Identification of Bacteria-Selective Threonyl-tRNA Synthetase Substrate Inhibitors by Structure-Based Design

Author:

Teng Min1,Hilgers Mark T.1,Cunningham Mark L.1,Borchardt Allen1,Locke Jeffrey B.1,Abraham Sunny1,Haley Gregory1,Kwan Bryan P.1,Hall Courtney1,Hough Grayson W.1,Shaw Karen J.1,Finn John1

Affiliation:

1. Medicinal Chemistry, ‡Structural Biology, §Biology, and ∥Analytical Chemistry, Trius Therapeutics, Inc., 6310 Nancy Ridge Drive, San Diego, California 92121, United States

Publisher

American Chemical Society (ACS)

Subject

Drug Discovery,Molecular Medicine

Reference38 articles.

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3. Bacterial resistance to aminoglycoside antibiotics

4. aFinn, J.; Tao, J.InAminoacyl-tRNA Synthetase as Drug Targets in Aminoacyl-tRNA Synthetases;Ibba, M., Ed.Landes BioScience Press:Georgetown, TX, 2004; pp405–413.

5. Nanomolar Inhibitors of Staphylococcus aureus Methionyl tRNA Synthetase with Potent Antibacterial Activity against Gram-Positive Pathogens

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