Id: | acc1552 |
Group: | 2sens |
Protein: | ERBB4 |
Gene Symbol: | ERBB4 |
Protein Id: | Q15303 |
Protein Name: | ERBB4_HUMAN |
PTM: | phosphorylation |
Site: | unclear |
Site Sequence: | |
Disease Category: | Cancer |
Disease: | Ovarian Cancer |
Disease Subtype: | |
Disease Cellline: | SK-OV-3 |
Disease Info: | |
Drug: | Y-142 |
Drug Info: | - |
Effect: | modulate |
Effect Info: | "Y-142 can also neutralize the phosphorylation of epidermal growth factor receptor and ERBB4 induced by HB-EGF, and inhibit the proliferation of cancer cells and endothelial cells induced by HB-EGF." |
Note: | |
Score: | 4.0 |
Pubmed(PMID): | 23251664 |
Sentence Index: | 23251664_9-10 |
Sentence: | "In addition, Y-142 neutralized HB-EGF-induced phosphorylation of EGFR and ERBB4, and blocked their downstream ERK1/2 and AKT signaling. We also found that Y-142 inhibited HB-EGF-induced cancer cell proliferation, endothelial cell proliferation, tube formation, and VEGF production more effectively than cetuximab and CRM197 and that Y-142 was superior to bevacizumab in the inhibition of HB-EGF-induced tube formation." |
Sequence & Structure:
MKPATGLWVWVSLLVAAGTVQPSDSQSVCAGTENKLSSLSDLEQQYRALRKYYENCEVVMGNLEITSIEHNRDLSFLRSVREVTGYVLVALNQFRYLPLENLRIIRGTKLYEDRYALAIFLNYRKDGNFGLQELGLKNLTEILNGGVYVDQNKFLCYADTIHWQDIVRNPWPSNLTLVSTNGSSGCGRCHKSCTGRCWGPTENHCQTLTRTVCAEQCDGRCYGPYVSDCCHRECAGGCSGPKDTDCFACMNFNDSGACVTQCPQTFVYNPTTFQLEHNFNAKYTYGAFCVKKCPHNFVVDSSSCVRACPSSKMEVEENGIKMCKPCTDICPKACDGIGTGSLMSAQTVDSSNIDKFINCTKINGNLIFLVTGIHGDPYNAIEAIDPEKLNVFRTVREITGFLNIQSWPPNMTDFSVFSNLVTIGGRVLYSGLSLLILKQQGITSLQFQSLKEISAGNIYITDNSNLCYYHTINWTTLFSTINQRIVIRDNRKAENCTAEGMVCNHLCSSDGCWGPGPDQCLSCRRFSRGRICIESCNLYDGEFREFENGSICVECDPQCEKMEDGLLTCHGPGPDNCTKCSHFKDGPNCVEKCPDGLQGANSFIFKYADPDRECHPCHPNCTQGCNGPTSHDCIYYPWTGHSTLPQHARTPLIAAGVIGGLFILVIVGLTFAVYVRRKSIKKKRALRRFLETELVEPLTPSGTAPNQAQLRILKETELKRVKVLGSGAFGTVYKGIWVPEGETVKIPVAIKILNETTGPKANVEFMDEALIMASMDHPHLVRLLGVCLSPTIQLVTQLMPHGCLLEYVHEHKDNIGSQLLLNWCVQIAKGMMYLEERRLVHRDLAARNVLVKSPNHVKITDFGLARLLEGDEKEYNADGGKMPIKWMALECIHYRKFTHQSDVWSYGVTIWELMTFGGKPYDGIPTREIPDLLEKGERLPQPPICTIDVYMVMVKCWMIDADSRPKFKELAAEFSRMARDPQRYLVIQGDDRMKLPSPNDSKFFQNLLDEEDLEDMMDAEEYLVPQAFNIPPPIYTSRARIDSNRSEIGHSPPPAYTPMSGNQFVYRDGGFAAEQGVSVPYRAPTSTIPEAPVAQGATAEIFDDSCCNGTLRKPVAPHVQEDSSTQRYSADPTVFAPERSPRGELDEEGYMTPMRDKPKQEYLNPVEENPFVSRRKNGDLQALDNPEYHNASNGPPKAEDEYVNEPLYLNTFANTLGKAEYLKNNILSMPEKAKKAFDNPDYWNHSLPPRSTLQHPDYLQEYSTKYFYKQNGRIRPIVAENPEYLSEFSLKPGTVLPPPPYRHRNTVV
Select PDB:
Target | Drug name | MOA | Phase | Status | Disease | Source |
---|---|---|---|---|---|---|
ERBB4 | NERATINIB MALEATE | Receptor protein-tyrosine kinase erbB-4 inhibitor | 4 | - | breast carcinoma | FDA |
ERBB4 | DACOMITINIB | Receptor protein-tyrosine kinase erbB-4 inhibitor | 4 | - | neoplasm | ATC |
ERBB4 | VANDETANIB | Epidermal growth factor receptor inhibitor | 4 | - | neoplasm | ATC |
ERBB4 | VANDETANIB | Epidermal growth factor receptor inhibitor | 4 | - | thyroid carcinoma | DailyMed |
ERBB4 | DACOMITINIB | Receptor protein-tyrosine kinase erbB-4 inhibitor | 4 | - | non-small cell lung carcinoma | EMA FDA |
ERBB4 | AFATINIB DIMALEATE | Receptor protein-tyrosine kinase erbB-4 inhibitor | 4 | - | non-small cell lung carcinoma | DailyMed |
ERBB4 | AFATINIB DIMALEATE | Receptor protein-tyrosine kinase erbB-4 inhibitor | 4 | Not yet recruiting | non-small cell lung carcinoma | ClinicalTrials |
ERBB4 | VANDETANIB | Epidermal growth factor receptor inhibitor | 4 | - | thyroid neoplasm | EMA |
ERBB4 | VANDETANIB | Epidermal growth factor receptor inhibitor | 4 | Active, not recruiting | thyroid cancer | ClinicalTrials |
ERBB4 | NERATINIB MALEATE | Receptor protein-tyrosine kinase erbB-4 inhibitor | 4 | - | breast cancer | DailyMed |
ERBB4 | VANDETANIB | Epidermal growth factor receptor inhibitor | 4 | - | medullary thyroid gland carcinoma | DailyMed |
ERBB4 | AFATINIB | Receptor protein-tyrosine kinase erbB-4 inhibitor | 3 | Completed | head and neck squamous cell carcinoma | ClinicalTrials |
ERBB4 | AFATINIB | Receptor protein-tyrosine kinase erbB-4 inhibitor | 3 | - | neoplasm | ATC |
ERBB4 | NERATINIB | Receptor protein-tyrosine kinase erbB-4 inhibitor | 3 | - | neoplasm | ATC |
ERBB4 | AFATINIB | Receptor protein-tyrosine kinase erbB-4 inhibitor | 3 | Completed | non-small cell lung carcinoma | ClinicalTrials ClinicalTrials ClinicalTrials ClinicalTrials ClinicalTrials ClinicalTrials ClinicalTrials |
ERBB4 | VANDETANIB | Epidermal growth factor receptor inhibitor | 3 | Completed | non-small cell lung carcinoma | ClinicalTrials ClinicalTrials ClinicalTrials ClinicalTrials |
ERBB4 | DACOMITINIB ANHYDROUS | Receptor protein-tyrosine kinase erbB-4 inhibitor | 3 | Completed | non-small cell lung carcinoma | ClinicalTrials ClinicalTrials |
ERBB4 | POZIOTINIB | Epidermal growth factor receptor inhibitor | 3 | Suspended | non-small cell lung carcinoma | ClinicalTrials |
ERBB4 | AFATINIB | Receptor protein-tyrosine kinase erbB-4 inhibitor | 3 | Completed | breast neoplasm | ClinicalTrials |
ERBB4 | NERATINIB | Receptor protein-tyrosine kinase erbB-4 inhibitor | 3 | Recruiting | biliary tract neoplasm | ClinicalTrials |
ERBB4 | AFATINIB | Receptor protein-tyrosine kinase erbB-4 inhibitor | 3 | Active, not recruiting | upper aerodigestive tract neoplasm | ClinicalTrials |
ERBB4 | AFATINIB | Receptor protein-tyrosine kinase erbB-4 inhibitor | 3 | Terminated | upper aerodigestive tract neoplasm | ClinicalTrials ClinicalTrials |
ERBB4 | VANDETANIB | Epidermal growth factor receptor inhibitor | 3 | Active, not recruiting | thyroid cancer | ClinicalTrials |
ERBB4 | VANDETANIB | Epidermal growth factor receptor inhibitor | 3 | Completed | thyroid cancer | ClinicalTrials |
ERBB4 | NERATINIB | Receptor protein-tyrosine kinase erbB-4 inhibitor | 3 | Completed | breast cancer | ClinicalTrials ClinicalTrials |
Note: Only show clinically investigational or approved drugs with protein targets.
Protein Tractability:
source: Open TargetsPTM Intensity:
source: CPTACNo intensity data of this site,
show all other sites!
ERBB4-Ser1124 | |||||
---|---|---|---|---|---|
Cancer | Intensity | ||||
BRCA | |||||
COAD | |||||
HGSC | |||||
ccRCC | |||||
GBM | -0.707 | ||||
HNSC | |||||
LUAD | |||||
LUSC | |||||
non_ccRCC | |||||
PDAC | |||||
UCEC | 0.707 |
ERBB4-Ser726 | |||||
---|---|---|---|---|---|
Cancer | Intensity | ||||
BRCA | |||||
COAD | |||||
HGSC | 1.005 | ||||
ccRCC | |||||
GBM | -0.995 | ||||
HNSC | |||||
LUAD | |||||
LUSC | |||||
non_ccRCC | |||||
PDAC | |||||
UCEC | -0.01 |
ERBB4-Thr699 | |
---|---|
Cancer | Intensity |
BRCA | |
COAD | |
HGSC | -1.155 |
ccRCC | |
GBM | 0.595 |
HNSC | |
LUAD | |
LUSC | |
non_ccRCC | |
PDAC | |
UCEC | 0.56 |
PTM-Disease Association:
source: PTMDResidue | Position | State | Disease | Class | PMID |
---|---|---|---|---|---|
- | - | P | Breast cancer/tumor/carcinoma | Phosphorylation | 11389077 |
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.