EC Number   |
Inhibitors |
Structure  |
|---|
   7.4.2.1 | more |
cycling of Gap1p-GFP to the plasma membrane is blocked by high amino acid concentrations |
 |
| 7.4.2.1 | more |
permease activity can be rapidly and reversibly inactivated by the presence of most amino acids, except alanine or phenylalanine, mixtures of amino acids are less toxic than single amino acids, the toxicity appears to be the consequence of uptake of unusually large quantities of a single amino acid |
|
| 7.4.2.1 | more |
brefeldin A decreases uptake of L-Leu, substance probably acts via direct or indirect modification of the transporting protein, which affects the kinetic parameters |
|
| 7.4.2.1 | more |
inhibition of agonist activity by the inhibitor molecules, overveiw |
|
| 7.4.2.1 | more |
no or poor inhibition by L-alanine, L-asparagine, L-arginine, L-proline, L-serine, glycine, L-methionine, L-threonine, L-histidine, and L-cysteine |
|
| 7.4.2.1 | more |
no inhibition by L-aspartate, L-arginine, L-asparagine, L-alanine, and L-serine |
|
| 7.4.2.1 | more |
reversible inactivation of intrinsic Gap1p activity at the cell surface by amino acids requires active transport through Gap1p |
|
| 7.4.2.1 | ADP |
inhibits ATPase activity |
  |
| 7.4.2.1 | ADP |
dimeric HisP protein with a carboxy-terminal extension of 8 amino acids |
|
| 7.4.2.1 | ADP |
- |
|
