9NKF

Structure of human substrate-free 26S proteasome in the presence of ATPgS and MG-132,SA-like state (composite map)

これはPDB形式変換不可エントリーです。

9NKF の概要

• エントリーDOI: 10.2210/pdb9nkf/pdb
• EMDBエントリー: 49507
• 分子名称: 26S proteasome regulatory subunit 7, Proteasome subunit alpha type-5, Proteasome subunit alpha type-1, ... (37 entities in total)
• 機能のキーワード: apo state, proteasome, midnolin, substrate-free 26s, mg-132, immune system
• 由来する生物種: Homo sapiens (human); 詳細
• タンパク質・核酸の鎖数: 46
• 化学式量合計: 1670602.65

構造登録者

Peddada, N.,Beutler, B. (登録日: 2025-02-28, 公開日: 2025-05-07, 最終更新日: 2025-05-21)

主引用文献

Peddada, N.,Zhong, X.,Yin, Y.,Lazaro, D.R.,Wang, J.,Lyon, S.,Choi, J.H.,Bai, X.C.,Moresco, E.M.Y.,Beutler, B.
Structural insights into the ubiquitin-independent midnolin-proteasome pathway.
Proc.Natl.Acad.Sci.USA, 122:e2505345122-e2505345122, 2025

PubMed Abstract: The protein midnolin (MIDN) augments proteasome activity in lymphocytes and dramatically facilitates the survival and proliferation of B-lymphoid malignancies. MIDN binds both to proteasomes and to substrates, but the mode of interaction with the proteasome is unknown, and the mechanism by which MIDN facilitates substrate degradation in a ubiquitin-independent manner is incompletely understood. Here, we present cryoelectron microscopy (cryo-EM) structures of the substrate-engaged, MIDN-bound human proteasome in two conformational states. MIDN induces proteasome conformations similarly to ubiquitinated substrates by using its ubiquitin-like domain to bind to the deubiquitinase RPN11 (PSMD14). By simultaneously binding to RPN1 (PSMD2) with its C-terminal α-helix, MIDN positions its substrate-carrying Catch domain above the proteasome ATPase channel through which substrates are translocated before degradation. Our findings suggest that both ubiquitin-like domain and C-terminal α-helix must bind to the proteasome for MIDN to stimulate proteasome activity.

PubMed: 40339123
DOI: 10.1073/pnas.2505345122

実験手法

ELECTRON MICROSCOPY (2.9 Å)