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Such a metabolite-protein interaction seeding and stabilizing an assembled oligomeric state is a potent mode of regulation for GS given the nature of a composite active site that is completely inactive in the monomeric state (Figure 2)

and Battisti, D

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WB revealed that the protein expression levels of ILF3, p-mTOR, PD-L1, SLC7A11, and GPX4 were lower in the oe-ILF3 group treated with LY294002, which is an inhibitor of the mTOR signaling pathway, than in the oe-ILF3 group (Fig