5o7t

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m (Protected "5o7t" [edit=sysop:move=sysop])
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'''Unreleased structure'''
 
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The entry 5o7t is ON HOLD until Paper Publication
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==Crystal structure of KlenTaq mutant M747K in a closed ternary complex with a dG:dCTP base pair==
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<StructureSection load='5o7t' size='340' side='right' caption='[[5o7t]], [[Resolution|resolution]] 1.80&Aring;' scene=''>
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== Structural highlights ==
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<table><tr><td colspan='2'>[[5o7t]] is a 3 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=5O7T OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=5O7T FirstGlance]. <br>
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</td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=DCP:2-DEOXYCYTIDINE-5-TRIPHOSPHATE'>DCP</scene>, <scene name='pdbligand=GOL:GLYCEROL'>GOL</scene>, <scene name='pdbligand=MG:MAGNESIUM+ION'>MG</scene></td></tr>
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<tr id='NonStdRes'><td class="sblockLbl"><b>[[Non-Standard_Residue|NonStd Res:]]</b></td><td class="sblockDat"><scene name='pdbligand=DDG:2,3-DIDEOXY-GUANOSINE-5-MONOPHOSPHATE'>DDG</scene></td></tr>
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<tr id='activity'><td class="sblockLbl"><b>Activity:</b></td><td class="sblockDat"><span class='plainlinks'>[http://en.wikipedia.org/wiki/DNA-directed_DNA_polymerase DNA-directed DNA polymerase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=2.7.7.7 2.7.7.7] </span></td></tr>
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<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=5o7t FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5o7t OCA], [http://pdbe.org/5o7t PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=5o7t RCSB], [http://www.ebi.ac.uk/pdbsum/5o7t PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=5o7t 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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The possibility to sequence cytotoxic O(6)-alkylG DNA adducts would greatly benefit research. Recently we reported a benzimidazole-derived nucleotide that is selectively incorporated opposite the damaged site by a mutated DNA polymerase. Here we provide the structural basis for this reaction which may spur future developments in DNA damage sequencing.
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Authors: Betz, K., Diederichs, K., Marx, A.
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Structural basis for the selective incorporation of an artificial nucleotide opposite a DNA adduct by a DNA polymerase.,Betz K, Nilforoushan A, Wyss LA, Diederichs K, Sturla SJ, Marx A Chem Commun (Camb). 2017 Nov 23;53(94):12704-12707. doi: 10.1039/c7cc07173f. PMID:29136072<ref>PMID:29136072</ref>
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Description: Crystal structure of KlenTaq mutant M747K in a closed ternary complex with a dG:dCTP base pair
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From MEDLINE&reg;/PubMed&reg;, a database of the U.S. National Library of Medicine.<br>
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[[Category: Unreleased Structures]]
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</div>
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[[Category: Diederichs, K]]
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<div class="pdbe-citations 5o7t" style="background-color:#fffaf0;"></div>
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== References ==
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<references/>
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__TOC__
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</StructureSection>
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[[Category: DNA-directed DNA polymerase]]
[[Category: Betz, K]]
[[Category: Betz, K]]
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[[Category: Diederichs, K]]
[[Category: Marx, A]]
[[Category: Marx, A]]
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[[Category: Dna polymerase]]
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[[Category: Transferase]]

Revision as of 06:08, 29 November 2017

Crystal structure of KlenTaq mutant M747K in a closed ternary complex with a dG:dCTP base pair

5o7t, resolution 1.80Å

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