Curated Information
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Home > Curated Information Page > PubMed Id: 37670785
Ghobashi AH, et al. (2023) Activation of AKT induces EZH2-mediated β-catenin trimethylation in colorectal cancer. iScience 26, 107630 37670785
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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S473-p - Akt1 (human)
Modsite: RPHFPQFsysAsGtA SwissProt Entrez-Gene
Orthologous residues
Akt1 (human): S473‑p, Akt1 iso2 (human): S411‑p, Akt1 (mouse): S473‑p, Akt1 (rat): S473‑p, Akt1 (fruit fly): S586‑p, Akt1 (cow): S473‑p
Characterization
Methods used to characterize site in vivo immunoprecipitation, phospho-antibody, western blotting
Disease tissue studied:  colorectal cancer, colorectal carcinoma
Relevant cell lines - cell types - tissues:  Caco-2 (intestinal), HEK293T (epithelial), RKO (intestinal)
Cellular systems studied:  cell lines
Species studied:  human
Upstream Regulation
Treatments, proteins and their effect on site modification: 
Treatments Referenced Treatments Manipulated Protein Referenced Protein Effect Notes
H2O2 increase
EZH2 (human) no change compared to control EZH2 KD has no effect on AKT pS473
GSK690693 H2O2 inhibit treatment-induced increase
PTEN (human) decrease PTEN KD increases AKT1 pS473
H2O2 PTEN (human) inhibit treatment-induced increase PTEN KD induces effect of H2O2
Downstream Regulation
Effect of modification (function):  activity, induced, molecular association, regulation
Modification regulates interactions with: 
Interacting molecule Interacting domains Effect Consequences (function) Consequences (process) Detection assays
EZH2 (human) Induces phosphorylation co-immunoprecipitation

K49-me - CTNNB1 (human)
Modsite: TAPsLsGkGNPEEED SwissProt Entrez-Gene
Orthologous residues
CTNNB1 (human): K49‑me, CTNNB1 (mouse): K49‑me, CTNNB1 (rat): K49‑me, CTNNB1 (rabbit): K49‑me
Characterization
Methods used to characterize site in vivo immunoprecipitation, mutation of modification site
Disease tissue studied:  colorectal cancer, colorectal carcinoma
Relevant cell lines - cell types - tissues:  SW480 (intestinal)
Cellular systems studied:  cell lines
Species studied:  human
Upstream Regulation
Treatments, proteins and their effect on site modification: 
Treatments Referenced Treatments Manipulated Protein Referenced Protein Effect Notes
H2O2 increase
PTEN (human) decrease PTEN KD increases CTNNB1 me-K49
decrease GSK-503 inhibits CTNNB1 K49-me
Downstream Regulation
Effect of modification (function):  intracellular localization, methylation, molecular association, regulation
Effect of modification (process):  transcription, induced
Modification regulates interactions with: 
Interacting molecule Interacting domains Effect Consequences (function) Consequences (process) Detection assays
POLR2A (human) Induces co-immunoprecipitation
HNF1A (human) Induces co-immunoprecipitation

S21-p - EZH2 (human)
Modsite: CWRKRVksEyMRLRQ SwissProt Entrez-Gene
Orthologous residues
EZH2 (human): S21‑p, EZH2 iso2 (human): S21‑p, EZH2 (mouse): S21‑p, EZH2 (rat): S21‑p
Characterization
Methods used to characterize site in vivo immunoprecipitation, mutation of modification site, phospho-antibody, western blotting
Disease tissue studied:  colorectal cancer, colorectal carcinoma
Relevant cell lines - cell types - tissues:  LoVo (intestinal), RKO (intestinal), SW480 (intestinal)
Cellular systems studied:  cell lines, tissue
Species studied:  human
Upstream Regulation
Potential in vivo enzymes for site: 
Type Enzyme Evidence Notes
KINASE Akt1 (human) phospho-antibody, co-immunoprecipitation, activation of upstream enzyme, modification site within consensus motif, pharmacological inhibitor of upstream enzyme
Treatments, proteins and their effect on site modification: 
Treatments Referenced Treatments Manipulated Protein Referenced Protein Effect Notes
H2O2 increase
GSK690693 H2O2 inhibit treatment-induced increase
Downstream Regulation
Effect of modification (function):  enzymatic activity, induced, molecular association, regulation, phosphorylation
Effect of modification (process):  cell motility, inhibited, chromatin organization, altered
Modification regulates interactions with: 
Interacting molecule Interacting domains Effect Consequences (function) Consequences (process) Detection assays
POLR2A (human) Induces co-immunoprecipitation
CTNNB1 (human) Induces co-immunoprecipitation