2q0r: Difference between revisions
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==Structure of Pectenotoxin-2 Bound to Actin== | ==Structure of Pectenotoxin-2 Bound to Actin== | ||
<StructureSection load='2q0r' size='340' side='right' caption='[[2q0r]], [[Resolution|resolution]] 1.70Å' scene=''> | <StructureSection load='2q0r' size='340' side='right'caption='[[2q0r]], [[Resolution|resolution]] 1.70Å' scene=''> | ||
== Structural highlights == | == Structural highlights == | ||
<table><tr><td colspan='2'>[[2q0r]] is a 1 chain structure with sequence from [http://en.wikipedia.org/wiki/European_rabbit European rabbit]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2Q0R OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=2Q0R FirstGlance]. <br> | <table><tr><td colspan='2'>[[2q0r]] is a 1 chain structure with sequence from [http://en.wikipedia.org/wiki/European_rabbit European rabbit]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2Q0R OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=2Q0R FirstGlance]. <br> | ||
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</div> | </div> | ||
<div class="pdbe-citations 2q0r" style="background-color:#fffaf0;"></div> | <div class="pdbe-citations 2q0r" style="background-color:#fffaf0;"></div> | ||
==See Also== | |||
*[[Actin 3D structures|Actin 3D structures]] | |||
== References == | == References == | ||
<references/> | <references/> | ||
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</StructureSection> | </StructureSection> | ||
[[Category: European rabbit]] | [[Category: European rabbit]] | ||
[[Category: Large Structures]] | |||
[[Category: Allingham, J S]] | [[Category: Allingham, J S]] | ||
[[Category: Miles, C O]] | [[Category: Miles, C O]] | ||
Revision as of 10:51, 31 July 2019
Structure of Pectenotoxin-2 Bound to ActinStructure of Pectenotoxin-2 Bound to Actin
Structural highlights
Function[ACTS_RABIT] Actins are highly conserved proteins that are involved in various types of cell motility and are ubiquitously expressed in all eukaryotic cells. Publication Abstract from PubMed(PTXs) are polyether macrolides found in certain dinoflagellates, sponges and shellfish, and have been associated with diarrhetic shellfish poisoning. In addition to their in vivo toxicity, some PTXs are potently cytotoxic in human cancer cell lines. Recent studies have demonstrated that disruption of the actin cytoskeleton may be a key function of these compounds, although no clarification of their mechanism of action at a molecular level was available. We have obtained an X-ray crystal structure of PTX-2 bound to actin, which, in combination with analyses of the effect of PTX-2 on purified actin filament dynamics, provides a molecular explanation for its effects on actin. PTX-2 formed a 1:1 complex with actin and engaged a novel site between subdomains 1 and 3. Based on models of the actin filament, PTX binding would disrupt key lateral contacts between the PTX-bound actin monomer and the lower lateral actin monomer within the filament, thereby capping the barbed-end. The location of this binding position within the interior of the filament indicates that it may not be accessible once polymerization has occurred, a hypothesis supported by our observation that PTX-2 caused filament capping without inducing filament severing. This mode of action is unique, as other actin filament destabilizing toxins appear to exclusively disrupt longitudinal monomer contacts, allowing many of them to sever filaments in addition to capping them. Examination of the PTX-binding site on actin provides a rationalization for the structure-activity relationships observed in vivo and in vitro, and may provide a basis for predicting toxicity of PTX analogues. A structural basis for regulation of actin polymerization by pectenotoxins.,Allingham JS, Miles CO, Rayment I J Mol Biol. 2007 Aug 24;371(4):959-70. Epub 2007 May 25. PMID:17599353[1] From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine. See AlsoReferences
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