Inhibition and Mechanism of Plasmodium falciparum Hypoxanthine–Guanine–Xanthine Phosphoribosyltransferase
Author:
Affiliation:
1. Department of Biochemistry, Albert Einstein College of Medicine, Bronx, New York 10461, United States
2. Ferrier Research Institute, Victoria University of Wellington, Gracefield, Lower Hutt 5010, New Zealand
Funder
Ministry of Business, Innovation and Employment
National Cancer Institute
National Institute of Allergy and Infectious Diseases
National Institutes of Health
National Institute of General Medical Sciences
Publisher
American Chemical Society (ACS)
Subject
Molecular Medicine,General Medicine,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acschembio.2c00546
Reference52 articles.
1. Potential Mechanisms Connecting Purine Metabolism and Cancer Therapy
2. Regulation of mammalian nucleotide metabolism and biosynthesis
3. Erythrocytic Adenosine Monophosphate as an Alternative Purine Source in Plasmodium falciparum
4. Purine and Pyrimidine Pathways as Targets in Plasmodium falciparum
5. Plasmodium falciparum Parasites Are Killed by a Transition State Analogue of Purine Nucleoside Phosphorylase in a Primate Animal Model
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1. Kinetic and Structural Characterization of Trypanosoma cruzi Hypoxanthine–Guanine–Xanthine Phosphoribosyltransferases and Repurposing of Transition-State Analogue Inhibitors;Biochemistry;2023-07-07
2. N2′‐Branched Acyclic Nucleoside Phosphonates Containing 9‐Deazahypoxanthine as Inhibitors of Plasmodium falciparum 6‐Oxopurine Phosphoribosyltransferase;ChemMedChem;2023-06-20
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