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Mutants of the candidate residues were subsequently compared with wild-type ScGrx7 in steady-state kinetic measurements using HEDS and GSSCys as a non-glutathione and glutathione disulfide substrate, respectively
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This addition will help identify proteins that uniquely interact with the target protein compared to other, general, zinc finger-binding proteins present
(PubMed) Ben S, Du M, Ma G, et al
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