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This iso-peptide bond is important because it renders GSH relatively resistant to intracellular proteases that cleave eu-peptide bonds [38]

It plays a crucial role in postprandial glucose regulation and satiety signaling that is entirely separate from the incretin system

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Evidence and Clinical Research Evidence-Level Definitions: Established clinical evidence: Supported by multiple peer-reviewed human studies

In contrast, FBXL5-dependent IRPs degradation will decrease in iron-deficient cells, and thus, the interaction between IRPs and the IRE motif in the 5-UTR of ferritin and FPN will inhibit the translation, while the binding of IRPs to an IRE at the 3-UTR of TfR1 can protect mRNA against endonuclease cleavage [67]

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