4xvk

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'''Unreleased structure'''
 
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The entry 4xvk is ON HOLD until Paper Publication
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==Binary complex of human polymerase nu and DNA with the finger domain closed==
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<StructureSection load='4xvk' size='340' side='right'caption='[[4xvk]], [[Resolution|resolution]] 2.95&Aring;' scene=''>
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== Structural highlights ==
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<table><tr><td colspan='2'>[[4xvk]] is a 3 chain structure with sequence from [https://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4XVK OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=4XVK 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">X-ray diffraction, [[Resolution|Resolution]] 2.95&#8491;</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=MES:2-(N-MORPHOLINO)-ETHANESULFONIC+ACID'>MES</scene>, <scene name='pdbligand=NA:SODIUM+ION'>NA</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=4xvk FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4xvk OCA], [https://pdbe.org/4xvk PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=4xvk RCSB], [https://www.ebi.ac.uk/pdbsum/4xvk PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=4xvk ProSAT]</span></td></tr>
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</table>
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== Function ==
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[https://www.uniprot.org/uniprot/DPOLN_HUMAN DPOLN_HUMAN]
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<div style="background-color:#fffaf0;">
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== Publication Abstract from PubMed ==
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All DNA replicases achieve high fidelity by a conserved mechanism, but each translesion polymerase carries out mutagenic DNA synthesis in its own way. Here we report crystal structures of human DNA polymerase nu (Pol nu), which is homologous to high-fidelity replicases yet is error prone. Instead of a simple open-to-closed movement of the O helix upon binding of a correct incoming nucleotide, Pol nu has a different open state and requires the finger domain to swing sideways and undergo both opening and closing motions to accommodate the nascent base pair. A single-amino acid substitution in the O helix of the finger domain improves the fidelity of Pol nu nearly ten-fold. A unique cavity and the flexibility of the thumb domain allow Pol nu to generate and accommodate a looped-out primer strand. Primer loop-out may be a mechanism for DNA trinucloetide-repeat expansion.
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Authors: Lee, Y.-S., Yang, W.
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How a homolog of high-fidelity replicases conducts mutagenic DNA synthesis.,Lee YS, Gao Y, Yang W Nat Struct Mol Biol. 2015 Mar 16. doi: 10.1038/nsmb.2985. PMID:25775266<ref>PMID:25775266</ref>
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Description: Binary complex of human polymerase nu and DNA with the finger domain closed
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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: Yang, W]]
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<div class="pdbe-citations 4xvk" style="background-color:#fffaf0;"></div>
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[[Category: Lee, Y.-S]]
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==See Also==
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*[[DNA polymerase 3D structures|DNA polymerase 3D structures]]
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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: Homo sapiens]]
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[[Category: Large Structures]]
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[[Category: Lee Y-S]]
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[[Category: Yang W]]

Current revision

Binary complex of human polymerase nu and DNA with the finger domain closed

PDB ID 4xvk

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