| Literature DB >> 27158836 |
Nathan A Bruender1, Vahe Bandarian1.
Abstract
Ribosomally synthesized post-translationally modified peptides (RiPPs) are encoded in the genomes of a wide variety of microorganisms, in the proximity of open reading frames that encode enzymes that conduct extensive modifications, many of which are novel. Recently, members of the radical S-adenosyl-l-methionine (SAM) superfamily have been identified in these biosynthetic clusters. Herein, we demonstrate the putative radical SAM enzyme, MftC, oxidatively decarboxylates the C-terminus of the MftA peptide in the presence of the accessory protein MftB. The reaction catalyzed by MftC expands the repertoire of peptide-based radical SAM chemistry beyond the intramolecular cross-links.Entities:
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Year: 2016 PMID: 27158836 PMCID: PMC5331333 DOI: 10.1021/acs.biochem.6b00355
Source DB: PubMed Journal: Biochemistry ISSN: 0006-2960 Impact factor: 3.162