| Literature DB >> 15103135 |
Katherine A Kantardjieff1, Chang Yub Kim, Cleo Naranjo, Geoffry S Waldo, Timothy Lekin, Brent W Segelke, Adam Zemla, Min S Park, Thomas C Terwilliger, Bernhard Rupp.
Abstract
The Mycobacterium tuberculosis rmlC gene encodes dTDP-4-keto-6-deoxyglucose epimerase, the third enzyme in the M. tuberculosis dTDP-L-rhamnose pathway which is essential for mycobacterial cell-wall synthesis. Because it is structurally unique, highly substrate-specific and does not require a cofactor, RmlC is considered to be the most promising drug target in the pathway, and the M. tuberculosis rmlC gene was selected in the initial round of TB Structural Genomics Consortium targets for structure determination. The 1.7 A native structure determined by the consortium facilities is reported and implications for in silico screening of ligands for structure-guided drug design are discussed.Entities:
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Year: 2004 PMID: 15103135 DOI: 10.1107/S0907444904005323
Source DB: PubMed Journal: Acta Crystallogr D Biol Crystallogr ISSN: 0907-4449