Cloned (Comment) | Organism |
---|---|
expressed in Escherichia coli strain BH110 | African swine fever virus |
Inhibitors | Comment | Organism | Structure |
---|---|---|---|
beta-mercaptoethanol | complete inhibition at 10 mM and higher | African swine fever virus | |
dithiothreitol | at 1 mM and higher dithiothreitol concentrations AP site incision is strongly inhibited with less than 10% of the activity remaining, the inhibition by dithiothreitol is reverted by H2O2 in a dose-dependent manner, the inhibition by dithiothreitol is not reverted by divalent cations, including Zn2+, Co2+, Ca2+, and Ni+ | African swine fever virus |
Organism | UniProt | Comment | Textmining |
---|---|---|---|
African swine fever virus | - |
- |
- |
Purification (Comment) | Organism |
---|---|
Ni-NTA column chromatography and HisTrap chelating column chromatography | African swine fever virus |
Source Tissue | Comment | Organism | Textmining |
---|
Substrates | Comment Substrates | Organism | Products | Comment (Products) | Rev. | Reac. |
---|---|---|---|---|---|---|
DNA | AP endonuclease pE296R has strong preference for mispaired and oxidative base lesions at the 3'-termini of single-strand breaks, the 3'-terminal damaged pyrimidines (uracil, 5,6-dihydrouracil, and 5-hydroxycytosine) are removed with higher efficiency than damaged purines inosine and 7,8-dihydro-8-oxoguanine | African swine fever virus | fragments of DNA | - |
? |
Synonyms | Comment | Organism |
---|---|---|
AP endonuclease | - |
African swine fever virus |
apurinic-apyrimidinic endonuclease | - |
African swine fever virus |
pE296R | - |
African swine fever virus |
General Information | Comment | Organism |
---|---|---|
physiological function | AP endonuclease pE296R is essential for virus growth in swine macrophages. DNA repair functions of pE296R are AP endonucleolytic, 3'-5' exonuclease, 3-diesterase and nucleotide incision repair activities | African swine fever virus |