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3OQC

Ubiquitin-fold modifier 1 Specific Protease, UfSP2

3OQC の概要
エントリーDOI10.2210/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
Ha, B.H.,Chung, C.H.,Kim, E.E. (登録日: 2010-09-02, 公開日: 2011-01-12, 最終更新日: 2024-03-20)
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: 21228277
DOI: 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
Validation report summary of 3oqc
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2024-11-06に公開中

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