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RPE-retinal G protein-coupled receptor (RGR)

Function: - receptor for all-trans-retinal & 11-cis-retinal - preferentially binds all-trans-retinal - may catalyze the isomerization of the retinal by a retinochrome-like mechanism - covalently binds all-trans-retinal & 11-cis-retinal Structure: - belongs to the G-protein coupled receptor 1 family Opsin subfamily Compartment: membrane Alternative splicing: named isoforms=3 Expression: - preferentially expressed at high levels in the retinal pigment epithelium (RPE) & Mueller cells of the neural retina Pathology: - defects in RGR are a cause of retinitis pigmentosa

General

glycoprotein G-protein coupled receptor; serpentine receptor

Properties

SIZE: entity length = 291 aa MW = 32 kD COMPARTMENT: cellular membrane MOTIF: exoplasmic domain {1-15} transmembrane domain {16-36} cytoplasmic loop {37-52} transmembrane domain {53-73} exoplasmic loop {74-91} MOTIF: cysteine residue {C88} MODIFICATION: cysteine residue {C162} transmembrane domain {92-112} cytoplasmic loop {113-130} transmembrane domain {131-151} exoplasmic loop {152-175} MOTIF: cysteine residue {C162} MODIFICATION: cysteine residue {C88} N-glycosylation site {N172} transmembrane domain {176-196} cytoplasmic loop {197-219} transmembrane domain {220-240} exoplasmic loop {241-247} transmembrane domain {248-268} cytoplasmic domain {269-291}

Database Correlations

OMIM correlations MORBIDMAP 600342 UniProt P47804 Pfam PF00001 Entrez Gene 5995 Kegg hsa:5995

References

  1. UniProt :accession P47804
  2. Mutations of the RGR gene; Retina International's scientific newsletter http://www.retina-international.com/sci-news/rgrmut.htm
  3. GeneReviews http://www.ncbi.nlm.nih.gov/sites/genetests/lab/gene/RGR