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8PHE

ACAD9-WT in complex with ECSIT-CTER

8PHE の概要
エントリーDOI10.2210/pdb8phe/pdb
EMDBエントリー17659
分子名称Complex I assembly factor ACAD9, mitochondrial, Evolutionarily conserved signaling intermediate in Toll pathway, mitochondrial (3 entities in total)
機能のキーワードoxidative phosphorylation (oxphos), fatty acid oxidation (fao), mitochondrial complex i assembly complex (mcia), amyloid-beta, ecsit phosphorylation, signaling protein
由来する生物種Homo sapiens (human)
詳細
タンパク質・核酸の鎖数4
化学式量合計182197.11
構造登録者
主引用文献McGregor, L.,Acajjaoui, S.,Desfosses, A.,Saidi, M.,Bacia-Verloop, M.,Schwarz, J.J.,Juyoux, P.,von Velsen, J.,Bowler, M.W.,McCarthy, A.A.,Kandiah, E.,Gutsche, I.,Soler-Lopez, M.
The assembly of the Mitochondrial Complex I Assembly complex uncovers a redox pathway coordination.
Nat Commun, 14:8248-8248, 2023
Cited by
PubMed Abstract: The Mitochondrial Complex I Assembly (MCIA) complex is essential for the biogenesis of respiratory Complex I (CI), the first enzyme in the respiratory chain, which has been linked to Alzheimer's disease (AD) pathogenesis. However, how MCIA facilitates CI assembly, and how it is linked with AD pathogenesis, is poorly understood. Here we report the structural basis of the complex formation between the MCIA subunits ECSIT and ACAD9. ECSIT binding induces a major conformational change in the FAD-binding loop of ACAD9, releasing the FAD cofactor and converting ACAD9 from a fatty acid β-oxidation (FAO) enzyme to a CI assembly factor. We provide evidence that ECSIT phosphorylation downregulates its association with ACAD9 and is reduced in neuronal cells upon exposure to amyloid-β (Aβ) oligomers. These findings advance our understanding of the MCIA complex assembly and suggest a possible role for ECSIT in the reprogramming of bioenergetic pathways linked to Aβ toxicity, a hallmark of AD.
PubMed: 38086790
DOI: 10.1038/s41467-023-43865-0
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 8phe
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2026-04-08に公開中

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