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1p0u

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(New page: 200px<br /><applet load="1p0u" size="450" color="white" frame="true" align="right" spinBox="true" caption="1p0u" /> '''Sheared G/C Base Pair'''<br /> ==Overview==...)
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'''Sheared G/C Base Pair'''<br />
'''Sheared G/C Base Pair'''<br />
==Overview==
==Overview==
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Stable DNA loop structures closed by a novel G.C base-pair have been, determined for the single-residue d(GXC) loops (X=A, T, G or C) in, low-salt solution by high-resolution nuclear magnetic resonance (NMR), techniques. The closing G.C base-pair in these loops is not of the, canonical Watson-Crick type, but adopts instead a unique sheared-type, (trans Watson-Crick/sugar-edge) pairing, like those occurring in the, sheared mismatched G.A or A.C base-pair, to draw the two opposite strands, together. The cytidine residue in the closing base-pair is transformed, into the rare syn domain to form two H-bonds with the guanine base and to, prevent the steric clash between the G 2NH(2) and the C H-5 protons., Besides, the sugar pucker of the syn cytidine is still located in the, regular C2'-endo domain, unlike the C3'-endo domain adopted for the, pyrimidines of the out-of-alternation left-handed Z-DNA structure. The, facile formation of the compact d(GXC) loops closed by a unique, sheared-type G(anti).C(syn) base-pair demonstrates the great potential of, the single-stranded d(GXC) triplet repeats to fold into stable hairpins.
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Stable DNA loop structures closed by a novel G.C base-pair have been determined for the single-residue d(GXC) loops (X=A, T, G or C) in low-salt solution by high-resolution nuclear magnetic resonance (NMR) techniques. The closing G.C base-pair in these loops is not of the canonical Watson-Crick type, but adopts instead a unique sheared-type (trans Watson-Crick/sugar-edge) pairing, like those occurring in the sheared mismatched G.A or A.C base-pair, to draw the two opposite strands together. The cytidine residue in the closing base-pair is transformed into the rare syn domain to form two H-bonds with the guanine base and to prevent the steric clash between the G 2NH(2) and the C H-5 protons. Besides, the sugar pucker of the syn cytidine is still located in the regular C2'-endo domain, unlike the C3'-endo domain adopted for the pyrimidines of the out-of-alternation left-handed Z-DNA structure. The facile formation of the compact d(GXC) loops closed by a unique sheared-type G(anti).C(syn) base-pair demonstrates the great potential of the single-stranded d(GXC) triplet repeats to fold into stable hairpins.
==About this Structure==
==About this Structure==
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1P0U 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=1P0U OCA].
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1P0U 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=1P0U OCA].
==Reference==
==Reference==
Sheared-type G(anti).C(syn) base-pair: a unique d(GXC) loop closure motif., Chin KH, Chou SH, J Mol Biol. 2003 May 30;329(2):351-61. PMID:[http://ispc.weizmann.ac.il//pmbin/getpm?pmid=12758081 12758081]
Sheared-type G(anti).C(syn) base-pair: a unique d(GXC) loop closure motif., Chin KH, Chou SH, J Mol Biol. 2003 May 30;329(2):351-61. PMID:[http://ispc.weizmann.ac.il//pmbin/getpm?pmid=12758081 12758081]
[[Category: Protein complex]]
[[Category: Protein complex]]
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[[Category: Chin, K.H.]]
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[[Category: Chin, K H.]]
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[[Category: Chou, S.H.]]
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[[Category: Chou, S H.]]
[[Category: nmr]]
[[Category: nmr]]
[[Category: sheared gc base pair]]
[[Category: sheared gc base pair]]
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[[Category: syn cytidine]]
[[Category: syn cytidine]]
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''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Sun Nov 25 01:46:47 2007''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 14:23:48 2008''

Revision as of 12:23, 21 February 2008


1p0u

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Sheared G/C Base Pair

Overview

Stable DNA loop structures closed by a novel G.C base-pair have been determined for the single-residue d(GXC) loops (X=A, T, G or C) in low-salt solution by high-resolution nuclear magnetic resonance (NMR) techniques. The closing G.C base-pair in these loops is not of the canonical Watson-Crick type, but adopts instead a unique sheared-type (trans Watson-Crick/sugar-edge) pairing, like those occurring in the sheared mismatched G.A or A.C base-pair, to draw the two opposite strands together. The cytidine residue in the closing base-pair is transformed into the rare syn domain to form two H-bonds with the guanine base and to prevent the steric clash between the G 2NH(2) and the C H-5 protons. Besides, the sugar pucker of the syn cytidine is still located in the regular C2'-endo domain, unlike the C3'-endo domain adopted for the pyrimidines of the out-of-alternation left-handed Z-DNA structure. The facile formation of the compact d(GXC) loops closed by a unique sheared-type G(anti).C(syn) base-pair demonstrates the great potential of the single-stranded d(GXC) triplet repeats to fold into stable hairpins.

About this Structure

1P0U is a Protein complex structure of sequences from [1]. Full crystallographic information is available from OCA.

Reference

Sheared-type G(anti).C(syn) base-pair: a unique d(GXC) loop closure motif., Chin KH, Chou SH, J Mol Biol. 2003 May 30;329(2):351-61. PMID:12758081

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