<p>Different length versions of peptide15 were tested for Kly18 inhibitory activity. All peptides were screened in a relatively high single concentration (87 µM) to reveal if omission of single amino acid residues displayed dramatic effects on Kly18 inhibition. The data demonstrated that peptide15 can be limited to (NH<sub>2</sub>)-SWFP-(CONH<sub>2</sub>) (structure 15-7) and still inhibit Kly18.</p
A novel class of peptide α-ketoamides useful for selectively inhibiting serine proteases, selectivel...
We explored the unique substrate specificity of the primary S1 subsite of human urinary kallikrein (...
<p>The <i>K</i><sub>i</sub> values (in µM) for inhibition of the indicated enzymes by the indicated ...
<p>Shown are 1/V-1/S plot of peptide15 inhibition of Kly18. Kly18 was pre-incubated with fixed conce...
<p>Peptide15 was pre-incubated with Kly18 in varying concentrations followed by addition of the subs...
Analogs of potent CaMKinase II inhibitor, CaM-KNtide, were prepared to explore new structural requir...
Analogs of potent CaMKinase II inhibitor, CaM-KNtide, were prepared to explore new structural requir...
Analogs of potent CaMKinase II inhibitor, CaM-KNtide, were prepared to explore new structural requir...
Analogs of potent CaMKinase II inhibitor, CaM-KNtide, were prepared to explore new structural requir...
Analogs of potent CaMKinase II inhibitor, CaM-KNtide, were prepared to explore new structural requir...
<p>The peptide15-MBP fusion protein interacted exclusively with Kly18, thereby demonstrating that pe...
ABSTRACT: Caspases are fundamental to many essential biological processes, including apoptosis, diff...
A novel class of peptide α-ketoamides useful for selectively inhibiting serine proteases, selectivel...
<p>(A) Peptide residues identified as tolerating positions for peptoid substitution are shown in sha...
In the selection or design of antimicrobial peptides, the key role played by cationic amino acids an...
A novel class of peptide α-ketoamides useful for selectively inhibiting serine proteases, selectivel...
We explored the unique substrate specificity of the primary S1 subsite of human urinary kallikrein (...
<p>The <i>K</i><sub>i</sub> values (in µM) for inhibition of the indicated enzymes by the indicated ...
<p>Shown are 1/V-1/S plot of peptide15 inhibition of Kly18. Kly18 was pre-incubated with fixed conce...
<p>Peptide15 was pre-incubated with Kly18 in varying concentrations followed by addition of the subs...
Analogs of potent CaMKinase II inhibitor, CaM-KNtide, were prepared to explore new structural requir...
Analogs of potent CaMKinase II inhibitor, CaM-KNtide, were prepared to explore new structural requir...
Analogs of potent CaMKinase II inhibitor, CaM-KNtide, were prepared to explore new structural requir...
Analogs of potent CaMKinase II inhibitor, CaM-KNtide, were prepared to explore new structural requir...
Analogs of potent CaMKinase II inhibitor, CaM-KNtide, were prepared to explore new structural requir...
<p>The peptide15-MBP fusion protein interacted exclusively with Kly18, thereby demonstrating that pe...
ABSTRACT: Caspases are fundamental to many essential biological processes, including apoptosis, diff...
A novel class of peptide α-ketoamides useful for selectively inhibiting serine proteases, selectivel...
<p>(A) Peptide residues identified as tolerating positions for peptoid substitution are shown in sha...
In the selection or design of antimicrobial peptides, the key role played by cationic amino acids an...
A novel class of peptide α-ketoamides useful for selectively inhibiting serine proteases, selectivel...
We explored the unique substrate specificity of the primary S1 subsite of human urinary kallikrein (...
<p>The <i>K</i><sub>i</sub> values (in µM) for inhibition of the indicated enzymes by the indicated ...