EC Number | Cloned (Comment) | Organism |
---|---|---|
6.1.1.21 | gene hisS, expression of HisRS active site fragments, HisRS1-HisRS4, as maltose-binding proteins fusion proteins in Escherichia coli strain BL21(DE3)pLysS | Escherichia coli |
EC Number | Protein Variants | Comment | Organism |
---|---|---|---|
6.1.1.21 | additional information | construction of four minimal, active site fragments, urzymes, of Escherichia coli class II HisRS by PCR-based subcloning, the fragments comprise: HisRS1 residues 16-134, HisRS2 residues 10-134, HisRS3 residues 16-134 and 301-320, and HisRS4 residues 10-134 and 301-320. HisRS-3 binds ATP far more tightly and histidine less strongly than native, full-length HisRS or its intact catalytic domain. HisRS-3 urzyme steady-state kinetic parameters differ substantially from those of native full-length HisRS. All urzymes show relative rate enhancements compared to the wild-type enzyme, overview | Escherichia coli |
EC Number | KM Value [mM] | KM Value Maximum [mM] | Substrate | Comment | Organism | Structure |
---|---|---|---|---|---|---|
6.1.1.21 | additional information | - |
additional information | Michaelis-Menten kinetics for the wild-type enzyme and recombinant HisRS active site fragments, HisRS1-HisRS4, overview | Escherichia coli |
EC Number | Metals/Ions | Comment | Organism | Structure |
---|---|---|---|---|
6.1.1.21 | Mg2+ | required | Escherichia coli |
EC Number | Natural Substrates | Organism | Comment (Nat. Sub.) | Natural Products | Comment (Nat. Pro.) | Rev. | Reac. |
---|---|---|---|---|---|---|---|
6.1.1.21 | ATP + L-histidine + tRNAHis | Escherichia coli | - |
AMP + diphosphate + L-histidyl-tRNAHis | - |
? |
EC Number | Organism | UniProt | Comment | Textmining |
---|---|---|---|---|
6.1.1.21 | Escherichia coli | - |
gene hisS | - |
EC Number | Purification (Comment) | Organism |
---|---|---|
6.1.1.21 | recombinant maltose-binding fusion HisRS active site fragments, HisRS1-HisRS4, from Escherichia coli strain BL21(DE3)pLysS by amylose affinity chromatography, fusion protein cleavage by TEV. The fusion protein does not affect urzyme activity | Escherichia coli |
EC Number | Substrates | Comment Substrates | Organism | Products | Comment (Products) | Rev. | Reac. |
---|---|---|---|---|---|---|---|
6.1.1.21 | ATP + L-histidine + tRNAHis | - |
Escherichia coli | AMP + diphosphate + L-histidyl-tRNAHis | - |
? |
EC Number | Synonyms | Comment | Organism |
---|---|---|---|
6.1.1.21 | class II histidyl-tRNA synthetase | - |
Escherichia coli |
6.1.1.21 | HisRS | - |
Escherichia coli |
6.1.1.21 | HisRS-1 | - |
Escherichia coli |
6.1.1.21 | HisRS-2 | - |
Escherichia coli |
6.1.1.21 | Histidyl-tRNA synthetase | - |
Escherichia coli |
EC Number | Cofactor | Comment | Organism | Structure |
---|---|---|---|---|
6.1.1.21 | ATP | - |
Escherichia coli |
EC Number | General Information | Comment | Organism |
---|---|---|---|
6.1.1.21 | evolution | significantly different rate enhancements by four HisRS urzymes demonstrate that amino acid activation provides an experimental metric for recapitulating very early evolutionary events. Catalytic activities of HisRS-1 and HisRS-2 provide complementary support for Rodin-Ohno hypothesis that ancestral class I and II aaRS were encoded on opposite strands of same gene | Escherichia coli |