|
gptkbp:instanceOf
|
gptkb:protein
gptkb:G_protein-coupled_receptor
|
|
gptkbp:absorption_maximum
|
~498 nm
|
|
gptkbp:activatedBy
|
light
|
|
gptkbp:alternativeName
|
visual purple
|
|
gptkbp:chromophore
|
gptkb:11-cis-retinal
|
|
gptkbp:deactivatedBy
|
phosphorylation
arrestin binding
|
|
gptkbp:degradedBy
|
lysosomal proteases
|
|
gptkbp:discoveredBy
|
gptkb:Franz_Boll
|
|
gptkbp:discoveredIn
|
1876
|
|
gptkbp:EC_number
|
7.1.1.1
|
|
gptkbp:Entrez_Gene_ID
|
ENSG00000163914
|
|
gptkbp:expressedIn
|
vertebrates
|
|
gptkbp:form
|
gptkb:opsin
gptkb:all-trans-retinal
gptkb:metarhodopsin_II
|
|
gptkbp:foundIn
|
retina
rod cells
|
|
gptkbp:function
|
photoreceptor activity
|
|
gptkbp:gene
|
gptkb:RHO
|
|
gptkbp:GO_term
|
GO:0007602
|
|
gptkbp:HGNC_ID
|
10012
|
|
https://www.w3.org/2000/01/rdf-schema#label
|
rhodopsin
|
|
gptkbp:ligand
|
retinal
|
|
gptkbp:location
|
outer segment of rod cells
|
|
gptkbp:molecularWeight
|
~40 kDa
|
|
gptkbp:mutationAssociatedWith
|
retinitis pigmentosa
congenital stationary night blindness
|
|
gptkbp:OMIM
|
180380
|
|
gptkbp:orthologIn
|
gptkb:bacteriorhodopsin
gptkb:melanopsin
cone opsins
|
|
gptkbp:PDB
|
1F88
|
|
gptkbp:postTranslationalModification
|
palmitoylation
phosphorylation
glycosylation
|
|
gptkbp:RefSeq
|
NM_000539
|
|
gptkbp:relatedTo
|
night vision
color vision
phototransduction
|
|
gptkbp:roleInVision
|
scotopic vision
|
|
gptkbp:species
|
gptkb:Bos_taurus
gptkb:Mus_musculus
gptkb:Homo_sapiens
|
|
gptkbp:structure
|
seven transmembrane helices
|
|
gptkbp:subcellularLocation
|
gptkb:plasma_membrane
|
|
gptkbp:UniProtID
|
P08100
|
|
gptkbp:bfsParent
|
gptkb:G_protein-coupled_receptor
gptkb:G_protein-coupled_receptors
|
|
gptkbp:bfsLayer
|
5
|