| Literature DB >> 12097137 |
Sophie Lanone1, Philippe Manivet, Jacques Callebert, Jean-Marie Launay, Didier Payen, Michel Aubier, Jorge Boczkowski, Alexandre Mebazaa.
Abstract
Tyrosine nitration is a post-translational protein modification with potentially significant biological implications. In the present study we demonstrate, for the first time, that tyrosine residues of human inducible nitric oxide synthase (NOS2) can be nitrated by peroxynitrite in vitro, leading to a decreased activity. Moreover, we show that NOS2 expressed in a skeletal muscle from septic patients is nitrated on selective tyrosine residues belonging to a canonic sequence. This phenomenon could be an endogenous mechanism of in vivo modulation of NOS2 enzymic activity.Entities:
Mesh:
Substances:
Year: 2002 PMID: 12097137 PMCID: PMC1222810 DOI: 10.1042/BJ20020339
Source DB: PubMed Journal: Biochem J ISSN: 0264-6021 Impact factor: 3.857