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The nature of the amino acids contributing to the substrate recognition in this H-site has not been identified so often since it generally requires the crystal structure of complexes

Usually, the next step is to use mass spectrometry to identify those interacting proteins (Kassa et al, 2023)

The molecule is engineered with a trans-3-hexenoic acid moiety covalently attached at the N-terminal tyrosine, a modification that confers significant resistance to enzymatic cleavage by dipeptidyl peptidase-4 (DPP-4)

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