Molecule Information
General Information of the Molecule (ID: Mol02074)
Name |
Chloramphenicol acetyltransferase (CAT)
,Clostridioides difficile
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Synonyms |
catD
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Molecule Type |
Protein
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Gene Name |
CAT
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Sequence |
MVFEKIDKNSWNRKEYFDHYFASVPCTYSMTVKVDITQIKEKGMKLYPAMLYYIAMIVNR
HSEFRTAINQDGELGIYDEMIPSYTIFHNDTETFSSLWTECKSDFKSFLADYESDTQRYG NNHRMEGKPNAPENIFNVSMIPWSTFDGFNLNLQKGYDYLIPIFTMGKIIKKDNKIILPL AIQVHHAVCDGFHICRFVNELQELIIVTQVCL Click to Show/Hide
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Function |
This enzyme is an effector of chloramphenicol resistance in bacteria.
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Uniprot ID | |||||
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Type(s) of Resistant Mechanism of This Molecule
DISM: Drug Inactivation by Structure Modification
Drug Resistance Data Categorized by Drug
Approved Drug(s)
1 drug(s) in total
Chloramphenicol
Drug Resistance Data Categorized by Their Corresponding Mechanisms | ||||
Drug Inactivation by Structure Modification (DISM) | ||||
Disease Class: Clostridium difficile infection | [1] | |||
Resistant Disease | Clostridium difficile infection [ICD-11: 1A04.0] | |||
Resistant Drug | Chloramphenicol | |||
Molecule Alteration | Expression | Inherence |
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Experimental Note | Discovered Using In-vivo Testing Model | |||
Mechanism Description | The inactivation of drug undergoes by the addition of side chain that generates a steric hindrance effect, which in turn disrupts the target-binding affinity. Two copies of catD gene encoding for CHL acetyltransferase locate at the mobile regions Tn4453a and Tn4453b of C. difficile. CHL acetyltransferase catalyses the relocation of acetyl group from acetyl-CoA to CHL, resulting in 3-O-acetyl CHL, which cannot bind to a ribosome and loses its antimicrobial action. |
References
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