AI Article Synopsis

  • The herbicide glyphosate effectively inhibits the enzyme EPSPS, highlighting the shikimate pathway as a target for developing new antimicrobial and herbicidal agents.
  • The final enzyme in this pathway, chorismate synthase (CS), was tested with various azo-dyes, leading to the identification of PH011669 as a significant inhibitor with specific dissociation and inhibition values.
  • The study utilized molecular docking and MD simulations to analyze how PH011669 interacts with CS, providing foundational insights for future development of novel enzyme inhibitors.

Article Abstract

The efficient inhibition of 5-enolpyruvylshikimate-3-phosphate synthase (EPSPS) by the broad-spectrum herbicide glyphosate validates the shikimate pathway as a promising target for developing antimicrobial, fungicidal and herbicidal agents. The last enzyme of this pathway, chorismate synthase (CS), catalyses an unusual reaction, making it an attractive target for novel inhibitors. Therefore, we tested a series of azo-dyes for their inhibitory potential against CS from the pathogenic fungus (CS) and identified the azo-dye PH011669 that exhibits a dissociation () and 50% inhibitory constant (IC) of 1.1 ± 0.1 and 10 ± 1 µM, respectively. Molecular docking and MD simulations provided insight into the mode of inhibition, showing that PH011669 binds to the enzyme's active site primarily through electrostatic interactions. Thus, our study is the first to integrate structural and computational methods to guide future efforts towards designing the next generation of CS inhibitors.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11633415PMC
http://dx.doi.org/10.1080/14756366.2024.2427175DOI Listing

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