2QIZ
Structure of the yeast U-box-containing ubiquitin ligase Ufd2p
2QIZ の概要
| エントリーDOI | 10.2210/pdb2qiz/pdb |
| 関連するPDBエントリー | 2QJ0 |
| 分子名称 | Ubiquitin conjugation factor E4, POTASSIUM ION (3 entities in total) |
| 機能のキーワード | helical hairpin, ligase |
| 由来する生物種 | Saccharomyces cerevisiae (baker's yeast) |
| 細胞内の位置 | Cytoplasm: P54860 |
| タンパク質・核酸の鎖数 | 1 |
| 化学式量合計 | 112268.05 |
| 構造登録者 | |
| 主引用文献 | Tu, D.,Li, W.,Ye, Y.,Brunger, A.T. Inaugural Article: Structure and function of the yeast U-box-containing ubiquitin ligase Ufd2p. Proc.Natl.Acad.Sci.Usa, 104:15599-15606, 2007 Cited by PubMed Abstract: Proteins conjugated by Lys-48-linked polyubiquitin chains are preferred substrates of the eukaryotic proteasome. Polyubiquitination requires an activating enzyme (E1), a conjugating enzyme (E2), and a ligase (E3). Occasionally, these enzymes only assemble short ubiquitin oligomers, and their extension to full length involves a ubiquitin elongating factor termed E4. Ufd2p, as the first E4 identified to date, is involved in the degradation of misfolded proteins of the endoplasmic reticulum and of a ubiquitin-beta-GAL fusion substrate in Saccharomyces cerevisiae. The mechanism of action of Ufd2p is unknown. Here we describe the crystal structure of the full-length yeast Ufd2p protein. Ufd2p has an elongated shape consisting of several irregular Armadillo-like repeats with two helical hairpins protruding from it and a U-box domain flexibly attached to its C terminus. The U-box of Ufd2p has a fold similar to that of the RING (Really Interesting New Gene) domain that is present in certain ubiquitin ligases. Accordingly, Ufd2p has all of the hallmarks of a RING finger-containing ubiquitin ligase: it associates with its cognate E2 Ubc4p via its U-box domain and catalyzes the transfer of ubiquitin from the E2 active site to Ufd2p itself or to an acceptor ubiquitin molecule to form unanchored diubiquitin oligomers. Thus, Ufd2p can function as a bona fide E3 ubiquitin ligase to promote ubiquitin chain elongation on a substrate. PubMed: 17890322DOI: 10.1073/pnas.0701369104 主引用文献が同じPDBエントリー |
| 実験手法 | X-RAY DIFFRACTION (2.56 Å) |
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