Entity Details

Primary name KAPCG_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionP22612
EntryNameKAPCG_HUMAN
FullNamecAMP-dependent protein kinase catalytic subunit gamma
TaxID9606
Evidenceevidence at protein level
Length351
SequenceStatuscomplete
DateCreated1991-08-01
DateModified2021-06-02

Ontological Relatives

GenesPRKACG

GO terms

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GOName
GO:0002223 stimulatory C-type lectin receptor signaling pathway
GO:0002250 adaptive immune response
GO:0002862 negative regulation of inflammatory response to antigenic stimulus
GO:0003091 renal water homeostasis
GO:0004679 AMP-activated protein kinase activity
GO:0004691 cAMP-dependent protein kinase activity
GO:0005524 ATP binding
GO:0005634 nucleus
GO:0005654 nucleoplasm
GO:0005829 cytosol
GO:0007268 chemical synaptic transmission
GO:0007283 spermatogenesis
GO:0007596 blood coagulation
GO:0008584 male gonad development
GO:0010737 protein kinase A signaling
GO:0034199 activation of protein kinase A activity
GO:0034237 protein kinase A regulatory subunit binding
GO:0034380 high-density lipoprotein particle assembly
GO:0045202 synapse
GO:0071377 cellular response to glucagon stimulus
GO:0097546 ciliary base
GO:0106310 protein serine kinase activity
GO:0106311 protein threonine kinase activity

Subcellular Location

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Domains

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DomainNameCategoryType
IPR000719 Protein kinase domainDomainDomain
IPR000961 AGC-kinase, C-terminalDomainDomain
IPR008271 Serine/threonine-protein kinase, active siteSiteActive site
IPR011009 Protein kinase-like domain superfamilyFamilyHomologous superfamily
IPR017441 Protein kinase, ATP binding siteSiteBinding site
IPR039084 cAMP-dependent protein kinase catalytic subunit gammaFamilyFamily
IPR044109 cAMP-dependent protein kinase catalytic subunitFamilyFamily

Diseases

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Disease IDSourceNameDescription
616176 OMIMBleeding disorder, platelet-type 19 (BDPLT19)A disorder characterized by increased bleeding tendency due to platelet dysfunction. Clinical features include epistaxis, hematomas, bleeding after tooth extraction, and menorrhagia. The disease is caused by variants affecting the gene represented in this entry.