1xj9

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(New page: 200px<br /><applet load="1xj9" size="450" color="white" frame="true" align="right" spinBox="true" caption="1xj9, resolution 2.6&Aring;" /> '''Crystal structure of ...)
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[[Image:1xj9.jpg|left|200px]]<br /><applet load="1xj9" size="350" color="white" frame="true" align="right" spinBox="true"
caption="1xj9, resolution 2.6&Aring;" />
caption="1xj9, resolution 2.6&Aring;" />
'''Crystal structure of a partly self-complementary peptide nucleic acid (PNA) oligomer showing a duplex-triplex network'''<br />
'''Crystal structure of a partly self-complementary peptide nucleic acid (PNA) oligomer showing a duplex-triplex network'''<br />
==Overview==
==Overview==
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The X-ray structure of a partly self-complementary peptide nucleic acid, (PNA) decamer (H-GTAGATCACT-l-Lys-NH(2)) to 2.60 A resolution is reported., The structure is mainly controlled by the canonical Watson-Crick base, pairs formed by the self-complementary stretch of four bases in the middle, of the decamer (G(4)A(5)T(6)C(7)). One right- and one left-handed, Watson-Crick duplex are formed. The two PNA units C(9)T(10) change helical, handedness, so that each PNA strand contains both a right- and a, left-handed section. The changed handedness in C(9)T(10) allows formation, of Hoogsteen hydrogen bonding between C(9)T(10) and G(4)A(5) of a PNA, strand in an adjacent Watson-Crick double helix of the same handedness., Thereby, a PNA-PNA-PNA triplex is formed. The PNA unit A(3) forms a, noncanonical base pair with A(8) in a symmetry-related strand of opposite, handedness; the base pair is of the A-A reverse Hoogsteen type. The, structural diversity of this PNA demonstrates how the PNA backbone is able, to adapt to structures governed by the stacking and hydrogen-bonding, interactions between the nucleobases. The crystal structure further shows, how PNA oligomers containing limited sequence complementarity may form, complex hydrogen-bonding networks.
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The X-ray structure of a partly self-complementary peptide nucleic acid (PNA) decamer (H-GTAGATCACT-l-Lys-NH(2)) to 2.60 A resolution is reported. The structure is mainly controlled by the canonical Watson-Crick base pairs formed by the self-complementary stretch of four bases in the middle of the decamer (G(4)A(5)T(6)C(7)). One right- and one left-handed Watson-Crick duplex are formed. The two PNA units C(9)T(10) change helical handedness, so that each PNA strand contains both a right- and a left-handed section. The changed handedness in C(9)T(10) allows formation of Hoogsteen hydrogen bonding between C(9)T(10) and G(4)A(5) of a PNA strand in an adjacent Watson-Crick double helix of the same handedness. Thereby, a PNA-PNA-PNA triplex is formed. The PNA unit A(3) forms a noncanonical base pair with A(8) in a symmetry-related strand of opposite handedness; the base pair is of the A-A reverse Hoogsteen type. The structural diversity of this PNA demonstrates how the PNA backbone is able to adapt to structures governed by the stacking and hydrogen-bonding interactions between the nucleobases. The crystal structure further shows how PNA oligomers containing limited sequence complementarity may form complex hydrogen-bonding networks.
==About this Structure==
==About this Structure==
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1XJ9 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=1XJ9 OCA].
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1XJ9 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=1XJ9 OCA].
==Reference==
==Reference==
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[[Category: Protein complex]]
[[Category: Protein complex]]
[[Category: Gajhede, M.]]
[[Category: Gajhede, M.]]
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[[Category: Kastrup, J.S.]]
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[[Category: Kastrup, J S.]]
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[[Category: Larsen, I.K.]]
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[[Category: Larsen, I K.]]
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[[Category: Nielsen, B.B.]]
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[[Category: Nielsen, B B.]]
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[[Category: Nielsen, P.E.]]
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[[Category: Nielsen, P E.]]
[[Category: Petersson, B.]]
[[Category: Petersson, B.]]
[[Category: Rasmussen, H.]]
[[Category: Rasmussen, H.]]
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[[Category: right-handed]]
[[Category: right-handed]]
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''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Sun Nov 25 02:16:32 2007''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 15:55:33 2008''

Revision as of 13:55, 21 February 2008


1xj9, resolution 2.6Å

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Crystal structure of a partly self-complementary peptide nucleic acid (PNA) oligomer showing a duplex-triplex network

Overview

The X-ray structure of a partly self-complementary peptide nucleic acid (PNA) decamer (H-GTAGATCACT-l-Lys-NH(2)) to 2.60 A resolution is reported. The structure is mainly controlled by the canonical Watson-Crick base pairs formed by the self-complementary stretch of four bases in the middle of the decamer (G(4)A(5)T(6)C(7)). One right- and one left-handed Watson-Crick duplex are formed. The two PNA units C(9)T(10) change helical handedness, so that each PNA strand contains both a right- and a left-handed section. The changed handedness in C(9)T(10) allows formation of Hoogsteen hydrogen bonding between C(9)T(10) and G(4)A(5) of a PNA strand in an adjacent Watson-Crick double helix of the same handedness. Thereby, a PNA-PNA-PNA triplex is formed. The PNA unit A(3) forms a noncanonical base pair with A(8) in a symmetry-related strand of opposite handedness; the base pair is of the A-A reverse Hoogsteen type. The structural diversity of this PNA demonstrates how the PNA backbone is able to adapt to structures governed by the stacking and hydrogen-bonding interactions between the nucleobases. The crystal structure further shows how PNA oligomers containing limited sequence complementarity may form complex hydrogen-bonding networks.

About this Structure

1XJ9 is a Protein complex structure of sequences from [1]. Full crystallographic information is available from OCA.

Reference

Crystal structure of a partly self-complementary peptide nucleic acid (PNA) oligomer showing a duplex-triplex network., Petersson B, Nielsen BB, Rasmussen H, Larsen IK, Gajhede M, Nielsen PE, Kastrup JS, J Am Chem Soc. 2005 Feb 9;127(5):1424-30. PMID:15686374

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