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  2. Endonuclease - Wikipedia

    en.wikipedia.org/wiki/Endonuclease

    MUS81/EME1 is a structure specific endonuclease involved in converting interstrand crosslinks to double-strand breaks in a DNA replication-dependent manner. [12] After introduction of a double-strand break, further steps are required to complete the repair process. If a crosslink is not properly repaired it can block DNA replication. [citation ...

  3. DNA replication - Wikipedia

    en.wikipedia.org/wiki/DNA_replication

    Enzyme Function in DNA replication DNA helicase: Also known as helix destabilizing enzyme. Helicase separates the two strands of DNA at the Replication Fork behind the topoisomerase. DNA polymerase: The enzyme responsible for catalyzing the addition of nucleotide substrates to DNA in the 5′ to 3′ direction during DNA replication.

  4. Exonuclease - Wikipedia

    en.wikipedia.org/wiki/Exonuclease

    It acts as a 3’→5’ DNA directed proofreading exonuclease that removes incorrectly incorporated bases during replication. [10] Similarly, in Salmonella typhimurium bacteria, the 3’ to 5’ editing function employed during DNA replication is also encoded by a gene, dnaQ , which specifies a 3’ to 5’ exonuclease subunit, one of the ...

  5. Nuclease - Wikipedia

    en.wikipedia.org/wiki/Nuclease

    Depiction of the restriction enzyme (endonuclease) HindIII cleaving a double-stranded DNA molecule at a valid restriction site (5'–A|AGCTT–3').. In biochemistry, a nuclease (also archaically known as nucleodepolymerase or polynucleotidase) is an enzyme capable of cleaving the phosphodiester bonds that link nucleotides together to form nucleic acids.

  6. Restriction enzyme - Wikipedia

    en.wikipedia.org/wiki/Restriction_enzyme

    In this method, the restriction enzyme can be used to genotype a DNA sample without the need for expensive gene sequencing. The sample is first digested with the restriction enzyme to generate DNA fragments, and then the different sized fragments separated by gel electrophoresis. In general, alleles with correct restriction sites will generate ...

  7. DNA mismatch repair - Wikipedia

    en.wikipedia.org/wiki/DNA_mismatch_repair

    If, however, the nick is on the 3' end of the mismatch, ExoI (a 3' to 5' enzyme) is used. The entire process ends past the mismatch site - i.e., both the site itself and its surrounding nucleotides are fully excised. The single-strand gap created by the exonuclease can then be repaired by DNA Polymerase III (assisted by single-strand-binding ...

  8. Helicase - Wikipedia

    en.wikipedia.org/wiki/Helicase

    RecQ is a family of DNA helicase enzymes that are found in various organisms including bacteria, archaea, and eukaryotes (like humans). These enzymes play important roles in DNA metabolism during DNA replication, recombination, and repair. There are five known RecQ helicase proteins in humans: RecQ1, BLM, WRN, RecQ4, and RecQ5.

  9. Type II topoisomerase - Wikipedia

    en.wikipedia.org/wiki/Type_II_topoisomerase

    Type II topoisomerases are topoisomerases that cut both strands of the DNA helix simultaneously in order to manage DNA tangles and supercoils. They use the hydrolysis of ATP, unlike Type I topoisomerase. In this process, these enzymes change the linking number of circular DNA by ±2. Topoisomerases are ubiquitous enzymes, found in all living ...