1oxl
From Proteopedia
Line 1: | Line 1: | ||
[[Image:1oxl.gif|left|200px]] | [[Image:1oxl.gif|left|200px]] | ||
- | + | <!-- | |
- | + | The line below this paragraph, containing "STRUCTURE_1oxl", creates the "Structure Box" on the page. | |
- | + | You may change the PDB parameter (which sets the PDB file loaded into the applet) | |
- | + | or the SCENE parameter (which sets the initial scene displayed when the page is loaded), | |
- | + | or leave the SCENE parameter empty for the default display. | |
- | | | + | --> |
- | | | + | {{STRUCTURE_1oxl| PDB=1oxl | SCENE= }} |
- | + | ||
- | + | ||
- | }} | + | |
'''INHIBITION OF PHOSPHOLIPASE A2 (PLA2) BY (2-CARBAMOYLMETHYL-5-PROPYL-OCTAHYDRO-INDOL-7-YL)-ACETIC ACID (INDOLE): CRYSTAL STRUCTURE OF THE COMPLEX FORMED BETWEEN PLA2 FROM RUSSELL'S VIPER AND INDOLE AT 1.8 RESOLUTION''' | '''INHIBITION OF PHOSPHOLIPASE A2 (PLA2) BY (2-CARBAMOYLMETHYL-5-PROPYL-OCTAHYDRO-INDOL-7-YL)-ACETIC ACID (INDOLE): CRYSTAL STRUCTURE OF THE COMPLEX FORMED BETWEEN PLA2 FROM RUSSELL'S VIPER AND INDOLE AT 1.8 RESOLUTION''' | ||
Line 24: | Line 21: | ||
Crystal structure of the complex of the secretory phospholipase A2 from Daboia russelli pulchella with an endogenic indole derivative, 2-carbamoylmethyl-5-propyl-octahydro-indol-7-yl-acetic acid at 1.8 A resolution., Balasubramanya R, Chandra V, Kaur P, Singh TP, Biochim Biophys Acta. 2005 Sep 25;1752(2):177-85. PMID:[http://www.ncbi.nlm.nih.gov/pubmed/16122995 16122995] | Crystal structure of the complex of the secretory phospholipase A2 from Daboia russelli pulchella with an endogenic indole derivative, 2-carbamoylmethyl-5-propyl-octahydro-indol-7-yl-acetic acid at 1.8 A resolution., Balasubramanya R, Chandra V, Kaur P, Singh TP, Biochim Biophys Acta. 2005 Sep 25;1752(2):177-85. PMID:[http://www.ncbi.nlm.nih.gov/pubmed/16122995 16122995] | ||
[[Category: Daboia russellii russellii]] | [[Category: Daboia russellii russellii]] | ||
- | [[Category: Phospholipase A(2)]] | ||
[[Category: Single protein]] | [[Category: Single protein]] | ||
[[Category: Balasubramanya, R.]] | [[Category: Balasubramanya, R.]] | ||
Line 30: | Line 26: | ||
[[Category: Kaur, P.]] | [[Category: Kaur, P.]] | ||
[[Category: Singh, T P.]] | [[Category: Singh, T P.]] | ||
- | [[Category: | + | [[Category: Crystal structure]] |
- | [[Category: | + | [[Category: Indole derivative]] |
- | [[Category: | + | [[Category: Inhibition]] |
- | [[Category: | + | [[Category: Phospholipase a2]] |
- | + | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sat May 3 04:24:06 2008'' | |
- | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on | + |
Revision as of 01:24, 3 May 2008
INHIBITION OF PHOSPHOLIPASE A2 (PLA2) BY (2-CARBAMOYLMETHYL-5-PROPYL-OCTAHYDRO-INDOL-7-YL)-ACETIC ACID (INDOLE): CRYSTAL STRUCTURE OF THE COMPLEX FORMED BETWEEN PLA2 FROM RUSSELL'S VIPER AND INDOLE AT 1.8 RESOLUTION
Overview
Phospholipase A2 (PLA2) enzymes from snake venoms are approximately 14 kDa secretory proteins and catalyze the release of arachidonic acid which is the precursor of proinflammatory mediators such as prostaglandins, leukotrienes, thromboxanes and platelet-activating factors. The structure of the PLA2 enzyme purified from the venom of Daboia russelli pulchella was determined using molecular replacement method and refined to an R value of 18.3% for all the reflections to 1.8 A resolution. The structure contains two crystallographically independent molecules A and B which form an asymmetric homodimer. The Ca2+ ion was not detected in the present structure, however, a characteristic non-protein high quality electron density was observed at the substrate-binding site of molecule A which allowed a clear interpretation of a natural ligand identified as a derivative of indole, 2-carbamoylmethyl-5-propyl-octahydro-indol-7-yl)-acetic acid. The corresponding substrate-binding site in molecule B was empty. The ligand present in molecule A is involved in extensive interactions with the protein atoms including important catalytic residues such as Asp-49 and His-48. The results also show that the indole derivatives act as potent inhibitors of secretory group II PLA2 enzymes that can be further modified to be used as potential therapeutic agents.
About this Structure
1OXL is a Single protein structure of sequence from Daboia russellii russellii. Full crystallographic information is available from OCA.
Reference
Crystal structure of the complex of the secretory phospholipase A2 from Daboia russelli pulchella with an endogenic indole derivative, 2-carbamoylmethyl-5-propyl-octahydro-indol-7-yl-acetic acid at 1.8 A resolution., Balasubramanya R, Chandra V, Kaur P, Singh TP, Biochim Biophys Acta. 2005 Sep 25;1752(2):177-85. PMID:16122995 Page seeded by OCA on Sat May 3 04:24:06 2008