EC Number |
Substrates |
Organism |
Products |
Reversibility |
---|
2.7.9.1 | 2'-dAMP + phosphoenolpyruvate + diphosphate |
- |
[Clostridium] symbiosum |
2'-dATP + pyruvate + phosphate |
- |
? |
2.7.9.1 | AMP + phosphoenolpyruvate + diphosphate |
- |
Zea mays |
ATP + pyruvate + phosphate |
- |
? |
2.7.9.1 | AMP + phosphoenolpyruvate + diphosphate |
synthesis of ATP is not thermodynamically favorable in trophozoites of Entamoeba histolytica |
Entamoeba histolytica |
ATP + pyruvate + phosphate |
- |
? |
2.7.9.1 | AMP + phosphoenolpyruvate + diphosphate |
ordered steady-state mechanism, uni uni bi bi ping-pong mechanismsequential kinetic mechanism between AMP and pyrophosphate, phosphate is released before ATP |
Entamoeba histolytica |
ATP + pyruvate + phosphate |
- |
? |
2.7.9.1 | ATP + PPDK central domain construct of residues 381-512 (Cent-I) + phosphate |
- |
[Clostridium] symbiosum |
? |
- |
? |
2.7.9.1 | ATP + PPDK N-terminal domain construct of residues 1-340 (Tem-340) + phosphate |
- |
[Clostridium] symbiosum |
? |
- |
? |
2.7.9.1 | ATP + PPDK N-terminal domain construct of residues 1-553 (Tem340-Cent-I) + phosphate |
- |
[Clostridium] symbiosum |
? |
- |
? |
2.7.9.1 | ATP + pyruvate + arsenate |
the rate of phosphoenolpyruvate formation in the presence of arsenate is 65% lower than that obtained with phosphate |
Komagataeibacter xylinus |
? |
- |
? |
2.7.9.1 | ATP + pyruvate + phosphate |
- |
Triticum aestivum |
AMP + phosphoenolpyruvate + diphosphate |
- |
? |
2.7.9.1 | ATP + pyruvate + phosphate |
- |
Acetobacter aceti |
AMP + phosphoenolpyruvate + diphosphate |
- |
? |