print visible entries

print all entries

Ligand trans-feruloyl-CoA

Basic Ligand Information

Molecular Structure

Pathway Source

Pathways

BRENDA

phenylpropanoid biosynthesis, suberin monomers biosynthesis

KEGG

Arginine and proline metabolism, Biosynthesis of phenylpropanoids, Biosynthesis of secondary metabolites, Biosynthesis of various alkaloids, Biosynthesis of various plant secondary metabolites, Cutin, suberine and wax biosynthesis, Flavonoid biosynthesis, Phenylpropanoid biosynthesis, Stilbenoid, diarylheptanoid and gingerol biosynthesis more

MetaCyc

capsaicin biosynthesis, capsiconiate biosynthesis, chlorogenic acid biosynthesis I, coumarins biosynthesis (engineered), curcuminoid biosynthesis, esterified suberin biosynthesis, ferulate degradation, flavonol acylglucoside biosynthesis I - kaempferol derivatives, flavonol acylglucoside biosynthesis II - isorhamnetin derivatives, flavonol acylglucoside biosynthesis III - quercetin derivatives, hydroxycinnamic acid serotonin amides biosynthesis, hydroxycinnamic acid tyramine amides biosynthesis, phenylpropanoid biosynthesis, phenylpropanoids methylation (ice plant), scopoletin biosynthesis, spermidine hydroxycinnamic acid conjugates biosynthesis, suberin monomers biosynthesis more

Show all BRENDA pathways known for trans-feruloyl-CoA

close all tables

open all tables

Roles as Enzyme Ligand

In Vivo Substrate in Enzyme-catalyzed Reactions (22 results)

top print hide

Show Natural Substrate (22 entries)

EC NUMBER

PROVEN IN VIVO REACTION

REACTION DIAGRAM

LITERATURE

ENZYME 3D STRUCTURE

1.14.11.61

trans-feruloyl-CoA + 2-oxoglutarate + O2 = trans-6-hydroxyferuloyl-CoA + succinate + CO2

751858

-

1.14.11.62

trans-feruloyl-CoA + 2-oxoglutarate + O2 = trans-6-hydroxyferuloyl-CoA + succinate + CO2

751859

-

1.2.1.44

feruloyl-CoA + NADPH + H+ = coniferaldehyde + CoA + NADP+

725626, 743447, 700489, 743007, 742589, 743848, 743233, 743470, 725147, 725759, 743501, 743559, 743156, 724494, 726367

-

1.2.1.44

feruloyl-CoA + NADPH + H+ = ferulic aldehyde + CoA + NADP+

725148, 288234, 288231

-

1.2.1.44

2 entries

1.3.1.117

trans-feruloyl-CoA + NADPH + H+ = dihydroferuloyl-CoA + NADP+

745999

-

2.3.1.110

feruloyl-CoA + tyramine = CoA + feruloyltyramine

486130, 486133, 486126, 486127, 486129, 486132, 486128, 486134

-

2.3.1.211

2 feruloyl-CoA + malonyl-CoA + H2O = 3 CoA + curcumin + 2 CO2

721196

-

2.3.1.217

(4-coumaroyl)acetyl-CoA + feruloyl-CoA + H2O = demethoxycurcumin + CO2 + 2 CoA

719493

-

2.3.1.217

feruloyl-CoA + cinnamoyl-diketide-N-acetylcysteamine + H2O = CoA + cinnamoylferuloylmethane + N-acetylcysteamine + CO2

722740

-

2.3.1.217

feruloyl-CoA + feruloylacetyl-CoA + H2O = 2 CoA + curcumin + CO2

719850, 722740, 719493

-

2.3.1.217

3 entries

2.3.1.218

feruloyl-CoA + malonyl-CoA = feruloylacetyl-CoA + CO2 + CoA

719850

-

2.3.1.219

(4-coumaroyl)acetyl-CoA + feruloyl-CoA + H2O = demethoxycurcumin + CO2 + CoA

719850

-

2.3.1.64

feruloyl-CoA + agmatine = CoA + feruloyl agmatine

706386

-

2.3.1.64

feruloyl-CoA + agmatine = CoA + feruloylagmatine

758017

-

2.3.1.64

feruloyl-CoA + putrescine = CoA + feruloylputrescine

706386

-

4.1.2.61

4-feruloyl-CoA = 4-hydroxy-3-methoxybenzaldehyde + acetyl-CoA

653573

-

4.1.2.61

feruloyl-CoA + H2O = 4-hydroxy-3-methoxybenzaldehyde + acetyl-CoA

729753

-

4.1.2.61

feruloyl-CoA + H2O = vanillin + acetyl-CoA

755197, 754012

-

4.1.2.61

feruloyl-CoA = 4-hydroxy-3-methoxy-benzaldehyde + acetyl-CoA

682467

-

4.1.2.61

feruloyl-CoA = 4-hydroxy-3-methoxybenzaldehyde + acetyl-CoA

677312

-

4.1.2.61

trans-feruloyl-CoA + H2O = 4-hydroxy-3-methoxyphenyl-beta-hydroxypropionyl-CoA

207982, 210668, 285198, 663518, 210669

-

2.3.1.64

3 entries

4.1.2.61

6 entries

4.2.1.17

feruloyl-CoA + H2O = 3-(4-hydroxy-3-methoxyphenyl)propanoyl-CoA

746582

-

In Vivo Product in Enzyme-catalyzed Reactions (6 results)

top print hide

Show Natural Product (6 entries)

EC NUMBER

PROVEN IN VIVO REACTION

REACTION DIAGRAM

LITERATURE

ENZYME 3D STRUCTURE

1.2.1.44

coniferaldehyde + CoA + NADP+ = feruloyl-CoA + NADPH + H+

0

-

1.2.1.68

coniferaldehyde + CoA + NADP+ = feruloyl-CoA + NADPH + H+

0

-

2.1.1.104

S-adenosyl-L-methionine + caffeoyl-CoA = S-adenosyl-L-homocysteine + feruloyl-CoA

0

-

6.2.1.12

ATP + ferulate + CoA = AMP + diphosphate + feruloyl-CoA

0

-

6.2.1.12

ATP + ferulate + CoA = AMP + diphosphate + ferulyl-CoA

0

-

6.2.1.12

2 entries

6.2.1.34

ferulic acid + CoASH + ATP = trans-feruloyl-CoA + products of ATP breakdown

207982

-

Substrate in Enzyme-catalyzed Reactions (81 results)

top print hide

Show Substrate (81 entries)

EC NUMBER

REACTION

REACTION DIAGRAM

LITERATURE

ENZYME 3D STRUCTURE

1.14.11.61

trans-feruloyl-CoA + 2-oxoglutarate + O2 = trans-6-hydroxyferuloyl-CoA + succinate + CO2

751858, 751859, 751828

-

1.14.11.62

trans-feruloyl-CoA + 2-oxoglutarate + O2 = trans-6-hydroxyferuloyl-CoA + succinate + CO2

751859

-

1.2.1.44

feruloyl-CoA + NADPH + H+ = coniferaldehyde + CoA + NADP+

725626, 762841, 676643, 763766, 763522, 743447, 676451, 763103, 763599, 700489, 672472, 743007, 742589, 743848, 743233, 743470, 725147, 725759, 743501, 743559, 743156, 676843, 675132, 693407, 724494, 726367

-

1.2.1.44

feruloyl-CoA + NADPH + H+ = ferulic aldehyde + CoA + NADP+

725148, 288234, 288231

-

1.2.1.44

feruloyl-CoA + NADPH = ferulic aldehyde + CoA + NADP+

288230, 288233, 288239, 288234, 288228, 288235

-

1.2.1.44

3 entries

1.3.1.108

feruloyl-CoA + 2 NADH + 2 oxidized ferredoxin iron-sulfur cluster = ? + 2 NAD+ + 2 reduced ferredoxin iron-sulfur cluster

732091

-

1.3.1.117

trans-feruloyl-CoA + NADPH + H+ = dihydroferuloyl-CoA + NADP+

745999

-

2.1.1.104

S-adenosyl-L-methionine + feruloyl-CoA = S-adenosyl-L-homocysteine + ?

758087

-

2.3.1.106

feruloyl-CoA + tartronic acid = CoA + feruloyltartronic acid

486106

-

2.3.1.110

feruloyl-CoA + (4-hydroxyphenyl)propylamine = CoA + feruloyl-(4-hydroxyphenyl)propylamine

486132

-

2.3.1.110

feruloyl-CoA + 3'-methoxyoctopamine = CoA + feruloyl-3'-methoxyoctopamine

486133

-

2.3.1.110

feruloyl-CoA + 3-methoxytyramine = CoA + feruloyl-3-methoxytyramine

486126, 486132

-

2.3.1.110

feruloyl-CoA + beta-phenylethylamine = CoA + feruloyl-beta-phenylethylamine

486132

-

2.3.1.110

feruloyl-CoA + dopamine = CoA + feruloyldopamine

486130, 486126, 486127, 486132, 486134, 676598, 660244

-

2.3.1.110

feruloyl-CoA + homotyramine = CoA + feruloylhomotyramine

486126

-

2.3.1.110

feruloyl-CoA + N-methyltyramine = CoA + N-feruloyl-N-methyltyramine

486126

-

2.3.1.110

feruloyl-CoA + noradrenaline = CoA + feruloylnoradrenaline

486133, 486132, 486126

-

2.3.1.110

feruloyl-CoA + octopamine = CoA + feruloyloctopamine

486133, 486126, 486132, 486128

-

2.3.1.110

feruloyl-CoA + phenethylamine = CoA + feruloylphenethylamine

486130, 660244

-

2.3.1.110

feruloyl-CoA + synephrine = CoA + feruloylsynephrine

486126

-

2.3.1.110

feruloyl-CoA + tryptamine = CoA + feruloyltryptamine

486130, 676598

-

2.3.1.110

feruloyl-CoA + tyramine = CoA + feruloyltyramine

486130, 486133, 486126, 486127, 486129, 486132, 486128, 486134, 676598

-

2.3.1.110

feruloyl-CoA + tyramine = CoA + N-feruloyltyramine

720789

-

2.3.1.110

14 entries

2.3.1.126

feruloyl-CoA + isocitric acid = CoA + feruloylisocitric acid

486247

-

2.3.1.130

feruloyl-CoA + galactarate = CoA + O-feruloylgalactarate

486275

-

2.3.1.131

feruloyl-CoA + glucarate = CoA + feruloylglucarate

486275

-

2.3.1.132

feruloyl-CoA + glucarolactone = CoA + O-feruloylglucarolactone

486275

-

2.3.1.133

feruloyl-CoA + 2,3-dihydroxybenzoate = CoA + ?

720787

-

2.3.1.133

feruloyl-CoA + 3-aminobenzoate = CoA + ?

720787

-

2.3.1.133

feruloyl-CoA + 3-hydroxyanthranilate = CoA + 3-feruloyloxyanthranilate

720787

-

2.3.1.133

feruloyl-CoA + 3-hydroxybenzoate = CoA + 3-feruloyloxybenzoate

720787

-

2.3.1.133

feruloyl-CoA + glycerol = CoA + ?

720638

-

2.3.1.133

feruloyl-CoA + shikimate = CoA + 5-O-feruloylshikimate

486281, 486283, 720638, 486280, 486282, 486285, 720787, 758066, 486275

-

2.3.1.138

feruloyl-CoA + agmatine = CoA + N-feruloylagmatine

757363

-

2.3.1.138

feruloyl-CoA + putrescine = CoA + N-feruloylputrescine

486312, 486313, 486314, 486315, 720745

-

2.3.1.140

feruloyl-CoA + 3-(3,4-dihydroxyphenyl)lactate = CoA + 2-O-feruloyl-3-(3,4-dihydroxyphenyl)lactate

720787, 756266

-

2.3.1.140

feruloyl-CoA + 3-(4-hydroxyphenyl)lactate = CoA + 2-O-feruloyl-3-(4-hydroxyphenyl)lactate

720787, 756266, 720789

-

2.3.1.140

feruloyl-CoA + 3-phenyllactate = CoA + 2-O-feruloyl-3-(4-hydroxyphenyl)lactate

756266

-

2.3.1.144

feruloyl-CoA + 3-hydroxyanthranilate = CoA + N-feruloyl-3-hydroxyanthranilate

718662

-

2.3.1.144

feruloyl-CoA + anthranilate = CoA + N-feruloylanthranilate

718662

-

2.3.1.133

6 entries

2.3.1.138

2 entries

2.3.1.140

3 entries

2.3.1.144

2 entries

2.3.1.146

feruloyl-CoA + malonyl-CoA = rhapontigenin + CoA + CO2

637806

-

2.3.1.188

feruloyl-CoA + 1-dodecanol = CoA + (E)-dodecyl 3-(4-hydroxy-3-methoxyphenyl)acrylate

700658, 700854

-

2.3.1.188

feruloyl-CoA + 1-hexadecanol = CoA + (E)-hexadecyl 3-(4-hydroxy-3-methoxyphenyl)acrylate

700854, 700658

-

2.3.1.188

feruloyl-CoA + 1-pentadecanol = CoA + (E)-pentadecyl 3-(4-hydroxy-3-methoxyphenyl)acrylate

700658, 700854

-

2.3.1.188

feruloyl-CoA + 1-tetradecanol = CoA + (E)-tetradecyl 3-(4-hydroxy-3-methoxyphenyl)acrylate

700658, 700659, 700854

-

2.3.1.188

feruloyl-CoA + 15-hydroxypentadecanoic acid = CoA + (E)-15-(3-(4-hydroxy-3-methoxyphenyl)acryloyloxy)pentadecanoic acid

700658, 700854

-

2.3.1.188

feruloyl-CoA + 16-hydroxypalmitic acid = CoA + (E)-16-(3-(4-hydroxy-3-methoxyphenyl)acryloyloxy)hexadecanoic acid

700658, 700659, 700854

-

2.3.1.188

feruloyl-CoA + hexadecane-1,16-diol = CoA + (E)-16-hydroxyhexadecyl 3-(4-hydroxy-3-methoxyphenyl)acrylate

700854, 700658

-

2.3.1.211

2 feruloyl-CoA + malonyl-CoA + H2O = 3 CoA + 4-hydroxy-6-[(E)-2-(4-hydroxy-3-methoxyphenyl)ethenyl]-2H-pyran-2-one + curcumin

722655

-

2.3.1.211

2 feruloyl-CoA + malonyl-CoA + H2O = 3 CoA + curcumin + 2 CO2

721196

-

2.3.1.212

feruloyl-CoA + malonyl-CoA + H2O = 2 CoA + (3E)-4-(4-hydroxy-3-methoxyphenyl)but-3-en-2-one + 2 CO2

684699

-

2.3.1.212

feruloyl-CoA + malonyl-CoA + H2O = 2 CoA + ? + 2 CO2

723451

-

2.3.1.212

feruloyl-CoA + malonyl-CoA + H2O = ?

757487

-

2.3.1.217

(4-coumaroyl)acetyl-CoA + feruloyl-CoA + H2O = demethoxycurcumin + CO2 + 2 CoA

719493

-

2.3.1.217

feruloyl-CoA + 3-oxo-5-phenyl-4-pentenoic acid + H2O = CoA + cinnamoylferuloylmethane + CO2

722740

-

2.3.1.217

feruloyl-CoA + cinnamoyl-diketide-N-acetylcysteamine + H2O = CoA + cinnamoylferuloylmethane + N-acetylcysteamine + CO2

719850, 722740

-

2.3.1.217

feruloyl-CoA + feruloylacetyl-CoA + H2O = 2 CoA + curcumin + CO2

737235, 719850, 722740, 758333, 719493

-

2.3.1.188

7 entries

2.3.1.211

2 entries

2.3.1.212

3 entries

2.3.1.217

4 entries

2.3.1.218

feruloyl-CoA + malonyl-CoA = feruloylacetyl-CoA + CO2 + CoA

719850, 758333

-

2.3.1.219

(4-coumaroyl)acetyl-CoA + feruloyl-CoA + H2O = demethoxycurcumin + CO2 + CoA

719850

-

2.3.1.302

feruloyl-CoA + 5-hydroxyanthranilate = avenanthramide B + CoA

762520, 761938

-

2.3.1.302

feruloyl-CoA + L-phenylalanine = ? + CoA

762175

-

2.3.1.64

feruloyl-CoA + agmatine = CoA + feruloyl agmatine

487361, 487362, 487363, 706386

-

2.3.1.64

feruloyl-CoA + agmatine = CoA + feruloylagmatine

758017

-

2.3.1.64

feruloyl-CoA + putrescine = CoA + feruloylputrescine

706386

-

2.3.1.74

3 malonyl-CoA + feruloyl-CoA = ?

757784

-

2.3.1.74

feruloyl-CoA + malonyl-CoA = ?

757487

-

2.3.1.74

malonyl-CoA + feruloyl-CoA = ?

757784

-

2.3.1.74

ferulyl-CoA + malonyl-CoA = homoeriodictyol + CoA + CO2

487468, 487469, 487471, 684699, 487470, 487474, 487460, 487459

-

2.3.1.302

2 entries

2.3.1.64

3 entries

2.3.1.74

4 entries

2.3.1.95

feruloyl-CoA + malonyl-CoA = 3,4',5-trihydroxy-3'-methoxystilbene + CoA + CO2

487723

-

2.3.1.99

feruloyl-CoA + quinate = CoA + O-feruloylquinate

487784, 486280, 676373, 486281, 486282, 486275, 487783

-

2.3.1.99

feruloyl-CoA + shikimate = CoA + 5-O-feruloylshikimate

486285, 758066

-

4.1.2.61

4-feruloyl-CoA = 4-hydroxy-3-methoxybenzaldehyde + acetyl-CoA

653573

-

4.1.2.61

4-hydroxy-3-methoxycinnamoyl-CoA + H2O = 4-hydroxy-3-methoxybenzaldehyde + acetyl-CoA

701671

-

4.1.2.61

4-trans-feruloyl-CoA = 4-hydroxy-3-methoxybenzaldehyde + acetyl-CoA

653573

-

4.1.2.61

feruloyl-CoA + H2O = 4-hydroxy-3-methoxybenzaldehyde + acetyl-CoA

729753

-

4.1.2.61

feruloyl-CoA + H2O = 4-hydroxy-3-methoxyphenyl-beta-hydroxypropionyl-CoA

690831

-

4.1.2.61

feruloyl-CoA + H2O = vanillin + acetyl-CoA

285198, 757268, 754012, 755197, 690831

-

4.1.2.61

feruloyl-CoA = 4-hydroxy-3-methoxy-benzaldehyde + acetyl-CoA

682467

-

4.1.2.61

feruloyl-CoA = 4-hydroxy-3-methoxybenzaldehyde + acetyl-CoA

677312

-

4.1.2.61

trans-feruloyl-CoA + H2O = 4-hydroxy-3-methoxyphenyl-beta-hydroxypropionyl-CoA

207982, 210668, 285198, 663518, 210669

-

2.3.1.99

2 entries

4.1.2.61

9 entries

4.2.1.17

feruloyl-CoA + H2O = 3-(4-hydroxy-3-methoxyphenyl)propanoyl-CoA

746582

-

Product in Enzyme-catalyzed Reactions (14 results)

top print hide

Show Product (14 entries)

EC NUMBER

REACTION

REACTION DIAGRAM

LITERATURE

ENZYME 3D STRUCTURE

1.2.1.44

coniferaldehyde + CoA + NADP+ = feruloyl-CoA + NADPH + H+

0

-

1.2.1.68

coniferaldehyde + CoA + NADP+ = feruloyl-CoA + NADPH + H+

0

-

2.1.1.104

S-adenosyl-L-methionine + caffeoyl-CoA = S-adenosyl-L-homocysteine + feruloyl CoA

0

-

2.1.1.104

S-adenosyl-L-methionine + caffeoyl-CoA = S-adenosyl-L-homocysteine + feruloyl-CoA

0, 485077, 485078, 485079, 485063, 485067, 485065, 485073, 485074, 485080

-

2.1.1.104

2 entries

2.8.3.23

3,4-dihydroxyphenylpropanoyl-CoA + ferulate = 3,4-dihydroxyphenylpropanoate + feruloyl-CoA

0

-

4.1.2.61

4-hydroxy-3-methoxy-phenyl-beta-hydroxypropionyl-CoA + H2O = vanillin + acetylCoA + feruloylCoA

285198

-

6.2.1.12

ATP + ferulic acid + CoA = AMP + diphosphate + 4-feruloyl-CoA

0

-

6.2.1.12

ATP + ferulate + CoA = AMP + diphosphate + feruloyl-CoA

0, 607, 651117, 653477, 595, 653536, 652146, 653481, 653527, 653496, 652422, 653597

-

6.2.1.12

CTP + ferulate + CoA = CMP + diphosphate + feruloyl-CoA

0

-

6.2.1.12

GTP + ferulate + CoA = GMP + diphosphate + feruloyl-CoA

0

-

6.2.1.12

ITP + ferulate + CoA = IMP + diphosphate + feruloyl-CoA

0

-

6.2.1.12

UTP + ferulate + CoA = UMP + diphosphate + feruloyl-CoA

0

-

6.2.1.12

ATP + ferulate + CoA = AMP + diphosphate + ferulyl-CoA

0

-

6.2.1.12

7 entries

6.2.1.34

ferulic acid + CoASH + ATP = trans-feruloyl-CoA + products of ATP breakdown

207982

-

Inhibitor in Enzyme-catalyzed Reactions (3 results)

top print hide

Show Inhibitors (3 entries)

EC NUMBER

COMMENTARY

LITERATURE

ENZYME 3D STRUCTURE

1.2.1.44

competitive inhibitor

676451

-

1.2.1.44

substrate inhibition at high concentration above 60 microM; substrate inhibition at high concentration above 60 microM

700489

-

1.2.1.44

2 entries

2.1.1.104

competitive to caffeoyl-CoA, non-competitive to S-adenosyl-L-methionine

485078

-

Enzyme Kinetic Parameters

k_cat Value (Turnover Number) (53 results)

top print hide

Show Turnover Number (53 entries)

EC NUMBER

TURNOVER NUMBER [1/S]

TURNOVER NUMBER MAXIMUM [1/S]

COMMENTARY

LITERATURE

1.14.11.61

2.68

-

pH 6.5, 30°C

751828

1.14.11.61

2.84

-

pH 6.5, 30°C

751828

1.14.11.61

11

-

30°C, pH 6.5

751858

1.2.1.44

0.00234

-

pH 6.0, 25°C, recombinant GST-tagged enzyme

742589

1.2.1.44

0.0101

-

pH 6.0, 40°C, recombinant His-tagged mutant A132T

743559

1.2.1.44

0.0192

-

pH 6.0, 40°C, recombinant His-tagged mutant A132S

743559

1.2.1.44

0.027

-

isoform CCR21, at pH 6.3 and 30°C

763103

1.2.1.44

0.0372

-

recombinant fusion protein GST-AtCCR2

288239

1.2.1.44

0.038

-

recombinant fusion protein GST-AtCCR1

288239

1.2.1.44

0.063

-

100 mM sodium/potassium phosphate buffer pH 6.3, 250 mM NADPH

700489

1.2.1.44

0.136

-

mutant S123T of isoform CCR1, pH and temperature not specified in the publication

763599

1.2.1.44

0.1409

-

pH 6.0, 40°C, recombinant His-tagged mutant F155H

743559

1.2.1.44

0.18

-

pH 6.0, 40°C, recombinant His-tagged enzyme

743559

1.2.1.44

0.191

-

isoform CCR19, at pH 6.3 and 30°C

763103

1.2.1.44

0.24

-

isoform CCR2-1, pH and temperature not specified in the publication

763599

1.2.1.44

0.289

-

isoform CCR1, pH and temperature not specified in the publication

763599

1.2.1.44

0.377

-

isoform CCR20, at pH 6.3 and 30°C

763103

1.2.1.44

0.47

-

pH 6.5, 30°C, mutant Y310F

743501

1.2.1.44

0.74

-

pH 6.5, 30°C, mutant T154A

743501

1.2.1.44

0.8375

-

pH 6.0, 40°C, recombinant His-tagged mutant A43V

743559

1.2.1.44

1.033

-

pH 6.0, 40°C, recombinant His-tagged enzyme

743559

1.2.1.44

1.6

-

CCR2

675132

1.2.1.44

1.9

-

-

676643

1.2.1.44

1.905

-

pH 6.0, 40°C, recombinant His-tagged mutant L192M

743559

1.2.1.44

2.01

-

100 mM sodium/potassium phosphate buffer pH 6.3, 250 mM NADPH

700489

1.2.1.44

2.1

-

pH 6.0, 40°C, recombinant His-tagged mutant F155Y

743559

1.2.1.44

3.96

-

pH 6.5, 30°C, wild-type enzyme

743501

1.2.1.44

5.8

-

recombinant isozyme CCR1, pH 6.0, 25°C

743447

1.2.1.44

7.8

-

-

676451

1.2.1.44

14.2

-

CCR1

675132

1.2.1.44

17.24

-

pH 6.5, 30°C, mutant Y154Y

743501

1.2.1.44

24

-

mutant enzyme S212G, pH and temperature not specified in the publication

725148

1.2.1.44

44

-

mutant enzyme H215L, pH and temperature not specified in the publication

725148

1.2.1.44

84

-

mutant enzyme R51G/D77G, pH and temperature not specified in the publication

725148

1.2.1.44

100

-

mutant enzyme R51G, pH and temperature not specified in the publication

725148

1.2.1.44

108

-

mutant enzyme D77G, pH and temperature not specified in the publication

725148

1.2.1.44

122

-

mutant enzyme V200E, pH and temperature not specified in the publication

725148

1.2.1.44

137

-

mutant enzyme F30V, pH and temperature not specified in the publication

725148

1.2.1.44

142

-

mutant enzyme RF30V/I31N, pH and temperature not specified in the publication

725148

1.2.1.44

144

-

mutant enzyme S99G, pH and temperature not specified in the publication

725148

1.2.1.44

155

-

mutant enzyme I31N, pH and temperature not specified in the publication

725148

1.2.1.44

160

-

mutant enzyme L64W, pH and temperature not specified in the publication

725148

1.2.1.44

162

-

wild type enzyme, pH and temperature not specified in the publication

725148

1.2.1.44

164

-

in 100 mM phosphate buffer pH 6.5, at 30°C

725147

1.14.11.61

3 entries

1.2.1.44

41 entries

1.3.1.117

0.0042

-

pH 50, 35°C

745999

2.3.1.217

0.0032

-

pH 7.5, 37°C, CURS3

719493

2.3.1.217

0.0068

-

pH 7.5, 37°C, CURS2

719493

2.3.1.217

0.0183

-

pH 7.5, 37°C, CURS1

719493

2.3.1.217

0.0183

-

pH 8.0, 37°C, with cinnamoyl-diketide-N-acetylcysteaminyl-CoA

719850

2.3.1.217

4 entries

2.3.1.218

0.02

-

pH 7.5, 37°C, recombinant enzyme

719850

4.1.2.61

0.41

-

mutant enzyme Y239F

690831

4.1.2.61

0.96

-

mutant enzyme S123A

690831

4.1.2.61

3.72

-

wild-type

690831

4.1.2.61

3 entries

K_M Value (101 results)

top print hide

Show KM Value (101 entries)

EC NUMBER

KM VALUE [MM]

KM VALUE MAXIMUM [MM]

COMMENTARY

LITERATURE

1.14.11.61

0.0092

-

pH 6.5, 30°C

751828

1.14.11.61

0.0102

-

pH 6.5, 30°C

751828

1.14.11.61

0.036

-

30°C, pH 6.5

751858

1.14.11.61

0.037

-

pH 7.2, 30°C

751859

1.14.11.61

4 entries

1.14.11.62

0.05

-

pH 7.2, 30°C

751859

1.2.1.44

0.00042

-

-

676643

1.2.1.44

0.00098

-

recombinant fusion protein GST-AtCCR1

288239

1.2.1.44

0.00235

-

-

288228

1.2.1.44

0.0027

-

isoform CCR21, at pH 6.3 and 30°C

763103

1.2.1.44

0.0047

-

recombinant fusion protein GST-AtCCR2

288239

1.2.1.44

0.00926

-

pH and temperature not specified in the publication

725626

1.2.1.44

0.00986

-

pH 6.0, 40°C, recombinant His-tagged enzyme

743559

1.2.1.44

0.0137

-

-

676451

1.2.1.44

0.01431

-

pH 6.0, 40°C, recombinant His-tagged wild-type enzyme

743559

1.2.1.44

0.01571

-

isoform CCR20, at pH 6.3 and 30°C

763103

1.2.1.44

0.0161

-

pH 6.0, 25°C, recombinant GST-tagged enzyme

742589

1.2.1.44

0.01643

-

pH 6.0, 40°C, recombinant His-tagged mutant A132T

743559

1.2.1.44

0.01731

-

pH 6.0, 40°C, recombinant His-tagged mutant A132S

743559

1.2.1.44

0.022

-

-

288234

1.2.1.44

0.023

-

-

672472

1.2.1.44

0.0238

-

at pH 6.0, temperature not specified in the publication

763766

1.2.1.44

0.0254

-

100 mM sodium/potassium phosphate buffer pH 6.3, 250 mM NADPH

700489

1.2.1.44

0.02685

-

isoform CCR19, at pH 6.3 and 30°C

763103

1.2.1.44

0.02759

-

isoform CCR1, pH and temperature not specified in the publication

763599

1.2.1.44

0.03123

-

pH 6.0, 40°C, recombinant His-tagged mutant F155H

743559

1.2.1.44

0.032

-

mutant enzyme S99G, pH and temperature not specified in the publication

725148

1.2.1.44

0.0356

-

at pH 6.0, temperature not specified in the publication

763766

1.2.1.44

0.036

-

in 100 mM phosphate buffer pH 6.5, at 30°C

725147

1.2.1.44

0.036

-

wild type enzyme, pH and temperature not specified in the publication

725148

1.2.1.44

0.039

-

mutant enzyme L64W, pH and temperature not specified in the publication

725148

1.2.1.44

0.042

-

mutant enzyme H215L, pH and temperature not specified in the publication

725148

1.2.1.44

0.047

-

100 mM sodium/potassium phosphate buffer pH 6.3, 250 mM NADPH

700489

1.2.1.44

0.047

-

mutant enzyme R51G, pH and temperature not specified in the publication

725148

1.2.1.44

0.04887

-

pH 6.0, 40°C, recombinant His-tagged mutant A43V

743559

1.2.1.44

0.057

-

mutant enzyme D77G, pH and temperature not specified in the publication

725148

1.2.1.44

0.06

-

mutant enzyme V200E, pH and temperature not specified in the publication

725148

1.2.1.44

0.063

-

pH 6.5, 30°C, mutant Y154Y

743501

1.2.1.44

0.07

-

pH 6.5, 30°C, wild-type enzyme

743501

1.2.1.44

0.07042

-

at pH 6.0, temperature not specified in the publication

763766

1.2.1.44

0.0716

-

at pH 6.0, temperature not specified in the publication

763766

1.2.1.44

0.073

-

-

288230

1.2.1.44

0.07474

-

pH 6.0, 40°C, recombinant His-tagged mutant L192M

743559

1.2.1.44

0.07697

-

-

693407

1.2.1.44

0.079

-

mutant enzyme S212G, pH and temperature not specified in the publication

725148

1.2.1.44

0.0933

-

pH 6.0, 40°C, recombinant His-tagged mutant F155Y

743559

1.2.1.44

0.096

-

mutant enzyme F30V, pH and temperature not specified in the publication

725148

1.2.1.44

0.102

-

mutant enzyme I31N, pH and temperature not specified in the publication

725148

1.2.1.44

0.132

-

pH 6.5, 30°C, mutant Y310F

743501

1.2.1.44

0.13699

-

isoform CCR2-1, pH and temperature not specified in the publication

763599

1.2.1.44

0.155

-

pH 6.5, 30°C, mutant T154A

743501

1.2.1.44

0.166

-

mutant enzyme R51G/D77G, pH and temperature not specified in the publication

725148

1.2.1.44

0.244

-

mutant enzyme RF30V/I31N, pH and temperature not specified in the publication

725148

1.2.1.44

0.3076

-

recombinant isozyme CCR1, pH 6.0, 25°C

743447

1.2.1.44

0.323

-

pH 6.25, 37°C, recombinant His-tagged enzyme

743156

1.2.1.44

49 entries

1.3.1.117

0.093

-

pH 50, 35°C

745999

2.3.1.110

0.0006

-

-

486132

2.3.1.110

0.0035

-

pH 8.5, 30°C

660244

2.3.1.110

0.0048

-

with tyramine as acceptor

486130

2.3.1.110

0.0049

-

+ tyramine

486127

2.3.1.110

0.0062

-

+ tyramine

486126

2.3.1.110

0.053

-

30°C, pH 8.5, recombinant enzyme

676598

2.3.1.110

0.062

-

-

486134

2.3.1.110

0.1

-

-

486133

2.3.1.110

0.192

-

with tyramine, pH 7.5, 30°C, recombinant AAT1

720789

2.3.1.110

9 entries

2.3.1.126

0.163

-

-

486247

2.3.1.130

0.045

-

-

486275

2.3.1.133

0.0051

-

pH 7.0, 30°C, with shikimate

720787

2.3.1.133

0.006

-

-

486280, 486282

2.3.1.133

0.0721

-

pH 7.5, 37°C, with glycerol

720638

2.3.1.133

0.35

-

-

486285

2.3.1.133

1.9

-

-

486283

2.3.1.133

15.4

-

-

486281

2.3.1.133

55.5

-

-

486281

2.3.1.138

0.0125

-

with caffeoyl-CoA

486313

2.3.1.138

0.0194

-

cosubstrate agmatine, pH 7.5, 30°C

757363

2.3.1.138

0.0356

-

cosubstrate putrescine, pH 7.5, 30°C

757363

2.3.1.140

0.0191

-

pH 7.0, 30°C, with 3-(3,4-dihydroxyphenyl)lactate, recombinant RAS

720787

2.3.1.140

0.022

-

with 3-(4-hydroxyphenyl)lactate, pH 7.5, 30°C, recombinant AAT1

720789

2.3.1.140

0.0364

-

pH 7.0, 30°C, with 3-(4-hydroxyphenyl)lactate, recombinant RAS

720787

2.3.1.188

0.005

-

pH 7.0, 30°C

700658

2.3.1.188

0.015

-

pH 7.0, 30°C

700854

2.3.1.217

0.0022

-

pH 7.5, 37°C, CURS3

719493

2.3.1.217

0.0043

-

pH 7.5, 37°C, CURS2

719493

2.3.1.217

0.018

-

pH 7.5, 37°C, CURS1

719493

2.3.1.217

0.018

-

pH 8.0, 37°C, with cinnamoyl-diketide-N-acetylcysteaminyl-CoA

719850

2.3.1.133

7 entries

2.3.1.138

3 entries

2.3.1.140

3 entries

2.3.1.188

2 entries

2.3.1.217

4 entries

2.3.1.302

0.04

-

pH 7, temperature not specified in the publication

762520

2.3.1.64

0.0013

-

-

487362

2.3.1.64

0.0017

-

isoenzyme 3

487363

2.3.1.64

0.0041

-

isoenzyme 2

487363

2.3.1.64

0.0061

-

isoenzyme 1

487363

2.3.1.64

0.0066

-

recombinant enzyme

487363

2.3.1.74

0.001

-

-

487474

2.3.1.74

0.0025

-

-

487471

2.3.1.99

0.009

-

-

486280

2.3.1.99

0.05

-

-

486275

2.3.1.99

0.35

-

pH 6.6, 30°C, cosubstrate: shikimate

486285

2.3.1.99

11.4

-

-

486281

4.1.2.61

0.0118

-

wild-type

690831

4.1.2.61

0.0135

-

mutant enzyme S123A

690831

4.1.2.61

0.095

-

mutant enzyme Y239F

690831

4.1.2.61

2.4

-

-

210668

2.3.1.64

5 entries

2.3.1.74

2 entries

2.3.1.99

4 entries

4.1.2.61

4 entries

K_i Value (3 results)

top print hide

Show KI Value (3 entries)

EC NUMBER

KI VALUE [MM]

KI VALUE MAXIMUM [MM]

COMMENTARY

LITERATURE

1.2.1.44

0.0063

-

competitive inhibition of feruloyl-CoA on the 5-hydroxyferuloyl-CoA reaction

676451

1.2.1.44

0.0066

-

competitive inhibition of feruloyl-CoA on the sinapoyl-CoA reaction

676451

1.2.1.44

0.0083

-

competitive inhibition of feruloyl-CoA on the caffeoyl-CoA reaction

676451

1.2.1.44

3 entries

References & Links

Literature References (139)

top print hide

Show Reference (139 entries)

BRENDA REFERENCE ID

PUBMED ID

TITLE

YEAR

AUTHORS

JOURNAL

VOLUME

PAGES

595

9177055

3-Hydroxybenzoate:coenzyme A ligase and 4-coumarate:coenzyme A ligase from cultured cells of Centaurium erythraea

1997

Barillas, W.; Beerhues, L.

Planta

202

112-116

607

4364250

Isolation and properties of hydroxycinnamate:CoA ligase from lignifying tissues of Forsythia

1974

Gross, G.G.; Zenk, M.H.

Eur. J. Biochem.

42

453-459

207982

9611814

Metabolism of ferulic acid via vanillin using a novel CoA-dependent pathway in a newly isolated strain of Pseudomonas fluorescens

1998

Narbad, A.; Gasson, M.J.

Microbiology

144

1397-1405

210668

10222033

4-Hydroxycinnamoyl-CoA hydratase/lyase (HCHL)-an enzyme of phenylpropanoid chain cleavage from Pseudomonas

1999

Mitra, A.; Kitamura, Y.; Gasson, M.J.; Narbad, A.; Parr, A.J.; Pyne, J.; Rhodes, M.J.C.; Sewter, C.; Walton, N.J.

Arch. Biochem. Biophys.

365

10-16

210669

10543794

Biochemical and genetic analysis of ferulic acid catabolism in Pseudomonas sp. strain HR199

1999

Overhage, J.; Priefert, H.; Steinbuchel, A.

Appl. Environ. Microbiol.

65

4837-4847

285198

9461612

Metabolism of ferulic acid to vanillin. A bacterial gene of the enoyl-SCoA hydratase/isomerase superfamily encodes an enzyme for the hydration and cleavage of a hydroxycinnamic acid SCoA thioester

1998

Gasson, M.J.; Kitamura, Y.; McLauchlan, W.R.; Narbad, A.; Parr, A.J.; Parsons, E.L.; Payne, J.; Rhodes, M.J.; Walton, N.J.

J. Biol. Chem.

273

4163-4170

288228

6365550

Purification and properties of cinnamoyl-CoA reductase and cinnamyl alcohol dehydrogenase from poplar stems (Populus X euramericana)

1984

Sarni, F.; Grand, C.; Boudet, A.M.

Eur. J. Biochem.

139

259-265

288230

7454

Enzymic synthesis of lignin precursors. Purification and properties of a cinnamoyl-CoA: NADPH reductase from cell suspension cultures of soybean (Glycine max)

1976

Wengenmayer, H.; Ebel, J.; Grisebach, H.

Eur. J. Biochem.

65

529-536

288231

-

Stimulation of lignification in neoformed calli induced by Agrobacterium rhizogenes on bean hypocotyls

1989

Grima-Pettenati, J.; Chriqui, D.; Sarni-Manchado, P.; Prinsen, E.

Plant Sci.

61

179-188

288233

7042334

Enzymic synthesis of lignin precursors. Comparison of cinnamoyl-CoA reductase and cinnamyl alcohol:NADP+ dehydrogenase from spruce (Picea abies L.) and soybean (Glycine max L.)

1981

Luderitz, T.; Grisebach, H.

Eur. J. Biochem.

119

115-124

288234

236926

Reduction of coenzyme A thioesters of cinnamic acids with an enzyme preparation from lignifying tissue of Forsythia

1975

Gross, G.G.; Kreiten, W.

FEBS Lett.

54

259-262

288235

-

Purification and characterization of cinnamoyl-CoA reductase from Eucalyptus gunnii

1995

Goffner, D.; Campbell, M.M.; Boudet, A.M.

Colloq. Inst. Natl. Rech. Agron.

69

329-330

288239

11430991

Two cinnamoyl-CoA reductase (CCR) genes from Arabidopsis thaliana are differentially expressed during development and in response to infection with pathogenic bacteria

2001

Lauvergeat, V.; Lacomme, C.; Lacombe, E.; Lasserre, E.; Roby, D.; Grima-Pettenati, J.

Phytochemistry

57

1187-1195

485063

12475619

Structural and compositional modifications in lignin of transgenic alfalfa down-regulated in caffeic acid 3-O-methyltransferase and caffeoyl coenzyme A 3-O-methyltransferase

2003

Marita, J.M.; Ralph, J.; Hatfield, R.D.; Guo, D.; Chen, F.; Dixon, R.A.

Phytochemistry

62

53-65

485065

12060306

Caffeoyl-coenzyme A 3-O-methyltransferase enzyme activity, protein and transcript accumulation in flax (Linum usitatissimum) stem during development

2001

Day, A.; Dehorter, B.; Neutelings, G.; Czeszak, X.; Chabbert, B.; Belingheri, L.; David, H.

Physiol. Plant.

113

275-284

485067

11169195

Substrate preferences of O-methyltransferases in alfalfa suggest new pathways for 3-O-methylation of monolignols

2001

Parvathi, K.; Chen, F.; Guo, D.; Blount, J.W.; Dixon, R.A.

Plant J.

25

193-202

485073

9747797

Substrate profiles and expression of caffeoyl coenzyme A and caffeic acid O-methyltransferases in secondary xylem of aspen during seasonal development

1998

Meng, H.; Campbell, W.H.

Plant Mol. Biol.

38

513-520

485074

9662519

Developmental expression and substrate specificities of alfalfa caffeic acid 3-O-methyltransferase and caffeoyl coenzyme A 3-O-methyltransferase in relation to lignification

1998

Inoue, K.; Sewalt, V.J.H.; Ballance, G.M.; Ni, W.; Sturzer, C.; Dixon, R.A.

Plant Physiol.

117

761-770

485077

16667940

Elicitor-inducible caffeoyl-coenzyme A 3-O-methyltransferase from Petroselinum crispum cell suspensions

1991

Pakusch, A.E.; Matern, U.; Schiltz, E.

Plant Physiol.

95

137-143

485078

16668176

Kinetic characterization of caffeoyl-coenzyme A-specific 3-O-methyltransferase from elicited parsley cell suspensions

1991

Pakusch, A.E.; Matern, U.

Plant Physiol.

96

327-330

485079

1894629

Molecular cloning, induction and taxonomic distribution of caffeoyl-CoA 3-O-methyltransferase, an enzyme involved in disease resistance

1991

Schmidt, D.; Pakusch, A.E.; Matern, U.

J. Biol. Chem.

266

17416-17423

485080

2499260

S-Adenosyl-L-methionine:trans-caffeoyl-coenzyme A 3-O-methyltransferase from elicitor-treated parsley cell suspension cultures

1989

Pakusch, A.E.; Kneusel, R.E.; Matern, U.

Arch. Biochem. Biophys.

271

488-494

486106

-

Hydroxycinnamoyl-coenzyme-A:tartronate hydroxycinnamoyltransferase in protein preparations from mung bean

1986

Strack, D.; Ruhoff, R.; Gräwe, W.

Phytochemistry

25

833-837

486126

-

The biosynthesis of feruloyltyramine in Nicotiana tabacum

1984

Negrel, J.; Martin, C.

Phytochemistry

23

2797-2801

486127

-

Partial purification of tyramine feruloyl transferase from TMV inoculated tobacco leaves

1989

Fleurence, J.; Negrel, J.

Phytochemistry

28

733-736

486128

11382813

Cloning and characterization of a hydroxycinnamoyl-CoA: tyramine N-(hydroxycinnamoyl)transferase induced in response to UV-C and wounding from Capsicum annuum

2001

Back, K.; Jang, S.M.; Lee, B.C.; Schmidt, A.; Strack, D.; Kim, K.M.

Plant Cell Physiol.

42

475-481

486129

10469131

Identification and characterization of cDNA clones encoding hydroxycinnamoyl-CoA:tyramine N-hydroxycinnamoyltransferase from tobacco

1999

Farmer, M.J.; Czermic, P.; Michael, A.; Negrel, J.

Eur. J. Biochem.

263

686-694

486130

10879473

Induction of N-hydroxycinnamoyltyramine synthesis and tyramine N-hydroxycinnamoyltransferase (THT) activity by wounding in maize leaves

2000

Ishihara, A.; Kawata, N.; Matsukawa, T.; Iwamura, H.

Biosci. Biotechnol. Biochem.

64

1025-1031

486132

9288939

Purification, characterization and partial amino acid sequencing of hydroxycinnamoyl-CoA:tyramine N-(hydroxycinnamoyl)transferase from tobacco cell-suspension cultures

1997

Negrel, J.; Javelle, F.

Eur. J. Biochem.

247

1127-1135

486133

9933628

Cloning and expression of a potato cDNA encoding hydroxycinnamoyl-CoA:tyramine N-(hydroxycinnamoyl)transferase

1999

Schmidt, A.; Grimm, R.; Schmidt, J.; Scheel, D.; Strack, D.; Rosahl, S.

J. Biol. Chem.

274

4273-4280

486134

10467029

Purification, characterization, and immunolocalization of hydroxycinnamoyl-CoA: tyramine N-(hydroxycinnamoyl)transferase from opium poppy

1999

Yu, M.; Facchini, P.J.

Planta

209

33-44

486247

-

Hydroxycinnamic acid esters of isocitric acid: Accumulation and enzymatic synthesis in Amaranthus cruentus

1987

Strack, D.; Leicht, P.; Bokern, M.; Wray, V.; Grotjahn, L.

Phytochemistry

26

2919-2923

486275

-

Enzymatic synthesis of hydroxycinnamic acid esters of sugar acids and hydroaromatic acids by protein preparations from rye (Secale cereale) primary leaves

1987

Strack, D.; Keller, H.; Weissenböck, G.

J. Plant Physiol.

131

61-73

486280

-

Partial purification and characterization of hydroxycinnamoyl CoA:transferase from apple and date fruits

1992

Lotfy, L.; Fleuriet, A.; Macheix, J.J.

Phytochemistry

31

767-772

486281

-

Hydroxycinnamoyl-CoA: transferases in higher plants. II. Characterization in Cichorium endivia and Raphanus sativus and comparison with other plants

1994

Lotfy, S.; Fleuriet, A.; Macheix, J.J.

Plant Physiol. Biochem.

32

355-363

486282

-

Inactivation and kinetic characterization of hydroxycinnamoyl-CoA:hydroaromatic acid O-hydroxycinnamoyltransferases from Cichorium endivia and Phoenix dactylifera

1995

Lotfy, S.

Plant Physiol. Biochem.

33

423-431

486283

12226354

Hydroxycinnamoyltransferases Involved in the accumulation of caffeic acid esters in gametophytes and sporophytes of Equisetum arvense

1996

Hohlfeld, M.; Veit, M.; Strack, D.

Plant Physiol.

111

1153-1159

486285

12381722

Purification, cloning, and properties of an acyltransferase controlling shikimate and quinate ester intermediates in phenylpropanoid metabolism

2003

Hoffmann, L.; Maury, S.; Martz, F.; Geoffroy, P.; Legrand, M.

J. Biol. Chem.

278

95-103

486312

-

Separation of putrescine and spermidine hydroxycinnamoyl transferases extracted from tobacco callus

1991

Negrel, J.; Javelle, F.; Paynot, M.

Phytochemistry

30

1089-1092

486313

16668786

Purification and properties of putrescine hydroxycinnamoyl transferase from tobacco (Nicotiana tabaccum) cell suspensions

1992

Negrel, J.; Paynot, M.; Javelle, F.

Plant Physiol.

98

1264-1269

486314

16666570

Hydroxycinnamoyl-CoA:putrescine hydroxycinnamoyltransferase in tobacco cell cultures with high and low levels of caffeoylputrescine

1989

Meurer-Grimes, B.; Berlin, J.; Strack, D.

Plant Physiol.

89

488-492

486315

-

The biosynthesis of cinnamoylputrescines in callus tissue cultures of Nicotiana tabaccum

1989

Negrel, J.

Phytochemistry

28

477-481

487361

-

Agmatine coumaroyltransferase (barley seedlings)

1983

Bird, C.R.; Smith, T.A.

Methods Enzymol.

94

344-347

487362

-

Agmatine coumaroyltransferase from barley seedlings

1983

Bird, C.R.; Smith, T.A.

Phytochemistry

22

2401-2403

487363

12582168

A new class of N-hydroxycinnamoyltransferases. Purification, cloning, and expression of barley agmatine coumaroyltransferase (EC 2.3.1.64)

2003

Burhenne, K.; Kristensen, B.K.; Rasmussen, S.K.

J. Biol. Chem.

278

13919-13927

487459

-

Purification and properties of chalcone synthase from cell suspension cultures of soybean

1987

Welle, R.; Grisebach, H.

Z. Naturforsch. C

42c

1200-1206

487460

3087289

Isolation and characterization of buckwheat (Fagopyrum esculentum M.) chalcone synthase and its polyclonal antibodies

1986

Hrazdina, G.; Lifson, E.; Weeden, N.F.

Arch. Biochem. Biophys.

247

414-419

487468

7396511

Chalcone synthesis with enzyme extracts from tulip anther tapetum using a biphasic enzyme assay

1980

Sutfeld, R.; Wiermann, R.

Arch. Biochem. Biophys.

201

64-72

487469

-

Purification of chalcone synthase from tulip anthers and comparison with the synthase from cosmos petals

1981

Sutfeld, R.; Wiermann, R.

Z. Naturforsch. C

36c

30-34

487470

-

Flavanone synthase from cell suspension cultures of Haplopappus gracilis and comparison with the synthase from parsely

1978

Saleh, N.A.M.; Fritsch, H.; Kreuzaler, F.; Grisebach, H.

Phytochemistry

17

183-186

487471

-

Characterization and development and localization of Flavanone synthase in tulip anthers

1978

Sutfeld, R.; Kehrel, B.; Wiermann, R.

Z. Naturforsch. C

33c

841-846

487474

9678580

A chalcone synthase with an unusual substrate preference is expressed in barley leaves in response to UV light and pathogen attack

1998

Christensen, A.B.; Gregersen, P.L.; Schroder, J.; Collinge, D.B.

Plant Mol. Biol.

37

849-857

487723

6427224

Purification and properties of a stilbene synthase from induced cell suspension cultures of peanut

1984

Schöppner, A.; Kindl, H.

J. Biol. Chem.

259

6806-6811

487783

-

The enzymic conversion of hydroxycinnamic acids to p-coumarylquinic and chlorogenic acids in tomato fruits

1976

Rhodes, M.J.C.; Wooltorton, L.S.C.

Phytochemistry

15

947-951

487784

-

Purification and properties of hydroxycinnamoyl CoA quinate hydroxycinnamoyl transferase from potatoes

1979

Rhodes, M.J.C.; Wooltorton, L.S.C.; Lourencq, E.J.

Phytochemistry

18

1125-1129

637806

7698342

Molecular and enzymic characterization of two stilbene synthases from Eastern white pine (Pinus strobus). A single Arg/His difference determines the activity and the pH dependence of the enzymes

1995

Raiber, S.; Schroeder, G.; Schroeder, J.

FEBS Lett.

361

299-302

651117

11856365

Divergent members of a soybean (Glycine max L.) 4-coumarate:coenzyme A ligase gene family

2002

Lindermayr, C.; Mollers, B.; Fliegmann, J.; Uhlmann, A.; Lottspeich, F.; Meimberg, H.; Ebel, J.

Eur. J. Biochem.

269

1304-1315

652146

11323416

Identification of the substrate specificity-conferring amino acid residues of 4-coumarate:coenzyme A ligase allows the rational design of mutant enzymes with new catalytic properties

2001

Stuible, H.P.; Kombrink, E.

J. Biol. Chem.

276

26893-26897

652422

12421821

Deletion of a single amino acid residue from different 4-coumarate:CoA ligases from soybean results in the generation of new substrate specificities

2003

Lindermayr, C.; Fliegmann, J.; Ebel, J.

J. Biol. Chem.

278

2781-2786

653477

10417722

Three 4-coumarate:coenzyme A ligases in Arabidopsis thaliana represent two evolutionarily divergent classes in angiosperms

1999

Ehlting, J.; Buttner, D.; Wang, Q.; Douglas, C.J.; Somssich, I.E.; Kombrink, E.

Plant J.

19

9-20

653481

11576429

Identification of 4-coumarate:coenzyme A ligase (4CL) substrate recognition domains

2001

Ehlting, J.; Shin, J.J.; Douglas, C.J.

Plant J.

27

455-465

653496

9489021

4-Coumarate:coenzyme A ligase in hybrid poplar. Properties of native enzymes, cDNA cloning, and analysis of recombinant enzymes

1998

Allina, S.M.; Pri-Hadash, A.; Theilmann, D.A.; Ellis, B.E.; Douglas, C.J.

Plant Physiol.

116

743-754

653527

11842147

Differential substrate inhibition couples kinetically distinct 4-coumarate: coenzyme A ligases with spatially distinct metabolic roles in quaking aspen

2002

Harding, S.A.; Leshkevich, J.; Chiang, V.L.; Tsai, C.J.

Plant Physiol.

128

428-438

653536

12644689

4-Coumarate:coenzyme A ligase has the catalytic capacity to synthesize and reuse various (di)adenosine polyphosphates

2003

Pietrowska-Borek, M.; Stuible, H.P.; Kombrink, E.; Guranowski, A.

Plant Physiol.

131

1401-1410

653573

12012244

4-Hydroxycinnamoyl-CoA hydratase/lyase, an enzyme of phenylpropanoid cleavage from Pseudomonas, causes formation of C(6)-C(1) acid and alcohol glucose conjugates when expressed in hairy roots of Datura stramonium L.

2002

Mitra, A.; Mayer, M.J.; Mellon, F.A.; Michael, A.J.; Narbad, A.; Parr, A.J.; Waldron, K.W.; Walton, N.J.

Planta

215

79-89

653597

12819348

The substrate specificity-determining amino acid code of 4-coumarate:CoA ligase

2003

Schneider, K.; Hovel, K.; Witzel, K.; Hamberger, B.; Schomburg, D.; Kombrink, E.; Stuible, H.P.

Proc. Natl. Acad. Sci. USA

100

8601-8606

660244

15122017

Production of coumaroylserotonin and feruloylserotonin in transgenic rice expressing pepper hydroxycinnamoyl-coenzyme a:Serotonin N-(hydroxycinnamoyl)transferase

2004

Jang, S.M.; Ishihara, A.; Back, K.

Plant Physiol.

135

346-356

663518

15583385

Purification, crystallization and preliminary x-ray crystallographic analysis of hydroxycinnamoyl-coenzyme A hydratase-lyase (HCHL), a crotonase homologue active in phenylpropanoid metabolism

2004

Leonard, P.M.; Marshall, C.M.; Dodson, E.J.; Walton, N.J.; Grogan, G.

Acta Crystallogr. Sect. D

D60

2343-2345

672472

16006242

Biochemical characterization of a cinnamoyl-CoA reductase from wheat

2005

Ma, Q.H.; Tian, B.

Biol. Chem.

386

553-560

675132

16551686

Down-regulation of cinnamoyl-CoA reductase in tomato (Solanum lycopersicum L.) induces dramatic changes in soluble phenolic pools

2006

van der Rest, B.; Danoun, S.; Boudet, A.M.; Rochange, S.F.

J. Exp. Bot.

57

1399-1411

676373

16890967

Biosynthesis of curcuminoids and gingerols in turmeric (Curcuma longa) and ginger (Zingiber officinale): identification of curcuminoid synthase and hydroxycinnamoyl-CoA thioesterases

2006

Ramirez-Ahumada, M.d.e.l.C.; Timmermann, B.N.; Gang, D.R.

Phytochemistry

67

2017-2029

676451

15870094

Clarification of cinnamoyl co-enzyme A reductase catalysis in monolignol biosynthesis of Aspen

2005

Li, L.; Cheng, X.; Lu, S.; Nakatsubo, T.; Umezawa, T.; Chiang, V.L.

Plant Cell Physiol.

46

1073-1082

676598

16384907

Functional analysis of the amine substrate specificity domain of pepper tyramine and serotonin N-hydroxycinnamoyltransferases

2006

Kang, S.; Kang, K.; Chung, G.C.; Choi, D.; Ishihara, A.; Lee, D.; Back, K.

Plant Physiol.

140

704-715

676643

16122934

Kinetic and inhibition studies of cinnamoyl-CoA reductase 1 from Arabidopsis thaliana

2005

Baltas, M.; Lapeyre, C.; Bedos-Belval, F.; Maturano, M.; Saint-Aguet, P.; Roussel, L.; Duran, H.; Grima-Pettenati, J.

Plant Physiol. Biochem.

43

746-753

676843

16380417

Cinnamoyl-CoA reductase, a key enzyme in lignin biosynthesis, is an effector of small GTPase Rac in defense signaling in rice

2006

Kawasaki, T.; Koita, H.; Nakatsubo, T.; Hasegawa, K.; Wakabayashi, K.; Takahashi, H.; Umemura, K.; Umezawa, T.; Shimamoto, K.

Proc. Natl. Acad. Sci. USA

103

230-235

677312

17139085

The 1.8 A resolution structure of hydroxycinnamoyl-coenzyme A hydratase-lyase (HCHL) from Pseudomonas fluorescens, an enzyme that catalyses the transformation of feruloyl-coenzyme A to vanillin

2006

Leonard, P.M.; Brzozowski, A.M.; Lebedev, A.; Marshall, C.M.; Smith, D.J.; Verma, C.S.; Walton, N.J.; Grogan, G.

Acta Crystallogr. Sect. D

62

1494-1501

682467

17120022

Metabolic diversion of the phenylpropanoid pathway causes cell wall and morphological changes in transgenic tobacco stems

2007

Merali, Z.; Mayer, M.J.; Parker, M.L.; Michael, A.J.; Smith, A.C.; Waldron, K.W.

Planta

225

1165-1178

684699

18068110

Molecular and biochemical characterization of benzalacetone synthase and chalcone synthase genes and their proteins from raspberry (Rubus idaeus L.)

2008

Zheng, D.; Hrazdina, G.

Arch. Biochem. Biophys.

470

139-145

690831

18479250

A ternary complex of hydroxycinnamoyl-CoA hydratase-lyase (HCHL) with acetyl-CoA and vanillin gives insights into substrate specificity and mechanism

2008

Bennett, J.P.; Bertin, L.; Moulton, B.; Fairlamb, I.J.; Brzozowski, A.M.; Walton, N.J.; Grogan, G.

Biochem. J.

414

281-289

693407

17452751

Characterization of a cinnamoyl-CoA reductase that is associated with stem development in wheat

2007

Ma, Q.H.

J. Exp. Bot.

58

2011-2021

700489

19761442

Switchgrass (Panicum virgatum) possesses a divergent family of cinnamoyl CoA reductases with distinct biochemical properties

2009

Escamilla-Trevino, L.L.; Shen, H.; Uppalapati, S.R.; Ray, T.; Tang, Y.; Hernandez, T.; Yin, Y.; Xu, Y.; Dixon, R.A.

New Phytol.

185

143-155

700658

-

Formation of omega-feruloyloxypalmitic acid by an enzyme from wound-healing potato tuber disks

1994

Lotfy, S.; Negrel, J.; Javelle, F.

Phytochemistry

35

1419-1424

700659

-

Distribution of hydroxycinnamoyl-CoA: omega-Hydroxypalmitic acid O-hydroxycinnamoyltransferase in higher plants

1995

Lotfy, S.; Javelle, F.; Negrel, J.

Phytochemistry

40

389-391

700854

-

Purification and characterization of hydroxycinnamoyl-coenzyme A:omega-hydroxypalmitic acid O-hydroxycinnamoyltransferase from tobacco (Nicotiana tabacum) cell-suspension cultures

1996

Lotfy, S.; Javelle, F.; Negrel, J.

Planta

199

475-480

701671

19563771

Quantitative isotopic 13C nuclear magnetic resonance at natural abundance to probe enzyme reaction mechanisms via site-specific isotope fractionation: the case of the chain-shortening reaction for the bioconversion of ferulic acid to vanillin

2009

Botosoa, E.P.; Blumenstein, C.; MacKenzie, D.A.; Silvestre, V.; Remaud, G.S.; Kwiecien, R.A.; Robins, R.J.

Anal. Biochem.

393

182-188

706386

19521717

Accumulation of hydroxycinnamic acid amides induced by pathogen infection and identification of agmatine coumaroyltransferase in Arabidopsis thaliana

2009

Muroi, A.; Ishihara, A.; Tanaka, C.; Ishizuka, A.; Takabayashi, J.; Miyoshi, H.; Nishioka, T.

Planta

230

517-527

718662

20972784

Production of tranilast [N-(3,4-dimethoxycinnamoyl)-anthranilic acid] and its analogs in yeast Saccharomyces cerevisiae

2011

Eudes, A.; Baidoo, E.E.; Yang, F.; Burd, H.; Hadi, M.Z.; Collins, F.W.; Keasling, J.D.; Loque, D.

Appl. Microbiol. Biotechnol.

89

989-1000

719493

19622354

Identification and characterization of multiple curcumin synthases from the herb Curcuma longa

2009

Katsuyama, Y.; Kita, T.; Horinouchi, S.

FEBS Lett.

583

2799-2803

719850

19258320

Curcuminoid biosynthesis by two type III polyketide synthases in the herb Curcuma longa

2009

Katsuyama, Y.; Kita, T.; Funa, N.; Horinouchi, S.

J. Biol. Chem.

284

11160-11170

720638

22285622

Characterization of hydroxycinnamoyltransferase from rice and its application for biological synthesis of hydroxycinnamoyl glycerols

2012

Kim, I.; Kim, B.; Kim, M.; Ahn, J.

Phytochemistry

76

25-31

720745

22082505

MYB8 controls inducible phenolamide levels by activating three novel hydroxycinnamoyl-coenzyme A: polyamine transferases in Nicotiana attenuata

2012

Onkokesung, N.; Gaquerel, E.; Kotkar, H.; Kaur, H.; Baldwin, I.; Galis, I.

Plant Physiol.

158

389-407

720787

21318289

Distinct substrate specificities and unusual substrate flexibilities of two hydroxycinnamoyltransferases, rosmarinic acid synthase and hydroxycinnamoyl-CoA:shikimate hydroxycinnamoyl-transferase, from Coleus blumei Benth.

2011

Sander, M.; Petersen, M.

Planta

233

1157-1171

720789

21424826

Substrate promiscuity of a rosmarinic acid synthase from lavender (Lavandula angustifolia L.)

2011

Landmann, C.; Huecherig, S.; Fink, B.; Hoffmann, T.; Dittlein, D.; Coiner, H.A.; Schwab, W.

Planta

234

305-320

721196

20693677

Expression, purification and crystallization of a plant type III polyketide synthase that produces diarylheptanoids

2010

Morita, H.; Wanibuchi, K.; Kato, R.; Sugio, S.; Abe, I.

Acta Crystallogr. Sect. F

66

948-950

722655

17932040

In vitro synthesis of curcuminoids by type III polyketide synthase from Oryza sativa

2007

Katsuyama, Y.; Matsuzawa, M.; Funa, N.; Horinouchi, S.

J. Biol. Chem.

282

37702-37709

722740

21148316

Structural and biochemical elucidation of mechanism for decarboxylative condensation of beta-keto acid by curcumin synthase

2011

Katsuyama, Y.; Miyazono, K.; Tanokura, M.; Ohnishi, Y.; Horinouchi, S.

J. Biol. Chem.

286

6659-6668

723451

12226219

Aromatic polyketide synthases (purification, characterization, and antibody development to benzalacetone synthase from raspberry fruits)

1996

Borejsza-Wysocki, W.; Hrazdina, G.

Plant Physiol.

110

791-799

724494

23515358

In silico mutagenesis and docking studies of active site residues suggest altered substrate specificity and possible physiological role of cinnamoyl CoA reductase 1 (Ll-CCRH1)

2013

Sonawane, P.; Patel, K.; Vishwakarma, R.K.; Singh, S.; Khan, B.M.

Bioinformation

9

224-232

725147

23541561

Biochemical characterization of recombinant cinnamoyl CoA reductase 1 (Ll-CCRH1) from Leucaena leucocephala

2013

Sonawane, P.; Vishwakarma, R.K.; Khan, B.M.

Int. J. Biol. Macromol.

58

154-159

725148

23688416

Probing the active site of cinnamoyl CoA reductase 1 (Ll-CCRH1) from Leucaena leucocephala

2013

Sonawane, P.; Patel, K.; Vishwakarma, R.K.; Srivastava, S.; Singh, S.; Gaikwad, S.; Khan, B.M.

Int. J. Biol. Macromol.

60C

33-38

725626

21493812

Characterization of a cinnamoyl-CoA reductase 1 (CCR1) mutant in maize: effects on lignification, fibre development, and global gene expression

2011

Tamasloukht, B.; Wong Quai Lam, M.S.; Martinez, Y.; Tozo, K.; Barbier, O.; Jourda, C.; Jauneau, A.; Borderies, G.; Balzergue, S.; Renou, J.P.; Huguet, S.; Martinant, J.P.; Tatout, C.; Lapierre, C.; Barriere, Y.; Goffner, D.; Pichon, M.

J. Exp. Bot.

62

3837-3848

725759

20512516

Structural and docking studies of Leucaena leucocephala cinnamoyl CoA reductase

2011

Prasad, N.K.; Vindal, V.; Kumar, V.; Kabra, A.; Phogat, N.; Kumar, M.

J. Mol. Model.

17

533-541

726367

20876124

Distinct cinnamoyl CoA reductases involved in parallel routes to lignin in Medicago truncatula

2010

Zhou, R.; Jackson, L.; Shadle, G.; Nakashima, J.; Temple, S.; Chen, F.; Dixon, R.A.

Proc. Natl. Acad. Sci. USA

107

17803-17808

729753

22515452

Characterization of FerC, a MarR-type transcriptional regulator, involved in transcriptional regulation of the ferulate catabolic operon in Sphingobium sp. strain SYK-6

2012

Kasai, D.; Kamimura, N.; Tani, K.; Umeda, S.; Abe, T.; Fukuda, M.; Masai, E.

FEMS Microbiol. Lett.

332

68-75

732091

23479729

An electron-bifurcating caffeyl-CoA reductase

2013

Bertsch, J.; Parthasarathy, A.; Buckel, W.; Müller, V.

J. Biol. Chem.

288

11304-11311

737235

-

Identification of a new curcumin synthase from ginger and construction of a curcuminoid-producing unnatural fusion protein diketide-CoA synthase - curcumin synthase

2016

Zhang, L.; Gao, B.; Wang, X.; Zhang, Z.; Liu, X.; Wang, J.; Mo, T.; Liu, Y.; Shi, S.; Tu, P.

RSC Adv.

6

12519-12524

742589

25346738

FaPOD27 functions in the metabolism of polyphenols in strawberry fruit (Fragaria sp.)

2014

Yeh, S.Y.; Huang, F.C.; Hoffmann, T.; Mayershofer, M.; Schwab, W.

Front. Plant Sci.

5

518

743007

24322526

Steady state fluorescence studies of wild type recombinant cinnamoyl CoA reductase (Ll-CCRH1) and its active site mutants

2014

Sonawane, P.; Vishwakarma, R.K.; Singh, S.; Gaikwad, S.; Khan, B.M.

J. Fluoresc.

24

665-673

743156

-

Preparation of cinnamoyl-CoA and analysis of the enzyme activity of recombinant CCR protein from Populus tomentosa

2014

Han, B.; Liu, S.; Gai, Y.; Jiang, X.

J. Plant Biochem. Biotechnol.

23

348-357

743233

26264710

Overexpression of artificially fused bifunctional enzyme 4CL1-CCR a method for production of secreted 4-hydroxycinnamaldehydes in Escherichia coli

2015

Liu, S.; Qi, Q.; Chao, N.; Hou, J.; Rao, G.; Xie, J.; Lu, H.; Jiang, X.; Gai, Y.

Microb. Cell Fact.

14

118

743447

25217505

Structural studies of cinnamoyl-CoA reductase and cinnamyl-alcohol dehydrogenase, key enzymes of monolignol biosynthesis

2014

Pan, H.; Zhou, R.; Louie, G.V.; Muehlemann, J.K.; Bomati, E.K.; Bowman, M.E.; Dudareva, N.; Dixon, R.A.; Noel, J.P.; Wang, X.

Plant Cell

26

3709-3727

743470

26058952

CCR1, an enzyme required for lignin biosynthesis in Arabidopsis, mediates cell proliferation exit for leaf development

2015

Xue, J.; Luo, D.; Xu, D.; Zeng, M.; Cui, X.; Li, L.; Huang, H.

Plant J.

83

375-387

743501

27956488

Structural and biochemical characterization of cinnamoyl-CoA reductases

2017

Sattler, S.A.; Walker, A.M.; Vermerris, W.; Sattler, S.E.; Kang, C.

Plant Physiol.

173

1031-1044

743559

27580618

Characterization of the cinnamoyl-CoA reductase (CCR) gene family in Populus tomentosa reveals the enzymatic active sites and evolution of CCR

2017

Chao, N.; Li, N.; Qi, Q.; Li, S.; Lv, T.; Jiang, X.N.; Gai, Y.

Planta

245

61-75

743848

24723816

Characterization of developmental- and stress-mediated expression of cinnamoyl-CoA reductase in kenaf (Hibiscus cannabinus L.)

2014

Ghosh, R.; Choi, B.; Cho, B.K.; Lim, H.S.; Park, S.U.; Bae, H.J.; Natarajan, S.; Bae, H.

ScientificWorldJournal

2014

601845

745999

25152451

Identification and cloning of an NADPH-dependent hydroxycinnamoyl-CoA double bond reductase involved in dihydrochalcone formation in Malus x domestica Borkh

2014

Ibdah, M.; Berim, A.; Martens, S.; Valderrama, A.L.; Palmieri, L.; Lewinsohn, E.; Gang, D.R.

Phytochemistry

107

24-31

746582

-

Crotonases natures exceedingly convertible catalysts

2017

Lohans, C.; Wang, D.; Wang, J.; Hamed, R.; Schofield, C.

ACS Catal.

7

6587-6599

751828

22169019

Molecular cloning and functional analysis of the ortho-hydroxylases of p-coumaroyl coenzyme A/feruloyl coenzyme A involved in formation of umbelliferone and scopoletin in sweet potato, Ipomoea batatas (L.) Lam

2012

Matsumoto, S.; Mizutani, M.; Sakata, K.; Shimizu, B.

Phytochemistry

74

49-57

751858

18547395

Scopoletin is biosynthesized via ortho-hydroxylation of feruloyl CoA by a 2-oxoglutarate-dependent dioxygenase in Arabidopsis thaliana

2008

Kai, K.; Mizutani, M.; Kawamura, N.; Yamamoto, R.; Tamai, M.; Yamaguchi, H.; Sakata, K.; Shimizu, B.

Plant J.

55

989-999

751859

22168819

A 2-oxoglutarate-dependent dioxygenase from Ruta graveolens L. Exhibits p-coumaroyl CoA 2-hydroxylase activity (C2H) A missing step in the synthesis of umbelliferone in plants

2012

Vialart, G.; Hehn, A.; Olry, A.; Ito, K.; Krieger, C.; Larbat, R.; Paris, C.; Shimizu, B.; Sugimoto, Y.; Mizutani, M.; Bourgaud, F.

Plant J.

70

460-470

754012

22328668

Anaerobic p-coumarate degradation by Rhodopseudomonas palustris and identification of CouR, a MarR repressor protein that binds p-coumaroyl coenzyme A

2012

Hirakawa, H.; Schaefer, A.L.; Greenberg, E.P.; Harwood, C.S.

J. Bacteriol.

194

1960-1967

755197

23840666

Characterization of two Streptomyces enzymes that convert ferulic acid to vanillin

2013

Yang, W.; Tang, H.; Ni, J.; Wu, Q.; Hua, D.; Tao, F.; Xu, P.

PLoS One

8

e67339

756266

26667131

Synthesis of rosmarinic acid analogues in Escherichia coli

2016

Zhuang, Y.; Jiang, J.; Bi, H.; Yin, H.; Liu, S.; Liu, T.

Biotechnol. Lett.

38

619-627

757268

32192841

Bioproduction of glucose conjugates of 4-hydroxybenzoic and vanillic acids using bamboo cells transformed to express bacterial 4-hydroxycinnamoyl-CoA hydratase/lyase

2020

Kitaoka, N.; Nomura, T.; Ogita, S.; Kato, Y.

J. Biosci. Bioeng.

S1389-1723

30926-0

757363

27015846

Molecular evidence for biochemical diversification of phenolamide biosynthesis in rice plants

2016

Tanabe, K.; Hojo, Y.; Shinya, T.; Galis, I.

J. Integr. Plant Biol.

58

903-913

757487

-

A bifunctional type III polyketide synthase from raspberry (Rubus idaeus L.) with both chalcone synthase and benzalacetone synthase activity

2017

Guo, H.; Yang, Y.; Ma, Y.; Liu, W.; Feng, J.; Luo, Z.; Lu, H.; Liu, C.; Yang, M.; Wang, Y.; Ma, L.

J. Plant Biochem. Biotechnol.

26

80-90

757784

27534116

Cloning and functional analysis of three chalcone synthases from the flowers of safflowers Carthamus tinctorius

2016

Shinozaki, J.; Kenmoku, H.; Nihei, K.; Masuda, K.; Noji, M.; Konno, K.; Asakawa, Y.; Kazuma, K.

Nat. Prod. Commun.

11

787-790

758017

29752755

Jasmonic acid/ethylene signaling coordinates hydroxycinnamic acid amides biosynthesis through ORA59 transcription factor

2018

Li, J.; Zhang, K.; Meng, Y.; Hu, J.; Ding, M.; Bian, J.; Yan, M.; Han, J.; Zhou, M.

Plant J.

95

444-457

758066

30691636

Isolation and functional characterization of hydroxycinnamoyltransferases from the liverworts Plagiochasma appendiculatum and Marchantia paleacea

2018

Wu, Y.F.; Zhao, Y.; Liu, X.Y.; Gao, S.; Cheng, A.X.; Lou, H.X.

Plant Physiol. Biochem.

129

400-410

758087

25854602

Biochemical characterization of caffeoyl coenzyme A 3-O-methyltransferase from wheat

2015

Ma, Q.; Luo, H.

Planta

242

113-122

758333

-

Identification of a new curcumin synthase from ginger and construction of a curcuminoid-producing unnatural fusion protein diketide-CoA synthase curcumin synthase

2016

Zhang, L.; Gao, B.; Wang, X.; Zhang, Z.; Liu, X.; Wang, J.; Mo, T.; Liu, Y.; Shi, S.; Tu, P.

RSC Adv.

6

12519-12524

761938

14714871

Analysis of the involvement of hydroxyanthranilate hydroxycinnamoyltransferase and caffeoyl-CoA 3-O-methyltransferase in phytoalexin biosynthesis in oat

2004

Yang, Q.; Trinh, H.; Imai, S.; Ishihara, A.; Zhang, L.; Nakayashiki, H.; Tosa, Y.; Mayama, S.

Mol. Plant Microbe Interact.

17

81-89

762175

29606213

Spectrophotometric determination of reaction rates and kinetic parameters of a BAHD acyltransferase using DTNB (5,5'-dithio-bis-[2-nitrobenzoic acid])

2018

Sullivan, M.; Bonawitz, N.

Plant Sci.

269

148-152

762520

-

Induction of hydroxycinnamoyl-CoA hydroxyanthranilate N-hydroxycinnamoyl-transferase (HHT) activity in oat leaves by victorin C

1997

Ishihara, A.; Matsukawa, T.; Miyagawa, H.; Ueno, T.; Iwamura, H.; Mayama, S.; Ishihara, A.; Matsukawa, T.; Miyagawa, H.; Iwamura, H.

Z. Naturforsch. C

52

756-760

762841

28469705

Suppression of cinnamoyl-CoA reductase increases the level of monolignol ferulates incorporated into maize lignins

2017

Smith, R.A.; Cass, C.L.; Mazaheri, M.; Sekhon, R.S.; Heckwolf, M.; Kaeppler, H.; de Leon, N.; Mansfield, S.D.; Kaeppler, S.M.; Sedbrook, J.C.; Karlen, S.D.; Ralph, J.

Biotechnol. Biofuels

10

109

763103

29312373

Biochemical and expression analyses of the rice cinnamoyl-CoA reductase gene family

2017

Park, H.L.; Bhoo, S.H.; Kwon, M.; Lee, S.W.; Cho, M.H.

Front. Plant Sci.

8

2099

763522

30276825

CAD1 and CCR2 protein complex formation in monolignol biosynthesis in Populus trichocarpa

2019

Yan, X.; Liu, J.; Kim, H.; Liu, B.; Huang, X.; Yang, Z.; Lin, Y.J.; Chen, H.; Yang, C.; Wang, J.P.; Muddiman, D.C.; Ralph, J.; Sederoff, R.R.; Li, Q.; Chiang, V.L.

New Phytol.

222

244-260

763599

28321576

Two distinct cinnamoyl-CoA reductases in Selaginella moellendorffii offer insight into the divergence of CCRs in plants

2017

Chao, N.; Li, S.; Li, N.; Qi, Q.; Jiang, W.T.; Jiang, X.N.; Gai, Y.

Planta

246

33-43

763766

31748812

Novel motif is capable of determining CCR and CCR-like proteins based on the divergence of CCRs in plants

2019

Chao, N.; Jiang, W.T.; Wang, X.C.; Jiang, X.N.; Gai, Y.

Tree Physiol.

39

2019-2026