Id: | acc1913 |
Group: | 2sens |
Protein: | IGF1R |
Gene Symbol: | IGF1R |
Protein Id: | P08069 |
Protein Name: | IGF1R_HUMAN |
PTM: | phosphorylation |
Site: | Tyr1136 |
Site Sequence: | NANKFVHRDLAARNCMVAEDF |
Disease Category: | Cancer |
Disease: | Sarcoma |
Disease Subtype: | osteosarcoma |
Disease Cellline: | U2OS |
Disease Info: | |
Drug: | mitoxantrone |
Drug Info: | "Mitoxantrone is a synthetic anthracycline-derived antineoplastic agent that inhibits DNA and RNA synthesis by intercalating into DNA, inhibiting topoisomerase II, and disrupting cell cycle progression, primarily used in the treatment of malignant lymphoma, breast cancer, acute leukemia, and various solid tumors." |
Effect: | inhibit |
Effect Info: | PPP inhibits the phosphorylation of IGF1R protein and enhances the effects of chemotherapy drugs and immunotherapy. |
Note: | |
Score: | 5.0 |
Pubmed(PMID): | 34110249 |
Sentence Index: | 34110249_4-5 |
Sentence: | "This PPP effect was phenocopied by another IGF1R inhibitor, linsitinib. Moreover, in human triple-negative breast cancer, phosphorylation of IGF1R correlates with reduced autophagy, an unfavorable local immune profile and poor prognosis." |
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 |
---|---|---|---|---|---|
Y | 1136 | U | Ewing sarcoma | Phosphorylation | 36394520 |
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.