InnateDB Protein
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IDBP-45908.7
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Last Modified
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2014-10-13 [Report errors or provide feedback]
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Gene Symbol
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SLC7A5
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Protein Name
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solute carrier family 7 (amino acid transporter light chain, L system), member 5
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Synonyms
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4F2LC; CD98; D16S469E; E16; hLAT1; LAT1; MPE16;
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Species
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Homo sapiens
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Ensembl Protein
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ENSP00000261622
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InnateDB Gene
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IDBG-45906 (SLC7A5)
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Protein Structure
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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}.
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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}.
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Disease Associations |
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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}.
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Comments |
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Number of Interactions
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This gene and/or its encoded proteins are associated with 6 experimentally validated interaction(s) in this database.
Experimentally validated |
Total |
6
[view]
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Protein-Protein |
6
[view]
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Protein-DNA |
0
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Protein-RNA |
0
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DNA-DNA |
0
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RNA-RNA |
0
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DNA-RNA |
0
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Molecular Function |
Accession |
GO Term |
GO:0015171
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amino acid transmembrane transporter activity
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GO:0015175
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neutral amino acid transmembrane transporter activity
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GO:0015179
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L-amino acid transmembrane transporter activity
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GO:0042605
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peptide antigen binding
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Biological Process |
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Cellular Component |
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PDB ID |
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InterPro |
IPR002293
Amino acid/polyamine transporter I
IPR004760
L-type amino acid transporter
IPR004841
Amino acid permease/ SLC12A domain
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PFAM |
PF13520
PF00324
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PRINTS |
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PIRSF |
PIRSF006060
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SMART |
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TIGRFAMs |
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Modification |
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SwissProt |
Q01650
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PhosphoSite |
PhosphoSite-Q01650
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TrEMBL |
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UniProt Splice Variant |
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Entrez Gene |
8140
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UniGene |
Hs.646192
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RefSeq |
NP_003477
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HUGO |
HGNC:11063
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OMIM |
600182
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CCDS |
CCDS10964
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HPRD |
02552
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IMGT |
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EMBL |
AB017908
AB018009
AB018542
AF077866
AF104032
BC039692
BC042600
M80244
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GenPept |
AAA35780
AAC61479
AAD20464
AAH39692
AAH42600
BAA33851
BAA75746
BAA84648
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