Host metabolic pathways essential for malaria and related hemoparasites in the infection of nucleated cells bioRxiv The essential host genome for Cryptosporidium survival exposes metabolic dependencies that can be leveraged for treatment: Cell X ray structure of glutathione S transferase from the malarial parasite Plasmodium falciparum PNAS Antimalarial Dual Drugs Based on Potent Inhibitors of Glutathione Reductase from Plasmodium falciparum Journal of Medicinal Chemistry
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glutathione and parasites Reductive Activation of Artefenomel (OZ439) by Fe(II)-Heme, Related to Its Antimalarial Activity