1qkg

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(New page: 200px<br /><applet load="1qkg" size="450" color="white" frame="true" align="right" spinBox="true" caption="1qkg" /> '''DNA DECAMER DUPLEX CONTAINING T-T DEWAR PHOT...)
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[[Image:1qkg.gif|left|200px]]<br /><applet load="1qkg" size="350" color="white" frame="true" align="right" spinBox="true"
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'''DNA DECAMER DUPLEX CONTAINING T-T DEWAR PHOTOPRODUCT'''<br />
'''DNA DECAMER DUPLEX CONTAINING T-T DEWAR PHOTOPRODUCT'''<br />
==Overview==
==Overview==
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In contrast to the highly mutagenic pyrimidine(6-4)pyrimidone, photoproduct, its Dewar valence isomer (Dewar product) has low mutagenic, potential and produces a broad range of mutations [LeClerc, J. E., Borden, A. &amp; Lawrence, C. W. (1991) Proc. Natl. Acad. Sci. USA 88, 9685-9689]. To, determine the origin of the mutagenic property of the Dewar product, we, used experimental NMR restraints and molecular dynamics to determine the, solution structure of a Dewar-lesion DNA decamer duplex. This DNA decamer, duplex (DW/GA duplex) contains a mismatched base pair between the 3' T, residue of the Dewar lesion (T6) and an opposed G residue (G15). The 3' T, (T6) of the Dewar lesion formed stable hydrogen bonds with the opposing, G15 residue. However, the helical bending and unwinding angles of the, DW/GA duplex were much larger than those of a second duplex that contains, the Dewar lesion and opposing A15 and A16 residues (DW/AA duplex). The, DW/GA duplex showed poorer stacking interactions at the two bases of the, Dewar product and at the adjacent A7 small middle dotT14 base pair than, did the DW/AA duplex. These structural features imply that no thermal, stability or conformational benefit is obtained by incorporating a G, instead of an A opposite the 3' T of the Dewar lesion. These properties, may thus facilitate the preferential incorporation of an A in accordance, with the A rule during translesion replication and lead to the low, frequency of 3' T--&gt;C mutations observed at this site.
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In contrast to the highly mutagenic pyrimidine(6-4)pyrimidone photoproduct, its Dewar valence isomer (Dewar product) has low mutagenic potential and produces a broad range of mutations [LeClerc, J. E., Borden, A. &amp; Lawrence, C. W. (1991) Proc. Natl. Acad. Sci. USA 88, 9685-9689]. To determine the origin of the mutagenic property of the Dewar product, we used experimental NMR restraints and molecular dynamics to determine the solution structure of a Dewar-lesion DNA decamer duplex. This DNA decamer duplex (DW/GA duplex) contains a mismatched base pair between the 3' T residue of the Dewar lesion (T6) and an opposed G residue (G15). The 3' T (T6) of the Dewar lesion formed stable hydrogen bonds with the opposing G15 residue. However, the helical bending and unwinding angles of the DW/GA duplex were much larger than those of a second duplex that contains the Dewar lesion and opposing A15 and A16 residues (DW/AA duplex). The DW/GA duplex showed poorer stacking interactions at the two bases of the Dewar product and at the adjacent A7 small middle dotT14 base pair than did the DW/AA duplex. These structural features imply that no thermal stability or conformational benefit is obtained by incorporating a G instead of an A opposite the 3' T of the Dewar lesion. These properties may thus facilitate the preferential incorporation of an A in accordance with the A rule during translesion replication and lead to the low frequency of 3' T--&gt;C mutations observed at this site.
==About this Structure==
==About this Structure==
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1QKG is a [http://en.wikipedia.org/wiki/Protein_complex Protein complex] structure of sequences from [http://en.wikipedia.org/wiki/ ]. Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1QKG OCA].
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1QKG is a [http://en.wikipedia.org/wiki/Protein_complex Protein complex] structure of sequences from [http://en.wikipedia.org/wiki/ ]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1QKG OCA].
==Reference==
==Reference==
The Dewar photoproduct of thymidylyl(3'--&gt;5')- thymidine (Dewar product) exhibits mutagenic behavior in accordance with the "A rule"., Lee JH, Bae SH, Choi BS, Proc Natl Acad Sci U S A. 2000 Apr 25;97(9):4591-6. PMID:[http://ispc.weizmann.ac.il//pmbin/getpm?pmid=10758155 10758155]
The Dewar photoproduct of thymidylyl(3'--&gt;5')- thymidine (Dewar product) exhibits mutagenic behavior in accordance with the "A rule"., Lee JH, Bae SH, Choi BS, Proc Natl Acad Sci U S A. 2000 Apr 25;97(9):4591-6. PMID:[http://ispc.weizmann.ac.il//pmbin/getpm?pmid=10758155 10758155]
[[Category: Protein complex]]
[[Category: Protein complex]]
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[[Category: Bae, S.H.]]
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[[Category: Bae, S H.]]
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[[Category: Choi, B.S.]]
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[[Category: Choi, B S.]]
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[[Category: Choi, Y.J.]]
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[[Category: Choi, Y J.]]
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[[Category: Lee, J.H.]]
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[[Category: Lee, J H.]]
[[Category: (6-4) adduct]]
[[Category: (6-4) adduct]]
[[Category: dewar product]]
[[Category: dewar product]]
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[[Category: translesion replication]]
[[Category: translesion replication]]
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''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Sun Nov 25 04:10:31 2007''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 14:40:40 2008''

Revision as of 12:40, 21 February 2008


1qkg

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DNA DECAMER DUPLEX CONTAINING T-T DEWAR PHOTOPRODUCT

Overview

In contrast to the highly mutagenic pyrimidine(6-4)pyrimidone photoproduct, its Dewar valence isomer (Dewar product) has low mutagenic potential and produces a broad range of mutations [LeClerc, J. E., Borden, A. & Lawrence, C. W. (1991) Proc. Natl. Acad. Sci. USA 88, 9685-9689]. To determine the origin of the mutagenic property of the Dewar product, we used experimental NMR restraints and molecular dynamics to determine the solution structure of a Dewar-lesion DNA decamer duplex. This DNA decamer duplex (DW/GA duplex) contains a mismatched base pair between the 3' T residue of the Dewar lesion (T6) and an opposed G residue (G15). The 3' T (T6) of the Dewar lesion formed stable hydrogen bonds with the opposing G15 residue. However, the helical bending and unwinding angles of the DW/GA duplex were much larger than those of a second duplex that contains the Dewar lesion and opposing A15 and A16 residues (DW/AA duplex). The DW/GA duplex showed poorer stacking interactions at the two bases of the Dewar product and at the adjacent A7 small middle dotT14 base pair than did the DW/AA duplex. These structural features imply that no thermal stability or conformational benefit is obtained by incorporating a G instead of an A opposite the 3' T of the Dewar lesion. These properties may thus facilitate the preferential incorporation of an A in accordance with the A rule during translesion replication and lead to the low frequency of 3' T-->C mutations observed at this site.

About this Structure

1QKG is a Protein complex structure of sequences from [1]. Full crystallographic information is available from OCA.

Reference

The Dewar photoproduct of thymidylyl(3'-->5')- thymidine (Dewar product) exhibits mutagenic behavior in accordance with the "A rule"., Lee JH, Bae SH, Choi BS, Proc Natl Acad Sci U S A. 2000 Apr 25;97(9):4591-6. PMID:10758155

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