3N1B
C-terminal domain of Vps54 subunit of the GARP complex
3N1B の概要
エントリーDOI | 10.2210/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: 20615984DOI: 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) |
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