P04637

PTMD Annotation Information


※ Protein Information

Tag Content
UniProt Accession P53_HUMAN; P04637;
Entrez ID 7157
GenBank Protein ID NM_000546.5; NM_001126112.2; NM_001126113.2; NM_001126114.2; NM_001126115.1; NM_001126116.1; NM_001126117.1; NM_001126118.1; NM_001276695.1; NM_001276696.1; NM_001276697.1; NM_001276698.1; NM_001276699.1; NM_001276760.1; NM_001276761.1;
GenBank Nucleotide ID NP_000537.3; NP_001119584.1; NP_001119585.1; NP_001119586.1; NP_001119587.1; NP_001119588.1; NP_001119589.1; NP_001119590.1; NP_001263624.1; NP_001263625.1; NP_001263626.1; NP_001263627.1; NP_001263628.1; NP_001263689.1; NP_001263690.1;
Protein Name Cellular tumor antigen p53 (Antigen NY-CO-13) (Phosphoprotein p53) (Tumor suppressor p53)
Gene Name TP53; P53
Organism Homo sapiens
NCBI Taxa ID 9606
Functional DescriptionActs as a tumor suppressor in many tumor types; induces growth arrest or apoptosis depending on the physiological circumstances and cell type. Involved in cell cycle regulation as a trans-activator that acts to negatively regulate cell division by controlling a set of genes required for this process. One of the activated genes is an inhibitor of cyclin-dependent kinases. Apoptosis induction seems to be mediated either by stimulation of BAX and FAS antigen expression, or by repression of Bcl-2 expression. In cooperation with mitochondrial PPIF i(view all)
Sequence
(Fasta)
MEEPQSDPSV EPPLSQETFS DLWKLLPENN VLSPLPSQAM DDLMLSPDDI EQWFTEDPGP 60
DEAPRMPEAA PPVAPAPAAP TPAAPAPAPS WPLSSSVPSQ KTYQGSYGFR LGFLHSGTAK 120
SVTCTYSPAL NKMFCQLAKT CPVQLWVDST PPPGTRVRAM AIYKQSQHMT EVVRRCPHHE 180
RCSDSDGLAP PQHLIRVEGN LRVEYLDDRN TFRHSVVVPY EPPEVGSDCT TIHYNYMCNS 240
SCMGGMNRRP ILTIITLEDS SGNLLGRNSF EVRVCACPGR DRRTEEENLR KKGEPHHELP 300
PGSTKRALPN NTSSSPQPKK KPLDGEYFTL QIRGRERFEM FRELNEALEL KDAQAGKEPG 360
GSRAHSSHLK SKKGQSTSRH KKLMFKTEGP DSD 394

※ PTM-Disease Association

NumPTMDiseaseCell TypeTypePTM SitePMID
1AcetylationBreast cancer/tumor/carcinomaD24920214
[Reference]: Our results provide evidence that melatonin enhances p53 acetylation by modulating the MDM2/MDMX/p300 pathway, disclosing new insights for understanding its anticancer effect.
2UbiquitinationGastric cancerP24240108
[Reference]: Collectively, our novel findings indicate that AURKA promotes tumor growth and cell survival through regulation of HDM2-induced ubiquitination and inhibition of P53
3PhosphorylationPancreatic cancer/carcinoma/adenocarcinomaP23845906
[Reference]: Here, we found that cisplatin mainly induced non-apoptotic death of the pancreatic cancer cells (AsPC-1 and Capan-2), which was associated with a significant p53 activation (phosphorylation and accumulation).
4PhosphorylationHead and neck squamous cell carcinomaP23414419
[Reference]: P276-00 treatment suppressed cell proliferation through inhibition of CCND1 expression, reduced phosphorylation of retinoblastoma protein and abrogative transcription of E2F1 gene targets
5PhosphorylationMelanomaA375 cell lineP22968364
[Reference]: Ruthenium complexes containing 2,6-bis(benzimidazolyl)pyridine derivatives induce cancer cell apoptosis by triggering DNA damage-mediated p53 phosphorylation
6UbiquitinationHepatocellular carcinoma/Hepatocarcinoma/HepatomaU16581249
[Reference]: Gankyrin regulates the phosphorylation of the retinoblastoma protein (pRb) by CDK4 and enhances the ubiquitylation of p53 by the RING ubiquitin ligase MDM3.
7Serine PhosphorylationBreast cancer/tumor/carcinomaMCF7AS1515958581; 23798621
[Reference]: DACH1 phosphorylation at serine residue (S439) inhibited p53 binding and phosphorylation at p53 amino-terminal sites (S15, S20) enhanced DACH1 binding. DACH1 binding to p53 was inhibited by NAD-dependent deacetylation via DACH1 K628. DACH1 repressed p21CIP1 and induced RAD51, an association found in basal breast cancer. DACH1 inhibits breast cancer cellular growth in an NAD and p53-dependent manner through direct protein-protein association.
8Serine PhosphorylationAtaxia-telangiectasic cancerDS159733515
[Reference]: Ionizing radiation, but not ultraviolet radiation, rapidly enhanced this p53-directed kinase activity of endogenous ATM. These observations, along with the fact that phosphorylation of p53 on serine-15 in response to ionizing radiation is reduced in ataxia telangiectasia cells, suggest that ATM is a protein kinase that phosphorylates p53 in vivo.
9Serine PhosphorylationBrain cancer/tumorGBM8401 cell lineDS1523268709
[Reference]: P. indica root aqueous extracts suppress cancer cell proliferation and migration through the phosphorylated-p53 and p21 pathways
10Serine PhosphorylationProstate cancer/carcinoma/adenocarcinomacell linePS1523359208
[Reference]: AA can activate p53 through increasing the phosphorylation of p53 on Ser15 in LNCaP cells
11Serine PhosphorylationDown syndromeUS1520696760
[Reference]: Accordingly, brains from embryonic DYRK1A transgenic mice exhibited elevated levels of Dyrk1A, Ser-15 (mouse Ser-18)-phosphorylated p53, and p21(CIP1) as well as impaired neuronal proliferation.
12Serine PhosphorylationColon cancer/carcinomacell lineUS1525860929
[Reference]: FBXW7-mutated colorectal cancer cells exhibit aberrant expression of phosphorylated-p53 at Serine-15.
13Serine PhosphorylationNeuroblastomaUS1523824039
[Reference]: MPTQ-mediated apoptosis is associated with increased phosphorylation of p53 at Ser15 and Ser20 which correlates with the hyperphosphorylation of Ataxia-Telangiectasia mutated protein (ATM)
14Serine PhosphorylationBreast cancer/tumor/carcinomaMCF7AS2023798621
[Reference]: DACH1 phosphorylation at serine residue (S439) inhibited p53 binding and phosphorylation at p53 amino-terminal sites (S15, S20) enhanced DACH1 binding. DACH1 binding to p53 was inhibited by NAD-dependent deacetylation via DACH1 K628. DACH1 repressed p21CIP1 and induced RAD51, an association found in basal breast cancer. DACH1 inhibits breast cancer cellular growth in an NAD and p53-dependent manner through direct protein-protein association.
15Serine PhosphorylationOvarian cancer/carcinomaUS2020009884
[Reference]: In p53-positive ovarian carinomas, S392 phosphorylation was associated with advanced tumor stage and high tumor grade. S20 phosphorylation was associated with low tumor grade in p53-positive, and high tumor grade in p53-negative, ovarian carcinomas.
16Serine PhosphorylationNeuroblastomaUS2023824039
[Reference]: MPTQ-mediated apoptosis is associated with increased phosphorylation of p53 at Ser15 and Ser20 which correlates with the hyperphosphorylation of Ataxia-Telangiectasia mutated protein (ATM)
17Serine PhosphorylationB-cell tumorAS2315343266
[Reference]: Our finding that S23A/S23A animals are tumor prone suggests that Ser23 phosphorylation is important for the tumor suppressor function of p53.
18Serine PhosphorylationT cell lymphomaNS3711042698
[Reference]: A serine 37 mutation associated with two missense mutations at highly conserved regions of p53 affect pro-apoptotic genes expression in a T-lymphoblastoid drug resistant cell line.
19Serine PhosphorylationBreast cancer/tumor/carcinomaMCF7DS4617404016
[Reference]: Effect of distinct anticancer drugs on the phosphorylation of p53 protein at serine 46 in human MCF-7 breast cancer cells
20Serine PhosphorylationAcute lymphoblastic leukaemiaDS4623717325; 16377624
[Reference]: TP53INP1 Functions as a Tumor Suppressor and Induces Apoptosis through Phosphorylating p53 at Serine-46
21Serine PhosphorylationHuntington's diseaseUS4622011578
[Reference]: Mass spectrometry analysis of the post-translational modifications of alpha-enolase from pancreatic ductal adenocarcinoma cells.
22Arginine MethylationLung cancer/carcinomaH1299 cell linePR21324384472
[Reference]: It has been reported that p53 with R213Q mutation is exist in certain tumor cell lines and its methylation on R213 as well
23Serine PhosphorylationLymphomaDS31224173284
[Reference]: Our study shows that in addition to protecting against tumours caused by ionising radiation, phosphorylation of p53 on Ser312 also contributes to the suppression of carcinogen-mediated tumourigenesis
24Lysine MethylationGlioblastomaPK37022864287
[Reference]: We also found that endogenous full-length PHF20 interacted with endogenous p53 in cell lines U87 (glioblastoma) and MCF7 (breast cancer), which both express wild-type p53; PHF20 is an effector protein of p53 double lysine methylation that stabilizes and activates p53.
25Lysine MethylationBreast cancer/tumor/carcinomaMCF7PK37022864287
[Reference]: We also found that endogenous full-length PHF20 interacted with endogenous p53 in cell lines U87 (glioblastoma) and MCF7 (breast cancer), which both express wild-type p53; PHF20 is an effector protein of p53 double lysine methylation that stabilizes and activates p53.
26Lysine MethylationLymphomaDK37224189068
[Reference]: We also show that reduced PRMT5 expression leads to cyclin D1 transcriptional repression via loss of TP53K372 methylation, which results in decreased BCL3 expression and enhanced recruitment of NF-B p52-HDAC1 repressor complexes to the cyclin D1 promoter.
27Serine PhosphorylationBreast cancer/tumor/carcinomaMCF7AS39221084272
[Reference]: lack of phosphorylation at Ser392 may be important in breast cancer pathogenesis and inability to phosphorylate p53 at this site has been related to treatment response
28Serine PhosphorylationVestibular schwannomasPS39216299809
[Reference]: Our results suggest that age dependent phosphorylation of p53 protein and deregulation of p53 gene has a role in the development of human vestibular schwannomas.
29Serine PhosphorylationOvarian cancer/carcinomaUS39220009884
[Reference]: Expression of p53 protein phosphorylated at serine 20 and serine 392 in malignant and benign ovarian neoplasms: correlation with clinicopathological parameters of tumors.
30Serine PhosphorylationHepatocellular carcinoma/Hepatocarcinoma/HepatomaUS39221455220
[Reference]: Met ensures cell survival through a new path in which c-Abl and p38-MAPK are employed to elicit p53 phosphorylation on Ser(392) and Mdm2 upregulation. We found a clinical correlation between activated Met, phospho-p53, and Mdm2 levels in human tumors, supporting the role of this path in tumorigenesis.