View source for 9asl


==Human DNA polymerase theta helicase domain tetramer, apo-form==
<StructureSection load='9asl' size='340' side='right'caption='[[9asl]], [[Resolution|resolution]] 3.50&Aring;' scene=''>
== Structural highlights ==
<table><tr><td colspan='2'>[[9asl]] is a 4 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=9ASL OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=9ASL FirstGlance]. <br>
</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">Electron Microscopy, [[Resolution|Resolution]] 3.5&#8491;</td></tr>
<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=9asl FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=9asl OCA], [https://pdbe.org/9asl PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=9asl RCSB], [https://www.ebi.ac.uk/pdbsum/9asl PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=9asl ProSAT]</span></td></tr>
</table>
== Function ==
[https://www.uniprot.org/uniprot/DPOLQ_HUMAN DPOLQ_HUMAN] Has a DNA polymerase activity on nicked double-stranded DNA and on a singly primed DNA template. The enzyme activity is resistant to aphidicolin, and inhibited by dideoxynucleotides. Exhibites a single-stranded DNA-dependent ATPase activity. Could be involved in the repair of interstrand cross-links.<ref>PMID:14576298</ref> 
<div style="background-color:#fffaf0;">
== Publication Abstract from PubMed ==
DNA double-strand breaks (DSBs) present a critical threat to genomic integrity, often precipitating genomic instability and oncogenesis. Repair of DSBs predominantly occurs through homologous recombination (HR) and non-homologous end joining (NHEJ). In HR-deficient cells, DNA polymerase theta (Poltheta) becomes critical for DSB repair via microhomology-mediated end joining (MMEJ), also termed theta-mediated end joining (TMEJ). Thus, Poltheta is synthetically lethal with BRCA1/2 and other HR factors, underscoring its potential as a therapeutic target in HR-deficient cancers. However, the molecular mechanisms governing Poltheta-mediated MMEJ remain poorly understood. Here we present a series of cryo-electron microscopy structures of the Poltheta helicase domain (Poltheta-hel) in complex with DNA containing different 3'-ssDNA overhangs. The structures reveal the sequential conformations adopted by Poltheta-hel during the critical phases of DNA binding, microhomology searching, and microhomology annealing. The stepwise conformational changes within the Poltheta-hel subdomains and its functional dimeric state are pivotal for aligning the 3'-ssDNA overhangs, facilitating the microhomology search and subsequent annealing necessary for DSB repair via MMEJ. Our findings illustrate the essential molecular switches within Poltheta-hel that orchestrate the MMEJ process in DSB repair, laying the groundwork for the development of targeted therapies against the Poltheta-hel.

Structural basis for Poltheta-helicase DNA binding and microhomology-mediated end-joining.,Ito F, Li Z, Minakhin L, Khant HA, Pomerantz RT, Chen XS Nat Commun. 2025 Apr 19;16(1):3725. doi: 10.1038/s41467-025-58441-x. PMID:40253368<ref>PMID:40253368</ref>

From MEDLINE&reg;/PubMed&reg;, a database of the U.S. National Library of Medicine.<br>
</div>
<div class="pdbe-citations 9asl" style="background-color:#fffaf0;"></div>
== References ==
<references/>
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</StructureSection>
[[Category: Homo sapiens]]
[[Category: Large Structures]]
[[Category: Chen XS]]
[[Category: Ito F]]
[[Category: Li Z]]