4.4 Review

Specificity and disease in the ubiquitin system

Journal

BIOCHEMICAL SOCIETY TRANSACTIONS
Volume 44, Issue -, Pages 212-227

Publisher

PORTLAND PRESS LTD
DOI: 10.1042/BST20150209

Keywords

ubiquitin; E3 ligase; RING; RBR; Fanconi anemia; Parkin

Funding

  1. Cancer Research UK [17739]
  2. Medical Research Council [MC_UU_12016/12]
  3. EMBO Young Investigator Programme
  4. MRC [MC_UU_12016/12] Funding Source: UKRI
  5. Cancer Research UK [17739] Funding Source: researchfish
  6. Medical Research Council [MC_UU_12016/12] Funding Source: researchfish

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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.

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