Cook W J, Jeffrey L C, Carson M, Chen Z, Pickart C M
Department of Pathology, University of Alabama, Birmingham 35294.
J Biol Chem. 1992 Aug 15;267(23):16467-71. doi: 10.2210/pdb1aar/pdb.
Covalent ligation of multiubiquitin chains targets eukaryotic proteins for degradation. In such multiubiquitin chains, successive ubiquitins are linked by an isopeptide bond involving the side chain of Lys48 and the carboxyl group of Gly76. The crystal structure of a diubiquitin conjugate has been determined and refined at 2.3-A resolution. The molecule has internal approximate 2-fold symmetry with multiple hydrophobic and hydrophilic contacts along the 2-fold axis. The structure of the diubiquitin conjugate suggests determinants for recognition of multiubiquitin chains. A model for the interaction of diubiquitin and a ubiquitin conjugating enzyme (E2) is proposed.
多聚泛素链的共价连接将真核生物蛋白质靶向降解。在这种多聚泛素链中,连续的泛素通过涉及赖氨酸48侧链和甘氨酸76羧基的异肽键相连。已确定并以2.3埃分辨率精修了双泛素缀合物的晶体结构。该分子具有内部近似的二重对称性,沿二重轴有多个疏水和亲水接触。双泛素缀合物的结构提示了多聚泛素链识别的决定因素。提出了双泛素与泛素缀合酶(E2)相互作用的模型。