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3.1.26.5: ribonuclease P

This is an abbreviated version!
For detailed information about ribonuclease P, go to the full flat file.

Word Map on EC 3.1.26.5

Reaction

endonucleolytic cleavage of RNA, removing 5'-extranucleotides from tRNA precursor =

Synonyms

Aq_880, aRpp29, aRpp29 protein, AtPop1p, AtPRORP1, AtPRORP2, AtPRORP3, C5 protein, CrPRORP, hPOP1, hPOP4, hPOP7, M1 RNA, M1GS, M1GS RNA, mitochondrial RNase P protein 1, MRPP1, MRPP2, MRPP3, nuclear ribonclease P ribonucleoprotein, nuclease, ribo-, P, Pfu Pop5, PhoPRNA, POP1, Pop1p, Pop5, Pop6, Pop7, PRORP, PRORP1, PRORP2, PRORP3, Protein C5, protein-only ribonuclease P, protein-only RNase P, protein-only RNase P enzyme, proteinaceous RNase P, ribonuclease MRP, ribonuclease P, ribonuclease P ribozyme, ribosomal RNA processing ribonucleoprotein, Ribunuclease P, RNA processing protein POP1, RNA processing protein POP5, RNA processing protein POP6, RNA processing protein POP7, RNA processing protein POP8, RNase MRP, RNase P, RNase P holoenzyme, RNase P protein, RNase P ribozyme, RNase P RNA, RNase P/MRP, RNase P/MRP protein, RNaseP protein, RNaseP protein p20, RNaseP protein p30, RNaseP protein p38, RNaseP protein p40, RNases P, RNP, Rpm2p, RPP, RPP14, Rpp20, Rpp21, Rpp25, Rpp29, Rpp30, Rpp38, RPP40, RPR, RPR1, transfer RNA 5' maturation enzyme, transfer RNA processing enzyme, tRNA processing enzyme, tRNA-processing endonuclease, tRNA-processing enzyme

ECTree

     3 Hydrolases
         3.1 Acting on ester bonds
             3.1.26 Endoribonucleases producing 5'-phosphomonoesters
                3.1.26.5 ribonuclease P

Renatured

Renatured on EC 3.1.26.5 - ribonuclease P

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RENATURED/Commentary
ORGANISM
UNIPROT
LITERATURE
heterologous reconstitution of the holoenzyme using the RNA subunit from in vitro transcription and the recombinant protein subunit from overexpression in Escherichia coli, maximal activity at a ratio of 1:10 protein to RNA components
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reconstitution of a functional mini-enzyme from protein subunits Rpp21 and Rpp29 with the RNA subunit H1, all 3 coponents are essential for reconstitution
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reconstitution of a heterologous holoenzyme with a bacterial protein subunit and the plastid-encoded RNA subunit
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renaturation conditions for nearly 95% uniformly folded populations of enzyme or RNA substrate are: heating to 95°C for 3 min without divalent cation, cooling to 37°C and incubation in the presence of divalent cation for at least 15 min
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