General Information of Drug Therapeutic Target (DTT) (ID: TTESBNC)

DTT Name M-phase inducer phosphatase 3 (MPIP3)
Synonyms Dual specificity phosphatase Cdc25C; Cdc25C phosphatase
Gene Name CDC25C
DTT Type
Literature-reported target
[1]
BioChemical Class
Phosphoric monoester hydrolase
UniProt ID
MPIP3_HUMAN
TTD ID
T19011
3D Structure
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2D Sequence (FASTA)
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3D Structure (PDB)
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EC Number
EC 3.1.3.48
Sequence
MSTELFSSTREEGSSGSGPSFRSNQRKMLNLLLERDTSFTVCPDVPRTPVGKFLGDSANL
SILSGGTPKRCLDLSNLSSGEITATQLTTSADLDETGHLDSSGLQEVHLAGMNHDQHLMK
CSPAQLLCSTPNGLDRGHRKRDAMCSSSANKENDNGNLVDSEMKYLGSPITTVPKLDKNP
NLGEDQAEEISDELMEFSLKDQEAKVSRSGLYRSPSMPENLNRPRLKQVEKFKDNTIPDK
VKKKYFSGQGKLRKGLCLKKTVSLCDITITQMLEEDSNQGHLIGDFSKVCALPTVSGKHQ
DLKYVNPETVAALLSGKFQGLIEKFYVIDCRYPYEYLGGHIQGALNLYSQEELFNFFLKK
PIVPLDTQKRIIIVFHCEFSSERGPRMCRCLREEDRSLNQYPALYYPELYILKGGYRDFF
PEYMELCEPQSYCPMHHQDHKTELLRCRSQSKVQEGERQLREQIALLVKDMSP
Function
Tyrosine protein phosphatase required for progression of the cell cycle. When phosphorylated, highly effective in activating G2 cells into prophase. Directly dephosphorylates CDK1 and activates its kinase activity. Functions as a dosage-dependent inducer in mitotic control.
KEGG Pathway
Cell cycle (hsa04110 )
Oocyte meiosis (hsa04114 )
Progesterone-mediated oocyte maturation (hsa04914 )
MicroRNAs in cancer (hsa05206 )
Reactome Pathway
Cyclin B2 mediated events (R-HSA-157881 )
Activation of ATR in response to replication stress (R-HSA-176187 )
RHO GTPases activate PKNs (R-HSA-5625740 )
Cyclin A/B1 associated events during G2/M transition (R-HSA-69273 )
Chk1/Chk2(Cds1) mediated inactivation of Cyclin B (R-HSA-75035 )
Polo-like kinase mediated events (R-HSA-156711 )

Molecular Interaction Atlas (MIA) of This DTT

Molecular Interaction Atlas (MIA) Jump to Detail Molecular Interaction Atlas of This DTT
1 Discontinued Drug(s) Targeting This DTT
Drug Name Drug ID Indication ICD 11 Highest Status REF
MX-7065 DMP26BW Solid tumour/cancer 2A00-2F9Z Terminated [1]
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3 Investigative Drug(s) Targeting This DTT
Drug Name Drug ID Indication ICD 11 Highest Status REF
BN-82002 DMXY574 Solid tumour/cancer 2A00-2F9Z Investigative [2]
BN-82685 DMZME4N Discovery agent N.A. Investigative [3]
NSC-663284 DMEXW31 Discovery agent N.A. Investigative [3]
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References

1 Handbook of Assay Development in Drug Discovery, Lisa K. Minor, 2013. Page(11).
2 Synthesis of small molecule CDC25 phosphatases inhibitors. Bioorg Med Chem Lett. 2004 Dec 6;14(23):5809-12.
3 Synthesis and biological evaluation of novel heterocyclic quinones as inhibitors of the dual specificity protein phosphatase CDC25C. Bioorg Med Chem Lett. 2006 Jan 1;16(1):171-5.