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The Diverse Binding Modes Explain the Nanomolar Levels of Inhibitory Activities Against 1-Deoxy-d-Xylulose 5-Phosphate Reductoisomerase from Plasmodium falciparum Exhibited by Reverse Hydroxamate Analogs of Fosmidomycin with Varying N-Substituents.
Takada S, Abdullaziz MA, Höfmann S, Knak T, Ozawa SI, Sakamoto Y, Kurz T, Tanaka N. Takada S, et al. Among authors: abdullaziz ma. Molecules. 2024 Dec 28;30(1):72. doi: 10.3390/molecules30010072. Molecules. 2024. PMID: 39795129 Free PMC article.
1-Deoxy-d-xylulose 5-phosphate reductoisomerase as target for anti Toxoplasma gondii agents: crystal structure, biochemical characterization and biological evaluation of inhibitors.
Mazzone F, Hoeppner A, Reiners J, Gertzen CGW, Applegate V, Abdullaziz MA, Gottstein J, Degrandi D, Wesemann M, Kurz T, Smits SHJ, Pfeffer K. Mazzone F, et al. Among authors: abdullaziz ma. Biochem J. 2024 Aug 21;481(16):1075-1096. doi: 10.1042/BCJ20240110. Biochem J. 2024. PMID: 39105673 Free PMC article.
Reverse N-Substituted Hydroxamic Acid Derivatives of Fosmidomycin Target a Previously Unknown Subpocket of 1-Deoxy-d-xylulose 5-Phosphate Reductoisomerase (DXR).
Abdullaziz MA, Takada S, Illarionov B, Pessanha de Carvalho L, Sakamoto Y, Höfmann S, Knak T, Kiffe-Delf AL, Mazzone F, Pfeffer K, Kalscheuer R, Bacher A, Held J, Fischer M, Tanaka N, Kurz T. Abdullaziz MA, et al. ACS Infect Dis. 2024 May 10;10(5):1739-1752. doi: 10.1021/acsinfecdis.4c00100. Epub 2024 Apr 22. ACS Infect Dis. 2024. PMID: 38647213