| Literature DB >> 27382049 |
Christina M Gregg1, Sebastian Goetzl1, Jae-Hun Jeoung1, Holger Dobbek2.
Abstract
Acetyl-CoA synthase (ACS) catalyzes the reversible condensation of CO, CoA, and a methyl-cation to form acetyl-CoA at a unique Ni,Ni-[4Fe4S] cluster (the A-cluster). However, it was unknown which proteins support the assembly of the A-cluster. We analyzed the product of a gene from the cluster containing the ACS gene, cooC2 from Carboxydothermus hydrogenoformans, named AcsFCh, and showed that it acts as a maturation factor of ACS. AcsFCh and inactive ACS form a stable 2:1 complex that binds two nickel ions with higher affinity than the individual components. The nickel-bound ACS-AcsFCh complex remains inactive until MgATP is added, thereby converting inactive to active ACS. AcsFCh is a MinD-type ATPase and belongs to the CooC protein family, which can be divided into homologous subgroups. We propose that proteins of one subgroup are responsible for assembling the Ni,Ni-[4Fe4S] cluster of ACS, whereas proteins of a second subgroup mature the [Ni4Fe4S] cluster of carbon monoxide dehydrogenases.Entities:
Keywords: ATPase; biosynthesis; iron-sulfur protein; metal ion-protein interaction; metalloenzyme; nickel
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Year: 2016 PMID: 27382049 PMCID: PMC5000062 DOI: 10.1074/jbc.M116.731638
Source DB: PubMed Journal: J Biol Chem ISSN: 0021-9258 Impact factor: 5.157