| Literature DB >> 31591036 |
Aaron P Landry1, Sojin Moon1, Hanseong Kim1, Pramod K Yadav1, Arkajit Guha1, Uhn-Soo Cho2, Ruma Banerjee3.
Abstract
Mitochondrial sulfide quinone oxidoreductase (SQR) catalyzes the oxidation of H2S to glutathione persulfide with concomitant reduction of CoQ10. We report herein that the promiscuous activity of human SQR supported the conversion of CoA to CoA-SSH (CoA-persulfide), a potent inhibitor of butyryl-CoA dehydrogenase, and revealed a molecular link between sulfide and butyrate metabolism, which are known to interact. Three different CoQ1-bound crystal structures furnished insights into how diverse substrates access human SQR, and provided snapshots of the reaction coordinate. Unexpectedly, the active site cysteines in SQR are configured in a bridging trisulfide at the start and end of the catalytic cycle, and the presence of sulfane sulfur was confirmed biochemically. Importantly, our study leads to a mechanistic proposal for human SQR in which sulfide addition to the trisulfide cofactor eliminates 201Cys-SSH, forming an intense charge-transfer complex with flavin adenine dinucleotide, and 379Cys-SSH, which transfers sulfur to an external acceptor.Entities:
Keywords: butyrate; coenzyme Q; crystal structure; enzyme kinetics; flavin; hydrogen sulfide
Year: 2019 PMID: 31591036 PMCID: PMC6906606 DOI: 10.1016/j.chembiol.2019.09.010
Source DB: PubMed Journal: Cell Chem Biol ISSN: 2451-9448 Impact factor: 8.116