Literature summary extracted from
Amundsen, S.K.; Taylor, A.F.; Smith, G.R.
A domain of RecC required for assembly of the regulatory RecD subunit into the Escherichia coli RecBCD holoenzyme (2002), Genetics, 161, 483-492.
Cloned(Commentary)
EC Number |
Cloned (Comment) |
Organism |
---|
3.1.11.5 |
recC gene |
Escherichia coli |
Protein Variants
EC Number |
Protein Variants |
Comment |
Organism |
---|
3.1.11.5 |
additional information |
recBC1010D, recBC1041D and recBCD1013 mutants have less than 0.2% of the exonuclease activity of wild-type enzyme. recBC1010D and recBC1041D produce RecD but fail to assemble it into holoenzyme |
Escherichia coli |
Natural Substrates/ Products (Substrates)
EC Number |
Natural Substrates |
Organism |
Comment (Nat. Sub.) |
Natural Products |
Comment (Nat. Pro.) |
Rev. |
Reac. |
---|
3.1.11.5 |
douple-stranded DNA |
Escherichia coli |
the enzyme is required for the major pathway of double-strand DNA break repair and genetic exchange, the enzyme has potent nuclease and helicase activity |
? |
- |
? |
|
Organism
EC Number |
Organism |
UniProt |
Comment |
Textmining |
---|
3.1.11.5 |
Escherichia coli |
- |
- |
- |
Purification (Commentary)
EC Number |
Purification (Comment) |
Organism |
---|
3.1.11.5 |
RecC, RecBC and RecBCD, RecBC1041 mutant |
Escherichia coli |
Storage Stability
EC Number |
Storage Stability |
Organism |
---|
3.1.11.5 |
4°C, RecC, stable for several months |
Escherichia coli |
Substrates and Products (Substrate)
EC Number |
Substrates |
Comment Substrates |
Organism |
Products |
Comment (Products) |
Rev. |
Reac. |
---|
3.1.11.5 |
douple-stranded DNA |
the enzyme has potent nuclease and helicase activity |
Escherichia coli |
? |
- |
? |
|
3.1.11.5 |
douple-stranded DNA |
the enzyme is required for the major pathway of double-strand DNA break repair and genetic exchange, the enzyme has potent nuclease and helicase activity |
Escherichia coli |
? |
- |
? |
|
Subunits
EC Number |
Subunits |
Comment |
Organism |
---|
3.1.11.5 |
heterotrimer |
RecB, RecC and RecD, The C-terminus of RecC: 35000 Da, is required for assembly of the RecD subunit into enzyme holoenzyme but not for recombination proficiency. The N-terminus of RecC: 95000 Da, contains functions essential for recombination and is also required for chi activity. RecD is essential for nuclease activity, regulation by the recombination hotspot Chi, and high affinity for DNA ends. RecC interacts with RecD to form a heterotrimer only in the presence of RecB. |
Escherichia coli |