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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

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

The -methyl leucine at position 13 supports glucagon and GIP receptor activation

Deboever N, Zhou N, McGrail DJ, Tomczak K, Oliva JL, Feldman HA, Parra E, Zhang J, Lee PP, Antonoff MB, Hofstetter WL, Mehran RJ, Rajaram R, Rice DC , Roth JA, Swisher SS, Vaporciyan AA, Altan M, Weissferdt A, Tsao AS, Haymaker CL, Sepesi B

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