<p>The Cα B-factor for each residue in trypsin computed from MD simulation trajectories in the form of catechin-free (black) and complex with EC (red), ECG (blue), EGC (dark-cyan) and EGCG (magenta), respectively. The orange line represents the Cα B-factor from PDB file. The wiring diagram shows the secondary structure of trypsin. The bar chart at the bottom of picture shows the distance range of the Cα atom to the nearest heavy atom of catechins. The inset enlarges the sequence motifs in the S1 pocket.</p
<p>(<b>A</b>) The α-helix and β-strands of the modeled SdPI structure are displayed in red and blue,...
<p>(A) S1-S2 region of cathepsin K (shown as transparent surface and tan sticks) with a docked subst...
<p>(A) RMSFs as calculated from MD simulations for MHC and peptide residues (inset). Only positions ...
<p>Representative structure models clustered from MD simulation trajectories for trypsin complex wit...
<p>Time evolutions of a) the backbone RMSD and b) the radius of gyration (<i>R</i><sub><i>g</i></sub...
<p>(a) Superimposed proteins. Trypsin (PDBid:1A0J) is in blue and PI-PLC (PDBid:1PTD) is in grey. Af...
<p>The lower view is rotated 90 around the horizontal axis with respect to the upper view. Helices a...
<p>The empty molecule and the K<sup>b</sup>/C-terminally truncated peptide complex show high flexibi...
AbstractIt is now widely accepted that protein function depends not only on structure, but also on f...
<p><sup>a</sup> The possibility of ligand binding to the S1 pocket.</p><p><sup>b</sup> The possibili...
On the right side, the close view of trypsin active site (S1 pocket) and anti-protease loop of both ...
Residues 7 and 8 show higher levels of order in the KLK7 complex compared to the trypsin complex ref...
<p>Ribbon plot of SFTI-1 in complex with trypsin (A) with β-sheets and α-helices coloured in yellow ...
EFR are rendered in blue, functional residues are rendered in orange. (A) In the case of trypsin inh...
<p><b>(a)</b> The number of residue positions (see <a href="http://www.plosone.org/article/info:doi/...
<p>(<b>A</b>) The α-helix and β-strands of the modeled SdPI structure are displayed in red and blue,...
<p>(A) S1-S2 region of cathepsin K (shown as transparent surface and tan sticks) with a docked subst...
<p>(A) RMSFs as calculated from MD simulations for MHC and peptide residues (inset). Only positions ...
<p>Representative structure models clustered from MD simulation trajectories for trypsin complex wit...
<p>Time evolutions of a) the backbone RMSD and b) the radius of gyration (<i>R</i><sub><i>g</i></sub...
<p>(a) Superimposed proteins. Trypsin (PDBid:1A0J) is in blue and PI-PLC (PDBid:1PTD) is in grey. Af...
<p>The lower view is rotated 90 around the horizontal axis with respect to the upper view. Helices a...
<p>The empty molecule and the K<sup>b</sup>/C-terminally truncated peptide complex show high flexibi...
AbstractIt is now widely accepted that protein function depends not only on structure, but also on f...
<p><sup>a</sup> The possibility of ligand binding to the S1 pocket.</p><p><sup>b</sup> The possibili...
On the right side, the close view of trypsin active site (S1 pocket) and anti-protease loop of both ...
Residues 7 and 8 show higher levels of order in the KLK7 complex compared to the trypsin complex ref...
<p>Ribbon plot of SFTI-1 in complex with trypsin (A) with β-sheets and α-helices coloured in yellow ...
EFR are rendered in blue, functional residues are rendered in orange. (A) In the case of trypsin inh...
<p><b>(a)</b> The number of residue positions (see <a href="http://www.plosone.org/article/info:doi/...
<p>(<b>A</b>) The α-helix and β-strands of the modeled SdPI structure are displayed in red and blue,...
<p>(A) S1-S2 region of cathepsin K (shown as transparent surface and tan sticks) with a docked subst...
<p>(A) RMSFs as calculated from MD simulations for MHC and peptide residues (inset). Only positions ...