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1oci

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(New page: 200px<br /><applet load="1oci" size="450" color="white" frame="true" align="right" spinBox="true" caption="1oci" /> '''[3.2.0]BCANA:DNA'''<br /> ==Overview== [3.2...)
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'''[3.2.0]BCANA:DNA'''<br />
'''[3.2.0]BCANA:DNA'''<br />
==Overview==
==Overview==
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[3.2.0]bcANA is a D-arabino-configured bicyclic nucleotide with a, 2'-O,3'-C-methylene bridge. We here present the high-resolution NMR, structure of a [3.2.0]bcANA modified dsDNA nonamer with one modified, nucleotide incorporated. NOE restraints were obtained by analysis of NOESY, cross peak intensities using a full relaxation matrix approach, and, subsequently these restraints were incorporated into a simulated annealing, scheme for the structure determination. In addition, the furanose ring, puckers of the deoxyribose moieties were determined by analysis of COSY, cross peaks. The modified duplex adopts a B-like geometry with, Watson-Crick base pairing in all base pairs and all glycosidic angles in, the anti range. The stacking arrangement of the nucleobases appears to be, unperturbed relative to the normal B-like arrangement. The, 2'-O,3'-C-methylene bridge of the modified nucleotide is located at the, brim of the major groove where it fits well into the B-type duplex, framework. The sugar pucker of the [3.2.0]bcANA nucleotide is O4'-endo and, this sugar conformation causes a change in the delta backbone angle, relative to the C2'-endo deoxyribose sugar pucker. This change is absorbed, locally by slight changes in the epsilon and zeta angles of the modified, nucleotide. Overall, the [3.2.0]bcANA modifications fits very well into a, B-like duplex framework and only small and local perturbations are, observed relative to the unmodified dsDNA of identical base sequence.
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[3.2.0]bcANA is a D-arabino-configured bicyclic nucleotide with a 2'-O,3'-C-methylene bridge. We here present the high-resolution NMR structure of a [3.2.0]bcANA modified dsDNA nonamer with one modified nucleotide incorporated. NOE restraints were obtained by analysis of NOESY cross peak intensities using a full relaxation matrix approach, and subsequently these restraints were incorporated into a simulated annealing scheme for the structure determination. In addition, the furanose ring puckers of the deoxyribose moieties were determined by analysis of COSY cross peaks. The modified duplex adopts a B-like geometry with Watson-Crick base pairing in all base pairs and all glycosidic angles in the anti range. The stacking arrangement of the nucleobases appears to be unperturbed relative to the normal B-like arrangement. The 2'-O,3'-C-methylene bridge of the modified nucleotide is located at the brim of the major groove where it fits well into the B-type duplex framework. The sugar pucker of the [3.2.0]bcANA nucleotide is O4'-endo and this sugar conformation causes a change in the delta backbone angle relative to the C2'-endo deoxyribose sugar pucker. This change is absorbed locally by slight changes in the epsilon and zeta angles of the modified nucleotide. Overall, the [3.2.0]bcANA modifications fits very well into a B-like duplex framework and only small and local perturbations are observed relative to the unmodified dsDNA of identical base sequence.
==About this Structure==
==About this Structure==
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1OCI is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/ ]. Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1OCI OCA].
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1OCI is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/ ]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1OCI OCA].
==Reference==
==Reference==
NMR solution structure of dsDNA containing a bicyclic D-arabino-configured nucleotide fixed in an O4'-endo sugar conformation., Tommerholt HV, Christensen NK, Nielsen P, Wengel J, Stein PC, Jacobsen JP, Petersen M, Org Biomol Chem. 2003 May 21;1(10):1790-7. PMID:[http://ispc.weizmann.ac.il//pmbin/getpm?pmid=12926371 12926371]
NMR solution structure of dsDNA containing a bicyclic D-arabino-configured nucleotide fixed in an O4'-endo sugar conformation., Tommerholt HV, Christensen NK, Nielsen P, Wengel J, Stein PC, Jacobsen JP, Petersen M, Org Biomol Chem. 2003 May 21;1(10):1790-7. PMID:[http://ispc.weizmann.ac.il//pmbin/getpm?pmid=12926371 12926371]
[[Category: Single protein]]
[[Category: Single protein]]
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[[Category: Christensen, N.K.]]
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[[Category: Christensen, N K.]]
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[[Category: Jacobsen, J.P.]]
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[[Category: Jacobsen, J P.]]
[[Category: Nielsen, P.]]
[[Category: Nielsen, P.]]
[[Category: Petersen, M.]]
[[Category: Petersen, M.]]
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[[Category: Stein, P.C.]]
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[[Category: Stein, P C.]]
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[[Category: Tommerholt, H.V.]]
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[[Category: Tommerholt, H V.]]
[[Category: Wengel, J.]]
[[Category: Wengel, J.]]
[[Category: arabino nucleic acid]]
[[Category: arabino nucleic acid]]
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[[Category: rnase h]]
[[Category: rnase h]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 14:16:04 2008''

Revision as of 12:16, 21 February 2008


1oci

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[3.2.0]BCANA:DNA

Overview

[3.2.0]bcANA is a D-arabino-configured bicyclic nucleotide with a 2'-O,3'-C-methylene bridge. We here present the high-resolution NMR structure of a [3.2.0]bcANA modified dsDNA nonamer with one modified nucleotide incorporated. NOE restraints were obtained by analysis of NOESY cross peak intensities using a full relaxation matrix approach, and subsequently these restraints were incorporated into a simulated annealing scheme for the structure determination. In addition, the furanose ring puckers of the deoxyribose moieties were determined by analysis of COSY cross peaks. The modified duplex adopts a B-like geometry with Watson-Crick base pairing in all base pairs and all glycosidic angles in the anti range. The stacking arrangement of the nucleobases appears to be unperturbed relative to the normal B-like arrangement. The 2'-O,3'-C-methylene bridge of the modified nucleotide is located at the brim of the major groove where it fits well into the B-type duplex framework. The sugar pucker of the [3.2.0]bcANA nucleotide is O4'-endo and this sugar conformation causes a change in the delta backbone angle relative to the C2'-endo deoxyribose sugar pucker. This change is absorbed locally by slight changes in the epsilon and zeta angles of the modified nucleotide. Overall, the [3.2.0]bcANA modifications fits very well into a B-like duplex framework and only small and local perturbations are observed relative to the unmodified dsDNA of identical base sequence.

About this Structure

1OCI is a Single protein structure of sequence from [1]. Full crystallographic information is available from OCA.

Reference

NMR solution structure of dsDNA containing a bicyclic D-arabino-configured nucleotide fixed in an O4'-endo sugar conformation., Tommerholt HV, Christensen NK, Nielsen P, Wengel J, Stein PC, Jacobsen JP, Petersen M, Org Biomol Chem. 2003 May 21;1(10):1790-7. PMID:12926371

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