5CVO
WDR48:USP46~ubiquitin ternary complex
5CVO の概要
エントリーDOI | 10.2210/pdb5cvo/pdb |
関連するPDBエントリー | 5CVL 5CVM 5CVN |
分子名称 | WD repeat-containing protein 48, Ubiquitin carboxyl-terminal hydrolase 46, Polyubiquitin-B, ... (4 entities in total) |
機能のキーワード | wdr48, wd repeat, beta propeller, usp46, ubiquitin, covalent complex, dub, deubiquitinase, hydrolase-protein binding complex, hydrolase/protein binding |
由来する生物種 | Homo sapiens (Human) 詳細 |
細胞内の位置 | Nucleus: Q8TAF3 Ubiquitin: Cytoplasm : P0CG47 |
タンパク質・核酸の鎖数 | 6 |
化学式量合計 | 251340.77 |
構造登録者 | |
主引用文献 | Yin, J.,Schoeffler, A.J.,Wickliffe, K.,Newton, K.,Starovasnik, M.A.,Dueber, E.C.,Harris, S.F. Structural Insights into WD-Repeat 48 Activation of Ubiquitin-Specific Protease 46. Structure, 23:2043-2054, 2015 Cited by PubMed Abstract: Protein ubiquitination patterns are an important component of cellular signaling. The WD-repeat protein WDR48 (USP1-associated factor UAF-1) stimulates activity of ubiquitin-specific proteases USP1, USP12, and USP46. To understand how WDR48 exerts its effect on the USP scaffold, we determined structures of the ternary WDR48:USP46:ubiquitin complex. WDR48 interacts with the USP46 fingers subdomain via a relatively small, highly polar surface on the top center of the WDR48 β propeller. In addition, WDR48 has a novel ancillary domain and a C-terminal SUMO-like domain encircling the USP46-bound ubiquitin. Mutation of residues involved in the WDR48:USP46 interaction abrogated both binding and deubiquitinase activity of the complex. An analogous mutation in USP1 similarly blocked WDR48-dependent activation. Our data suggest a possible mechanism of deubiquitinase stimulation via stabilization and prolonged residence time of substrate. The unprecedented mode of interaction between the USP fingers domain and the WD-repeat β propeller serves as a prototypical example for this family of deubiquitinases. PubMed: 26388029DOI: 10.1016/j.str.2015.08.010 主引用文献が同じPDBエントリー |
実験手法 | X-RAY DIFFRACTION (3.885 Å) |
構造検証レポート
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