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PMID: 35358930 J Pharm Anal A highly efficient protein corona-based proteomic analysis strategy for the discovery of pharmacodynamic biomarkers
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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[Abstract] Acta Pharm Sin B
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