Structural basis for rifamycin resistance of bacterial RNA polymerase by the three most clinically important RpoB mutations found inMycobacterium tuberculosis-Reference-Cited by-同舟云学术

Structural basis for rifamycin resistance of bacterial RNA polymerase by the three most clinically important RpoB mutations found inMycobacterium tuberculosis

Published:2017-01-10 Issue:6 Volume:103 Page:1034-1045
ISSN:0950-382X
Container-title:Molecular Microbiology
language:en
Short-container-title:Molecular Microbiology

Author:

Molodtsov Vadim¹,Scharf Nathan T.²,Stefan Maxwell A.²,Garcia George A.²,Murakami Katsuhiko S.¹^ORCID

Affiliation:

1. Department of Biochemistry and Molecular Biology; The Center for RNA Molecular Biology, The Pennsylvania State University, University Park; PA 16802 USA

2. Department of Medicinal Chemistry, College of Pharmacy; University of Michigan; 428 Church St Ann Arbor MI 48109-1065 USA

Publisher

Wiley

Subject

Molecular Biology,Microbiology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/mmi.13606/fullpdf

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3. Rifamycins - Obstacles and Opportunities;Aristoff;Tuberculosis,2010

4. Allosteric modulation of the RNA polymerase catalytic reaction is an essential component of transcription control by rifamycins;Artsimovitch;Cell,2005

5. Phage T7 Gp2 inhibition of Escherichia coli RNA polymerase involves misappropriation of sigma70 domain 1.1;Bae;Proc Natl Acad Sci U S A,2013

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