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        <identifier>oai:figshare.com:article/34035555</identifier>
        <datestamp>2026-09-30T17:34:59Z</datestamp>
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          <dc:title>&lt;p&gt;Additional biochemical characterization of the ORC4R protein.&lt;/p&gt;</dc:title>
          <dc:creator>Luis E. Martínez-Rodríguez (25145346)</dc:creator>
          <dc:creator>Stephen P. Bell (25145349)</dc:creator>
          <dc:subject>Biochemistry</dc:subject>
          <dc:subject>Cell Biology</dc:subject>
          <dc:subject>Genetics</dc:subject>
          <dc:subject>Molecular Biology</dc:subject>
          <dc:subject>Biological Sciences not elsewhere classified</dc:subject>
          <dc:subject>origin recognition complex</dc:subject>
          <dc:subject>saccharomyces cerevisiae &lt;/</dc:subject>
          <dc:subject>helicase loading activity</dc:subject>
          <dc:subject>div &gt;&lt; p</dc:subject>
          <dc:subject>atpase interfaces within</dc:subject>
          <dc:subject>six orc subunits</dc:subject>
          <dc:subject>orc atp hydrolysis</dc:subject>
          <dc:subject>defective orc allele</dc:subject>
          <dc:subject>atp hydrolysis</dc:subject>
          <dc:subject>orc subunits</dc:subject>
          <dc:subject>defective orc</dc:subject>
          <dc:subject>vitro &lt;/</dc:subject>
          <dc:subject>toa2 &lt;/</dc:subject>
          <dc:subject>r267a &lt;/</dc:subject>
          <dc:subject>sixth allele</dc:subject>
          <dc:subject>reducing transcription</dc:subject>
          <dc:subject>orc4r ).</dc:subject>
          <dc:subject>lethal phenotype</dc:subject>
          <dc:subject>genetic screen</dc:subject>
          <dc:subject>essential role</dc:subject>
          <dc:subject>cdc6 complex</dc:subject>
          <dc:subject>binds origins</dc:subject>
          <dc:subject>although functions</dc:subject>
          <dc:description>&lt;p&gt;A) Comparison of DNA binding of WT ORC, ORC4R with and without the Orc4-&lt;i&gt;sofa&lt;/i&gt; mutation, and ORC1K in electrophoretic-mobility shift assay (EMSA). Binding in the presence of ATP or ATPγS is shown. B) Sequence specificity of ORC and ORC4R DNA binding. EMSA was used to measure wild-type ORC and ORC4R DNA binding to WT &lt;i&gt;ARS1&lt;/i&gt; or &lt;i&gt;ARS1&lt;/i&gt; lacking the strongest ORC binding site (A-). C) Titration of WT ORC, ORC4R, and ORC1K proteins in a helicase-loading assay (0.3 mM ATP). D) Salt titration and sequence-specific loading of the WT and ORC4R protein (R267A). Sequence specificity is tested using a WT &lt;i&gt;ARS1&lt;/i&gt; and an &lt;i&gt;ARS1&lt;/i&gt; lacking the two strongest ORC binding sites (A-/B2-).&lt;/p&gt; &lt;p&gt;(TIF)&lt;/p&gt;</dc:description>
          <dc:date>2026-09-30T17:34:54Z</dc:date>
          <dc:type>Image</dc:type>
          <dc:type>Figure</dc:type>
          <dc:identifier>10.1371/journal.pone.0349465.s005</dc:identifier>
          <dc:relation>https://figshare.com/articles/figure/_p_Additional_biochemical_characterization_of_the_ORC4R_protein_p_/34035555</dc:relation>
          <dc:rights>CC BY 4.0</dc:rights>
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