General Information of Drug Off-Target (DOT) (ID: OTTDFM1O)

DOT Name Amine oxidase B (MAOB)
Synonyms EC 1.4.3.21; EC 1.4.3.4; Monoamine oxidase type B; MAO-B
Gene Name MAOB
UniProt ID
AOFB_HUMAN
3D Structure
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2D Sequence (FASTA)
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3D Structure (PDB)
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PDB ID
1GOS ; 1OJ9 ; 1OJA ; 1OJC ; 1OJD ; 1S2Q ; 1S2Y ; 1S3B ; 1S3E ; 2BK3 ; 2BK4 ; 2BK5 ; 2BYB ; 2C64 ; 2C65 ; 2C66 ; 2C67 ; 2C70 ; 2C72 ; 2C73 ; 2C75 ; 2C76 ; 2V5Z ; 2V60 ; 2V61 ; 2VRL ; 2VRM ; 2VZ2 ; 2XCG ; 2XFN ; 2XFO ; 2XFP ; 2XFQ ; 2XFU ; 3PO7 ; 3ZYX ; 4A79 ; 4A7A ; 4CRT ; 5MRL ; 6FVZ ; 6FW0 ; 6FWC ; 6RKB ; 6RKP ; 6RLE ; 6YT2 ; 7B0V ; 7B0Z ; 7P4F ; 7P4H ; 7ZW3
EC Number
1.4.3.21; 1.4.3.4
Pfam ID
PF01593
Sequence
MSNKCDVVVVGGGISGMAAAKLLHDSGLNVVVLEARDRVGGRTYTLRNQKVKYVDLGGSY
VGPTQNRILRLAKELGLETYKVNEVERLIHHVKGKSYPFRGPFPPVWNPITYLDHNNFWR
TMDDMGREIPSDAPWKAPLAEEWDNMTMKELLDKLCWTESAKQLATLFVNLCVTAETHEV
SALWFLWYVKQCGGTTRIISTTNGGQERKFVGGSGQVSERIMDLLGDRVKLERPVIYIDQ
TRENVLVETLNHEMYEAKYVISAIPPTLGMKIHFNPPLPMMRNQMITRVPLGSVIKCIVY
YKEPFWRKKDYCGTMIIDGEEAPVAYTLDDTKPEGNYAAIMGFILAHKARKLARLTKEER
LKKLCELYAKVLGSLEALEPVHYEEKNWCEEQYSGGCYTTYFPPGILTQYGRVLRQPVDR
IYFAGTETATHWSGYMEGAVEAGERAAREILHAMGKIPEDEIWQSEPESVDVPAQPITTT
FLERHLPSVPGLLRLIGLTTIFSATALGFLAHKRGLLVRV
Function
Catalyzes the oxidative deamination of primary and some secondary amines such as neurotransmitters, and exogenous amines including the tertiary amine, neurotoxin 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP), with concomitant reduction of oxygen to hydrogen peroxide and participates in the metabolism of neuroactive and vasoactive amines in the central nervous system and peripheral tissues. Preferentially degrades benzylamine and phenylethylamine.
KEGG Pathway
Glycine, serine and threonine metabolism (hsa00260 )
Arginine and proline metabolism (hsa00330 )
Histidine metabolism (hsa00340 )
Tyrosine metabolism (hsa00350 )
Phenylalanine metabolism (hsa00360 )
Tryptophan metabolism (hsa00380 )
Drug metabolism - cytochrome P450 (hsa00982 )
Metabolic pathways (hsa01100 )
Serotonergic sy.pse (hsa04726 )
Dopaminergic sy.pse (hsa04728 )
Parkinson disease (hsa05012 )
Cocaine addiction (hsa05030 )
Amphetamine addiction (hsa05031 )
Alcoholism (hsa05034 )
Reactome Pathway
Biogenic amines are oxidatively deaminated to aldehydes by MAOA and MAOB (R-HSA-141333 )
BioCyc Pathway
MetaCyc:HS00966-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 Biotransformations of 4 Drug(s)
Drug Name Drug ID Highest Status Interaction REF
Dopamine DMPGUCF Approved Amine oxidase B (MAOB) decreases the amination of Dopamine. [27]
TRYPTAMINE DMAFPHB Phase 3 Amine oxidase B (MAOB) decreases the amination of TRYPTAMINE. [29]
Serotonin DMOFCRY Investigative Amine oxidase B (MAOB) decreases the amination of Serotonin. [27]
1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine DMPWB8G Investigative Amine oxidase B (MAOB) increases the oxidation of 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine. [12]
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This DOT Affected the Drug Response of 1 Drug(s)
Drug Name Drug ID Highest Status Interaction REF
Amphetamine DMSZQAK Approved Amine oxidase B (MAOB) decreases the response to substance of Amphetamine. [28]
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3 Drug(s) Affected the Post-Translational Modifications of This DOT
Drug Name Drug ID Highest Status Interaction REF
Valproate DMCFE9I Approved Valproate decreases the methylation of Amine oxidase B (MAOB). [1]
Benzo(a)pyrene DMN7J43 Phase 1 Benzo(a)pyrene increases the methylation of Amine oxidase B (MAOB). [20]
Bisphenol A DM2ZLD7 Investigative Bisphenol A decreases the methylation of Amine oxidase B (MAOB). [23]
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33 Drug(s) Affected the Gene/Protein Processing of This DOT
Drug Name Drug ID Highest Status Interaction REF
Ciclosporin DMAZJFX Approved Ciclosporin decreases the expression of Amine oxidase B (MAOB). [2]
Acetaminophen DMUIE76 Approved Acetaminophen decreases the expression of Amine oxidase B (MAOB). [3]
Doxorubicin DMVP5YE Approved Doxorubicin decreases the expression of Amine oxidase B (MAOB). [4]
Quercetin DM3NC4M Approved Quercetin decreases the expression of Amine oxidase B (MAOB). [5]
Calcitriol DM8ZVJ7 Approved Calcitriol increases the expression of Amine oxidase B (MAOB). [6]
Triclosan DMZUR4N Approved Triclosan decreases the expression of Amine oxidase B (MAOB). [7]
Carbamazepine DMZOLBI Approved Carbamazepine increases the expression of Amine oxidase B (MAOB). [8]
Methotrexate DM2TEOL Approved Methotrexate increases the expression of Amine oxidase B (MAOB). [9]
Phenobarbital DMXZOCG Approved Phenobarbital decreases the expression of Amine oxidase B (MAOB). [10]
Progesterone DMUY35B Approved Progesterone increases the expression of Amine oxidase B (MAOB). [11]
Menadione DMSJDTY Approved Menadione decreases the activity of Amine oxidase B (MAOB). [12]
Troglitazone DM3VFPD Approved Troglitazone decreases the activity of Amine oxidase B (MAOB). [13]
Rosiglitazone DMILWZR Approved Rosiglitazone decreases the activity of Amine oxidase B (MAOB). [13]
Diclofenac DMPIHLS Approved Diclofenac affects the expression of Amine oxidase B (MAOB). [14]
Selegiline DM6034S Approved Selegiline decreases the activity of Amine oxidase B (MAOB). [15]
Methylene blue DMJAPE7 Approved Methylene blue decreases the activity of Amine oxidase B (MAOB). [12]
Benzyl benzoate DMDPYI5 Approved Benzyl benzoate decreases the activity of Amine oxidase B (MAOB). [16]
Linezolid DMGFPU2 Approved Linezolid decreases the activity of Amine oxidase B (MAOB). [17]
Pargyline DMM0HR1 Approved Pargyline decreases the activity of Amine oxidase B (MAOB). [16]
Urethane DM7NSI0 Phase 4 Urethane decreases the expression of Amine oxidase B (MAOB). [18]
3,4-Dihydroxycinnamic Acid DMVZL26 Phase 4 3,4-Dihydroxycinnamic Acid decreases the activity of Amine oxidase B (MAOB). [16]
Fucoxanthin DMPQFTA Phase 2 Fucoxanthin decreases the activity of Amine oxidase B (MAOB). [19]
PMID28460551-Compound-2 DM4DOUB Patented PMID28460551-Compound-2 decreases the expression of Amine oxidase B (MAOB). [21]
Benzylcinnamate DMD7Z3H Patented Benzylcinnamate decreases the activity of Amine oxidase B (MAOB). [16]
Lazabemide DMCULK7 Patented Lazabemide decreases the activity of Amine oxidase B (MAOB). [22]
Trichostatin A DM9C8NX Investigative Trichostatin A decreases the expression of Amine oxidase B (MAOB). [24]
Aminohippuric acid DMUN54G Investigative Aminohippuric acid affects the expression of Amine oxidase B (MAOB). [25]
Chlorogenic acid DM2Y3P4 Investigative Chlorogenic acid decreases the activity of Amine oxidase B (MAOB). [16]
ROSMARINIC ACID DMQ6SJT Investigative ROSMARINIC ACID decreases the activity of Amine oxidase B (MAOB). [16]
NORHARMANE DMKYQWG Investigative NORHARMANE decreases the activity of Amine oxidase B (MAOB). [12]
1,2,3,4-tetrahydroisoquinoline DMZGCEQ Investigative 1,2,3,4-tetrahydroisoquinoline decreases the activity of Amine oxidase B (MAOB). [26]
5-Nitroindazole DMH7SIX Investigative 5-Nitroindazole decreases the activity of Amine oxidase B (MAOB). [12]
2-Methyl-beta-carboline-2-ium iodide DMQBF7J Investigative 2-Methyl-beta-carboline-2-ium iodide decreases the activity of Amine oxidase B (MAOB). [12]
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⏷ Show the Full List of 33 Drug(s)

References

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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 Increased mitochondrial ROS formation by acetaminophen in human hepatic cells is associated with gene expression changes suggesting disruption of the mitochondrial electron transport chain. Toxicol Lett. 2015 Apr 16;234(2):139-50.
4 Bringing in vitro analysis closer to in vivo: studying doxorubicin toxicity and associated mechanisms in 3D human microtissues with PBPK-based dose modelling. Toxicol Lett. 2018 Sep 15;294:184-192.
5 Comparison of phenotypic and transcriptomic effects of false-positive genotoxins, true genotoxins and non-genotoxins using HepG2 cells. Mutagenesis. 2011 Sep;26(5):593-604.
6 Identification of vitamin D3 target genes in human breast cancer tissue. J Steroid Biochem Mol Biol. 2016 Nov;164:90-97.
7 Transcriptome and DNA methylome dynamics during triclosan-induced cardiomyocyte differentiation toxicity. Stem Cells Int. 2018 Oct 29;2018:8608327.
8 Transcriptional profiling of genes induced in the livers of patients treated with carbamazepine. Clin Pharmacol Ther. 2006 Nov;80(5):440-456.
9 Functional gene expression profile underlying methotrexate-induced senescence in human colon cancer cells. Tumour Biol. 2011 Oct;32(5):965-76.
10 Xenobiotic CAR activators induce Dlk1-Dio3 locus noncoding RNA expression in mouse liver. Toxicol Sci. 2017 Aug 1;158(2):367-378.
11 Progesterone regulation of implantation-related genes: new insights into the role of oestrogen. Cell Mol Life Sci. 2007 Apr;64(7-8):1009-32.
12 Inhibition of the bioactivation of the neurotoxin MPTP by antioxidants, redox agents and monoamine oxidase inhibitors. Food Chem Toxicol. 2011 Aug;49(8):1773-81.
13 Molecular Insights into Human Monoamine Oxidase B Inhibition by the Glitazone Anti-Diabetes Drugs. ACS Med Chem Lett. 2011 Oct 15;3(1):39-42.
14 Drug-induced endoplasmic reticulum and oxidative stress responses independently sensitize toward TNF-mediated hepatotoxicity. Toxicol Sci. 2014 Jul;140(1):144-59. doi: 10.1093/toxsci/kfu072. Epub 2014 Apr 20.
15 Chromone, a privileged scaffold for the development of monoamine oxidase inhibitors. J Med Chem. 2011 Jul 28;54(14):5165-73.
16 Combining initro and in silico approaches to evaluate the multifunctional profile of rosmarinic acid from Blechnum brasiliense on targets related to neurodegeneration. Chem Biol Interact. 2016 Jul 25;254:135-45.
17 Nonclinical Evaluation of Antibacterial Oxazolidinones Contezolid and Contezolid Acefosamil with Low Serotonergic Neurotoxicity. Chem Res Toxicol. 2021 May 17;34(5):1348-1354. doi: 10.1021/acs.chemrestox.0c00524. Epub 2021 Apr 29.
18 Ethyl carbamate induces cell death through its effects on multiple metabolic pathways. Chem Biol Interact. 2017 Nov 1;277:21-32.
19 Characterizing fucoxanthin as a selective dopamine D(3)/D(4) receptor agonist: Relevance to Parkinson's disease. Chem Biol Interact. 2019 Sep 1;310:108757. doi: 10.1016/j.cbi.2019.108757. Epub 2019 Jul 16.
20 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.
21 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.
22 Safety study of lazabemide (Ro19-6327), a new MAO-B inhibitor, on cardiac arrhythmias and blood pressure of patients with Parkinson's disease. Clin Neuropharmacol. 1999 Nov-Dec;22(6):340-6.
23 DNA methylome-wide alterations associated with estrogen receptor-dependent effects of bisphenols in breast cancer. Clin Epigenetics. 2019 Oct 10;11(1):138. doi: 10.1186/s13148-019-0725-y.
24 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.
25 Identification of molecular signatures predicting the carcinogenicity of polycyclic aromatic hydrocarbons (PAHs). Toxicol Lett. 2012 Jul 7;212(1):18-28. doi: 10.1016/j.toxlet.2012.04.013. Epub 2012 May 1.
26 Inhibition of monoamine oxidases A and B by simple isoquinoline alkaloids: racemic and optically active 1,2,3,4-tetrahydro-, 3,4-dihydro-, and fully aromatic isoquinolines. J Med Chem. 1990 Jan;33(1):147-52. doi: 10.1021/jm00163a025.
27 Inhibition potential of 3,4-methylenedioxymethamphetamine (MDMA) and its metabolites on the in vitro monoamine oxidase (MAO)-catalyzed deamination of the neurotransmitters serotonin and dopamine. Toxicol Lett. 2016 Jan 22;243:48-55.
28 Differential effects of chronic amphetamine and baclofen administration on cAMP levels and phosphorylation of CREB in distinct brain regions of wild type and monoamine oxidase B-deficient mice. Synapse. 2006 Dec 15;60(8):573-84. doi: 10.1002/syn.20334.
29 Evidence for new light-independent pathways for generation of the endogenous aryl hydrocarbon receptor agonist FICZ. Chem Res Toxicol. 2016 Jan 19;29(1):75-86.