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| Title: |  | MOLECULAR TOPOLOGY OF POLYCYCLIC AROMATIC CARCINOGENS DETERMINES DNA ADDUCT CONFORMATION: A LINK TO TUMORIGENIC ACTIVITY |  |
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| Molecular Description: | 5'-D(CpCpApTpCpGpCpTpApCpC)-3' 5'-D(GpGpTpApGpCpGpApTpGpG)-3' |
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| Nucleic Acid Sequence: |
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| Chain | A: | |
(DC) (DC) (DA) (DT) (DC) (DG) (DC) (DT) (DA) (DC) (DC)
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| Chain | B: | |
(DG) (DG) (DT) (DA) (DG) (DC) (DG) (DA) (DT) (DG) (DG)
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| Primary Citation: | Lin, C.H., Huang, X., Kolbanovskii, A., Hingerty, B.E., Amin, S., Broyde, S., Geacintov, N.E., Patel, D.J.
Molecular topology of polycyclic aromatic carcinogens determines DNA adduct conformation: a link to tumorigenic activity.
J.Mol.Biol.
, 306,
pp. 1059 - 1080, 2001.
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Experimental Information: | NMR |
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Number of Models: | 7 STRUCTURES |
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| Sample Details: |
trans-anti-BPh (carcinogen) covalently bound to 11mer DNA duplex
aqueous solution with 100 mM NaCl
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