期刊
NATURE CHEMICAL BIOLOGY
卷 3, 期 6, 页码 323-324出版社
NATURE PUBLISHING GROUP
DOI: 10.1038/nchembio884
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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.
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