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Instead of relying on the K17 salt bridge, retatrutide utilizes a distinct set of polar and hydrophobic contacts to conquer the GIPR binding pocket: Hydrogen Bonding Network: In the GIPR binding pocket, Gln138 (1.40b), Glu135 (1.37b), and Glu288 (45.52b) form a powerful triad of hydrogen bonds with the hydroxyl group of Tyr10 and the side chain of Thr7 located on retatrutide
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