry Molecular Sequence Data Nickel/chemistry Protein Conformation Protein Processing, Post-Translational Protons
Chemicals
Iron-Sulfur Proteins Protons Nickel Iron nickel-iron hydrogenase Hydrogenase
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Volbeda A
Laboratoire de Cristallographie et de Cristallogénèse des Protéines, Institut de Biologie Structurale J. P. Ebel (CEA, CNRS), Grenoble, France.
Charon M H
Piras C
Hatchikian E C
Frey M
Fontecilla-Camps J C
Article Info
Journal
Nature
Abbr.
Nature
ISSN
0028-0836
Published
1995-02-16
Pages
580-7
Language
English
Region
England
NLM ID
0410462
Subset
IM
Corrections
CommentIn
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