| Literature DB >> 27471863 |
Molly A Silvers, Svetlana Pakhomova, David B Neau1,2, William C Silvers3, Nicholas Anzalone, Carol M Taylor, Grover L Waldrop.
Abstract
The dramatic increase in the prevalence of antibiotic-resistant bacteria has necessitated a search for new antiba<span class="Gene">cterial agents against novel targets. Moiramide B is a natural product, broad-spectrum antibiotic that inhibits the carboxyltransferase component of acetyl-CoA carboxylase, which catalyzes the first committed step in fatty acid synthesis. Herein, we report the 2.6 Å resolution crystal structure of moiramide B bound to carboxyltransferase. An unanticipated but significant finding was that moiramide B bound as the enol/enolate. Crystallographic studies demonstrate that the (4S)-methyl succinimide moiety interacts with the oxyanion holes of the enzyme, supporting the notion that an anionic enolate is the active form of the antibacterial agent. Structure-activity studies demonstrate that the unsaturated fatty acid tail of moiramide B is needed only for entry into the bacterial cell. These results will allow the design of new antibacterial agents against the bacterial form of carboxyltransferase.Entities:
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Year: 2016 PMID: 27471863 PMCID: PMC5226424 DOI: 10.1021/acs.biochem.6b00641
Source DB: PubMed Journal: Biochemistry ISSN: 0006-2960 Impact factor: 3.162