Id: | acc1834 |
Group: | 2sens |
Protein: | p53 |
Gene Symbol: | TP53 |
Protein Id: | P04637 |
Protein Name: | P53_HUMAN |
PTM: | acetylation |
Site: | Lys382 |
Site Sequence: | KGQSTSRHKKLMFKTEGPDSD |
Disease Category: | Cancer |
Disease: | Glioblastoma |
Disease Subtype: | |
Disease Cellline: | U251 |
Disease Info: | |
Drug: | DWP0016 |
Drug Info: | "DWP0016 is a novel histone deacetylase (HDAC) inhibitor that demonstrates inhibitory effects on lung cancer A549 cells and Lewis lung carcinoma in mice by modulating histone acetylation, PTEN expression, and Akt phosphorylation." |
Effect: | enhance |
Effect Info: | "DWP0016 promotes the acetylation of p53 at the lys382 site, inducing growth inhibition, cell cycle arrest, and apoptosis." |
Note: | |
Score: | 5.0 |
Pubmed(PMID): | 23297003 |
Sentence Index: | 23297003_4-5 |
Sentence: | "DWP0016 induced caspase-dependent and independent apoptosis in U251 cells, which was identified by flow cytometry analysis, caspases activity analysis, Western blotting assay, and caspases inhibition. Mechanisms research suggested that DWP0016 activated transcription and acetylation of tumor suppressor p53. DWP0016 regulated p300, CBP, and PCAF to facilitate p53 acetylation at lys382 in U251 cells." |
Sequence & Structure:
MEEPQSDPSVEPPLSQETFSDLWKLLPENNVLSPLPSQAMDDLMLSPDDIEQWFTEDPGPDEAPRMPEAAPPVAPAPAAPTPAAPAPAPSWPLSSSVPSQKTYQGSYGFRLGFLHSGTAKSVTCTYSPALNKMFCQLAKTCPVQLWVDSTPPPGTRVRAMAIYKQSQHMTEVVRRCPHHERCSDSDGLAPPQHLIRVEGNLRVEYLDDRNTFRHSVVVPYEPPEVGSDCTTIHYNYMCNSSCMGGMNRRPILTIITLEDSSGNLLGRNSFEVRVCACPGRDRRTEEENLRKKGEPHHELPPGSTKRALPNNTSSSPQPKKKPLDGEYFTLQIRGRERFEMFRELNEALELKDAQAGKEPGGSRAHSSHLKSKKGQSTSRHKKLMFKTEGPDSD
Select PDB:
Target | Drug name | MOA | Phase | Status | Disease | Source |
---|---|---|---|---|---|---|
TP53 | EPRENETAPOPT | Cellular tumor antigen p53 stabiliser | 3 | Completed | myelodysplastic syndrome | ClinicalTrials |
TP53 | IDASANUTLIN | Tumour suppressor p53/oncoprotein Mdm2 inhibitor | 3 | Terminated | acute myeloid leukemia | ClinicalTrials |
TP53 | CENERSEN SODIUM | p53 mRNA antisense inhibitor | 2 | Terminated | chronic lymphocytic leukemia | ClinicalTrials |
TP53 | CENERSEN | p53 mRNA antisense inhibitor | 2 | Completed | acute myeloid leukemia | ClinicalTrials |
TP53 | CENERSEN | p53 mRNA antisense inhibitor | 2 | Withdrawn | acute myeloid leukemia | ClinicalTrials |
TP53 | NAVTEMADLIN | Tumour suppressor p53/oncoprotein Mdm2 inhibitor | 2 | Recruiting | essential thrombocythemia | ClinicalTrials |
TP53 | SIREMADLIN | Tumour suppressor p53/oncoprotein Mdm2 inhibitor | 2 | Recruiting | neoplasm | ClinicalTrials |
TP53 | IDASANUTLIN | Tumour suppressor p53/oncoprotein Mdm2 inhibitor | 2 | Recruiting | neoplasm | ClinicalTrials |
TP53 | NAVTEMADLIN | Tumour suppressor p53/oncoprotein Mdm2 inhibitor | 2 | Terminated | small cell lung carcinoma | ClinicalTrials |
TP53 | NAVTEMADLIN | Tumour suppressor p53/oncoprotein Mdm2 inhibitor | 2 | Active, not recruiting | polycythemia vera | ClinicalTrials |
TP53 | NAVTEMADLIN | Tumour suppressor p53/oncoprotein Mdm2 inhibitor | 2 | Recruiting | polycythemia vera | ClinicalTrials |
TP53 | NAVTEMADLIN | Tumour suppressor p53/oncoprotein Mdm2 inhibitor | 2 | Recruiting | primary myelofibrosis | ClinicalTrials |
TP53 | IDASANUTLIN | Tumour suppressor p53/oncoprotein Mdm2 inhibitor | 2 | Terminated | polycythemia vera | ClinicalTrials |
TP53 | CONTUSUGENE LADENOVEC | Cellular tumor antigen p53 exogenous gene | 2 | Unknown status | non-small cell lung carcinoma | ClinicalTrials |
TP53 | APG115 | Tumour suppressor p53/oncoprotein Mdm2 inhibitor | 2 | Recruiting | lymphoid leukemia | ClinicalTrials |
TP53 | CONTUSUGENE LADENOVEC | Cellular tumor antigen p53 exogenous gene | 2 | Terminated | head and neck malignant neoplasia | ClinicalTrials |
TP53 | CONTUSUGENE LADENOVEC | Cellular tumor antigen p53 exogenous gene | 2 | Unknown status | head and neck malignant neoplasia | ClinicalTrials ClinicalTrials |
TP53 | EPRENETAPOPT | Cellular tumor antigen p53 stabiliser | 2 | Withdrawn | Mantle cell lymphoma | ClinicalTrials |
TP53 | TEPRASIRAN | p53 mRNA RNAi inhibitor | 2 | Completed | Acute kidney injury | ClinicalTrials |
TP53 | EPRENETAPOPT | Cellular tumor antigen p53 stabiliser | 2 | Completed | ovarian cancer | ClinicalTrials |
TP53 | CONTUSUGENE LADENOVEC | Cellular tumor antigen p53 exogenous gene | 2 | Completed | breast cancer | ClinicalTrials |
TP53 | NAVTEMADLIN | Tumour suppressor p53/oncoprotein Mdm2 inhibitor | 2 | Recruiting | endometrial cancer | ClinicalTrials |
TP53 | CENERSEN | p53 mRNA antisense inhibitor | 1 | Terminated | myelodysplastic syndrome | ClinicalTrials |
TP53 | NAVTEMADLIN | Tumour suppressor p53/oncoprotein Mdm2 inhibitor | 1 | Active, not recruiting | acute myeloid leukemia | ClinicalTrials ClinicalTrials |
TP53 | NAVTEMADLIN | Tumour suppressor p53/oncoprotein Mdm2 inhibitor | 1 | Completed | acute myeloid leukemia | ClinicalTrials |
Note: Only show clinically investigational or approved drugs with protein targets.
Protein Tractability:
source: Open TargetsPTM Intensity:
source: CPTACTP53-Lys382 | |
---|---|
Cancer | Intensity |
BRCA | |
COAD | |
HGSC | |
ccRCC | |
GBM | |
HNSC | |
LUAD | |
LUSC | |
non_ccRCC | |
PDAC | |
UCEC |
PTM-Disease Association:
source: PTMDResidue | Position | State | Disease | Class | PMID |
---|---|---|---|---|---|
K | 382 | A | Osteosarcoma | Acetylation | 30454890 |
K | 382 | D | Acute kidney injury | Acetylation | 37354967 |
K | 382 | D | Neuroblastoma | Acetylation | 29609003 |
K | 382 | D | Osteoporosis | Acetylation | 37023393 |
K | 382 | D | Cutaneous melanoma | Acetylation | 29235570 |
K | 382 | D | Cervical adenocarcinoma | Acetylation | 32976537 |
K | 382 | U | Hepatocellular carcinoma | Acetylation | 31440094 |
K | 382 | U | Non-small cell lung cancer | Acetylation | 29103158 |
K | 382 | U | Triple-negative breast cancer | Acetylation | 29334665 |
K | 382 | U | Lung cancer | Acetylation | 34947995 |
K | 382 | U | Epithelial ovarian cancer | Ubiquitination | 31002112 |
State Note: Based on the distinct PTM states in diseases, PTMD classified all disease-associated PTMs into six classes, including whether the up-regulation (U) or down-regulation (D) of PTM levels, the absence (A) or presence (P) of PTMs, and the creation (C) or disruption (N) of PTM sites are associated with diseases.
PTM-Drug Perturbation Response:
source: DecryptMNo data.
Function score:
source: funscoRNo data.