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1fv8

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(New page: 200px<br /><applet load="1fv8" size="450" color="white" frame="true" align="right" spinBox="true" caption="1fv8" /> '''NMR STUDY OF AN HETEROCHIRAL HAIRPIN'''<br /...)
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[[Image:1fv8.gif|left|200px]]<br /><applet load="1fv8" size="450" color="white" frame="true" align="right" spinBox="true"
 
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caption="1fv8" />
 
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'''NMR STUDY OF AN HETEROCHIRAL HAIRPIN'''<br />
 
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==Overview==
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==NMR STUDY OF AN HETEROCHIRAL HAIRPIN==
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We carried out a structural study of the DNA heterochiral strand d, (AGCTTATCAT(L)CGATAAGCT), -AT(L)C-, where T(L) (L thymine ) replaces T, (natural D-thymine). -AT(L)C- is a structural analog of -ATC- that belongs, to a strong topoisomerase II DNA cleavage site and which has been shown to, resolve into a hairpin structure with a stem formed by eight Waston-Crick, base-pairs and a single residue loop closed by an A.C sheared base-pair., Although - AT(L)C-, like its parent -ATC-, folds into a hairpin structure, at low and high DNA concentrations it displays a lower stability (Tm of 56, degrees C versus 58.5 degrees C). Several NMR features in -AT(L)C- account, for the disruption of the A.C pairing in the loop and a weakening of the, C.G base-pair stability at the stem-loop junction. For instance, the, exchange of the loop imino protons with solvent is accelerated compared, with the natural oligonucleotide -ATC-. The higher flexibility of the, heterochiral loop is confirmed by the results of NMR restrained molecular, dynamics. In the calculated final structures of -AT(L)C-, the T10(L), residue moves the A9 and C11 residues away, thus preventing the loop, closure through a C.A sheared base-pair and the achievement of a good, base-base or sugar-base stacking. Actually, most of the stabilizing, interactions present in -ATC- are lost in the heterochiral - AT(L)C-, explaining its weaker stability.
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<StructureSection load='1fv8' size='340' side='right'caption='[[1fv8]]' scene=''>
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== Structural highlights ==
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<table><tr><td colspan='2'>[[1fv8]] is a 1 chain structure. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1FV8 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=1FV8 FirstGlance]. <br>
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</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">Solution NMR</td></tr>
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<tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=0DT:2-DEOXY-L-RIBO-FURANOSYL+THYMIDINE-5-MONOPHOSPHATE'>0DT</scene></td></tr>
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<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=1fv8 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1fv8 OCA], [https://pdbe.org/1fv8 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=1fv8 RCSB], [https://www.ebi.ac.uk/pdbsum/1fv8 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=1fv8 ProSAT]</span></td></tr>
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</table>
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<div style="background-color:#fffaf0;">
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== Publication Abstract from PubMed ==
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We carried out a structural study of the DNA heterochiral strand d (AGCTTATCAT(L)CGATAAGCT), -AT(L)C-, where T(L) (L thymine ) replaces T (natural D-thymine). -AT(L)C- is a structural analog of -ATC- that belongs to a strong topoisomerase II DNA cleavage site and which has been shown to resolve into a hairpin structure with a stem formed by eight Waston-Crick base-pairs and a single residue loop closed by an A.C sheared base-pair. Although - AT(L)C-, like its parent -ATC-, folds into a hairpin structure at low and high DNA concentrations it displays a lower stability (Tm of 56 degrees C versus 58.5 degrees C). Several NMR features in -AT(L)C- account for the disruption of the A.C pairing in the loop and a weakening of the C.G base-pair stability at the stem-loop junction. For instance, the exchange of the loop imino protons with solvent is accelerated compared with the natural oligonucleotide -ATC-. The higher flexibility of the heterochiral loop is confirmed by the results of NMR restrained molecular dynamics. In the calculated final structures of -AT(L)C-, the T10(L) residue moves the A9 and C11 residues away, thus preventing the loop closure through a C.A sheared base-pair and the achievement of a good base-base or sugar-base stacking. Actually, most of the stabilizing interactions present in -ATC- are lost in the heterochiral - AT(L)C- explaining its weaker stability.
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==About this Structure==
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NMR study of a heterochiral DNA hairpin:impact of L-enantiomery in the loop.,El Amri C, Mauffret O, Santamariar F, Tevanian G, Rayner S, Fermandjian S J Biomol Struct Dyn. 2001 Dec;19(3):459-70. PMID:11790144<ref>PMID:11790144</ref>
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1FV8 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=1FV8 OCA].
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==Reference==
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From MEDLINE&reg;/PubMed&reg;, a database of the U.S. National Library of Medicine.<br>
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NMR study of a heterochiral DNA hairpin:impact of L-enantiomery in the loop., El Amri C, Mauffret O, Santamariar F, Tevanian G, Rayner S, Fermandjian S, J Biomol Struct Dyn. 2001 Dec;19(3):459-70. PMID:[http://ispc.weizmann.ac.il//pmbin/getpm?pmid=11790144 11790144]
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</div>
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[[Category: Protein complex]]
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<div class="pdbe-citations 1fv8" style="background-color:#fffaf0;"></div>
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[[Category: Amri, C.El.]]
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== References ==
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[[Category: Fermandjian, S.]]
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<references/>
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[[Category: Mauffret, O.]]
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__TOC__
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[[Category: Rayner, B.]]
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</StructureSection>
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[[Category: Santamaria, F.]]
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[[Category: Large Structures]]
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[[Category: antisense dna]]
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[[Category: El Amri C]]
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[[Category: flexibilty]]
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[[Category: Fermandjian S]]
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[[Category: hairpin]]
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[[Category: Mauffret O]]
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[[Category: heterochiral loop]]
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[[Category: Rayner B]]
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[[Category: Santamaria F]]
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''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Sun Nov 25 00:24:25 2007''
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NMR STUDY OF AN HETEROCHIRAL HAIRPIN

PDB ID 1fv8

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