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10.1016/j.exer.2021.108624 25 GuttenplanK

Researchers followed 327 participants for a full year after they stopped taking semaglutide 2.4 mg and ended the structured lifestyle program that accompanied it

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Regarding additional residues of ScGrx7 that could form an interaction site for GSH, we suggest Asp144 and Glu147 in helix 3 as well as the hydroxyl group of conserved Tyr110: First, helix 3 and Tyr110 are both replaced in enzymatically inactive glutaredoxins 11,12 (Fig