1h2a

From Proteopedia

proteopedia linkproteopedia link

spinqualitylabelsall models 1h2a, resolution 1.8Å Show:Asymmetric Unit Biological Assembly Drag the structure with the mouse to rotate   Export Animated Image

SINGLE CRYSTALS OF HYDROGENASE FROM DESULFOVIBRIO VULGARIS

Overview

BACKGROUND: The hydrogenase of Desulfovibrio sp. catalyzes the reversible, oxidoreduction of molecular hydrogen, in conjunction with a specific, electron acceptor, cytochrome c3. The Ni-Fe active center of Desulfovibrio, hydrogenase has an unusual ligand structure with non-protein ligands. An, atomic model at high resolution is required to make concrete assignment of, the ligands which coordinate the Ni-Fe center. These in turn will provide, insight into the mechanism of electron transfer, during the reaction, catalysed by hydrogenase. RESULTS: The X-ray structure of the hydrogenase, from Desulfovibrio vulgaris Miyazaki has been solved at 1.8 A resolution, and refined to a crystallographic R factor of 0.229. The overall folding, pattern and the spatial arrangement of the metal centers are very similar, to those found in Desulfovibrio gigas hydrogenase. This high resolution, crystal structure enabled us to assign the non-protein ligands to the Fe, atom in the Ni-Fe site and revealed the presence of a Mg center, located, approximately 13 A from the Ni-Fe active center. CONCLUSIONS: From the, nature of the electron-density map, stereochemical geometry and atomic, parameters of the refined structure, the most probable candidates for the, four ligands, coordinating the Ni-Fe center, have been proposed to be, diatomic S=O, C triple bond O and C triple bond N molecules and one sulfur, atom. The assignment was supported by pyrolysis mass spectrometry, measurements. These ligands may have a role as an electron sink during the, electron transfer reaction between the hydrogenase and its biological, counterparts, and they could stabilize the redox state of Fe(II), which, may not change during the catalytic cycle and is independent of the redox, transition of the Ni. The hydrogen-bonding system between the Ni-Fe and, the Mg centers suggests the possible.

About this Structure

1H2A is a Protein complex structure of sequences from Desulfovibrio vulgaris with MG, SF4, F3S and NFE as ligands. Active as Ferredoxin hydrogenase, with EC number 1.12.7.2 Full crystallographic information is available from OCA.

Reference

Unusual ligand structure in Ni-Fe active center and an additional Mg site in hydrogenase revealed by high resolution X-ray structure analysis., Higuchi Y, Yagi T, Yasuoka N, Structure. 1997 Dec 15;5(12):1671-80. PMID:9438867

Page seeded by OCA on Tue Nov 20 16:23:38 2007