Id: | acc0042 |
Group: | 1sens |
Protein: | FLT3 |
Gene Symbol: | FLT3 |
Protein Id: | P36888 |
Protein Name: | FLT3_HUMAN |
PTM: | methylation |
Site: | Arg973 |
Site Sequence: | ECPHTYQNRRPFSREMDLGLL |
Disease Category: | Cancer |
Disease: | Leukemia |
Disease Subtype: | AML |
Disease Cellline: | MV4-11 |
Disease Info: | |
Drug: | MS023 |
Drug Info: | "MS023 is a potent, cell-active, and selective inhibitor of human type I protein arginine methyltransferases (PRMTs) with IC50 values ranging from 4 to 119 nM against PRMT1, PRMT3, PRMT4, PRMT6, and PRMT8." |
Effect: | modulate |
Effect Info: | "The drug inhibits protein methylation, thereby enhancing cell killing ability." |
Note: | |
Score: | 4.0 |
Pubmed(PMID): | 31217189 |
Sentence Index: | 31217189_0 |
Sentence: | PRMT1-mediated FLT3 arginine methylation promotes maintenance of FLT3-ITD+ acute myeloid leukemia. |
Sequence & Structure:
MPALARDGGQLPLLVVFSAMIFGTITNQDLPVIKCVLINHKNNDSSVGKSSSYPMVSESPEDLGCALRPQSSGTVYEAAAVEVDVSASITLQVLVDAPGNISCLWVFKHSSLNCQPHFDLQNRGVVSMVILKMTETQAGEYLLFIQSEATNYTILFTVSIRNTLLYTLRRPYFRKMENQDALVCISESVPEPIVEWVLCDSQGESCKEESPAVVKKEEKVLHELFGTDIRCCARNELGRECTRLFTIDLNQTPQTTLPQLFLKVGEPLWIRCKAVHVNHGFGLTWELENKALEEGNYFEMSTYSTNRTMIRILFAFVSSVARNDTGYYTCSSSKHPSQSALVTIVEKGFINATNSSEDYEIDQYEEFCFSVRFKAYPQIRCTWTFSRKSFPCEQKGLDNGYSISKFCNHKHQPGEYIFHAENDDAQFTKMFTLNIRRKPQVLAEASASQASCFSDGYPLPSWTWKKCSDKSPNCTEEITEGVWNRKANRKVFGQWVSSSTLNMSEAIKGFLVKCCAYNSLGTSCETILLNSPGPFPFIQDNISFYATIGVCLLFIVVLTLLICHKYKKQFRYESQLQMVQVTGSSDNEYFYVDFREYEYDLKWEFPRENLEFGKVLGSGAFGKVMNATAYGISKTGVSIQVAVKMLKEKADSSEREALMSELKMMTQLGSHENIVNLLGACTLSGPIYLIFEYCCYGDLLNYLRSKREKFHRTWTEIFKEHNFSFYPTFQSHPNSSMPGSREVQIHPDSDQISGLHGNSFHSEDEIEYENQKRLEEEEDLNVLTFEDLLCFAYQVAKGMEFLEFKSCVHRDLAARNVLVTHGKVVKICDFGLARDIMSDSNYVVRGNARLPVKWMAPESLFEGIYTIKSDVWSYGILLWEIFSLGVNPYPGIPVDANFYKLIQNGFKMDQPFYATEEIYIIMQSCWAFDSRKRPSFPNLTSFLGCQLADAEEAMYQNVDGRVSECPHTYQNRRPFSREMDLGLLSPQAQVEDS
Select PDB:
Target | Drug name | MOA | Phase | Status | Disease | Source |
---|---|---|---|---|---|---|
FLT3 | MIDOSTAURIN | Tyrosine-protein kinase receptor FLT3 inhibitor | 4 | - | acute myeloid leukemia | FDA |
FLT3 | GILTERITINIB FUMARATE | Tyrosine-protein kinase receptor FLT3 inhibitor | 4 | - | acute myeloid leukemia | EMA FDA |
FLT3 | FEDRATINIB | Tyrosine-protein kinase receptor FLT3 inhibitor | 4 | - | neoplasm | ATC |
FLT3 | SUNITINIB | Tyrosine-protein kinase receptor FLT3 inhibitor | 4 | Completed | neoplasm | ClinicalTrials |
FLT3 | MIDOSTAURIN | Tyrosine-protein kinase receptor FLT3 inhibitor | 4 | - | neoplasm | ATC |
FLT3 | PEXIDARTINIB | Tyrosine-protein kinase receptor FLT3 inhibitor | 4 | - | neoplasm | ATC |
FLT3 | PACRITINIB | Tyrosine-protein kinase receptor FLT3 inhibitor | 4 | - | neoplasm | ATC |
FLT3 | GILTERITINIB | Tyrosine-protein kinase receptor FLT3 inhibitor | 4 | - | neoplasm | ATC |
FLT3 | SUNITINIB | Tyrosine-protein kinase receptor FLT3 inhibitor | 4 | - | neoplasm | ATC |
FLT3 | SUNITINIB | Tyrosine-protein kinase receptor FLT3 inhibitor | 4 | - | renal cell carcinoma | DailyMed EMA |
FLT3 | SORAFENIB TOSYLATE | Tyrosine-protein kinase receptor FLT3 inhibitor | 4 | - | renal cell carcinoma | DailyMed |
FLT3 | SUNITINIB MALATE | Tyrosine-protein kinase receptor FLT3 inhibitor | 4 | - | renal cell carcinoma | DailyMed |
FLT3 | SUNITINIB MALATE | Tyrosine-protein kinase receptor FLT3 inhibitor | 4 | Completed | renal cell carcinoma | ClinicalTrials |
FLT3 | SUNITINIB | Tyrosine-protein kinase receptor FLT3 inhibitor | 4 | Completed | renal cell carcinoma | ClinicalTrials ClinicalTrials |
FLT3 | SUNITINIB | Tyrosine-protein kinase receptor FLT3 inhibitor | 4 | Terminated | renal cell carcinoma | ClinicalTrials ClinicalTrials |
FLT3 | PACRITINIB CITRATE | Tyrosine-protein kinase receptor FLT3 inhibitor | 4 | - | polycythemia vera | FDA |
FLT3 | FEDRATINIB HYDROCHLORIDE | Tyrosine-protein kinase receptor FLT3 inhibitor | 4 | - | primary myelofibrosis | EMA FDA |
FLT3 | PACRITINIB CITRATE | Tyrosine-protein kinase receptor FLT3 inhibitor | 4 | - | primary myelofibrosis | FDA |
FLT3 | SORAFENIB TOSYLATE | Tyrosine-protein kinase receptor FLT3 inhibitor | 4 | - | thyroid carcinoma | DailyMed |
FLT3 | FEDRATINIB HYDROCHLORIDE | Tyrosine-protein kinase receptor FLT3 inhibitor | 4 | - | myeloproliferative disorder | EMA |
FLT3 | MIDOSTAURIN | Tyrosine-protein kinase receptor FLT3 inhibitor | 4 | - | mast-cell leukemia | DailyMed FDA |
FLT3 | MIDOSTAURIN | Tyrosine-protein kinase receptor FLT3 inhibitor | 4 | - | Mastocytosis | DailyMed |
FLT3 | PEXIDARTINIB HYDROCHLORIDE | Tyrosine-protein kinase receptor FLT3 inhibitor | 4 | - | Tenosynovial Giant Cell Tumor | DailyMed FDA |
FLT3 | SUNITINIB | Tyrosine-protein kinase receptor FLT3 inhibitor | 4 | Completed | pancreatic neuroendocrine tumor | ClinicalTrials |
FLT3 | SUNITINIB MALATE | Tyrosine-protein kinase receptor FLT3 inhibitor | 4 | - | neuroendocrine neoplasm | DailyMed |
Note: Only show clinically investigational or approved drugs with protein targets.
Protein Tractability:
source: Open TargetsPTM Intensity:
source: CPTACNo data.
PTM-Disease Association:
source: PTMDResidue | Position | State | Disease | Class | PMID |
---|---|---|---|---|---|
R | 973 | U | Acute lymphocytic leukemia | Methylation | 31395602 |
R | 973 | U | Acute myelogenous leukemia | Methylation | 31217189 |
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.