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Deubiquitylating enzymes and disease

dc.contributor.authorSinghal, Shweta
dc.contributor.authorTaylor, Matthew C
dc.contributor.authorBaker, Rohan
dc.date.accessioned2015-12-24T00:32:25Z
dc.date.available2015-12-24T00:32:25Z
dc.date.issued2008-10-21
dc.date.updated2016-02-24T10:53:37Z
dc.description.abstractDeubiquitylating enzymes (DUBs) can hydrolyze a peptide, amide, ester or thiolester bond at the C-terminus of UBIQ (ubiquitin), including the post-translationally formed branched peptide bonds in mono- or multi-ubiquitylated conjugates. DUBs thus have the potential to regulate any UBIQ-mediated cellular process, the two best characterized being proteolysis and protein trafficking. Mammals contain some 80-90 DUBs in five different subfamilies, only a handful of which have been characterized with respect to the proteins that they interact with and deubiquitylate. Several other DUBs have been implicated in various disease processes in which they are changed by mutation, have altered expression levels, and/or form part of regulatory complexes. Specific examples of DUB involvement in various diseases are presented. While no specific drugs targeting DUBs have yet been described, sufficient functional and structural information has accumulated in some cases to allow their rapid development. PUBLICATION HISTORY : Republished from Current BioData's Targeted Proteins database (TPdb; http://www.targetedproteinsdb.com).
dc.identifier.issn1471-2091en_AU
dc.identifier.urihttp://hdl.handle.net/1885/95199
dc.publisherBioMed Central
dc.rights© Singhal et al. 2008 This article is published under license to BioMed Central Ltd. This is an open access article distributed under the terms of the Creative Commons Attribution License (http://​creativecommons.​org/​licenses/​by/​2.​0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
dc.sourceBMC Biochemistry
dc.subjectanimals
dc.subjectendopeptidases
dc.subjecthumans
dc.subjecthydrolysis
dc.subjectmutation
dc.subjectneoplasms
dc.subjectubiquitin
dc.subjectvon hippel-lindau disease
dc.titleDeubiquitylating enzymes and disease
dc.typeJournal article
local.bibliographicCitation.issueSuppl 1en_AU
local.bibliographicCitation.startpageS3en_AU
local.contributor.affiliationSinghal, Shweta, College of Medicine, Biology and Environment, CMBE John Curtin School of Medical Research, Genome Sciences, The Australian National Universityen_AU
local.contributor.affiliationTaylor, Matthew C, CSIRO Entomology, Australiaen_AU
local.contributor.affiliationBaker, Rohan, College of Medicine, Biology and Environment, CMBE John Curtin School of Medical Research, Genome Sciences, The Australian National Universityen_AU
local.contributor.authoruidu4081675en_AU
local.description.notesImported from ARIESen_AU
local.identifier.absfor060199en_AU
local.identifier.ariespublicationu4292316xPUB28en_AU
local.identifier.citationvolume9en_AU
local.identifier.doi10.1186/1471-2091-9-S1-S3en_AU
local.identifier.essn1471-2091en_AU
local.identifier.scopusID2-s2.0-54249106271
local.identifier.thomsonID000263949700003
local.publisher.urlhttp://www.biomedcentral.com/en_AU
local.type.statusPublished Versionen_AU

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