General Information of Drug Off-Target (DOT) (ID: OTWFM5G0)

DOT Name Atos homolog protein A (ATOSA)
Gene Name ATOSA
UniProt ID
ATOSA_HUMAN
3D Structure
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2D Sequence (FASTA)
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3D Structure (PDB)
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Pfam ID
PF13889 ; PF13915
Sequence
MKPDRDTLDEYFEYDAEEFLVSLALLITEGRTPECSVKGRTESFHCPPAQSCYPVTTKHE
CSDKLAQCRQARRTRSEVTLLWKNNLPIMVEMMLLPDCCYSDDGPTTEGIDLNDPAIKQD
ALLLERWILEPVPRQNGDRFIEEKTLLLAVRSFVFFSQLSAWLSVSHGAIPRNILYRISA
ADVDLQWNFSQTPIEHVFPVPNVSHNVALKVSVQSLPRQSNYPVLTCSIHTNIGLYEKRI
QQHKLKTHQHHNPNEAEQCGTNSSQRLCSKQTWTMAPESVLHAKSGPSPEYTAAVKNIKL
YPGTGSKSDHGTSQANILGFSGIGDIKSQETSVRTLKSFSMVDSSISNRQSFWQSAGETN
PLIGSLIQERQEIIARIAQHLIHCDPSTSHVSGRPFNTQESSSLHSKLFRVSQENENVGK
GKEAFSMTFGSPEFSSPEDTNEGKIRLKPETPRSETCISNDFYSHMPVGETNPLIGSLLQ
ERQDVIARIAQHLEHIDPTASHIPRQSFNMHDSSSVASKVFRSSYEDKNLLKKNKDESSV
SISHTKCSLLGDISDGKNLVPNKCFTSFKNNSKEKCSLKHQTRNQCQNNPSEIIQSTYQE
TQNKSSSLSTSSILSQHKENNLDLTSRFKEQEMSNGIDKQYSNCTTIDKQICTNKYKEKI
INENYNPKFFGNLQSDDSKKNDSKIKVTVLEMSEYLNKYESMSSNKDSKRPKTCEQNTQL
NSIENYLNKDNEGFKCKKSDQLKNEQDKQEDPTNEKSQNYSQRRSIKDCLSTCEQPKNTE
VLRTTLKHSNVWRKHNFHSLDGTSTRAFHPQTGLPLLSSPVPQRKTQSGCFDLDSSLLHL
KSFSSRSPRPCLNIEDDPDIHEKPFLSSSAPPITSLSLLGNFEESVLNYRFDPLGIVDGF
TAEVGASGAFCPTHLTLPVEVSFYSVSDDNAPSPYMGVITLESLGKRGYRVPPSGTIQVT
LFNPNKTVVKMFVVIYDLRDMPANHQTFLRQRTFSVPVKQEVKRSVNKENIRHTEERLLR
YLIHLRFQSSKSGKIYLHRDVRLLFSRKSMEVDSGAAYELKSYTESPTNPQFSPRC
Function Transcription regulator that syncronizes transcriptional and translational programs to promote macrophage invasion of tissues.

Molecular Interaction Atlas (MIA) of This DOT

Molecular Interaction Atlas (MIA) Jump to Detail Molecular Interaction Atlas of This DOT
20 Drug(s) Affected the Gene/Protein Processing of This DOT
Drug Name Drug ID Highest Status Interaction REF
Ciclosporin DMAZJFX Approved Ciclosporin increases the expression of Atos homolog protein A (ATOSA). [1]
Cupric Sulfate DMP0NFQ Approved Cupric Sulfate increases the expression of Atos homolog protein A (ATOSA). [2]
Cisplatin DMRHGI9 Approved Cisplatin decreases the expression of Atos homolog protein A (ATOSA). [3]
Estradiol DMUNTE3 Approved Estradiol decreases the expression of Atos homolog protein A (ATOSA). [4]
Zoledronate DMIXC7G Approved Zoledronate increases the expression of Atos homolog protein A (ATOSA). [3]
Rosiglitazone DMILWZR Approved Rosiglitazone decreases the expression of Atos homolog protein A (ATOSA). [3]
Cidofovir DMA13GD Approved Cidofovir decreases the expression of Atos homolog protein A (ATOSA). [3]
Ifosfamide DMCT3I8 Approved Ifosfamide decreases the expression of Atos homolog protein A (ATOSA). [3]
Clodronate DM9Y6X7 Approved Clodronate decreases the expression of Atos homolog protein A (ATOSA). [3]
Urethane DM7NSI0 Phase 4 Urethane increases the expression of Atos homolog protein A (ATOSA). [5]
Dihydrotestosterone DM3S8XC Phase 4 Dihydrotestosterone increases the expression of Atos homolog protein A (ATOSA). [6]
GSK2110183 DMZHB37 Phase 2 GSK2110183 increases the expression of Atos homolog protein A (ATOSA). [7]
GDC0941 DM1YAK6 Phase 2 GDC0941 increases the expression of Atos homolog protein A (ATOSA). [8]
GDC-0980/RG7422 DMF3MV1 Phase 2 GDC-0980/RG7422 increases the expression of Atos homolog protein A (ATOSA). [8]
Benzo(a)pyrene DMN7J43 Phase 1 Benzo(a)pyrene increases the expression of Atos homolog protein A (ATOSA). [1]
(+)-JQ1 DM1CZSJ Phase 1 (+)-JQ1 increases the expression of Atos homolog protein A (ATOSA). [9]
Trichostatin A DM9C8NX Investigative Trichostatin A affects the expression of Atos homolog protein A (ATOSA). [10]
Milchsaure DM462BT Investigative Milchsaure decreases the expression of Atos homolog protein A (ATOSA). [11]
Coumestrol DM40TBU Investigative Coumestrol decreases the expression of Atos homolog protein A (ATOSA). [12]
methyl p-hydroxybenzoate DMO58UW Investigative methyl p-hydroxybenzoate increases the expression of Atos homolog protein A (ATOSA). [13]
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⏷ Show the Full List of 20 Drug(s)

References

1 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.
2 Physiological and toxicological transcriptome changes in HepG2 cells exposed to copper. Physiol Genomics. 2009 Aug 7;38(3):386-401.
3 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.
4 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.
5 Ethyl carbamate induces cell death through its effects on multiple metabolic pathways. Chem Biol Interact. 2017 Nov 1;277:21-32.
6 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.
7 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.
8 Phosphoinositide 3-kinase (PI3K) pathway alterations are associated with histologic subtypes and are predictive of sensitivity to PI3K inhibitors in lung cancer preclinical models. Clin Cancer Res. 2012 Dec 15;18(24):6771-83. doi: 10.1158/1078-0432.CCR-12-2347. Epub 2012 Nov 7.
9 Inhibition of BRD4 attenuates tumor cell self-renewal and suppresses stem cell signaling in MYC driven medulloblastoma. Oncotarget. 2014 May 15;5(9):2355-71.
10 A trichostatin A expression signature identified by TempO-Seq targeted whole transcriptome profiling. PLoS One. 2017 May 25;12(5):e0178302. doi: 10.1371/journal.pone.0178302. eCollection 2017.
11 Transcriptional profiling of lactic acid treated reconstructed human epidermis reveals pathways underlying stinging and itch. Toxicol In Vitro. 2019 Jun;57:164-173.
12 Pleiotropic combinatorial transcriptomes of human breast cancer cells exposed to mixtures of dietary phytoestrogens. Food Chem Toxicol. 2009 Apr;47(4):787-95.
13 Transcriptome dynamics of alternative splicing events revealed early phase of apoptosis induced by methylparaben in H1299 human lung carcinoma cells. Arch Toxicol. 2020 Jan;94(1):127-140. doi: 10.1007/s00204-019-02629-w. Epub 2019 Nov 20.