General Information of Drug Off-Target (DOT) (ID: OT8MCRNY)

DOT Name ATPase family AAA domain-containing protein 2 (ATAD2)
Synonyms EC 3.6.1.-; AAA nuclear coregulator cancer-associated protein; ANCCA
Gene Name ATAD2
UniProt ID
ATAD2_HUMAN
3D Structure
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2D Sequence (FASTA)
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3D Structure (PDB)
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PDB ID
3DAI ; 4QSP ; 4QSQ ; 4QSR ; 4QSS ; 4QST ; 4QSU ; 4QSV ; 4QSW ; 4QSX ; 4QUT ; 4QUU ; 4TT2 ; 4TT4 ; 4TT6 ; 4TTE ; 4TU4 ; 4TU6 ; 4TYL ; 4TZ2 ; 4TZ8 ; 5A5N ; 5A5O ; 5A5P ; 5A5Q ; 5A5R ; 5A81 ; 5A82 ; 5A83 ; 5EPB ; 5F36 ; 5F3A ; 5LJ0 ; 5QXI ; 5QXJ ; 5QXK ; 5QXL ; 5QXM ; 5QXN ; 5QXO ; 5QXP ; 5QXQ ; 5QXR ; 5QXS ; 5QXT ; 5QXU ; 5QXV ; 5QXW ; 5QXX ; 5QXY ; 5QXZ ; 5QY0 ; 5R4E ; 5R4F ; 5R4V ; 5R4W ; 5R4X ; 5R4Y ; 5R4Z ; 6CPS ; 6EPJ ; 6EPR ; 6EPS ; 6EPT ; 6EPU ; 6EPV ; 6EPW ; 6EPX ; 6HDN ; 6HDO ; 6HI3 ; 6HI4 ; 6HI5 ; 6HI6 ; 6HI7 ; 6HI8 ; 6HIA ; 6HIB ; 6HIC ; 6HID ; 6HIE ; 6S55 ; 6S56 ; 6S57 ; 6YB4 ; 7M98 ; 7PPX ; 7PX5 ; 7Q6T ; 7Q6U ; 7Q6V ; 7Q6W ; 7QU7 ; 7QUK ; 7QUM ; 7QWO ; 7QX1 ; 7QXT ; 7QYK ; 7QYL ; 7QZM ; 7QZY ; 7QZZ ; 7R00 ; 7R05 ; 7R0Y ; 7Z9H ; 7Z9I ; 7Z9J ; 7Z9N ; 7Z9O ; 7Z9S ; 7Z9U ; 8H3H ; 8JUW ; 8JUY ; 8JUZ
EC Number
3.6.1.-
Pfam ID
PF00004 ; PF17862 ; PF00439
Sequence
MVVLRSSLELHNHSAASATGSLDLSSDFLSLEHIGRRRLRSAGAAQKKPAATTAKAGDGS
SVKEVETYHRTRALRSLRKDAQNSSDSSFEKNVEITEQLANGRHFTRQLARQQADKKKEE
HREDKVIPVTRSLRARNIVQSTEHLHEDNGDVEVRRSCRIRSRYSGVNQSMLFDKLITNT
AEAVLQKMDDMKKMRRQRMRELEDLGVFNETEESNLNMYTRGKQKDIQRTDEETTDNQEG
SVESSEEGEDQEHEDDGEDEDDEDDDDDDDDDDDDDDEDDEDEEDGEEENQKRYYLRQRK
ATVYYQAPLEKPRHQRKPNIFYSGPASPARPRYRLSSAGPRSPYCKRMNRRRHAIHSSDS
TSSSSSEDEQHFERRRKRSRNRAINRCLPLNFRKDELKGIYKDRMKIGASLADVDPMQLD
SSVRFDSVGGLSNHIAALKEMVVFPLLYPEVFEKFKIQPPRGCLFYGPPGTGKTLVARAL
ANECSQGDKRVAFFMRKGADCLSKWVGESERQLRLLFDQAYQMRPSIIFFDEIDGLAPVR
SSRQDQIHSSIVSTLLALMDGLDSRGEIVVIGATNRLDSIDPALRRPGRFDREFLFSLPD
KEARKEILKIHTRDWNPKPLDTFLEELAENCVGYCGADIKSICAEAALCALRRRYPQIYT
TSEKLQLDLSSINISAKDFEVAMQKMIPASQRAVTSPGQALSTVVKPLLQNTVDKILEAL
QRVFPHAEFRTNKTLDSDISCPLLESDLAYSDDDVPSVYENGLSQKSSHKAKDNFNFLHL
NRNACYQPMSFRPRILIVGEPGFGQGSHLAPAVIHALEKFTVYTLDIPVLFGVSTTSPEE
TCAQVIREAKRTAPSIVYVPHIHVWWEIVGPTLKATFTTLLQNIPSFAPVLLLATSDKPH
SALPEEVQELFIRDYGEIFNVQLPDKEERTKFFEDLILKQAAKPPISKKKAVLQALEVLP
VAPPPEPRSLTAEEVKRLEEQEEDTFRELRIFLRNVTHRLAIDKRFRVFTKPVDPDEVPD
YVTVIKQPMDLSSVISKIDLHKYLTVKDYLRDIDLICSNALEYNPDRDPGDRLIRHRACA
LRDTAYAIIKEELDEDFEQLCEEIQESRKKRGCSSSKYAPSYYHVMPKQNSTLVGDKRSD
PEQNEKLKTPSTPVACSTPAQLKRKIRKKSNWYLGTIKKRRKISQAKDDSQNAIDHKIES
DTEETQDTSVDHNETGNTGESSVEENEKQQNASESKLELRNNSNTCNIENELEDSRKTTA
CTELRDKIACNGDASSSQIIHISDENEGKEMCVLRMTRARRSQVEQQQLITVEKALAILS
QPTPSLVVDHERLKNLLKTVVKKSQNYNIFQLENLYAVISQCIYRHRKDHDKTSLIQKME
QEVENFSCSR
Function
May be a transcriptional coactivator of the nuclear receptor ESR1 required to induce the expression of a subset of estradiol target genes, such as CCND1, MYC and E2F1. May play a role in the recruitment or occupancy of CREBBP at some ESR1 target gene promoters. May be required for histone hyperacetylation. Involved in the estrogen-induced cell proliferation and cell cycle progression of breast cancer cells.
Tissue Specificity Highly expressed in estrogen receptor positive breast tumors and in osteosarcoma tumors.
Reactome Pathway
TFAP2 (AP-2) family regulates transcription of growth factors and their receptors (R-HSA-8866910 )

Molecular Interaction Atlas (MIA) of This DOT

Molecular Interaction Atlas (MIA) Jump to Detail Molecular Interaction Atlas of This DOT
31 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 ATPase family AAA domain-containing protein 2 (ATAD2). [1]
Ciclosporin DMAZJFX Approved Ciclosporin decreases the expression of ATPase family AAA domain-containing protein 2 (ATAD2). [2]
Tretinoin DM49DUI Approved Tretinoin decreases the expression of ATPase family AAA domain-containing protein 2 (ATAD2). [3]
Acetaminophen DMUIE76 Approved Acetaminophen increases the expression of ATPase family AAA domain-containing protein 2 (ATAD2). [4]
Doxorubicin DMVP5YE Approved Doxorubicin decreases the expression of ATPase family AAA domain-containing protein 2 (ATAD2). [5]
Cupric Sulfate DMP0NFQ Approved Cupric Sulfate decreases the expression of ATPase family AAA domain-containing protein 2 (ATAD2). [6]
Cisplatin DMRHGI9 Approved Cisplatin decreases the expression of ATPase family AAA domain-containing protein 2 (ATAD2). [7]
Estradiol DMUNTE3 Approved Estradiol increases the expression of ATPase family AAA domain-containing protein 2 (ATAD2). [8]
Ivermectin DMDBX5F Approved Ivermectin decreases the expression of ATPase family AAA domain-containing protein 2 (ATAD2). [9]
Arsenic trioxide DM61TA4 Approved Arsenic trioxide increases the expression of ATPase family AAA domain-containing protein 2 (ATAD2). [11]
Triclosan DMZUR4N Approved Triclosan decreases the expression of ATPase family AAA domain-containing protein 2 (ATAD2). [12]
Progesterone DMUY35B Approved Progesterone increases the expression of ATPase family AAA domain-containing protein 2 (ATAD2). [13]
Demecolcine DMCZQGK Approved Demecolcine decreases the expression of ATPase family AAA domain-containing protein 2 (ATAD2). [14]
Azathioprine DMMZSXQ Approved Azathioprine decreases the expression of ATPase family AAA domain-containing protein 2 (ATAD2). [15]
Piroxicam DMTK234 Approved Piroxicam decreases the expression of ATPase family AAA domain-containing protein 2 (ATAD2). [16]
Dasatinib DMJV2EK Approved Dasatinib decreases the expression of ATPase family AAA domain-containing protein 2 (ATAD2). [17]
Cidofovir DMA13GD Approved Cidofovir increases the expression of ATPase family AAA domain-containing protein 2 (ATAD2). [18]
Clodronate DM9Y6X7 Approved Clodronate increases the expression of ATPase family AAA domain-containing protein 2 (ATAD2). [18]
Lucanthone DMZLBUO Approved Lucanthone decreases the expression of ATPase family AAA domain-containing protein 2 (ATAD2). [19]
Adefovir dipivoxil DMMAWY1 Approved Adefovir dipivoxil increases the expression of ATPase family AAA domain-containing protein 2 (ATAD2). [18]
Urethane DM7NSI0 Phase 4 Urethane decreases the expression of ATPase family AAA domain-containing protein 2 (ATAD2). [20]
Dihydrotestosterone DM3S8XC Phase 4 Dihydrotestosterone increases the expression of ATPase family AAA domain-containing protein 2 (ATAD2). [21]
Resveratrol DM3RWXL Phase 3 Resveratrol increases the expression of ATPase family AAA domain-containing protein 2 (ATAD2). [22]
Genistein DM0JETC Phase 2/3 Genistein increases the expression of ATPase family AAA domain-containing protein 2 (ATAD2). [8]
GSK2110183 DMZHB37 Phase 2 GSK2110183 decreases the expression of ATPase family AAA domain-containing protein 2 (ATAD2). [23]
Benzo(a)pyrene DMN7J43 Phase 1 Benzo(a)pyrene decreases the expression of ATPase family AAA domain-containing protein 2 (ATAD2). [24]
PMID28460551-Compound-2 DM4DOUB Patented PMID28460551-Compound-2 decreases the expression of ATPase family AAA domain-containing protein 2 (ATAD2). [26]
THAPSIGARGIN DMDMQIE Preclinical THAPSIGARGIN decreases the expression of ATPase family AAA domain-containing protein 2 (ATAD2). [28]
Bisphenol A DM2ZLD7 Investigative Bisphenol A decreases the expression of ATPase family AAA domain-containing protein 2 (ATAD2). [29]
Trichostatin A DM9C8NX Investigative Trichostatin A decreases the expression of ATPase family AAA domain-containing protein 2 (ATAD2). [30]
Coumestrol DM40TBU Investigative Coumestrol increases the expression of ATPase family AAA domain-containing protein 2 (ATAD2). [22]
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⏷ Show the Full List of 31 Drug(s)
4 Drug(s) Affected the Post-Translational Modifications of This DOT
Drug Name Drug ID Highest Status Interaction REF
Arsenic DMTL2Y1 Approved Arsenic affects the methylation of ATPase family AAA domain-containing protein 2 (ATAD2). [10]
TAK-243 DM4GKV2 Phase 1 TAK-243 decreases the sumoylation of ATPase family AAA domain-containing protein 2 (ATAD2). [25]
PMID28870136-Compound-52 DMFDERP Patented PMID28870136-Compound-52 affects the phosphorylation of ATPase family AAA domain-containing protein 2 (ATAD2). [27]
Coumarin DM0N8ZM Investigative Coumarin decreases the phosphorylation of ATPase family AAA domain-containing protein 2 (ATAD2). [27]
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References

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8 Convergent transcriptional profiles induced by endogenous estrogen and distinct xenoestrogens in breast cancer cells. Carcinogenesis. 2006 Aug;27(8):1567-78.
9 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.
10 Prenatal arsenic exposure and the epigenome: identifying sites of 5-methylcytosine alterations that predict functional changes in gene expression in newborn cord blood and subsequent birth outcomes. Toxicol Sci. 2015 Jan;143(1):97-106. doi: 10.1093/toxsci/kfu210. Epub 2014 Oct 10.
11 Combination of arsenic trioxide and Dasatinib: a new strategy to treat Philadelphia chromosome-positive acute lymphoblastic leukaemia. J Cell Mol Med. 2018 Mar;22(3):1614-1626.
12 Transcriptome and DNA methylome dynamics during triclosan-induced cardiomyocyte differentiation toxicity. Stem Cells Int. 2018 Oct 29;2018:8608327.
13 Progesterone regulation of implantation-related genes: new insights into the role of oestrogen. Cell Mol Life Sci. 2007 Apr;64(7-8):1009-32.
14 Characterization of formaldehyde's genotoxic mode of action by gene expression analysis in TK6 cells. Arch Toxicol. 2013 Nov;87(11):1999-2012.
15 A transcriptomics-based in vitro assay for predicting chemical genotoxicity in vivo. Carcinogenesis. 2012 Jul;33(7):1421-9.
16 Apoptosis induced by piroxicam plus cisplatin combined treatment is triggered by p21 in mesothelioma. PLoS One. 2011;6(8):e23569.
17 Dasatinib reverses cancer-associated fibroblasts (CAFs) from primary lung carcinomas to a phenotype comparable to that of normal fibroblasts. Mol Cancer. 2010 Jun 27;9:168.
18 Transcriptomics hit the target: monitoring of ligand-activated and stress response pathways for chemical testing. Toxicol In Vitro. 2015 Dec 25;30(1 Pt A):7-18.
19 Lucanthone is a novel inhibitor of autophagy that induces cathepsin D-mediated apoptosis. J Biol Chem. 2011 Feb 25;286(8):6602-13.
20 Ethyl carbamate induces cell death through its effects on multiple metabolic pathways. Chem Biol Interact. 2017 Nov 1;277:21-32.
21 LSD1 activates a lethal prostate cancer gene network independently of its demethylase function. Proc Natl Acad Sci U S A. 2018 May 1;115(18):E4179-E4188.
22 Pleiotropic combinatorial transcriptomes of human breast cancer cells exposed to mixtures of dietary phytoestrogens. Food Chem Toxicol. 2009 Apr;47(4):787-95.
23 Novel ATP-competitive Akt inhibitor afuresertib suppresses the proliferation of malignant pleural mesothelioma cells. Cancer Med. 2017 Nov;6(11):2646-2659. doi: 10.1002/cam4.1179. Epub 2017 Sep 27.
24 Transcriptional signature of human macrophages exposed to the environmental contaminant benzo(a)pyrene. Toxicol Sci. 2010 Apr;114(2):247-59.
25 Inhibiting ubiquitination causes an accumulation of SUMOylated newly synthesized nuclear proteins at PML bodies. J Biol Chem. 2019 Oct 18;294(42):15218-15234. doi: 10.1074/jbc.RA119.009147. Epub 2019 Jul 8.
26 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.
27 Quantitative phosphoproteomics reveal cellular responses from caffeine, coumarin and quercetin in treated HepG2 cells. Toxicol Appl Pharmacol. 2022 Aug 15;449:116110. doi: 10.1016/j.taap.2022.116110. Epub 2022 Jun 7.
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29 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.
30 A transcriptome-based classifier to identify developmental toxicants by stem cell testing: design, validation and optimization for histone deacetylase inhibitors. Arch Toxicol. 2015 Sep;89(9):1599-618.