Crystallization (Comment) | Organism |
---|---|
- |
Saccharolobus solfataricus |
Protein Variants | Comment | Organism |
---|---|---|
C210S | decrease in melting temperature by 12 degrees | Saccharolobus solfataricus |
Localization | Comment | Organism | GeneOntology No. | Textmining |
---|
Molecular Weight [Da] | Molecular Weight Maximum [Da] | Comment | Organism |
---|---|---|---|
37000 | - |
2 * 37000, calculated and dynamic light scattering | Saccharolobus solfataricus |
42000 | - |
gel filtration, Tris-HCl buffer, presence of 2-mercaptoethanol | Saccharolobus solfataricus |
52000 | - |
gel filtration, sodium phosphate buffer | Saccharolobus solfataricus |
Organism | UniProt | Comment | Textmining |
---|---|---|---|
Saccharolobus solfataricus | Q97UL5 | - |
- |
Saccharolobus solfataricus DSM 1617 | Q97UL5 | - |
- |
Posttranslational Modification | Comment | Organism |
---|---|---|
side-chain modification | subunits of the enzyme homodimer are connected via an intersubunit disulfide bond between the Cys210 residues. When mutagenesis replaces the disulfide-forming cysteine residue with serine, the thermostability of the enzyme is significantly lowered. In the presence of 2-mercaptoethanol, the wild-type enzyme is less stable to heat. The disulfide bond is predominantly formed in the cells | Saccharolobus solfataricus |
Subunits | Comment | Organism |
---|---|---|
dimer | 2 * 37000, calculated and dynamic light scattering | Saccharolobus solfataricus |
Synonyms | Comment | Organism |
---|---|---|
SSO2989 | - |
Saccharolobus solfataricus |
Temperature Stability Minimum [°C] | Temperature Stability Maximum [°C] | Comment | Organism |
---|---|---|---|
78 | - |
melting temperature, mutant C210S | Saccharolobus solfataricus |
80 | - |
1 h, complete loss of activity in presence of 2-mercaptoethanol | Saccharolobus solfataricus |
90 | - |
melting temperature, wild-type | Saccharolobus solfataricus |