10.1002/hep.20948 43 LeBlancA.ShiaoT
We show (i) that PfGrx-catalyzed redox reactions outcompete uncatalyzed reactions between roGFP2 and GSH or GSSG by several orders of magnitude, (ii) that the PfGrx-catalyzed reduction and oxidation of roGFP2 occur via a mono- and not a dithiol mechanism, and (iii) that the reduction of roGFP2(S 2 ) as a model non-glutathione disulfide substrate most likely involves a rate-limiting glutathionylation in a ternary complex with a GSH molecule that is activated at the 1st glutathione-interaction site of PfGrx
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(PubMed) Mennella JA, Beauchamp GK
Mechanism and Significance of Increased Glutathione Level in Human Hepatocellular Carcinoma and Liver Regeneration. The FASEB Journal, vol