Entity Details

Primary name PPM1D_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionO15297
EntryNamePPM1D_HUMAN
FullNameProtein phosphatase 1D
TaxID9606
Evidenceevidence at protein level
Length605
SequenceStatuscomplete
DateCreated2000-12-01
DateModified2021-06-02

Ontological Relatives

GenesPPM1D

GO terms

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GOName
GO:0000086 G2/M transition of mitotic cell cycle
GO:0004722 protein serine/threonine phosphatase activity
GO:0005634 nucleus
GO:0005654 nucleoplasm
GO:0005730 nucleolus
GO:0005829 cytosol
GO:0006306 DNA methylation
GO:0006342 chromatin silencing
GO:0006470 protein dephosphorylation
GO:0008285 negative regulation of cell population proliferation
GO:0009267 cellular response to starvation
GO:0009314 response to radiation
GO:0009617 response to bacterium
GO:0030330 DNA damage response, signal transduction by p53 class mediator
GO:0035970 peptidyl-threonine dephosphorylation
GO:0045814 negative regulation of gene expression, epigenetic
GO:0046872 metal ion binding
GO:0051019 mitogen-activated protein kinase binding
GO:0060260 regulation of transcription initiation from RNA polymerase II promoter
GO:0106306 protein serine phosphatase activity
GO:0106307 protein threonine phosphatase activity

Subcellular Location

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Subcellular Location
Cytoplasm
Nucleus

Domains

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DomainNameCategoryType
IPR000222 PPM-type phosphatase, divalent cation bindingSiteBinding site
IPR001932 PPM-type phosphatase domainDomainDomain
IPR036457 PPM-type phosphatase domain superfamilyFamilyHomologous superfamily

Diseases

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Disease IDSourceNameDescription
617450 OMIMJansen-de Vries syndrome (JDVS)An autosomal dominant neurodevelopmental disorder characterized by mild to severe intellectual disability, psychomotor developmental delay, speech delay, and behavioral manifestations including attention deficit-hyperactivity disorder, autism and anxiety disorders. Most patients have variable additional features, including feeding and gastrointestinal difficulties, high pain threshold, hypersensitivity to sound, hypotonia, broad-based gait, and dysmorphic features, including mild facial abnormalities, strabismus, and small hands and feet. The disease is caused by variants affecting the gene represented in this entry.
114480 OMIMBreast cancer (BC)A common malignancy originating from breast epithelial tissue. Breast neoplasms can be distinguished by their histologic pattern. Invasive ductal carcinoma is by far the most common type. Breast cancer is etiologically and genetically heterogeneous. Important genetic factors have been indicated by familial occurrence and bilateral involvement. Mutations at more than one locus can be involved in different families or even in the same case. Disease susceptibility may be associated with variants affecting the gene represented in this entry.
167000 OMIMOvarian cancer (OC)The term ovarian cancer defines malignancies originating from ovarian tissue. Although many histologic types of ovarian tumors have been described, epithelial ovarian carcinoma is the most common form. Ovarian cancers are often asymptomatic and the recognized signs and symptoms, even of late-stage disease, are vague. Consequently, most patients are diagnosed with advanced disease. Disease susceptibility may be associated with variants affecting the gene represented in this entry.

Interactions

29 interactions

InteractorPartnerSourcesPublicationsLink
PPM1D_HUMANMDM2_HUMANBioGRID, HPRD, IntAct17936559 details
PPM1D_HUMANH2AX_HUMANBioGRID, MINT20101220 20118229 20460517 details
PPM1D_HUMANBEX2_HUMANBioGRID, MINT25640309 details
PPM1D_HUMANCASZ1_HUMANBioGRID, MINT25640309 details
PPM1D_HUMANDIRA3_HUMANBioGRID, MINT25640309 details
PPM1D_HUMANDKK3_HUMANBioGRID, MINT25640309 details
PPM1D_HUMANESIP1_HUMANBioGRID, MINT25640309 details
PPM1D_HUMANERRFI_HUMANBioGRID, MINT25640309 details
PPM1D_HUMANGLCE_HUMANBioGRID, MINT25640309 details
PPM1D_HUMANITIH5_HUMANBioGRID, MINT25640309 details
PPM1D_HUMANMRC2_HUMANBioGRID, MINT25640309 details
PPM1D_HUMANLYPD3_HUMANBioGRID, MINT25640309 details
PPM1D_HUMANARY2_HUMANBioGRID, MINT25640309 details
PPM1D_HUMANOSGI1_HUMANBioGRID, MINT25640309 details
PPM1D_HUMANRHBT2_HUMANBioGRID, MINT25640309 details
PPM1D_HUMANNSD3_HUMANBioGRID, MINT25640309 details
PPM1D_HUMANRUNX2_HUMANDIP22065775 details
PPM1D_HUMANUBC_HUMANBioGRID23314748 details
PPM1D_HUMANKDM1A_HUMANBioGRID25999347 details
PPM1D_HUMANCHK2_HUMANBioGRID16311512 28027003 details
PPM1D_HUMANH31_HUMANBioGRID23828041 details
PPM1D_HUMANH33_HUMANBioGRID23828041 details
PPM1D_HUMANP53_HUMANBioGRID, HPRD17936559 28027003 32807901 details
PPM1D_HUMANMK11_HUMANBioGRID28027003 details
PPM1D_HUMANRL5_HUMANHPRD7649987 details
PPM1D_HUMANCDC5L_HUMANBioGRID, MINT11101529 20467437 details
PPM1D_HUMANPP4C_HUMANIntAct18614045 details
PPM1D_HUMANCK5P3_HUMANBioGRID28027003 details
PPM1D_HUMANNUCL_HUMANHPRD12185196 details