General Information of Drug Transporter (DTP) (ID: DT0UQDA)

DTP Name Putative sodium-coupled neutral amino acid transporter 8 (SLC38A8)
Gene Name SLC38A8
UniProt ID
A6NNN8 (S38A8_HUMAN)
VARIDT ID
DTD0335
3D Structure
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2D Sequence (FASTA)
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3D Structure (PDB)
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Synonyms FVH2; SLC38A8; Solute carrier family 38 member 8
DTP Family Amino Acid/Auxin Permease (AAAP) Family ;
Tissue Specificity Expressed in fetal and adult brain, and spinalcord. In the brain, it is localized in the cell body and axon ofthe majority of neuronal cells and in a subset of glial cells.Found throughout the neuronal retina, with higher expressionlevels in the inner and outer plexiform layers and thephotoreceptor layer. Very weak expression is also present in thekidneys, thymus, and testes.
Sequence
MEGQTPGSRGLPEKPHPATAAATLSSMGAVFILMKSALGAGLLNFPWAFSKAGGVVPAFL
VELVSLVFLISGLVILGYAAAVSGQATYQGVVRGLCGPAIGKLCEACFLLNLLMISVAFL
RVIGDQLEKLCDSLLSGTPPAPQPWYADQRFTLPLLSVLVILPLSAPREIAFQKYTSILG
TLAACYLALVITVQYYLWPQGLVRESHPSLSPASWTSVFSVFPTICFGFQCHEAAVSIYC
SMRKRSLSHWALVSVLSLLACCLIYSLTGVYGFLTFGTEVSADVLMSYPGNDMVIIVARV
LFAVSIVTVYPIVLFLGRSVMQDFWRRSCLGGWGPSALADPSGLWVRMPLTILWVTVTLA
MALFMPDLSEIVSIIGGISSFFIFIFPGLCLICAMGVEPIGPRVKCCLEVWGVVSVLVGT
FIFGQSTAAAVWEMF
Function This transporter is putative sodium-dependent amino acid/proton antiporter.
Endogenous Substrate(s) Amino acids; Proton
TCDB ID
2.A.18.6.12
Gene ID
146167

Molecular Interaction Atlas (MIA) of This DTP

Molecular Interaction Atlas (MIA) Jump to Detail Molecular Interaction Atlas of This DTP
1 Approved Drug(s) Transported by This DTP
Drug Name Drug ID Indication ICD 11 Highest Status REF
L-Glutamic Acid DM4PUDW Schizophrenia 6A20 Approved [1]
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References

1 Structural modeling of a novel SLC38A8 mutation that causes foveal hypoplasia. Mol Genet Genomic Med. 2017 Feb 26;5(3):202-209.