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In these models, we take into account the reaction geometry of common thiol-disulfide exchange reactions and distinguish hypothetical protein areas that might either interact with the disulfide substrate (a scaffold site) or the reducing agent (an activator site) (Fig
Wash hands, face, and/or body 3
So now we come to our original question
A natural question: if both are heptapeptides with overlapping monoaminergic effects, are they substitutable, or do they address different things