Homo sapiens Protein: SLC29A4
Summary
InnateDB Protein IDBP-7461.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol SLC29A4
Protein Name solute carrier family 29 (nucleoside transporters), member 4
Synonyms
Species Homo sapiens
Ensembl Protein ENSP00000297195
InnateDB Gene IDBG-7459 (SLC29A4)
Protein Structure
UniProt Annotation
Function Functions as a polyspecific organic cation transporter, efficiently transporting many organic cations such as monoamine neurotransmitters 1-methyl-4-phenylpyridinium and biogenic amines including serotonin, dopamine, norepinephrine and epinephrine. May play a role in regulating central nervous system homeostasis of monoamine neurotransmitters. May be involved in luminal transport of organic cations in the kidney and seems to use luminal proton gradient to drive organic cation reabsorption. Does not seem to transport nucleoside and nucleoside analogs such as uridine, cytidine, thymidine, adenosine, inosine, guanosine, and azidothymidine. In (PubMed:16873718) adenosine is efficiently transported but in a fashion highly sensitive to extracellular pH, with maximal activity in the pH range 5.5 to 6.5. Glu-206 is essential for the cation selectivity and may function as the charge sensor for cationic substrates. Transport is chloride and sodium-independent but appears to be sensitive to changes in membrane potential. Weakly inhibited by the classical inhibitors of equilibrative nucleoside transport, dipyridamole, dilazep, and nitrobenzylthioinosine. May play a role in the regulation of extracellular adenosine concentrations in cardiac tissues, in particular during ischemia. {ECO:0000269PubMed:15448143, ECO:0000269PubMed:16873718, ECO:0000269PubMed:17018840, ECO:0000269PubMed:17121826}.
Subcellular Localization Cell membrane {ECO:0000305}; Multi-pass membrane protein {ECO:0000305}. Apical cell membrane {ECO:0000305}; Multi-pass membrane protein {ECO:0000305}. Note=Located to the plasma membranes of ventricular myocytes and vascular endothelial cells. Targeted to the apical membranes of differentiated kidney epithelial cells. {ECO:0000269PubMed:15448143, ECO:0000269PubMed:16873718}.
Disease Associations
Tissue Specificity Expressed abundantly in the heart, in both cardiomyocytes and vascular endothelial cells (at protein level). Highly expressed in brain, kidney and skeletal muscle. In the brain expressed in cerebellum, cerebral cortex, medulla, occipital pole, frontal and temporal lobes putamen and in the spinal cord. Lower expression in liver, pancreas, and liver. Expressed in endometrial tissue, exclusively in the stroma. Expression is high in the proliferative phase, decreases during the secretory phase, and is no longer detectable in the menstrual phase. {ECO:0000269PubMed:15448143, ECO:0000269PubMed:16873718, ECO:0000269PubMed:17018840, ECO:0000269PubMed:17393420}.
Comments
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 0 experimentally validated interaction(s) in this database.
Gene Ontology

Molecular Function
Accession GO Term
GO:0005337 nucleoside transmembrane transporter activity
Biological Process
GO:0006810 transport
GO:0055085 transmembrane transport
GO:1901642 nucleoside transmembrane transport
Cellular Component
GO:0005886 plasma membrane
GO:0016021 integral component of membrane
GO:0016324 apical plasma membrane
Protein Structure and Domains
PDB ID
InterPro IPR002259 Equilibrative nucleoside transporter
IPR016196 Major facilitator superfamily domain, general substrate transporter
PFAM PF01733
PRINTS PR01130
PIRSF PIRSF016379
SMART
TIGRFAMs
Post-translational Modifications
Modification
Cross-References
SwissProt Q7RTT9
PhosphoSite PhosphoSite-Q7RTT9
TrEMBL C9IYM7
UniProt Splice Variant
Entrez Gene 222962
UniGene Hs.4302
RefSeq NP_694979
HUGO HGNC:23097
OMIM 609149
CCDS CCDS5340
HPRD 15362
IMGT
EMBL AC093376 AK075422 AK092242 AY485959 BC025325 BC047592 BK000627 CH471144
GenPept AAH25325 AAH47592 AAS65965 BAC03836 BAC11612 DAA00308 EAW87329 EAW87330