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8BF9

Molecular view of ER membrane remodeling by the Sec61/TRAP translocon.

8BF9 の概要
エントリーDOI10.2210/pdb8bf9/pdb
EMDBエントリー16017
分子名称RNA (1766), Ribosomal protein L23/L25 N-terminal domain-containing protein, RL26 protein (Fragment), ... (19 entities in total)
機能のキーワードmembrane protein, protein translocation, protein biogenesis., transport protein
由来する生物種Ovis aries
詳細
タンパク質・核酸の鎖数19
化学式量合計1548686.85
構造登録者
Karki, S.,Javanainen, M.,Tranter, D.,Rehan, S.,Huiskonen, J.,Happonen, L.,Paavilainen, V. (登録日: 2022-10-24, 公開日: 2023-11-01, 最終更新日: 2025-07-02)
主引用文献Karki, S.,Javanainen, M.,Rehan, S.,Tranter, D.,Kellosalo, J.,Huiskonen, J.T.,Happonen, L.,Paavilainen, V.
Molecular view of ER membrane remodeling by the Sec61/TRAP translocon.
Embo Rep., 24:e57910-e57910, 2023
Cited by
PubMed Abstract: Protein translocation across the endoplasmic reticulum (ER) membrane is an essential step during protein entry into the secretory pathway. The conserved Sec61 protein-conducting channel facilitates polypeptide translocation and coordinates cotranslational polypeptide-processing events. In cells, the majority of Sec61 is stably associated with a heterotetrameric membrane protein complex, the translocon-associated protein complex (TRAP), yet the mechanism by which TRAP assists in polypeptide translocation remains unknown. Here, we present the structure of the core Sec61/TRAP complex bound to a mammalian ribosome by cryogenic electron microscopy (cryo-EM). Ribosome interactions anchor the Sec61/TRAP complex in a conformation that renders the ER membrane locally thinner by significantly curving its lumenal leaflet. We propose that TRAP stabilizes the ribosome exit tunnel to assist nascent polypeptide insertion through Sec61 and provides a ratcheting mechanism into the ER lumen mediated by direct polypeptide interactions.
PubMed: 37983950
DOI: 10.15252/embr.202357910
主引用文献が同じPDBエントリー
実験手法
ELECTRON MICROSCOPY (2.69 Å)
構造検証レポート
Validation report summary of 8bf9
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2026-01-28に公開中

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