Fuchs Katharina, Totaro Massimo G, Toplak Marina, Bijelic Aleksandar, Macheroux Peter
Institute of Biochemistry, Graz University of Technology, Graz, Austria.
J Enzyme Inhib Med Chem. 2024 Dec;39(1):2427175. doi: 10.1080/14756366.2024.2427175. Epub 2024 Dec 10.
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.
广谱除草剂草甘膦对5-烯醇丙酮酰莽草酸-3-磷酸合酶(EPSPS)的有效抑制,证实了莽草酸途径是开发抗菌、杀真菌和除草剂的一个有前景的靶点。该途径的最后一种酶,分支酸合酶(CS),催化一种不同寻常的反应,使其成为新型抑制剂的一个有吸引力的靶点。因此,我们测试了一系列偶氮染料对致病真菌分支酸合酶(CS)的抑制潜力,并鉴定出偶氮染料PH011669,其解离常数()和50%抑制常数(IC)分别为1.1±0.1和10±1μM。分子对接和分子动力学模拟提供了对抑制模式的深入了解,表明PH011669主要通过静电相互作用与酶的活性位点结合。因此,我们的研究首次整合了结构和计算方法,以指导未来设计下一代CS抑制剂的工作。