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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

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187 Since the NETs have been proven to aggravate or even lead to diseases, like stroke, diabetes, and tumors when they over-generate, 188,189,190 the inhibition of ROS may prevent disease progression caused by NETs