Id: | acc3536 |
Group: | 2sens |
Protein: | FAK |
Gene Symbol: | PTK2 |
Protein Id: | Q05397 |
Protein Name: | FAK1_HUMAN |
PTM: | phosphorylation |
Site: | Tyr397 |
Site Sequence: | AVSVSETDDYAEIIDEEDTYT |
Disease Category: | Cancer |
Disease: | Hemangioma |
Disease Subtype: | Infantile Hemangiomas |
Disease Cellline: | HUVECs |
Disease Info: | |
Drug: | Propranolol |
Drug Info: | "Propranolol is a beta - blocker used to treat high blood pressure, irregular heart rhythms, and other heart - related conditions." |
Effect: | modulate |
Effect Info: | "The drug inhibits phosphorylated signaling proteins, indicating that it achieves the therapeutic effect on IHs by inhibiting the angiogenesis signaling pathway mediated by VEGF." |
Note: | |
Score: | 4.0 |
Pubmed(PMID): | 33575332 |
Sentence Index: | 33575332_8-9 |
Sentence: | "Further studies showed that it could not only inhibit the migration, invasion, and tube formation ability of HUVECs after VEGF induction but also inhibit the phosphorylated protein expressions of angiogenesis-related signaling molecules like AKT, mTOR, ERK, and FAK in HUVECs, with a concentration-dependent inhibitory effect. Conclusion: Propranolol can inhibit the proliferation, migration, invasion, adhesion, and tube formation of hemangioma endothelial cells; block VEGF-mediated angiogenesis signaling pathway; suppress the expressions of downstream angiogenesis-related signaling molecules; and ultimately achieve the effect of treatment of IHs." |
Sequence & Structure:
MAAAYLDPNLNHTPNSSTKTHLGTGMERSPGAMERVLKVFHYFESNSEPTTWASIIRHGDATDVRGIIQKIVDSHKVKHVACYGFRLSHLRSEEVHWLHVDMGVSSVREKYELAHPPEEWKYELRIRYLPKGFLNQFTEDKPTLNFFYQQVKSDYMLEIADQVDQEIALKLGCLEIRRSYWEMRGNALEKKSNYEVLEKDVGLKRFFPKSLLDSVKAKTLRKLIQQTFRQFANLNREESILKFFEILSPVYRFDKECFKCALGSSWIISVELAIGPEEGISYLTDKGCNPTHLADFTQVQTIQYSNSEDKDRKGMLQLKIAGAPEPLTVTAPSLTIAENMADLIDGYCRLVNGTSQSFIIRPQKEGERALPSIPKLANSEKQGMRTHAVSVSETDDYAEIIDEEDTYTMPSTRDYEIQRERIELGRCIGEGQFGDVHQGIYMSPENPALAVAIKTCKNCTSDSVREKFLQEALTMRQFDHPHIVKLIGVITENPVWIIMELCTLGELRSFLQVRKYSLDLASLILYAYQLSTALAYLESKRFVHRDIAARNVLVSSNDCVKLGDFGLSRYMEDSTYYKASKGKLPIKWMAPESINFRRFTSASDVWMFGVCMWEILMHGVKPFQGVKNNDVIGRIENGERLPMPPNCPPTLYSLMTKCWAYDPSRRPRFTELKAQLSTILEEEKAQQEERMRMESRRQATVSWDSGGSDEAPPKPSRPGYPSPRSSEGFYPSPQHMVQTNHYQVSGYPGSHGITAMAGSIYPGQASLLDQTDSWNHRPQEIAMWQPNVEDSTVLDLRGIGQVLPTHLMEERLIRQQQEMEEDQRWLEKEERFLKPDVRLSRGSIDREDGSLQGPIGNQHIYQPVGKPDPAAPPKKPPRPGAPGHLGSLASLSSPADSYNEGVKLQPQEISPPPTANLDRSNDKVYENVTGLVKAVIEMSSKIQPAPPEEYVPMVKEVGLALRTLLATVDETIPLLPASTHREIEMAQKLLNSDLGELINKMKLAQQYVMTSLQQEYKKQMLTAAHALAVDAKNLLDVIDQARLKMLGQTRPH
Select PDB:
Target | Drug name | MOA | Phase | Status | Disease | Source |
---|---|---|---|---|---|---|
PTK2 | DEFACTINIB | Focal adhesion kinase 1 inhibitor | 3 | Recruiting | ovarian cancer | ClinicalTrials |
PTK2 | DEFACTINIB | Focal adhesion kinase 1 inhibitor | 2 | Terminated | malignant pleural mesothelioma | ClinicalTrials ClinicalTrials |
PTK2 | DEFACTINIB | Focal adhesion kinase 1 inhibitor | 2 | Active, not recruiting | multiple myeloma | ClinicalTrials |
PTK2 | DEFACTINIB | Focal adhesion kinase 1 inhibitor | 2 | Recruiting | pancreatic carcinoma | ClinicalTrials |
PTK2 | DEFACTINIB | Focal adhesion kinase 1 inhibitor | 2 | Recruiting | thyroid carcinoma | ClinicalTrials |
PTK2 | DEFACTINIB | Focal adhesion kinase 1 inhibitor | 2 | Completed | non-small cell lung carcinoma | ClinicalTrials ClinicalTrials |
PTK2 | DEFACTINIB | Focal adhesion kinase 1 inhibitor | 2 | Active, not recruiting | ovarian serous adenocarcinoma | ClinicalTrials |
PTK2 | DEFACTINIB | Focal adhesion kinase 1 inhibitor | 2 | Recruiting | pancreatic adenocarcinoma | ClinicalTrials |
PTK2 | GSK-2256098 | Focal adhesion kinase 1 inhibitor | 2 | Completed | pancreatic adenocarcinoma | ClinicalTrials |
PTK2 | DEFACTINIB | Focal adhesion kinase 1 inhibitor | 2 | Active, not recruiting | Uveal Melanoma | ClinicalTrials |
PTK2 | DEFACTINIB | Focal adhesion kinase 1 inhibitor | 2 | Recruiting | pancreatic ductal adenocarcinoma | ClinicalTrials |
PTK2 | DEFACTINIB | Focal adhesion kinase 1 inhibitor | 2 | Not yet recruiting | colorectal cancer | ClinicalTrials |
PTK2 | DEFACTINIB | Focal adhesion kinase 1 inhibitor | 2 | Active, not recruiting | ovarian cancer | ClinicalTrials |
PTK2 | DEFACTINIB | Focal adhesion kinase 1 inhibitor | 2 | Recruiting | ovarian cancer | ClinicalTrials |
PTK2 | IFEBEMTINIB | Focal adhesion kinase 1 inhibitor | 2 | Recruiting | ovarian cancer | ClinicalTrials |
PTK2 | DEFACTINIB | Focal adhesion kinase 1 inhibitor | 2 | Completed | lung cancer | ClinicalTrials |
PTK2 | GSK-2256098 | Focal adhesion kinase 1 inhibitor | 2 | Recruiting | meningioma | ClinicalTrials |
PTK2 | DEFACTINIB | Focal adhesion kinase 1 inhibitor | 2 | Recruiting | female reproductive system neoplasm | ClinicalTrials |
PTK2 | GSK-2256098 | Focal adhesion kinase 1 inhibitor | 2 | Recruiting | intracranial meningioma | ClinicalTrials |
PTK2 | VS-4718 | Focal adhesion kinase 1 inhibitor | 1 | Withdrawn | B-cell acute lymphoblastic leukemia | ClinicalTrials |
PTK2 | VS-4718 | Focal adhesion kinase 1 inhibitor | 1 | Withdrawn | acute myeloid leukemia | ClinicalTrials |
PTK2 | DEFACTINIB | Focal adhesion kinase 1 inhibitor | 1 | Active, not recruiting | endometrioid carcinoma | ClinicalTrials |
PTK2 | IFEBEMTINIB | Focal adhesion kinase 1 inhibitor | 1 | Not yet recruiting | neoplasm | ClinicalTrials |
PTK2 | IFEBEMTINIB | Focal adhesion kinase 1 inhibitor | 1 | Recruiting | neoplasm | ClinicalTrials ClinicalTrials |
PTK2 | CEP-37440 | Focal adhesion kinase 1 inhibitor | 1 | Completed | neoplasm | ClinicalTrials |
Note: Only show clinically investigational or approved drugs with protein targets.
Protein Tractability:
source: Open TargetsPTM Intensity:
source: CPTACPTK2-Tyr397 | |
---|---|
Cancer | Intensity |
BRCA | |
COAD | 0.587 |
HGSC | -1.155 |
ccRCC | |
GBM | |
HNSC | |
LUAD | |
LUSC | |
non_ccRCC | |
PDAC | |
UCEC | 0.567 |
PTM-Disease Association:
source: PTMDResidue | Position | State | Disease | Class | PMID |
---|---|---|---|---|---|
Y | 397 | D | Skin cancer | Phosphorylation | 23799510 |
Y | 397 | D | Colorectal cancer | Phosphorylation | 12871985 ;  12871985 |
Y | 397 | D | Lung cancer/carcinoma | Phosphorylation | 23799510 |
Y | 397 | D | Lung cancer | Phosphorylation | 21876001 |
Y | 397 | D | Hepatocellular carcinoma | Phosphorylation | 36209205 |
Y | 397 | P | Gastric cancer | Phosphorylation | 23109808 |
Y | 397 | U | Papillary thyroid carcinoma | Phosphorylation | 37443754 |
Y | 397 | U | Melanoma | Phosphorylation | 24098450 |
Y | 397 | U | Lung squamous cell carcinoma | Phosphorylation | 23906871 |
Y | 397 | U | Breast cancer | Phosphorylation | 37846507 |
Y | 397 | U | Oral squamous cell carcinoma | Phosphorylation | 22766511 |
Y | 397 | U | Ovarian cancer/carcinoma | Phosphorylation | 24062525 |
Y | 397 | U | Ovarian epithelial carcinoma | Phosphorylation | 24655477 |
Y | 397 | U | Non-small cell lung cancer | Phosphorylation | 36209201 |
Y | 397 | U | Glioblastoma | Phosphorylation | 23243059 |
Y | 397 | U | Ewing sarcoma | Phosphorylation | 31811703 |
Y | 397 | U | Ovarian epithelial carcinoma | Phosphorylation | 24655477 |
Y | 397 | U | Ovarian cancer/carcinoma | Phosphorylation | 24655477 |
Y | 397 | U | Squamous cell carcinoma | Phosphorylation | 14603053 ;  14603053 ;  14603053 |
Y | 397 | U | Osteosarcoma | Phosphorylation | 37013056 |
Y | 397 | U | Diffuse gastric cancer | Phosphorylation | 35471457 |
Y | 397 | U | Clear cell renal cell carcinoma | Phosphorylation | 35257717 |
Y | 397 | U | Cancer | Phosphorylation | 14603053 ;  14603053 |
Y | 397 | U | Non-small cell lung cancer | Phosphorylation | 35131384 |
Y | 397 | U | Hepatocellular carcinoma/hepatocarcinoma/hepatoma | Phosphorylation | 23525457 ;  20180147 |
Y | 397 | U | Esophageal squamous cell carcinoma | Phosphorylation | 33532186 |
Y | 397 | U | Ovarian cancer | Phosphorylation | 37221403 ;  35201437 |
Y | 397 | U | Pancreatic ductal adenocarcinoma | Phosphorylation | 35982848 ;  36228156 |
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.