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Next, we examined the enzymatic activities of AsGGT1, AsGGT2, and AsGGT3 toward -glutamyl- S -allyl-L-cysteine and -glutamyl- S -allyl-L-cysteine sulfoxide, which are two possible biosynthetic intermediates in alliin biosynthesis, as potential -glutamyl donor substrates ( Figures 3 and 4 )

Cagrilintides refined structure demonstrates how minimal sequence alterations can yield significant gains in receptor affinity and stability, making it a cornerstone model in modern peptide research