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Literature summary extracted from

  • Takasawa, K.; Masutani, C.; Hanaoka, F.; Iwai, S.
    Chemical synthesis and translesion replication of a cis-syn cyclobutane thymine-uracil dimer (2004), Nucleic Acids Res., 32, 1738-1745.
    View publication on PubMedView publication on EuropePMC

Metals/Ions

EC Number Metals/Ions Comment Organism Structure
3.1.25.1 NaCl
-
Tequatrovirus T4

Organism

EC Number Organism UniProt Comment Textmining
3.1.25.1 Tequatrovirus T4
-
-
-

Substrates and Products (Substrate)

EC Number Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
3.1.25.1 dsDNA + H2O excision of cyclobutane pyrimidine dimers TT and TU, the latter being a cis-syn cyclobutane thymine-uracil dimer, produced within duplex DNA by UV radiation with equal efficiency, U is derived from C which becomes deaminated by UV radiation Tequatrovirus T4 ?
-
?
3.1.25.1 additional information synthesis of cis-syn cyclobutane thymine-uracil dimer, determination of cyclobutane dimer structure by NMR spectroscopy Tequatrovirus T4 ?
-
?

Synonyms

EC Number Synonyms Comment Organism
3.1.25.1 bacteriophage T4 endonuclease V
-
Tequatrovirus T4
3.1.25.1 T4 endonuclease V
-
Tequatrovirus T4

Temperature Optimum [°C]

EC Number Temperature Optimum [°C] Temperature Optimum Maximum [°C] Comment Organism
3.1.25.1 37
-
assay at Tequatrovirus T4

pH Optimum

EC Number pH Optimum Minimum pH Optimum Maximum Comment Organism
3.1.25.1 7.5
-
assay at Tequatrovirus T4