General Information of Drug Off-Target (DOT) (ID: OT08KS8J)

DOT Name Solute carrier family 45 member 3 (SLC45A3)
Synonyms Prostate cancer-associated protein 6; Prostein
Gene Name SLC45A3
UniProt ID
S45A3_HUMAN
3D Structure
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2D Sequence (FASTA)
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3D Structure (PDB)
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Pfam ID
PF07690
Sequence
MVQRLWVSRLLRHRKAQLLLVNLLTFGLEVCLAAGITYVPPLLLEVGVEEKFMTMVLGIG
PVLGLVCVPLLGSASDHWRGRYGRRRPFIWALSLGILLSLFLIPRAGWLAGLLCPDPRPL
ELALLILGVGLLDFCGQVCFTPLEALLSDLFRDPDHCRQAYSVYAFMISLGGCLGYLLPA
IDWDTSALAPYLGTQEECLFGLLTLIFLTCVAATLLVAEEAALGPTEPAEGLSAPSLSPH
CCPCRARLAFRNLGALLPRLHQLCCRMPRTLRRLFVAELCSWMALMTFTLFYTDFVGEGL
YQGVPRAEPGTEARRHYDEGVRMGSLGLFLQCAISLVFSLVMDRLVQRFGTRAVYLASVA
AFPVAAGATCLSHSVAVVTASAALTGFTFSALQILPYTLASLYHREKQVFLPKYRGDTGG
ASSEDSLMTSFLPGPKPGAPFPNGHVGAGGSGLLPPPPALCGASACDVSVRVVVGEPTEA
RVVPGRGICLDLAILDSAFLLSQVAPSLFMGSIVQLSQSVTAYMVSAAGLGLVAIYFATQ
VVFDKSDLAKYSA
Function Proton-associated sucrose transporter. May be able to transport also glucose and fructose.
Tissue Specificity Prostate specific. Expressed in all prostatic glandular cells. Expressed both in normal and cancerous prostates.
KEGG Pathway
Transcriptio.l misregulation in cancer (hsa05202 )
MicroR.s in cancer (hsa05206 )
Reactome Pathway
Cellular hexose transport (R-HSA-189200 )

Molecular Interaction Atlas (MIA) of This DOT

Molecular Interaction Atlas (MIA) Jump to Detail Molecular Interaction Atlas of This DOT
8 Drug(s) Affected the Gene/Protein Processing of This DOT
Drug Name Drug ID Highest Status Interaction REF
Tretinoin DM49DUI Approved Tretinoin affects the expression of Solute carrier family 45 member 3 (SLC45A3). [1]
Acetaminophen DMUIE76 Approved Acetaminophen decreases the expression of Solute carrier family 45 member 3 (SLC45A3). [2]
Estradiol DMUNTE3 Approved Estradiol increases the expression of Solute carrier family 45 member 3 (SLC45A3). [3]
Triclosan DMZUR4N Approved Triclosan increases the expression of Solute carrier family 45 member 3 (SLC45A3). [4]
Zoledronate DMIXC7G Approved Zoledronate decreases the expression of Solute carrier family 45 member 3 (SLC45A3). [5]
Dihydrotestosterone DM3S8XC Phase 4 Dihydrotestosterone increases the expression of Solute carrier family 45 member 3 (SLC45A3). [6]
(+)-JQ1 DM1CZSJ Phase 1 (+)-JQ1 decreases the expression of Solute carrier family 45 member 3 (SLC45A3). [8]
[3H]methyltrienolone DMTSGOW Investigative [3H]methyltrienolone increases the expression of Solute carrier family 45 member 3 (SLC45A3). [9]
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⏷ Show the Full List of 8 Drug(s)
1 Drug(s) Affected the Post-Translational Modifications of This DOT
Drug Name Drug ID Highest Status Interaction REF
Benzo(a)pyrene DMN7J43 Phase 1 Benzo(a)pyrene decreases the methylation of Solute carrier family 45 member 3 (SLC45A3). [7]
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References

1 Molecular characterization of a toxicological tipping point during human stem cell differentiation. Reprod Toxicol. 2020 Jan;91:1-13. doi: 10.1016/j.reprotox.2019.10.001. Epub 2019 Oct 7.
2 Gene expression analysis of precision-cut human liver slices indicates stable expression of ADME-Tox related genes. Toxicol Appl Pharmacol. 2011 May 15;253(1):57-69.
3 17-Estradiol Activates HSF1 via MAPK Signaling in ER-Positive Breast Cancer Cells. Cancers (Basel). 2019 Oct 11;11(10):1533. doi: 10.3390/cancers11101533.
4 Transcriptome and DNA methylome dynamics during triclosan-induced cardiomyocyte differentiation toxicity. Stem Cells Int. 2018 Oct 29;2018:8608327.
5 Interleukin-19 as a translational indicator of renal injury. Arch Toxicol. 2015 Jan;89(1):101-6.
6 Androgen-induced TOP2B-mediated double-strand breaks and prostate cancer gene rearrangements. Nat Genet. 2010 Aug;42(8):668-75. doi: 10.1038/ng.613. Epub 2010 Jul 4.
7 Air pollution and DNA methylation alterations in lung cancer: A systematic and comparative study. Oncotarget. 2017 Jan 3;8(1):1369-1391. doi: 10.18632/oncotarget.13622.
8 CCAT1 is an enhancer-templated RNA that predicts BET sensitivity in colorectal cancer. J Clin Invest. 2016 Feb;126(2):639-52.
9 Analysis of the prostate cancer cell line LNCaP transcriptome using a sequencing-by-synthesis approach. BMC Genomics. 2006 Sep 29;7:246. doi: 10.1186/1471-2164-7-246.