General Information of Drug Off-Target (DOT) (ID: OTUJ93MN)

DOT Name Glutathione S-transferase omega-1 (GSTO1)
Synonyms
GSTO-1; EC 2.5.1.18; Glutathione S-transferase omega 1-1; GSTO 1-1; Glutathione-dependent dehydroascorbate reductase; EC 1.8.5.1; Monomethylarsonic acid reductase; MMA(V) reductase; EC 1.20.4.2; S-(Phenacyl)glutathione reductase; SPG-R
Gene Name GSTO1
UniProt ID
GSTO1_HUMAN
3D Structure
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2D Sequence (FASTA)
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3D Structure (PDB)
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PDB ID
1EEM; 3LFL; 3VLN; 4IS0; 4YQM; 4YQU; 4YQV; 5UEH; 5V3Q; 5YVN; 5YVO; 6MHB; 6MHC; 6MHD; 6PNM; 6PNN; 6PNO
EC Number
1.20.4.2; 1.8.5.1; 2.5.1.18
Pfam ID
PF14497 ; PF13409
Sequence
MSGESARSLGKGSAPPGPVPEGSIRIYSMRFCPFAERTRLVLKAKGIRHEVININLKNKP
EWFFKKNPFGLVPVLENSQGQLIYESAITCEYLDEAYPGKKLLPDDPYEKACQKMILELF
SKVPSLVGSFIRSQNKEDYAGLKEEFRKEFTKLEEVLTNKKTTFFGGNSISMIDYLIWPW
FERLEAMKLNECVDHTPKLKLWMAAMKEDPTVSALLTSEKDWQGFLELYLQNSPEACDYG
L
Function
Exhibits glutathione-dependent thiol transferase and dehydroascorbate reductase activities. Has S-(phenacyl)glutathione reductase activity. Has also glutathione S-transferase activity. Participates in the biotransformation of inorganic arsenic and reduces monomethylarsonic acid (MMA) and dimethylarsonic acid.
Tissue Specificity Ubiquitous. Highest expression in liver, pancreas, skeletal muscle, spleen, thymus, colon, blood leukocyte and heart. Lowest expression in brain, placenta and lung.
KEGG Pathway
Glutathione metabolism (hsa00480 )
Metabolism of xenobiotics by cytochrome P450 (hsa00980 )
Drug metabolism - cytochrome P450 (hsa00982 )
Drug metabolism - other enzymes (hsa00983 )
Metabolic pathways (hsa01100 )
Platinum drug resistance (hsa01524 )
Pathways in cancer (hsa05200 )
Chemical carcinogenesis - D. adducts (hsa05204 )
Chemical carcinogenesis - receptor activation (hsa05207 )
Chemical carcinogenesis - reactive oxygen species (hsa05208 )
Hepatocellular carcinoma (hsa05225 )
Fluid shear stress and atherosclerosis (hsa05418 )
Reactome Pathway
Glutathione conjugation (R-HSA-156590 )
Vitamin C (ascorbate) metabolism (R-HSA-196836 )
Gene and protein expression by JAK-STAT signaling after Interleukin-12 stimulation (R-HSA-8950505 )
Methylation (R-HSA-156581 )
BioCyc Pathway
MetaCyc:HS07564-MONOMER

Molecular Interaction Atlas (MIA) of This DOT

Molecular Interaction Atlas (MIA) Jump to Detail Molecular Interaction Atlas of This DOT
This DOT Affected the Drug Response of 1 Drug(s)
Drug Name Drug ID Highest Status Interaction REF
Arsenic DMTL2Y1 Approved Glutathione S-transferase omega-1 (GSTO1) increases the response to substance of Arsenic. [27]
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30 Drug(s) Affected the Gene/Protein Processing of This DOT
Drug Name Drug ID Highest Status Interaction REF
Valproate DMCFE9I Approved Valproate decreases the expression of Glutathione S-transferase omega-1 (GSTO1). [1]
Ciclosporin DMAZJFX Approved Ciclosporin decreases the expression of Glutathione S-transferase omega-1 (GSTO1). [2]
Tretinoin DM49DUI Approved Tretinoin increases the expression of Glutathione S-transferase omega-1 (GSTO1). [3]
Acetaminophen DMUIE76 Approved Acetaminophen decreases the expression of Glutathione S-transferase omega-1 (GSTO1). [4]
Doxorubicin DMVP5YE Approved Doxorubicin affects the expression of Glutathione S-transferase omega-1 (GSTO1). [5]
Cupric Sulfate DMP0NFQ Approved Cupric Sulfate decreases the expression of Glutathione S-transferase omega-1 (GSTO1). [6]
Cisplatin DMRHGI9 Approved Cisplatin increases the expression of Glutathione S-transferase omega-1 (GSTO1). [7]
Ivermectin DMDBX5F Approved Ivermectin decreases the expression of Glutathione S-transferase omega-1 (GSTO1). [8]
Temozolomide DMKECZD Approved Temozolomide decreases the expression of Glutathione S-transferase omega-1 (GSTO1). [9]
Triclosan DMZUR4N Approved Triclosan decreases the expression of Glutathione S-transferase omega-1 (GSTO1). [10]
Decitabine DMQL8XJ Approved Decitabine increases the expression of Glutathione S-transferase omega-1 (GSTO1). [11]
Menadione DMSJDTY Approved Menadione affects the expression of Glutathione S-transferase omega-1 (GSTO1). [12]
Aspirin DM672AH Approved Aspirin decreases the expression of Glutathione S-transferase omega-1 (GSTO1). [13]
Menthol DMG2KW7 Approved Menthol increases the expression of Glutathione S-transferase omega-1 (GSTO1). [14]
Cocaine DMSOX7I Approved Cocaine affects the expression of Glutathione S-transferase omega-1 (GSTO1). [15]
Phenytoin DMNOKBV Approved Phenytoin decreases the expression of Glutathione S-transferase omega-1 (GSTO1). [16]
Vitamin C DMXJ7O8 Approved Vitamin C increases the expression of Glutathione S-transferase omega-1 (GSTO1). [17]
Urethane DM7NSI0 Phase 4 Urethane decreases the expression of Glutathione S-transferase omega-1 (GSTO1). [18]
Tamibarotene DM3G74J Phase 3 Tamibarotene increases the expression of Glutathione S-transferase omega-1 (GSTO1). [3]
Benzo(a)pyrene DMN7J43 Phase 1 Benzo(a)pyrene decreases the expression of Glutathione S-transferase omega-1 (GSTO1). [19]
PMID28460551-Compound-2 DM4DOUB Patented PMID28460551-Compound-2 decreases the expression of Glutathione S-transferase omega-1 (GSTO1). [20]
PMID28870136-Compound-52 DMFDERP Patented PMID28870136-Compound-52 decreases the expression of Glutathione S-transferase omega-1 (GSTO1). [4]
MG-132 DMKA2YS Preclinical MG-132 increases the expression of Glutathione S-transferase omega-1 (GSTO1). [21]
Bisphenol A DM2ZLD7 Investigative Bisphenol A decreases the expression of Glutathione S-transferase omega-1 (GSTO1). [22]
Trichostatin A DM9C8NX Investigative Trichostatin A increases the expression of Glutathione S-transferase omega-1 (GSTO1). [23]
Milchsaure DM462BT Investigative Milchsaure increases the expression of Glutathione S-transferase omega-1 (GSTO1). [24]
chloropicrin DMSGBQA Investigative chloropicrin increases the expression of Glutathione S-transferase omega-1 (GSTO1). [25]
3R14S-OCHRATOXIN A DM2KEW6 Investigative 3R14S-OCHRATOXIN A decreases the expression of Glutathione S-transferase omega-1 (GSTO1). [26]
Protoporphyrin IX DMWYE7A Investigative Protoporphyrin IX increases the expression of Glutathione S-transferase omega-1 (GSTO1). [21]
ROSMARINIC ACID DMQ6SJT Investigative ROSMARINIC ACID increases the expression of Glutathione S-transferase omega-1 (GSTO1). [17]
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⏷ Show the Full List of 30 Drug(s)

References

1 Human embryonic stem cell-derived test systems for developmental neurotoxicity: a transcriptomics approach. Arch Toxicol. 2013 Jan;87(1):123-43.
2 Comparison of HepG2 and HepaRG by whole-genome gene expression analysis for the purpose of chemical hazard identification. Toxicol Sci. 2010 May;115(1):66-79.
3 Differential modulation of PI3-kinase/Akt pathway during all-trans retinoic acid- and Am80-induced HL-60 cell differentiation revealed by DNA microarray analysis. Biochem Pharmacol. 2004 Dec 1;68(11):2177-86.
4 Gene expression changes associated with cytotoxicity identified using cDNA arrays. Funct Integr Genomics. 2000 Sep;1(2):114-26.
5 Identification of novel biomarkers for doxorubicin-induced toxicity in human cardiomyocytes derived from pluripotent stem cells. Toxicology. 2015 Feb 3;328:102-11. doi: 10.1016/j.tox.2014.12.018. Epub 2014 Dec 18.
6 Physiological and toxicological transcriptome changes in HepG2 cells exposed to copper. Physiol Genomics. 2009 Aug 7;38(3):386-401.
7 Activation of AIFM2 enhances apoptosis of human lung cancer cells undergoing toxicological stress. Toxicol Lett. 2016 Sep 6;258:227-236.
8 Quantitative proteomics reveals a broad-spectrum antiviral property of ivermectin, benefiting for COVID-19 treatment. J Cell Physiol. 2021 Apr;236(4):2959-2975. doi: 10.1002/jcp.30055. Epub 2020 Sep 22.
9 Temozolomide induces activation of Wnt/-catenin signaling in glioma cells via PI3K/Akt pathway: implications in glioma therapy. Cell Biol Toxicol. 2020 Jun;36(3):273-278. doi: 10.1007/s10565-019-09502-7. Epub 2019 Nov 22.
10 Transcriptome and DNA methylome dynamics during triclosan-induced cardiomyocyte differentiation toxicity. Stem Cells Int. 2018 Oct 29;2018:8608327.
11 Downregulation of glutathione S-transferase M1 protein in N-butyl-N-(4-hydroxybutyl)nitrosamine-induced mouse bladder carcinogenesis. Toxicol Appl Pharmacol. 2014 Sep 15;279(3):322-330.
12 Global gene expression analysis reveals differences in cellular responses to hydroxyl- and superoxide anion radical-induced oxidative stress in caco-2 cells. Toxicol Sci. 2010 Apr;114(2):193-203. doi: 10.1093/toxsci/kfp309. Epub 2009 Dec 31.
13 DNA array analysis of the effects of aspirin on colon cancer cells: involvement of Rac1. Carcinogenesis. 2004 Jul;25(7):1293-8.
14 Repurposing L-menthol for systems medicine and cancer therapeutics? L-menthol induces apoptosis through caspase 10 and by suppressing HSP90. OMICS. 2016 Jan;20(1):53-64.
15 Proteomic analysis of the nucleus accumbens of rats with different vulnerability to cocaine addiction. Neuropharmacology. 2009 Jul;57(1):41-8. doi: 10.1016/j.neuropharm.2009.04.005. Epub 2009 Apr 22.
16 Role of phenytoin in wound healing: microarray analysis of early transcriptional responses in human dermal fibroblasts. Biochem Biophys Res Commun. 2004 Feb 13;314(3):661-6. doi: 10.1016/j.bbrc.2003.12.146.
17 Identification of lead-produced lipid hydroperoxides in human HepG2 cells and protection using rosmarinic and ascorbic acids with a reference to their regulatory roles on Nrf2-Keap1 antioxidant pathway. Chem Biol Interact. 2019 Dec 1;314:108847. doi: 10.1016/j.cbi.2019.108847. Epub 2019 Oct 11.
18 Ethyl carbamate induces cell death through its effects on multiple metabolic pathways. Chem Biol Interact. 2017 Nov 1;277:21-32.
19 Identification of a transcriptomic signature of food-relevant genotoxins in human HepaRG hepatocarcinoma cells. Food Chem Toxicol. 2020 Jun;140:111297. doi: 10.1016/j.fct.2020.111297. Epub 2020 Mar 28.
20 Cell-based two-dimensional morphological assessment system to predict cancer drug-induced cardiotoxicity using human induced pluripotent stem cell-derived cardiomyocytes. Toxicol Appl Pharmacol. 2019 Nov 15;383:114761. doi: 10.1016/j.taap.2019.114761. Epub 2019 Sep 15.
21 Differential effects of arsenic species on Nrf2 and Bach1 nuclear localization in cultured hepatocytes. Toxicol Appl Pharmacol. 2021 Feb 15;413:115404. doi: 10.1016/j.taap.2021.115404. Epub 2021 Jan 9.
22 Bisphenol A induces DSB-ATM-p53 signaling leading to cell cycle arrest, senescence, autophagy, stress response, and estrogen release in human fetal lung fibroblasts. Arch Toxicol. 2018 Apr;92(4):1453-1469.
23 From transient transcriptome responses to disturbed neurodevelopment: role of histone acetylation and methylation as epigenetic switch between reversible and irreversible drug effects. Arch Toxicol. 2014 Jul;88(7):1451-68.
24 Transcriptional profiling of lactic acid treated reconstructed human epidermis reveals pathways underlying stinging and itch. Toxicol In Vitro. 2019 Jun;57:164-173.
25 Transcriptomic analysis of human primary bronchial epithelial cells after chloropicrin treatment. Chem Res Toxicol. 2015 Oct 19;28(10):1926-35.
26 Ochratoxin a lowers mRNA levels of genes encoding for key proteins of liver cell metabolism. Cancer Genomics Proteomics. 2008 Nov-Dec;5(6):319-32.
27 Association between arsenic metabolism gene polymorphisms and arsenic-induced skin lesions in individuals exposed to high-dose inorganic arsenic in northwest China. Sci Rep. 2018 Jan 11;8(1):413. doi: 10.1038/s41598-017-18925-3.