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These included a cluster of phosphosites in which the basal phosphorylation was higher in WT-IR than in L973F-IR (II-B, 141 sites), a cluster in which ligand-dependent reduction of phosphorylation was greater in WT-IR than in L973F-IR (II-C, 41 sites), and a cluster in which phosphorylation of proteins was downregulated more by ligands in WT-IR than in L973F-IR (II-D, 28 sites)

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Thiazolidinedione (TZD) compounds, such as rosiglitazone (ROSI), pioglitazone (PIO), and troglitazone (TRO), reduced the mortality of mice after GPX4 was loss by inhibiting the action of ACSL4, indicating that these compounds may show potential therapeutic effects on AKI [43, 48]