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Diabetologia 16 , 7585 (1979)
GLP-1, GIP, and exenatide seem to have the same patterns here: Phe 22 is centered to specifically interact with the receptor and the adjacent hydrophobic residues of positions 23, 25, and 26 are used to form a hydrophobic region
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Fatty di-acids that had a proximal fatty acid for amide connectivity to the linker, as well as a distal fatty acid, were shown to be the solution to obtaining high albumin binding and GLP-1R potency
