Tu Daqi, Li Wei, Ye Yihong, Brunger Axel T
Department of Molecular and Cellular Physiology, Stanford University and Howard Hughes Medical Institute, Stanford, CA 94305, USA.
Proc Natl Acad Sci U S A. 2007 Oct 2;104(40):15599-606. doi: 10.1073/pnas.0701369104. Epub 2007 Sep 21.
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.
由赖氨酸-48连接的多聚泛素链共轭的蛋白质是真核蛋白酶体的首选底物。多聚泛素化需要一种激活酶(E1)、一种共轭酶(E2)和一种连接酶(E3)。偶尔,这些酶仅组装短的泛素寡聚物,而将它们延伸至全长涉及一种称为E4的泛素延伸因子。Ufd2p作为迄今为止鉴定出的首个E4,参与酿酒酵母中内质网错误折叠蛋白和泛素-β-半乳糖苷融合底物的降解。Ufd2p的作用机制尚不清楚。在此,我们描述了全长酵母Ufd2p蛋白的晶体结构。Ufd2p呈细长形,由几个不规则的犰狳样重复序列组成,有两个螺旋发夹从中伸出,一个U-box结构域灵活地连接在其C末端。Ufd2p的U-box结构域折叠与某些泛素连接酶中存在的RING(真有趣新基因)结构域相似。因此,Ufd2p具有含RING结构域的泛素连接酶的所有特征:它通过其U-box结构域与其同源E2 Ubc4p结合,并催化泛素从E2活性位点转移至Ufd2p自身或受体泛素分子,以形成非锚定的双泛素寡聚物。因此,Ufd2p可作为一种真正的E3泛素连接酶,促进底物上泛素链的延伸。