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6MAT

Cryo-EM structure of the essential ribosome assembly AAA-ATPase Rix7

6MAT の概要
エントリーDOI10.2210/pdb6mat/pdb
EMDBエントリー9063
分子名称Rix7 mutant, unknown protein, ADENOSINE-5'-TRIPHOSPHATE (3 entities in total)
機能のキーワードaaa-atpase, ribosomal protein
由来する生物種Chaetomium thermophilum (strain DSM 1495 / CBS 144.50 / IMI 039719)
詳細
タンパク質・核酸の鎖数7
化学式量合計544404.43
構造登録者
Lo, Y.H.,Sobhany, M.,Hsu, A.L.,Ford, B.L.,Krahn, J.M.,Borgnia, M.J.,Stanley, R.E. (登録日: 2018-08-28, 公開日: 2019-02-06, 最終更新日: 2024-03-13)
主引用文献Lo, Y.H.,Sobhany, M.,Hsu, A.L.,Ford, B.L.,Krahn, J.M.,Borgnia, M.J.,Stanley, R.E.
Cryo-EM structure of the essential ribosome assembly AAA-ATPase Rix7.
Nat Commun, 10:513-513, 2019
Cited by
PubMed Abstract: Rix7 is an essential type II AAA-ATPase required for the formation of the large ribosomal subunit. Rix7 has been proposed to utilize the power of ATP hydrolysis to drive the removal of assembly factors from pre-60S particles, but the mechanism of release is unknown. Rix7's mammalian homolog, NVL2 has been linked to cancer and mental illness disorders, highlighting the need to understand the molecular mechanisms of this essential machine. Here we report the cryo-EM reconstruction of the tandem AAA domains of Rix7 which form an asymmetric stacked homohexameric ring. We trapped Rix7 with a polypeptide in the central channel, revealing Rix7's role as a molecular unfoldase. The structure establishes that type II AAA-ATPases lacking the aromatic-hydrophobic motif within the first AAA domain can engage a substrate throughout the entire central channel. The structure also reveals that Rix7 contains unique post-α7 insertions within both AAA domains important for Rix7 function.
PubMed: 30705282
DOI: 10.1038/s41467-019-08373-0
主引用文献が同じPDBエントリー
実験手法
ELECTRON MICROSCOPY (4.5 Å)
構造検証レポート
Validation report summary of 6mat
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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