3OQC
Ubiquitin-fold modifier 1 Specific Protease, UfSP2
3OQC の概要
エントリーDOI | 10.2210/pdb3oqc/pdb |
分子名称 | Ufm1-specific protease 2 (2 entities in total) |
機能のキーワード | dph motif cys protease, hydrolase |
由来する生物種 | Mus musculus (mouse) |
細胞内の位置 | Cytoplasm: Q99K23 |
タンパク質・核酸の鎖数 | 2 |
化学式量合計 | 109348.38 |
構造登録者 | |
主引用文献 | Ha, B.H.,Jeon, Y.J.,Shin, S.C.,Tatsumi, K.,Komatsu, M.,Tanaka, K.,Watson, C.M.,Wallis, G.,Chung, C.H.,Kim, E.E. Structure of ubiquitin-fold modifier 1-specific protease UfSP2 J.Biol.Chem., 286:10248-10257, 2011 Cited by PubMed Abstract: Ubiquitin-fold modifier 1 (Ufm1)-specific protease 2 (UfSP2) is a cysteine protease that is responsible for the release of Ufm1 from Ufm1-conjugated cellular proteins, as well as for the generation of mature Ufm1 from its precursor. The 2.6 Å resolution crystal structure of mouse UfSP2 reveals that it is composed of two domains. The C-terminal catalytic domain is similar to UfSP1 with Cys(294), Asp(418), His(420), Tyr(282), and a regulatory loop participating in catalysis. The novel N-terminal domain shows a unique structure and plays a role in the recognition of its cellular substrate C20orf116 and thus in the recruitment of UfSP2 to the endoplasmic reticulum, where C20orf116 predominantly localizes. Mutagenesis studies were carried out to provide the structural basis for understanding the loss of catalytic activity observed in a recently identified UfSP2 mutation that is associated with an autosomal dominant form of hip dysplasia. PubMed: 21228277DOI: 10.1074/jbc.M110.172171 主引用文献が同じPDBエントリー |
実験手法 | X-RAY DIFFRACTION (2.6 Å) |
構造検証レポート
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