藤黄固氮菌
固氮酶
化学
蛋白质亚单位
ATP水解
结晶学
核苷酸
生物化学
固氮
立体化学
ATP酶
酶
氮气
有机化学
基因
作者
Millie M. Georgiadis,H. Komiya,Pinak Chakrabarti,D. Woo,J. J. Kornuc,Douglas C. Rees
出处
期刊:Science
[American Association for the Advancement of Science (AAAS)]
日期:1992-09-18
卷期号:257 (5077): 1653-1659
被引量:665
标识
DOI:10.1126/science.1529353
摘要
The nitrogenase enzyme system catalyzes the ATP (adenosine triphosphate)-dependent reduction of dinitrogen to ammonia during the process of nitrogen fixation. Nitrogenase consists of two proteins: the iron (Fe)-protein, which couples hydrolysis of ATP to electron transfer, and the molybdenum-iron (MoFe)-protein, which contains the dinitrogen binding site. In order to address the role of ATP in nitrogen fixation, the crystal structure of the nitrogenase Fe-protein from Azotobacter vinelandii has been determined at 2.9 angstrom (Å) resolution. Fe-protein is a dimer of two identical subunits that coordinate a single 4Fe:4S cluster. Each subunit folds as a single α/β type domain, which together symmetrically ligate the surface exposed 4Fe:4S cluster through two cysteines from each subunit. A single bound ADP (adenosine diphosphate) molecule is located in the interface region between the two subunits. Because the phosphate groups of this nucleotide are ∼20 Å from the 4Fe:4S cluster, it is unlikely that ATP hydrolysis and electron transfer are directly coupled. Instead, it appears that interactions between the nucleotide and cluster sites must be indirectly coupled by allosteric changes occurring at the subunit interface. The coupling between protein conformation and nucleotide hydrolysis in Fe-protein exhibits general similarities to the H-Ras p21 and recA proteins that have been recently characterized structurally. The Fe-protein structure may be relevant to the functioning of other biochemical energy-transducing systems containing two nucleotide-binding sites, including membrane transport proteins.
科研通智能强力驱动
Strongly Powered by AbleSci AI