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3EH2

Crystal structure of the human COPII-coat protein Sec24c

3EH2 の概要
エントリーDOI10.2210/pdb3eh2/pdb
関連するPDBエントリー3EFO 3EG9 3EGD 3EGX 3EH1
分子名称Protein transport protein Sec24C, ZINC ION (3 entities in total)
機能のキーワードcopii-coat protein, vesicle transport, cytoplasm, endoplasmic reticulum, er-golgi transport, golgi apparatus, membrane, phosphoprotein, protein transport, transport
由来する生物種Homo sapiens (Human)
細胞内の位置Cytoplasm: P53992
タンパク質・核酸の鎖数3
化学式量合計257068.74
構造登録者
Goldberg, J.,Mancias, J.D. (登録日: 2008-09-11, 公開日: 2008-10-21, 最終更新日: 2024-02-21)
主引用文献Mancias, J.D.,Goldberg, J.
Structural basis of cargo membrane protein discrimination by the human COPII coat machinery.
Embo J., 27:2918-2928, 2008
Cited by
PubMed Abstract: Genomic analysis shows that the increased complexity of trafficking pathways in mammalian cells involves an expansion of the number of SNARE, Rab and COP proteins. Thus, the human genome encodes four forms of Sec24, the cargo selection subunit of the COPII vesicular coat, and this is proposed to increase the range of cargo accommodated by human COPII-coated vesicles. In this study, we combined X-ray crystallographic and biochemical analysis with functional assays of cargo packaging into COPII vesicles to establish molecular mechanisms for cargo discrimination by human Sec24 subunits. A conserved IxM packaging signal binds in a surface groove of Sec24c and Sec24d, but the groove is occluded in the Sec24a and Sec24b subunits. Conversely, LxxLE class transport signals and the DxE signal of VSV glycoprotein are selectively bound by Sec24a and Sec24b subunits. A comparative analysis of crystal structures of the four human Sec24 isoforms establishes the structural determinants for discrimination among these transport signals, and provides a framework to understand how an expansion of coat subunits extends the range of cargo proteins packaged into COPII-coated vesicles.
PubMed: 18843296
DOI: 10.1038/emboj.2008.208
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (2.35 Å)
構造検証レポート
Validation report summary of 3eh2
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2025-12-31に公開中

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