Inhibitors | Comment | Organism | Structure |
---|---|---|---|
3-Methyladenine | product inhibition | Escherichia coli | |
additional information | free adenine, 1 methyladenine, 7-methylguanine, caffeine or uracil fails to inhibit the enzyme | Escherichia coli |
KM Value [mM] | KM Value Maximum [mM] | Substrate | Comment | Organism | Structure |
---|---|---|---|---|---|
0.000006 | - |
3-methyladenine residues in alkylated DNA | pH 7.6, 37°C, release of 3-methyladenine | Escherichia coli |
Metals/Ions | Comment | Organism | Structure |
---|---|---|---|
Mg2+ | slight stimulation about 30% with 5-15 mM MgCl2 | Escherichia coli | |
additional information | does not require divalent metal ions | Escherichia coli |
Molecular Weight [Da] | Molecular Weight Maximum [Da] | Comment | Organism |
---|---|---|---|
19000 | - |
sucrose densitiy gradient centrifugation | Escherichia coli |
Natural Substrates | Organism | Comment (Nat. Sub.) | Natural Products | Comment (Nat. Pro.) | Rev. | Reac. |
---|---|---|---|---|---|---|
alkylated DNA + H2O | Escherichia coli | double-stranded DNA is an effective substrate, enzyme is less efficient in excision of base damage from single-stranded regions transiently formed in DNA during transcription and replication | 3-methyladenine + ? | - |
? | |
alkylated DNA + H2O | Escherichia coli | reaction of the enzyme with alkylated DNA leads to introduction of apurinic sites but no chain breaks | 3-methyladenine + ? | - |
? |
Organism | UniProt | Comment | Textmining |
---|---|---|---|
Escherichia coli | - |
- |
- |
Purification (Comment) | Organism |
---|---|
- |
Escherichia coli |
Specific Activity Minimum [µmol/min/mg] | Specific Activity Maximum [µmol/min/mg] | Comment | Organism |
---|---|---|---|
0.0093 | - |
- |
Escherichia coli |
Storage Stability | Organism |
---|---|
-70°C, stable | Escherichia coli |
Substrates | Comment Substrates | Organism | Products | Comment (Products) | Rev. | Reac. |
---|---|---|---|---|---|---|
3-methyladenine residues in alkylated DNA + H2O | - |
Escherichia coli | 3-methyladenine + ? | - |
? | |
alkylated DNA + H2O | - |
Escherichia coli | 3-methyladenine + ? | releases 3-methyladenine and 3-ethyladenine | ? | |
alkylated DNA + H2O | double-stranded DNA is an effective substrate, enzyme is less efficient in excision of base damage from single-stranded regions transiently formed in DNA during transcription and replication | Escherichia coli | 3-methyladenine + ? | - |
? | |
alkylated DNA + H2O | reaction of the enzyme with alkylated DNA leads to introduction of apurinic sites but no chain breaks | Escherichia coli | 3-methyladenine + ? | - |
? | |
additional information | does not liberate 7-methylguanine, O6-methylguanine, 7-methyladenine, 7-ethylguanine, O6-ethylguanine, and arylalkylated purine derivatives obtained by treatment of DNA with 7-bromomethyl-12-methylbenz[alpha]anthracene, no detectable nuclease activity with native DNA, depurinated DNA, ultraviolet-irradiated DNA, or X-irradiated DNA as potential substrates, enzyme does not release hypoxanthine or xanthine in free form from by nitrous acid treatment partly demainated DNA | Escherichia coli | ? | - |
? |
pH Optimum Minimum | pH Optimum Maximum | Comment | Organism |
---|---|---|---|
7.2 | 7.8 | similar activity in either HEPES-KOH or Tris-HCl buffers | Escherichia coli |
Cofactor | Comment | Organism | Structure |
---|---|---|---|
additional information | no absolute cofactor requirement | Escherichia coli |