<p>The PDB structure 3N7O was used to visualize specificity-conferring triplet (S1 pocket) of residues 189, 216 and 226, chymotrypsinogen numbering, highlighted in red. The catalytic triad residues His57, Asp102 and Ser195 and shown in blue. The bound inhibitor is highlighted in green in both ribbon and space-filling models to visualize how it sits into the S1 pocket. UCSF Chimera program was used to construct the image with further annotation in Adobe Illustrator (CS6).</p
<p>(<b>A</b>). The pharmacophore mapping of the same compound is also depicted. HBA, hydrogen bond a...
Chymotrypsin is a member of the trypsin family of serine proteases and is one of the first proteins ...
<p>Five different patented inhibitors of the HC originating from 5 different companies were synthesi...
<p>Overall 3D structure of human chymase and the zoomed view which clearly shows the important catal...
<p>(A) Overlay of the binding modes of all the inhibitors at the active site of human chymase enzyme...
<p>The 2D chemical structures of human chymase inhibitors used in this study along with their IC<sub...
Human chymase catalyzes the hydrolysis of peptide bonds. Three chymase inhibitors with very similar ...
<p>(<b>A</b>) SB_Model1 mapped to N7O, (<b>B</b>) SB_Model2 mapped to OHH, (<b>C</b>) SB_Model4 mapp...
A panel of mammalian alpha and beta chymases were aligned using the DNA Star Megalign program and us...
Background: Inhibitors of chymase appear to be interesting compounds to develop drugs for the treatm...
Background: Inhibitors of chymase appear to be interesting compounds to develop drugs for the treatm...
Background: Inhibitors of chymase appear to be interesting compounds to develop drugs for the treatm...
Background: Inhibitors of chymase appear to be interesting compounds to develop drugs for the treatm...
Background: Inhibitors of chymase appear to be interesting compounds to develop drugs for the treatm...
Chymotrypsin is a member of the trypsin family of serine proteases and is one of the first proteins ...
<p>(<b>A</b>). The pharmacophore mapping of the same compound is also depicted. HBA, hydrogen bond a...
Chymotrypsin is a member of the trypsin family of serine proteases and is one of the first proteins ...
<p>Five different patented inhibitors of the HC originating from 5 different companies were synthesi...
<p>Overall 3D structure of human chymase and the zoomed view which clearly shows the important catal...
<p>(A) Overlay of the binding modes of all the inhibitors at the active site of human chymase enzyme...
<p>The 2D chemical structures of human chymase inhibitors used in this study along with their IC<sub...
Human chymase catalyzes the hydrolysis of peptide bonds. Three chymase inhibitors with very similar ...
<p>(<b>A</b>) SB_Model1 mapped to N7O, (<b>B</b>) SB_Model2 mapped to OHH, (<b>C</b>) SB_Model4 mapp...
A panel of mammalian alpha and beta chymases were aligned using the DNA Star Megalign program and us...
Background: Inhibitors of chymase appear to be interesting compounds to develop drugs for the treatm...
Background: Inhibitors of chymase appear to be interesting compounds to develop drugs for the treatm...
Background: Inhibitors of chymase appear to be interesting compounds to develop drugs for the treatm...
Background: Inhibitors of chymase appear to be interesting compounds to develop drugs for the treatm...
Background: Inhibitors of chymase appear to be interesting compounds to develop drugs for the treatm...
Chymotrypsin is a member of the trypsin family of serine proteases and is one of the first proteins ...
<p>(<b>A</b>). The pharmacophore mapping of the same compound is also depicted. HBA, hydrogen bond a...
Chymotrypsin is a member of the trypsin family of serine proteases and is one of the first proteins ...
<p>Five different patented inhibitors of the HC originating from 5 different companies were synthesi...