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7BEF

Structures of class II bacterial transcription complexes

7BEF の概要
エントリーDOI10.2210/pdb7bef/pdb
EMDBエントリー12156
分子名称DNA-directed RNA polymerase subunit alpha, DNA-directed RNA polymerase subunit beta, DNA-directed RNA polymerase subunit beta', ... (8 entities in total)
機能のキーワードantibiotic resistance, bacterial transcription activator, cryoem, transcription
由来する生物種Escherichia coli (strain K12)
詳細
タンパク質・核酸の鎖数9
化学式量合計522474.51
構造登録者
Hao, M.,Ye, F.Z.,Zhang, X.D. (登録日: 2020-12-23, 公開日: 2021-12-01, 最終更新日: 2024-07-10)
主引用文献Hao, M.,Ye, F.,Jovanovic, M.,Kotta-Loizou, I.,Xu, Q.,Qin, X.,Buck, M.,Zhang, X.,Wang, M.
Structures of Class I and Class II Transcription Complexes Reveal the Molecular Basis of RamA-Dependent Transcription Activation.
Adv Sci, 9:e2103669-e2103669, 2022
Cited by
PubMed Abstract: Transcription activator RamA is linked to multidrug resistance of Klebsiella pneumoniae through controlling genes that encode efflux pumps (acrA) and porin-regulating antisense RNA (micF). In bacteria, σ , together with activators, controls the majority of genes by recruiting RNA polymerase (RNAP) to the promoter regions. RNAP and σ form a holoenzyme that recognizes -35 and -10 promoter DNA consensus sites. Many activators bind upstream from the holoenzyme and can be broadly divided into two classes. RamA acts as a class I activator on acrA and class II activator on micF, respectively. The authors present biochemical and structural data on RamA in complex with RNAP-σ at the two promoters and the data reveal the molecular basis for how RamA assembles and interacts with core RNAP and activates transcription that contributes to antibiotic resistance. Further, comparing with CAP/TAP complexes reveals common and activator-specific features in activator binding and uncovers distinct roles of the two C-terminal domains of RNAP α subunit.
PubMed: 34761556
DOI: 10.1002/advs.202103669
主引用文献が同じPDBエントリー
実験手法
ELECTRON MICROSCOPY (4.5 Å)
構造検証レポート
Validation report summary of 7bef
検証レポート(詳細版)ダウンロードをダウンロード

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件を2024-10-30に公開中

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