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New page: left|200px<br /><applet load="2asm" size="450" color="white" frame="true" align="right" spinBox="true" caption="2asm, resolution 1.60Å" /> '''Structure of Rabbit ...
 
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[[Image:2asm.gif|left|200px]]<br /><applet load="2asm" size="450" color="white" frame="true" align="right" spinBox="true"  
[[Image:2asm.gif|left|200px]]<br /><applet load="2asm" size="350" color="white" frame="true" align="right" spinBox="true"  
caption="2asm, resolution 1.60&Aring;" />
caption="2asm, resolution 1.60&Aring;" />
'''Structure of Rabbit Actin In Complex With Reidispongiolide A'''<br />
'''Structure of Rabbit Actin In Complex With Reidispongiolide A'''<br />


==Overview==
==Overview==
Marine macrolides that disrupt the actin cytoskeleton are promising, candidates for cancer treatment. Here, we present the actin-bound x-ray, crystal structures of reidispongiolide A and C and sphinxolide B, three, marine macrolides found among a recently discovered family of cytotoxic, compounds. Their structures allow unequivocal assignment of the absolute, configuration for each compound. A comparison of their actin-binding site, to macrolides found in the trisoxazole family, as well as the divalent, macrolide, swinholide A, reveals the existence of a common binding surface, for a defined segment of their macrocyclic ring. This surface is located, on a hydrophobic patch adjacent to the cleft separating domains 1 and 3 at, the barbed-end of actin. The large area surrounding this surface, accommodates a wide variety of conformations and designs observed in the, macrocyclic component of barbed-end-targeting macrolides. Conversely, the, binding pocket for the macrolide tail, located within the cleft itself, shows very limited variation. Functional characterization of these, macrolides by using in vitro actin filament severing and polymerization, assays demonstrate the necessity of the N-methyl-vinylformamide moiety at, the terminus of the macrolide tail for toxin potency. These analyses also, show the importance of stable interactions between the macrocyclic ring, and the hydrophobic patch on actin for modifying filament structure and, how this stability can be compromised by subtle changes in macrolactone, ring composition. By identifying the essential components of these complex, natural products that underlie their high actin affinity, we have, established a framework for designing new therapeutic agents.
Marine macrolides that disrupt the actin cytoskeleton are promising candidates for cancer treatment. Here, we present the actin-bound x-ray crystal structures of reidispongiolide A and C and sphinxolide B, three marine macrolides found among a recently discovered family of cytotoxic compounds. Their structures allow unequivocal assignment of the absolute configuration for each compound. A comparison of their actin-binding site to macrolides found in the trisoxazole family, as well as the divalent macrolide, swinholide A, reveals the existence of a common binding surface for a defined segment of their macrocyclic ring. This surface is located on a hydrophobic patch adjacent to the cleft separating domains 1 and 3 at the barbed-end of actin. The large area surrounding this surface accommodates a wide variety of conformations and designs observed in the macrocyclic component of barbed-end-targeting macrolides. Conversely, the binding pocket for the macrolide tail, located within the cleft itself, shows very limited variation. Functional characterization of these macrolides by using in vitro actin filament severing and polymerization assays demonstrate the necessity of the N-methyl-vinylformamide moiety at the terminus of the macrolide tail for toxin potency. These analyses also show the importance of stable interactions between the macrocyclic ring and the hydrophobic patch on actin for modifying filament structure and how this stability can be compromised by subtle changes in macrolactone ring composition. By identifying the essential components of these complex natural products that underlie their high actin affinity, we have established a framework for designing new therapeutic agents.


==About this Structure==
==About this Structure==
2ASM is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Oryctolagus_cuniculus Oryctolagus cuniculus] with CA, ATP, RGA and EDO as [http://en.wikipedia.org/wiki/ligands ligands]. Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=2ASM OCA].  
2ASM is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Oryctolagus_cuniculus Oryctolagus cuniculus] with <scene name='pdbligand=CA:'>CA</scene>, <scene name='pdbligand=ATP:'>ATP</scene>, <scene name='pdbligand=RGA:'>RGA</scene> and <scene name='pdbligand=EDO:'>EDO</scene> as [http://en.wikipedia.org/wiki/ligands ligands]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2ASM OCA].  


==Reference==
==Reference==
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[[Category: Oryctolagus cuniculus]]
[[Category: Oryctolagus cuniculus]]
[[Category: Single protein]]
[[Category: Single protein]]
[[Category: Allingham, J.S.]]
[[Category: Allingham, J S.]]
[[Category: Auria, M.V.D.]]
[[Category: Auria, M V.D.]]
[[Category: Rayment, I.]]
[[Category: Rayment, I.]]
[[Category: Zampella, A.]]
[[Category: Zampella, A.]]
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[[Category: toxin]]
[[Category: toxin]]


''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Wed Nov 21 08:20:30 2007''
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 16:30:34 2008''