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Here, we reveal that while the peptides form similar interactions in the fully active, G s -coupled state of the receptor, exendin-4 and oxyntomodulin-occupied receptors are more dynamic, which may, in part, be linked to the more transient nature of their interactions with the TMD observed in MD simulations

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The hyperglycemia buffer of dual-incretin action is a particularly important property, as it allows for more potent development of the glucagon constituent in compound formulation