Homo sapiens Protein: SLC7A8
Summary
InnateDB Protein IDBP-3106.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol SLC7A8
Protein Name solute carrier family 7 (amino acid transporter light chain, L system), member 8
Synonyms LAT2; LPI-PC1;
Species Homo sapiens
Ensembl Protein ENSP00000320378
InnateDB Gene IDBG-3104 (SLC7A8)
Protein Structure
UniProt Annotation
Function Sodium-independent, high-affinity transport of small and large neutral amino acids such as alanine, serine, threonine, cysteine, phenylalanine, tyrosine, leucine, arginine and tryptophan, when associated with SLC3A2/4F2hc. Acts as an amino acid exchanger. Has higher affinity for L-phenylalanine than LAT1 but lower affinity for glutamine and serine. L-alanine is transported at physiological concentrations. Plays a role in basolateral (re)absorption of neutral amino acids. Involved in the uptake of methylmercury (MeHg) when administered as the L-cysteine or D,L-homocysteine complexes, and hence plays a role in metal ion homeostasis and toxicity. Involved in the cellular activity of small molecular weight nitrosothiols, via the stereoselective transport of L-nitrosocysteine (L-CNSO) across the transmembrane. Plays an essential role in the reabsorption of neutral amino acids from the epithelial cells to the bloodstream in the kidney. {ECO:0000269PubMed:10391915, ECO:0000269PubMed:10574970, ECO:0000269PubMed:11311135, ECO:0000269PubMed:12117417, ECO:0000269PubMed:12716892, ECO:0000269PubMed:15081149, ECO:0000269PubMed:15769744, ECO:0000269PubMed:15918515}.
Subcellular Localization Cytoplasm. Basolateral cell membrane; Multi- pass membrane protein. Note=Localized to the cytoplasm when expressed alone but when coexpressed with SLC3A2/4F2hc, is localized to the plasma membrane. Colocalized with SLC3A2/4F2hc at the basolateral membrane of kidney cortex proximal tubules and small intestine epithelia of the villi.
Disease Associations
Tissue Specificity Strongest expression is observed in kidney and moderate expression in placenta and brain, followed by liver, prostate, testis, ovary, lymph node, thymus, spleen, skeletal muscle and heart. Also expressed in fetal liver as well as in the retinal pigment epithelial cell line ARPE-19 and the intestinal epithelial cell line Caco-2. {ECO:0000269PubMed:10391915, ECO:0000269PubMed:15081149, ECO:0000269PubMed:15918515, ECO:0000269PubMed:16027961}.
Comments
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 2 experimentally validated interaction(s) in this database.
They are also associated with 1 interaction(s) predicted by orthology.
Experimentally validated
Total 2 [view]
Protein-Protein 2 [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:0005515 protein binding
GO:0015101 organic cation transmembrane transporter activity
GO:0015171 amino acid transmembrane transporter activity
GO:0015175 neutral amino acid transmembrane transporter activity
GO:0015179 L-amino acid transmembrane transporter activity
GO:0019534 toxin transporter activity
GO:0042605 peptide antigen binding
Biological Process
GO:0003333 amino acid transmembrane transport
GO:0006520 cellular amino acid metabolic process
GO:0006810 transport
GO:0006811 ion transport
GO:0006865 amino acid transport
GO:0007596 blood coagulation
GO:0009636 response to toxic substance
GO:0015695 organic cation transport
GO:0015804 neutral amino acid transport
GO:0015807 L-amino acid transport
GO:0050900 leukocyte migration
GO:0055065 metal ion homeostasis
GO:0055085 transmembrane transport
GO:1901998 toxin transport
GO:1902475 L-alpha-amino acid transmembrane transport
Cellular Component
GO:0005737 cytoplasm
GO:0005886 plasma membrane
GO:0005887 integral component of plasma membrane
GO:0016020 membrane
GO:0016021 integral component of membrane
GO:0016323 basolateral plasma membrane
GO:0070062 extracellular vesicular exosome
Protein Structure and Domains
PDB ID
InterPro IPR002293 Amino acid/polyamine transporter I
IPR004760 L-type amino acid transporter
IPR004841 Amino acid permease/ SLC12A domain
PFAM PF13520
PF00324
PRINTS
PIRSF PIRSF006060
SMART
TIGRFAMs
Post-translational Modifications
Modification
Cross-References
SwissProt Q9UHI5
PhosphoSite PhosphoSite-Q9UHI5
TrEMBL E9PQT4
UniProt Splice Variant
Entrez Gene 23428
UniGene Hs.735363
RefSeq NP_036376
HUGO HGNC:11066
OMIM 604235
CCDS CCDS9590
HPRD 11971
IMGT
EMBL AB037669 AF135828 AF135829 AF135830 AF171669 AK094550 AK296702 AK300384 AK313465 AL117258 BC052250 BX248288 CH471078 Y18483
GenPept AAF05695 AAF05696 AAF05697 AAF20381 AAH52250 BAB21519 BAG36251 BAG52886 BAG59296 BAG62118 CAB40137 CAD62616 EAW66181 EAW66182