Curated Information
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Home > Curated Information Page > PubMed Id: 25568665
Benavides-Serrato A, et al. (2014) mTORC2 modulates feedback regulation of p38 MAPK activity via DUSP10/MKP5 to confer differential responses to PP242 in glioblastoma. Genes Cancer 5, 393-406 25568665
This page summarizes selected information from the record referenced above and curated into PhosphoSitePlus®, a comprehensive online resource for the study of protein post-translational modifications (NAR, 2015, 43:D512-20). To learn more about the scope of PhosphoSitePlus®, click here.
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S224-p - DUSP10 (human)
Modsite: SCREGKDsFKRIFsK SwissProt Entrez-Gene
Orthologous residues
DUSP10 (human): S224‑p, DUSP10 (mouse): S225‑p
Characterization
Methods used to characterize site in vivo mutation of modification site
Disease tissue studied:  brain cancer, glioblastoma, glioma
Relevant cell lines - cell types - tissues:  U87MG (glial)
Cellular systems studied:  cell lines
Species studied:  human
Enzymes shown to modify site in vitro
Type Enzyme
KINASE mTOR (human)
Downstream Regulation
Effect of modification (process):  apoptosis, induced, cell growth, inhibited

S230-p - DUSP10 (human)
Modsite: DsFKRIFsKEIIVyD SwissProt Entrez-Gene
Orthologous residues
DUSP10 (human): S230‑p, DUSP10 (mouse): S231‑p
Characterization
Methods used to characterize site in vivo mutation of modification site
Disease tissue studied:  brain cancer, glioblastoma, glioma
Relevant cell lines - cell types - tissues:  U87MG (glial)
Cellular systems studied:  cell lines
Species studied:  human
Enzymes shown to modify site in vitro
Type Enzyme
KINASE mTOR (human)
Downstream Regulation
Effect of modification (process):  apoptosis, induced, cell growth, inhibited