2lgm

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==Structure of DNA Containing an Aristolactam II-dA Lesion==
==Structure of DNA Containing an Aristolactam II-dA Lesion==
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<StructureSection load='2lgm' size='340' side='right' caption='[[2lgm]], [[NMR_Ensembles_of_Models | 26 NMR models]]' scene=''>
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<StructureSection load='2lgm' size='340' side='right'caption='[[2lgm]]' scene=''>
== Structural highlights ==
== Structural highlights ==
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[[2lgm]] is a 2 chain structure. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2LGM OCA]. <br>
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<table><tr><td colspan='2'>[[2lgm]] is a 2 chain structure. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2LGM OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=2LGM FirstGlance]. <br>
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<b>Activity:</b> <span class='plainlinks'>[http://en.wikipedia.org/wiki/Glucokinase Glucokinase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=2.7.1.2 2.7.1.2] </span><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=A4A:[1,3]BENZODIOXOLO[6,5,4-CD]BENZO[F]INDOL-5(6H)-ONE'>A4A</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=2lgm FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2lgm OCA], [https://pdbe.org/2lgm PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=2lgm RCSB], [https://www.ebi.ac.uk/pdbsum/2lgm PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=2lgm ProSAT]</span></td></tr>
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</table>
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<div style="background-color:#fffaf0;">
== Publication Abstract from PubMed ==
== Publication Abstract from PubMed ==
Aristolochic acids I and II are prevalent plant toxicants found in the Aristolochiaceae plant family. Metabolic activation of the aristolochic acids leads to the formation of a cyclic N-hydroxylactam product that can react with the peripheral amino group of purine bases generating bulky DNA adducts. These lesions are mutagenic and established human carcinogens. Interestingly, although AL-dG adducts progressively disappear from the DNA of laboratory animals, AL-dA lesions has lasting persistence in the genome. We describe here NMR structural studies of an undecameric duplex damaged at its center by the presence of an ALII-dA adduct. Our data establish a locally perturbed double helical structure that accommodates the bulky adduct by displacing the counter residue into the major groove and stacking the ALII moiety between flanking bases. The presence of the ALII-dA perturbs the conformation of the 5'-side flanking base pair, but all other pairs of the duplex adopt standard conformations. Thermodynamic studies reveal that the lesion slightly decreases the energy of duplex formation in a sequence-dependent manner. We discuss our results in terms of its implications for the repair of ALII-dA adducts in mammalian cells.
Aristolochic acids I and II are prevalent plant toxicants found in the Aristolochiaceae plant family. Metabolic activation of the aristolochic acids leads to the formation of a cyclic N-hydroxylactam product that can react with the peripheral amino group of purine bases generating bulky DNA adducts. These lesions are mutagenic and established human carcinogens. Interestingly, although AL-dG adducts progressively disappear from the DNA of laboratory animals, AL-dA lesions has lasting persistence in the genome. We describe here NMR structural studies of an undecameric duplex damaged at its center by the presence of an ALII-dA adduct. Our data establish a locally perturbed double helical structure that accommodates the bulky adduct by displacing the counter residue into the major groove and stacking the ALII moiety between flanking bases. The presence of the ALII-dA perturbs the conformation of the 5'-side flanking base pair, but all other pairs of the duplex adopt standard conformations. Thermodynamic studies reveal that the lesion slightly decreases the energy of duplex formation in a sequence-dependent manner. We discuss our results in terms of its implications for the repair of ALII-dA adducts in mammalian cells.
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Structure and stability of DNA containing an aristolactam II-dA lesion: implications for the NER recognition of bulky adducts.,Lukin M, Zaliznyak T, Johnson F, de Los Santos C Nucleic Acids Res. 2012 Mar 1;40(6):2759-70. Epub 2011 Nov 25. PMID:22121223<ref>PMID:22121223</ref>
Structure and stability of DNA containing an aristolactam II-dA lesion: implications for the NER recognition of bulky adducts.,Lukin M, Zaliznyak T, Johnson F, de Los Santos C Nucleic Acids Res. 2012 Mar 1;40(6):2759-70. Epub 2011 Nov 25. PMID:22121223<ref>PMID:22121223</ref>
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From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.<br>
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From MEDLINE&reg;/PubMed&reg;, a database of the U.S. National Library of Medicine.<br>
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</div>
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<div class="pdbe-citations 2lgm" style="background-color:#fffaf0;"></div>
== References ==
== References ==
<references/>
<references/>
__TOC__
__TOC__
</StructureSection>
</StructureSection>
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[[Category: Johnson, F.]]
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[[Category: Large Structures]]
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[[Category: Lukin, M.]]
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[[Category: Johnson F]]
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[[Category: Santos, C de los.]]
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[[Category: Lukin M]]
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[[Category: Zaliznyak, T.]]
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[[Category: Zaliznyak T]]
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[[Category: Dna]]
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[[Category: De los Santos C]]
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[[Category: Duplex stability]]
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[[Category: Ner recognition]]
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Structure of DNA Containing an Aristolactam II-dA Lesion

PDB ID 2lgm

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