General Information of Drug Off-Target (DOT) (ID: OTAHB98A)

DOT Name Cytochrome b (CYTB)
Synonyms Complex III subunit 3; Complex III subunit III; Cytochrome b-c1 complex subunit 3; Ubiquinol-cytochrome-c reductase complex cytochrome b subunit
Gene Name CYTB
Related Disease
Multiple sclerosis ( )
Pediculus capitis infestation ( )
Advanced cancer ( )
Alzheimer disease ( )
Arteriosclerosis ( )
Atherosclerosis ( )
Bladder cancer ( )
Carcinoma of esophagus ( )
Cardiovascular disease ( )
Chagas disease ( )
Cutaneous leishmaniasis ( )
Epilepsy ( )
Epithelial ovarian cancer ( )
Esophageal cancer ( )
Gastric cancer ( )
Hepatocellular carcinoma ( )
Lactic acidosis ( )
Leber hereditary optic neuropathy ( )
leukaemia ( )
Leukemia ( )
Melanoma ( )
MELAS syndrome ( )
Mitochondrial disease ( )
Mitochondrial encephalomyopathy ( )
Mitochondrial myopathy ( )
Myopathy ( )
Neoplasm ( )
Non-insulin dependent diabetes ( )
Parkinson disease ( )
Parkinsonian disorder ( )
Pneumonia ( )
Stomach cancer ( )
Thyrotoxicosis ( )
Triple negative breast cancer ( )
Type-1/2 diabetes ( )
Ulcerative colitis ( )
Urinary bladder cancer ( )
Urinary bladder neoplasm ( )
Granulomatous disease, chronic, X-linked ( )
Head-neck squamous cell carcinoma ( )
Obesity ( )
Visceral leishmaniasis ( )
Pneumocystis pneumonia ( )
Coronary heart disease ( )
Intellectual disability ( )
Leigh syndrome ( )
Mitochondrial myopathy with reversible cytochrome C oxidase deficiency ( )
Type-1 diabetes ( )
UniProt ID
CYB_HUMAN
3D Structure
Download
2D Sequence (FASTA)
Download
3D Structure (PDB)
Download
PDB ID
5XTE; 5XTH; 5XTI
Pfam ID
PF00032 ; PF00033
Sequence
MTPMRKTNPLMKLINHSFIDLPTPSNISAWWNFGSLLGACLILQITTGLFLAMHYSPDAS
TAFSSIAHITRDVNYGWIIRYLHANGASMFFICLFLHIGRGLYYGSFLYSETWNIGIILL
LATMATAFMGYVLPWGQMSFWGATVITNLLSAIPYIGTDLVQWIWGGYSVDSPTLTRFFT
FHFILPFIIAALATLHLLFLHETGSNNPLGITSHSDKITFHPYYTIKDALGLLLFLLSLM
TLTLFSPDLLGDPDNYTLANPLNTPPHIKPEWYFLFAYTILRSVPNKLGGVLALLLSILI
LAMIPILHMSKQQSMMFRPLSQSLYWLLAADLLILTWIGGQPVSYPFTIIGQVASVLYFT
TILILMPTISLIENKMLKWA
Function
Component of the ubiquinol-cytochrome c reductase complex (complex III or cytochrome b-c1 complex) that is part of the mitochondrial respiratory chain. The b-c1 complex mediates electron transfer from ubiquinol to cytochrome c. Contributes to the generation of a proton gradient across the mitochondrial membrane that is then used for ATP synthesis.
KEGG Pathway
Oxidative phosphorylation (hsa00190 )
Metabolic pathways (hsa01100 )
Cardiac muscle contraction (hsa04260 )
Thermogenesis (hsa04714 )
Non-alcoholic fatty liver disease (hsa04932 )
Alzheimer disease (hsa05010 )
Parkinson disease (hsa05012 )
Amyotrophic lateral sclerosis (hsa05014 )
Huntington disease (hsa05016 )
Prion disease (hsa05020 )
Pathways of neurodegeneration - multiple diseases (hsa05022 )
Chemical carcinogenesis - reactive oxygen species (hsa05208 )
Diabetic cardiomyopathy (hsa05415 )
Reactome Pathway
Respiratory electron transport (R-HSA-611105 )
BioCyc Pathway
MetaCyc:HS00029-MONOMER

Molecular Interaction Atlas (MIA) of This DOT

48 Disease(s) Related to This DOT
Disease Name Disease ID Evidence Level Mode of Inheritance REF
Multiple sclerosis DISB2WZI Definitive Biomarker [1]
Pediculus capitis infestation DISLZYDI Definitive Genetic Variation [2]
Advanced cancer DISAT1Z9 Strong Biomarker [3]
Alzheimer disease DISF8S70 Strong Altered Expression [4]
Arteriosclerosis DISK5QGC Strong Genetic Variation [5]
Atherosclerosis DISMN9J3 Strong Genetic Variation [5]
Bladder cancer DISUHNM0 Strong Genetic Variation [6]
Carcinoma of esophagus DISS6G4D Strong Genetic Variation [7]
Cardiovascular disease DIS2IQDX Strong Genetic Variation [8]
Chagas disease DIS8KNVF Strong Genetic Variation [9]
Cutaneous leishmaniasis DISRK7TS Strong Genetic Variation [10]
Epilepsy DISBB28L Strong Genetic Variation [11]
Epithelial ovarian cancer DIS56MH2 Strong Altered Expression [12]
Esophageal cancer DISGB2VN Strong Genetic Variation [7]
Gastric cancer DISXGOUK Strong Biomarker [13]
Hepatocellular carcinoma DIS0J828 Strong Altered Expression [14]
Lactic acidosis DISZI1ZK Strong Genetic Variation [15]
Leber hereditary optic neuropathy DIS7Y2EE Strong Genetic Variation [16]
leukaemia DISS7D1V Strong Genetic Variation [17]
Leukemia DISNAKFL Strong Genetic Variation [17]
Melanoma DIS1RRCY Strong Biomarker [18]
MELAS syndrome DIS81Z3S Strong Genetic Variation [19]
Mitochondrial disease DISKAHA3 Strong Genetic Variation [20]
Mitochondrial encephalomyopathy DISA6PTN Strong Genetic Variation [21]
Mitochondrial myopathy DIS9SA7V Strong Genetic Variation [22]
Myopathy DISOWG27 Strong Genetic Variation [23]
Neoplasm DISZKGEW Strong Altered Expression [24]
Non-insulin dependent diabetes DISK1O5Z Strong Biomarker [25]
Parkinson disease DISQVHKL Strong Genetic Variation [26]
Parkinsonian disorder DISHGY45 Strong Genetic Variation [27]
Pneumonia DIS8EF3M Strong Biomarker [28]
Stomach cancer DISKIJSX Strong Biomarker [13]
Thyrotoxicosis DISWH7BV Strong Biomarker [29]
Triple negative breast cancer DISAMG6N Strong Altered Expression [30]
Type-1/2 diabetes DISIUHAP Strong Biomarker [31]
Ulcerative colitis DIS8K27O Strong Biomarker [32]
Urinary bladder cancer DISDV4T7 Strong Genetic Variation [6]
Urinary bladder neoplasm DIS7HACE Strong Genetic Variation [6]
Granulomatous disease, chronic, X-linked DISNTTS3 moderate Genetic Variation [33]
Head-neck squamous cell carcinoma DISF7P24 moderate Altered Expression [24]
Obesity DIS47Y1K moderate Genetic Variation [34]
Visceral leishmaniasis DISTKEYK moderate Genetic Variation [35]
Pneumocystis pneumonia DISFSOM3 Disputed Biomarker [28]
Coronary heart disease DIS5OIP1 Limited Biomarker [36]
Intellectual disability DISMBNXP Limited Genetic Variation [37]
Leigh syndrome DISWQU45 Limited CausalMutation [21]
Mitochondrial myopathy with reversible cytochrome C oxidase deficiency DISW3XTC Limited CausalMutation [38]
Type-1 diabetes DIS7HLUB Limited Biomarker [31]
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⏷ Show the Full List of 48 Disease(s)
Molecular Interaction Atlas (MIA) Jump to Detail Molecular Interaction Atlas of This DOT
14 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 Cytochrome b (CYTB). [39]
Doxorubicin DMVP5YE Approved Doxorubicin decreases the expression of Cytochrome b (CYTB). [40]
Ivermectin DMDBX5F Approved Ivermectin decreases the expression of Cytochrome b (CYTB). [41]
Hydrogen peroxide DM1NG5W Approved Hydrogen peroxide decreases the expression of Cytochrome b (CYTB). [42]
Zidovudine DM4KI7O Approved Zidovudine affects the expression of Cytochrome b (CYTB). [43]
Urethane DM7NSI0 Phase 4 Urethane increases the expression of Cytochrome b (CYTB). [44]
Fialuridine DMCIGRB Phase 2 Fialuridine decreases the expression of Cytochrome b (CYTB). [45]
Benzo(a)pyrene DMN7J43 Phase 1 Benzo(a)pyrene decreases the expression of Cytochrome b (CYTB). [46]
THAPSIGARGIN DMDMQIE Preclinical THAPSIGARGIN decreases the expression of Cytochrome b (CYTB). [47]
Bisphenol A DM2ZLD7 Investigative Bisphenol A decreases the expression of Cytochrome b (CYTB). [48]
methyl p-hydroxybenzoate DMO58UW Investigative methyl p-hydroxybenzoate decreases the expression of Cytochrome b (CYTB). [49]
D-glucose DMMG2TO Investigative D-glucose decreases the expression of Cytochrome b (CYTB). [50]
2-AMINO-1-METHYL-6-PHENYLIMIDAZO[4,5-B]PYRIDINE DMNQL17 Investigative 2-AMINO-1-METHYL-6-PHENYLIMIDAZO[4,5-B]PYRIDINE decreases the expression of Cytochrome b (CYTB). [51]
Ethidium DMMEQUR Investigative Ethidium decreases the expression of Cytochrome b (CYTB). [52]
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⏷ Show the Full List of 14 Drug(s)

References

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17 Tumor necrosis factor and immune interferon synergistically induce cytochrome b-245 heavy-chain gene expression and nicotinamide-adenine dinucleotide phosphate hydrogenase oxidase in human leukemic myeloid cells.J Clin Invest. 1989 May;83(5):1570-9. doi: 10.1172/JCI114054.
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20 Mitochondrial disease-related mutations at the cytochrome b-iron-sulfur protein (ISP) interface: Molecular effects on the large-scale motion of ISP and superoxide generation studied in Rhodobacter capsulatus cytochrome bc1.Biochim Biophys Acta. 2016 Aug;1857(8):1102-1110. doi: 10.1016/j.bbabio.2016.03.022. Epub 2016 Mar 28.
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22 A novel mutation in the mitochondrial DNA cytochrome b gene (MTCYB) in a patient with Prader Willi syndrome.J Child Neurol. 2015 Mar;30(3):378-81. doi: 10.1177/0883073814530499. Epub 2014 Apr 25.
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24 Down-regulation of mitochondrial NADH and cytochrome b gene associated with high tumor stages in head and neck squamous cell carcinoma.Arch Oral Biol. 2019 Mar;99:107-112. doi: 10.1016/j.archoralbio.2019.01.005. Epub 2019 Jan 10.
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