Cloned (Comment) | Organism |
---|---|
EcoR124I methylase is purified from Escherichia coli strain JM109(DE3) harboring plasmid pJS4M | Escherichia coli |
Crystallization (Comment) | Organism |
---|---|
sitting-drop vapor diffusion, crystal structures of three mutants of EcoR124I HsdR are designed to probe this mechanism. The results indicate that interdomain engagement via ATP is responsible for signal transmission between the endonuclease and helicase domains of the motor subunit | Escherichia coli |
Protein Variants | Comment | Organism |
---|---|---|
K220A | the mutant enzyme shows a 5fold reduction in restriction activity. The mutant motor subunit is not defective in interacting with the methyltransferase to form the endonuclease complex | Escherichia coli |
K220Q | the mutant enzyme shows a 400fold reduction in restriction activity. The mutant motor subunit is not defective in interacting with the methyltransferase to form the endonuclease complex | Escherichia coli |
K220R | the mutant motor subunit is not defective in interacting with the methyltransferase to form the endonuclease complex | Escherichia coli |
Organism | UniProt | Comment | Textmining |
---|---|---|---|
Escherichia coli | P10486 | HsdR subunit of the Escherichia coli type I restriction-modification system EcoR124; plasmid R124 | - |
Purification (Comment) | Organism |
---|---|
EcoR124I methylase is purified from Escherichia coli strain JM109(DE3) harboring plasmid pJS4M | Escherichia coli |
Synonyms | Comment | Organism |
---|---|---|
HsdR | subunit of the Escherichia coli type I restriction-modification system EcoR124 | Escherichia coli |