1iey

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(New page: 200px<br /><applet load="1iey" size="450" color="white" frame="true" align="right" spinBox="true" caption="1iey" /> '''SOLUTION STRUCTURE OF THE DNA DUPLEX D(CCACC...)
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[[Image:1iey.gif|left|200px]]<br /><applet load="1iey" size="450" color="white" frame="true" align="right" spinBox="true"
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[[Image:1iey.gif|left|200px]]<br /><applet load="1iey" size="350" color="white" frame="true" align="right" spinBox="true"
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'''SOLUTION STRUCTURE OF THE DNA DUPLEX D(CCACCGGAAC).(GTTCCGGTGG) WITH A CHIRAL ALKYL-PHOSPHONATE MOIETY (DIAESTEREOISOMER R)'''<br />
'''SOLUTION STRUCTURE OF THE DNA DUPLEX D(CCACCGGAAC).(GTTCCGGTGG) WITH A CHIRAL ALKYL-PHOSPHONATE MOIETY (DIAESTEREOISOMER R)'''<br />
==Overview==
==Overview==
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The solution structures of two DNA decamers of sequence, d(CCACCpxGGAAC).(GTTCCGGTGG) with a chiral alkyl phosphonate moiety (px), have been determined using NMR and restrained molecular dynamics, simulations and compared with the solution structure of the unmodified, duplex. The (1)H NMR spectra of two samples with pure stereochemistry in, the modified phosphate have been assigned. The structures of both, diastereoisomers, as well as the unmodified control duplex, have been, determined from NMR-derived distance and torsion angle constraints., Accurate distance constraints were obtained from a complete relaxation, matrix analysis of the NOE intensities. The structures have been refined, with state of the art molecular dynamics methods, including explicit, solvent and applying the particle mesh Ewald method to properly evaluate, the long-range electrostatic interactions. In both cases, the calculations, converge to well-defined structures, with RMSDs of approximately 1 A. The, resulting structures belong to the general B family of DNA structures, even though the presence of the alkyl phosphonate moiety induces some, slight displacement to the A-form in the neighborhood of the modified, phosphate. Partial neutralization of this phosphate and the steric effect, of the alkyl moiety provoke moderate bending in the DNA. This effect is, more pronounced in the S diastereoisomer, where the alkyl group points, inwards to the double helix.
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The solution structures of two DNA decamers of sequence d(CCACCpxGGAAC).(GTTCCGGTGG) with a chiral alkyl phosphonate moiety (px) have been determined using NMR and restrained molecular dynamics simulations and compared with the solution structure of the unmodified duplex. The (1)H NMR spectra of two samples with pure stereochemistry in the modified phosphate have been assigned. The structures of both diastereoisomers, as well as the unmodified control duplex, have been determined from NMR-derived distance and torsion angle constraints. Accurate distance constraints were obtained from a complete relaxation matrix analysis of the NOE intensities. The structures have been refined with state of the art molecular dynamics methods, including explicit solvent and applying the particle mesh Ewald method to properly evaluate the long-range electrostatic interactions. In both cases, the calculations converge to well-defined structures, with RMSDs of approximately 1 A. The resulting structures belong to the general B family of DNA structures, even though the presence of the alkyl phosphonate moiety induces some slight displacement to the A-form in the neighborhood of the modified phosphate. Partial neutralization of this phosphate and the steric effect of the alkyl moiety provoke moderate bending in the DNA. This effect is more pronounced in the S diastereoisomer, where the alkyl group points inwards to the double helix.
==About this Structure==
==About this Structure==
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1IEY is a [http://en.wikipedia.org/wiki/Protein_complex Protein complex] structure of sequences from [http://en.wikipedia.org/wiki/ ] with OCT as [http://en.wikipedia.org/wiki/ligand ligand]. Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1IEY OCA].
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1IEY is a [http://en.wikipedia.org/wiki/Protein_complex Protein complex] structure of sequences from [http://en.wikipedia.org/wiki/ ] with <scene name='pdbligand=OCT:'>OCT</scene> as [http://en.wikipedia.org/wiki/ligand ligand]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1IEY OCA].
==Reference==
==Reference==
Solution structure of a DNA duplex with a chiral alkyl phosphonate moiety., Soliva R, Monaco V, Gomez-Pinto I, Meeuwenoord NJ, Marel GA, Boom JH, Gonzalez C, Orozco M, Nucleic Acids Res. 2001 Jul 15;29(14):2973-85. PMID:[http://ispc.weizmann.ac.il//pmbin/getpm?pmid=11452022 11452022]
Solution structure of a DNA duplex with a chiral alkyl phosphonate moiety., Soliva R, Monaco V, Gomez-Pinto I, Meeuwenoord NJ, Marel GA, Boom JH, Gonzalez C, Orozco M, Nucleic Acids Res. 2001 Jul 15;29(14):2973-85. PMID:[http://ispc.weizmann.ac.il//pmbin/getpm?pmid=11452022 11452022]
[[Category: Protein complex]]
[[Category: Protein complex]]
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[[Category: Boom, J.H.van.]]
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[[Category: Boom, J H.van.]]
[[Category: Gomez-Pinto, I.]]
[[Category: Gomez-Pinto, I.]]
[[Category: Gonzalez, C.]]
[[Category: Gonzalez, C.]]
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[[Category: Marel, G.A.van.der.]]
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[[Category: Marel, G A.van der.]]
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[[Category: Meeuwenoord, N.J.]]
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[[Category: Meeuwenoord, N J.]]
[[Category: Monaco, V.]]
[[Category: Monaco, V.]]
[[Category: Orozco, M.]]
[[Category: Orozco, M.]]
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[[Category: modified oligonucleotide]]
[[Category: modified oligonucleotide]]
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''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Sat Nov 24 21:55:04 2007''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 13:11:13 2008''

Revision as of 11:11, 21 February 2008


1iey

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SOLUTION STRUCTURE OF THE DNA DUPLEX D(CCACCGGAAC).(GTTCCGGTGG) WITH A CHIRAL ALKYL-PHOSPHONATE MOIETY (DIAESTEREOISOMER R)

Overview

The solution structures of two DNA decamers of sequence d(CCACCpxGGAAC).(GTTCCGGTGG) with a chiral alkyl phosphonate moiety (px) have been determined using NMR and restrained molecular dynamics simulations and compared with the solution structure of the unmodified duplex. The (1)H NMR spectra of two samples with pure stereochemistry in the modified phosphate have been assigned. The structures of both diastereoisomers, as well as the unmodified control duplex, have been determined from NMR-derived distance and torsion angle constraints. Accurate distance constraints were obtained from a complete relaxation matrix analysis of the NOE intensities. The structures have been refined with state of the art molecular dynamics methods, including explicit solvent and applying the particle mesh Ewald method to properly evaluate the long-range electrostatic interactions. In both cases, the calculations converge to well-defined structures, with RMSDs of approximately 1 A. The resulting structures belong to the general B family of DNA structures, even though the presence of the alkyl phosphonate moiety induces some slight displacement to the A-form in the neighborhood of the modified phosphate. Partial neutralization of this phosphate and the steric effect of the alkyl moiety provoke moderate bending in the DNA. This effect is more pronounced in the S diastereoisomer, where the alkyl group points inwards to the double helix.

About this Structure

1IEY is a Protein complex structure of sequences from [1] with as ligand. Full crystallographic information is available from OCA.

Reference

Solution structure of a DNA duplex with a chiral alkyl phosphonate moiety., Soliva R, Monaco V, Gomez-Pinto I, Meeuwenoord NJ, Marel GA, Boom JH, Gonzalez C, Orozco M, Nucleic Acids Res. 2001 Jul 15;29(14):2973-85. PMID:11452022

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