Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/117364
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dc.contributor.authorManning, J.A.-
dc.contributor.authorKumar, S.-
dc.date.issued2018-
dc.identifier.citationTrends in Biochemical Sciences, 2018; 43(8):635-647-
dc.identifier.issn0968-0004-
dc.identifier.issn1362-4326-
dc.identifier.urihttp://hdl.handle.net/2440/117364-
dc.description.abstractProtein modification by ubiquitination plays a key evolutionarily conserved role in regulating membrane proteins. Nedd4-2, a ubiquitin ligase, targets membrane proteins such as ion channels and transporters for ubiquitination. This Nedd4-2-mediated ubiquitination provides a crucial step in controlling the membrane availability of these proteins, thus affecting their signaling and physiological outcomes. In one well-studied example, Nedd4-2 fine-tunes the physiological function of the epithelial sodium channel (ENaC), thus modulating Na+ reabsorption by epithelia to maintain whole-body Na+ homeostasis. This review summarizes the key signaling pathways regulated by Nedd4-2 and the possible implications of such regulation in various pathologies.-
dc.description.statementofresponsibilityJantina A. Manning, Sharad Kumar-
dc.language.isoen-
dc.publisherElsevier-
dc.rights© 2018 Elsevier Ltd. All rights reserved.-
dc.source.urihttp://dx.doi.org/10.1016/j.tibs.2018.06.004-
dc.subjectENaC-
dc.subjectNedd4-2-
dc.subjection channels-
dc.subjectpathophysiology-
dc.subjectsodium-
dc.subjectubiquitination-
dc.titlePhysiological functions of nedd4-2: lessons from knockout mouse models-
dc.typeJournal article-
dc.identifier.doi10.1016/j.tibs.2018.06.004-
dc.relation.granthttp://purl.org/au-research/grants/nhmrc/1103006-
dc.relation.granthttp://purl.org/au-research/grants/nhmrc/1020755-
dc.relation.granthttp://purl.org/au-research/grants/nhmrc/1099307-
pubs.publication-statusPublished-
dc.identifier.orcidKumar, S. [0000-0001-7126-9814]-
Appears in Collections:Aurora harvest 8
Chemistry publications

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