EC Number |
Substrates |
Organism |
Products |
Reversibility |
---|
4.2.1.108 | N-alpha-acetyl-L-2,4-diaminobutanoate |
- |
Sphingopyxis alaskensis |
L-ectoine + H2O |
- |
? |
4.2.1.108 | N-alpha-acetyl-L-2,4-diaminobutanoate |
- |
Sphingopyxis alaskensis DSM 13593 / LMG 18877 / RB2256 |
L-ectoine + H2O |
- |
? |
4.2.1.108 | N4-acetyl-L-2,4-diaminobutanoate |
an intramolecular condensation reaction |
Halomonas elongata |
L-ectoine + H2O |
- |
r |
4.2.1.108 | N4-acetyl-L-2,4-diaminobutanoate |
an intramolecular condensation reaction |
Halomonas elongata |
L-ectoine + H2O |
i.e. 1,4,5,6-tetrahydro-2-methyl-4-pyrimidine carboxylic acid, over 95% conversion by the recombinant ectoine synthase |
r |
4.2.1.108 | N4-acetyl-L-2,4-diaminobutanoate |
an intramolecular condensation reaction |
Halomonas elongata DSM 2581 |
L-ectoine + H2O |
- |
r |
4.2.1.108 | N4-acetyl-L-2,4-diaminobutanoate |
an intramolecular condensation reaction |
Halomonas elongata DSM 2581 |
L-ectoine + H2O |
i.e. 1,4,5,6-tetrahydro-2-methyl-4-pyrimidine carboxylic acid, over 95% conversion by the recombinant ectoine synthase |
r |
4.2.1.108 | N4-acetyl-L-2,4-diaminobutyrate |
- |
Halalkalibacterium halodurans |
2-methyl-1,4,5,6-tetrahydropyrimidine-4-carboxylic acid + H2O |
- |
? |
4.2.1.108 | N4-acetyl-L-2,4-diaminobutyrate |
- |
Halalkalibacterium halodurans TCJAR021 |
2-methyl-1,4,5,6-tetrahydropyrimidine-4-carboxylic acid + H2O |
- |
? |
4.2.1.108 | N4-acetyl-L-2,4-diaminobutyrate |
- |
Halalkalibacterium halodurans |
L-ectoine + H2O |
- |
? |
4.2.1.108 | N4-acetyl-L-2,4-diaminobutyrate |
- |
Halalkalibacterium halodurans TCJAR021 |
L-ectoine + H2O |
- |
? |