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5UH6

Crystal structure of Mycobacterium tuberculosis transcription initiation complex containing 2ntRNA in complex with Rifampin

Summary for 5UH6
Entry DOI10.2210/pdb5uh6/pdb
Related5UH7 5UH8 5UHA 5UHB 5UHC 5UHD 5UHE 5UHF 5UHG
DescriptorDNA-directed RNA polymerase subunit alpha, ZINC ION, MAGNESIUM ION, ... (11 entities in total)
Functional Keywordsrna polymerase complex, transcription, dna, rna, transcription-dna-rna complex, transcription-dna-rna-antibiotic complex, transcription/dna/rna/antibiotic
Biological sourceMycobacterium tuberculosis (strain ATCC 25618 / H37Rv)
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Cellular locationCytoplasm : P9WGI1
Total number of polymer chains9
Total formula weight435874.08
Authors
Lin, W.,Das, K.,Feng, Y.,Ebright, R.H. (deposition date: 2017-01-11, release date: 2017-04-12, Last modification date: 2017-11-22)
Primary citationLin, W.,Mandal, S.,Degen, D.,Liu, Y.,Ebright, Y.W.,Li, S.,Feng, Y.,Zhang, Y.,Mandal, S.,Jiang, Y.,Liu, S.,Gigliotti, M.,Talaue, M.,Connell, N.,Das, K.,Arnold, E.,Ebright, R.H.
Structural Basis of Mycobacterium tuberculosis Transcription and Transcription Inhibition.
Mol. Cell, 66:169-179.e8, 2017
Cited by
PubMed Abstract: Mycobacterium tuberculosis (Mtb) is the causative agent of tuberculosis, which kills 1.8 million annually. Mtb RNA polymerase (RNAP) is the target of the first-line antituberculosis drug rifampin (Rif). We report crystal structures of Mtb RNAP, alone and in complex with Rif, at 3.8-4.4 Å resolution. The results identify an Mtb-specific structural module of Mtb RNAP and establish that Rif functions by a steric-occlusion mechanism that prevents extension of RNA. We also report non-Rif-related compounds-Nα-aroyl-N-aryl-phenylalaninamides (AAPs)-that potently and selectively inhibit Mtb RNAP and Mtb growth, and we report crystal structures of Mtb RNAP in complex with AAPs. AAPs bind to a different site on Mtb RNAP than Rif, exhibit no cross-resistance with Rif, function additively when co-administered with Rif, and suppress resistance emergence when co-administered with Rif.
PubMed: 28392175
DOI: 10.1016/j.molcel.2017.03.001
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (3.837 Å)
Structure validation

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數據於2024-11-06公開中

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