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Group by :Switch typeMotif classProteinEnzymePathway         Hide inferred   Group Index    Colouring Info              Filtered: UNIPROT:P04637 (12 hits) x


x  Coloured by: Pathway evidence source
          Curated          inferred


x  Index
Cell cycleG1/S DNA Damage CheckpointsNeurotrophin signaling pathway
PI3K-Akt signaling pathwayWnt signaling pathwayp53 signaling pathway
p53-Dependent G1/S DNA damage checkpoint


MotifProteinStartEndSwitch TypeSwitch SubtypeSwitch descriptionInformationEvidence

Cell cycle (KEGG - hsa04110)
MOD_GSK3_1 P53_HUMAN3037BinaryPhysicochemical compatibilityPhosphorylation of Cellular tumor antigen p53 (TP53) at S37 primes the protein for phosphorylation at S33 by Glycogen synthase kinase-3 beta (GSK3B).
details
Inferred
DEG_MDM2_1 P53_HUMAN1926BinaryPhysicochemical compatibilityPhosphorylation of Cellular tumor antigen p53 (TP53) on T18 (in vitro by Casein kinase I subfamily, requiring prior phosphorylation of S15) inhibits its binding to E3 ubiquitin-protein ligase Mdm2 (MDM2). In vivo, T18 is phosphorylated in response to DNA damage.
details
Curated
LIG_TAZ2 P53_HUMAN1925CumulativeRheostaticMultisite phosphorylation of S15 and T18 and S20 and S33 and S37 and S46 in the TAD region of Cellular tumor antigen p53 (TP53) additively enhances its affinity for CREB-binding protein (CREBBP).
details
Curated
DEG_MDM2_1 P53_HUMAN1926BinaryPre‑translationalAlternative promoter usage and alternative splicing removes the E3 ubiquitin ligase MDM2-binding motif of Cellular tumor antigen p53 (TP53), abrogating binding to E3 ubiquitin-protein ligase Mdm2 (MDM2). The splice variant without this motif is resistant to MDM2-mediated degradation, leading to a longer half-life.
details
Curated

G1/S DNA Damage Checkpoints (Reactome - 69615)
LIG_TAZ2 P53_HUMAN1925CumulativeRheostaticMultisite phosphorylation of S15 and T18 and S20 and S33 and S37 and S46 in the TAD region of Cellular tumor antigen p53 (TP53) additively enhances its affinity for CREB-binding protein (CREBBP).
details
Curated

Neurotrophin signaling pathway (KEGG - hsa04722)
MOD_GSK3_1 P53_HUMAN3037BinaryPhysicochemical compatibilityPhosphorylation of Cellular tumor antigen p53 (TP53) at S37 primes the protein for phosphorylation at S33 by Glycogen synthase kinase-3 beta (GSK3B).
details
Inferred

PI3K-Akt signaling pathway (KEGG - hsa04151)
MOD_GSK3_1 P53_HUMAN3037BinaryPhysicochemical compatibilityPhosphorylation of Cellular tumor antigen p53 (TP53) at S37 primes the protein for phosphorylation at S33 by Glycogen synthase kinase-3 beta (GSK3B).
details
Inferred

Wnt signaling pathway (KEGG - hsa04310)
MOD_GSK3_1 P53_HUMAN3037BinaryPhysicochemical compatibilityPhosphorylation of Cellular tumor antigen p53 (TP53) at S37 primes the protein for phosphorylation at S33 by Glycogen synthase kinase-3 beta (GSK3B).
details
Inferred

p53 signaling pathway (KEGG - hsa04115)
DEG_MDM2_1 P53_HUMAN1926BinaryPhysicochemical compatibilityPhosphorylation of Cellular tumor antigen p53 (TP53) on T18 (in vitro by Casein kinase I subfamily, requiring prior phosphorylation of S15) inhibits its binding to E3 ubiquitin-protein ligase Mdm2 (MDM2). In vivo, T18 is phosphorylated in response to DNA damage.
details
Curated
DEG_MDM2_1 P53_HUMAN1926BinaryPre‑translationalAlternative promoter usage and alternative splicing removes the E3 ubiquitin ligase MDM2-binding motif of Cellular tumor antigen p53 (TP53), abrogating binding to E3 ubiquitin-protein ligase Mdm2 (MDM2). The splice variant without this motif is resistant to MDM2-mediated degradation, leading to a longer half-life.
details
Curated

p53-Dependent G1/S DNA damage checkpoint (Reactome - 69580)
DEG_MDM2_1 P53_HUMAN1926BinaryPhysicochemical compatibilityPhosphorylation of Cellular tumor antigen p53 (TP53) on T18 (in vitro by Casein kinase I subfamily, requiring prior phosphorylation of S15) inhibits its binding to E3 ubiquitin-protein ligase Mdm2 (MDM2). In vivo, T18 is phosphorylated in response to DNA damage.
details
Curated
DEG_MDM2_1 P53_HUMAN1926BinaryPre‑translationalAlternative promoter usage and alternative splicing removes the E3 ubiquitin ligase MDM2-binding motif of Cellular tumor antigen p53 (TP53), abrogating binding to E3 ubiquitin-protein ligase Mdm2 (MDM2). The splice variant without this motif is resistant to MDM2-mediated degradation, leading to a longer half-life.
details
Curated
           
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