HCSGD entry for AKT1S1


1. General information

Official gene symbolAKT1S1
Entrez ID84335
Gene full nameAKT1 substrate 1 (proline-rich)
Other gene symbolsLobe PRAS40
Links to Entrez GeneLinks to Entrez Gene

2. Neighbors in the network

color bar
This gene isn't in Literature mining network.

3. Gene ontology annotation

GO ID

GO term

Evidence

Category

GO:0005515Protein bindingIPImolecular_function
GO:0005634NucleusIEAcellular_component
GO:0005829CytosolIEA ISS TAScellular_component
GO:0006469Negative regulation of protein kinase activityIDAbiological_process
GO:0007173Epidermal growth factor receptor signaling pathwayTASbiological_process
GO:0008543Fibroblast growth factor receptor signaling pathwayTASbiological_process
GO:0031931TORC1 complexIDAcellular_component
GO:0032007Negative regulation of TOR signalingIDA IEAbiological_process
GO:0038095Fc-epsilon receptor signaling pathwayTASbiological_process
GO:0043234Protein complexIEAcellular_component
GO:0043523Regulation of neuron apoptotic processIEA ISSbiological_process
GO:0045087Innate immune responseTASbiological_process
GO:0045792Negative regulation of cell sizeIDAbiological_process
GO:0048011Neurotrophin TRK receptor signaling pathwayIEA TASbiological_process
GO:0048015Phosphatidylinositol-mediated signalingTASbiological_process
Entries Per Page
Displaying Page of

4. Expression levels in datasets

  • Meta-analysis result

p-value upp-value downFDR upFDR down
0.00612346800.89728061620.20663564101.0000000000

  • Individual experiment result
    ( "-" represent NA in the specific microarray platform )

Data sourceUp or downLog fold change
GSE11954Up0.4757454956
GSE13712_SHEARDown-0.0808769992
GSE13712_STATICDown-0.0208306026
GSE19018Up0.6169120317
GSE19899_A1Down-0.0006394497
GSE19899_A2Up1.2899612610
PubMed_21979375_A1Up0.5069881999
PubMed_21979375_A2Up1.3270496293
GSE35957Up0.3427887851
GSE36640Up0.4709024141
GSE54402Up0.3831827054
GSE9593Up0.6272645636
GSE43922Up0.3480583738
GSE24585Down-0.3247829463
GSE37065Down-0.2678501218
GSE28863_A1Down-0.3941802852
GSE28863_A2Down-0.3751263502
GSE28863_A3Up0.3537453978
GSE28863_A4Up0.1532670759
GSE48662Up0.7789741101

5. Regulation relationships with compounds/drugs/microRNAs

  • Compounds

Not regulated by compounds

  • Drugs

Not regulated by drugs

  • MicroRNAs

  • mirTarBase

MiRNA_name

mirBase ID

miRTarBase ID

Experiment

Support type

References (Pubmed ID)

hsa-miR-124-3pMIMAT0000422MIRT022786MicroarrayFunctional MTI (Weak)18668037
hsa-miR-484MIMAT0002174MIRT041919CLASHFunctional MTI (Weak)23622248
hsa-miR-185-5pMIMAT0000455MIRT045373CLASHFunctional MTI (Weak)23622248
Entries Per Page
Displaying Page of
  • mirRecord
No target information from mirRecord

6. Text-mining results about the gene

Gene occurances in abstracts of cellular senescence-associated articles: 2 abstracts the gene occurs.


PubMed ID of the article

Sentenece the gene occurs

25077541Importantly, we found that MKP7 inhibited senescence by dephosphorylating PRAS40 at Thr246 and mTOR at Ser2248, facilitating the interaction and loss of function of both molecules
24704832Nuclear PRAS40 couples the Akt/mTORC1 signaling axis to the RPL11-HDM2-p53 nucleolar stress response pathway
24704832The proline-rich Akt substrate of 40 kDa (PRAS40) has recently been identified as a binding partner and inhibitor of the mechanistic (formerly referred to as mammalian) target of rapamycin complex 1 (mTORC1)
24704832Importantly, silencing of PRAS40 induces upregulation of p53 in a manner dependent on RPL11
24704832This effect is rescued by wild-type PRAS40, but not by the RPL11-binding-null PRAS40T246A mutant
24704832We found that PRAS40 negatively regulates the RPL11-HDM2-p53 nucleolar stress response pathway and suppresses induction of p53-mediated cellular senescence
24704832This work identifies nuclear PRAS40 as a dual-input signaling checkpoint that links cell growth and proliferation to inhibition of cellular senescence
24704832These findings may help to explain the protumorigenic effect of PRAS40 and identify the PRAS40-RPL11 complex as a promising target for p53-restorative anticancer drug discovery
Entries Per Page
Displaying Page of