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Computer-aided design of a cyclic di-AMP synthesizing enzyme CdaA inhibitor
by
Ficner, Ralf
, Neumann, Piotr
, Kloskowski, Patrick
in
Antibiotics
/ Antimicrobial agents
/ Bacteria
/ Bacterial infections
/ Cell walls
/ COVID-19
/ Disease transmission
/ Drug resistance
/ Enzymes
/ Homeostasis
/ Pathogens
/ Public health
/ Therapeutic targets
2023
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Computer-aided design of a cyclic di-AMP synthesizing enzyme CdaA inhibitor
by
Ficner, Ralf
, Neumann, Piotr
, Kloskowski, Patrick
in
Antibiotics
/ Antimicrobial agents
/ Bacteria
/ Bacterial infections
/ Cell walls
/ COVID-19
/ Disease transmission
/ Drug resistance
/ Enzymes
/ Homeostasis
/ Pathogens
/ Public health
/ Therapeutic targets
2023
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Do you wish to request the book?
Computer-aided design of a cyclic di-AMP synthesizing enzyme CdaA inhibitor
by
Ficner, Ralf
, Neumann, Piotr
, Kloskowski, Patrick
in
Antibiotics
/ Antimicrobial agents
/ Bacteria
/ Bacterial infections
/ Cell walls
/ COVID-19
/ Disease transmission
/ Drug resistance
/ Enzymes
/ Homeostasis
/ Pathogens
/ Public health
/ Therapeutic targets
2023
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Computer-aided design of a cyclic di-AMP synthesizing enzyme CdaA inhibitor
Journal Article
Computer-aided design of a cyclic di-AMP synthesizing enzyme CdaA inhibitor
2023
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Overview
Abstract
Cyclic di-AMP (c-di-AMP) is an essential secondary messenger regulating cell wall homeostasis and myriads of physiological processes in several Gram-positive and mycobacteria, including human pathogens. Hence, c-di-AMP synthesizing enzymes (DACs) have become a promising antibacterial drug target. To overcome a scarcity of small molecule inhibitors of c-di-AMP synthesizing enzyme CdaA, a computer-aided design of a new compound that should block the enzyme has been performed. This has led to the identification of a molecule comprising two thiazole rings and showing inhibitory potential based on ITC measurements. Thiazole scaffold is a good pharmacophore nucleus known due to its various pharmaceutical applications. It is contained in more than 18 FDA-approved drugs as well as in dozens of experimental drugs. Hence, the designed inhibitor can serve as a potent lead compound for further development of inhibitor against CdaA.
Publisher
Oxford University Press
Subject
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