Cloned (Comment) | Organism |
---|---|
the enzyme is cloned into pMal-c2 vector with N-terminal or with N- as well as C-terminal flanking sequences, and expressed in fusion with maltose binding protein. The proteinase self-processes itself from the fusion protein during expression and forms inclusion bodies | bovine leukemia virus |
KM Value [mM] | KM Value Maximum [mM] | Substrate | Comment | Organism | Structure |
---|---|---|---|---|---|
0.019 | - |
KGPPVILPIQAP | pH 5.6, 37°C | bovine leukemia virus | |
0.023 | - |
PPMVGVLDAP | pH 5.6, 37°C | bovine leukemia virus |
Localization | Comment | Organism | GeneOntology No. | Textmining |
---|---|---|---|---|
additional information | enzyme is purified from inclusion bodies of Escherichia coli | bovine leukemia virus | - |
- |
Organism | UniProt | Comment | Textmining |
---|---|---|---|
bovine leukemia virus | - |
- |
- |
Purification (Comment) | Organism |
---|---|
- |
bovine leukemia virus |
Substrates | Comment Substrates | Organism | Products | Comment (Products) | Rev. | Reac. |
---|---|---|---|---|---|---|
APQVLPVMHP + H2O | - |
bovine leukemia virus | APQVL + PVMHP | - |
? | |
KGPPVILPIQAP + H2O | - |
bovine leukemia virus | KGPPVIL + PIQAP | - |
? | |
KQPAILVHTPG + H2O | - |
bovine leukemia virus | KQPAIL + VHTPG | - |
? | |
KTKVLVVQPK + H2O | - |
bovine leukemia virus | KTKVL + VVQPK | - |
? | |
PPAILPIISE + H2O | - |
bovine leukemia virus | PPAIL + PIISE | - |
? | |
PPMVGVLDAP + H2O | - |
bovine leukemia virus | PPMVG + VLDAP | - |
? |
Turnover Number Minimum [1/s] | Turnover Number Maximum [1/s] | Substrate | Comment | Organism | Structure |
---|---|---|---|---|---|
0.01 | - |
PPMVGVLDAP | pH 5.6, 37°C | bovine leukemia virus | |
0.02 | - |
KGPPVILPIQAP | pH 5.6, 37°C | bovine leukemia virus | |
0.04 | - |
PPAILPIISE | pH 5.6, 37°C | bovine leukemia virus | |
0.07 | - |
APQVLPVMHP | pH 5.6, 37°C | bovine leukemia virus | |
0.17 | - |
KTKVLVVQPK | pH 5.6, 37°C | bovine leukemia virus | |
0.18 | - |
KQPAILVHTPG | pH 5.6, 37°C | bovine leukemia virus |