Id: | acc1346 |
Group: | 2sens |
Protein: | mTOR |
Gene Symbol: | MTOR |
Protein Id: | P42345 |
Protein Name: | MTOR_HUMAN |
PTM: | phosphorylation |
Site: | Ser2481 |
Site Sequence: | GTTVPESIHSFIGDGLVKPEA |
Disease Category: | Cancer |
Disease: | Breast Cancer |
Disease Subtype: | |
Disease Cellline: | MDA-MB-231 |
Disease Info: | |
Drug: | IBP OV |
Drug Info: | - |
Effect: | modulate |
Effect Info: | "Overexpression of IBP promotes the phosphorylation of mTOR, Akt, and FOXO3a, thereby promoting the growth of breast cancer cells." |
Note: | Non-conventional drugs |
Score: | 3.0 |
Pubmed(PMID): | 24113176 |
Sentence Index: | 24113176_4-5 |
Sentence: | "In this study, we for the first time, reported that upregulation of IBP expression significantly suppressed the autophagy of breast cancer cells, and downregulation of IBP expression markedly induced autophagy of these cells. Further investigation revealed that IBP effectively counteracted autophagy by directly activating mammalian target of rapamycin complex 2 (mTORC2) and upregulating phosphorylation of Akt on ser473 and FOXO3a on Thr32." |
Sequence & Structure:
MLGTGPAAATTAATTSSNVSVLQQFASGLKSRNEETRAKAAKELQHYVTMELREMSQEESTRFYDQLNHHIFELVSSSDANERKGGILAIASLIGVEGGNATRIGRFANYLRNLLPSNDPVVMEMASKAIGRLAMAGDTFTAEYVEFEVKRALEWLGADRNEGRRHAAVLVLRELAISVPTFFFQQVQPFFDNIFVAVWDPKQAIREGAVAALRACLILTTQREPKEMQKPQWYRHTFEEAEKGFDETLAKEKGMNRDDRIHGALLILNELVRISSMEGERLREEMEEITQQQLVHDKYCKDLMGFGTKPRHITPFTSFQAVQPQQSNALVGLLGYSSHQGLMGFGTSPSPAKSTLVESRCCRDLMEEKFDQVCQWVLKCRNSKNSLIQMTILNLLPRLAAFRPSAFTDTQYLQDTMNHVLSCVKKEKERTAAFQALGLLSVAVRSEFKVYLPRVLDIIRAALPPKDFAHKRQKAMQVDATVFTCISMLARAMGPGIQQDIKELLEPMLAVGLSPALTAVLYDLSRQIPQLKKDIQDGLLKMLSLVLMHKPLRHPGMPKGLAHQLASPGLTTLPEASDVGSITLALRTLGSFEFEGHSLTQFVRHCADHFLNSEHKEIRMEAARTCSRLLTPSIHLISGHAHVVSQTAVQVVADVLSKLLVVGITDPDPDIRYCVLASLDERFDAHLAQAENLQALFVALNDQVFEIRELAICTVGRLSSMNPAFVMPFLRKMLIQILTELEHSGIGRIKEQSARMLGHLVSNAPRLIRPYMEPILKALILKLKDPDPDPNPGVINNVLATIGELAQVSGLEMRKWVDELFIIIMDMLQDSSLLAKRQVALWTLGQLVASTGYVVEPYRKYPTLLEVLLNFLKTEQNQGTRREAIRVLGLLGALDPYKHKVNIGMIDQSRDASAVSLSESKSSQDSSDYSTSEMLVNMGNLPLDEFYPAVSMVALMRIFRDQSLSHHHTMVVQAITFIFKSLGLKCVQFLPQVMPTFLNVIRVCDGAIREFLFQQLGMLVSFVKSHIRPYMDEIVTLMREFWVMNTSIQSTIILLIEQIVVALGGEFKLYLPQLIPHMLRVFMHDNSPGRIVSIKLLAAIQLFGANLDDYLHLLLPPIVKLFDAPEAPLPSRKAALETVDRLTESLDFTDYASRIIHPIVRTLDQSPELRSTAMDTLSSLVFQLGKKYQIFIPMVNKVLVRHRINHQRYDVLICRIVKGYTLADEEEDPLIYQHRMLRSGQGDALASGPVETGPMKKLHVSTINLQKAWGAARRVSKDDWLEWLRRLSLELLKDSSSPSLRSCWALAQAYNPMARDLFNAAFVSCWSELNEDQQDELIRSIELALTSQDIAEVTQTLLNLAEFMEHSDKGPLPLRDDNGIVLLGERAAKCRAYAKALHYKELEFQKGPTPAILESLISINNKLQQPEAAAGVLEYAMKHFGELEIQATWYEKLHEWEDALVAYDKKMDTNKDDPELMLGRMRCLEALGEWGQLHQQCCEKWTLVNDETQAKMARMAAAAAWGLGQWDSMEEYTCMIPRDTHDGAFYRAVLALHQDLFSLAQQCIDKARDLLDAELTAMAGESYSRAYGAMVSCHMLSELEEVIQYKLVPERREIIRQIWWERLQGCQRIVEDWQKILMVRSLVVSPHEDMRTWLKYASLCGKSGRLALAHKTLVLLLGVDPSRQLDHPLPTVHPQVTYAYMKNMWKSARKIDAFQHMQHFVQTMQQQAQHAIATEDQQHKQELHKLMARCFLKLGEWQLNLQGINESTIPKVLQYYSAATEHDRSWYKAWHAWAVMNFEAVLHYKHQNQARDEKKKLRHASGANITNATTAATTAATATTTASTEGSNSESEAESTENSPTPSPLQKKVTEDLSKTLLMYTVPAVQGFFRSISLSRGNNLQDTLRVLTLWFDYGHWPDVNEALVEGVKAIQIDTWLQVIPQLIARIDTPRPLVGRLIHQLLTDIGRYHPQALIYPLTVASKSTTTARHNAANKILKNMCEHSNTLVQQAMMVSEELIRVAILWHEMWHEGLEEASRLYFGERNVKGMFEVLEPLHAMMERGPQTLKETSFNQAYGRDLMEAQEWCRKYMKSGNVKDLTQAWDLYYHVFRRISKQLPQLTSLELQYVSPKLLMCRDLELAVPGTYDPNQPIIRIQSIAPSLQVITSKQRPRKLTLMGSNGHEFVFLLKGHEDLRQDERVMQLFGLVNTLLANDPTSLRKNLSIQRYAVIPLSTNSGLIGWVPHCDTLHALIRDYREKKKILLNIEHRIMLRMAPDYDHLTLMQKVEVFEHAVNNTAGDDLAKLLWLKSPSSEVWFDRRTNYTRSLAVMSMVGYILGLGDRHPSNLMLDRLSGKILHIDFGDCFEVAMTREKFPEKIPFRLTRMLTNAMEVTGLDGNYRITCHTVMEVLREHKDSVMAVLEAFVYDPLLNWRLMDTNTKGNKRSRTRTDSYSAGQSVEILDGVELGEPAHKKTGTTVPESIHSFIGDGLVKPEALNKKAIQIINRVRDKLTGRDFSHDDTLDVPTQVELLIKQATSHENLCQCYIGWCPFW
Select PDB:
Target | Drug name | MOA | Phase | Status | Disease | Source |
---|---|---|---|---|---|---|
MTOR | PERHEXILINE | Serine/threonine-protein kinase mTOR inhibitor | 4 | - | cardiovascular disease | ATC |
MTOR | PERHEXILINE | Serine/threonine-protein kinase mTOR inhibitor | 3 | Withdrawn | hypertrophic cardiomyopathy | ClinicalTrials |
MTOR | DACTOLISIB | Serine/threonine-protein kinase mTOR inhibitor | 3 | Completed | infection | ClinicalTrials |
MTOR | RIDAFOROLIMUS | Serine/threonine-protein kinase mTOR inhibitor | 3 | - | neoplasm | ATC |
MTOR | RIDAFOROLIMUS | Serine/threonine-protein kinase mTOR inhibitor | 3 | Completed | soft tissue sarcoma | ClinicalTrials |
MTOR | GEDATOLISIB | Serine/threonine-protein kinase mTOR inhibitor | 3 | Recruiting | breast cancer | ClinicalTrials |
MTOR | RIDAFOROLIMUS | Serine/threonine-protein kinase mTOR inhibitor | 3 | Completed | bone sarcoma | ClinicalTrials |
MTOR | SF-1126 | Serine/threonine-protein kinase mTOR inhibitor | 2 | Terminated | head and neck squamous cell carcinoma | ClinicalTrials |
MTOR | ONATASERTIB | Serine/threonine-protein kinase mTOR inhibitor | 2 | Terminated | hepatocellular carcinoma | ClinicalTrials |
MTOR | INDOXIMOD | mTORC1 activator | 2 | Completed | metastatic prostate cancer | ClinicalTrials |
MTOR | RIDAFOROLIMUS | Serine/threonine-protein kinase mTOR inhibitor | 2 | Completed | myelodysplastic syndrome | ClinicalTrials |
MTOR | GEDATOLISIB | Serine/threonine-protein kinase mTOR inhibitor | 2 | Terminated | myelodysplastic syndrome | ClinicalTrials |
MTOR | GEDATOLISIB | Serine/threonine-protein kinase mTOR inhibitor | 2 | Terminated | acute myeloid leukemia | ClinicalTrials |
MTOR | SAPANISERTIB | Serine/threonine-protein kinase mTOR inhibitor | 2 | Active, not recruiting | T-cell acute lymphoblastic leukemia | ClinicalTrials |
MTOR | VISTUSERTIB | Serine/threonine-protein kinase mTOR inhibitor | 2 | Active, not recruiting | adenocarcinoma | ClinicalTrials |
MTOR | VISTUSERTIB | Serine/threonine-protein kinase mTOR inhibitor | 2 | Terminated | clear cell renal carcinoma | ClinicalTrials |
MTOR | VISTUSERTIB | Serine/threonine-protein kinase mTOR inhibitor | 2 | Terminated | gastric adenocarcinoma | ClinicalTrials |
MTOR | PERHEXILINE | Serine/threonine-protein kinase mTOR inhibitor | 2 | Terminated | hypertrophic cardiomyopathy | ClinicalTrials |
MTOR | RIDAFOROLIMUS | Serine/threonine-protein kinase mTOR inhibitor | 2 | Completed | leiomyosarcoma | ClinicalTrials |
MTOR | DACTOLISIB | Serine/threonine-protein kinase mTOR inhibitor | 2 | Active, not recruiting | infection | ClinicalTrials |
MTOR | RIDAFOROLIMUS | Serine/threonine-protein kinase mTOR inhibitor | 2 | Completed | lymphoma | ClinicalTrials |
MTOR | VOXTALISIB | Serine/threonine-protein kinase mTOR inhibitor | 2 | Completed | lymphoma | ClinicalTrials |
MTOR | PERHEXILINE | Serine/threonine-protein kinase mTOR inhibitor | 2 | Completed | hypertrophic cardiomyopathy | ClinicalTrials |
MTOR | PERHEXILINE | Serine/threonine-protein kinase mTOR inhibitor | 2 | Recruiting | hypertrophic cardiomyopathy | ClinicalTrials |
MTOR | RIDAFOROLIMUS | Serine/threonine-protein kinase mTOR inhibitor | 2 | Completed | leukemia | ClinicalTrials |
Note: Only show clinically investigational or approved drugs with protein targets.
Protein Tractability:
source: Open TargetsPTM Intensity:
source: CPTACMTOR-Ser2481 | |
---|---|
Cancer | Intensity |
BRCA | 0.302 |
COAD | -0.364 |
HGSC | 2.451 |
ccRCC | -0.257 |
GBM | 0.596 |
HNSC | -0.341 |
LUAD | -0.327 |
LUSC | 0.493 |
non_ccRCC | -1.381 |
PDAC | -0.206 |
UCEC | -0.964 |
PTM-Disease Association:
source: PTMDResidue | Position | State | Disease | Class | PMID |
---|---|---|---|---|---|
S | 2481 | U | Breast cancer | Phosphorylation | 27721400 |
S | 2481 | U | Breast cancer/tumor/carcinoma | Phosphorylation | 19956839 |
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: DecryptMProtein | Gene | PTM | Position | Modified sequence | Cell | Drug | pEC50 | Regulation | Experiment |
---|---|---|---|---|---|---|---|---|---|
P42345 | MTOR | P | Ser2481 | TGTTVPESIHS(ph)FIGDGLVKPEALNKK | HeLa | A486 | 6.001 | - |
pEC50 Note: pEC50 is the negative logarithm of EC50 (half-maximal effective concentration, dosage unit Mol), calculated as pEC50 = -log10(EC50), which quantifies the potency of a drug or compound.
Function score:
source: funscoRNo data.