1e1a

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[[Image:1e1a.jpg|left|200px]]
[[Image:1e1a.jpg|left|200px]]
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{{Structure
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|PDB= 1e1a |SIZE=350|CAPTION= <scene name='initialview01'>1e1a</scene>, resolution 1.8&Aring;
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The line below this paragraph, containing "STRUCTURE_1e1a", creates the "Structure Box" on the page.
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|SITE= <scene name='pdbsite=DFP:Ca+Binding+Site+For+Chain+A'>DFP</scene>
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You may change the PDB parameter (which sets the PDB file loaded into the applet)
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|LIGAND= <scene name='pdbligand=CA:CALCIUM+ION'>CA</scene>
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or the SCENE parameter (which sets the initial scene displayed when the page is loaded),
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|ACTIVITY= <span class='plainlinks'>[http://en.wikipedia.org/wiki/Diisopropyl-fluorophosphatase Diisopropyl-fluorophosphatase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.1.8.2 3.1.8.2] </span>
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{{STRUCTURE_1e1a| PDB=1e1a | SCENE= }}
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|RELATEDENTRY=
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|RESOURCES=<span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=1e1a FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1e1a OCA], [http://www.ebi.ac.uk/pdbsum/1e1a PDBsum], [http://www.rcsb.org/pdb/explore.do?structureId=1e1a RCSB]</span>
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'''CRYSTAL STRUCTURE OF DFPASE FROM LOLIGO VULGARIS'''
'''CRYSTAL STRUCTURE OF DFPASE FROM LOLIGO VULGARIS'''
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[[Category: Rueterjans, H.]]
[[Category: Rueterjans, H.]]
[[Category: Scharff, E I.]]
[[Category: Scharff, E I.]]
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[[Category: beta-propeller]]
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[[Category: Beta-propeller]]
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[[Category: calcium-binding site]]
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[[Category: Calcium-binding site]]
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[[Category: phosphotriesterase (pte)]]
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[[Category: Selenometionine]]
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[[Category: selenometionine]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Fri May 2 14:32:06 2008''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun Mar 30 19:53:02 2008''
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Revision as of 11:32, 2 May 2008

Template:STRUCTURE 1e1a

CRYSTAL STRUCTURE OF DFPASE FROM LOLIGO VULGARIS


Overview

BACKGROUND: Phosphotriesterases (PTE) are enzymes capable of detoxifying organophosphate-based chemical warfare agents by hydrolysis. One subclass of these enzymes comprises the family of diisopropylfluorophosphatases (DFPases). The DFPase reported here was originally isolated from squid head ganglion of Loligo vulgaris and can be characterized as squid-type DFPase. It is capable of hydrolyzing the organophosphates diisopropylfluorophosphate, soman, sarin, tabun, and cyclosarin. RESULTS: Crystals were grown of both the native and the selenomethionine-labeled enzyme. The X-ray crystal structure of the DFPase from Loligo vulgaris has been solved by MAD phasing and refined to a crystallographic R value of 17.6% at a final resolution of 1.8 A. Using site-directed mutagenesis, we have structurally and functionally characterized essential residues in the active site of the enzyme. CONCLUSIONS: The crystal structure of the DFPase from Loligo vulgaris is the first example of a structural characterization of a squid-type DFPase and the second crystal structure of a PTE determined to date. Therefore, it may serve as a structural model for squid-type DFPases in general. The overall structure of this protein represents a six-fold beta propeller with two calcium ions bound in a central water-filled tunnel. The consensus motif found in the blades of this beta propeller has not yet been observed in other beta propeller structures. Based on the results obtained from mutants of active-site residues, a mechanistic model for the DFP hydrolysis has been developed.

About this Structure

1E1A is a Single protein structure of sequence from Loligo vulgaris. Full crystallographic information is available from OCA.

Reference

Crystal structure of diisopropylfluorophosphatase from Loligo vulgaris., Scharff EI, Koepke J, Fritzsch G, Lucke C, Ruterjans H, Structure. 2001 Jun;9(6):493-502. PMID:11435114 Page seeded by OCA on Fri May 2 14:32:06 2008

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