We're sorry, but BRENDA doesn't work properly without JavaScript. Please make sure you have JavaScript enabled in your browser settings.
Please wait a moment until all data is loaded. This message will disappear when all data is loaded.
IUBMB Comments Isolated from the bacterium Streptomyces pristinaespiralis .
Synonyms
Please wait a moment until the data is sorted. This message will disappear when the data is sorted.
pentalenene synthase
-
Please wait a moment until the data is sorted. This message will disappear when the data is sorted.
(2E,6E)-farnesyl diphosphate + H2O = (+)-(2S,3R,9R)-pristinol + diphosphate
-
-
-
-
Please wait a moment until the data is sorted. This message will disappear when the data is sorted.
(2E,6E)-farnesyl-diphosphate diphosphate-lyase [cyclizing, (+)-(2S,3R,9R)-pristinol-forming]
Isolated from the bacterium Streptomyces pristinaespiralis.
Please wait a moment until the data is sorted. This message will disappear when the data is sorted.
(2E,6E)-farnesyl diphosphate + H2O
(+)-(2S,3R,9R)-pristinol + diphosphate
additional information
?
-
(2E,6E)-farnesyl diphosphate + H2O
(+)-(2S,3R,9R)-pristinol + diphosphate
Substrates: -
?
(2E,6E)-farnesyl diphosphate + H2O
(+)-(2S,3R,9R)-pristinol + diphosphate
Substrates: -
?
additional information
?
-
Substrates: possible reaction mechanisms start with the cyclization of farnesyl diphosphate to the humulyl cation, a 1,2-hydride shift, and capture with water to (R)-hyemalol. No substrates: geranyl diphosphate and geranylgeranyl diphosphate
?
additional information
?
-
Substrates: possible reaction mechanisms start with the cyclization of farnesyl diphosphate to the humulyl cation, a 1,2-hydride shift, and capture with water to (R)-hyemalol. No substrates: geranyl diphosphate and geranylgeranyl diphosphate
?
Please wait a moment until the data is sorted. This message will disappear when the data is sorted.
(2E,6E)-farnesyl diphosphate + H2O
(+)-(2S,3R,9R)-pristinol + diphosphate
additional information
?
-
(2E,6E)-farnesyl diphosphate + H2O
(+)-(2S,3R,9R)-pristinol + diphosphate
Substrates: -
?
(2E,6E)-farnesyl diphosphate + H2O
(+)-(2S,3R,9R)-pristinol + diphosphate
Substrates: -
?
additional information
?
-
Substrates: possible reaction mechanisms start with the cyclization of farnesyl diphosphate to the humulyl cation, a 1,2-hydride shift, and capture with water to (R)-hyemalol. No substrates: geranyl diphosphate and geranylgeranyl diphosphate
?
additional information
?
-
Substrates: possible reaction mechanisms start with the cyclization of farnesyl diphosphate to the humulyl cation, a 1,2-hydride shift, and capture with water to (R)-hyemalol. No substrates: geranyl diphosphate and geranylgeranyl diphosphate
?
Please wait a moment until the data is sorted. This message will disappear when the data is sorted.
-
UniProt
brenda
-
UniProt
brenda
Highest Expressing Human Cell Lines
Filter by:
Cell Line Links
Gene Links
Please wait a moment until the data is sorted. This message will disappear when the data is sorted.
TATC6_HYPAT
386
0
44939
Swiss-Prot
other Location (Reliability: 4 )
PRISS_STRE2
Streptomyces pristinaespiralis (strain ATCC 25486 / DSM 40338 / CBS 914.69 / JCM 4507 / KCC S-0507 / NBRC 13074 / NRRL 2958 / 5647)
372
0
41393
Swiss-Prot
-
Please wait a moment until the data is sorted. This message will disappear when the data is sorted.
Please wait a moment until the data is sorted. This message will disappear when the data is sorted.
expression in Escherichia coli
Please wait a moment until the data is sorted. This message will disappear when the data is sorted.
Klapschinski, T.A.; Rabe, P.; Dickschat, J.S.
Pristinol, a sesquiterpene alcohol with an unusual skeleton from Streptomyces pristinaespiralis
Angew. Chem. Int. Ed. Engl.
55
10141-10144
2016
Streptomyces pristinaespiralis (B5H7H3), Streptomyces pristinaespiralis ATCC 25 486 (B5H7H3)
brenda
html completed
show
top
