7O7Z

Rabbit 80S ribosome stalled close to the mutated SARS-CoV-2 slippery site by a pseudoknot (classified for pseudoknot)

これはPDB形式変換不可エントリーです。

7O7Z の概要

• エントリーDOI: 10.2210/pdb7o7z/pdb
• EMDBエントリー: 12757
• 分子名称: 18S rRNA, E-site tRNA, P-site Phe-tRNA(Phe), ... (92 entities in total)
• 機能のキーワード: frameshift, virus, pseudoknot, ribosome
• 由来する生物種: Severe acute respiratory syndrome coronavirus 2 (2019-nCoV, SARS-CoV-2); 詳細
• タンパク質・核酸の鎖数: 86
• 化学式量合計: 4071783.04

構造登録者

Bhatt, P.R.,Scaiola, A.,Leibundgut, M.A.,Atkins, J.F.,Ban, N. (登録日: 2021-04-14, 公開日: 2021-06-02, 最終更新日: 2024-04-24)

主引用文献

Bhatt, P.R.,Scaiola, A.,Loughran, G.,Leibundgut, M.,Kratzel, A.,Meurs, R.,Dreos, R.,O'Connor, K.M.,McMillan, A.,Bode, J.W.,Thiel, V.,Gatfield, D.,Atkins, J.F.,Ban, N.
Structural basis of ribosomal frameshifting during translation of the SARS-CoV-2 RNA genome.
Science, 372:1306-1313, 2021

PubMed Abstract: Programmed ribosomal frameshifting is a key event during translation of the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) RNA genome that allows synthesis of the viral RNA-dependent RNA polymerase and downstream proteins. Here, we present the cryo-electron microscopy structure of a translating mammalian ribosome primed for frameshifting on the viral RNA. The viral RNA adopts a pseudoknot structure that lodges at the entry to the ribosomal messenger RNA (mRNA) channel to generate tension in the mRNA and promote frameshifting, whereas the nascent viral polyprotein forms distinct interactions with the ribosomal tunnel. Biochemical experiments validate the structural observations and reveal mechanistic and regulatory features that influence frameshifting efficiency. Finally, we compare compounds previously shown to reduce frameshifting with respect to their ability to inhibit SARS-CoV-2 replication, establishing coronavirus frameshifting as a target for antiviral intervention.

PubMed: 34029205
DOI: 10.1126/science.abf3546

実験手法

ELECTRON MICROSCOPY (2.4 Å)