Improving the selectivity of engineered protease inhibitors: optimizing the P2 prime residue using a versatile cyclic peptide library
Standard mechanism inhibitors are attractive design templates for engineering reversible
serine protease inhibitors. When optimizing interactions between the inhibitor and target
protease, many studies focus on the nonprimed segment of the inhibitor's binding loop …
serine protease inhibitors. When optimizing interactions between the inhibitor and target
protease, many studies focus on the nonprimed segment of the inhibitor's binding loop …
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