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To determine if the increase in enzymatic activity of glutathione peroxidases was due to increased gene expression, qPCR was again conducted to determine if there was any change in abundance of glutathione peroxidase transcripts

In conclusion, we revealed novel structurefunction relationships of glutaredoxins, gained insights regarding the enzymatic conversion of glutathione- and non-glutathione disulfide substrates, and identified two distinct substrate interaction sites that include a scaffold residue and the conserved dual activator Lys105 in ScGrx7 and Lys26 in PfGrx

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