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3-phenylpropionate + NADH + H+ + O2
3-(2,3-dihydroxyphenyl)propionate + NAD+
3-phenylpropionate + NADH + H+ + O2
3-(cis-5,6-dihydroxycyclohexa-1,3-dien-1-yl)propanoate + NAD+
3-phenylpropionate + NADH + H+ + O2
3-[(5S,6R)-5,6-dihydroxycyclohexa-1,3-dien-1-yl]propanoic acid + NAD+
cinnamic acid + NADH + H+ + O2
cinnamic acid-2,3-dihydrodiol + NAD+
3-phenylpropionate + NADH + H+ + O2
3-(2,3-dihydroxyphenyl)propionate + NAD+
-
Substrates: -
Products: -
?
3-phenylpropionate + NADH + H+ + O2
3-(2,3-dihydroxyphenyl)propionate + NAD+
-
Substrates: enables utilization of 3-phenylpropionate as carbon source
Products: -
?
3-phenylpropionate + NADH + H+ + O2
3-(2,3-dihydroxyphenyl)propionate + NAD+
-
Substrates: -
Products: -
?
3-phenylpropionate + NADH + H+ + O2
3-(2,3-dihydroxyphenyl)propionate + NAD+
-
Substrates: enables utilization of 3-phenylpropionate as carbon source
Products: -
?
3-phenylpropionate + NADH + H+ + O2
3-(cis-5,6-dihydroxycyclohexa-1,3-dien-1-yl)propanoate + NAD+
-
Substrates: -
Products: -
?
3-phenylpropionate + NADH + H+ + O2
3-(cis-5,6-dihydroxycyclohexa-1,3-dien-1-yl)propanoate + NAD+
-
Substrates: enables utilization of 3-phenylpropionate as carbon source
Products: -
?
3-phenylpropionate + NADH + H+ + O2
3-[(5S,6R)-5,6-dihydroxycyclohexa-1,3-dien-1-yl]propanoic acid + NAD+
-
Substrates: -
Products: -
?
3-phenylpropionate + NADH + H+ + O2
3-[(5S,6R)-5,6-dihydroxycyclohexa-1,3-dien-1-yl]propanoic acid + NAD+
-
Substrates: enables utilization of 3-phenylpropionate as carbon source
Products: -
?
3-phenylpropionate + NADH + H+ + O2
3-[(5S,6R)-5,6-dihydroxycyclohexa-1,3-dien-1-yl]propanoic acid + NAD+
-
Substrates: enables utilization of 3-phenylpropionate as carbon source, important role in wine making, aging and storage
Products: -
?
3-phenylpropionate + NADH + H+ + O2
3-[(5S,6R)-5,6-dihydroxycyclohexa-1,3-dien-1-yl]propanoic acid + NAD+
-
Substrates: involved in oxidative stress response
Products: -
?
3-phenylpropionate + NADH + H+ + O2
3-[(5S,6R)-5,6-dihydroxycyclohexa-1,3-dien-1-yl]propanoic acid + NAD+
-
Substrates: -
Products: -
?
3-phenylpropionate + NADH + H+ + O2
3-[(5S,6R)-5,6-dihydroxycyclohexa-1,3-dien-1-yl]propanoic acid + NAD+
-
Substrates: -
Products: -
?
cinnamic acid + NADH + H+ + O2
cinnamic acid-2,3-dihydrodiol + NAD+
-
Substrates: -
Products: -
?
cinnamic acid + NADH + H+ + O2
cinnamic acid-2,3-dihydrodiol + NAD+
-
Substrates: HcaE is involved in degradation of endogenous cinnamic acid
Products: -
?
cinnamic acid + NADH + H+ + O2
cinnamic acid-2,3-dihydrodiol + NAD+
-
Substrates: HcaE is involved in degradation of endogenous cinnamic acid
Products: -
?
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3-phenylpropionate + NADH + H+ + O2
3-(2,3-dihydroxyphenyl)propionate + NAD+
3-phenylpropionate + NADH + H+ + O2
3-(cis-5,6-dihydroxycyclohexa-1,3-dien-1-yl)propanoate + NAD+
-
Substrates: enables utilization of 3-phenylpropionate as carbon source
Products: -
?
3-phenylpropionate + NADH + H+ + O2
3-[(5S,6R)-5,6-dihydroxycyclohexa-1,3-dien-1-yl]propanoic acid + NAD+
3-phenylpropionate + NADH + H+ + O2
3-(2,3-dihydroxyphenyl)propionate + NAD+
-
Substrates: enables utilization of 3-phenylpropionate as carbon source
Products: -
?
3-phenylpropionate + NADH + H+ + O2
3-(2,3-dihydroxyphenyl)propionate + NAD+
-
Substrates: enables utilization of 3-phenylpropionate as carbon source
Products: -
?
3-phenylpropionate + NADH + H+ + O2
3-[(5S,6R)-5,6-dihydroxycyclohexa-1,3-dien-1-yl]propanoic acid + NAD+
-
Substrates: enables utilization of 3-phenylpropionate as carbon source
Products: -
?
3-phenylpropionate + NADH + H+ + O2
3-[(5S,6R)-5,6-dihydroxycyclohexa-1,3-dien-1-yl]propanoic acid + NAD+
-
Substrates: enables utilization of 3-phenylpropionate as carbon source, important role in wine making, aging and storage
Products: -
?
3-phenylpropionate + NADH + H+ + O2
3-[(5S,6R)-5,6-dihydroxycyclohexa-1,3-dien-1-yl]propanoic acid + NAD+
-
Substrates: involved in oxidative stress response
Products: -
?
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11328
-
gene products from hcaA1, hcaA2, hcaC and hcaD, 1 * 51109 + 1 * 20579 + 1 * 11328 + 1 * 43978, subunit masses calculated from deduced amino acid sequences
20579
-
gene products from hcaA1, hcaA2, hcaC and hcaD, 1 * 51109 + 1 * 20579 + 1 * 11328 + 1 * 43978, subunit masses calculated from deduced amino acid sequences
43978
-
gene products from hcaA1, hcaA2, hcaC and hcaD, 1 * 51109 + 1 * 20579 + 1 * 11328 + 1 * 43978, subunit masses calculated from deduced amino acid sequences
51109
-
gene products from hcaA1, hcaA2, hcaC and hcaD, 1 * 51109 + 1 * 20579 + 1 * 11328 + 1 * 43978, subunit masses calculated from deduced amino acid sequences
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Burlingame, R.; Chapmen, P.J.
Catabolism of phenylpropionic acid and its 3-hydroxy-derivative by Escherichia coli
J. Bacteriol.
155
113-121
1983
Escherichia coli, Escherichia coli KK334
brenda
Burlingame, R.P.; Wyman, L.; Chapman, P.J.
Isolation and characterization of Escherichia coli mutants defective for phenylpropionate degradation
J. Bacteriol.
168
55-64
1986
Escherichia coli
brenda
Diaz, E.; Ferrandez, A.; Garcia, J.L.
Characterization of the hca cluster encoding the dioxygenolytic pathway for initial catabolism of 3-phenylpropionic acid in Escherichia coli K-12
J. Bacteriol.
180
2915-2923
1998
Escherichia coli
brenda
Turlin, E.; Perrotte-Piquemal, M.; Danchin, A.; Biville, F.
Regulation of the early steps of 3-phenylpropionate catabolism in Escherichia coli
J. Mol. Microbiol. Biotechnol.
3
127-133
2001
Escherichia coli
brenda
Turlin, E.; Sismeiro, O.; Le Caer, J.P.; Labas, V.; Danchin, A.; Biville, F.
3-phenylpropionate catabolism and the Escherichia coli oxidative stress response
Res. Microbiol.
156
312-321
2005
Escherichia coli
brenda
Chalabaev, S.; Turlin, E.; Bay, S.; Ganneau, C.; Brito-Fravallo, E.; Charles, J.F.; Danchin, A.; Biville, F.
Cinnamic acid, an autoinducer of its own biosynthesis, is processed via Hca enzymes in Photorhabdus luminescens
Appl. Environ. Microbiol.
74
1717-1725
2008
Photorhabdus luminescens, Photorhabdus luminescens TT01R
brenda
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