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dc.contributor.authorWeirich, Sarade
dc.contributor.authorKusevic, Denisde
dc.contributor.authorKudithipudi, Srikanthde
dc.contributor.authorJeltsch, Albertde
dc.date.accessioned2015-11-30de
dc.date.accessioned2016-03-31T07:48:56Z-
dc.date.available2015-11-30de
dc.date.available2016-03-31T07:48:56Z-
dc.date.issued2015de
dc.identifier.other452686369de
dc.identifier.urihttp://nbn-resolving.de/urn:nbn:de:bsz:93-opus-103860de
dc.identifier.urihttp://elib.uni-stuttgart.de/handle/11682/1481-
dc.identifier.urihttp://dx.doi.org/10.18419/opus-1464-
dc.description.abstractIt has been reported that the Numb protein is methylated at lysine 158 and 163 and that this methylation is introduced by the SET8 protein lysine methyltransferase [Dhami et al., (2013) Molecular Cell 50, 565-576]. We studied this methylation in vitro using peptide arrays and recombinant Numb protein as substrates. Numb peptides and protein were incubated with recombinant SET8 purified after expression in E. coli or human HEK293 cells. However, no methylation of Numb by SET8 was detectable. SET8 methylation of Histone H4 and p53 peptides and proteins, which were used as positive controls, was readily observed. While SET8 methylation of Numb in cells cannot be ruled out, based on our findings, more evidence is needed to Support this claim. It appears likely that another not yet identified PKMT is responsible for the reported methylation of Numb in cells.en
dc.language.isoende
dc.rightsinfo:eu-repo/semantics/openAccessde
dc.subject.classificationEnzym , Proteinede
dc.subject.ddc570de
dc.subject.otherProtein Lysine Methyltransferase , Enzyme specificity , SET8en
dc.titleInvestigation of the methylation of Numb by the SET8 protein lysine methyltransferaseen
dc.typearticlede
dc.date.updated2015-11-30de
ubs.fakultaetFakultät Chemiede
ubs.institutInstitut für Biochemiede
ubs.opusid10386de
ubs.publikation.sourceScientific reports 5 (2015), Nr. 13813. URL http://dx.doi.org./10.1038/srep13813de
ubs.publikation.typZeitschriftenartikelde
Enthalten in den Sammlungen:03 Fakultät Chemie

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