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10.1084/jem.20191094 J
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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
Substrate-induced conformational changes in human UMP/CMP kinase
Alpha-lipoic acid as a new treatment option for Alzheimer's disease--a 48 months follow-up analysis
COX-2 specific inhibitors (e.g., coxibs) preferentially reduce amounts of PGI2, tipping the balance toward thrombosis (Vonkeman 2010)
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