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1YQW

Structure of the Oxidized Unready Form of Ni-Fe Hydrogenase

Summary for 1YQW
Entry DOI10.2210/pdb1yqw/pdb
Related1FRF 1YRQ
DescriptorPeriplasmic [NiFe] hydrogenase small subunit, CARBONMONOXIDE-(DICYANO) IRON, PEROXIDE ION, ... (12 entities in total)
Functional Keywordsni-fe hydrogenase unready state, oxidoreductase
Biological sourceDesulfovibrio fructosovorans
More
Total number of polymer chains6
Total formula weight269725.91
Authors
Volbeda, A. (deposition date: 2005-02-02, release date: 2005-04-19, Last modification date: 2024-10-30)
Primary citationVolbeda, A.,Martin, L.,Cavazza, C.,Matho, M.,Faber, B.W.,Roseboom, W.,Albracht, S.P.,Garcin, E.,Rousset, M.,Fontecilla-Camps, J.C.
Structural differences between the ready and unready oxidized states of [NiFe] hydrogenases.
J.Biol.Inorg.Chem., 10:239-249, 2005
Cited by
PubMed Abstract: [NiFe] hydrogenases catalyze the reversible heterolytic cleavage of molecular hydrogen. Several oxidized, inactive states of these enzymes are known that are distinguishable by their very different activation properties. So far, the structural basis for this difference has not been understood because of lack of relevant crystallographic data. Here, we present the crystal structure of the ready Ni-B state of Desulfovibrio fructosovorans [NiFe] hydrogenase and show it to have a putative mu-hydroxo Ni-Fe bridging ligand at the active site. On the other hand, a new, improved refinement procedure of the X-ray diffraction data obtained for putative unready Ni-A/Ni-SU states resulted in a more elongated electron density for the bridging ligand, suggesting that it is a diatomic species. The slow activation of the Ni-A state, compared with the rapid activation of the Ni-B state, is therefore proposed to result from the different chemical nature of the ligands in the two oxidized species. Our results along with very recent electrochemical studies suggest that the diatomic ligand could be hydro-peroxide.
PubMed: 15803334
DOI: 10.1007/s00775-005-0632-x
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.83 Å)
Structure validation

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数据于2024-11-13公开中

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