Volbeda A, Charon M H, Piras C, Hatchikian E C, Frey M, Fontecilla-Camps J C
Laboratoire de Cristallographie et de Cristallogénèse des Protéines, Institut de Biologie Structurale J. P. Ebel (CEA, CNRS), Grenoble, France.
Nature. 1995 Feb 16;373(6515):580-7. doi: 10.1038/373580a0.
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.
来自巨大脱硫弧菌的异二聚体镍铁氢化酶的X射线结构已在2.85埃分辨率下解析出来,该酶负责分子氢的代谢。活性位点除了镍之外似乎还含有第二种金属离子,它埋藏在60K亚基中。28K亚基配位一个[3铁-4硫]和两个[4铁-4硫]簇,包含一个与氧化还原蛋白黄素氧还蛋白相似的氨基末端结构域。该结构表明了合理的电子和质子转移途径。