General Information of Drug Off-Target (DOT) (ID: OTSYQN71)

DOT Name Calumenin (CALU)
Synonyms Crocalbin; IEF SSP 9302
Gene Name CALU
Related Disease
Lung adenocarcinoma ( )
Arteriosclerosis ( )
Asthma ( )
Atherosclerosis ( )
Breast cancer ( )
Breast carcinoma ( )
Colon cancer ( )
Colon carcinoma ( )
Cystic fibrosis ( )
Familial hypertrophic cardiomyopathy ( )
Lung carcinoma ( )
Atrial fibrillation ( )
Familial atrial fibrillation ( )
Filarial disease ( )
Metastatic malignant neoplasm ( )
Advanced cancer ( )
Lung cancer ( )
Neoplasm ( )
UniProt ID
CALU_HUMAN
3D Structure
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2D Sequence (FASTA)
Download
3D Structure (PDB)
Download
Pfam ID
PF13202
Sequence
MDLRQFLMCLSLCTAFALSKPTEKKDRVHHEPQLSDKVHNDAQSFDYDHDAFLGAEEAKT
FDQLTPEESKERLGKIVSKIDGDKDGFVTVDELKDWIKFAQKRWIYEDVERQWKGHDLNE
DGLVSWEEYKNATYGYVLDDPDPDDGFNYKQMMVRDERRFKMADKDGDLIATKEEFTAFL
HPEEYDYMKDIVVQETMEDIDKNADGFIDLEEYIGDMYSHDGNTDEPEWVKTEREQFVEF
RDKNRDGKMDKEETKDWILPSDYDHAEAEARHLVYESDQNKDGKLTKEEIVDKYDLFVGS
QATDFGEALVRHDEF
Function Involved in regulation of vitamin K-dependent carboxylation of multiple N-terminal glutamate residues. Seems to inhibit gamma-carboxylase GGCX. Binds 7 calcium ions with a low affinity.
Tissue Specificity Ubiquitously expressed. Expressed at high levels in heart, placenta and skeletal muscle, at lower levels in lung, kidney and pancreas and at very low levels in brain and liver.
Reactome Pathway
Regulation of Insulin-like Growth Factor (IGF) transport and uptake by Insulin-like Growth Factor Binding Proteins (IGFBPs) (R-HSA-381426 )
Post-translational protein phosphorylation (R-HSA-8957275 )
Platelet degranulation (R-HSA-114608 )

Molecular Interaction Atlas (MIA) of This DOT

18 Disease(s) Related to This DOT
Disease Name Disease ID Evidence Level Mode of Inheritance REF
Lung adenocarcinoma DISD51WR Definitive Biomarker [1]
Arteriosclerosis DISK5QGC Strong Biomarker [2]
Asthma DISW9QNS Strong Altered Expression [3]
Atherosclerosis DISMN9J3 Strong Biomarker [2]
Breast cancer DIS7DPX1 Strong Biomarker [4]
Breast carcinoma DIS2UE88 Strong Biomarker [4]
Colon cancer DISVC52G Strong Biomarker [5]
Colon carcinoma DISJYKUO Strong Biomarker [5]
Cystic fibrosis DIS2OK1Q Strong Genetic Variation [6]
Familial hypertrophic cardiomyopathy DISQ89HN Strong Altered Expression [3]
Lung carcinoma DISTR26C Strong Biomarker [7]
Atrial fibrillation DIS15W6U moderate Biomarker [8]
Familial atrial fibrillation DISL4AGF moderate Biomarker [8]
Filarial disease DISWBRRN moderate Biomarker [9]
Metastatic malignant neoplasm DIS86UK6 moderate Biomarker [10]
Advanced cancer DISAT1Z9 Limited Biomarker [11]
Lung cancer DISCM4YA Limited Biomarker [7]
Neoplasm DISZKGEW Limited Biomarker [12]
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⏷ Show the Full List of 18 Disease(s)
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
Warfarin DMJYCVW Approved Calumenin (CALU) affects the response to substance of Warfarin. [34]
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23 Drug(s) Affected the Gene/Protein Processing of This DOT
Drug Name Drug ID Highest Status Interaction REF
Valproate DMCFE9I Approved Valproate increases the expression of Calumenin (CALU). [13]
Ciclosporin DMAZJFX Approved Ciclosporin decreases the expression of Calumenin (CALU). [14]
Tretinoin DM49DUI Approved Tretinoin decreases the expression of Calumenin (CALU). [15]
Acetaminophen DMUIE76 Approved Acetaminophen decreases the expression of Calumenin (CALU). [16]
Doxorubicin DMVP5YE Approved Doxorubicin decreases the expression of Calumenin (CALU). [17]
Ivermectin DMDBX5F Approved Ivermectin decreases the expression of Calumenin (CALU). [18]
Temozolomide DMKECZD Approved Temozolomide decreases the expression of Calumenin (CALU). [19]
Hydrogen peroxide DM1NG5W Approved Hydrogen peroxide affects the expression of Calumenin (CALU). [20]
Selenium DM25CGV Approved Selenium increases the expression of Calumenin (CALU). [21]
Clozapine DMFC71L Approved Clozapine decreases the expression of Calumenin (CALU). [22]
Benzatropine DMF7EXL Approved Benzatropine decreases the expression of Calumenin (CALU). [22]
Dihydrotestosterone DM3S8XC Phase 4 Dihydrotestosterone increases the expression of Calumenin (CALU). [23]
Phenol DM1QSM3 Phase 2/3 Phenol decreases the expression of Calumenin (CALU). [25]
Tocopherol DMBIJZ6 Phase 2 Tocopherol increases the expression of Calumenin (CALU). [21]
PMID28870136-Compound-52 DMFDERP Patented PMID28870136-Compound-52 decreases the expression of Calumenin (CALU). [16]
THAPSIGARGIN DMDMQIE Preclinical THAPSIGARGIN decreases the expression of Calumenin (CALU). [27]
Bisphenol A DM2ZLD7 Investigative Bisphenol A decreases the expression of Calumenin (CALU). [28]
Trichostatin A DM9C8NX Investigative Trichostatin A increases the expression of Calumenin (CALU). [29]
Formaldehyde DM7Q6M0 Investigative Formaldehyde decreases the expression of Calumenin (CALU). [30]
Coumestrol DM40TBU Investigative Coumestrol increases the expression of Calumenin (CALU). [31]
chloropicrin DMSGBQA Investigative chloropicrin decreases the expression of Calumenin (CALU). [32]
Deguelin DMXT7WG Investigative Deguelin decreases the expression of Calumenin (CALU). [33]
1,4-Dithiothreitol DMIFOXE Investigative 1,4-Dithiothreitol increases the expression of Calumenin (CALU). [27]
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⏷ Show the Full List of 23 Drug(s)
2 Drug(s) Affected the Protein Interaction/Cellular Processes of This DOT
Drug Name Drug ID Highest Status Interaction REF
Resveratrol DM3RWXL Phase 3 Resveratrol affects the secretion of Calumenin (CALU). [24]
D-glucose DMMG2TO Investigative D-glucose decreases the secretion of Calumenin (CALU). [24]
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1 Drug(s) Affected the Post-Translational Modifications of This DOT
Drug Name Drug ID Highest Status Interaction REF
TAK-243 DM4GKV2 Phase 1 TAK-243 increases the sumoylation of Calumenin (CALU). [26]
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References

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8 Biobank-driven genomic discovery yields new insight into atrial fibrillation biology.Nat Genet. 2018 Sep;50(9):1234-1239. doi: 10.1038/s41588-018-0171-3. Epub 2018 Jul 30.
9 Novel Findings of Anti-Filarial Drug Target and Structure-Based Virtual Screening for Drug Discovery.Int J Mol Sci. 2018 Nov 13;19(11):3579. doi: 10.3390/ijms19113579.
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11 Proteomic characterization of early lung response to breast cancer metastasis in mice.Exp Mol Pathol. 2019 Apr;107:129-140. doi: 10.1016/j.yexmp.2019.02.001. Epub 2019 Feb 11.
12 RETRACTED: Antitumor activity of bortezomib in human cancer cells with acquired resistance to anti-epidermal growth factor receptor tyrosine kinase inhibitors.Lung Cancer. 2011 Mar;71(3):283-90. doi: 10.1016/j.lungcan.2010.06.005.
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19 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.
20 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.
21 Selenium and vitamin E: cell type- and intervention-specific tissue effects in prostate cancer. J Natl Cancer Inst. 2009 Mar 4;101(5):306-20.
22 Cannabidiol Displays Proteomic Similarities to Antipsychotics in Cuprizone-Exposed Human Oligodendrocytic Cell Line MO3.13. Front Mol Neurosci. 2021 May 28;14:673144. doi: 10.3389/fnmol.2021.673144. eCollection 2021.
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24 Calorie restriction-induced changes in the secretome of human adipocytes, comparison with resveratrol-induced secretome effects. Biochim Biophys Acta. 2014 Sep;1844(9):1511-22. doi: 10.1016/j.bbapap.2014.04.023. Epub 2014 May 5.
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26 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.
27 Proteomic signatures in thapsigargin-treated hepatoma cells. Chem Res Toxicol. 2011 Aug 15;24(8):1215-22. doi: 10.1021/tx200109y. Epub 2011 Jul 1.
28 Bisphenol A Exposure Changes the Transcriptomic and Proteomic Dynamics of Human Retinoblastoma Y79 Cells. Genes (Basel). 2021 Feb 11;12(2):264. doi: 10.3390/genes12020264.
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