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However, aGLP1-E2 decreased fasting and fed blood glucose to a greater extent than aGLP1 and iGLP1-E2 alone

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We therefore sought to investigate the molecular mechanisms by which GLP-1, oxyntomodulin, exendin-4 and exendin-P5 bind and activate the GLP-1R using a combination of structural biology, molecular dynamics simulations and pharmacological studies combined with extensive receptor mutagenesis

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