Specificity and disease in the ubiquitin system

被引:48
作者
Chaugule, Viduth K. [1 ]
Walden, Helen [1 ]
机构
[1] Univ Dundee, Coll Life Sci, MRC Prot Phosphorylat & Ubiquitylat Unit, Dow St, Dundee DD1 5EH, Scotland
基金
英国医学研究理事会;
关键词
ubiquitin; E3; ligase; RING; RBR; Fanconi anemia; Parkin; ANAPHASE-PROMOTING COMPLEX; FANCONI-ANEMIA PATHWAY; DNA-REPAIR PATHWAY; LINEAR POLYUBIQUITIN CHAINS; CELL-CYCLE CONTROL; RING-RING COMPLEX; E3 LIGASE PARKIN; CONJUGATING ENZYMES; CRYSTAL-STRUCTURE; STRUCTURAL BASIS;
D O I
10.1042/BST20150209
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Post-translational modification (PTM) of proteins by ubiquitination is an essential cellular regulatory process. Such regulation drives the cell cycle and cell division, signalling and secretory pathways, DNA replication and repair processes and protein quality control and degradation pathways. A huge range of ubiquitin signals can be generated depending on the specificity and catalytic activity of the enzymes required for attachment of ubiquitin to a given target. As a consequence of its importance to eukaryotic life, dysfunction in the ubiquitin system leads to many disease states, including cancers and neurodegeneration. This review takes a retrospective look at our progress in understanding the molecular mechanisms that govern the specificity of ubiquitin conjugation.
引用
收藏
页码:212 / 227
页数:16
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