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IID00954
UniprotP60484
ProteinPhosphatidylinositol 3,4,5-trisphosphate 3-phosphatase and dual-specificity protein phosphatase PTEN
GenePTEN
OrganismHomo sapiens
Sequence LLPS PhaSepDB
PhaSePro
LLPSDB
DrLLPS
Network xml rdf
Structure
Experiment
  :order   disorder   conflict   PDB cluster   ProS   Pfam Domain   SEG
403
 order/disorder by at least rule
     disorder by at least rule
     order by at least rule
 order/disorder by majority rule
Seq 1-403 Monomer :
 Evidence X-RAY 1d5r A Reference
       Region 1d5r A 8-13 disorder
       Region 1d5r A 14-281 order
       Region 1d5r A 282-285 disorder
       Region 1d5r A 309-312 disorder
       Region 1d5r A 313-351 order
       Region 1d5r A 352-353 disorder
 Evidence X-RAY 5bug A Reference
       Region 5bug A 14-285 order
       Region 5bug A 310-351 order
 Evidence X-RAY 5bug B Reference
       Region 5bug B 14-285 order
       Region 5bug B 310-351 order
 Evidence X-RAY 5bug C Reference
       Region 5bug C 14-285 order
       Region 5bug C 310-351 order
 Evidence X-RAY 5bug D Reference
       Region 5bug D 14-285 order
       Region 5bug D 310-351 order
 Evidence X-RAY 5bzx A Reference
       Region 5bzx A 14-285 order
       Region 5bzx A 310-351 order
 Evidence X-RAY 5bzx B Reference
       Region 5bzx B 14-285 order
       Region 5bzx B 310-351 order
 Evidence X-RAY 5bzx C Reference
       Region 5bzx C 14-285 order
       Region 5bzx C 310-351 order
 Evidence X-RAY 5bzx D Reference
       Region 5bzx D 14-285 order
       Region 5bzx D 310-351 order
 Evidence X-RAY 5bzz A Reference
       Region 5bzz A 14-285 order
       Region 5bzz A 310-351 order
 Evidence X-RAY 5bzz B Reference
       Region 5bzz B 14-285 order
       Region 5bzz B 310-351 order
 Evidence X-RAY 5bzz C Reference
       Region 5bzz C 14-285 order
       Region 5bzz C 310-351 order
 Evidence X-RAY 5bzz D Reference
       Region 5bzz D 14-285 order
       Region 5bzz D 310-351 order
 Evidence X-RAY 7jtx A Reference
       Region 7jtx A 7-22 disorder
       Region 7jtx A 23-37 order
       Region 7jtx A 38-49 disorder
       Region 7jtx A 50-73 order
       Region 7jtx A 74-82 disorder
       Region 7jtx A 83-282 order
       Region 7jtx A 283-285 disorder
       Region 7jtx A 310-311 disorder
       Region 7jtx A 312-351 order
       Region 7jtx A 352-358 disorder
       Region 7jtx A 359-358 order
       Region 7jtx A 359-374 disorder
       Region 7jtx A 380-395 disorder
 Evidence X-RAY 7juk A Reference
       Region 7juk A 7-281 order
       Region 7juk A 282-285 disorder
       Region 7juk A 310-313 disorder
       Region 7juk A 314-351 order
       Region 7juk A 352-353 disorder
       Region 7juk A 378-390 disorder
 Evidence X-RAY 7jul A Reference
       Region 7jul A 7-281 order
       Region 7jul A 282-285 disorder
       Region 7jul A 310-312 disorder
       Region 7jul A 313-351 order
       Region 7jul A 352-353 disorder
       Region 7jul A 378-390 disorder
 Evidence X-RAY 7jvx A Reference
       Region 7jvx A 1-6 disorder
       Region 7jvx A 7-282 order
       Region 7jvx A 283-313 disorder
       Region 7jvx A 314-351 order
       Region 7jvx A 352-380 disorder
       Region 7jvx A 381-380 order
       Region 7jvx A 381-403 disorder
Seq 354-368 Hetero dimer : IID00529Complex
 Evidence X-RAY 4o1v B Reference
       Region 4o1v B 354-356 disorder
       Region 4o1v B 357-363 order
       Region 4o1v B 364-368 disorder
Seq 391-403 Hetero dimer : Q6P0Q8
 Evidence NMR 2kyl B Reference
       Region 2kyl B 391-403 order
       Region 2kyl B 391-391 high_rmsd
Seq 394-403 Hetero hexamer : IID00700Complex,Q9NSN8
 Evidence X-RAY 7pc7 E Reference
       Region 7pc7 E 394-403 order
 Evidence X-RAY 7pc7 F Reference
       Region 7pc7 F 394-399 disorder
       Region 7pc7 F 400-403 order
SeqProS predicted 357-363 This region is predicted to be disordered by NeProc and AlphaFold (pLDDT < 68.5). Hetero dimer : IID00529Complex
       Region 4o1v B 357-363 order
SeqProS predicted 394-403 This region is predicted to be disordered by NeProc and AlphaFold (pLDDT < 68.5). Hetero hexamer : IID00700Complex,Q9NSN8
       Region 7pc7 E 394-403 order
       Region 7pc7 F 400-403 order
Seqphosphorylation
    401-401 Phosphothreonine
    385-385 Phosphoserine; by CK2
    383-383 Phosphothreonine; by ROCK1 and CK2
    382-382 Phosphothreonine; by ROCK1 and CK2
    380-380 Phosphoserine; by ROCK1 and CK2
    370-370 Phosphoserine; by CK2 and PLK3
    366-366 Phosphothreonine; by GSK3-beta and PLK3
    336-336 Phosphotyrosine; by FRK
    321-321 Phosphothreonine
    319-319 Phosphothreonine
    294-294 Phosphoserine
Seqacetylation
    2-2 N-acetylthreonine
 
Prediction
NeProc
Disorder 1-14,293-306,351-403
Order 15-285,290-292,307-350
ProS 1-14,293-306,366-383,395-403
AlphaFold
Disorder 1-2,10-10,44-45,282-304,308-312,352-403
Order 3-9,11-43,46-281,305-307,313-351
SEG 322-334 ,360-371
Function
Function in SwissProt
Dual-specificity protein phosphatase, dephosphorylating tyrosine-, serine- and threonine-phosphorylated proteins (PubMed:9187108, PubMed:9256433, PubMed:9616126). Also functions as a lipid phosphatase, removing the phosphate in the D3 position of the inositol ring of PtdIns(3,4,5)P3/phosphatidylinositol 3,4,5-trisphosphate, PtdIns(3,4)P2/phosphatidylinositol 3,4-diphosphate and PtdIns3P/phosphatidylinositol 3-phosphate with a preference for PtdIns(3,4,5)P3 (PubMed:9811831, PubMed:16824732, PubMed:26504226, PubMed:9593664). Furthermore, this enzyme can also act as a cytosolic inositol 3-phosphatase acting on Ins(1,3,4,5,6)P5/inositol 1,3,4,5,6 pentakisphosphate and possibly Ins(1,3,4,5)P4/1D-myo-inositol 1,3,4,5-tetrakisphosphate (PubMed:11418101, PubMed:15979280). Antagonizes the PI3K-AKT/PKB signaling pathway by dephosphorylating phosphoinositides and thereby modulating cell cycle progression and cell survival (PubMed:31492966, PubMed:37279284). The unphosphorylated form cooperates with MAGI2 to suppress AKT1 activation (PubMed:11707428). In motile cells, suppresses the formation of lateral pseudopods and thereby promotes cell polarization and directed movement (PubMed:22279049). Dephosphorylates tyrosine-phosphorylated focal adhesion kinase and inhibits cell migration and integrin-mediated cell spreading and focal adhesion formation (PubMed:22279049). Required for growth factor-induced epithelial cell migration; growth factor stimulation induces PTEN phosphorylation which changes its binding preference from the p85 regulatory subunit of the PI3K kinase complex to DLC1 and results in translocation of the PTEN-DLC1 complex to the posterior of migrating cells to promote RHOA activation (PubMed:26166433). Meanwhile, TNS3 switches binding preference from DLC1 to p85 and the TNS3-p85 complex translocates to the leading edge of migrating cells to activate RAC1 activation (PubMed:26166433). Plays a role as a key modulator of the AKT-mTOR signaling pathway controlling the tempo of the process of newborn neurons integration during adult neurogenesis, including correct neuron positioning, dendritic development and synapse formation (By similarity). Involved in the regulation of synaptic function in excitatory hippocampal synapses. Recruited to the postsynaptic membrane upon NMDA receptor activation, is required for the modulation of synaptic activity during plasticity. Enhancement of lipid phosphatase activity is able to drive depression of AMPA receptor-mediated synaptic responses, activity required for NMDA receptor-dependent long-term depression (LTD) (By similarity). May be a negative regulator of insulin signaling and glucose metabolism in adipose tissue. The nuclear monoubiquitinated form possesses greater apoptotic potential, whereas the cytoplasmic nonubiquitinated form induces less tumor suppressive ability (PubMed:10468583, PubMed:18716620).
Functional kinase, like isoform 1 it antagonizes the PI3K-AKT/PKB signaling pathway. Plays a role in mitochondrial energetic metabolism by promoting COX activity and ATP production, via collaboration with isoform 1 in increasing protein levels of PINK1.