Id: | acc0263 |
Group: | 1sens |
Protein: | EGFR |
Gene Symbol: | EGFR |
Protein Id: | P00533 |
Protein Name: | EGFR_HUMAN |
PTM: | phosphorylation |
Site: | Tyr1173 |
Site Sequence: | QISLDNPDYQQDFFPKEAKPN |
Disease Category: | Cancer |
Disease: | Hepatocellular Carcinoma |
Disease Subtype: | |
Disease Cellline: | HAK1-B |
Disease Info: | |
Drug: | vandetanib |
Drug Info: | "Vandetanib is an oral multikinase inhibitor targeting RET, EGFR, and VEGFR, approved for the treatment of symptomatic or progressive medullary thyroid cancer in patients with unresectable locally advanced or metastatic disease." |
Effect: | modulate |
Effect Info: | "Vandetanib inhibits the phosphorylation of VEGFR - 2 and EGFR in tumor tissues, significantly reduces tumor vascular density, enhances tumor cell apoptosis, and inhibits tumor growth." |
Note: | |
Score: | 4.0 |
Pubmed(PMID): | 22611027 |
Sentence Index: | 22611027_10 |
Sentence: | "In tumor-bearing mice, vandetanib suppressed phosphorylation of VEGFR-2 and EGFR in tumor tissues, significantly reduced tumor vessel density, enhanced tumor cell apoptosis, suppressed tumor growth, improved survival, reduced number of intrahepatic metastases, and upregulated VEGF, TGF-alpha, and EGF in tumor tissues." |
Sequence & Structure:
MRPSGTAGAALLALLAALCPASRALEEKKVCQGTSNKLTQLGTFEDHFLSLQRMFNNCEVVLGNLEITYVQRNYDLSFLKTIQEVAGYVLIALNTVERIPLENLQIIRGNMYYENSYALAVLSNYDANKTGLKELPMRNLQEILHGAVRFSNNPALCNVESIQWRDIVSSDFLSNMSMDFQNHLGSCQKCDPSCPNGSCWGAGEENCQKLTKIICAQQCSGRCRGKSPSDCCHNQCAAGCTGPRESDCLVCRKFRDEATCKDTCPPLMLYNPTTYQMDVNPEGKYSFGATCVKKCPRNYVVTDHGSCVRACGADSYEMEEDGVRKCKKCEGPCRKVCNGIGIGEFKDSLSINATNIKHFKNCTSISGDLHILPVAFRGDSFTHTPPLDPQELDILKTVKEITGFLLIQAWPENRTDLHAFENLEIIRGRTKQHGQFSLAVVSLNITSLGLRSLKEISDGDVIISGNKNLCYANTINWKKLFGTSGQKTKIISNRGENSCKATGQVCHALCSPEGCWGPEPRDCVSCRNVSRGRECVDKCNLLEGEPREFVENSECIQCHPECLPQAMNITCTGRGPDNCIQCAHYIDGPHCVKTCPAGVMGENNTLVWKYADAGHVCHLCHPNCTYGCTGPGLEGCPTNGPKIPSIATGMVGALLLLLVVALGIGLFMRRRHIVRKRTLRRLLQERELVEPLTPSGEAPNQALLRILKETEFKKIKVLGSGAFGTVYKGLWIPEGEKVKIPVAIKELREATSPKANKEILDEAYVMASVDNPHVCRLLGICLTSTVQLITQLMPFGCLLDYVREHKDNIGSQYLLNWCVQIAKGMNYLEDRRLVHRDLAARNVLVKTPQHVKITDFGLAKLLGAEEKEYHAEGGKVPIKWMALESILHRIYTHQSDVWSYGVTVWELMTFGSKPYDGIPASEISSILEKGERLPQPPICTIDVYMIMVKCWMIDADSRPKFRELIIEFSKMARDPQRYLVIQGDERMHLPSPTDSNFYRALMDEEDMDDVVDADEYLIPQQGFFSSPSTSRTPLLSSLSATSNNSTVACIDRNGLQSCPIKEDSFLQRYSSDPTGALTEDSIDDTFLPVPEYINQSVPKRPAGSVQNPVYHNQPLNPAPSRDPHYQDPHSTAVGNPEYLNTVQPTCVNSTFDSPAHWAQKGSHQISLDNPDYQQDFFPKEAKPNGIFKGSTAENAEYLRVAPQSSEFIGA
Select PDB:
Target | Drug name | MOA | Phase | Status | Disease | Source |
---|---|---|---|---|---|---|
EGFR | LAPATINIB DITOSYLATE | Epidermal growth factor receptor erbB1 inhibitor | 4 | - | breast carcinoma | FDA |
EGFR | NERATINIB MALEATE | Epidermal growth factor receptor erbB1 inhibitor | 4 | - | breast carcinoma | FDA |
EGFR | CETUXIMAB | Epidermal growth factor receptor erbB1 inhibitor | 4 | - | colorectal adenocarcinoma | DailyMed |
EGFR | PANITUMUMAB | Epidermal growth factor receptor erbB1 inhibitor | 4 | - | colorectal adenocarcinoma | DailyMed |
EGFR | NECITUMUMAB | Epidermal growth factor receptor erbB1 inhibitor | 4 | - | neoplasm | ATC |
EGFR | AMIVANTAMAB | Epidermal growth factor receptor inhibitor | 4 | - | neoplasm | ATC |
EGFR | CETUXIMAB | Epidermal growth factor receptor erbB1 inhibitor | 4 | - | neoplasm | ATC |
EGFR | CETUXIMAB | Epidermal growth factor receptor erbB1 inhibitor | 4 | Recruiting | neoplasm | ClinicalTrials |
EGFR | VANDETANIB | Epidermal growth factor receptor inhibitor | 4 | - | neoplasm | ATC |
EGFR | PANITUMUMAB | Epidermal growth factor receptor erbB1 inhibitor | 4 | - | neoplasm | ATC |
EGFR | GEFITINIB | Epidermal growth factor receptor erbB1 inhibitor | 4 | - | neoplasm | ATC |
EGFR | DACOMITINIB | Epidermal growth factor receptor erbB1 inhibitor | 4 | - | neoplasm | ATC |
EGFR | MOBOCERTINIB | Epidermal growth factor receptor erbB1 inhibitor | 4 | - | neoplasm | ATC |
EGFR | OSIMERTINIB | Epidermal growth factor receptor erbB1 inhibitor | 4 | - | neoplasm | ATC |
EGFR | BRIGATINIB | Epidermal growth factor receptor erbB1 inhibitor | 4 | - | neoplasm | ATC |
EGFR | CETUXIMAB | Epidermal growth factor receptor erbB1 inhibitor | 4 | - | squamous cell carcinoma | DailyMed |
EGFR | VANDETANIB | Epidermal growth factor receptor inhibitor | 4 | - | thyroid carcinoma | DailyMed |
EGFR | NECITUMUMAB | Epidermal growth factor receptor erbB1 inhibitor | 4 | - | non-small cell lung carcinoma | EMA DailyMed |
EGFR | AFATINIB DIMALEATE | Epidermal growth factor receptor erbB1 inhibitor | 4 | - | non-small cell lung carcinoma | DailyMed |
EGFR | AFATINIB DIMALEATE | Epidermal growth factor receptor erbB1 inhibitor | 4 | Not yet recruiting | non-small cell lung carcinoma | ClinicalTrials |
EGFR | DACOMITINIB | Epidermal growth factor receptor erbB1 inhibitor | 4 | - | non-small cell lung carcinoma | FDA EMA |
EGFR | OSIMERTINIB MESYLATE | Epidermal growth factor receptor erbB1 inhibitor | 4 | - | non-small cell lung carcinoma | EMA DailyMed |
EGFR | ERLOTINIB HYDROCHLORIDE | Epidermal growth factor receptor erbB1 inhibitor | 4 | - | non-small cell lung carcinoma | DailyMed |
EGFR | BRIGATINIB | Epidermal growth factor receptor erbB1 inhibitor | 4 | - | non-small cell lung carcinoma | EMA FDA |
EGFR | AMIVANTAMAB | Epidermal growth factor receptor inhibitor | 4 | - | non-small cell lung carcinoma | EMA FDA |
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!
EGFR-Ser1012 | |||||
---|---|---|---|---|---|
Cancer | Intensity | ||||
BRCA | |||||
COAD | |||||
HGSC | |||||
ccRCC | -0.224 | ||||
GBM | |||||
HNSC | |||||
LUAD | 1.093 | ||||
LUSC | -0.869 | ||||
non_ccRCC | |||||
PDAC | |||||
UCEC |
EGFR-Ser1019 | |||||
---|---|---|---|---|---|
Cancer | Intensity | ||||
BRCA | -0.162 | ||||
COAD | 0.525 | ||||
HGSC | 1.91 | ||||
ccRCC | -0.216 | ||||
GBM | |||||
HNSC | |||||
LUAD | -1.07 | ||||
LUSC | -1.597 | ||||
non_ccRCC | -0.132 | ||||
PDAC | 0.291 | ||||
UCEC | 0.453 |
EGFR-Ser1026 | |||||
---|---|---|---|---|---|
Cancer | Intensity | ||||
BRCA | |||||
COAD | 0.707 | ||||
HGSC | |||||
ccRCC | |||||
GBM | |||||
HNSC | |||||
LUAD | -0.707 | ||||
LUSC | |||||
non_ccRCC | |||||
PDAC | |||||
UCEC |
EGFR-Ser1121 | |||||
---|---|---|---|---|---|
Cancer | Intensity | ||||
BRCA | |||||
COAD | 0.33 | ||||
HGSC | 0.793 | ||||
ccRCC | -1.123 | ||||
GBM | |||||
HNSC | |||||
LUAD | |||||
LUSC | |||||
non_ccRCC | |||||
PDAC | |||||
UCEC |
EGFR-Ser650 | |||||
---|---|---|---|---|---|
Cancer | Intensity | ||||
BRCA | |||||
COAD | -0.529 | ||||
HGSC | 1.453 | ||||
ccRCC | -0.792 | ||||
GBM | |||||
HNSC | |||||
LUAD | -1.019 | ||||
LUSC | -0.082 | ||||
non_ccRCC | |||||
PDAC | |||||
UCEC | 0.969 |
EGFR-Ser675 | |||||
---|---|---|---|---|---|
Cancer | Intensity | ||||
BRCA | -2.294 | ||||
COAD | |||||
HGSC | 0.643 | ||||
ccRCC | 0.535 | ||||
GBM | |||||
HNSC | |||||
LUAD | -0.009 | ||||
LUSC | -0.232 | ||||
non_ccRCC | 0.66 | ||||
PDAC | 0.738 | ||||
UCEC | -0.041 |
EGFR-Ser946 | |||||
---|---|---|---|---|---|
Cancer | Intensity | ||||
BRCA | 0.751 | ||||
COAD | 0.597 | ||||
HGSC | 1.404 | ||||
ccRCC | -0.059 | ||||
GBM | |||||
HNSC | |||||
LUAD | 0.114 | ||||
LUSC | -0.811 | ||||
non_ccRCC | -2.003 | ||||
PDAC | 0.462 | ||||
UCEC | -0.456 |
EGFR-Ser991 | |||||
---|---|---|---|---|---|
Cancer | Intensity | ||||
BRCA | |||||
COAD | |||||
HGSC | |||||
ccRCC | 0.707 | ||||
GBM | -0.707 | ||||
HNSC | |||||
LUAD | |||||
LUSC | |||||
non_ccRCC | |||||
PDAC | |||||
UCEC |
EGFR-Ser992 | |||||
---|---|---|---|---|---|
Cancer | Intensity | ||||
BRCA | |||||
COAD | |||||
HGSC | |||||
ccRCC | -0.707 | ||||
GBM | |||||
HNSC | 0.707 | ||||
LUAD | |||||
LUSC | |||||
non_ccRCC | |||||
PDAC | |||||
UCEC |
EGFR-Ser994 | |||||
---|---|---|---|---|---|
Cancer | Intensity | ||||
BRCA | |||||
COAD | 0.623 | ||||
HGSC | -0.784 | ||||
ccRCC | -0.58 | ||||
GBM | |||||
HNSC | |||||
LUAD | -0.129 | ||||
LUSC | |||||
non_ccRCC | -1.376 | ||||
PDAC | 0.785 | ||||
UCEC | 1.461 |
EGFR-Ser997 | |||||
---|---|---|---|---|---|
Cancer | Intensity | ||||
BRCA | 1.611 | ||||
COAD | 0.359 | ||||
HGSC | -2.065 | ||||
ccRCC | -0.131 | ||||
GBM | |||||
HNSC | |||||
LUAD | 0.009 | ||||
LUSC | -0.098 | ||||
non_ccRCC | 0.862 | ||||
PDAC | -0.488 | ||||
UCEC | -0.059 |
EGFR-Thr648 | |||||
---|---|---|---|---|---|
Cancer | Intensity | ||||
BRCA | 1.108 | ||||
COAD | 0.434 | ||||
HGSC | 1.068 | ||||
ccRCC | 0.044 | ||||
GBM | |||||
HNSC | |||||
LUAD | 0.416 | ||||
LUSC | -1.175 | ||||
non_ccRCC | -1.717 | ||||
PDAC | -0.77 | ||||
UCEC | 0.592 |
EGFR-Thr948 | |||||
---|---|---|---|---|---|
Cancer | Intensity | ||||
BRCA | |||||
COAD | 0.914 | ||||
HGSC | 0.483 | ||||
ccRCC | -0.006 | ||||
GBM | |||||
HNSC | |||||
LUAD | -1.39 | ||||
LUSC | |||||
non_ccRCC | |||||
PDAC | |||||
UCEC |
EGFR-Thr996 | |||||
---|---|---|---|---|---|
Cancer | Intensity | ||||
BRCA | 1.232 | ||||
COAD | -0.247 | ||||
HGSC | |||||
ccRCC | -1.249 | ||||
GBM | |||||
HNSC | |||||
LUAD | -0.683 | ||||
LUSC | -0.608 | ||||
non_ccRCC | 1.709 | ||||
PDAC | -0.291 | ||||
UCEC | 0.136 |
EGFR-Tyr1047 | |||||
---|---|---|---|---|---|
Cancer | Intensity | ||||
BRCA | |||||
COAD | 0.614 | ||||
HGSC | |||||
ccRCC | 0.139 | ||||
GBM | |||||
HNSC | |||||
LUAD | -0.763 | ||||
LUSC | -1.224 | ||||
non_ccRCC | |||||
PDAC | |||||
UCEC | 1.234 |
EGFR-Tyr1127 | |||||
---|---|---|---|---|---|
Cancer | Intensity | ||||
BRCA | 0.853 | ||||
COAD | 0.567 | ||||
HGSC | 1.203 | ||||
ccRCC | -0.756 | ||||
GBM | |||||
HNSC | |||||
LUAD | -0.922 | ||||
LUSC | -0.649 | ||||
non_ccRCC | -1.614 | ||||
PDAC | 0.354 | ||||
UCEC | 0.964 |
EGFR-Tyr1152 | |
---|---|
Cancer | Intensity |
BRCA | 0.302 |
COAD | 0.15 |
HGSC | 0.898 |
ccRCC | -0.139 |
GBM | |
HNSC | |
LUAD | -0.637 |
LUSC | -1.754 |
non_ccRCC | -0.871 |
PDAC | 0.427 |
UCEC | 1.624 |
PTM-Disease Association:
source: PTMDResidue | Position | State | Disease | Class | PMID |
---|---|---|---|---|---|
Y | 1173 | U | Non-small cell lung cancer/carcinoma | Phosphorylation | 19002495 |
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.