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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

Haqqani AS, Blanger K, Stanimirovic DB (2024) Receptor-mediated transcytosis for brain delivery of therapeutics: receptor classes and criteria

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The study monitored for erythema, itching, scarring, atrophy, telangiectasias, and post-inflammatory hyperpigmentation, none of which were observed