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1d26

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(New page: 200px<br /><applet load="1d26" size="450" color="white" frame="true" align="right" spinBox="true" caption="1d26, resolution 2.120&Aring;" /> '''EFFECT OF A SINGLE ...)
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caption="1d26, resolution 2.120&Aring;" />
'''EFFECT OF A SINGLE 3'-METHYLENE PHOSPHONATE LINKAGE ON THE CONFORMATION OF AN A-DNA OCTAMER DOUBLE HELIX'''<br />
'''EFFECT OF A SINGLE 3'-METHYLENE PHOSPHONATE LINKAGE ON THE CONFORMATION OF AN A-DNA OCTAMER DOUBLE HELIX'''<br />
==Overview==
==Overview==
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The three-dimensional structure of the self-complementary DNA octamer, d(GCCCGpGGC) has been determined in the crystalline state using X-ray, diffraction data to a nominal resolutoin of 2.12 measured from a very, small crystal at DESY, Hamburg. The structure was refined with, stereochemical restraints to an R value of 17.1%. d(GCCCGpGGC), containing, one single 3'-methylene phosphonate linkage (denoted p), forms an A-DNA, double helix with strict dyad symmetry, that is distinct from canonical, A-DNA by a wide open major groove and a small average base-pair, inclination against the helix axis. The conformation of the unmodified, control d(GCCCGGGC) is known from an X-ray analysis of isomorphous, crystals (Heinemann et al. (1987) Nucleic Acids Res. 15, 9531-9550)., Comparison of the two structures reveals only minor conformational, differences, most notably in the pucker of the reduced deoxyribose. It is, suggested that oligonucleotides with charged 3'-methylene phosphonate, groups may form stable duplexes with complementary DNA or RNA strands, rendering them candidates for use as gene-regulatory antisense probes.
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The three-dimensional structure of the self-complementary DNA octamer d(GCCCGpGGC) has been determined in the crystalline state using X-ray diffraction data to a nominal resolutoin of 2.12 measured from a very small crystal at DESY, Hamburg. The structure was refined with stereochemical restraints to an R value of 17.1%. d(GCCCGpGGC), containing one single 3'-methylene phosphonate linkage (denoted p), forms an A-DNA double helix with strict dyad symmetry, that is distinct from canonical A-DNA by a wide open major groove and a small average base-pair inclination against the helix axis. The conformation of the unmodified control d(GCCCGGGC) is known from an X-ray analysis of isomorphous crystals (Heinemann et al. (1987) Nucleic Acids Res. 15, 9531-9550). Comparison of the two structures reveals only minor conformational differences, most notably in the pucker of the reduced deoxyribose. It is suggested that oligonucleotides with charged 3'-methylene phosphonate groups may form stable duplexes with complementary DNA or RNA strands rendering them candidates for use as gene-regulatory antisense probes.
==About this Structure==
==About this Structure==
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1D26 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=1D26 OCA].
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1D26 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=1D26 OCA].
==Reference==
==Reference==
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 12:12:08 2008''

Revision as of 10:12, 21 February 2008


1d26, resolution 2.120Å

Drag the structure with the mouse to rotate

EFFECT OF A SINGLE 3'-METHYLENE PHOSPHONATE LINKAGE ON THE CONFORMATION OF AN A-DNA OCTAMER DOUBLE HELIX

Overview

The three-dimensional structure of the self-complementary DNA octamer d(GCCCGpGGC) has been determined in the crystalline state using X-ray diffraction data to a nominal resolutoin of 2.12 measured from a very small crystal at DESY, Hamburg. The structure was refined with stereochemical restraints to an R value of 17.1%. d(GCCCGpGGC), containing one single 3'-methylene phosphonate linkage (denoted p), forms an A-DNA double helix with strict dyad symmetry, that is distinct from canonical A-DNA by a wide open major groove and a small average base-pair inclination against the helix axis. The conformation of the unmodified control d(GCCCGGGC) is known from an X-ray analysis of isomorphous crystals (Heinemann et al. (1987) Nucleic Acids Res. 15, 9531-9550). Comparison of the two structures reveals only minor conformational differences, most notably in the pucker of the reduced deoxyribose. It is suggested that oligonucleotides with charged 3'-methylene phosphonate groups may form stable duplexes with complementary DNA or RNA strands rendering them candidates for use as gene-regulatory antisense probes.

About this Structure

1D26 is a Protein complex structure of sequences from [1]. Full crystallographic information is available from OCA.

Reference

Effect of a single 3'-methylene phosphonate linkage on the conformation of an A-DNA octamer double helix., Heinemann U, Rudolph LN, Alings C, Morr M, Heikens W, Frank R, Blocker H, Nucleic Acids Res. 1991 Feb 11;19(3):427-33. PMID:2011517

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