Cloned (Comment) | Organism |
---|---|
expression in Escherichia coli | Arabidopsis thaliana |
Inhibitors | Comment | Organism | Structure |
---|---|---|---|
GDP | potent competitive inhibitor | Arabidopsis thaliana | |
GDP-D-glucose | potent competitive inhibitor | Arabidopsis thaliana | |
GDP-L-fucose | complex type of inhibition, IC50: 0.07 mM | Arabidopsis thaliana | |
L-ascorbic acid | 1 mM, 15% inhibition | Arabidopsis thaliana | |
L-galactono-1,4-lactone | 1 mM, 14% inhibition | Arabidopsis thaliana | |
NADH | - |
Arabidopsis thaliana | |
NADPH | - |
Arabidopsis thaliana |
KM Value [mM] | KM Value Maximum [mM] | Substrate | Comment | Organism | Structure |
---|---|---|---|---|---|
0.0045 | - |
GDP-D-mannose | native enzyme | Arabidopsis thaliana | |
0.018 | - |
GDP-D-mannose | recombinant enzyme with N-terminal His-tag | Arabidopsis thaliana | |
0.031 | - |
GDP-D-mannose | recombinant enzyme with N-terminal glutathione-S-transferase tag | Arabidopsis thaliana |
Natural Substrates | Organism | Comment (Nat. Sub.) | Natural Products | Comment (Nat. Pro.) | Rev. | Reac. |
---|---|---|---|---|---|---|
GDP-D-mannose | Arabidopsis thaliana | the enzyme catalyzes a reversible epimerization that precedes the committed step in the biosynthesis of vitamin C, resulting in the hydrolysis of the highly energetic glycosyl-diphosphoryl linkage. The plant enzyme undergoes a complex regulation and could control the carbonflux into the vitamin C pathway in response to the redox state of thecell, stress conditions, and GDP-sugar demand for the cell wall glycoprotein biosynthesis | GDP-L-galactose | - |
r |
Organism | UniProt | Comment | Textmining |
---|---|---|---|
Arabidopsis thaliana | - |
- |
- |
Substrates | Comment Substrates | Organism | Products | Comment (Products) | Rev. | Reac. |
---|---|---|---|---|---|---|
GDP-D-mannose | the reaction mixture contains at equilibrium GDP-D-mannose, GDP-L-galactose and GDP-L-gulose in a ratio of 1:0.4:0.2 | Arabidopsis thaliana | GDP-L-galactose | - |
r | |
GDP-D-mannose | the enzyme catalyzes a reversible epimerization that precedes the committed step in the biosynthesis of vitamin C, resulting in the hydrolysis of the highly energetic glycosyl-diphosphoryl linkage. The plant enzyme undergoes a complex regulation and could control the carbonflux into the vitamin C pathway in response to the redox state of thecell, stress conditions, and GDP-sugar demand for the cell wall glycoprotein biosynthesis | Arabidopsis thaliana | GDP-L-galactose | - |
r |
Turnover Number Minimum [1/s] | Turnover Number Maximum [1/s] | Substrate | Comment | Organism | Structure |
---|---|---|---|---|---|
0.007 | - |
GDP-D-mannose | recombinant enzyme with N-terminal His-tag | Arabidopsis thaliana | |
0.01 | - |
GDP-D-mannose | recombinant enzyme with N-terminal glutathione-S-transferase tag | Arabidopsis thaliana | |
0.041 | - |
GDP-D-mannose | native enzyme | Arabidopsis thaliana |
Cofactor | Comment | Organism | Structure |
---|---|---|---|
NAD+ | stimulates | Arabidopsis thaliana | |
NADP+ | stimulates | Arabidopsis thaliana |
IC50 Value | IC50 Value Maximum | Comment | Organism | Inhibitor | Structure |
---|---|---|---|---|---|
0.07 | - |
complex type of inhibition, IC50: 0.07 mM | Arabidopsis thaliana | GDP-L-fucose |