Mus musculus Protein: Slc7a8
Summary
InnateDB Protein IDBP-162170.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol Slc7a8
Protein Name solute carrier family 7 (cationic amino acid transporter, y+ system), member 8
Synonyms AA408822; LAT2;
Species Mus musculus
Ensembl Protein ENSMUSP00000022787
InnateDB Gene IDBG-162168 (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:10574970}.
Subcellular Localization Cytoplasm {ECO:0000250}. Basolateral cell membrane {ECO:0000269PubMed:10574970}; Multi-pass membrane protein {ECO:0000269PubMed:10574970}. Note=Localized to the cytoplasm when expressed alone (By similarity). 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. {ECO:0000250}.
Disease Associations
Tissue Specificity Strongly expressed in kidney and small intestine. Moderately present in placenta, ovary and brain. {ECO:0000269PubMed:10574970}.
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 1 [view]
Protein-DNA 1 [view]
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:0005275 amine transmembrane transporter activity
GO:0005515 protein binding
GO:0015101 organic cation transmembrane transporter activity
GO:0015171 amino acid transmembrane transporter activity
GO:0015179 L-amino acid transmembrane transporter activity
GO:0019534 toxin transporter activity
Biological Process
GO:0003333 amino acid transmembrane transport
GO:0006810 transport
GO:0006865 amino acid transport
GO:0015695 organic cation transport
GO:0015807 L-amino acid transport
GO:0015837 amine transport
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:0016020 membrane
GO:0016021 integral component of membrane
GO:0016323 basolateral plasma membrane
GO:0070062 extracellular vesicular exosome
Protein Structure and Domains
PDB ID MGI:1355323
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 Q9QXW9
PhosphoSite PhosphoSite-Q9QXW9
TrEMBL
UniProt Splice Variant
Entrez Gene 50934
UniGene Mm.276831
RefSeq NP_058668
MGI ID
MGI Symbol Slc7a8
OMIM
CCDS CCDS27101
HPRD
IMGT
EMBL AF171668 BC059004 Y19022
GenPept AAF20380 AAH59004 CAB69072