000249924 001__ 249924
000249924 005__ 20240118161500.0
000249924 037__ $$aDZNE-2023-00239
000249924 1001_ $$0P:(DE-2719)2811291$$aGloeckner, Christian Johannes$$b0$$eLast author
000249924 245__ $$aDataset: USP9X phosphopeptide mapping
000249924 260__ $$bPRoteomics IDEntifications Database$$c2020
000249924 3367_ $$2BibTeX$$aMISC
000249924 3367_ $$0PUB:(DE-HGF)32$$2PUB:(DE-HGF)$$aDataset$$bdataset$$mdataset$$s1705590871_9225
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000249924 3367_ $$2DataCite$$aDataset
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000249924 3367_ $$2DINI$$aResearchData
000249924 520__ $$aWe previously identified the deubiquitylase USP9X as a G2/M-specific CDC14B interactor (PXD012732). The functional connection of these proteins has been further investigated by a quantitative comparison of USP9X phosphorylation in WT vs CDC14B-overexpressing HEK 293Tcells (ATCC® CRL-3216™). The approach identified USP9X serine 2563 as a specific CDC14B target. Phosphorylation at USP9XS2563 has been confirmed by in-house phosphospecific antibodies.
000249924 536__ $$0G:(DE-HGF)POF4-352$$a352 - Disease Mechanisms (POF4-352)$$cPOF4-352$$fPOF IV$$x0
000249924 7870_ $$0DZNE-2020-01409$$aDietachmayr, Michael et.al.$$d[London] : Nature Publishing Group UK, 2020$$iRelatedTo$$r$$tAntagonistic activities of CDC14B and CDK1 on USP9X regulate WT1-dependent mitotic transcription and survival.
000249924 8564_ $$uhttps://www.ebi.ac.uk/pride/archive/projects/PXD012733
000249924 909CO $$ooai:pub.dzne.de:249924$$pVDB
000249924 9101_ $$0I:(DE-588)1065079516$$6P:(DE-2719)2811291$$aDeutsches Zentrum für Neurodegenerative Erkrankungen$$b0$$kDZNE
000249924 9131_ $$0G:(DE-HGF)POF4-352$$1G:(DE-HGF)POF4-350$$2G:(DE-HGF)POF4-300$$3G:(DE-HGF)POF4$$4G:(DE-HGF)POF$$aDE-HGF$$bGesundheit$$lNeurodegenerative Diseases$$vDisease Mechanisms$$x0
000249924 9141_ $$y2020
000249924 9201_ $$0I:(DE-2719)1210007$$kAG Gloeckner$$lFunctional Neuroproteomics and Translational Biomarkers in Neurodegenerative Diseases$$x0
000249924 980__ $$adataset
000249924 980__ $$aVDB
000249924 980__ $$aI:(DE-2719)1210007
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