EC Number |
Substrates |
Organism |
Products |
Reversibility |
---|
1.3.1.119 | 3-chloro-5-methylbenzene dihydrodiol + NAD+ |
- |
Cupriavidus sp. PS12 |
3-chloro-5-methylcatechol + NADH + H+ |
- |
? |
1.3.1.119 | 5-chloro-3-methylbenzene dihydrodiol + NAD+ |
- |
Cupriavidus sp. PS12 |
5-chloro-3-methylcatechol + NADH + H+ |
- |
? |
1.3.1.119 | (+)-cis-2',3'-dihydroxy-2',3'-dihydro-2-chlorobiphenyl + NAD+ |
- |
Pseudomonas sp. P51 |
2,3-dihydroxy-2'-chlorobiphenyl + NADH + H+ |
- |
? |
1.3.1.119 | (+)-cis-2',3'-dihydroxy-2',3'-dihydro-3-chlorobiphenyl + NAD+ |
- |
Pseudomonas sp. P51 |
2,3-dihydroxy-3'-chlorobiphenyl + NADH + H+ |
- |
? |
1.3.1.119 | (+)-cis-2',3'-dihydroxy-2',3'-dihydro-4-chlorobiphenyl + NAD+ |
- |
Pseudomonas sp. P51 |
2,3-dihydroxy-4'-chlorobiphenyl + NADH + H+ |
- |
? |
1.3.1.119 | (1S)-1-indanol + NAD+ |
with racemic 1-indanol, the enzyme enantioselectively transforms the (1S) enantiomer to 1-indanone |
Pseudomonas sp. P51 |
1-indanone + NADH + H+ |
- |
? |
1.3.1.119 | cis-(1R,2S)-1,2-dihydroxy-1,2,3,4-tetrahydronaphthalene + NAD+ |
the enzyme oxidizes both enantiomers of cis-1,2-dihydroxy-1,2,3,4-tetrahydronaphthalene, but oxidation of the cis-(1S,2R) enantiomer is delayed until the cis-(1R,2S) enantiomer is completely depleted |
Pseudomonas sp. P51 |
1,2-dihydroxy-3,4-dihydronaphthalene + NADH + H+ |
- |
? |
1.3.1.119 | cis-(1R,2S)-1,2-indandiol + NAD+ |
no activity with the cis-(1S,2R) enantiomer |
Pseudomonas sp. P51 |
1,2-indenediol + NADH + H+ |
- |
? |
1.3.1.119 | cis-(1S,2R)-1,2-dihydroxy-1,2,3,4-tetrahydronaphthalene + NAD+ |
the enzyme oxidizes both enantiomers of cis-1,2-dihydroxy-1,2,3,4-tetrahydronaphthalene, but oxidation of the cis-(1S,2R) enantiomer is delayed until the cis-(1R,2S) enantiomer is completely depleted |
Pseudomonas sp. P51 |
1,2-dihydroxy-3,4-dihydronaphthalene + NADH + H+ |
- |
? |
1.3.1.119 | cis-toluene dihydrodiol + NAD+ |
- |
Pseudomonas sp. P51 |
3-methylcatechol + NADH + H+ |
- |
? |