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Nat Chem Biol ; 3(6): 323-4, 2007 Jun.
Article in English | MEDLINE | ID: mdl-17496888

ABSTRACT

The diarylquinoline R207910 (TMC207) is a promising candidate in clinical development for the treatment of tuberculosis. Though R207910-resistant mycobacteria bear mutations in ATP synthase, the compound's precise target is not known. Here we establish by genetic, biochemical and binding assays that the oligomeric subunit c (AtpE) of ATP synthase is the target of R207910. Thus targeting energy metabolism is a new, promising approach for antibacterial drug discovery.


Subject(s)
ATP Synthetase Complexes/metabolism , Antitubercular Agents/pharmacology , Quinolines/pharmacology , ATP Synthetase Complexes/chemistry , ATP Synthetase Complexes/drug effects , Bacterial Proteins/chemistry , Bacterial Proteins/drug effects , Bacterial Proteins/metabolism , Bacterial Proton-Translocating ATPases , Binding Sites , Diarylquinolines , Electrophoresis, Gel, Two-Dimensional , Kinetics , Mycobacterium smegmatis/drug effects , Mycobacterium smegmatis/enzymology , Protein Subunits/drug effects , Protein Subunits/isolation & purification , Protein Subunits/metabolism
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