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Studies on -synuclein demonstrate that methionine residues near the N-terminus are more susceptible to copper-mediated oxidation than internal residues, with Met1 substitution decreasing Cu-peptide reduction potential by approximately 80 mV

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BPC-157's action profile in treating side effects caused by NSAIDs is based on protein phosphorylation, inhibition of protein denaturation, stabilization of lysosomal and cellular membranes, inhibition of complement activation, inhibition of proteases and protein kinases, and fibrinolytic activity

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