5.3.99.6: allene-oxide cyclase
This is an abbreviated version!
For detailed information about allene-oxide cyclase, go to the full flat file.
Word Map on EC 5.3.99.6
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5.3.99.6
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jasmonic
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12-oxo-phytodienoic
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oxylipins
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octadecanoids
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13s-lipoxygenase
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phytodienoic
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ja-deficient
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hebiba
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12-opda
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ja-ile
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agriculture
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12-oxo-pda
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tulipae
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biotechnology
- 5.3.99.6
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jasmonic
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12-oxo-phytodienoic
- oxylipins
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octadecanoids
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13s-lipoxygenase
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phytodienoic
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ja-deficient
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hebiba
- 12-opda
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ja-ile
- agriculture
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12-oxo-pda
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tulipae
- biotechnology
Reaction
Synonyms
AaAOC, Allene oxide cyclase, allene oxide oxidase, allene oxide oxidase 3, AOC, AOC1, AOC2, AOC3, Cyclase, allene oxide, EC 5.3.99.1, JcAOC, OsAOC, PnAOC
ECTree
5.3.99.6 allene-oxide cyclaseAdvanced search results
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results (Substrates Products
Substrates Products on EC 5.3.99.6 - allene-oxide cyclase
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SUBSTRATE 
PRODUCT
REACTION DIAGRAM
ORGANISM
UNIPROT
COMMENTARY
(Substrate)
(Substrate)
LITERATURE
(Substrate)
(Substrate)
COMMENTARY
(Product)
(Product)
LITERATURE
(Product)
(Product)
Reversibility
r=reversible
ir=irreversible
?=not specified
r=reversible
ir=irreversible
?=not specified
(12,13S)-epoxy-(9Z,11,15Z)-octadecatrienoic acid
(9S,13S)-12-oxo-(10,15Z)-phytodienoic acid
(12,13S)-epoxy-(9Z,11E,15Z)-octadecatrienoic acid
12-oxo-phytodienoic acid
-
-
-
-
?
(12S)-hydroperoxy eicosatetraenoic acid
11-oxoprostatrienoic acid
20:4(n-6)-derived (12S)-hydroperoxy eicosatetraenoic acid
-
-
?
(12Z)-9,10-epoxy-10,12-octadecadienoic acid
rac-cis-10-oxo-11-phytoenoic acid
-
CYP74C3 catalyzes the synthesis, hydrolysis and cyclization of allene oxide
in addition, formation of some alpha-ketol
-
?
(5Z,8Z,10Z)-10-[3-[(2Z)-oct-2-en-1-yl]oxiran-2-ylidene]deca-5,8-dienoic acid
(5Z,14Z)-11-oxoprosta-5,9,14-trien-1-oic acid
-
substrate for isoenzyme PpAOC2
-
-
?
(9Z,11E)-11-[(3S)-3-[(2Z)-pent-2-en-1-yl]oxiran-2-ylidene]undec-9-enoic acid
8-[(1R,5S)-4-oxo-5-[(2Z)-pent-2-en-1-yl]cyclopent-2-en-1-yl]octanoic acid
-
-
i.e. cis-(+)-OPDA
-
?
(9Z,13S,15Z)-12,13-epoxy-9,11,15-octadecatrienoic acid
(9S,13S)-12-oxo-phytodienoic acid
-
-
-
-
?
(9Z,13S,15Z)-12,13-epoxyoctadeca-9,11,15-trienoate
(9S,13S,15Z)-12-oxophyto-10,15-dienoate
(12,13S)-epoxy-(9Z,11,15Z)-octadecatrienoic acid
(9S,13S)-12-oxo-(10,15Z)-phytodienoic acid
-
-
-
?
(12,13S)-epoxy-(9Z,11,15Z)-octadecatrienoic acid
(9S,13S)-12-oxo-(10,15Z)-phytodienoic acid
-
-
-
?
(12,13S)-epoxy-(9Z,11,15Z)-octadecatrienoic acid
(9S,13S)-12-oxo-(10,15Z)-phytodienoic acid
-
-
-
?
(12,13S)-epoxy-(9Z,11,15Z)-octadecatrienoic acid
(9S,13S)-12-oxo-(10,15Z)-phytodienoic acid
-
-
-
?
(12,13S)-epoxy-(9Z,11,15Z)-octadecatrienoic acid
(9S,13S)-12-oxo-(10,15Z)-phytodienoic acid
-
-
-
?
(12,13S)-epoxy-(9Z,11,15Z)-octadecatrienoic acid
(9S,13S)-12-oxo-(10,15Z)-phytodienoic acid
-
-
-
?
(12,13S)-epoxy-(9Z,11,15Z)-octadecatrienoic acid
(9S,13S)-12-oxo-(10,15Z)-phytodienoic acid
-
-
-
?
(12,13S)-epoxy-(9Z,11,15Z)-octadecatrienoic acid
(9S,13S)-12-oxo-(10,15Z)-phytodienoic acid
-
-
-
?
(12,13S)-epoxy-(9Z,11,15Z)-octadecatrienoic acid
(9S,13S)-12-oxo-(10,15Z)-phytodienoic acid
-
-
-
?
(12,13S)-epoxy-(9Z,11,15Z)-octadecatrienoic acid
(9S,13S)-12-oxo-(10,15Z)-phytodienoic acid
-
-
-
?
(12,13S)-epoxy-(9Z,11,15Z)-octadecatrienoic acid
(9S,13S)-12-oxo-(10,15Z)-phytodienoic acid
-
-
-
?
(12,13S)-epoxy-(9Z,11,15Z)-octadecatrienoic acid
(9S,13S)-12-oxo-(10,15Z)-phytodienoic acid
-
-
-
?
(9Z)-(13S)-12,13-epoxyoctadeca-9,11,15-trienoate
(15Z)-12-oxophyto-10,15-dienoate
-
-
-
-
?
(9Z)-(13S)-12,13-epoxyoctadeca-9,11,15-trienoate
(15Z)-12-oxophyto-10,15-dienoate
-
-
-
?
(9Z)-(13S)-12,13-epoxyoctadeca-9,11,15-trienoate
(15Z)-12-oxophyto-10,15-dienoate
-
-
-
-
?
(9Z)-(13S)-12,13-epoxyoctadeca-9,11,15-trienoate
(15Z)-12-oxophyto-10,15-dienoate
-
-
-
-
?
(9Z)-(13S)-12,13-epoxyoctadeca-9,11,15-trienoate
(15Z)-12-oxophyto-10,15-dienoate
-
-
-
?
(9Z)-(13S)-12,13-epoxyoctadeca-9,11,15-trienoate
(15Z)-12-oxophyto-10,15-dienoate
-
-
-
-
?
(9Z)-(13S)-12,13-epoxyoctadeca-9,11,15-trienoate
(15Z)-12-oxophyto-10,15-dienoate
-
-
-
-
?
(9Z)-(13S)-12,13-epoxyoctadeca-9,11,15-trienoate
(15Z)-12-oxophyto-10,15-dienoate
-
-
-
?
(9Z)-(13S)-12,13-epoxyoctadeca-9,11,15-trienoate
(15Z)-12-oxophyto-10,15-dienoate
-
-
-
-
?
(9Z)-(13S)-12,13-epoxyoctadeca-9,11,15-trienoate
(15Z)-12-oxophyto-10,15-dienoate
-
-
-
-
?
(9Z)-(13S)-12,13-epoxyoctadeca-9,11,15-trienoate
(15Z)-12-oxophyto-10,15-dienoate
-
-
-
-
?
(9Z)-(13S)-12,13-epoxyoctadeca-9,11,15-trienoate
(15Z)-12-oxophyto-10,15-dienoate
-
-
-
-
?
(9Z)-(13S)-12,13-epoxyoctadeca-9,11,15-trienoate
(15Z)-12-oxophyto-10,15-dienoate
Q8L6H4
-
-
-
?
(9Z)-(13S)-12,13-epoxyoctadeca-9,11,15-trienoate
(15Z)-12-oxophyto-10,15-dienoate
Q8L6H4
enzyme catalyzes a late step in the jasmonic acid biosynthetic pathway
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-
?
(9Z)-(13S)-12,13-epoxyoctadeca-9,11,15-trienoate
(15Z)-12-oxophyto-10,15-dienoate
-
-
-
?
(9Z)-(13S)-12,13-epoxyoctadeca-9,11,15-trienoate
(15Z)-12-oxophyto-10,15-dienoate
-
-
-
-
?
(9Z)-(13S)-12,13-epoxyoctadeca-9,11,15-trienoate
(15Z)-12-oxophyto-10,15-dienoate
-
-
-
-
?
(9Z,13S,15Z)-12,13-epoxyoctadeca-9,11,15-trienoate
(9S,13S,15Z)-12-oxophyto-10,15-dienoate
-
-
-
?
(9Z,13S,15Z)-12,13-epoxyoctadeca-9,11,15-trienoate
(9S,13S,15Z)-12-oxophyto-10,15-dienoate
-
-
-
?
13(S)-hydroperoxy-9(Z),11(E),15(Z)-octadecatrienoic acid
cis-(+)-12-oxophytodienoic acid
-
93.9% of cis-(+)-12-oxophytodienoic acid
-
?
13(S)-hydroperoxy-9(Z),11(E),15(Z)-octadecatrienoic acid
cis-(+)-12-oxophytodienoic acid
-
94.1% of cis-(+)-12-oxophytodienoic acid
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?
13(S)-hydroperoxy-9(Z),11(E),15(Z)-octadecatrienoic acid
cis-(+)-12-oxophytodienoic acid
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isoform AOC1, 91.3% of cis-(+)-12-oxophytodienoic acid
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?
13(S)-hydroperoxy-9(Z),11(E),15(Z)-octadecatrienoic acid
cis-(+)-12-oxophytodienoic acid
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isoforms AOC2, 93.6%of cis-(+)-12-oxophytodienoic acid
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?
additional information
?
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all Arabidopsis allene oxide cyclase isoforms may contribute to jasmonate biosynthesis
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-
?
additional information
?
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all Arabidopsis allene oxide cyclase isoforms may contribute to jasmonate biosynthesis
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-
?
additional information
?
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all Arabidopsis allene oxide cyclase isoforms may contribute to jasmonate biosynthesis
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-
?
additional information
?
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all Arabidopsis allene oxide cyclase isoforms may contribute to jasmonate biosynthesis
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?
additional information
?
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all Arabidopsis allene oxide cyclase isoforms may contribute to jasmonate biosynthesis
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?
additional information
?
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allene oxides formed by the action of EC 4.2.1.92 are converted into cyclopentanone derivatives
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?
additional information
?
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enzyme of a branch leading specifically from (13S)-hydroperoxy-(9Z,11E,15Z)-octatrienoic acid to 12-oxo-phytodienoic acid, the precursor of jasmonic acid
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?
additional information
?
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role for jasmonic acid in the transfer of the assimilate to seeds
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?
additional information
?
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enzyme plays an essential role in formation of jasmonic acid induced by theobroxide
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?
additional information
?
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the plant contains two isozymes, PpAOC1 and PpAOC2, with different substrate specificities for C18- and C20-derived substrates, respectively. Comparison of complex structures of the C18 substrate analogue with in silico modeling of the C20 substrate analogue bound to the enzyme allows identification of the three major molecular determinants responsible for the different substrate specificities, i.e. larger active site diameter, an elongated cavity of PpAOC2, and two nonidentical residues at the entrance of the active site
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-
?
additional information
?
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the plant contains two isozymes, PpAOC1 and PpAOC2, with different substrate specificities for C18- and C20-derived substrates, respectively. Comparison of complex structures of the C18 substrate analogue with in silico modeling of the C20 substrate analogue bound to the enzyme allows identification of the three major molecular determinants responsible for the different substrate specificities, i.e. larger active site diameter, an elongated cavity of PpAOC2, and two nonidentical residues at the entrance of the active site
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-
?
additional information
?
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the plant contains two isozymes, PpAOC1 and PpAOC2, with different substrate specificities for C18- and C20-derived substrates, respectively. Comparison of complex structures of the C18 substrate analogue with in silico modeling of the C20 substrate analogue bound to the enzyme allows identification of the three major molecular determinants responsible for the different substrate specificities, i.e. larger active site diameter, an elongated cavity of PpAOC2, and two nonidentical residues at the entrance of the active site
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-
?
additional information
?
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substrate specificity of isozyme AOC2, overview
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?
additional information
?
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substrate specificity of isozyme AOC2, overview
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?
additional information
?
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substrate specificity of isozyme AOC2, overview
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?
additional information
?
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substrate specificity of wild-type and mutant isozymes AOC1, overview. The substrate dihydro analogue cis-12,13S-epoxy-9Z,15Z-octadecadienoic acid does not cyclize in the presence of PpAOC1, but when bound to the enzyme, it undergoes isomerization into the corresponding trans-epoxide. AOc1 shows no activity with 20:4(n-6)-derived (12S)-hydroperoxy eicosatetraenoic acid
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-
?
additional information
?
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substrate specificity of wild-type and mutant isozymes AOC1, overview. The substrate dihydro analogue cis-12,13S-epoxy-9Z,15Z-octadecadienoic acid does not cyclize in the presence of PpAOC1, but when bound to the enzyme, it undergoes isomerization into the corresponding trans-epoxide. AOc1 shows no activity with 20:4(n-6)-derived (12S)-hydroperoxy eicosatetraenoic acid
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-
?
additional information
?
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substrate specificity of wild-type and mutant isozymes AOC1, overview. The substrate dihydro analogue cis-12,13S-epoxy-9Z,15Z-octadecadienoic acid does not cyclize in the presence of PpAOC1, but when bound to the enzyme, it undergoes isomerization into the corresponding trans-epoxide. AOc1 shows no activity with 20:4(n-6)-derived (12S)-hydroperoxy eicosatetraenoic acid
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-
?
