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To investigate the potential ligating Cys in GSDME, AlphaFold structure of GSDME (AF-O60443-F1-model_v2) was used as the initial structure in view that the experimental GSDME structure remains still unresolved

doi: 10.1016/j.pccm.2025.05.004 4 de OcaMMPerez-PadillaRCelliBAaronSDWehrmeisterFCAmaralAFSet al

Pharmacokinetics of biological drugs The biological basis of pharmacokinetics General considerations Absorption Absorption from the gut Absorption from other routes Distribution Reversible protein binding Irreversible protein binding Distribution to specific organs Elimination Metabolism Excretion The mathematical basis of pharmacokinetics General considerations Absorption Rate of absorption Extent of absorption Distribution Rate of distribution Extent of distribution Elimination Rate of elimination Extent of elimination Chronic administration Time to reach steady-state Plasma concentration at steady-state Oral administration Loading dose Pharmacokinetics of biological drugs Genetic variation and drug kinetics Pharmacokinetics of biological drugs The type of response experienced by an individual to a particular drug depends on the inherent pharmacological properties of the drug at its site of action

Du Vigneaud was awarded the Nobel Prize in Chemistry for his work on the synthesis of essential biological substances, including his research on methionine and homocysteine [5]

This process is different from other conjugation reactions because glucuronic acid, sulfate and amino acid conjugations take place at nucleophilic centres

121, 879888.10.1104/pp.121.3.879 32 MaughanS