Homo sapiens Protein: PDE6B
Summary
InnateDB Protein IDBP-484508.3
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol PDE6B
Protein Name phosphodiesterase 6B, cGMP-specific, rod, beta
Synonyms CSNB3; CSNBAD2; PDEB; rd1; RP40;
Species Homo sapiens
Ensembl Protein ENSP00000420295
InnateDB Gene IDBG-5946 (PDE6B)
Protein Structure
UniProt Annotation
Function This protein participates in processes of transmission and amplification of the visual signal. Necessary for the formation of a functional phosphodiesterase holoenzyme.
Subcellular Localization Membrane; Lipid-anchor.
Disease Associations Retinitis pigmentosa 40 (RP40) [MIM:613801]: A retinal dystrophy belonging to the group of pigmentary retinopathies. Retinitis pigmentosa is characterized by retinal pigment deposits visible on fundus examination and primary loss of rod photoreceptor cells followed by secondary loss of cone photoreceptors. Patients typically have night vision blindness and loss of midperipheral visual field. As their condition progresses, they lose their far peripheral visual field and eventually central vision as well. {ECO:0000269PubMed:22334370, ECO:0000269PubMed:8394174, ECO:0000269PubMed:8557257, ECO:0000269PubMed:8595886, ECO:0000269PubMed:8698075, ECO:0000269PubMed:8956055, ECO:0000269PubMed:9543643}. Note=The disease is caused by mutations affecting the gene represented in this entry.Night blindness, congenital stationary, autosomal dominant 2 (CSNBAD2) [MIM:163500]: A non-progressive retinal disorder characterized by impaired night vision, often associated with nystagmus and myopia. {ECO:0000269PubMed:8075643}. Note=The disease is caused by mutations affecting the gene represented in this entry.
Tissue Specificity
Comments
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 2 experimentally validated interaction(s) in this database.
Experimentally validated
Total 2 [view]
Protein-Protein 1 [view]
Protein-DNA 1 [view]
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Gene Ontology

Molecular Function
Accession GO Term
GO:0004114 3',5'-cyclic-nucleotide phosphodiesterase activity
GO:0005515 protein binding
GO:0046872 metal ion binding
GO:0047555 3',5'-cyclic-GMP phosphodiesterase activity
Biological Process
GO:0007165 signal transduction
GO:0007601 visual perception
GO:0007603 phototransduction, visible light
GO:0008152 metabolic process
GO:0009583 detection of light stimulus
GO:0016056 rhodopsin mediated signaling pathway
GO:0022400 regulation of rhodopsin mediated signaling pathway
GO:0046037 GMP metabolic process
GO:0051480 cytosolic calcium ion homeostasis
GO:0060041 retina development in camera-type eye
Cellular Component
GO:0005886 plasma membrane
GO:0097381 photoreceptor disc membrane
Protein Structure and Domains
PDB ID
InterPro IPR002073 3\'5\'-cyclic nucleotide phosphodiesterase, catalytic domain
IPR003018 GAF domain
IPR003607 HD/PDEase domain
IPR023088 3\'5\'-cyclic nucleotide phosphodiesterase
IPR029016 GAF domain-like
PFAM PF00233
PF01590
PF13185
PF13492
PRINTS PR00387
PIRSF
SMART SM00065
SM00471
TIGRFAMs
Post-translational Modifications
Modification
Cross-References
SwissProt P35913
PhosphoSite PhosphoSite-P35913
TrEMBL V9H1J2
UniProt Splice Variant
Entrez Gene 5158
UniGene Hs.654544
RefSeq NP_000274
HUGO HGNC:8786
OMIM 180072
CCDS CCDS33932
HPRD 01571
IMGT
EMBL AC107464 AK316054 BC000249 BT009794 S41458 X62692 X62693 X62694 X62695 X66142 X90587 X90588 X90589 X90590
GenPept AAB22690 AAH00249 AAP88796 BAH14425 CAA44569 CAA44570 CAA44571 CAA46932 CAA62215