Ac-Asp-Tyr(2-malonyl)-Val-Pro-Met-Leu-NH2 carries an N-terminal acetylation and a malonyl-modified tyrosine that alters electronic properties and steric behavior. These modifications influence peptide-protein association and enhance analytical detectability. The sequence provides a model for studying post-translational-like modifications. Researchers employ it to explore residue contributions to structural stability and recognition events.
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