Introduction Glucagon-like peptide-1 receptor agonists (GLP-1 RAs) represent one of the most transformative pharmacologic developments in metabolic medicine
Moreover, while all the complexes displayed common and extensive interactions between the GLP-1R and the 5 helix of G s , the persistence of interactions with individual residues differed in the exendin-P5 and oxyntomodulin bound complex (and to a lesser extent exendin-4), relative to GLP-1 over the time-course of the simulation (Figure 8B, Supplemental Table 4)
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