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Sep. 10, 2014:
A total of 174 experimentally verified S-nitrosylation sites on 94 S-nitrosylated proteins from individualized human colorectal cancer tissues using a label-free quantitation strategy.

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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 :
( If your security settings prevent Jmol from running, please register http://140.138.144.145/ as a safe location in your Java settings. )

Protein 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
Network with metabolic pathway:
Kegg map ID Pathway Link
map05014Amyotrophic lateral sclerosis (ALS)
map05213Endometrial cancer
map05216Thyroid cancer
map05217Basal cell carcinoma
map05219Bladder cancer
map05223Non-small cell lung cancer
map04115p53 signaling pathway
map04210Apoptosis
map04722Neurotrophin signaling pathway
map05160Hepatitis C
map05162Measles
map05210Colorectal cancer
map05212Pancreatic cancer
map05214Glioma
map05215Prostate cancer
map05218Melanoma
map05220Chronic myeloid leukemia
map05222Small cell lung cancer
map04010MAPK signaling pathway
map04110Cell cycle
map04151PI3K-Akt signaling pathway
map04310Wnt signaling pathway
map05016Huntington's disease
map05161Hepatitis B
map05166HTLV-I infection
map05168Herpes simplex infection
map05169Epstein-Barr virus infection
map05200Pathways in cancer
map05202Transcriptional misregulation in cancer
map05203Viral carcinogenesis
Graphical Visualization of S-nitrosylation Sites:
Overview of Protein S-nitrosylation Sites with Functional and Structural Information
InterPro ID Domain
IPR002117
IPR008967
IPR010991
IPR011615
IPR012346
IPR013872
IPR015551

The S-nitrosylation sites of P53_HUMAN

No. Position S-nitrosylated Peptide Secondary Structure of S-nitrosylated Peptide Solvent Accessibility of nitrosylated Site Substrate Motifs PubMed ID Experiment
1124LHSGTAKSVT C TYSPALNKMF CCCCCCCEEE E EECCHHHHHH 2.93%HC127791795-
2124LHSGTAKSVT C TYSPALNKMF CCCCCCCEEE E EECCHHHHHH 2.93%HC1223796488-
3124LHSGTAKSVT C TYSPALNKMF CCCCCCCEEE E EECCHHHHHH 2.93%HC1215998249-
4141NKMFCQLAKT C PVQLWVDSTP HHHHHHHCCC C CEEEEECCCC 2.83%HC037791795-
5141NKMFCQLAKT C PVQLWVDSTP HHHHHHHCCC C CEEEEECCCC 2.83%HC0323796488-
6141NKMFCQLAKT C PVQLWVDSTP HHHHHHHCCC C CEEEEECCCC 2.83%HC0315998249-
7182VVRRCPHHER C SDSDGLAPPQ HHHHCCCCCC C CCCCCCCCCC 4.89%HC017791795-
8182VVRRCPHHER C SDSDGLAPPQ HHHHCCCCCC C CCCCCCCCCC 4.89%HC0123796488-
9182VVRRCPHHER C SDSDGLAPPQ HHHHCCCCCC C CCCCCCCCCC 4.89%HC0115998249-