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Literature summary for 3.1.26.5 extracted from

  • Bai, Y.; Sunkara, N.; Liu, F.
    Targeting mRNAs by engineered sequence-specific RNase P ribozymes (2012), Methods Mol. Biol., 848, 357-368.
    View publication on PubMed

Application

Application Comment Organism
biotechnology RNase P of Escherichia coli contains a catalytic RNA subunit (M1 RNA) that can be engineered to cleave tRNA-like substrates and other target RNAs, including specific mRNAs. The enzyme can be expressed in infected human U373MG cells or fibroblasts, or in murine PA317 cells, and therein be used for inhibition of targeting and cleavage of host RNA by Human cytomegalovirus enzyme, HCMV strain AD169, through blocking substrate mRNA expression, methods of using engineered RNase P catalytic RNA for in vitro and in vivo in trans-cleavage of target viral mRNA, overview. customized M1GS RNA and full-length RNase P are effective in cleaving both viral and cellular mRNAs and blocking their expression in cultured cells Escherichia coli

Metals/Ions

Metals/Ions Comment Organism Structure
Mg2+ required Escherichia coli

Organism

Organism UniProt Comment Textmining
Escherichia coli
-
-
-

Posttranslational Modification

Posttranslational Modification Comment Organism
ribonucleoprotein
-
Escherichia coli

Substrates and Products (Substrate)

Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
additional information method development for the engineered catalytic RNA subunit of Escherichia coli RNase P to cleave tRNA-like substrates and other target RNAs, including specific mRNAs, detailed overview Escherichia coli ?
-
?

Synonyms

Synonyms Comment Organism
RNase P
-
Escherichia coli

Temperature Optimum [°C]

Temperature Optimum [°C] Temperature Optimum Maximum [°C] Comment Organism
37
-
assay at Escherichia coli

pH Optimum

pH Optimum Minimum pH Optimum Maximum Comment Organism
7 7.4 assay at Escherichia coli

General Information

General Information Comment Organism
additional information RNase P-mediated inhibition of gene expression represents a novel and promising nucleic acid-based gene interference strategy for specific inhibition of target mRNA, overview Escherichia coli