| Literature DB >> 18494460 |
Joseph A Ippolito1, Zoltan F Kanyo, Deping Wang, Francois J Franceschi, Peter B Moore, Thomas A Steitz, Erin M Duffy.
Abstract
The oxazolidinone antibacterials target the 50S subunit of prokaryotic ribosomes. To gain insight into their mechanism of action, the crystal structure of the canonical oxazolidinone, linezolid, has been determined bound to the Haloarcula marismortui 50S subunit. Linezolid binds the 50S A-site, near the catalytic center, which suggests that inhibition involves competition with incoming A-site substrates. These results provide a structural basis for the discovery of improved oxazolidinones active against emerging drug-resistant clinical strains.Entities:
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Year: 2008 PMID: 18494460 DOI: 10.1021/jm800379d
Source DB: PubMed Journal: J Med Chem ISSN: 0022-2623 Impact factor: 7.446