Entity Details

Primary name KPBB_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionQ93100
EntryNameKPBB_HUMAN
FullNamePhosphorylase b kinase regulatory subunit beta
TaxID9606
Evidenceevidence at protein level
Length1093
SequenceStatuscomplete
DateCreated1997-11-01
DateModified2021-06-02

Ontological Relatives

GenesPHKB

GO terms

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GOName
GO:0005516 calmodulin binding
GO:0005829 cytosol
GO:0005886 plasma membrane
GO:0005964 phosphorylase kinase complex
GO:0005977 glycogen metabolic process
GO:0005980 glycogen catabolic process
GO:0006091 generation of precursor metabolites and energy
GO:0006468 protein phosphorylation

Subcellular Location

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Subcellular Location
Cell membrane

Domains

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DomainNameCategoryType
IPR008734 Phosphorylase kinase alpha/beta subunitFamilyFamily
IPR008928 Six-hairpin glycosidase superfamilyFamilyHomologous superfamily
IPR011613 GH15-like domainDomainDomain

Diseases

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Disease IDSourceNameDescription
261750 OMIMGlycogen storage disease 9B (GSD9B)A metabolic disorder characterized by hepatomegaly, only slightly elevated transaminases and plasma lipids, clinical improvement with increasing age, and remarkably no clinical muscle involvement. Biochemical observations suggest that this mild phenotype is caused by an incomplete holoenzyme that lacks the beta subunit, but that may possess residual activity. The disease is caused by variants affecting the gene represented in this entry.