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Literature summary extracted from
- Combining recombinant ribonuclease U2 and protein phosphatase for RNA modification mapping by liquid chromatography-mass spectrometry (2015), Anal. Biochem., 478, 52-58 .
Application
| EC Number | Application | Comment | Organism |
|---|---|---|---|
| 4.6.1.20 | analysis | bacteriophage lambda protein phosphatase and recombinant RNase U2 can be used to generate RNase digestion products amenable to liquid chromatography-tandem mass spectrometry analysis, which can be used to determine the presence and location of modified ribonucleosides in RNA samples | synthetic construct |
Cloned(Commentary)
| EC Number | Cloned (Comment) | Organism |
|---|---|---|
| 4.6.1.20 | overexpression of the synthetic gene for RNase U2 in Escherichia coli | synthetic construct |
Organism
| EC Number | Organism | UniProt | Comment | Textmining |
|---|---|---|---|---|
| 4.6.1.20 | synthetic construct | KP779641 | derived from Ustilago sphaerogena | - |
Purification (Commentary)
| EC Number | Purification (Comment) | Organism |
|---|---|---|
| 4.6.1.20 | - |
synthetic construct |
Synonyms
| EC Number | Synonyms | Comment | Organism |
|---|---|---|---|
| 4.6.1.20 | RNase U2 | - |
synthetic construct |
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Release 2023.1 (January 2023)
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