DNA Polymerase I: Difference between revisions

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<StructureSection load='1KLN_pymol.pdb' size='400' side='right' scene='Sandbox_dvoet/DNA_polymerase/Klenow-dna/4' caption='' >
<StructureSection load='1KLN_pymol.pdb' size='400' side='right' scene='Sandbox_dvoet/DNA_polymerase/Klenow-dna/4' caption='' >
==Overview==
==Overview==
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==Structure of the whole ''Thermus aquaticus'' DNA polymerase I==
==Structure of the whole ''Thermus aquaticus'' DNA polymerase I==
<applet load='1taq.pdb' size='400' frame='true' align='right' caption='Thermus aquaticus Pol I ([[1taq]])' scene= 'Sandbox_dvoet/DNA_polymerase/Taq_pol_i/1'/>


As mentioned above, Pol I's primary and essential function is to excise the RNA primers from newly synthesized Okazaki fragments with its 5' → 3' exonuclease function and replace them with DNA using its polymerase function. This yields a double-stranded DNA (dsDNA) with a single strand nick between successive Okazaki fragments, a nick that is eventually sealed through the action of DNA ligase.
As mentioned above, Pol I's primary and essential function is to excise the RNA primers from newly synthesized Okazaki fragments with its 5' → 3' exonuclease function and replace them with DNA using its polymerase function. This yields a double-stranded DNA (dsDNA) with a single strand nick between successive Okazaki fragments, a nick that is eventually sealed through the action of DNA ligase.

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Donald Voet, Eran Hodis, David Canner, Michal Harel, Alexander Berchansky