Entity Details

Primary name KCC2G_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionQ13555
EntryNameKCC2G_HUMAN
FullNameCalcium/calmodulin-dependent protein kinase type II subunit gamma
TaxID9606
Evidenceevidence at protein level
Length558
SequenceStatuscomplete
DateCreated1997-11-01
DateModified2021-06-02

Ontological Relatives

GenesCAMK2G

GO terms

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GOName
GO:0004683 calmodulin-dependent protein kinase activity
GO:0004723 calcium-dependent protein serine/threonine phosphatase activity
GO:0005516 calmodulin binding
GO:0005524 ATP binding
GO:0005654 nucleoplasm
GO:0005737 cytoplasm
GO:0005829 cytosol
GO:0005954 calcium- and calmodulin-dependent protein kinase complex
GO:0007399 nervous system development
GO:0010975 regulation of neuron projection development
GO:0014733 regulation of skeletal muscle adaptation
GO:0016020 membrane
GO:0030073 insulin secretion
GO:0030154 cell differentiation
GO:0030666 endocytic vesicle membrane
GO:0033017 sarcoplasmic reticulum membrane
GO:0042802 identical protein binding
GO:0042803 protein homodimerization activity
GO:0043005 neuron projection
GO:0051924 regulation of calcium ion transport
GO:0060333 interferon-gamma-mediated signaling pathway
GO:0106310 protein serine kinase activity
GO:0106311 protein threonine kinase activity
GO:1900034 regulation of cellular response to heat

Subcellular Location

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Subcellular Location
Sarcoplasmic reticulum membrane

Domains

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DomainNameCategoryType
IPR000719 Protein kinase domainDomainDomain
IPR008271 Serine/threonine-protein kinase, active siteSiteActive site
IPR011009 Protein kinase-like domain superfamilyFamilyHomologous superfamily
IPR013543 Calcium/calmodulin-dependent protein kinase II, association-domainDomainDomain
IPR017441 Protein kinase, ATP binding siteSiteBinding site
IPR032710 NTF2-like domain superfamilyFamilyHomologous superfamily

Diseases

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Disease IDSourceNameDescription
618522 OMIMIntellectual developmental disorder, autosomal dominant 59 (MRD59)An autosomal dominant form of mental retardation, a disorder characterized by significantly below average general intellectual functioning associated with impairments in adaptive behavior and manifested during the developmental period. The disease may be caused by variants affecting the gene represented in this entry.

Drugs

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DrugNameSourceType
DB06616 BosutinibDrugbanksmall molecule
DB08699 1-tert-butyl-3-(3-methylbenzyl)-1H-pyrazolo[3,4-d]pyrimidin-4-amineDrugbanksmall molecule
DB12010 FostamatinibDrugbanksmall molecule

Interactions

40 interactions

InteractorPartnerSourcesPublicationsLink
KCC2G_HUMANKCC2A_HUMANBioGRID, IntAct25852190 31980649 32296183 details
KCC2G_HUMANLOX5_HUMANMINT24860872 details
KCC2G_HUMANKR193_HUMANBioGRID, IntAct32296183 details
KCC2G_HUMANTTC5_HUMANBioGRID, IntAct32296183 details
KCC2G_HUMANKCC2D_HUMANBioGRID, DIP, IntAct20668654 28514442 29426014 32296183 details
KCC2G_HUMANKRA61_HUMANBioGRID, IntAct32296183 details
KCC2G_HUMANTNPO3_HUMANBioGRID, IntAct32296183 details
KCC2G_HUMANSTRBP_HUMANBioGRID, IntAct32296183 details
KCC2G_HUMANTNPO2_HUMANBioGRID, IntAct32296183 details
KCC2G_HUMANPSB1_HUMANBioGRID, IntAct32296183 details
KCC2G_HUMANRM11_HUMANBioGRID, IntAct32296183 details
KCC2G_HUMANKCC2G_HUMANDIP20668654 details
KCC2G_HUMANNXF1_HUMANBioGRID, IntAct32296183 details
KCC2G_HUMANCALM2_HUMANBioGRID, DIP10860555 20668654 details
KCC2G_HUMANCDC37_HUMANBioGRID, IntAct32296183 details
KCC2G_HUMANCALM3_HUMANBioGRID10860555 details
KCC2G_HUMANDUS1L_HUMANBioGRID, IntAct32296183 details
KCC2G_HUMANNTF2_HUMANBioGRID, IntAct32296183 details
KCC2G_HUMANRAD_HUMANBioGRID9115241 9677319 details
KCC2G_HUMANKANK2_HUMANBioGRID, IntAct32296183 details
KCC2G_HUMANZN363_HUMANBioGRID17568776 details
KCC2G_HUMANKCC2B_HUMANBioGRID, IntAct32296183 details
KCC2G_HUMANERR3_HUMANBioGRID, IntAct32296183 details
KCC2G_HUMANNMDE2_HUMANBioGRID28636948 9670010 details
KCC2G_HUMANCALM1_HUMANBioGRID10860555 details
KCC2G_HUMANPTEN_HUMANBioGRID28636948 details
KCC2G_HUMANNR1H2_HUMANDIP21331046 details
KCC2G_HUMANPCNA_HUMANUniProt26030842 details
KCC2G_HUMANSMAD2_HUMANBioGRID11027280 details
KCC2G_HUMANSMAD4_HUMANBioGRID11027280 details
KCC2G_HUMANNMDZ1_HUMANBioGRID9670010 details
KCC2G_HUMANSTMN1_HUMANBioGRID21768358 details
KCC2G_HUMANUBC9_HUMANBioGRID32296183 details
KCC2G_HUMANFXR2_HUMANBioGRID, MINT21653829 29395067 details
KCC2G_HUMANHS90B_HUMANIntAct22939624 details
KCC2G_HUMANFXR1_HUMANMINT21653829 details
KCC2G_HUMANSIVA_HUMANBioGRID21768358 details
KCC2G_HUMANMALT1_HUMANBioGRID21513986 details
KCC2G_HUMANBCL10_HUMANBioGRID21513986 details
KCC2G_HUMANBECN1_HUMANBioGRID29079782 details