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5DCN

Crystal structure of LC3 in complex with TECPR2 LIR

5DCN の概要
エントリーDOI10.2210/pdb5dcn/pdb
分子名称Microtubule-associated proteins 1A/1B light chain 3B, SULFATE ION (3 entities in total)
機能のキーワードlc3, autophagy, cell cycle
由来する生物種Homo sapiens (Human)
細胞内の位置Cytoplasm, cytoskeleton: Q9GZQ8
タンパク質・核酸の鎖数1
化学式量合計15232.21
構造登録者
Stadel, D.,Huber, J.,Dotsch, V.,Rogov, V.V.,Behrends, C.,Akutsu, M. (登録日: 2015-08-24, 公開日: 2016-03-09, 最終更新日: 2024-05-08)
主引用文献Stadel, D.,Millarte, V.,Tillmann, K.D.,Huber, J.,Tamin-Yecheskel, B.C.,Akutsu, M.,Demishtein, A.,Ben-Zeev, B.,Anikster, Y.,Perez, F.,Dotsch, V.,Elazar, Z.,Rogov, V.V.,Farhan, H.,Behrends, C.
TECPR2 Cooperates with LC3C to Regulate COPII-Dependent ER Export.
Mol.Cell, 60:89-104, 2015
Cited by
PubMed Abstract: Hereditary spastic paraplegias (HSPs) are a diverse group of neurodegenerative diseases that are characterized by axonopathy of the corticospinal motor neurons. A mutation in the gene encoding for Tectonin β-propeller containing protein 2 (TECPR2) causes HSP that is complicated by neurological symptoms. While TECPR2 is a human ATG8 binding protein and positive regulator of autophagy, the exact function of TECPR2 is unknown. Here, we show that TECPR2 associates with several trafficking components, among them the COPII coat protein SEC24D. TECPR2 is required for stabilization of SEC24D protein levels, maintenance of functional ER exit sites (ERES), and efficient ER export in a manner dependent on binding to lipidated LC3C. TECPR2-deficient HSP patient cells display alterations in SEC24D abundance and ER export efficiency. Additionally, TECPR2 and LC3C are required for autophagosome formation, possibly through maintaining functional ERES. Collectively, these results reveal that TECPR2 functions as molecular scaffold linking early secretion pathway and autophagy.
PubMed: 26431026
DOI: 10.1016/j.molcel.2015.09.010
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (2 Å)
構造検証レポート
Validation report summary of 5dcn
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2026-02-04に公開中

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