1p4z

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(New page: 200px<br /><applet load="1p4z" size="450" color="white" frame="true" align="right" spinBox="true" caption="1p4z, resolution 2.00&Aring;" /> '''Effect of Sequence o...)
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'''Effect of Sequence on the Conformational Geometry of DNA Holliday Junctions'''<br />
'''Effect of Sequence on the Conformational Geometry of DNA Holliday Junctions'''<br />
==Overview==
==Overview==
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Structures of the DNA sequences d(CCGGCGCCGG) and d(CCAGTACbr(5)UGG) are, presented here as four-way Holliday junctions in their compact stacked-X, forms, with antiparallel alignment of the DNA strands. Thus, the, ACC-trinucleotide motif, previously identified as important for, stabilizing the junction, is now extended to PuCPy, where Pu is either an, adenine or guanine, and Py is either a cytosine, 5-methylcytosine, or, 5-bromouracil but not thymine nucleotide. We see that both sequence and, base substituents affect the geometry of the junction in terms of the, interduplex angle as well as the previously defined conformational, variables, J(roll) (the rotation of the stacked duplexes about their, respective helical axis) and J(slide) (the translational displacement of, the stacked duplexes along their respective helical axis). The structures, of the GCC and parent ACC containing junctions fall into a distinct, conformational class that is relatively undistorted in terms of J(slide), and J(roll), with interduplex angles of 40-43 degrees. The substituted, ACbr(5)U structure, however, is more akin to that of the distorted, methylated ACm(5)C containing junction, with J(slide) (&gt;or=2.3 A) and a, similar J(roll) (164 degrees) opening the major groove-side of the, junction, but shows a reduced interduplex angle. In contrast, the, analogous d(CCAGTACTGG) sequence has to date been crystallized only as, resolved B-DNA duplexes. This suggests that there is an electronic effect, of substituents at the pyrimidine Py position on the stability of, four-stranded junctions. The single-crystal structures presented here, therefore, show how sequence affects the detailed geometry, and, subsequently, the associated stability and conformational dynamics of the, Holliday junction.
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Structures of the DNA sequences d(CCGGCGCCGG) and d(CCAGTACbr(5)UGG) are presented here as four-way Holliday junctions in their compact stacked-X forms, with antiparallel alignment of the DNA strands. Thus, the ACC-trinucleotide motif, previously identified as important for stabilizing the junction, is now extended to PuCPy, where Pu is either an adenine or guanine, and Py is either a cytosine, 5-methylcytosine, or 5-bromouracil but not thymine nucleotide. We see that both sequence and base substituents affect the geometry of the junction in terms of the interduplex angle as well as the previously defined conformational variables, J(roll) (the rotation of the stacked duplexes about their respective helical axis) and J(slide) (the translational displacement of the stacked duplexes along their respective helical axis). The structures of the GCC and parent ACC containing junctions fall into a distinct conformational class that is relatively undistorted in terms of J(slide) and J(roll), with interduplex angles of 40-43 degrees. The substituted ACbr(5)U structure, however, is more akin to that of the distorted methylated ACm(5)C containing junction, with J(slide) (&gt;or=2.3 A) and a similar J(roll) (164 degrees) opening the major groove-side of the junction, but shows a reduced interduplex angle. In contrast, the analogous d(CCAGTACTGG) sequence has to date been crystallized only as resolved B-DNA duplexes. This suggests that there is an electronic effect of substituents at the pyrimidine Py position on the stability of four-stranded junctions. The single-crystal structures presented here, therefore, show how sequence affects the detailed geometry, and subsequently, the associated stability and conformational dynamics of the Holliday junction.
==About this Structure==
==About this Structure==
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1P4Z is a [http://en.wikipedia.org/wiki/Protein_complex Protein complex] structure of sequences from [http://en.wikipedia.org/wiki/ ] with NA as [http://en.wikipedia.org/wiki/ligand ligand]. Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1P4Z OCA].
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1P4Z is a [http://en.wikipedia.org/wiki/Protein_complex Protein complex] structure of sequences from [http://en.wikipedia.org/wiki/ ] with <scene name='pdbligand=NA:'>NA</scene> as [http://en.wikipedia.org/wiki/ligand ligand]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1P4Z OCA].
==Reference==
==Reference==
Effect of sequence on the conformation of DNA holliday junctions., Hays FA, Vargason JM, Ho PS, Biochemistry. 2003 Aug 19;42(32):9586-97. PMID:[http://ispc.weizmann.ac.il//pmbin/getpm?pmid=12911300 12911300]
Effect of sequence on the conformation of DNA holliday junctions., Hays FA, Vargason JM, Ho PS, Biochemistry. 2003 Aug 19;42(32):9586-97. PMID:[http://ispc.weizmann.ac.il//pmbin/getpm?pmid=12911300 12911300]
[[Category: Protein complex]]
[[Category: Protein complex]]
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[[Category: Hays, F.A.]]
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[[Category: Hays, F A.]]
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[[Category: Ho, P.S.]]
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[[Category: Ho, P S.]]
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[[Category: Vargason, J.M.]]
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[[Category: Vargason, J M.]]
[[Category: NA]]
[[Category: NA]]
[[Category: b-dna]]
[[Category: b-dna]]
[[Category: double helix]]
[[Category: double helix]]
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''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Sun Nov 25 02:00:02 2007''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 14:25:10 2008''

Revision as of 12:25, 21 February 2008


1p4z, resolution 2.00Å

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Effect of Sequence on the Conformational Geometry of DNA Holliday Junctions

Overview

Structures of the DNA sequences d(CCGGCGCCGG) and d(CCAGTACbr(5)UGG) are presented here as four-way Holliday junctions in their compact stacked-X forms, with antiparallel alignment of the DNA strands. Thus, the ACC-trinucleotide motif, previously identified as important for stabilizing the junction, is now extended to PuCPy, where Pu is either an adenine or guanine, and Py is either a cytosine, 5-methylcytosine, or 5-bromouracil but not thymine nucleotide. We see that both sequence and base substituents affect the geometry of the junction in terms of the interduplex angle as well as the previously defined conformational variables, J(roll) (the rotation of the stacked duplexes about their respective helical axis) and J(slide) (the translational displacement of the stacked duplexes along their respective helical axis). The structures of the GCC and parent ACC containing junctions fall into a distinct conformational class that is relatively undistorted in terms of J(slide) and J(roll), with interduplex angles of 40-43 degrees. The substituted ACbr(5)U structure, however, is more akin to that of the distorted methylated ACm(5)C containing junction, with J(slide) (>or=2.3 A) and a similar J(roll) (164 degrees) opening the major groove-side of the junction, but shows a reduced interduplex angle. In contrast, the analogous d(CCAGTACTGG) sequence has to date been crystallized only as resolved B-DNA duplexes. This suggests that there is an electronic effect of substituents at the pyrimidine Py position on the stability of four-stranded junctions. The single-crystal structures presented here, therefore, show how sequence affects the detailed geometry, and subsequently, the associated stability and conformational dynamics of the Holliday junction.

About this Structure

1P4Z is a Protein complex structure of sequences from [1] with as ligand. Full crystallographic information is available from OCA.

Reference

Effect of sequence on the conformation of DNA holliday junctions., Hays FA, Vargason JM, Ho PS, Biochemistry. 2003 Aug 19;42(32):9586-97. PMID:12911300

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