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Molecular Architecture of GLP-1 Receptor Drug Binding Reveals Dynamic Activation Mechanisms Evolving cryo-EM structural approaches for GPCR drug discovery Deep Pocket Architecture: The orthosteric binding pocket comprises Y152 (TM1), K197 (TM2), Q234/Y241 (TM3), W306/R310 (TM5), E364/H363 (TM6), and L384 (TM7), with His1 of peptide agonists forming critical contacts deep within this cavity that stabilize the

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