EC Number |
Inhibitors |
Structure |
---|
5.4.99.30 | EDTA |
5 mM, complete inhibition; 5 mM, complete inhibition |
|
5.4.99.30 | Mn2+ |
activates, best divalent metal ion, optimal at 0.08 mM, about 20% of maximal activity at 1 mM, complete inhibition at 5 mM; activates, best divalent metal ion, optimal at 0.08 mM, about 20% of maximal activity at 1 mM, complete inhibition at 5 mM; activates, best divalent metal ion, optimal at 0.08 mM, about 25% of maximal activity at 1 mM, complete inhibition at 5 mM |
|
5.4.99.30 | more |
no affect: CaCl2, MgCl2, CuSO4, ZnCl2, and CoCl2 at 5 mM; no affect: CaCl2, MgCl2, CuSO4, ZnCl2, and CoCl2 at 5 mM |
|
5.4.99.30 | n-butanol |
- |
|
5.4.99.30 | UDP |
competitive inhibition, lower affinity for enzyme than substrate |
|
5.4.99.30 | UDP-Gal |
activity decreases by 40% under pretreatment for 3 h |
|
5.4.99.30 | UDP-Gal |
decrease in mutase activity, when the nucleotide sugar reacts with the enzyme prior to the addition of beta-L-arabinofuranose; decrease in mutase activity, when the nucleotide sugar reacts with the enzyme prior to the addition of beta-L-arabinofuranose |
|
5.4.99.30 | UDP-Glc |
activity decreases by 40% under pretreatment for 3 h |
|
5.4.99.30 | UDP-Glc |
decrease in mutase activity, when the nucleotide sugar reacts with the enzyme prior to the addition of beta-L-arabinofuranose; decrease in mutase activity, when the nucleotide sugar reacts with the enzyme prior to the addition of beta-L-arabinofuranose |
|
5.4.99.30 | UDP-Xyl |
activity decreases by 40% under pretreatment for 3 h |
|