IndraLab

Statements


TP53 is methylated on lysine. 12 / 12
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sparser
"Mono- or di-methylation of TP53 at four C-terminal lysine residues by at least six different lysine methyltransferases facilitates binding by TIP60, PHF20, L3MBTL1 and 53BP1 to TP53 ( xref , xref , xref ) ( xref ; xref )."

sparser
"To further the analogy to histone modification, the same p53 lysine residues that are methylated are also subject to other modifications like acetylation, sumoylation and ubiquitylation [ xref ]."

sparser
"P53 is methylated at C-terminal lysine residues: K370, K372 and K382."

sparser
"For example, methyltransferase Set 9 can specifically methylate lysine residues in p53 to regulate its target gene expression [ xref ]."

sparser
"To this point, three different methyltransferases have been shown to be able to methylate C-terminal lysine residues of p53."

sparser
"These results disfavour a role for JMJD3 in the regulation of p53 C-terminal methylation, however, we cannot rule out that JMJD3 is involved in regulating p53 methylation at other lysine residues than the tested ones, or that additional co-factors are required for an efficient enzymatic removal of methylation."

sparser
"The p53 protein is methylated at lysine residues in its C-terminal regulatory region p53, which stabilizes it, restricts it to the nucleus, and enhances its ability to transcriptionally transactivate target genes (reviewed in xref )."

sparser
"Interestingly, some lysine residues of p53 that are modified by acetylation can also be methylated [ xref ]."

sparser
"Genotoxic stress can induce methylation of p53 in at least three different lysine residues, which mediate activation or repression of p53-dependent apoptosis ( Chuikov et al., 2004; Huang et al., 2006[MISSING/INVALID CREDENTIALS: limited to 200 char for Elsevier]"

sparser
"Some HMTs (SETD8 and SMYD2) have been found to regulate the methylation of non-histone proteins in particular p53 in lysine residues."

sparser
"For instance, histone lysine methyltransferases KMT5 (Set9), KMT3C (Smyd2), and KMT5A (Set8) were reported to methylate p53 at specific C-terminal lysine residues."

sparser
"Thus, methylation and acetylation at different lysine residues of p53 and their interplay govern cellular response to spontaneous/endogenous and exogenous damage, respectively."