EC Number |
Inhibitors |
Structure |
---|
7.1.2.1 | 2-phenylbenzisothiazol-3(2H)-one |
- |
|
7.1.2.1 | adenosine 5'-(beta,gamma-imido)-triphosphate |
5 mM, 60% inhibition |
|
7.1.2.1 | adenosine 5'-monophosphate |
decreases the interaction between the phosphorylated Vha2 and the 14-3-3 protein, followed by a reduction of the H+-ATPase activity and citrate exudation under Al stress conditions |
|
7.1.2.1 | ADP |
5 mM, 60% inhibition, Kd value 0.8 mM |
|
7.1.2.1 | Al3+ |
inhibition of H+-ATPase activity, Mg2+ partly prevents |
|
7.1.2.1 | Al3+ |
the proton transport activity of the enzyme is inhibited by 50% in the presence of 100 mM Al3+ at pH 6.5 and 10% at pH 7.5 |
|
7.1.2.1 | aluminium |
the activity of plasma membrane H+-ATPase is affected by aluminium at the transcription, translation, and post-translation levels |
|
7.1.2.1 | aluminum fluoride |
- |
|
7.1.2.1 | ATP |
competitive inhibitor, the enzyme activity decreases in the presence of Mg2+-free ATP. ATP inhibition also occurs at pH 7.5. Upon increasing Mg2+ concentration from 5 mM to 15 mM, the decrease in ATPase activity at high ATP concentration is prevented |
|
7.1.2.1 | bafilomycin |
- |
|