Activating Compound | Comment | Organism | Structure |
---|---|---|---|
S-adenosyl methionine | stimulates DNA cleavage activity | Escherichia coli |
Application | Comment | Organism |
---|---|---|
biotechnology | potential uses for EcoR124I as a nanoactuator within a biosensor in the field of bionanotechnology. It may be used as a molecular dynamo that can measure events from single molecules of DNA, providing a highly sensitive biosensor for detecting events that interrupt translocation events | Escherichia coli |
Cloned (Comment) | Organism |
---|---|
- |
Escherichia coli |
recombinant plasmid pJS4M overproducing HsdM compared to HsdS | Escherichia coli |
Protein Variants | Comment | Organism |
---|---|---|
additional information | point mutation within the hsdS gene or insertional mutagenesis using the Tn5 transposon, both show new DNA specificities. Both new specificities are due to the production of a truncated HsdS subunit, which is able to dimerize, producing the recognition sequence GAAn7TTC in the case of the point mutation of EcoR124I, which produces a stop codon and hence the truncated subunit | Escherichia coli |
Localization | Comment | Organism | GeneOntology No. | Textmining |
---|---|---|---|---|
membrane | the EcoR124I holoenzyme is particularly exposed on the periplasmic side of the cytoplasmic membrane | Escherichia coli | 16020 | - |
Molecular Weight [Da] | Molecular Weight Maximum [Da] | Comment | Organism |
---|---|---|---|
43000 | - |
x * 116000, HsdR, x * 55000, HsdM, x * 43000, HsdS | Escherichia coli |
55000 | - |
x * 116000, HsdR, x * 55000, HsdM, x * 43000, HsdS | Escherichia coli |
116000 | - |
x * 116000, HsdR, x * 55000, HsdM, x * 43000, HsdS | Escherichia coli |
Organism | UniProt | Comment | Textmining |
---|---|---|---|
Escherichia coli | - |
- |
- |
Purification (Comment) | Organism |
---|---|
- |
Escherichia coli |
Substrates | Comment Substrates | Organism | Products | Comment (Products) | Rev. | Reac. |
---|---|---|---|---|---|---|
DNA + H2O | HsdR subunit can produce only a single cleavage of the phosphodiester backbone of the DNA but can cooperate with another HsdR subunit to produce full DNA cleavage, producing DNA with overhanging ends of single-stranded DNA. On a single-site plasmid, cleavage requires the association of HsdR, from solution, to the cleavage complex in order to produce double-strand cleavage | Escherichia coli | ? | - |
? | |
duplex DNA + ATP | - |
Escherichia coli | double-stranded DNA fragments with terminal 5'-phosphate + ADP + inorganic phosphate | - |
? |
Subunits | Comment | Organism |
---|---|---|
? | x * 116000, HsdR, x * 55000, HsdM, x * 43000, HsdS | Escherichia coli |
Synonyms | Comment | Organism |
---|---|---|
EcoR124I | - |
Escherichia coli |
type I R-M enzyme | - |
Escherichia coli |
type I restriction-modification enzyme | - |
Escherichia coli |
Cofactor | Comment | Organism | Structure |
---|---|---|---|
ATP | - |
Escherichia coli | |
ATP | required | Escherichia coli | |
S-adenosyl-L-methionine | activity is stimulated by S-adenosyl-L-methionine | Escherichia coli |