1k8j

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(New page: 200px<br /><applet load="1k8j" size="450" color="white" frame="true" align="right" spinBox="true" caption="1k8j" /> '''NMR STRUCTURE OF THE CK14 DNA DUPLEX: A PORT...)
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[[Image:1k8j.gif|left|200px]]<br /><applet load="1k8j" size="350" color="white" frame="true" align="right" spinBox="true"
caption="1k8j" />
caption="1k8j" />
'''NMR STRUCTURE OF THE CK14 DNA DUPLEX: A PORTION OF THE KNOWN NF-kB SEQUENCE CK1'''<br />
'''NMR STRUCTURE OF THE CK14 DNA DUPLEX: A PORTION OF THE KNOWN NF-kB SEQUENCE CK1'''<br />
==Overview==
==Overview==
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A variety of monothio- and dithiosubstituted duplex aptamers targeting, NF-kappaB have been synthesized and designed. The specificity and affinity, of the dithioate aptamers of p50 and RelA(p65) NF-kappaB homodimers was, determined by gel shift experiments. The NMR solution structures for, several unmodified and dithioate backbone modified 14-base paired duplex, aptamers have been determined by a hybrid, complete matrix, (MORASS)/restrained molecular dynamics method. Structural perturbations of, the dithioate substitutions support our hypothesis that the dithioate, binds cations less tightly than phosphoryl groups. This increases the, electrostatic repulsion across the B-form narrow minor groove and enlarges, the minor groove, similar to that found in A-form duplexes. Structural, analysis of modeled aptamer complexes with NF-kappaB homo- and, heterodimers suggests that the dithioate backbone substitution can, increase the aptamer's relative affinity to basic groups in proteins such, as NF-kappaB by helping to "strip" the cations from the aptamer backbone.
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A variety of monothio- and dithiosubstituted duplex aptamers targeting NF-kappaB have been synthesized and designed. The specificity and affinity of the dithioate aptamers of p50 and RelA(p65) NF-kappaB homodimers was determined by gel shift experiments. The NMR solution structures for several unmodified and dithioate backbone modified 14-base paired duplex aptamers have been determined by a hybrid, complete matrix (MORASS)/restrained molecular dynamics method. Structural perturbations of the dithioate substitutions support our hypothesis that the dithioate binds cations less tightly than phosphoryl groups. This increases the electrostatic repulsion across the B-form narrow minor groove and enlarges the minor groove, similar to that found in A-form duplexes. Structural analysis of modeled aptamer complexes with NF-kappaB homo- and heterodimers suggests that the dithioate backbone substitution can increase the aptamer's relative affinity to basic groups in proteins such as NF-kappaB by helping to "strip" the cations from the aptamer backbone.
==About this Structure==
==About this Structure==
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1K8J is a [http://en.wikipedia.org/wiki/Protein_complex Protein complex] structure of sequences from [http://en.wikipedia.org/wiki/ ]. Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1K8J OCA].
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1K8J is a [http://en.wikipedia.org/wiki/Protein_complex Protein complex] structure of sequences from [http://en.wikipedia.org/wiki/ ]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1K8J OCA].
==Reference==
==Reference==
Solution structure and design of dithiophosphate backbone aptamers targeting transcription factor NF-kappaB., Volk DE, Yang X, Fennewald SM, King DJ, Bassett SE, Venkitachalam S, Herzog N, Luxon BA, Gorenstein DG, Bioorg Chem. 2002 Dec;30(6):396-419. PMID:[http://ispc.weizmann.ac.il//pmbin/getpm?pmid=12642125 12642125]
Solution structure and design of dithiophosphate backbone aptamers targeting transcription factor NF-kappaB., Volk DE, Yang X, Fennewald SM, King DJ, Bassett SE, Venkitachalam S, Herzog N, Luxon BA, Gorenstein DG, Bioorg Chem. 2002 Dec;30(6):396-419. PMID:[http://ispc.weizmann.ac.il//pmbin/getpm?pmid=12642125 12642125]
[[Category: Protein complex]]
[[Category: Protein complex]]
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[[Category: Bassett, S.E.]]
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[[Category: Bassett, S E.]]
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[[Category: Fennewald, S.M.]]
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[[Category: Fennewald, S M.]]
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[[Category: Gorenstein, D.G.]]
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[[Category: Gorenstein, D G.]]
[[Category: Herzog, N.]]
[[Category: Herzog, N.]]
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[[Category: King, D.J.]]
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[[Category: King, D J.]]
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[[Category: Luxon, B.A.]]
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[[Category: Luxon, B A.]]
[[Category: Venkitachalam, S.]]
[[Category: Venkitachalam, S.]]
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[[Category: Volk, D.E.]]
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[[Category: Volk, D E.]]
[[Category: Yang, X.]]
[[Category: Yang, X.]]
[[Category: ck1]]
[[Category: ck1]]
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[[Category: nf-kb]]
[[Category: nf-kb]]
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''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Sun Nov 25 00:55:25 2007''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 13:31:14 2008''

Revision as of 11:31, 21 February 2008


1k8j

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NMR STRUCTURE OF THE CK14 DNA DUPLEX: A PORTION OF THE KNOWN NF-kB SEQUENCE CK1

Overview

A variety of monothio- and dithiosubstituted duplex aptamers targeting NF-kappaB have been synthesized and designed. The specificity and affinity of the dithioate aptamers of p50 and RelA(p65) NF-kappaB homodimers was determined by gel shift experiments. The NMR solution structures for several unmodified and dithioate backbone modified 14-base paired duplex aptamers have been determined by a hybrid, complete matrix (MORASS)/restrained molecular dynamics method. Structural perturbations of the dithioate substitutions support our hypothesis that the dithioate binds cations less tightly than phosphoryl groups. This increases the electrostatic repulsion across the B-form narrow minor groove and enlarges the minor groove, similar to that found in A-form duplexes. Structural analysis of modeled aptamer complexes with NF-kappaB homo- and heterodimers suggests that the dithioate backbone substitution can increase the aptamer's relative affinity to basic groups in proteins such as NF-kappaB by helping to "strip" the cations from the aptamer backbone.

About this Structure

1K8J is a Protein complex structure of sequences from [1]. Full crystallographic information is available from OCA.

Reference

Solution structure and design of dithiophosphate backbone aptamers targeting transcription factor NF-kappaB., Volk DE, Yang X, Fennewald SM, King DJ, Bassett SE, Venkitachalam S, Herzog N, Luxon BA, Gorenstein DG, Bioorg Chem. 2002 Dec;30(6):396-419. PMID:12642125

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