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208d

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(New page: 200px<br /><applet load="208d" size="350" color="white" frame="true" align="right" spinBox="true" caption="208d, resolution 2.050&Aring;" /> '''HIGH-RESOLUTION STR...)
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==Overview==
==Overview==
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Triple helices result from interaction between single- and double-stranded, nucleic acids. Their formation is a possible mechanism for recombination, of homologous gene sequences in nature and provides, inter alia, a basis, for artificial control of gene activity. Triple-helix motifs have been, extensively studied by a variety of techniques, but few high-resolution, structural data are available. The only triplet structures characterized, so far by X-ray diffraction were in protein-DNA complexes studied at about, 3 A resolution. We report here the X-ray analysis of a DNA nonamer, d(GCGAATTCG), to a resolution of 2.05 A, in which the extended crystal, structure contains (C.G)*G triplets as a fragment of triple helix. The, guanosine-containing chains are in a parallel orientation. This, arrangement is a necessary feature of models for homologous recombination, which results ultimately in replacement of one length of DNA by another of, similar sequence. The present-structure agrees with many published, predictions of triplex organization, and provides an accurate, representation of an element that allows sequence-specific association, between single- and double-stranded nucleic acids.
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Triple helices result from interaction between single- and double-stranded nucleic acids. Their formation is a possible mechanism for recombination of homologous gene sequences in nature and provides, inter alia, a basis for artificial control of gene activity. Triple-helix motifs have been extensively studied by a variety of techniques, but few high-resolution structural data are available. The only triplet structures characterized so far by X-ray diffraction were in protein-DNA complexes studied at about 3 A resolution. We report here the X-ray analysis of a DNA nonamer, d(GCGAATTCG), to a resolution of 2.05 A, in which the extended crystal structure contains (C.G)*G triplets as a fragment of triple helix. The guanosine-containing chains are in a parallel orientation. This arrangement is a necessary feature of models for homologous recombination which results ultimately in replacement of one length of DNA by another of similar sequence. The present-structure agrees with many published predictions of triplex organization, and provides an accurate representation of an element that allows sequence-specific association between single- and double-stranded nucleic acids.
==About this Structure==
==About this Structure==
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[[Category: Gallois, B.]]
[[Category: Gallois, B.]]
[[Category: Kennard, O.]]
[[Category: Kennard, O.]]
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[[Category: Meervelt, L.Van.]]
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[[Category: Meervelt, L Van.]]
[[Category: Precigoux, G.]]
[[Category: Precigoux, G.]]
[[Category: Vlieghe, D.]]
[[Category: Vlieghe, D.]]
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[[Category: double helix]]
[[Category: double helix]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Tue Jan 29 17:47:05 2008''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 16:20:51 2008''

Revision as of 14:20, 21 February 2008


208d, resolution 2.050Å

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HIGH-RESOLUTION STRUCTURE OF A DNA HELIX FORMING (C.G)*G BASE TRIPLETS

Overview

Triple helices result from interaction between single- and double-stranded nucleic acids. Their formation is a possible mechanism for recombination of homologous gene sequences in nature and provides, inter alia, a basis for artificial control of gene activity. Triple-helix motifs have been extensively studied by a variety of techniques, but few high-resolution structural data are available. The only triplet structures characterized so far by X-ray diffraction were in protein-DNA complexes studied at about 3 A resolution. We report here the X-ray analysis of a DNA nonamer, d(GCGAATTCG), to a resolution of 2.05 A, in which the extended crystal structure contains (C.G)*G triplets as a fragment of triple helix. The guanosine-containing chains are in a parallel orientation. This arrangement is a necessary feature of models for homologous recombination which results ultimately in replacement of one length of DNA by another of similar sequence. The present-structure agrees with many published predictions of triplex organization, and provides an accurate representation of an element that allows sequence-specific association between single- and double-stranded nucleic acids.

About this Structure

208D is a Protein complex structure of sequences from [1] with as ligand. Full crystallographic information is available from OCA.

Reference

High-resolution structure of a DNA helix forming (C.G)*G base triplets., Van Meervelt L, Vlieghe D, Dautant A, Gallois B, Precigoux G, Kennard O, Nature. 1995 Apr 20;374(6524):742-4. PMID:7715732

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