| Literature DB >> 7048060 |
M Brufani, L Cellai, S Cerrini, W Fedeli, A Segre, A Vaciago.
Abstract
The X-ray and NMR structural study of 3-carbomethoxy rifamycin S5 was undertaken in order to determine whether its low antimicrobial activity was related to a conformation of the molecule which was unfavorable for interaction with bacterial DNA-dependent RNA polymerase. However, the molecule assumes a conformation similar to that of the active rifamycins. Indeed the compound was found to be active on the isolated enzyme, so that its low activity on whole bacteria has to be attributed to factors affecting its penetration through the bacterial cell wall.Entities:
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Year: 1982 PMID: 7048060
Source DB: PubMed Journal: Mol Pharmacol ISSN: 0026-895X Impact factor: 4.436