Cloned (Comment) | Organism |
---|---|
expression in Escherichia coli | Geobacillus stearothermophilus |
Crystallization (Comment) | Organism |
---|---|
sitting drop vapor diffusion method at 19°C | Geobacillus stearothermophilus |
Organism | UniProt | Comment | Textmining |
---|---|---|---|
Geobacillus stearothermophilus | Q6UQ65 | - |
- |
Purification (Comment) | Organism |
---|---|
- |
Geobacillus stearothermophilus |
Substrates | Comment Substrates | Organism | Products | Comment (Products) | Rev. | Reac. |
---|---|---|---|---|---|---|
DNA + H2O | the enzyme recognizes a degenerated sequence 5'-W/CCGGW-3' (W stands for A or T and / denotes the cleavage site). It belongs to a large family of restriction enzymes that contain a conserved CCGG tetranucleotide in their target sites. It requires binding of two target sites for the optimal catalytic activity | Geobacillus stearothermophilus | ? | - |
? |
Subunits | Comment | Organism |
---|---|---|
dimer | in solution the BsaWI protein exists in a dimer-tetramer-oligomer equilibrium, but in the presence of specific DNA forms a tetramer bound to two target sites. Site-directed mutagenesis and kinetic experiments show that BsaWI is active as a tetramer and requires two target sites for optimal activity | Geobacillus stearothermophilus |
tetramer | in solution the BsaWI protein exists in a dimer-tetramer-oligomer equilibrium, but in the presence of specific DNA forms a tetramer bound to two target sites. Site-directed mutagenesis and kinetic experiments show that BsaWI is active as a tetramer and requires two target sites for optimal activity | Geobacillus stearothermophilus |
Synonyms | Comment | Organism |
---|---|---|
BsaWI | - |
Geobacillus stearothermophilus |
type IIF restriction endonuclease | - |
Geobacillus stearothermophilus |