Id: | acc1619 |
Group: | 2sens |
Protein: | EGFR |
Gene Symbol: | EGFR |
Protein Id: | P00533 |
Protein Name: | EGFR_HUMAN |
PTM: | phosphorylation |
Site: | Tyr1068 |
Site Sequence: | PIKEDSFLQRYSSDPTGALTE |
Disease Category: | Cancer |
Disease: | Lung Cancer |
Disease Subtype: | NSCLC |
Disease Cellline: | |
Disease Info: | |
Drug: | erlotinib |
Drug Info: | "Erlotinib is a medication used in the treatment of certain types of lung cancer, particularly non-small cell lung cancer (NSCLC), and pancreatic cancer, often as a maintenance therapy or after chemotherapy failure." |
Effect: | activate |
Effect Info: | EGFR tyr1068 may represent a potential candidate biomarker for predicting the erlotinib response in EGFR - WT lung cancer patients at the CSC (lung cancer stem cell) level. |
Note: | |
Score: | 5.0 |
Pubmed(PMID): | 26247735 |
Sentence Index: | 26247735_5-6 |
Sentence: | "Here, we investigated erlotinib response of lung CSCs with WT-EGFR and identified EGFR phosphorylation at tyrosine1068 (EGFRtyr1068) as a powerful biomarker associated with erlotinib sensitivity both in vitro and in preclinical CSC-generated xenografts. In contrast to the preferential cytotoxicity of chemotherapy against the more differentiated cells, in EGFRtyr1068 cells, erlotinib was even more active against the LCSCs compared with their differentiated counterpart, acquiring potential value as CSC-directed therapeutics in the context of WT-EGFR lung cancer." |
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 | 1068 | D | Glioblastoma multiforme | Phosphorylation | 35915159 |
Y | 1068 | P | Gastric cancer | Phosphorylation | 23613900 |
Y | 1068 | P | Tonsillar cancer | Phosphorylation | 23564800 |
Y | 1068 | U | Non-small cell lung cancer/carcinoma | Phosphorylation | 22901364 ;  18687633 |
Y | 1068 | U | Prostate cancer/carcinoma/adenocarcinoma | Phosphorylation | 22307624 |
Y | 1068 | U | Squamous cell carcinoma | Phosphorylation | 37109043 |
Y | 1068 | U | Pancreatic cancer | Phosphorylation | 31851779 |
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.