EC Number | General Stability | Organism |
---|---|---|
2.7.7.79 | the enzyme shows a drastically shortened half-life in the absence of divalent metal ions | Saccharomyces cerevisiae |
EC Number | Inhibitors | Comment | Organism | Structure |
---|---|---|---|---|
2.7.7.79 | 5,5'-dithiobis(2-nitrobenzoic)acid | progressive loss of activity with increasing amounts of DTNB. Thus, sulfhydryl groups are involved in maintaining the active state of the enzyme or are involved in the mechanism | Saccharomyces cerevisiae |
EC Number | Metals/Ions | Comment | Organism | Structure |
---|---|---|---|---|
2.7.7.79 | Co2+ | the requirement for a divalent metal ion can be satisfied by Mg2+, Mn2+, and to a lesser extent by Co2+ and Zn2+. Activity in presence of 10 mM Co2+ is 13% compared to the activity in presence of 10 mM Mg2+ | Saccharomyces cerevisiae | |
2.7.7.79 | Mg2+ | the requirement for a divalent metal ion can be satisfied by Mg2+, Mn2+, and to a lesser extent by Co2+ and Zn2+. Maximal activity by 10 mM Mg2+ | Saccharomyces cerevisiae | |
2.7.7.79 | Mn2+ | the requirement for a divalent metal ion can be satisfied by Mg2+, Mn2+, and to a lesser extent by Co2+ and Zn2+. Activity in presence of 10 mM Mn2+ is 70% compared to the activity in presence of 10 mM Mg2+ | Saccharomyces cerevisiae | |
2.7.7.79 | Zn2+ | the requirement for a divalent metal ion can be satisfied by Mg2+, Mn2+, and to a lesser extent by Co2+ and Zn2+. Activity in presence of 10 mM Zn2+ is 15% compared to the activity in presence of 10 mM Mg2+ | Saccharomyces cerevisiae |
EC Number | Molecular Weight [Da] | Molecular Weight Maximum [Da] | Comment | Organism |
---|---|---|---|---|
2.7.7.79 | 58000 | - |
2 * 58000, SDS-PAGE | Saccharomyces cerevisiae |
2.7.7.79 | 120000 | - |
gel filtration | Saccharomyces cerevisiae |
EC Number | Natural Substrates | Organism | Comment (Nat. Sub.) | Natural Products | Comment (Nat. Pro.) | Rev. | Reac. |
---|---|---|---|---|---|---|---|
2.7.7.79 | p-tRNAHis + ATP + GTP | Saccharomyces cerevisiae | - |
pppGp-tRNAHis + AMP + diphosphate | - |
? |
EC Number | Organism | UniProt | Comment | Textmining |
---|---|---|---|---|
2.7.7.79 | Saccharomyces cerevisiae | P53215 | - |
- |
EC Number | Purification (Comment) | Organism |
---|---|---|
2.7.7.79 | - |
Saccharomyces cerevisiae |
EC Number | Substrates | Comment Substrates | Organism | Products | Comment (Products) | Rev. | Reac. |
---|---|---|---|---|---|---|---|
2.7.7.79 | p-tRNAHis + ATP + GTP | - |
Saccharomyces cerevisiae | pppGp-tRNAHis + AMP + diphosphate | - |
? | |
2.7.7.79 | p-tRNAHis + ATP + GTP | among all acceptor tRNAs in unfractionatedt RNA only tRNAHis is a substrate for the purified enzyme. tRNA from plant and prokaryotes are better substrates than mammalian and insect tRNAs | Saccharomyces cerevisiae | pppGp-tRNAHis + AMP + diphosphate | - |
? |
EC Number | Subunits | Comment | Organism |
---|---|---|---|
2.7.7.79 | dimer | 2 * 58000, SDS-PAGE | Saccharomyces cerevisiae |
EC Number | Synonyms | Comment | Organism |
---|---|---|---|
2.7.7.79 | histidine tRNA guanylyltransferase | - |
Saccharomyces cerevisiae |
EC Number | Temperature Optimum [°C] | Temperature Optimum Maximum [°C] | Comment | Organism |
---|---|---|---|---|
2.7.7.79 | 22 | - |
assay at room temperature | Saccharomyces cerevisiae |
EC Number | pH Minimum | pH Maximum | Comment | Organism |
---|---|---|---|---|
2.7.7.79 | 8 | - |
assay at | Saccharomyces cerevisiae |