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The methylthiolation reaction mediated by the Radical-SAM enzymes.
Atta, Mohamed; Arragain, Simon; Fontecave, Marc; Mulliez, Etienne; Hunt, John F; Luff, Jon D; Forouhar, Farhad.
Afiliação
  • Atta M; Institut de Recherches en Technologie et Sciences pour le Vivant IRTSV-LCBM, UMR 5249 CEA/CNRS/UJF, CEA-Grenoble, 17 avenue des Martyrs, 38054, Grenoble Cedex 09, France. mohamed.atta@cea.fr
Biochim Biophys Acta ; 1824(11): 1223-30, 2012 Nov.
Article em En | MEDLINE | ID: mdl-22178611
Over the past 10 years, considerable progress has been made in our understanding of the mechanistic enzymology of the Radical-SAM enzymes. It is now clear that these enzymes appear to be involved in a remarkably wide range of chemically challenging reactions. This review article highlights mechanistic and structural aspects of the methylthiotransferases (MTTases) sub-class of the Radical-SAM enzymes. The mechanism of methylthio insertion, now observed to be performed by three different enzymes is an exciting unsolved problem. This article is part of a Special Issue entitled: Radical SAM enzymes and Radical Enzymology.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: S-Adenosilmetionina / Sulfurtransferases / Proteínas Ferro-Enxofre / Metiltransferases Idioma: En Ano de publicação: 2012 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: S-Adenosilmetionina / Sulfurtransferases / Proteínas Ferro-Enxofre / Metiltransferases Idioma: En Ano de publicação: 2012 Tipo de documento: Article