1d19

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[[Image:1d19.gif|left|200px]]
[[Image:1d19.gif|left|200px]]
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{{Structure
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|PDB= 1d19 |SIZE=350|CAPTION= <scene name='initialview01'>1d19</scene>
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The line below this paragraph, containing "STRUCTURE_1d19", creates the "Structure Box" on the page.
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|SITE=
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You may change the PDB parameter (which sets the PDB file loaded into the applet)
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|LIGAND= <scene name='pdbligand=DA:2&#39;-DEOXYADENOSINE-5&#39;-MONOPHOSPHATE'>DA</scene>, <scene name='pdbligand=DC:2&#39;-DEOXYCYTIDINE-5&#39;-MONOPHOSPHATE'>DC</scene>, <scene name='pdbligand=DG:2&#39;-DEOXYGUANOSINE-5&#39;-MONOPHOSPHATE'>DG</scene>, <scene name='pdbligand=DT:THYMIDINE-5&#39;-MONOPHOSPHATE'>DT</scene>
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|ACTIVITY=
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|GENE=
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|DOMAIN=
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{{STRUCTURE_1d19| PDB=1d19 | SCENE= }}
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|RELATEDENTRY=[[1d18|1D18]]
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|RESOURCES=<span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=1d19 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1d19 OCA], [http://www.ebi.ac.uk/pdbsum/1d19 PDBsum], [http://www.rcsb.org/pdb/explore.do?structureId=1d19 RCSB]</span>
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}}
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'''SOLUTION CONFORMATION OF PURINE-PYRIMIDINE DNA OCTAMERS USING NUCLEAR MAGNETIC RESONANCE, RESTRAINED MOLECULAR DYNAMICS AND NOE-BASED REFINEMENT'''
'''SOLUTION CONFORMATION OF PURINE-PYRIMIDINE DNA OCTAMERS USING NUCLEAR MAGNETIC RESONANCE, RESTRAINED MOLECULAR DYNAMICS AND NOE-BASED REFINEMENT'''
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==About this Structure==
==About this Structure==
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1D19 is a [[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=1D19 OCA].
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Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1D19 OCA].
==Reference==
==Reference==
Solution conformation of purine-pyrimidine DNA octamers using nuclear magnetic resonance, restrained molecular dynamics and NOE-based refinement., Baleja JD, Germann MW, van de Sande JH, Sykes BD, J Mol Biol. 1990 Oct 5;215(3):411-28. PMID:[http://www.ncbi.nlm.nih.gov/pubmed/2231713 2231713]
Solution conformation of purine-pyrimidine DNA octamers using nuclear magnetic resonance, restrained molecular dynamics and NOE-based refinement., Baleja JD, Germann MW, van de Sande JH, Sykes BD, J Mol Biol. 1990 Oct 5;215(3):411-28. PMID:[http://www.ncbi.nlm.nih.gov/pubmed/2231713 2231713]
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[[Category: Protein complex]]
 
[[Category: Baleja, J D.]]
[[Category: Baleja, J D.]]
[[Category: Sykes, B D.]]
[[Category: Sykes, B D.]]
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[[Category: dna]]
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[[Category: Dna]]
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[[Category: double helix]]
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[[Category: Double helix]]
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[[Category: nmr]]
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[[Category: Nmr]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Fri May 2 13:20:07 2008''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun Mar 30 19:32:32 2008''
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Revision as of 10:20, 2 May 2008

Image:1d19.gif

Template:STRUCTURE 1d19

SOLUTION CONFORMATION OF PURINE-PYRIMIDINE DNA OCTAMERS USING NUCLEAR MAGNETIC RESONANCE, RESTRAINED MOLECULAR DYNAMICS AND NOE-BASED REFINEMENT


Overview

The solution structures of two alternating purine-pyrimidine octamers, [d(G-T-A-C-G-T-A-C)]2 and the reverse sequence [d(C-A-T-G-C-A-T-G)]2, are investigated by using nuclear magnetic resonance spectroscopy and restrained molecular dynamics calculations. Chemical shift assignments are obtained for non-exchangeable protons by a combination of two-dimensional correlation and nuclear Overhauser enhancement (NOE) spectroscopy experiments. Distances between protons are estimated by extrapolating distances derived from time-dependent NOE measurements to zero mixing time. Approximate dihedral angles are determined within the deoxyribose ring from coupling constants observed in one and two-dimensional spectra. Sets of distance and dihedral determinations for each of the duplexes form the bases for structure determination. Molecular dynamics is then used to generate structures that satisfy the experimental restraints incorporated as effective potentials into the total energy. Separate runs start from classical A and B-form DNA and converge to essentially identical structures. To circumvent the problems of spin diffusion and differential motion associated with distance measurements within molecules, models are improved by NOE-based refinement in which observed NOE intensities are compared to those calculated using a full matrix analysis procedure. The refined structures generally have the global features of B-type DNA. Some, but not all, variations in dihedral angles and in the spatial relationships of adjacent base-pairs are observed to be in synchrony with the alternating purine-pyrimidine sequence.

About this Structure

Full crystallographic information is available from OCA.

Reference

Solution conformation of purine-pyrimidine DNA octamers using nuclear magnetic resonance, restrained molecular dynamics and NOE-based refinement., Baleja JD, Germann MW, van de Sande JH, Sykes BD, J Mol Biol. 1990 Oct 5;215(3):411-28. PMID:2231713 Page seeded by OCA on Fri May 2 13:20:07 2008

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