Literature DB >> 17291766

S-adenosylmethionine as an oxidant: the radical SAM superfamily.

Susan C Wang1, Perry A Frey.   

Abstract

A recently discovered superfamily of enzymes function using chemically novel mechanisms, in which S-adenosylmethionine (SAM) serves as an oxidizing agent in DNA repair and the biosynthesis of vitamins, coenzymes and antibiotics. Members of this superfamily, the radical SAM enzymes, are related by the cysteine motif CxxxCxxC, which nucleates the [4Fe-4S] cluster found in each. A common thread in the novel chemistry of these proteins is the use of a strong reducing agent--a low-potential [4Fe-4S](1+) cluster--to generate a powerful oxidizing agent, the 5'-deoxyadenosyl radical, from SAM. Recent results are beginning to determine the unique biochemistry for some of the radical SAM enzymes, for example, lysine 2,3 aminomutase, pyruvate formate lyase activase and biotin synthase.

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Year:  2007        PMID: 17291766     DOI: 10.1016/j.tibs.2007.01.002

Source DB:  PubMed          Journal:  Trends Biochem Sci        ISSN: 0968-0004            Impact factor:   13.807


  58 in total

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Authors:  Abhishek Chatterjee; Yue Li; Yang Zhang; Tyler L Grove; Michael Lee; Carsten Krebs; Squire J Booker; Tadhg P Begley; Steven E Ealick
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Authors:  Squire J Booker
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Review 9.  Marine-derived metabolites of S-adenosylmethionine as templates for new anti-infectives.

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10.  Insights into the structure, function and evolution of the radical-SAM 23S rRNA methyltransferase Cfr that confers antibiotic resistance in bacteria.

Authors:  Katarzyna H Kaminska; Elzbieta Purta; Lykke H Hansen; Janusz M Bujnicki; Birte Vester; Katherine S Long
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