Homo sapiens Protein: SLC7A5
Summary
InnateDB Protein IDBP-45908.7
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol SLC7A5
Protein Name solute carrier family 7 (amino acid transporter light chain, L system), member 5
Synonyms 4F2LC; CD98; D16S469E; E16; hLAT1; LAT1; MPE16;
Species Homo sapiens
Ensembl Protein ENSP00000261622
InnateDB Gene IDBG-45906 (SLC7A5)
Protein Structure
UniProt Annotation
Function Sodium-independent, high-affinity transport of large neutral amino acids such as phenylalanine, tyrosine, leucine, arginine and tryptophan, when associated with SLC3A2/4F2hc. Involved in cellular amino acid uptake. Acts as an amino acid exchanger. Involved in the transport of L-DOPA across the blood- brain barrier, and that of thyroid hormones triiodothyronine (T3) and thyroxine (T4) across the cell membrane in tissues such as placenta. Plays a role in neuronal cell proliferation (neurogenesis) in brain. 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. May play an important role in high-grade gliomas. Mediates blood-to-retina L- leucine transport across the inner blood-retinal barrier which in turn may play a key role in maintaining large neutral amino acids as well as neurotransmitters in the neural retina. Acts as the major transporter of tyrosine in fibroblasts. {ECO:0000269PubMed:10049700, ECO:0000269PubMed:10391915, ECO:0000269PubMed:10574970, ECO:0000269PubMed:11311135, ECO:0000269PubMed:11389679, ECO:0000269PubMed:11557028, ECO:0000269PubMed:11564694, ECO:0000269PubMed:11742812, ECO:0000269PubMed:12117417, ECO:0000269PubMed:12225859, ECO:0000269PubMed:15769744, ECO:0000269PubMed:16496379, ECO:0000269PubMed:18262359, ECO:0000269PubMed:9751058}.
Subcellular Localization Cytoplasm, cytosol. Apical cell membrane; Multi-pass membrane protein. Note=Located to the plasma membrane by SLC3A2/4F2hc. Localized to the apical membrane of placental syncytiophoblastic cells. Expressed in both luminal and abluminal membranes of brain capillary endothelial cells (By similarity). {ECO:0000250}.
Disease Associations
Tissue Specificity Expressed abundantly in adult lung, liver, brain, skeletal muscle, placenta, bone marrow, testis, resting lymphocytes and monocytes, and in fetal liver. Weaker expression in thymus, cornea, retina, peripheral leukocytes, spleen, kidney, colon and lymph node. During gestation, expression in the placenta was significantly stronger at full-term than at the mid-trimester stage. Also expressed in all human tumor cell lines tested and in the astrocytic process of primary astrocytic gliomas. Expressed in retinal endothelial cells and in the intestinal epithelial cell line Caco-2. {ECO:0000269PubMed:10049700, ECO:0000269PubMed:10072483, ECO:0000269PubMed:11389679, ECO:0000269PubMed:11557028, ECO:0000269PubMed:11742812, ECO:0000269PubMed:12824232, ECO:0000269PubMed:1597461, ECO:0000269PubMed:16027961, ECO:0000269PubMed:16496379}.
Comments
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 6 experimentally validated interaction(s) in this database.
Experimentally validated
Total 6 [view]
Protein-Protein 6 [view]
Protein-DNA 0
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Gene Ontology

Molecular Function
Accession GO Term
GO:0015171 amino acid transmembrane transporter activity
GO:0015175 neutral amino acid transmembrane transporter activity
GO:0015179 L-amino acid transmembrane 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:0007399 nervous system development
GO:0007596 blood coagulation
GO:0015804 neutral amino acid transport
GO:0015807 L-amino acid transport
GO:0030154 cell differentiation
GO:0050900 leukocyte migration
GO:0055085 transmembrane transport
GO:1902475 L-alpha-amino acid transmembrane transport
Cellular Component
GO:0005634 nucleus
GO:0005730 nucleolus
GO:0005829 cytosol
GO:0005886 plasma membrane
GO:0016020 membrane
GO:0016021 integral component of membrane
GO:0016324 apical 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 Q01650
PhosphoSite PhosphoSite-Q01650
TrEMBL
UniProt Splice Variant
Entrez Gene 8140
UniGene Hs.646192
RefSeq NP_003477
HUGO HGNC:11063
OMIM 600182
CCDS CCDS10964
HPRD 02552
IMGT
EMBL AB017908 AB018009 AB018542 AF077866 AF104032 BC039692 BC042600 M80244
GenPept AAA35780 AAC61479 AAD20464 AAH39692 AAH42600 BAA33851 BAA75746 BAA84648