InnateDB Protein
|
IDBP-140477.6
|
Last Modified
|
2014-10-13 [Report errors or provide feedback]
|
Gene Symbol
|
Slc3a2
|
Protein Name
|
solute carrier family 3 (activators of dibasic and neutral amino acid transport), member 2
|
Synonyms
|
4F2; 4F2HC; AI314110; Cd98; Ly-10; Ly-m10; Ly10; Mdu1; Mgp-2hc; NACAE;
|
Species
|
Mus musculus
|
Ensembl Protein
|
ENSMUSP00000010239
|
InnateDB Gene
|
IDBG-140475 (Slc3a2)
|
Protein Structure
|
|
Function |
Required for the function of light chain amino-acid transporters. Involved in sodium-independent, high-affinity transport of large neutral amino acids such as phenylalanine, tyrosine, leucine, arginine and tryptophan. Involved in guiding and targeting of LAT1 and LAT2 to the plasma membrane. When associated with SLC7A6 or SLC7A7 acts as an arginine/glutamine exchanger, following an antiport mechanism for amino acid transport, influencing arginine release in exchange for extracellular amino acids. Plays a role in nitric oxide synthesis in human umbilical vein endothelial cells (HUVECs) via transport of L-arginine. Required for normal and neoplastic cell growth. When associated with SLC7A5/LAT1, is also 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. 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. When associated with SLC7A5 or SLC7A8, involved in the cellular activity of small molecular weight nitrosothiols, via the stereoselective transport of L- nitrosocysteine (L-CNSO) across the transmembrane. Together with ICAM1, regulates the transport activity LAT2 in polarized intestinal cells, by generating and delivering intracellular signals. When associated with SLC7A5, plays an important role in transporting L-leucine from the circulating blood to the retina across the inner blood-retinal barrier. {ECO:0000269PubMed:10391915, ECO:0000269PubMed:11011012, ECO:0000269PubMed:9915839}.
|
Subcellular Localization |
Apical cell membrane; Single-pass type II membrane protein. Melanosome {ECO:0000250}. Note=Identified by mass spectrometry in melanosome fractions from stage I to stage IV (By similarity). Localized to the plasma membrane when associated with SLC7A5 or SLC7A8 (By similarity). Localized to the placental apical membrane (By similarity). Located selectively at cell-cell adhesion sites. Colocalized with SLC7A8/LAT2 at the basolateral membrane of kidney proximal tubules and small intestine epithelia. Expressed in both luminal and abluminal membranes of brain capillary endothelial cells (By similarity). {ECO:0000250}.
|
Disease Associations |
|
Tissue Specificity |
Observed in all adult tissues tested with strongest expression in kidney, small intestine, spleen, thymus and liver. Moderate expression in brain, stomach, heart, testis, lung, skin, pancreas and skeletal muscle. Expressed on the surface of epithelial cells of most embryonic tissues including epidermis, choroid plexus in the brain, retina, as well as intestinal, renal, and thymic epithelium. In brain expressed on capillary endothelia in cerebral cortex. {ECO:0000269PubMed:10574970, ECO:0000269PubMed:2928113, ECO:0000269PubMed:9915839}.
|
Comments |
|
Number of Interactions
|
This gene and/or its encoded proteins are associated with 8 experimentally validated interaction(s) in this database.
They are also associated with 31 interaction(s) predicted by orthology.
Experimentally validated |
Total |
8
[view]
|
Protein-Protein |
8
[view]
|
Protein-DNA |
0
|
Protein-RNA |
0
|
DNA-DNA |
0
|
RNA-RNA |
0
|
DNA-RNA |
0
|
|
Predicted by orthology |
Total |
31 [view]
|
|
|
Molecular Function |
|
Biological Process |
|
Cellular Component |
|
PDB ID |
MGI:96955
|
InterPro |
IPR006047
Glycosyl hydrolase, family 13, catalytic domain
IPR006589
Glycosyl hydrolase, family 13, subfamily, catalytic domain
IPR017853
Glycoside hydrolase, superfamily
|
PFAM |
PF00128
|
PRINTS |
|
PIRSF |
|
SMART |
SM00642
|
TIGRFAMs |
|
Modification |
|
SwissProt |
P10852
|
PhosphoSite |
PhosphoSite-P10852
|
TrEMBL |
Q3TIP1
|
UniProt Splice Variant |
|
Entrez Gene |
17254
|
UniGene |
Mm.4114
|
RefSeq |
NP_032603
|
MGI ID |
|
MGI Symbol |
Slc3a2
|
OMIM |
|
CCDS |
CCDS29540
|
HPRD |
|
IMGT |
|
EMBL |
AB023408
AC025794
AK161280
AK165417
AK167773
BC065173
CH466612
X14309
|
GenPept |
AAH65173
BAA90555
BAE36291
BAE38172
BAE39805
CAA32490
EDL33352
|
|
|