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6RIC

Structure of the core Vaccinia Virus DNA-dependent RNA polymerase complex

6RIC の概要
エントリーDOI10.2210/pdb6ric/pdb
関連するPDBエントリー6RFL 6RID 6RIE
EMDBエントリー4868 4888
分子名称DNA-dependent RNA polymerase subunit rpo147, MAGNESIUM ION, ZINC ION, ... (11 entities in total)
機能のキーワードvaccinia, rna polymerase, transcription, gene expression, viral protein
由来する生物種Vaccinia virus GLV-1h68
詳細
タンパク質・核酸の鎖数9
化学式量合計505343.91
構造登録者
主引用文献Hillen, H.S.,Bartuli, J.,Grimm, C.,Dienemann, C.,Bedenk, K.,Szalay, A.A.,Fischer, U.,Cramer, P.
Structural Basis of Poxvirus Transcription: Transcribing and Capping Vaccinia Complexes.
Cell, 179:1525-, 2019
Cited by
PubMed Abstract: Poxviruses use virus-encoded multisubunit RNA polymerases (vRNAPs) and RNA-processing factors to generate mG-capped mRNAs in the host cytoplasm. In the accompanying paper, we report structures of core and complete vRNAP complexes of the prototypic Vaccinia poxvirus (Grimm et al., 2019; in this issue of Cell). Here, we present the cryo-electron microscopy (cryo-EM) structures of Vaccinia vRNAP in the form of a transcribing elongation complex and in the form of a co-transcriptional capping complex that contains the viral capping enzyme (CE). The trifunctional CE forms two mobile modules that bind the polymerase surface around the RNA exit tunnel. RNA extends from the vRNAP active site through this tunnel and into the active site of the CE triphosphatase. Structural comparisons suggest that growing RNA triggers large-scale rearrangements on the surface of the transcription machinery during the transition from transcription initiation to RNA capping and elongation. Our structures unravel the basis for synthesis and co-transcriptional modification of poxvirus RNA.
PubMed: 31835031
DOI: 10.1016/j.cell.2019.11.023
主引用文献が同じPDBエントリー
実験手法
ELECTRON MICROSCOPY (2.8 Å)
構造検証レポート
Validation report summary of 6ric
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2025-12-31に公開中

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