Co-Target(s) Information
Target General Information | Top | ||||
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Target ID | T31230 | Target Info | |||
Target Name | Bacterial Fumarate reductase flavoprotein (Bact frdA) | ||||
Synonyms |
Fumarate reductase; FRDA
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Target Type | Successful Target | ||||
Gene Name | Bact frdA | ||||
Biochemical Class | CH-CH donor oxidoreductase | ||||
UniProt ID |
Co-Targets of This Target | Top | |||||
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Co-Target Name | Bacterial Methionine aminopeptidase (Bact map) | Co-Target | ||||
UniProt ID | MAP1_ECOLI | |||||
Gene Name | Bact map | |||||
Synonyms |
Bact MAP; Bact MetAP
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Representative Drug(s) | Thiabendazole | Drug Info | IC50 = 472 nM | [1] | ||
Co-Target Name | Cytochrome P450 1A2 (CYP1A2) | Co-Target | ||||
UniProt ID | CP1A2_HUMAN | |||||
Gene Name | CYP1A2 | |||||
Synonyms |
Cholesterol 25-hydroxylase; Hydroperoxy icosatetraenoate dehydratase; CYPIA2; Cytochrome P(3)450; Cytochrome P450 4; Cytochrome P450-P3
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Representative Drug(s) | Thiabendazole | Drug Info | IC50 = 800 nM | [2] |
References | Top | ||||
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REF 1 | Metal-mediated inhibition of Escherichia coli methionine aminopeptidase: structure-activity relationships and development of a novel scoring function for metal-ligand interactions. J Med Chem. 2006 Jan 26;49(2):511-22. | ||||
REF 2 | DrugMatrix in vitro pharmacology data. National Toxicology Program |
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