1B5K
3,N4-ETHENO-2'-DEOXYCYTIDINE OPPOSITE THYMIDINE IN AN 11-MER DUPLEX, SOLUTION STRUCTURE FROM NMR AND MOLECULAR DYNAMICS
1B5K の概要
| エントリーDOI | 10.2210/pdb1b5k/pdb |
| 分子名称 | DNA (5'-D(*CP*GP*TP*AP*CP*EDCP*CP*AP*TP*GP*C)-3'), DNA (5'-D(*GP*CP*AP*TP*GP*TP*GP*TP*AP*CP*G)-3') (2 entities in total) |
| 機能のキーワード | ethenodc, edc, exocyclic lesion, dna |
| タンパク質・核酸の鎖数 | 2 |
| 化学式量合計 | 6707.41 |
| 構造登録者 | Cullinan, D.,Korobka, A.,Grollman, A.P.,Patel, D.J.,Eisenberg, M.,De Santos, C.L. (登録日: 1999-01-07, 公開日: 1999-01-13, 最終更新日: 2023-12-27) |
| 主引用文献 | Cullinan, D.,Korobka, A.,Grollman, A.P.,Patel, D.J.,Eisenberg, M.,De Los Santos, C. NMR solution structure of an oligodeoxynucleotide duplex containing the exocyclic lesion 3,N4-etheno-2'-deoxycytidine opposite thymidine: comparison with the duplex containing deoxyadenosine opposite the adduct. Biochemistry, 35:13319-13327, 1996 Cited by PubMed Abstract: The exocyclic 3,N4-etheno-2'-deoxycytidine adduct was incorporated at the center of the oligodeoxynucleotide duplex d(C-G-T-A-C-epsilon C-C-A-T-G-C).d (G-C-A-T-G-T-G-T-A-C-G), and its solution structure was analyzed using high-resolution proton NMR spectroscopy and molecular dynamics simulations. The experimental data indicate that the oligodeoxynucleotide duplex adopts a right-handed helical structure with sugar puckers in the C2'-endo/C3'-exo range and Watson-Crick hydrogen bond alignments for all base pairs. NOE connectivities established a syn orientation for the glycosidic torsion angle of the exocyclic adduct. Restrained molecular dynamics simulations, using the full relaxation matrix approach, produced a three-dimensional model in agreement with the experimental data. The structure shows only minor perturbations in the sugar-phosphate backbone and a 27 degrees bend of the helical axis at the lesion site. On the refined model a well-formed hydrogen bond between T (N3H) and epsilon C(N4) stabilizes the epsilon C(syn).T(anti) base pair alignment, reflecting the preference of the adduct for the syn orientation. Furthermore, the epsilon C(syn).T(anti) base pair stacks with flanking base pairs. We discuss a correlation between the mutagenic properties of the adduct and the three-dimensional structure of the epsilon C.dA and epsilon C.T duplexes. PubMed: 8873598DOI: 10.1021/bi9605705 主引用文献が同じPDBエントリー |
| 実験手法 | SOLUTION NMR |
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