1aok

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|PDB= 1aok |SIZE=350|CAPTION= <scene name='initialview01'>1aok</scene>, resolution 2.0&Aring;
|PDB= 1aok |SIZE=350|CAPTION= <scene name='initialview01'>1aok</scene>, resolution 2.0&Aring;
|SITE=
|SITE=
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|LIGAND= <scene name='pdbligand=ACT:ACETATE ION'>ACT</scene>
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|LIGAND= <scene name='pdbligand=ACT:ACETATE+ION'>ACT</scene>
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|ACTIVITY= [http://en.wikipedia.org/wiki/Phospholipase_A(2) Phospholipase A(2)], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.1.1.4 3.1.1.4]
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|ACTIVITY= <span class='plainlinks'>[http://en.wikipedia.org/wiki/Phospholipase_A(2) Phospholipase A(2)], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.1.1.4 3.1.1.4] </span>
|GENE=
|GENE=
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|DOMAIN=
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|RELATEDENTRY=
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|RESOURCES=<span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=1aok FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1aok OCA], [http://www.ebi.ac.uk/pdbsum/1aok PDBsum], [http://www.rcsb.org/pdb/explore.do?structureId=1aok RCSB]</span>
}}
}}
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[[Category: Perbandt, M.]]
[[Category: Perbandt, M.]]
[[Category: Wilson, J C.]]
[[Category: Wilson, J C.]]
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[[Category: ACT]]
 
[[Category: hydrolase]]
[[Category: hydrolase]]
[[Category: phospholipase]]
[[Category: phospholipase]]
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[[Category: vipoxin]]
[[Category: vipoxin]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Mar 20 10:00:19 2008''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun Mar 30 18:44:33 2008''

Revision as of 15:44, 30 March 2008


PDB ID 1aok

Drag the structure with the mouse to rotate
, resolution 2.0Å
Ligands:
Activity: Phospholipase A(2), with EC number 3.1.1.4
Resources: FirstGlance, OCA, PDBsum, RCSB
Coordinates: save as pdb, mmCIF, xml



VIPOXIN COMPLEX


Overview

Vipoxin is the main toxic component in the venom of the Bulgarian snake Vipera ammodytes meridionalis, the most toxic snake in Europe. Vipoxin is a complex between a toxic phospholipase A2 (PLA2) and a non-toxic protein inhibitor. The structure is of genetic interest due to the high degree of sequence homology (62%) between the two functionally different components. The structure shows that the formation of the complex in vipoxin is significantly different to that seen in many known structures of phospholipases and contradicts the assumptions made in earlier studies. The modulation of PLA2 activity is of great pharmacological interest, and the present structure will be a model for structure-based drug design.

About this Structure

1AOK is a Protein complex structure of sequences from Vipera ammodytes meridionalis. Full crystallographic information is available from OCA.

Reference

Crystal structure of vipoxin at 2.0 A: an example of regulation of a toxic function generated by molecular evolution., Perbandt M, Wilson JC, Eschenburg S, Mancheva I, Aleksiev B, Genov N, Willingmann P, Weber W, Singh TP, Betzel C, FEBS Lett. 1997 Aug 4;412(3):573-7. PMID:9276469

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