4.2.1.127: linalool dehydratase
This is an abbreviated version!
For detailed information about linalool dehydratase, go to the full flat file.
Word Map on EC 4.2.1.127
-
4.2.1.127
-
castellaniella
-
defragrans
-
isomerization
-
monoterpene
-
acyclic
-
s-+-linalool
-
alkene
-
in-frame
-
terpene
-
betaproteobacterium
-
beta-myrcene
-
biotechnology
-
synthesis
- 4.2.1.127
- castellaniella
- defragrans
-
isomerization
-
monoterpene
-
acyclic
-
s-+-linalool
- alkene
-
in-frame
-
terpene
-
betaproteobacterium
- beta-myrcene
- biotechnology
- synthesis
Reaction
Synonyms
bifunctional linalool dehydratase isomerase, LDI, ldi/LDI, linalool dehydratase isomerase, linalool dehydratase-isomerase, linalool dehydratase/isomerase, LinD, LIS, More
ECTree
Advanced search results
Reaction
Reaction on EC 4.2.1.127 - linalool dehydratase
Please wait a moment until all data is loaded. This message will disappear when all data is loaded.
(3S)-linalool = myrcene + H2O
catalytic mechanism of enzyme LinD by a combined quantum mechanics and molecular mechanics (QM/MM), computational modeling
(3S)-linalool = myrcene + H2O
reaction mechanism via one acid-base mechanism via a carbocation intermediate. Residues C171, Y45 and D39 act as general acid and base for the protonation of the hydroxyl leaving group of the substrate (S)-linalool and the dehydration at the chiral carbon atom. Water is activated by H129 or C180 and added to the covalent or carbocation intermediate
(3S)-linalool = myrcene + H2O
the substrates are embedded inside a hydrophobic channel between two monomers of the (alpha,alpha)6 barrel fold class and flanked by three clusters of polar residues involved in acid-base catalysis. Catalytic mechanism, structure-function analysis, overview
(3S)-linalool = myrcene + H2O
reaction mechanism via one acid-base mechanism via a carbocation intermediate. Residues C171, Y45 and D39 act as general acid and base for the protonation of the hydroxyl leaving group of the substrate (S)-linalool and the dehydration at the chiral carbon atom. Water is activated by H129 or C180 and added to the covalent or carbocation intermediate
-
-
(3S)-linalool = myrcene + H2O
the substrates are embedded inside a hydrophobic channel between two monomers of the (alpha,alpha)6 barrel fold class and flanked by three clusters of polar residues involved in acid-base catalysis. Catalytic mechanism, structure-function analysis, overview
-
-