Application | Comment | Organism |
---|---|---|
drug development | the enzyme is a primary target in the development of antiviral agents against HIV-1 | Human immunodeficiency virus 1 |
Cloned (Comment) | Organism |
---|---|
expression of untagged or C-terminally intein- and biotin-tagged enzyme in Escherichia coli strain BL21 (DE3) | Human immunodeficiency virus 1 |
Metals/Ions | Comment | Organism | Structure |
---|---|---|---|
Mg2+ | required | Human immunodeficiency virus 1 |
Organism | UniProt | Comment | Textmining |
---|---|---|---|
Human immunodeficiency virus 1 | - |
- |
- |
Purification (Comment) | Organism |
---|---|
purification method development, one-step purification 157fold using an affinity column prepared by conjugating an RNase H specific inhibitor with NHS-activated resin, washing with Mn2+, and elution with EDTA, or purification using a C-terminal intein and a biotin tag for avidin affinty chromatography, followed by reductive cleavage of the Mxe intein, overview. Purification of recombinant enzyme from Escherichia coli strain BL21 (DE3). RNase inhibitors have a greater affinity for the RNase H active site in the presence of Mn2+ than in the presence of Mg2+ | Human immunodeficiency virus 1 |
Synonyms | Comment | Organism |
---|---|---|
HIV-1 R | - |
Human immunodeficiency virus 1 |
HIV-1 reverse transcriptase | - |
Human immunodeficiency virus 1 |
human immunodeficiency virus type 1 reverse transcriptase | - |
Human immunodeficiency virus 1 |
Temperature Optimum [°C] | Temperature Optimum Maximum [°C] | Comment | Organism |
---|---|---|---|
37 | - |
assay at | Human immunodeficiency virus 1 |
pH Optimum Minimum | pH Optimum Maximum | Comment | Organism |
---|---|---|---|
7.8 | - |
assay at | Human immunodeficiency virus 1 |
General Information | Comment | Organism |
---|---|---|
physiological function | HIV-1 reverse transcriptase plays an essential role in the life cycle of the virus | Human immunodeficiency virus 1 |