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Protein Name: Cellular tumor antigen p53

UniprotKB/SwissProt ID: P53_HUMAN (P04637)

Gene Name: TP53

Synonyms: P53

Organism: Homo sapiens (Human).

Function: Acts 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 is involved in activating oxidative stress-induced necrosis; the function is largely independent of transcription. Induces the transcription of long intergenic non-coding RNA p21 (lincRNA-p21) and lincRNA- Mkln1. LincRNA-p21 participates in TP53-dependent transcriptional repression leading to apoptosis and seem to have to effect on cell-cycle regulation. Implicated in Notch signaling cross-over. Prevents CDK7 kinase activity when associated to CAK complex in response to DNA damage, thus stopping cell cycle progression. Isoform 2 enhances the transactivation activity of isoform 1 from some but not all TP53-inducible promoters. Isoform 4 suppresses transactivation activity and impairs growth suppression mediated by isoform 1. Isoform 7 inhibits isoform 1-mediated apoptosis.

Other Modifications: View all modification sites in dbPTM

Protein Subcellular Localization: Cytoplasm. Nucleus. Nucleus, PML body. Endoplasmic reticulum. Mitochondrion matrix. Note=Interaction with BANP promotes nuclear localization. Recruited into PML bodies together with CHEK2. Translocates to mitochondria upon oxidative stress. Isoform 1: Nu

PDB :
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Graphical Visualization of Ubiquitination Sites:
Overview of Protein Ubiquitination Sites with Functional and Structural Information
InterPro ID Domain
IPR002117
IPR008967
IPR010991
IPR011615
IPR012346
IPR013872
IPR015551


The ubiquitination sites of P53_HUMAN

No. Position Ubiquitinated Peptide Secondary Structure Solvent Accessibility Substrate Motifs PubMed ID
140NEATGG K YVPRAI CCCCCC H HHHHCC 2.98%21890473
283PVVPAH K DKSGAP CCCCCC C CCCCCC 28.67%2190698
3101SSVPSQ K TYQGSY CCCCCC C CCCCCC 54.24%17371868
4120LHSGTA K SVTCTY CCCCCC C EEEEEE 45.34%17371868
5132YSPALN K MFCQLA ECCHHH H HHHHHC 33.92%17371868
6139MFCQLA K TCPVQL HHHHHC C CCCEEE 60.29%17371868
7164RAMAIY K QSQHMT EEEHHH H HHHHHH 37.04%17371868
8279QQVFDA K NMMAAC EEEECC C CCCCCC 43.96%21890473
9291EEENLR K KGEPHH CHHHHH C CCCCCC 69.19%19536131
10291EEENLR K KGEPHH CHHHHH C CCCCCC 69.19%19536131
11292EENLRK K GEPHHE HHHHHC C CCCCCC 63.17%19536131
12292EENLRK K GEPHHE HHHHHC C CCCCCC 63.17%19536131
13305LPPGST K RALPNN CCCCCC C CCCCCC 37.05%19857530
14319SSSPQP K KKPLDG CCCCCC C CCCCCC 69.08%19927155
15319SSSPQP K KKPLDG CCCCCC C CCCCCC 69.08%19927155
16320SSPQPK K KPLDGE CCCCCC C CCCCCC 67.32%19857530
17320SSPQPK K KPLDGE CCCCCC C CCCCCC 67.32%19857530
18321SPQPKK K PLDGEY CCCCCC C CCCCCE 57.87%19857530
19321SPQPKK K PLDGEY CCCCCC C CCCCCE 57.87%19857530
20351NEALEL K DAQAGK HHHHHH H HCCCCC 41.46%11046142
21357KDAQAG K EPGGSR HHCCCC C CCCCCC 64.85%21906983
22357KDAQAG K EPGGSR HHCCCC C CCCCCC 64.85%21906983
23361AIQELF K RISEQF CCCCCC C CCCCCC 25.36%2189047
24370AHSSHL K SKKGQS CCCCCC C CCCCCC 55.60%11046142
25370AHSSHL K SKKGQS CCCCCC C CCCCCC 55.60%11046142
26372SSHLKS K KGQSTS CCCCCC C CCCCCC 60.37%11046142
27372SSHLKS K KGQSTS CCCCCC C CCCCCC 60.37%11046142
28373SHLKSK K GQSTSR CCCCCC C CCCCCC 70.08%11046142
29373SHLKSK K GQSTSR CCCCCC C CCCCCC 70.08%11046142
30381QSTSRH K KLMFKT CCCCCC C EEEEEC 46.63%11046142
31381QSTSRH K KLMFKT CCCCCC C EEEEEC 46.63%11046142
32382STSRHK K LMFKTE CCCCCC E EEEECC 38.77%11046142
33386HKKLMF K TEGPDS CCEEEE E CCCCCC 31.53%10562557
34386HKKLMF K TEGPDS CCEEEE E CCCCCC 31.53%10562557
35386HKKLMF K TEGPDS CCEEEE E CCCCCC 31.53%10562557

The interacting network mediated by proteins: P53_HUMAN


Disease:
Disease database Database Entry Disease information
KEGGH00020 Colorectal cancer
HPRD01859Adrenocortical carcinoma, pediatric
HPRD01859Breast cancer
HPRD01859Choroid plexus papilloma
HPRD01859Colon tumors, concurrent multiple primary
HPRD01859Hepatoblastoma
HPRD01859Hepatocellular carcinoma
HPRD01859Histiocytoma, malignant fibrous
HPRD01859Li-Fraumeni syndrome
HPRD01859Li-Fraumeni syndrome 1
HPRD01859Multiple malignancy syndrome
HPRD01859Nasopharyngeal carcinoma
HPRD01859Osteosarcoma
HPRD01859Pancreatic cancer
HPRD01859Tp53 polymorphism
Metabolic pathway:
Kegg map ID Pathway
map03008Ribosome biogenesis in eukaryotes