| Literature DB >> 24972661 |
Joan B Broderick1, Amanda S Byer, Kaitlin S Duschene, Benjamin R Duffus, Jeremiah N Betz, Eric M Shepard, John W Peters.
Abstract
The organometallic H-cluster at the active site of the [FeFe]-hydrogenase serves as the site of reversible binding and reduction of protons to produce H2. The H-cluster is unique in biology, and consists of a 2Fe subcluster tethered to a typical [4Fe-4S] cluster by a single cysteine ligand. The remaining ligands to the 2Fe subcluster include three carbon monoxides, two cyanides, and a dithiomethylamine. This mini-review will focus on the significant advances in recent years in understanding the pathway for H-cluster biosynthesis, as well as the structures, roles, and mechanisms of the three enzymes directly involved.Entities:
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Year: 2014 PMID: 24972661 DOI: 10.1007/s00775-014-1168-8
Source DB: PubMed Journal: J Biol Inorg Chem ISSN: 0949-8257 Impact factor: 3.358