EC Number | Activating Compound | Comment | Organism | Structure |
---|---|---|---|---|
2.7.7.48 | GTP | flaviviral RdRps require high concentrations of the second incoming nucleotide GTP to catalyze de novo template-dependent RNA synthesis. GTP stimulates de novo RNA synthesis by RdRp from Japanese encephalitis virus | Japanese encephalitis virus |
EC Number | Cloned (Comment) | Organism |
---|---|---|
2.7.7.48 | the gene segment corresponding to the RdRp module corresponds to amino acid 272905 of the NS5 protein, recombinant expression of the enzyme as N-terminally GST-tagged protein in Escherichia coli strain C41(DE3) | Japanese encephalitis virus |
EC Number | Crystallization (Comment) | Organism |
---|---|---|
2.7.7.48 | purified recombinant enzyme in apo-form or in complex with ATP or GTP, jRdRp (0.08 mM) is incubated with GTP/ATP (5 mM) for 30 min before setting crystallization trials, screening and method optimization, hanging drop vapour diffusion method, mixing of protein-ATP/GTP with 10-18% w/v PEG 4000, 100 mM Tris-Cl buffer, pH 8.0, and 7% v/v 1-propanol, 25°C, for the apo-enzyme mixing of 0.096 mM protein with 10-15% PEG 5000 mono methyl ether, 100 mM Tris-Cl, pH 8.0, and 200mM NaSCN, 25°C, X-ray diffraction structure determination and analysis at 2.28-3.65 A resolution, molecular replacement using the apo-enzyme structures of WNV and DENV, PDB IDs 2HFZ and 2J7W, as search models | Japanese encephalitis virus |
EC Number | Protein Variants | Comment | Organism |
---|---|---|---|
2.7.7.48 | D541A | site-directed mutagenesis, the mutant's elongation activity is marginally reduced compared to the wild-type enzyme | Japanese encephalitis virus |
2.7.7.48 | R734A | site-directed mutagenesis, the mutant catalyzes elongation almost identically to the wild-type enzyme | Japanese encephalitis virus |
2.7.7.48 | R742A | site-directed mutagenesis, the mutant catalyzes elongation almost identically to the wild-type enzyme | Japanese encephalitis virus |
2.7.7.48 | S604A | site-directed mutagenesis, the mutant's elongation activity is marginally reduced compared to the wild-type enzyme | Japanese encephalitis virus |
2.7.7.48 | S604A-D541A | site-directed mutagenesis, the mutant shows no detectable primer extension activity | Japanese encephalitis virus |
2.7.7.48 | S799A | site-directed mutagenesis, the mutant catalyzes elongation almost identically to the wild-type enzyme | Japanese encephalitis virus |
2.7.7.48 | S799Y | site-directed mutagenesis, the mutant catalyzes elongation almost identically to the wild-type enzyme | Japanese encephalitis virus |
EC Number | KM Value [mM] | KM Value Maximum [mM] | Substrate | Comment | Organism | Structure |
---|---|---|---|---|---|---|
2.7.7.48 | additional information | - |
additional information | dissociation constants for the interaction of jRdRp with RNA in the presence/absence of NTPs and Mn2+ | Japanese encephalitis virus |
EC Number | Metals/Ions | Comment | Organism | Structure |
---|---|---|---|---|
2.7.7.48 | Mn2+ | required, GTP binding reduces the affinity of jRdRp for RNA in the absence of Mn2+, binding affinity of jRdRp toward RNA in the presence of GTP/ATP is restored when Mn2+ ion is included in the reaction buffer | Japanese encephalitis virus |
EC Number | Natural Substrates | Organism | Comment (Nat. Sub.) | Natural Products | Comment (Nat. Pro.) | Rev. | Reac. |
---|---|---|---|---|---|---|---|
2.7.7.48 | additional information | Japanese encephalitis virus | flaviviral RNA-dependent RNA polymerases initiate replication of the single-stranded RNA genome in the absence of a primer. The template sequence 5'-CU-3' at the 3'-end of the flaviviral genome is highly conserved. Flaviviral RdRps require high concentrations of the second incoming nucleotide GTP to catalyze de novo template-dependent RNA synthesis. the conserved motif F of jRdRp occupies multiple conformations in absence of GTP. Motif F becomes ordered on GTP binding and occludes the nucleotide triphosphate entry tunnel | ? | - |
? | |
2.7.7.48 | additional information | Japanese encephalitis virus P20778 | flaviviral RNA-dependent RNA polymerases initiate replication of the single-stranded RNA genome in the absence of a primer. The template sequence 5'-CU-3' at the 3'-end of the flaviviral genome is highly conserved. Flaviviral RdRps require high concentrations of the second incoming nucleotide GTP to catalyze de novo template-dependent RNA synthesis. the conserved motif F of jRdRp occupies multiple conformations in absence of GTP. Motif F becomes ordered on GTP binding and occludes the nucleotide triphosphate entry tunnel | ? | - |
? | |
2.7.7.48 | nucleoside triphosphate + RNAn | Japanese encephalitis virus | - |
diphosphate + RNAn+1 | - |
? | |
2.7.7.48 | nucleoside triphosphate + RNAn | Japanese encephalitis virus P20778 | - |
diphosphate + RNAn+1 | - |
? |
EC Number | Organism | UniProt | Comment | Textmining |
---|---|---|---|---|
2.7.7.48 | Japanese encephalitis virus | O90417 | polyprotein; a flavivirus | - |
2.7.7.48 | Japanese encephalitis virus P20778 | O90417 | polyprotein; a flavivirus | - |
EC Number | Purification (Comment) | Organism |
---|---|---|
2.7.7.48 | recombinant N-terminally GST-tagged enzyme from Escherichia coli strain C41(DE3) by glutathione affinity chromatography and gel filtration | Japanese encephalitis virus |
EC Number | Substrates | Comment Substrates | Organism | Products | Comment (Products) | Rev. | Reac. |
---|---|---|---|---|---|---|---|
2.7.7.48 | additional information | flaviviral RNA-dependent RNA polymerases initiate replication of the single-stranded RNA genome in the absence of a primer. The template sequence 5'-CU-3' at the 3'-end of the flaviviral genome is highly conserved. Flaviviral RdRps require high concentrations of the second incoming nucleotide GTP to catalyze de novo template-dependent RNA synthesis. the conserved motif F of jRdRp occupies multiple conformations in absence of GTP. Motif F becomes ordered on GTP binding and occludes the nucleotide triphosphate entry tunnel | Japanese encephalitis virus | ? | - |
? | |
2.7.7.48 | additional information | ATP and GTP enzyme binding structures, detailed overview. The triphosphate moiety of GTP interacts with the side chains of basic residues from motif F (R460, K463, K471 and R474) and from motif E (R734 and R742) | Japanese encephalitis virus | ? | - |
? | |
2.7.7.48 | additional information | flaviviral RNA-dependent RNA polymerases initiate replication of the single-stranded RNA genome in the absence of a primer. The template sequence 5'-CU-3' at the 3'-end of the flaviviral genome is highly conserved. Flaviviral RdRps require high concentrations of the second incoming nucleotide GTP to catalyze de novo template-dependent RNA synthesis. the conserved motif F of jRdRp occupies multiple conformations in absence of GTP. Motif F becomes ordered on GTP binding and occludes the nucleotide triphosphate entry tunnel | Japanese encephalitis virus P20778 | ? | - |
? | |
2.7.7.48 | additional information | ATP and GTP enzyme binding structures, detailed overview. The triphosphate moiety of GTP interacts with the side chains of basic residues from motif F (R460, K463, K471 and R474) and from motif E (R734 and R742) | Japanese encephalitis virus P20778 | ? | - |
? | |
2.7.7.48 | nucleoside triphosphate + RNAn | - |
Japanese encephalitis virus | diphosphate + RNAn+1 | - |
? | |
2.7.7.48 | nucleoside triphosphate + RNAn | primer-free initiation assay with 13-nt RNA template, and ATP, CTP, FAM-UTP, and GTP, and additionally with a primer (5'-GUUCACACAGAUAAACUUCU-3') with a 6-FAM-labeled at the 5'-end in the primer extension assay | Japanese encephalitis virus | diphosphate + RNAn+1 | - |
? | |
2.7.7.48 | nucleoside triphosphate + RNAn | - |
Japanese encephalitis virus P20778 | diphosphate + RNAn+1 | - |
? | |
2.7.7.48 | nucleoside triphosphate + RNAn | primer-free initiation assay with 13-nt RNA template, and ATP, CTP, FAM-UTP, and GTP, and additionally with a primer (5'-GUUCACACAGAUAAACUUCU-3') with a 6-FAM-labeled at the 5'-end in the primer extension assay | Japanese encephalitis virus P20778 | diphosphate + RNAn+1 | - |
? |
EC Number | Synonyms | Comment | Organism |
---|---|---|---|
2.7.7.48 | jRdRp | - |
Japanese encephalitis virus |
2.7.7.48 | RDRP | - |
Japanese encephalitis virus |
2.7.7.48 | RNA-dependent RNA polymerase | - |
Japanese encephalitis virus |
EC Number | Temperature Optimum [°C] | Temperature Optimum Maximum [°C] | Comment | Organism |
---|---|---|---|---|
2.7.7.48 | 30 | 37 | assay at | Japanese encephalitis virus |
EC Number | pH Optimum Minimum | pH Optimum Maximum | Comment | Organism |
---|---|---|---|---|
2.7.7.48 | 8 | - |
assay at | Japanese encephalitis virus |