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Uridine-based inhibitors as new leads for antibiotics targeting E. coli LpxC

The UDP-3-O-(R-3-hydroxyacyl)-N-acetylglucosamine deacetylase LpxC catalyzes the committed reaction of lipid A (endotoxin) biosynthesis in Gram-negative bacteria and is a validated antibiotic target. Although several previously described compounds bind to the unique acyl chain binding passage of Lpx...

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Bibliografski detalji
Glavni autori: Barb, Adam W., Leavy, Tanya M., Robins, Lori I., Guan, Ziqiang, Six, David A., Zhou, Pei, Bertozzi, Carolyn R., Raetz, Christian R.H.
Format: Artigo
Jezik:Inglês
Izdano: 2009
Teme:
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC2709817/
https://ncbi.nlm.nih.gov/pubmed/19256534
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1021/bi900167q
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