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Preprint at (2023)

Raun et al., 1998 European Journal of Endocrinology Researchers tested different peptides to see how strongly (and selectively) they stimulated GH release

To address this question, we mutated Tyr110 in the CPYS-motif of ScGrx7 as a candidate residue that might contribute to the glutathione activator site (see Discussion for details) and performed a preliminary study with wild-type ScGrx7 as a control