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Literature summary for 3.1.21.10 extracted from

  • Symington, L.S.; Kolodner, R.
    Partial purification of an enzyme from Saccharomyces cerevisiae that cleaves Holliday junctions (1985), Proc. Natl. Acad. Sci. USA, 82, 7247-7251.
    View publication on PubMedView publication on EuropePMC

Natural Substrates/ Products (Substrates)

Natural Substrates Organism Comment (Nat. Sub.) Natural Products Comment (Nat. Pro.) Rev. Reac.
DNA + H2O Saccharomyces cerevisiae holliday structure hydrolyzed DNA
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Organism

Organism UniProt Comment Textmining
Saccharomyces cerevisiae
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Purification (Commentary)

Purification (Comment) Organism
500-1000fold Saccharomyces cerevisiae

Specific Activity [micromol/min/mg]

Specific Activity Minimum [µmol/min/mg] Specific Activity Maximum [µmol/min/mg] Comment Organism
0.00000583
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Saccharomyces cerevisiae

Storage Stability

Storage Stability Organism
-20°C, 0.6 ml enzyme solution were diluted with 0.6 ml glycerol Saccharomyces cerevisiae

Substrates and Products (Substrate)

Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
DNA + H2O specifically cleaves Holliday junctions, e.g. in bacteriophage G4 figure-8 molecules, cleavage at either of two sites present in the stem of the cruciform, not at the end of the stem Saccharomyces cerevisiae hydrolyzed DNA
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DNA + H2O holliday structure Saccharomyces cerevisiae hydrolyzed DNA
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