1qby
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(New page: 200px<br /><applet load="1qby" size="450" color="white" frame="true" align="right" spinBox="true" caption="1qby" /> '''THE SOLUTION STRUCTURE OF A BAY-REGION 1R-BE...)
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Revision as of 01:48, 25 November 2007
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THE SOLUTION STRUCTURE OF A BAY-REGION 1R-BENZ[A]ANTHRACENE OXIDE ADDUCT AT THE N6 POSITION OF ADENINE OF AN OLIGODEOXYNUCLEOTIDE CONTAINING THE HUMAN N-RAS CODON 61 SEQUENCE
Overview
The solution structure of the (-)-(1R,2S,3R,4S)-N6-[1-(1,2,3, 4-tetrahydroxy-benz[a]anthracenyl)]-2'-deoxyadenosyl adduct at X6 of, 5'-d(CGGACXAGAAG)-3'.5'-d(CTTCTTGTCCG)-3', incorporating codons 60, 61(italic), and 62 of the human N-ras protooncogene, was determined. This, adduct results from the trans opening of 1S,2R,3R,4S-1, 2-epoxy-1,2,3,4-tetrahydro-benz[a]anthracenyl-3,4-diol by the exocyclic N6, of adenine. Molecular dynamics simulations were restrained by 509 NOEs, from 1H NMR. The precision of the refined structures was monitored by, pairwise root-mean-square deviations which were <1.2 A; accuracy was, measured by complete relaxation matrix calculations, which yielded a sixth, root R factor of 9.1 x 10(-)2 at 250 ms. The refined structure was a, right-handed duplex, in which the benz[a]anthracene moiety intercalated, from the major groove between C5.G18 and R,S,R,SA6.T17. In this, orientation, the saturated ring of BA was oriented in the major groove of, the duplex, with the aromatic rings inserted into the duplex such that the, terminal ring of BA threaded the duplex and faced toward the minor groove, direction. The duplex suffered localized distortion at and immediately, adjacent to the adduct site, evidenced by the increased rise of 8.8 A as, compared to the value of 3.5 A normally observed for B-DNA between base, pairs C5.G18 and R,S,R,SA6.T17. These two base pairs also buckled in, opposite directions away from the intercalated BA moiety. The refined, structure was similar to the (-)-(7S,8R,9S,10R)-N6-[10-(7,8,9, 10)-tetrahydrobenzo[a]pyrenyl)]-2'-deoxyadenosyl adduct of corresponding, stereochemistry at X6 of the same oligodeoxynucleotide [Zegar, I. S., Kim, S. J., Johansen, T. N., Horton, P. J., Harris, C. M., Harris, T. M., and, Stone, M. P. (1996) Biochemistry 35, 6212-6224]. Both adducts intercalated, toward the 5'-direction from the site of adduction. The similarities in, solution structures were reflected in similar biological responses, when, repair-deficient AB2480 Escherichia coli were transformed with M13mp7L2, DNA site-specifically modified with these two adducts.
About this Structure
1QBY is a Protein complex structure of sequences from [1] with BZA as ligand. Full crystallographic information is available from OCA.
Reference
Intercalation of the (-)-(1R,2S,3R, 4S)-N6-[1-benz[a]anthracenyl]-2'-deoxyadenosyl adduct in an oligodeoxynucleotide containing the human N-ras codon 61 sequence., Li Z, Mao H, Kim HY, Tamura PJ, Harris CM, Harris TM, Stone MP, Biochemistry. 1999 Mar 9;38(10):2969-81. PMID:10074349[[Category: benz[a]anthracene-dna duplex]]
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Categories: Protein complex | Harris, C.M. | Harris, T.M. | Kim, H.Y. | Li, Z. | Mao, H. | Stone, M.P. | Tamura, P.J. | BZA | Intercalation