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TitleNuclear Magnetic Resonance Studies of an N(2)-Guanine Adduct Derived from the Tumorigen Dibenzo[a,l]pyrene in DNA: Impact of Adduct Stereochemistry, Size, and Local DNA Sequence on Solution Conformations.
Journal, issue, pagesBiochemistry, Vol. 53, Page 1827-1841, Year 2014
Publish dateDec 20, 2013 (structure data deposition date)
AuthorsRodriguez, F.A. / Liu, Z. / Lin, C.H. / Ding, S. / Cai, Y. / Kolbanovskiy, A. / Kolbanovskiy, M. / Amin, S. / Broyde, S. / Geacintov, N.E.
External linksBiochemistry / PubMed:24617538
MethodsNMR (solution)
Structure data

PDB-2miv:
NMR studies of N2-guanine adducts derived from the tumorigen dibenzo[a,l]pyrene in DNA: Impact of adduct stereochemistry, size, and local DNA structure on solution conformations
Method: SOLUTION NMR

PDB-2miw:
Nuclear magnetic resonance studies of N2-guanine adducts derived from the tumorigen dibenzo[a,l]pyrene in DNA: Impact of adduct stereochemistry, size, and local DNA structure on solution conformations
Method: SOLUTION NMR

Chemicals

ChemComp-2QL:
(11R,12R,13R)-11,12,13,14-tetrahydronaphtho[1,2,3,4-pqr]tetraphene-11,12,13-triol

KeywordsDNA / 14S(-)-trans-anti-DB[a / l]P-N2-dG / DNA adduct / 14S (-)-trans-anti-DB[a

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