Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/23361
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dc.contributor.authorFotia, A.-
dc.contributor.authorCook, D.-
dc.contributor.authorKumar, S.-
dc.date.issued2006-
dc.identifier.citationThe International Journal of Biochemistry and Cell Biology, 2006; 38(3):472-479-
dc.identifier.issn1357-2725-
dc.identifier.issn1878-5875-
dc.identifier.urihttp://hdl.handle.net/2440/23361-
dc.description.abstractNedd4 and Nedd4-2 are closely related HECT-type ubiquitin-protein ligases (E3) implicated in the regulation of a number of proteins and pathways. Given the close homology between these E3 enzymes it would be predicted that a conserved ubiquitin-conjugating enzyme (E2) specificity exists between the two proteins. However, E2 specificities for Nedd4 and Nedd4-2 are not well established. In the present studies we aimed at clarifying the E2-specificities of Nedd4 and Nedd4-2 using in vitro ubiquitination assays. We demonstrate strong substrate ubiquitination in the presence of UbcH5b by both Nedd4 and Nedd4-2. We also found that Ube2e3, an E2 previously shown to be used by Nedd4-2, is used less efficiently than UbcH5b. Our results suggest that for optimal ubiquitination Nedd4 and Nedd4-2 require the same E2 enzymes.-
dc.language.isoen-
dc.publisherPergamon-Elsevier Science Ltd-
dc.source.urihttp://dx.doi.org/10.1016/j.biocel.2005.11.006-
dc.subjectE2-
dc.subjectE3-
dc.subjectubiquitination-
dc.subjectubiquitin-protein ligase-
dc.subjectubiquitin-conjugating enzyme-
dc.subjectsodium channel-
dc.subjectsubstrates-
dc.subjectN4BP1-
dc.titleThe ubiquitin-protein ligases Nedd4 and Nedd4-2 show similar ubiquitin-conjugating enzyme specificities-
dc.typeJournal article-
dc.identifier.doi10.1016/j.biocel.2005.11.006-
pubs.publication-statusPublished-
dc.identifier.orcidKumar, S. [0000-0001-7126-9814]-
Appears in Collections:Aurora harvest 2
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