General Information of Target

Target ID LDTP09588
Target Name Sodium-coupled neutral amino acid transporter 5 (SLC38A5)
Gene Name SLC38A5
Gene ID 92745
Synonyms
JM24; SN2; SNAT5; Sodium-coupled neutral amino acid transporter 5; Solute carrier family 38 member 5; System N transporter 2
3D Structure
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2D Sequence (FASTA)
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3D Structure (PDB)
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Sequence
MELQDPKMNGALPSDAVGYRQEREGFLPSRGPAPGSKPVQFMDFEGKTSFGMSVFNLSNA
IMGSGILGLAYAMAHTGVIFFLALLLCIALLSSYSIHLLLTCAGIAGIRAYEQLGQRAFG
PAGKVVVATVICLHNVGAMSSYLFIIKSELPLVIGTFLYMDPEGDWFLKGNLLIIIVSVL
IILPLALMKHLGYLGYTSGLSLTCMLFFLVSVIYKKFQLGCAIGHNETAMESEALVGLPS
QGLNSSCEAQMFTVDSQMSYTVPIMAFAFVCHPEVLPIYTELCRPSKRRMQAVANVSIGA
MFCMYGLTATFGYLTFYSSVKAEMLHMYSQKDPLILCVRLAVLLAVTLTVPVVLFPIRRA
LQQLLFPGKAFSWPRHVAIALILLVLVNVLVICVPTIRDIFGVIGSTSAPSLIFILPSIF
YLRIVPSEVEPFLSWPKIQALCFGVLGVLFMAVSLGFMFANWATGQSRMSGH
Target Type
Literature-reported
Target Bioclass
Transporter and channel
Family
Amino acid/polyamine transporter 2 family
Subcellular location
Cell membrane
Function
Symporter that cotransports neutral amino acids and sodium ions, coupled to an H(+) antiporter activity. Releases L-glutamine and glycine from astroglial cells and may participate in the glutamate/GABA-L-glutamine cycle and the NMDA receptors activation. In addition, contributes significantly to L-glutamine uptake in retina, namely in ganglion and Mueller cells therefore, participates in the retinal glutamate-glutamine cycle. The transport activity is pH sensitive and Li(+) tolerant. Moreover functions in both direction and is associated with large uncoupled fluxes of protons. The transport is electroneutral coupled to the cotransport of 1 Na(+) and the antiport of 1 H(+). May have a particular importance for modulation of net hepatic glutamine flux.
TTD ID
T86817
Uniprot ID
Q8WUX1
DrugMap ID
TTC8YPT
Ensemble ID
ENST00000595796.5
HGNC ID
HGNC:18070

Target Site Mutations in Different Cell Lines

Cell line Mutation details Probe for labeling this protein in this cell
HCT15 SNV: p.W373Ter .
NCIH2170 SNV: p.D43V .
OVKATE SNV: p.M451I .
SNGM SNV: p.N135S .
SW756 SNV: p.A360T .

Probe(s) Labeling This Target

ABPP Probe
Click To Hide/Show 2 Probe Related to This Target
Probe name Structure Binding Site(Ratio) Interaction ID Ref
IA-alkyne
 Probe Info 
C337(2.23)  LDD2186  [1]
IPM
 Probe Info 
C283(3.04)  LDD1701  [2]
PAL-AfBPP Probe
Click To Hide/Show 1 Probe Related to This Target
Probe name Structure Binding Site(Ratio) Interaction ID Ref
VE-P
 Probe Info 
N.A.  LDD0396  [3]

Competitor(s) Related to This Target

Competitor ID Name Cell line Binding Site(Ratio) Interaction ID Ref
 LDCM0625  F8 Ramos C337(0.98)  LDD2187  [1]
 LDCM0573  Fragment11 Ramos C337(1.96)  LDD2190  [1]
 LDCM0575  Fragment13 Ramos C337(1.01)  LDD2192  [1]
 LDCM0580  Fragment21 Ramos C337(1.41)  LDD2195  [1]
 LDCM0582  Fragment23 Ramos C337(1.36)  LDD2196  [1]
 LDCM0578  Fragment27 Ramos C337(0.87)  LDD2197  [1]
 LDCM0586  Fragment28 Ramos C337(0.79)  LDD2198  [1]
 LDCM0588  Fragment30 Ramos C337(1.79)  LDD2199  [1]
 LDCM0589  Fragment31 Ramos C337(1.26)  LDD2200  [1]
 LDCM0468  Fragment33 Ramos C337(1.22)  LDD2202  [1]
 LDCM0596  Fragment38 Ramos C337(1.20)  LDD2203  [1]
 LDCM0610  Fragment52 Ramos C337(1.15)  LDD2204  [1]
 LDCM0614  Fragment56 Ramos C337(0.89)  LDD2205  [1]
 LDCM0569  Fragment7 Ramos C337(2.23)  LDD2186  [1]
 LDCM0023  KB03 MDA-MB-231 C283(3.04)  LDD1701  [2]

The Interaction Atlas With This Target

The Drug(s) Related To This Target

Investigative
Click To Hide/Show 2 Drug(s) Interacting with This Target
Drug Name Drug Type External ID
[14c]Histidine Small molecular drug D0XT2X
[3h]Histidine Small molecular drug D07UTZ

References

1 Site-specific quantitative cysteine profiling with data-independent acquisition-based mass spectrometry. Methods Enzymol. 2023;679:295-322. doi: 10.1016/bs.mie.2022.07.037. Epub 2022 Sep 7.
Mass spectrometry data entry: PXD027578
2 Nucleophilic covalent ligand discovery for the cysteine redoxome. Nat Chem Biol. 2023 Nov;19(11):1309-1319. doi: 10.1038/s41589-023-01330-5. Epub 2023 May 29.
Mass spectrometry data entry: PXD039908 , PXD029761
3 Pharmacological Targeting of Vacuolar H(+)-ATPase via Subunit V1G Combats Multidrug-Resistant Cancer. Cell Chem Biol. 2020 Nov 19;27(11):1359-1370.e8. doi: 10.1016/j.chembiol.2020.06.011. Epub 2020 Jul 9.