EC Number |
Inhibitors |
Structure |
---|
2.7.1.33 | (2E)-3-[[(2R)-2,4-dihydroxy-3,3-dimethylbutanoyl]amino]prop-2-enoic acid |
CJ-15,801, an enamide analogue of pantothenate isolated from the fungus Seimatosporium sp. CL28611. CJ-15,801 is phosphorylated by pantothenate kinase (PanK). Subsequently, phospho-CJ-15,801 is accepted as a substrate by the next enzyme in the pathway (phosphopantothenoylcysteine synthetase, PPCS), and reacts to become cytidylylated. The cytidylylated phospho-CJ-15,801, which closely mimics the natural reaction intermediate and binds tightly and reversibly to the enzyme, does not react further and instead inhibits the enzyme |
|
2.7.1.33 | (2E)-3-[[(2R)-2,4-dihydroxy-3,3-dimethylbutanoyl]amino]prop-2-enoic acid |
- |
|
2.7.1.33 | (2E)-3-[[(2S)-2,4-dihydroxy-3,3-dimethylbutanoyl]amino]prop-2-enoic acid |
- |
|
2.7.1.33 | (2R)-2,4-dihydroxy-3,3-dimethyl-N'-phenylbutanohydrazide |
competitive, pantothenic acid analogue with 2,4-dihydroxy-3,3-dimethylbutyramide core of pantothenate, inhibition mechanism |
|
2.7.1.33 | (2R)-2,4-dihydroxy-3,3-dimethylbutanohydrazide |
competitive, pantothenic acid analogue with 2,4-dihydroxy-3,3-dimethylbutyramide core of pantothenate, inhibition mechanism |
|
2.7.1.33 | (2R)-2,4-dihydroxy-N-(2-hydroxyethyl)-3,3-dimethylbutanamide |
competitive, pantothenic acid analogue with 2,4-dihydroxy-3,3-dimethylbutyramide core of pantothenate, inhibition mechanism |
|
2.7.1.33 | (2R)-N-(2,3-dihydroxypropyl)-2,4-dihydroxy-3,3-dimethylbutanamide |
competitive, pantothenic acid analogue with 2,4-dihydroxy-3,3-dimethylbutyramide core of pantothenate, inhibition mechanism |
|
2.7.1.33 | (2R)-N-allyl-2,4-dihydroxy-3,3-dimethylbutanamide |
competitive, pantothenic acid analogue with 2,4-dihydroxy-3,3-dimethylbutyramide core of pantothenate, inhibition mechanism |
|
2.7.1.33 | (2Z)-3-[[(2R)-2,4-dihydroxy-3,3-dimethylbutanoyl]amino]prop-2-enoic acid |
- |
|
2.7.1.33 | (2Z)-3-[[(2S)-2,4-dihydroxy-3,3-dimethylbutanoyl]amino]prop-2-enoic acid |
- |
|