Id: | acc1634 |
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: | Head and Neck Cancer |
Disease Subtype: | HNSCC |
Disease Cellline: | |
Disease Info: | |
Drug: | Lysophosphatidic acid (LPA) |
Drug Info: | "1-Oleoyl-sn-glycero-3-phosphate sodium salt: A sodium salt form of lysophosphatidic acid (LPA) used in research to study its biological activities, including cell proliferation and signaling pathways. " |
Relation: |
Lysophosphatidic acid (LPA)
➜
EGFR-Tyr1068
UP
➜
Head and Neck Cancer
Aggravate
|
Effect: | modulate |
Effect Info: | Lysophosphatidic acid (LPA) promotes the proliferation and migration of head and neck squamous cell carcinoma (HNSCC) cells through the transactivation of epidermal growth factor receptor (EGFR). |
Note: | site unclear |
Score: | 4.0 |
Pubmed(PMID): | 12414665 |
Sentence Index: | 12414665_4-5 |
Sentence: | "Using the metalloprotease inhibitor batimastat, the EGFR-specific tyrphostin AG1478, and a dominant-negative EGFR mutant, we show that in HNSCC cell lines, EGFR tyrosine phosphorylation, recruitment of the adaptor proteins SHC and Gab1, and activation of the ERK/mitogen-activated protein kinase pathway in response to LPA depend both on metalloprotease function and EGFR tyrosine kinase activity. Most importantly, critical characteristics of HNSCC cell lines such as DNA synthesis, cell cycle progression and tumor cell migration are stimulated by LPA and can be abrogated by interfering with EGFR signal transmission." |
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.