Entity Details

Primary name GRK1_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionQ15835
EntryNameGRK1_HUMAN
FullNameRhodopsin kinase GRK1
TaxID9606
Evidenceevidence at protein level
Length563
SequenceStatuscomplete
DateCreated1997-11-01
DateModified2021-06-02

Ontological Relatives

GenesGRK1

GO terms

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GOName
GO:0004672 protein kinase activity
GO:0004703 G protein-coupled receptor kinase activity
GO:0005524 ATP binding
GO:0007601 visual perception
GO:0008277 regulation of G protein-coupled receptor signaling pathway
GO:0016056 rhodopsin mediated signaling pathway
GO:0022400 regulation of rhodopsin mediated signaling pathway
GO:0046777 protein autophosphorylation
GO:0050254 rhodopsin kinase activity
GO:0097381 photoreceptor disc membrane

Subcellular Location

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Subcellular Location
Cell projection
Membrane

Domains

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DomainNameCategoryType
IPR000239 GPCR kinaseFamilyFamily
IPR000719 Protein kinase domainDomainDomain
IPR000961 AGC-kinase, C-terminalDomainDomain
IPR008271 Serine/threonine-protein kinase, active siteSiteActive site
IPR011009 Protein kinase-like domain superfamilyFamilyHomologous superfamily
IPR016137 RGS domainDomainDomain
IPR017441 Protein kinase, ATP binding siteSiteBinding site
IPR032965 Rhodopsin kinase GRK1FamilyFamily
IPR036305 RGS domain superfamilyFamilyHomologous superfamily
IPR037716 Rhodopsin kinase, catalytic domainDomainDomain

Diseases

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Disease IDSourceNameDescription
613411 OMIMNight blindness, congenital stationary, Oguchi type 2 (CSNBO2)A non-progressive retinal disorder characterized by impaired night vision, often associated with nystagmus and myopia. Congenital stationary night blindness Oguchi type is associated with fundus discoloration and abnormally slow dark adaptation. The disease is caused by variants affecting the gene represented in this entry.