1n1k

Revision as of 23:16, 24 November 2007 by OCA (talk | contribs) (New page: left|200px<br /><applet load="1n1k" size="450" color="white" frame="true" align="right" spinBox="true" caption="1n1k" /> '''NMR Structure for d(CCGCGG)2'''<br /> ==Ove...)
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NMR Structure for d(CCGCGG)2

File:1n1k.gif


1n1k

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OverviewOverview

Long repeated stretches of d(CCG) and tri-nucleotide are crucial mutations, that cause hereditary forms of mental retardation (fragile X-syndrome)., Moreover, the alternating (CG) di-nucleotide is one of the candidates for, Z-DNA conformation. Solution NMR structure of d(CCGCGG)(2) has been solved, and is discussed. The determined NMR solution structure is a distorted, highly bent B-DNA conformation with increased flexibility in both terminal, residues. This conformation differs significantly from the Z-DNA tetramer, structure reported for the same hexamer in the crystal state at similar, ionic strength by Malinina and co-workers. Crystal structure of, d(CCGCGG)(2) at high salt concentration includes a central alternating, tetramer in Z-DNA conformation, while the initial cytosine swings out and, forms a Watson-Crick base-pair with the terminal guanine of a, symmetry-related molecule. In solution, NMR data for sugar ring puckering, combined with restrained molecular dynamics simulations starting from a, Z-DNA form show that terminal furanose residues could adopt the, conformation required for aromatic bases swinging out. Therefore, tetramer, formation could be considered possible once the hexanucleotide had, previously adopted the Z-DNA form. This work gives some insight into, correlations between anomalous crystal structures and their accessibility, in the solution state.

About this StructureAbout this Structure

1N1K is a Protein complex structure of sequences from [1]. Full crystallographic information is available from OCA.

ReferenceReference

NMR study of hexanucleotide d(CCGCGG)2 containing two triplet repeats of fragile X syndrome., Monleon D, Esteve V, Celda B, Biochem Biophys Res Commun. 2003 Mar 28;303(1):81-90. PMID:12646170

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