1nxn: Difference between revisions

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New page: left|200px<br /><applet load="1nxn" size="450" color="white" frame="true" align="right" spinBox="true" caption="1nxn" /> '''SOLUTION STRUCTURE OF CONTRYPHAN-VN'''<br />...
 
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[[Image:1nxn.gif|left|200px]]<br /><applet load="1nxn" size="450" color="white" frame="true" align="right" spinBox="true"  
[[Image:1nxn.gif|left|200px]]<br /><applet load="1nxn" size="350" color="white" frame="true" align="right" spinBox="true"  
caption="1nxn" />
caption="1nxn" />
'''SOLUTION STRUCTURE OF CONTRYPHAN-VN'''<br />
'''SOLUTION STRUCTURE OF CONTRYPHAN-VN'''<br />


==Overview==
==Overview==
The solution structure of contryphan-Vn, a cyclic peptide with a double, cysteine S-S bridge and containing a D-tryptophan extracted from the venom, of the cone snail Conus ventricosus, has been determined by NMR, spectroscopy using a variety of homonuclear and heteronuclear NMR methods, and restrained molecular dynamics simulations. The main conformational, features of backbone contryphan-Vn are a type IV beta-turn from Gly 1 to, Lys 6 and a type I beta-turn from Lys 6 to Cys 9. As already found in, other contryphans, one of the two prolines--the Pro4--is mainly in the cis, conformation while Pro7 is trans. A small hydrophobic region probably, partly shielded from solvent constituted from the close proximity of side, chains of Pro7 and Trp8 was observed together with a persistent salt, bridge between Asp2 and Lys6, which has been revealed by the diagnostic, observation of specific nuclear Overhauser effects. The salt bridge was, used as a restraint in the molecular dynamics in vacuum but without, inserting explicit electrostatic contribution in the calculations. The, backbone of the unique conformational family found of contryphan-Vn, superimposes well with those of contryphan-Sm and contryphan-R. This, result indicates that the contryphan structural motif represents a robust, and conserved molecular scaffold whose main structural determinants are, the size of the intercysteine loop and the presence and location in the, sequence of the D-Trp and the two Pro residues.
The solution structure of contryphan-Vn, a cyclic peptide with a double cysteine S-S bridge and containing a D-tryptophan extracted from the venom of the cone snail Conus ventricosus, has been determined by NMR spectroscopy using a variety of homonuclear and heteronuclear NMR methods and restrained molecular dynamics simulations. The main conformational features of backbone contryphan-Vn are a type IV beta-turn from Gly 1 to Lys 6 and a type I beta-turn from Lys 6 to Cys 9. As already found in other contryphans, one of the two prolines--the Pro4--is mainly in the cis conformation while Pro7 is trans. A small hydrophobic region probably partly shielded from solvent constituted from the close proximity of side chains of Pro7 and Trp8 was observed together with a persistent salt bridge between Asp2 and Lys6, which has been revealed by the diagnostic observation of specific nuclear Overhauser effects. The salt bridge was used as a restraint in the molecular dynamics in vacuum but without inserting explicit electrostatic contribution in the calculations. The backbone of the unique conformational family found of contryphan-Vn superimposes well with those of contryphan-Sm and contryphan-R. This result indicates that the contryphan structural motif represents a robust and conserved molecular scaffold whose main structural determinants are the size of the intercysteine loop and the presence and location in the sequence of the D-Trp and the two Pro residues.


==About this Structure==
==About this Structure==
1NXN is a [http://en.wikipedia.org/wiki/Protein_complex Protein complex] structure of sequences from [http://en.wikipedia.org/wiki/ ] with NH2 as [http://en.wikipedia.org/wiki/ligand ligand]. This structure superseeds the now removed PDB entry 1N3V. Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1NXN OCA].  
1NXN is a [http://en.wikipedia.org/wiki/Protein_complex Protein complex] structure of sequences from [http://en.wikipedia.org/wiki/ ] with <scene name='pdbligand=NH2:'>NH2</scene> as [http://en.wikipedia.org/wiki/ligand ligand]. This structure supersedes the now removed PDB entry 1N3V. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1NXN OCA].  


==Reference==
==Reference==
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[[Category: Protein complex]]
[[Category: Protein complex]]
[[Category: Ascenzi, P.]]
[[Category: Ascenzi, P.]]
[[Category: Cicero, D.O.]]
[[Category: Cicero, D O.]]
[[Category: Eliseo, T.]]
[[Category: Eliseo, T.]]
[[Category: Massilia, G.R.]]
[[Category: Massilia, G R.]]
[[Category: Paci, M.]]
[[Category: Paci, M.]]
[[Category: Polticelli, F.]]
[[Category: Polticelli, F.]]
[[Category: Schinina, M.E.]]
[[Category: Schinina, M E.]]
[[Category: NH2]]
[[Category: NH2]]
[[Category: cis-trans isomerism]]
[[Category: cis-trans isomerism]]
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[[Category: toxin]]
[[Category: toxin]]


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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 14:11:17 2008''