| Literature DB >> 24958726 |
Cédric Eichmann1, Christos Tzitzilonis2, Enrica Bordignon1, Innokentiy Maslennikov3, Senyon Choe3, Roland Riek4.
Abstract
The solution NMR structure of the α-helical integral membrane protein YgaP from Escherichia coli in mixed 1,2-diheptanoyl-sn-glycerol-3-phosphocholine/1-myristoyl-2-hydroxy-sn-glycero-3-phospho-(1'-rac-glycerol) micelles is presented. In these micelles, YgaP forms a homodimer with the two transmembrane helices being the dimer interface, whereas the N-terminal cytoplasmic domain includes a rhodanese-fold in accordance to its sequence homology to the rhodanese family of sulfurtransferases. The enzymatic sulfur transfer activity of full-length YgaP as well as of the N-terminal rhodanese domain only was investigated performing a series of titrations with sodium thiosulfate and potassium cyanide monitored by NMR and EPR. The data indicate the thiosulfate concentration-dependent addition of several sulfur atoms to the catalytic Cys-63, which process can be reversed by the addition of potassium cyanide. The catalytic reaction induces thereby conformational changes within the rhodanese domain, as well as on the transmembrane α-helices of YgaP. These results provide insights into a potential mechanism of YgaP during the catalytic thiosulfate activity in vivo.Entities:
Keywords: Enzyme Catalysis; Membrane Enzyme; Membrane Protein; Nuclear Magnetic Resonance (NMR); Rhodanese; Structural Biology; Sulfotransferase; Sulfurtransferase; Three-dimensional Structure
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Year: 2014 PMID: 24958726 PMCID: PMC4156090 DOI: 10.1074/jbc.M114.571935
Source DB: PubMed Journal: J Biol Chem ISSN: 0021-9258 Impact factor: 5.157