1n1k: Difference between revisions

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[[Image:1n1k.gif|left|200px]]
[[Image:1n1k.gif|left|200px]]


{{Structure
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|SITE=
You may change the PDB parameter (which sets the PDB file loaded into the applet)
|LIGAND= <scene name='pdbligand=DC:2&#39;-DEOXYCYTIDINE-5&#39;-MONOPHOSPHATE'>DC</scene>, <scene name='pdbligand=DG:2&#39;-DEOXYGUANOSINE-5&#39;-MONOPHOSPHATE'>DG</scene>
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{{STRUCTURE_1n1k| PDB=1n1k  | SCENE= }}  
|RELATEDENTRY=
|RESOURCES=<span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=1n1k FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1n1k OCA], [http://www.ebi.ac.uk/pdbsum/1n1k PDBsum], [http://www.rcsb.org/pdb/explore.do?structureId=1n1k RCSB]</span>
}}


'''NMR Structure for d(CCGCGG)2'''
'''NMR Structure for d(CCGCGG)2'''
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==About this Structure==
==About this Structure==
1N1K is a [[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=1N1K OCA].  
Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1N1K OCA].  


==Reference==
==Reference==
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:[http://www.ncbi.nlm.nih.gov/pubmed/12646170 12646170]
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:[http://www.ncbi.nlm.nih.gov/pubmed/12646170 12646170]
[[Category: Protein complex]]
[[Category: Celda, B.]]
[[Category: Celda, B.]]
[[Category: Monleon, D.]]
[[Category: Monleon, D.]]
[[Category: ccgcgg]]
[[Category: Ccgcgg]]
[[Category: nmr]]
[[Category: Nmr]]
[[Category: recombination-like]]
[[Category: Recombination-like]]
 
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Revision as of 01:58, 3 May 2008

File:1n1k.gif

Template:STRUCTURE 1n1k

NMR Structure for d(CCGCGG)2


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

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 Page seeded by OCA on Sat May 3 01:58:34 2008

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