| Literature DB >> 27473602 |
Cédric Eichmann1, Christos Tzitzilonis2, Tomohiro Nakamura3, Witek Kwiatkowski2, Innokentiy Maslennikov2, Senyon Choe2, Stuart A Lipton4, Roland Riek5.
Abstract
S-Nitrosylation is well established as an important post-translational regulator in protein function and signaling. However, relatively little is known about its structural and dynamical consequences. We have investigated the effects of S-nitrosylation on the rhodanese domain of the Escherichia coli integral membrane protein YgaP by NMR, X-ray crystallography, and mass spectrometry. The results show that the active cysteine in the rhodanese domain of YgaP is subjected to two competing modifications: S-nitrosylation and S-sulfhydration, which are naturally occurring in vivo. It has been observed that in addition to inhibition of the sulfur transfer activity, S-nitrosylation of the active site residue Cys63 causes an increase in slow motion and a displacement of helix 5 due to a weakening of the interaction between the active site and the helix dipole. These findings provide an example of how nitrosative stress can exert action at the atomic level.Entities:
Keywords: X-ray crystallography; mass spectrometry; nuclear magnetic resonance (NMR); post-translational modification; rhodanese
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Year: 2016 PMID: 27473602 PMCID: PMC5260856 DOI: 10.1016/j.jmb.2016.07.010
Source DB: PubMed Journal: J Mol Biol ISSN: 0022-2836 Impact factor: 5.469