1q5t

From Proteopedia

(Difference between revisions)
Jump to: navigation, search
Line 1: Line 1:
[[Image:1q5t.gif|left|200px]]
[[Image:1q5t.gif|left|200px]]
-
{{Structure
+
<!--
-
|PDB= 1q5t |SIZE=350|CAPTION= <scene name='initialview01'>1q5t</scene>, resolution 1.90&Aring;
+
The line below this paragraph, containing "STRUCTURE_1q5t", creates the "Structure Box" on the page.
-
|SITE=
+
You may change the PDB parameter (which sets the PDB file loaded into the applet)
-
|LIGAND= <scene name='pdbligand=SO4:SULFATE+ION'>SO4</scene>
+
or the SCENE parameter (which sets the initial scene displayed when the page is loaded),
-
|ACTIVITY=
+
or leave the SCENE parameter empty for the default display.
-
|GENE=
+
-->
-
|DOMAIN=
+
{{STRUCTURE_1q5t| PDB=1q5t | SCENE= }}
-
|RELATEDENTRY=
+
-
|RESOURCES=<span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=1q5t FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1q5t OCA], [http://www.ebi.ac.uk/pdbsum/1q5t PDBsum], [http://www.rcsb.org/pdb/explore.do?structureId=1q5t RCSB]</span>
+
-
}}
+
'''Gln48 PLA2 separated from Vipoxin from the venom of Vipera ammodytes meridionalis.'''
'''Gln48 PLA2 separated from Vipoxin from the venom of Vipera ammodytes meridionalis.'''
Line 31: Line 28:
[[Category: Perbandt, M.]]
[[Category: Perbandt, M.]]
[[Category: Rypniewski, W.]]
[[Category: Rypniewski, W.]]
-
[[Category: toxin]]
+
[[Category: Toxin]]
-
 
+
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sat May 3 05:54:02 2008''
-
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun Mar 30 23:09:10 2008''
+

Revision as of 02:54, 3 May 2008

Template:STRUCTURE 1q5t

Gln48 PLA2 separated from Vipoxin from the venom of Vipera ammodytes meridionalis.


Overview

Phospholipase A2 is an "interfacial" enzyme and its binding to negatively charged surfaces is an important step during catalysis. The Gln48 phospholipase A2 from the venom of Vipera ammodytes meridionalis plays the role of chaperone and directs a toxic His48 PLA2 onto its acceptor. In the venom the two phospholipases A2 exist as a postsynaptic neurotoxic complex, Vipoxin. The X-ray structure of Gln48 PLA2, complexed to sulphate ions, which mimic the negatively charged groups of anionic membranes, has been determined by the molecular replacement method and refined to 1.9A resolution. The protein forms a homodimer stabilized by ionic, hydrophobic, and hydrogen-bond interactions. The structure reveals two anion-binding sites per subunit. These sites are probably involved in interactions with the negatively charged membrane surface and, in this way, in the "targeting" of the toxic component to the receptors of the postsynaptic membranes. In the absence of the chaperone subunit the toxin changes the target of the physiological attack. A comparison of the homodimeric Gln48 PLA2 structure with that of the heterodimeric Vipoxin reveals differences in regions involved in the pharmacological activity of the toxin. This fact, except the active site histidine substitution, can explain the absence of toxicity in the Gln48 protein in comparison to the His48 phospholipase A2.

About this Structure

1Q5T is a Single protein structure of sequence from Vipera ammodytes meridionalis. Full crystallographic information is available from OCA.

Reference

The X-ray structure of a snake venom Gln48 phospholipase A2 at 1.9A resolution reveals anion-binding sites., Georgieva DN, Perbandt M, Rypniewski W, Hristov K, Genov N, Betzel C, Biochem Biophys Res Commun. 2004 Mar 26;316(1):33-8. PMID:15003507 Page seeded by OCA on Sat May 3 05:54:02 2008

Proteopedia Page Contributors and Editors (what is this?)

OCA

Personal tools