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3N1B

C-terminal domain of Vps54 subunit of the GARP complex

3N1B の概要
エントリーDOI10.2210/pdb3n1b/pdb
関連するPDBエントリー2a2f 2fji 2pfv 3N1E 3fhn 3hr0
分子名称Vacuolar protein sorting-associated protein 54 (2 entities in total)
機能のキーワードspinal muscular atrophy, vesicle trafficking, golgi apparatus, tethering complex, garp, transport protein
由来する生物種Mus musculus (mouse)
細胞内の位置Golgi apparatus, trans-Golgi network : Q5SPW0
タンパク質・核酸の鎖数2
化学式量合計32998.68
構造登録者
Perez-Victoria, F.J.,Abascal-Palacios, G.,Tascon, I.,Kajava, A.,Pioro, E.P.,Bonifacino, J.S.,Hierro, A. (登録日: 2010-05-15, 公開日: 2010-07-14, 最終更新日: 2024-11-06)
主引用文献Perez-Victoria, F.J.,Abascal-Palacios, G.,Tascon, I.,Kajava, A.,Magadan, J.G.,Pioro, E.P.,Bonifacino, J.S.,Hierro, A.
Structural basis for the wobbler mouse neurodegenerative disorder caused by mutation in the Vps54 subunit of the GARP complex.
Proc.Natl.Acad.Sci.USA, 107:12860-12865, 2010
Cited by
PubMed Abstract: The multisubunit Golgi-associated retrograde protein (GARP) complex is required for tethering and fusion of endosome-derived transport vesicles to the trans-Golgi network. Mutation of leucine-967 to glutamine in the Vps54 subunit of GARP is responsible for spinal muscular atrophy in the wobbler mouse, an animal model of amyotrophic lateral sclerosis. The crystal structure at 1.7 A resolution of the mouse Vps54 C-terminal fragment harboring leucine-967, in conjunction with comparative sequence analysis, reveals that Vps54 has a continuous alpha-helical bundle organization similar to that of other multisubunit tethering complexes. The structure shows that leucine-967 is buried within the alpha-helical bundle through predominantly hydrophobic interactions that are critical for domain stability and folding in vitro. Mutation of this residue to glutamine does not prevent integration of Vps54 into the GARP complex but greatly reduces the half-life and levels of the protein in vivo. Severely reduced levels of mutant Vps54 and, consequently, of the whole GARP complex underlie the phenotype of the wobbler mouse.
PubMed: 20615984
DOI: 10.1073/pnas.1004756107
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (2.398 Å)
構造検証レポート
Validation report summary of 3n1b
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2025-05-07に公開中

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