Id: | acc0293 |
Group: | 1sens |
Protein: | IGF-IR |
Gene Symbol: | IGF1R |
Protein Id: | P08069 |
Protein Name: | IGF1R_HUMAN |
PTM: | phosphorylation |
Site: | Tyr1131 |
Site Sequence: | GMAYLNANKFVHRDLAARNCM |
Disease Category: | Cancer |
Disease: | Sarcoma |
Disease Subtype: | synovial sarcoma |
Disease Cellline: | CME-1 |
Disease Info: | |
Drug: | dasatinib |
Drug Info: | "Dasatinib is a tyrosine kinase inhibitor that targets BCR-ABL and SRC family kinases, used in the treatment of chronic myeloid leukemia (CML) and Philadelphia chromosome-positive acute lymphoblastic leukemia (Ph+ ALL), particularly in patients resistant or intolerant to prior therapy including imatinib." |
Effect: | modulate |
Effect Info: | "Dasatinib reduces the levels of p-(Tyr416)-SRC, p-(Ser473)-AKT, p-(Tyr576/577)-FAK, p-(Tyr705)-STAT3, and p-(Tyr1131)-IGF-IR, thereby inhibiting tumors." |
Note: | |
Score: | 4.0 |
Pubmed(PMID): | 23580575 |
Sentence Index: | 23580575_10 |
Sentence: | "Treatment of synovial sarcoma cells with dasatinib led to apoptosis and inhibition of cellular proliferation, associated with reduced phosphorylation of FAK (PTK2), STAT3, IGF-IR, and AKT." |
Sequence & Structure:
MKSGSGGGSPTSLWGLLFLSAALSLWPTSGEICGPGIDIRNDYQQLKRLENCTVIEGYLHILLISKAEDYRSYRFPKLTVITEYLLLFRVAGLESLGDLFPNLTVIRGWKLFYNYALVIFEMTNLKDIGLYNLRNITRGAIRIEKNADLCYLSTVDWSLILDAVSNNYIVGNKPPKECGDLCPGTMEEKPMCEKTTINNEYNYRCWTTNRCQKMCPSTCGKRACTENNECCHPECLGSCSAPDNDTACVACRHYYYAGVCVPACPPNTYRFEGWRCVDRDFCANILSAESSDSEGFVIHDGECMQECPSGFIRNGSQSMYCIPCEGPCPKVCEEEKKTKTIDSVTSAQMLQGCTIFKGNLLINIRRGNNIASELENFMGLIEVVTGYVKIRHSHALVSLSFLKNLRLILGEEQLEGNYSFYVLDNQNLQQLWDWDHRNLTIKAGKMYFAFNPKLCVSEIYRMEEVTGTKGRQSKGDINTRNNGERASCESDVLHFTSTTTSKNRIIITWHRYRPPDYRDLISFTVYYKEAPFKNVTEYDGQDACGSNSWNMVDVDLPPNKDVEPGILLHGLKPWTQYAVYVKAVTLTMVENDHIRGAKSEILYIRTNASVPSIPLDVLSASNSSSQLIVKWNPPSLPNGNLSYYIVRWQRQPQDGYLYRHNYCSKDKIPIRKYADGTIDIEEVTENPKTEVCGGEKGPCCACPKTEAEKQAEKEEAEYRKVFENFLHNSIFVPRPERKRRDVMQVANTTMSSRSRNTTAADTYNITDPEELETEYPFFESRVDNKERTVISNLRPFTLYRIDIHSCNHEAEKLGCSASNFVFARTMPAEGADDIPGPVTWEPRPENSIFLKWPEPENPNGLILMYEIKYGSQVEDQRECVSRQEYRKYGGAKLNRLNPGNYTARIQATSLSGNGSWTDPVFFYVQAKTGYENFIHLIIALPVAVLLIVGGLVIMLYVFHRKRNNSRLGNGVLYASVNPEYFSAADVYVPDEWEVAREKITMSRELGQGSFGMVYEGVAKGVVKDEPETRVAIKTVNEAASMRERIEFLNEASVMKEFNCHHVVRLLGVVSQGQPTLVIMELMTRGDLKSYLRSLRPEMENNPVLAPPSLSKMIQMAGEIADGMAYLNANKFVHRDLAARNCMVAEDFTVKIGDFGMTRDIYETDYYRKGGKGLLPVRWMSPESLKDGVFTTYSDVWSFGVVLWEIATLAEQPYQGLSNEQVLRFVMEGGLLDKPDNCPDMLFELMRMCWQYNPKMRPSFLEIISSIKEEMEPGFREVSFYYSEENKLPEPEELDLEPENMESVPLDPSASSSSLPLPDRHSGHKAENGPGPGVLVLRASFDERQPYAHMNGGRKNERALPLPQSSTC
Select PDB:
Target | Drug name | MOA | Phase | Status | Disease | Source |
---|---|---|---|---|---|---|
IGF1R | TEPROTUMUMAB | Insulin-like growth factor I receptor antagonist | 4 | - | immune system disease | ATC |
IGF1R | MASOPROCOL | Insulin-like growth factor I receptor inhibitor | 4 | - | neoplasm | ATC |
IGF1R | MECASERMIN | Insulin-like growth factor I receptor agonist | 4 | - | hypothyroidism | DailyMed |
IGF1R | TEPROTUMUMAB | Insulin-like growth factor I receptor antagonist | 4 | - | Graves ophthalmopathy | DailyMed FDA |
IGF1R | TEPROTUMUMAB | Insulin-like growth factor I receptor antagonist | 4 | Completed | Graves ophthalmopathy | ClinicalTrials |
IGF1R | MECASERMIN | Insulin-like growth factor I receptor agonist | 4 | - | Growth delay | DailyMed |
IGF1R | MECASERMIN | Insulin-like growth factor I receptor agonist | 4 | - | Laron syndrome | EMA |
IGF1R | MECASERMIN | Insulin-like growth factor I receptor agonist | 3 | Completed | diabetes mellitus | ClinicalTrials |
IGF1R | FIGITUMUMAB | Insulin-like growth factor I receptor antagonist | 3 | Terminated | squamous cell carcinoma | ClinicalTrials ClinicalTrials |
IGF1R | FIGITUMUMAB | Insulin-like growth factor I receptor antagonist | 3 | Terminated | non-small cell lung carcinoma | ClinicalTrials ClinicalTrials |
IGF1R | FIGITUMUMAB | Insulin-like growth factor I receptor antagonist | 3 | Withdrawn | non-small cell lung carcinoma | ClinicalTrials |
IGF1R | FIGITUMUMAB | Insulin-like growth factor I receptor antagonist | 3 | Terminated | large cell lung carcinoma | ClinicalTrials ClinicalTrials |
IGF1R | TEPROTUMUMAB | Insulin-like growth factor I receptor antagonist | 3 | Recruiting | eye disease | ClinicalTrials |
IGF1R | TEPROTUMUMAB | Insulin-like growth factor I receptor antagonist | 3 | Completed | eye disease | ClinicalTrials |
IGF1R | LINSITINIB | Insulin-like growth factor I receptor inhibitor | 3 | Completed | adrenal cortex carcinoma | ClinicalTrials |
IGF1R | TEPROTUMUMAB | Insulin-like growth factor I receptor antagonist | 3 | Completed | Graves ophthalmopathy | ClinicalTrials |
IGF1R | MECASERMIN | Insulin-like growth factor I receptor agonist | 3 | Completed | Growth abnormality | ClinicalTrials |
IGF1R | MECASERMIN | Insulin-like growth factor I receptor agonist | 3 | Terminated | Growth abnormality | ClinicalTrials |
IGF1R | MECASERMIN | Insulin-like growth factor I receptor agonist | 3 | Completed | amyotrophic lateral sclerosis | ClinicalTrials |
IGF1R | CIXUTUMUMAB | Insulin-like growth factor I receptor antagonist | 2 | Completed | hepatocellular carcinoma | ClinicalTrials |
IGF1R | CIXUTUMUMAB | Insulin-like growth factor I receptor antagonist | 2 | Completed | head and neck squamous cell carcinoma | ClinicalTrials |
IGF1R | LINSITINIB | Insulin-like growth factor I receptor inhibitor | 2 | Completed | Ewing sarcoma | ClinicalTrials |
IGF1R | GANITUMAB | Insulin-like growth factor I receptor antagonist | 2 | Completed | Ewing sarcoma | ClinicalTrials |
IGF1R | LINSITINIB | Insulin-like growth factor I receptor inhibitor | 2 | Terminated | hepatocellular carcinoma | ClinicalTrials |
IGF1R | CIXUTUMUMAB | Insulin-like growth factor I receptor antagonist | 2 | Completed | alveolar rhabdomyosarcoma | ClinicalTrials |
Note: Only show clinically investigational or approved drugs with protein targets.
Protein Tractability:
source: Open TargetsPTM Intensity:
source: CPTACIGF1R-Ser1339 | |
---|---|
Cancer | Intensity |
BRCA | 0.418 |
COAD | |
HGSC | |
ccRCC | |
GBM | |
HNSC | 0.723 |
LUAD | |
LUSC | -1.141 |
non_ccRCC | |
PDAC | |
UCEC |
PTM-Disease Association:
source: PTMDResidue | Position | State | Disease | Class | PMID |
---|---|---|---|---|---|
- | - | P | Prostate cancer/carcinoma/adenocarcinoma | Glycosylation | 23724116 |
Y | 1165 | U | Breast cancer/tumor/carcinoma | Phosphorylation | 23663564 |
Y | 1166 | U | Breast cancer/tumor/carcinoma | Phosphorylation | 23663564 |
Y | 980 | U | Ewing sarcoma | Phosphorylation | 36394520 |
Y | 1135 | U | Ewing sarcoma | Phosphorylation | 36394520 |
Y | 1136 | U | Ewing sarcoma | Phosphorylation | 36394520 |
Y | 1161 | U | Neuroblastoma | Phosphorylation | 24349301 |
- | - | U | Barrett's neoplasia | Phosphorylation | 14608530 |
K | 1025 | U | Acute myelogenous leukemia | SUMOylation | 25448401 |
K | 1100 | U | Acute myelogenous leukemia | SUMOylation | 25448401 |
- | - | U | Non-small cell lung cancer | Ubiquitination | 33415003 |
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.