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In catalase and peroxidase, analysis of the crystal structure indicates strongly that amino-acid side chains are situated to aid in the cleavage by stabilizing a charge-separated transition state (Figure 5.14)

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The PfGrx C88S -catalyzed deglutathionylation of monothiol roGFP2 C208S (SSG) is therefore two orders of magnitudes faster than the glutathionylation of roGFP2 C208S (SH) by PfGrx C88S (SSG) (Table 1) corresponding to the strongly shifted equilibrium towards glutathionylated PfGrx C88S and reduced roGFP2 C208S in the redox mobility shift assays (Fig