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Mechanistic studies of inactivation of glutathione S-transferase Pi isozyme by a haloenol lactone derivative

Notably, many proteins interacting with our cytosolic or mitochondrial Pf Prx were not located in the same subcellular compartment and are therefore listed separately in the figures and tables of this manuscript

The resulting nanosponge network is susceptible to degradation by endogenous biomolecules, including glutathione and esterase enzymes, enabling a triggered structural breakdown that releases the antimicrobial payload at the infection site