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3PHD

Crystal structure of human HDAC6 in complex with ubiquitin

3PHD の概要
エントリーDOI10.2210/pdb3phd/pdb
関連するPDBエントリー2ZNV 3C5K 3GV4 3NHE
分子名称Histone deacetylase 6, Polyubiquitin, ZINC ION, ... (4 entities in total)
機能のキーワードhdac6, ubiquitin, structural genomics, structural genomics consortium, sgc, protein binding
由来する生物種Homo sapiens (human)
詳細
細胞内の位置Nucleus: Q9UBN7
タンパク質・核酸の鎖数8
化学式量合計83187.19
構造登録者
主引用文献Ouyang, H.,Ali, Y.O.,Ravichandran, M.,Dong, A.,Qiu, W.,Mackenzie, F.,Dhe-Paganon, S.,Arrowsmith, C.H.,Zhai, R.G.
Protein Aggregates Are Recruited to Aggresome by Histone Deacetylase 6 via Unanchored Ubiquitin C Termini.
J.Biol.Chem., 287:2317-2327, 2012
Cited by
PubMed Abstract: The aggresome pathway is activated when proteasomal clearance of misfolded proteins is hindered. Misfolded polyubiquitinated protein aggregates are recruited and transported to the aggresome via the microtubule network by a protein complex consisting of histone deacetylase 6 (HDAC6) and the dynein motor complex. The current model suggests that HDAC6 recognizes protein aggregates by binding directly to polyubiquitinated proteins. Here, we show that there are substantial amounts of unanchored ubiquitin in protein aggregates with solvent-accessible C termini. The ubiquitin-binding domain (ZnF-UBP) of HDAC6 binds exclusively to the unanchored C-terminal diglycine motif of ubiquitin instead of conjugated polyubiquitin. The unanchored ubiquitin C termini in the aggregates are generated in situ by aggregate-associated deubiquitinase ataxin-3. These results provide structural and mechanistic bases for the role of HDAC6 in aggresome formation and further suggest a novel ubiquitin-mediated signaling pathway, where the exposure of ubiquitin C termini within protein aggregates enables HDAC6 recognition and transport to the aggresome.
PubMed: 22069321
DOI: 10.1074/jbc.M111.273730
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (3 Å)
構造検証レポート
Validation report summary of 3phd
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2025-05-28に公開中

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