Ac-Tyr-Val-Lys-Asp-aldehyde (pseudo acid) is a reversible inhibitory peptide applied to examine protease-substrate docking. Its aldehyde group forms transient covalent interactions facilitating mechanistic insight. Researchers evaluate its structure to explore sequence contributions to binding. The molecule enhances studies of peptide-based inhibitory strategies.
1. Store-operated Ca2+ entry sustains the fertilization Ca2+ signal in pig eggs
3. TMEM16F and dynamins control expansive plasma membrane reservoirs
4. Adipose tissue is a key organ for the beneficial effects of GLP-2 metabolic function
5. C-Peptide replacement therapy and sensory nerve function in type 1 diabetic neuropathy
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