1xxs

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(New page: 200px<br /><applet load="1xxs" size="450" color="white" frame="true" align="right" spinBox="true" caption="1xxs, resolution 1.8&Aring;" /> '''Structural insights f...)
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[[Image:1xxs.gif|left|200px]]<br /><applet load="1xxs" size="450" color="white" frame="true" align="right" spinBox="true"
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[[Image:1xxs.gif|left|200px]]<br /><applet load="1xxs" size="350" color="white" frame="true" align="right" spinBox="true"
caption="1xxs, resolution 1.8&Aring;" />
caption="1xxs, resolution 1.8&Aring;" />
'''Structural insights for fatty acid binding in a Lys49 phospholipase A2: crystal structure of myotoxin II from Bothrops moojeni complexed with stearic acid'''<br />
'''Structural insights for fatty acid binding in a Lys49 phospholipase A2: crystal structure of myotoxin II from Bothrops moojeni complexed with stearic acid'''<br />
==Overview==
==Overview==
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The crystal structure of dimeric Lys49-phospholipase A2 myotoxin-II from, Bothrops moojeni (MjTX-II) co-crystallized with stearic acid, (C(18)H(36)O(2)) has been determined at a resolution of 1.8 A. The, electron density maps permitted the unambiguous inclusion of six stearic, acid molecules in the refinement. Two stearic acid molecules could be, located in the substrate-binding cleft of each monomer in positions, which, favor the interaction of their carboxyl groups with active site residues., The way of binding of stearic acids to this Lys49-PLA(2)s is analogous to, phospholipids and transition state analogues to catalytically active, PLA(2)s. Two additional stearic acid molecules were located at the dimer, interface region, defining a hitherto unidentified acyl-binding site on, the protein surface. The strictly conserved Lys122 for Lys49-PLA(2)s may, play a fundamental role for stabilization of legend-protein complex. The, comparison of MjTX-II/satiric acid complex with other Lys-PLA(2)s, structures whose putative fatty acids were located at their active site is, also analysed. Molecular details of the stearic acid/protein interactions, provide insights to binding in group I/II PLA(2)s, and to the possible, interactions of Lys49-PLA(2)s with target membranes.
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The crystal structure of dimeric Lys49-phospholipase A2 myotoxin-II from Bothrops moojeni (MjTX-II) co-crystallized with stearic acid (C(18)H(36)O(2)) has been determined at a resolution of 1.8 A. The electron density maps permitted the unambiguous inclusion of six stearic acid molecules in the refinement. Two stearic acid molecules could be located in the substrate-binding cleft of each monomer in positions, which favor the interaction of their carboxyl groups with active site residues. The way of binding of stearic acids to this Lys49-PLA(2)s is analogous to phospholipids and transition state analogues to catalytically active PLA(2)s. Two additional stearic acid molecules were located at the dimer interface region, defining a hitherto unidentified acyl-binding site on the protein surface. The strictly conserved Lys122 for Lys49-PLA(2)s may play a fundamental role for stabilization of legend-protein complex. The comparison of MjTX-II/satiric acid complex with other Lys-PLA(2)s structures whose putative fatty acids were located at their active site is also analysed. Molecular details of the stearic acid/protein interactions provide insights to binding in group I/II PLA(2)s, and to the possible interactions of Lys49-PLA(2)s with target membranes.
==About this Structure==
==About this Structure==
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1XXS is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Bothrops_moojeni Bothrops moojeni] with SO4 and STE as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [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] Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1XXS OCA].
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1XXS is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Bothrops_moojeni Bothrops moojeni] with <scene name='pdbligand=SO4:'>SO4</scene> and <scene name='pdbligand=STE:'>STE</scene> as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [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] Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1XXS OCA].
==Reference==
==Reference==
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[[Category: Phospholipase A(2)]]
[[Category: Phospholipase A(2)]]
[[Category: Single protein]]
[[Category: Single protein]]
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[[Category: Arni, R.K.]]
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[[Category: Arni, R K.]]
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[[Category: Fontes, M.R.]]
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[[Category: Fontes, M R.]]
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[[Category: Soares, A.M.]]
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[[Category: Soares, A M.]]
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[[Category: Ward, R.J.]]
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[[Category: Ward, R J.]]
[[Category: Watanabe, L.]]
[[Category: Watanabe, L.]]
[[Category: SO4]]
[[Category: SO4]]
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[[Category: stearic acid]]
[[Category: stearic acid]]
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''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Wed Nov 21 06:25:13 2007''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 15:59:46 2008''

Revision as of 13:59, 21 February 2008


1xxs, resolution 1.8Å

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Structural insights for fatty acid binding in a Lys49 phospholipase A2: crystal structure of myotoxin II from Bothrops moojeni complexed with stearic acid

Overview

The crystal structure of dimeric Lys49-phospholipase A2 myotoxin-II from Bothrops moojeni (MjTX-II) co-crystallized with stearic acid (C(18)H(36)O(2)) has been determined at a resolution of 1.8 A. The electron density maps permitted the unambiguous inclusion of six stearic acid molecules in the refinement. Two stearic acid molecules could be located in the substrate-binding cleft of each monomer in positions, which favor the interaction of their carboxyl groups with active site residues. The way of binding of stearic acids to this Lys49-PLA(2)s is analogous to phospholipids and transition state analogues to catalytically active PLA(2)s. Two additional stearic acid molecules were located at the dimer interface region, defining a hitherto unidentified acyl-binding site on the protein surface. The strictly conserved Lys122 for Lys49-PLA(2)s may play a fundamental role for stabilization of legend-protein complex. The comparison of MjTX-II/satiric acid complex with other Lys-PLA(2)s structures whose putative fatty acids were located at their active site is also analysed. Molecular details of the stearic acid/protein interactions provide insights to binding in group I/II PLA(2)s, and to the possible interactions of Lys49-PLA(2)s with target membranes.

About this Structure

1XXS is a Single protein structure of sequence from Bothrops moojeni with and as ligands. Active as Phospholipase A(2), with EC number 3.1.1.4 Full crystallographic information is available from OCA.

Reference

Structural insights for fatty acid binding in a Lys49-phospholipase A2: crystal structure of myotoxin II from Bothrops moojeni complexed with stearic acid., Watanabe L, Soares AM, Ward RJ, Fontes MR, Arni RK, Biochimie. 2005 Feb;87(2):161-7. PMID:15760708

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