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1ONM

Solution Structure of a DNA duplex containing A:G mismatch. d(GCTTCAGTCGT):d(ACGACGGAAGC)

Summary for 1ONM
Entry DOI10.2210/pdb1onm/pdb
NMR InformationBMRB: 5714
Descriptor5'-D(*GP*CP*TP*TP*CP*AP*GP*TP*CP*GP*T)-3', 5'-D(*AP*CP*GP*AP*CP*GP*GP*AP*AP*GP*C)-3' (2 entities in total)
Functional Keywordsa/g mismatch, a:g mismatch, a/g mispair, a:g mispair, dna
Total number of polymer chains2
Total formula weight6732.42
Authors
Sanchez, A.M.,Volk, D.E.,Gorenstein, D.G.,Lloyd, R.S. (deposition date: 2003-02-28, release date: 2003-11-04, Last modification date: 2024-05-22)
Primary citationSanchez, A.M.,Volk, D.E.,Gorenstein, D.G.,Lloyd, R.S.
Initiation of repair of A/G mismatches is modulated by sequence context
DNA REPAIR, 2:863-878, 2003
Cited by
PubMed Abstract: The efficiency of DNA glycosylases to initiate base excision repair (BER) has been demonstrated to be modulated by the precise sequence context in which the lesion or mismatch is located. In the case of DNA containing an A/G mismatch, in which the recognition and excision of adenine from the mismatch is mediated by the Escherichia coli MutY enzyme, not only does the local sequence context affect the strength of base stacking interactions, but it also modulates the syn/anti conformation around the glycosyl bond of the bases in the mispair. Utilizing prior NMR data to identify DNA sequence contexts that adopt either an anti/anti or a syn/anti configuration at an A/G mismatch, we tested the hypothesis that the initial equilibrium of the mismatched base orientations would modulate the overall efficiency of glycosyl bond scission. By systematically varying the sequence context around a central A/G mismatch within a 30-mer duplex DNA, significant kinetic differences were observed that were consistent with this hypothesis. Since the relative efficiency of the kinetics fell into only two groupings, a NMR study was conducted on a DNA sequence context of unknown syn/anti conformation. These data established that the relative syn/anti conformation did not correlate with the excision efficiency, as well as there being a lack of correlation between kinetics and thermal stability of these DNAs.
PubMed: 12893083
DOI: 10.1016/S1568-7864(03)00067-3
PDB entries with the same primary citation
Experimental method
SOLUTION NMR
Structure validation

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