Literature DB >> 26540123

SAM/SAH Analogs as Versatile Tools for SAM-Dependent Methyltransferases.

Jing Zhang1, Yujun George Zheng1.   

Abstract

S-Adenosyl-L-methionine (SAM) is a sulfonium molecule with a structural hybrid of methionine and adenosine. As the second largest cofactor in the human body, its major function is to serve as methyl donor for SAM-dependent methyltransferases (MTases). The resultant transmethylation of biomolecules constitutes a significant biochemical mechanism in epigenetic regulation, cellular signaling, and metabolite degradation. Recently, numerous SAM analogs have been developed as synthetic cofactors to transfer the activated groups on MTase substrates for downstream ligation and identification. Meanwhile, new compounds built upon or derived from the SAM scaffold have been designed and tested as selective inhibitors for important MTase targets. Here, we summarized the recent development and application of SAM analogs as chemical biology tools for MTases.

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Year:  2015        PMID: 26540123      PMCID: PMC5772741          DOI: 10.1021/acschembio.5b00812

Source DB:  PubMed          Journal:  ACS Chem Biol        ISSN: 1554-8929            Impact factor:   5.100


  133 in total

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5.  [New syntheses of S-adenosyl homocysteine analogues, potential methyltransferase inhibitors].

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