No, DNA polymerase does not have the ability to remove DNA adducts. Adducts are chemical modifications that occur on the DNA molecule, and they typically require specialized DNA repair enzymes to be removed. DNA polymerase is primarily responsible for synthesizing new DNA strands during replication and repair processes.
DNA polymerase has a proofreading function that allows it to detect errors during DNA replication. If the enzyme detects a mismatched base pair, it can reverse its catalytic activity and remove the incorrect nucleotide before continuing with DNA synthesis. This proofreading process helps maintain the accuracy of DNA replication.
Efficiency in proofreading activity of DNA polymerase is achieved through its ability to recognize and remove incorrectly paired nucleotides during DNA synthesis. This process involves the exonuclease activity of DNA polymerase, which allows it to backtrack, excise the mismatched base, and replace it with the correct one. This proofreading mechanism helps ensure high fidelity in DNA replication.
DNA polymerase proofreading is a process in which the enzyme checks for errors in the newly synthesized DNA strand during DNA replication. If an incorrect nucleotide is added, the enzyme has the ability to remove the incorrect nucleotide and replace it with the correct one. This helps ensure the fidelity of DNA replication.
When the replication fork is moving towards DNA double strand in the direction 5'- 3', a "Single-strand Binding Protein" (or SSB) -a dnaB gene product- must be removed in order to allow DNA polymerase to add the following nucleotide.
A RNA primer in DNA replication is removed by an enzyme called DNA polymerase I in prokaryotes and DNA polymerase δ in eukaryotes. These enzymes have exonuclease activity that can remove RNA primers and replace them with DNA nucleotides.
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DNA polymerase has a proofreading function that allows it to detect errors during DNA replication. If the enzyme detects a mismatched base pair, it can reverse its catalytic activity and remove the incorrect nucleotide before continuing with DNA synthesis. This proofreading process helps maintain the accuracy of DNA replication.
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The process by which DNA polymerase is able to correct mismatched nucleotides is called proofreading. DNA polymerase has a built-in proofreading mechanism that allows it to recognize and remove incorrect nucleotides during DNA replication, thereby increasing the accuracy of DNA synthesis.
Efficiency in proofreading activity of DNA polymerase is achieved through its ability to recognize and remove incorrectly paired nucleotides during DNA synthesis. This process involves the exonuclease activity of DNA polymerase, which allows it to backtrack, excise the mismatched base, and replace it with the correct one. This proofreading mechanism helps ensure high fidelity in DNA replication.
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DNA polymerase proofreading is a process in which the enzyme checks for errors in the newly synthesized DNA strand during DNA replication. If an incorrect nucleotide is added, the enzyme has the ability to remove the incorrect nucleotide and replace it with the correct one. This helps ensure the fidelity of DNA replication.
DNA polymerase 1 is involved in replication when proofreading and repairing of the DNA sequence as well as removal of RNA primers placed by primase so that DNA polymerase 3 can successfully attach the complementary strand of DNA