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6VWL

70S ribosome bound to HIV frameshifting stem-loop (FSS) and P/E tRNA (rotated conformation)

これはPDB形式変換不可エントリーです。
6VWL の概要
エントリーDOI10.2210/pdb6vwl/pdb
EMDBエントリー21420
分子名称50S ribosomal protein L2, 50S ribosomal protein L16, 50S ribosomal protein L17, ... (54 entities in total)
機能のキーワードhiv fss, frameshifting, ribosome
由来する生物種Escherichia coli
詳細
タンパク質・核酸の鎖数53
化学式量合計2186735.14
構造登録者
Loerch, S.,Bao, C.,Ling, C.,Korostelev, A.A.,Grigorieff, N.,Ermolenko, D.M. (登録日: 2020-02-20, 公開日: 2020-06-03, 最終更新日: 2024-10-23)
主引用文献Bao, C.,Loerch, S.,Ling, C.,Korostelev, A.A.,Grigorieff, N.,Ermolenko, D.N.
mRNA stem-loops can pause the ribosome by hindering A-site tRNA binding.
Elife, 9:-, 2020
Cited by
PubMed Abstract: Although the elongating ribosome is an efficient helicase, certain mRNA stem-loop structures are known to impede ribosome movement along mRNA and stimulate programmed ribosome frameshifting via mechanisms that are not well understood. Using biochemical and single-molecule Förster resonance energy transfer (smFRET) experiments, we studied how frameshift-inducing stem-loops from mRNA and the transcript of Human Immunodeficiency Virus (HIV) perturb translation elongation. We find that upon encountering the ribosome, the stem-loops strongly inhibit A-site tRNA binding and ribosome intersubunit rotation that accompanies translation elongation. Electron cryo-microscopy (cryo-EM) reveals that the HIV stem-loop docks into the A site of the ribosome. Our results suggest that mRNA stem-loops can transiently escape the ribosome helicase by binding to the A site. Thus, the stem-loops can modulate gene expression by sterically hindering tRNA binding and inhibiting translation elongation.
PubMed: 32427100
DOI: 10.7554/eLife.55799
主引用文献が同じPDBエントリー
実験手法
ELECTRON MICROSCOPY (3.1 Å)
構造検証レポート
Validation report summary of 6vwl
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2026-04-15に公開中

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