Journal:FLS:1

From Proteopedia

(Difference between revisions)
Jump to: navigation, search
Line 1: Line 1:
-
<StructureSection load='3HSWa.pdb' size='500' side='right' scene='' caption=''>
+
<Structure load='3HSWa.pdb' size='500' frame='true' align='right' caption='Insert caption here' scene='Insert optional scene name here' />
-
=== Crystal structure of porcine pancreatic phospholipase A2 in complex with 2-methoxycyclohexa-2-5-diene-1,4-dione ===
+
=== Crystal structure of porcine pancreatic phospholipase A<sub>2</sub> in complex with 2-methoxycyclohexa-2-5-diene-1,4-dione ===
<big>K V Dileep, I Tintu, P K Mandal, P Karthe, M Haridas and C Sadasivan</big><ref >none yet</ref>
<big>K V Dileep, I Tintu, P K Mandal, P Karthe, M Haridas and C Sadasivan</big><ref >none yet</ref>
<hr/>
<hr/>
<b>Molecular Tour</b><br>
<b>Molecular Tour</b><br>
-
Curcumin possess anti-inflammatory activity. The binding of curcumin with PLA2 was studied using X-ray crystallography. Since the electron density found in the active site did not match with curcumin, 2-methoxycyclohexa-2-5-diene-1,4-dione (MCW) (the photo-degraded product of curcumin) was fitted in the unexplained electron density. To understand the binding mode of actual curcumin, molecular docking studies was carried out. Both crystallographic and docked structures were superimposed with respect to the ligand position and identified that curcumin is binding in the hydrophobic cavity of PLA2 with a binding energy -16.81 Kcal/mol. The binding mode is in such a manner that it can prevent the entry of substrate to the hydrophobic active site. These studies indicate that curcumin can be act as an inhibitor to PLA2.
+
Curcumin possess anti-inflammatory activity. The binding of curcumin with PLA2 was studied using X-ray crystallography. Since the electron density found in the active site did not match with curcumin, 2-methoxycyclohexa-2-5-diene-1,4-dione (MCW) (the photo-degraded product of curcumin) was fitted in the unexplained electron density. To understand the binding mode of actual curcumin, molecular docking studies was carried out. Both crystallographic and docked structures were superimposed with respect to the ligand position and identified that curcumin is binding in the hydrophobic cavity of PLA<sub>2</sub> with a binding energy -16.81 Kcal/mol. The binding mode is in such a manner that it can prevent the entry of substrate to the hydrophobic active site. These studies indicate that curcumin can be act as an inhibitor to PLA<sub>2</sub>.

Revision as of 10:04, 20 June 2012

Insert caption here

Drag the structure with the mouse to rotate

Crystal structure of porcine pancreatic phospholipase A2 in complex with 2-methoxycyclohexa-2-5-diene-1,4-dione

K V Dileep, I Tintu, P K Mandal, P Karthe, M Haridas and C Sadasivan[1]


Molecular Tour
Curcumin possess anti-inflammatory activity. The binding of curcumin with PLA2 was studied using X-ray crystallography. Since the electron density found in the active site did not match with curcumin, 2-methoxycyclohexa-2-5-diene-1,4-dione (MCW) (the photo-degraded product of curcumin) was fitted in the unexplained electron density. To understand the binding mode of actual curcumin, molecular docking studies was carried out. Both crystallographic and docked structures were superimposed with respect to the ligand position and identified that curcumin is binding in the hydrophobic cavity of PLA2 with a binding energy -16.81 Kcal/mol. The binding mode is in such a manner that it can prevent the entry of substrate to the hydrophobic active site. These studies indicate that curcumin can be act as an inhibitor to PLA2.


  1. none yet

Proteopedia Page Contributors and Editors (what is this?)

Alexander Berchansky, Jaime Prilusky

This page complements a publication in scientific journals and is one of the Proteopedia's Interactive 3D Complement pages. For aditional details please see I3DC.
Personal tools