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Here we determined the rate constants for the individual redox reactions between the two redox-sensitive cysteinyl residues of roGFP2 and the active-site cysteinyl residues of the model class I glutaredoxin PfGrx from the malaria parasite Plasmodium falciparum using stopped-flow kinetic measurements in combination with redox mobility shift assays

Exploring the O-GlcNAc proteome: direct identification of O-GlcNAc-modified proteins from the brain

What does 98% purity mean