Gene interactions and pathways from curated databases and text-mining

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EP300 — TP53

Pathways - manually collected, often from reviews:

Protein-Protein interactions - manually collected from original source literature:

Studies that report less than 10 interactions are marked with *

Text-mined interactions from Literome

Grossman et al., Eur J Biochem 2001 : p300/CBP/p53 interaction and regulation of the p53 response ... Through physical interaction with p53, p300/CBP can both positively and negatively regulate p53 transactivation, as well as p53 protein turnover depending on cellular context and environmental stimuli, such as DNA damage
Sabbatini et al., DNA Cell Biol 2002 : We demonstrate that MDMX dramatically inhibits the acetylation of p53 induced by both endogenous and ectopically expressed p300/CBP
Deng et al., Cancer Res 2005 (Cell Transformation, Neoplastic) : We further showed that p300/CBP were essential for ras induced p53 activity, providing a potential mechanism underlying the important role of p300/CBP in senescence
Li et al., Biochem Biophys Res Commun 2007 : ZNF307 might suppress p53-p21 pathway through activating MDM2 and EP300 expression and inducing p53 degradation
Kim et al., PloS one 2009 : Suppression of p300 histone acetyltransferase (p300HAT) activity by the p300HAT inhibitor anacardic acid ( AA ) or by down-regulation of p300 by siRNA prevented UV-induced MMP-1 expression and inhibited UV-enhanced gamma-H2AX, p53 level, and acetyl-H3
Sang et al., J Cell Biochem 1997 : Our data suggest that p300/CBP and TBP but not the pocket proteins, pRb, p107, and pRb2/p130 are functional targets of E1A in transcriptional regulation and that p53 transactivation requires the function of the p300/TBP/TFIIB complex, thus delineating a new pathway by which E1A may exert its transforming activity
Ravi et al., Cancer Res 1998 : p53 dependent transactivation and transrepression require its interaction with p300/CBP , a coactivator that also interacts with the RelA subunit of nuclear factor-kappaB