Homo sapiens Protein: SLC6A4
Summary
InnateDB Protein IDBP-38867.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol SLC6A4
Protein Name solute carrier family 6 (neurotransmitter transporter, serotonin), member 4
Synonyms 5-HTT; 5-HTTLPR; 5HTT; hSERT; HTT; OCD1; SERT; SERT1;
Species Homo sapiens
Ensembl Protein ENSP00000261707
InnateDB Gene IDBG-38865 (SLC6A4)
Protein Structure
UniProt Annotation
Function Serotonin transporter whose primary function in the central nervous system involves the regulation of serotonergic signaling via transport of serotonin molecules from the synaptic cleft back into the pre-synaptic terminal for re-utilization. Plays a key role in mediating regulation of the availability of serotonin to other receptors of serotonergic systems. Terminates the action of serotonin and recycles it in a sodium-dependent manner. {ECO:0000269PubMed:17506858, ECO:0000269PubMed:18227069, ECO:0000269PubMed:19270731}.
Subcellular Localization Cell membrane; Multi-pass membrane protein. Endomembrane system; Multi-pass membrane protein. Endosome membrane; Multi-pass membrane protein. Note=Translocates from intracellular locations to the plasma membrane. Density of transporter molecules on the plasma membrane is itself regulated by serotonin.
Disease Associations
Tissue Specificity Expressed in platelets (at protein level). {ECO:0000269PubMed:17506858}.
Comments
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 10 experimentally validated interaction(s) in this database.
They are also associated with 1 interaction(s) predicted by orthology.
Experimentally validated
Total 10 [view]
Protein-Protein 10 [view]
Protein-DNA 0
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Predicted by orthology
Total 1 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0005328 neurotransmitter:sodium symporter activity
GO:0005335 serotonin:sodium symporter activity
GO:0005515 protein binding
GO:0008504 monoamine transmembrane transporter activity
GO:0015222 serotonin transmembrane transporter activity
GO:0017022 myosin binding
GO:0017075 syntaxin-1 binding
GO:0017137 Rab GTPase binding
GO:0019811 cocaine binding
GO:0042803 protein homodimerization activity
GO:0050998 nitric-oxide synthase binding
GO:0051015 actin filament binding
Biological Process
GO:0001666 response to hypoxia
GO:0006836 neurotransmitter transport
GO:0006837 serotonin transport
GO:0007420 brain development
GO:0007584 response to nutrient
GO:0007613 memory
GO:0007623 circadian rhythm
GO:0009636 response to toxic substance
GO:0010033 response to organic substance
GO:0010628 positive regulation of gene expression
GO:0015844 monoamine transport
GO:0021794 thalamus development
GO:0021941 negative regulation of cerebellar granule cell precursor proliferation
GO:0032227 negative regulation of synaptic transmission, dopaminergic
GO:0032355 response to estradiol
GO:0035176 social behavior
GO:0042310 vasoconstriction
GO:0042493 response to drug
GO:0042713 sperm ejaculation
GO:0045665 negative regulation of neuron differentiation
GO:0045787 positive regulation of cell cycle
GO:0046621 negative regulation of organ growth
GO:0048854 brain morphogenesis
GO:0051259 protein oligomerization
GO:0051260 protein homooligomerization
GO:0051610 serotonin uptake
GO:0055085 transmembrane transport
GO:0071300 cellular response to retinoic acid
GO:0071310 cellular response to organic substance
GO:0071321 cellular response to cGMP
Cellular Component
GO:0005829 cytosol
GO:0005886 plasma membrane
GO:0005887 integral component of plasma membrane
GO:0010008 endosome membrane
GO:0012505 endomembrane system
GO:0016021 integral component of membrane
GO:0043005 neuron projection
GO:0045121 membrane raft
Protein Structure and Domains
PDB ID
InterPro IPR000175 Sodium:neurotransmitter symporter
IPR013086 Sodium:neurotransmitter symporter, serotonin, N-terminal
PFAM PF00209
PF03491
PRINTS PR00176
PR01203
PIRSF
SMART
TIGRFAMs
Post-translational Modifications
Modification
Cross-References
SwissProt P31645
PhosphoSite PhosphoSite-P31645
TrEMBL Q9NYN7
UniProt Splice Variant
Entrez Gene 6532
UniGene Hs.29792
RefSeq NP_001036
HUGO HGNC:11050
OMIM 182138
CCDS CCDS11256
HPRD 01640
IMGT
EMBL AC104984 AF233399 AK308014 AY902473 BC069484 EU099989 EU796564 EU796569 EU796574 EU796579 EU796584 EU796589 EU796594 EU796604 EU796609 EU796614 EU796619 EU796624 L05568 U79746 X70697
GenPept AAA35492 AAB93475 AAF61945 AAH69484 AAW80933 ABV02581 ACE96158 ACE96163 ACE96168 ACE96173 ACE96178 ACE96188 ACE96193 ACE96198 ACE96203 ACE96208 ACE96213 ACE96218 CAA50029