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(-)-maackiain biosynthesis
-
-
PWY-2464
(-)-medicarpin biosynthesis
-
-
PWY-2463
(1,4)-beta-D-xylan degradation
-
-
PWY-6717
(3R)-linalool biosynthesis
-
-
PWY-7709
(3R)-N-[(2S)-1-hydroxy-6-[(3R)-3-isocyanobutanamido]hexan-2-yl]-3-isocyanobutanamide biosynthesis
-
-
PWY-8320
(3S)-linalool biosynthesis
-
-
PWY-7141
(4S)-carvone biosynthesis
-
-
PWY-7443
(4Z,7Z,10Z,13Z,16Z)-docosa-4,7,10,13,16-pentaenoate biosynthesis II (4-desaturase)
-
-
PWY-7728
(4Z,7Z,10Z,13Z,16Z)-docosapentaenoate biosynthesis (6-desaturase)
-
-
PWY-7726
(5R)-carbapenem carboxylate biosynthesis
(5Z)-dodecenoate biosynthesis I
-
-
PWY0-862
(5Z)-dodecenoate biosynthesis II
-
-
PWY-7858
(7Z,10Z,13Z)-hexadecatrienoate biosynthesis
-
-
PWY-7590
(8E,10E)-dodeca-8,10-dienol biosynthesis
-
-
PWY-7654
(9Z)-tricosene biosynthesis
-
-
PWY-7035
(aminomethyl)phosphonate degradation
-
-
PWY-7805
(E,E)-4,8,12-trimethyltrideca-1,3,7,11-tetraene biosynthesis
-
-
PWY-6668
(R)- and (S)-3-hydroxybutanoate biosynthesis (engineered)
-
-
PWY-7216
(R)-cysteate degradation
-
-
PWY-6642
(S)-lactate fermentation to propanoate, acetate and hydrogen
-
-
PWY-8086
(S)-propane-1,2-diol degradation
-
-
PWY-7013
(S)-reticuline biosynthesis
-
-
(S)-reticuline biosynthesis I
-
-
PWY-3581
(S)-reticuline biosynthesis II
-
-
PWY-6133
(Z)-butanethial-S-oxide biosynthesis
-
-
PWY-6900
(Z)-phenylmethanethial S-oxide biosynthesis
-
-
PWY-6539
1,2-dichloroethane degradation
-
-
12DICHLORETHDEG-PWY
1,3-beta-D-glucan biosynthesis
-
-
PWY-6773
1,3-propanediol biosynthesis (engineered)
-
-
PWY-7385
1,5-anhydrofructose degradation
-
-
PWY-6992
1-butanol autotrophic biosynthesis (engineered)
-
-
PWY-6886
1-methylpyrrolinium biosynthesis
-
-
PWY-5315
10-cis-heptadecenoyl-CoA degradation (yeast)
-
-
PWY-7337
10-trans-heptadecenoyl-CoA degradation (MFE-dependent, yeast)
-
-
PWY-7339
10-trans-heptadecenoyl-CoA degradation (reductase-dependent, yeast)
-
-
PWY-7338
11-oxyandrogens biosynthesis
-
-
PWY-8202
15-epi-lipoxin biosynthesis
-
-
PWY66-393
1D-myo-inositol hexakisphosphate biosynthesis I (from Ins(1,4,5)P3)
-
-
PWY-6361
1D-myo-inositol hexakisphosphate biosynthesis II (mammalian)
-
-
PWY-6362
1D-myo-inositol hexakisphosphate biosynthesis III (Spirodela polyrrhiza)
-
-
PWY-4661
1D-myo-inositol hexakisphosphate biosynthesis IV (Dictyostelium)
-
-
PWY-6372
1D-myo-inositol hexakisphosphate biosynthesis V (from Ins(1,3,4)P3)
-
-
PWY-6554
2'-deoxymugineic acid phytosiderophore biosynthesis
-
-
PWY-5912
2,3-dihydroxybenzoate biosynthesis
-
-
PWY-5901
2-arachidonoylglycerol biosynthesis
-
-
PWY-8052
2-carboxy-1,4-naphthoquinol biosynthesis
-
-
PWY-5837
2-chloroacrylate degradation I
-
-
PWY-7425
2-deoxy-D-glucose 6-phosphate degradation
-
-
PWY-8121
2-deoxy-D-ribose degradation II
-
-
PWY-8058
2-methyl-branched fatty acid beta-oxidation
-
-
PWY-8181
2-methylpropene degradation
-
-
PWY-7778
2-nitrotoluene degradation
-
-
PWY-5641
2-oxoglutarate decarboxylation to succinyl-CoA
-
-
PWY-5084
24-epi-campesterol, fucosterol, and clionasterol biosynthesis (diatoms)
-
-
PWY-8238
3,5-dimethoxytoluene biosynthesis
-
-
PWY-7076
3,8-divinyl-chlorophyllide a biosynthesis I (aerobic, light-dependent)
-
-
CHLOROPHYLL-SYN
3,8-divinyl-chlorophyllide a biosynthesis II (anaerobic)
-
-
PWY-5531
3,8-divinyl-chlorophyllide a biosynthesis III (aerobic, light independent)
-
-
PWY-7159
3-(4-hydroxyphenyl)pyruvate biosynthesis
-
-
PWY-5886
3-dehydroquinate biosynthesis I
-
-
PWY-6164
3-dehydroquinate biosynthesis II (archaea)
-
-
PWY-6160
3-hydroxy-4-methyl-anthranilate biosynthesis I
-
-
PWY-7717
3-hydroxy-4-methyl-anthranilate biosynthesis II
-
-
PWY-7765
3-hydroxypropanoate cycle
-
-
PWY-5743
3-hydroxypropanoate/4-hydroxybutanate cycle
-
-
PWY-5789
3-methyl-branched fatty acid alpha-oxidation
-
-
PWY66-387
3-methylbutanol biosynthesis (engineered)
-
-
PWY-6871
3-methylthiopropanoate biosynthesis
-
-
PWY-5389
3-phenylpropanoate degradation
-
-
P281-PWY
3-phenylpropionate degradation
-
-
3-phosphoinositide biosynthesis
-
-
PWY-6352
3-phosphoinositide degradation
-
-
PWY-6368
4-amino-2-methyl-5-diphosphomethylpyrimidine biosynthesis I
-
-
PWY-6890
4-aminobenzoate biosynthesis I
-
-
PWY-6543
4-aminobenzoate biosynthesis II
-
-
PWY-8276
4-aminobutanoate degradation I
-
-
PWY-6535
4-aminobutanoate degradation II
-
-
PWY-6537
4-aminobutanoate degradation III
-
-
PWY-6536
4-aminobutanoate degradation IV
-
-
PWY-6473
4-aminobutanoate degradation V
-
-
PWY-5022
4-coumarate degradation (aerobic)
-
-
PWY-8002
4-coumarate degradation (anaerobic)
-
-
PWY-7046
4-ethylphenol degradation (anaerobic)
-
-
PWY-6080
4-hydroxy-2(1H)-quinolone biosynthesis
-
-
PWY-6661
4-hydroxy-2-nonenal detoxification
-
-
PWY-7112
4-hydroxybenzoate biosynthesis I (eukaryotes)
-
-
PWY-5754
4-hydroxybenzoate biosynthesis III (plants)
-
-
PWY-6435
4-hydroxymandelate degradation
4-hydroxyphenylacetate degradation
4-oxopentanoate degradation
-
-
PWY-7948
5'-deoxyadenosine degradation I
-
-
PWY-8130
5'-deoxyadenosine degradation II
-
-
PWY-8131
5-deoxystrigol biosynthesis
-
-
PWY-7101
5-nitroanthranilate degradation
-
-
PWY-7044
5-oxo-L-proline metabolism
-
-
PWY-7942
6-gingerol analog biosynthesis (engineered)
-
-
PWY-6920
6-hydroxymethyl-dihydropterin diphosphate biosynthesis
-
-
6-hydroxymethyl-dihydropterin diphosphate biosynthesis I
-
-
PWY-6147
6-hydroxymethyl-dihydropterin diphosphate biosynthesis II (Methanocaldococcus)
-
-
PWY-6797
6-hydroxymethyl-dihydropterin diphosphate biosynthesis III (Chlamydia)
-
-
PWY-7539
6-hydroxymethyl-dihydropterin diphosphate biosynthesis IV (Plasmodium)
-
-
PWY-7852
7-dehydroporiferasterol biosynthesis
-
-
PWY-7155
8-amino-7-oxononanoate biosynthesis I
-
-
PWY-6519
8-amino-7-oxononanoate biosynthesis IV
-
-
PWY-8203
9-cis, 11-trans-octadecadienoyl-CoA degradation (isomerase-dependent, yeast)
-
-
PWY-7340
9-lipoxygenase and 9-allene oxide synthase pathway
-
-
PWY-5407
9-lipoxygenase and 9-hydroperoxide lyase pathway
-
-
PWY-5408
ABH and Lewis epitopes biosynthesis from type 1 precursor disaccharide
-
-
PWY-7832
ABH and Lewis epitopes biosynthesis from type 2 precursor disaccharide
-
-
PWY-7831
abietic acid biosynthesis
-
-
PWY-5411
abscisic acid biosynthesis
-
-
PWY-695
acetaldehyde biosynthesis I
-
-
PWY-6333
acetaldehyde biosynthesis II
-
-
PWY-6330
acetate and ATP formation from acetyl-CoA I
-
-
PWY0-1312
acetate and ATP formation from acetyl-CoA III
-
-
PWY-8328
acetate conversion to acetyl-CoA
-
-
PWY0-1313
acetoacetate degradation (to acetyl CoA)
-
-
ACETOACETATE-DEG-PWY
acetone degradation I (to methylglyoxal)
-
-
PWY-5451
acetone degradation III (to propane-1,2-diol)
-
-
PWY-7466
acetyl CoA biosynthesis
-
-
acetyl-CoA fermentation to butanoate
-
-
PWY-5676
acetylene degradation (anaerobic)
-
-
P161-PWY
acridone alkaloid biosynthesis
-
-
PWY-5958
acrylonitrile degradation I
-
-
PWY-7308
acyl carrier protein activation
-
-
PWY-6012-1
acyl carrier protein metabolism
-
-
PWY-6012
acyl-[acyl-carrier protein] thioesterase pathway
-
-
PWY-5142
adenine and adenosine salvage I
-
-
P121-PWY
adenine and adenosine salvage II
-
-
PWY-6605
adenine and adenosine salvage III
-
-
PWY-6609
adenine and adenosine salvage V
-
-
PWY-6611
adenine and adenosine salvage VI
-
-
PWY-6619
adenine salvage
-
-
PWY-6610
adenosine deoxyribonucleotides de novo biosynthesis I
-
-
PWY-7227
adenosine deoxyribonucleotides de novo biosynthesis II
-
-
PWY-7220
adenosine nucleotides degradation I
-
-
PWY-6596
adenosine nucleotides degradation II
-
-
SALVADEHYPOX-PWY
adenosine ribonucleotides de novo biosynthesis
-
-
PWY-7219
adipate biosynthesis
-
-
PWY-8347
adlupulone and adhumulone biosynthesis
-
-
PWY-7857
aerobic respiration I (cytochrome c)
-
-
PWY-3781
aerobic respiration II (cytochrome c) (yeast)
-
-
PWY-7279
aerobic respiration III (alternative oxidase pathway)
-
-
PWY-4302
aerobic toluene degradation
-
-
Aflatoxin biosynthesis
-
-
ajmaline and sarpagine biosynthesis
-
-
PWY-5301
Alanine, aspartate and glutamate metabolism
-
-
aldoxime degradation
-
-
P345-PWY
alginate degradation
-
-
PWY-6986
alkane biosynthesis II
-
-
PWY-7033
alkane oxidation
-
-
PWY-2724
all-trans-decaprenyl diphosphate biosynthesis
-
-
PWY-5806
all-trans-farnesol biosynthesis
-
-
PWY-6859
allantoin degradation
-
-
alliin metabolism
-
-
PWY-5706
allopregnanolone biosynthesis
-
-
PWY-7455
alpha-amyrin biosynthesis
-
-
PWY-5377
alpha-carotene biosynthesis
-
-
PWY-5946
alpha-linolenate biosynthesis I (plants and red algae)
-
-
PWY-5997
alpha-linolenate metabolites biosynthesis
-
-
PWY-8398
alpha-Linolenic acid metabolism
-
-
alpha-tomatine degradation
-
-
PWY18C3-5
Amaryllidacea alkaloids biosynthesis
-
-
PWY-7826
Amino sugar and nucleotide sugar metabolism
-
-
Aminoacyl-tRNA biosynthesis
-
-
Aminobenzoate degradation
-
-
aminopropylcadaverine biosynthesis
-
-
PWY0-1303
ammonia assimilation cycle I
-
-
PWY-6963
ammonia assimilation cycle II
-
-
PWY-6964
ammonia assimilation cycle III
-
-
AMMASSIM-PWY
ammonia oxidation II (anaerobic)
-
-
P303-PWY
amygdalin and prunasin degradation
-
-
PWY-6011
anaerobic energy metabolism (invertebrates, cytosol)
-
-
PWY-7383
anaerobic energy metabolism (invertebrates, mitochondrial)
-
-
PWY-7384
anandamide biosynthesis I
-
-
PWY-8051
anandamide biosynthesis II
-
-
PWY-8053
anandamide lipoxygenation
-
-
PWY-8056
anapleurotic synthesis of oxalacetate
-
-
androgen and estrogen metabolism
-
-
androgen biosynthesis
-
-
PWY66-378
androstenedione degradation I (aerobic)
-
-
PWY-6944
androstenedione degradation II (anaerobic)
-
-
PWY-8152
anteiso-branched-chain fatty acid biosynthesis
-
-
PWY-8173
anthocyanin biosynthesis
-
-
PWY-5125
anthocyanin biosynthesis (pelargonidin 3-O-glucoside)
-
-
PWY-7267
apratoxin A biosynthesis
-
-
PWY-8361
arachidonate biosynthesis
-
-
arachidonate biosynthesis I (6-desaturase, lower eukaryotes)
-
-
PWY-5353
arachidonate biosynthesis III (6-desaturase, mammals)
-
-
PWY-7592
arachidonate biosynthesis IV (8-detaturase, lower eukaryotes)
-
-
PWY-7601
arachidonate biosynthesis V (8-detaturase, mammals)
-
-
PWY-7725
arachidonate metabolites biosynthesis
-
-
PWY-8397
Arachidonic acid metabolism
-
-
arachidonic acid metabolism
-
-
Arg/N-end rule pathway (eukaryotic)
-
-
PWY-7799
Arginine and proline metabolism
-
-
Arginine biosynthesis
-
-
arginine dependent acid resistance
-
-
PWY0-1299
aromatic glucosinolate activation
-
-
PWY-6684
aromatic biogenic amine degradation (bacteria)
-
-
PWY-7431
aromatic polyketides biosynthesis
-
-
PWY-6316
arsenate detoxification I
-
-
PWY-8264
arsenate detoxification III
-
-
PWY-8263
arsenic detoxification (plants)
-
-
PWY-8259
arsenic detoxification (yeast)
-
-
PWY-4621
arsenite to oxygen electron transfer
-
-
PWY-4521
arsenite to oxygen electron transfer (via azurin)
-
-
PWY-7429
Ascorbate and aldarate metabolism
-
-
ascorbate glutathione cycle
-
-
PWY-2261
ascorbate recycling (cytosolic)
-
-
PWY-6370
aspartate and asparagine metabolism
-
-
aspirin triggered resolvin D biosynthesis
-
-
PWY66-395
aspirin triggered resolvin E biosynthesis
-
-
PWY66-394
assimilatory sulfate reduction I
-
-
SO4ASSIM-PWY
assimilatory sulfate reduction II
-
-
SULFMETII-PWY
assimilatory sulfate reduction III
-
-
PWY-6683
assimilatory sulfate reduction IV
-
-
PWY1ZNC-1
astaxanthin biosynthesis (bacteria, fungi, algae)
-
-
PWY-5288
ATP biosynthesis
-
-
PWY-7980
atromentin biosynthesis
-
-
PWY-7518
autoinducer AI-1 biosynthesis
-
-
PWY-6157
autoinducer AI-2 biosynthesis I
-
-
PWY-6153
autoinducer AI-2 biosynthesis II (Vibrio)
-
-
PWY-6154
avenacin A-1 biosynthesis
-
-
PWY-7473
avenanthramide biosynthesis
-
-
PWY-8157
bacilysin biosynthesis
-
-
PWY-7626
backdoor pathway of androgen biosynthesis
-
-
PWY-8200
bacterial bioluminescence
-
-
PWY-7723
baicalein degradation (hydrogen peroxide detoxification)
-
-
PWY-7214
benzoate biosynthesis I (CoA-dependent, beta-oxidative)
-
-
PWY-6443
benzoate biosynthesis II (CoA-independent, non-beta-oxidative)
-
-
PWY-6444
benzoate biosynthesis III (CoA-dependent, non-beta-oxidative)
-
-
PWY-6446
Benzoxazinoid biosynthesis
-
-
benzoxazinoid glucosides biosynthesis
-
-
benzoyl-CoA biosynthesis
-
-
PWY-6458
benzoyl-CoA degradation I (aerobic)
-
-
PWY-1361
bergamotene biosynthesis II
-
-
PWY-6244
beta-(1,4)-mannan degradation
-
-
PWY-7456
beta-1,4-D-mannosyl-N-acetyl-D-glucosamine degradation
-
-
PWY-7586
beta-alanine biosynthesis I
-
-
PWY-3981
beta-alanine biosynthesis IV
-
-
PWY-5760
beta-Alanine metabolism
-
-
beta-carboline biosynthesis
-
-
PWY-5877
beta-carotene biosynthesis
-
-
PWY-5943
beta-caryophyllene biosynthesis
-
-
PWY-6275
beta-D-glucuronide and D-glucuronate degradation
-
-
PWY-7247
Betalain biosynthesis
-
-
betalamic acid biosynthesis
-
-
PWY-5394
betanidin degradation
-
-
PWY-5461
betaxanthin biosynthesis
-
-
PWY-5426
betaxanthin biosynthesis (via dopamine)
-
-
PWY-5403
Bifidobacterium shunt
-
-
P124-PWY
bile acid biosynthesis, neutral pathway
Biosynthesis of 12-, 14- and 16-membered macrolides
-
-
Biosynthesis of ansamycins
-
-
Biosynthesis of enediyne antibiotics
-
-
biosynthesis of Lewis epitopes (H. pylori)
-
-
PWY-7833
Biosynthesis of secondary metabolites
-
-
Biosynthesis of siderophore group nonribosomal peptides
-
-
Biosynthesis of unsaturated fatty acids
-
-
Biosynthesis of vancomycin group antibiotics
-
-
Biosynthesis of various secondary metabolites - part 1
-
-
Biosynthesis of various secondary metabolites - part 2
-
-
biotin-carboxyl carrier protein assembly
-
-
PWY0-1264
biphenyl degradation
-
-
PWY5F9-12
bisabolene biosynthesis (engineered)
-
-
PWY-7102
bisbenzylisoquinoline alkaloid biosynthesis
-
-
PWY-5472
Bisphenol degradation
-
-
bisucaberin biosynthesis
-
-
PWY-6381
brassicicene C biosynthesis
-
-
PWY-7517
brassinolide biosynthesis I
-
-
PWY-699
brassinolide biosynthesis II
-
-
PWY-2582
Brassinosteroid biosynthesis
-
-
bryostatin biosynthesis
-
-
PWY-8047
bupropion degradation
-
-
PWY66-241
butachlor degradation
-
-
PWY-7771
butanoate fermentation
-
-
butanol and isobutanol biosynthesis (engineered)
-
-
PWY-7396
C20 prostanoid biosynthesis
-
-
PWY66-374
C25,25 CDP-archaeol biosynthesis
-
-
PWY-8365
C4 and CAM-carbon fixation
-
-
C4 photosynthetic carbon assimilation cycle, NAD-ME type
-
-
PWY-7115
C4 photosynthetic carbon assimilation cycle, NADP-ME type
-
-
PWY-241
C4 photosynthetic carbon assimilation cycle, PEPCK type
-
-
PWY-7117
C5-Branched dibasic acid metabolism
-
-
cadaverine biosynthesis
-
-
PWY0-1601
caffeine degradation III (bacteria, via demethylation)
-
-
PWY-6538
caffeoylglucarate biosynthesis
-
-
PWY-6673
calonectrin biosynthesis
-
-
PWY-7711
Calvin-Benson-Bassham cycle
-
-
CALVIN-PWY
camalexin biosynthesis
-
-
CAMALEXIN-SYN
canavanine biosynthesis
-
-
PWY-5
canavanine degradation
-
-
PWY-31
cannabinoid biosynthesis
-
-
PWY-5140
Caprolactam degradation
-
-
capsaicin biosynthesis
-
-
PWY-5710
capsanthin and capsorubin biosynthesis
-
-
PWY-5174
capsiconiate biosynthesis
-
-
PWY-6027
Carbapenem biosynthesis
-
-
Carbon fixation in photosynthetic organisms
-
-
Carbon fixation pathways in prokaryotes
-
-
cardenolide glucosides biosynthesis
-
-
PWY-6036
cardiolipin biosynthesis
-
-
cardiolipin biosynthesis I
-
-
PWY-5668
cardiolipin biosynthesis II
-
-
PWY-5269
cardiolipin biosynthesis III
-
-
PWY0-1545
carnosate bioynthesis
-
-
PWY-7680
Carotenoid biosynthesis
-
-
carotenoid biosynthesis
-
-
carotenoid cleavage
-
-
PWY-6806
casbene biosynthesis
-
-
PWY-6304
catechol degradation to 2-hydroxypentadienoate I
-
-
P183-PWY
catechol degradation to 2-hydroxypentadienoate II
-
-
PWY-5419
catecholamine biosynthesis
CDP-6-deoxy-D-gulose biosynthesis
-
-
PWY-8139
CDP-diacylglycerol biosynthesis
-
-
CDP-diacylglycerol biosynthesis I
-
-
PWY-5667
CDP-diacylglycerol biosynthesis II
-
-
PWY0-1319
cell-surface glycoconjugate-linked phosphocholine biosynthesis
-
-
PWY-7886
cellulose and hemicellulose degradation (cellulolosome)
-
-
PWY-6784
cellulose biosynthesis
-
-
PWY-1001
cellulose degradation
-
-
cellulose degradation II (fungi)
-
-
PWY-6788
ceramide and sphingolipid recycling and degradation (yeast)
-
-
PWY-7119
ceramide biosynthesis
-
-
ceramide de novo biosynthesis
-
-
PWY3DJ-12
ceramide degradation (generic)
-
-
PWY-6483
ceramide degradation by alpha-oxidation
-
-
PWY66-388
chitin biosynthesis
-
-
PWY-6981
chitin deacetylation
-
-
PWY-7118
chitin degradation I (archaea)
-
-
PWY-6855
chitin degradation II (Vibrio)
-
-
PWY-6902
chitin degradation III (Serratia)
-
-
PWY-7822
chitin derivatives degradation
-
-
PWY-6906
chloramphenicol biosynthesis
-
-
PWY-8032
Chloroalkane and chloroalkene degradation
-
-
chlorobactene biosynthesis
-
-
PWY-7939
Chlorocyclohexane and chlorobenzene degradation
-
-
chlorogenic acid biosynthesis I
-
-
PWY-6039
chlorogenic acid biosynthesis II
-
-
PWY-6040
chlorogenic acid degradation
-
-
PWY-6781
chlorophyll a degradation I
-
-
PWY-5098
chlorophyll a degradation II
-
-
PWY-6927
chlorophyll a degradation III
-
-
PWY-7164
chlorophyll metabolism
-
-
chlorosalicylate degradation
-
-
PWY-6107
chlorpyrifos degradation
-
-
PWY-8065
cholesterol biosynthesis
-
-
cholesterol biosynthesis (algae, late side-chain reductase)
-
-
PWY-8191
cholesterol biosynthesis (diatoms)
-
-
PWY-8239
cholesterol biosynthesis (plants, early side-chain reductase)
-
-
PWY18C3-1
cholesterol biosynthesis I
-
-
PWY66-341
cholesterol biosynthesis II (via 24,25-dihydrolanosterol)
-
-
PWY66-3
cholesterol biosynthesis III (via desmosterol)
-
-
PWY66-4
cholesterol degradation to androstenedione I (cholesterol oxidase)
-
-
PWY-6945
cholesterol degradation to androstenedione II (cholesterol dehydrogenase)
-
-
PWY-6946
cholesterol degradation to androstenedione III (anaerobic)
-
-
PWY-8151
choline biosynthesis III
-
-
PWY-3561
choline degradation I
-
-
CHOLINE-BETAINE-ANA-PWY
choline degradation IV
-
-
PWY-7494
chorismate biosynthesis from 3-dehydroquinate
-
-
PWY-6163
chorismate metabolism
-
-
chrysin biosynthesis
-
-
PWY-5363
chrysoeriol biosynthesis
-
-
PWY-6232
cinnamoyl-CoA biosynthesis
-
-
PWY-6457
cis-abienol biosynthesis
-
-
PWY18C3-13
cis-geranyl-CoA degradation
-
-
PWY-6672
cis-vaccenate biosynthesis
cis-zeatin biosynthesis
-
-
PWY-2781
Citrate cycle (TCA cycle)
-
-
CMP phosphorylation
-
-
PWY-7205
CMP-3-deoxy-D-manno-octulosonate biosynthesis
-
-
PWY-1269
CMP-8-amino-3,8-dideoxy-D-manno-octulosonate biosynthesis
-
-
PWY-7674
CO2 fixation in Crenarchaeota
-
-
CO2 fixation into oxaloacetate (anaplerotic)
-
-
PWYQT-4429
coenzyme B biosynthesis
-
-
P241-PWY
coenzyme M biosynthesis
-
-
coenzyme M biosynthesis II
-
-
PWY-6643
colanic acid building blocks biosynthesis
-
-
COLANSYN-PWY
colupulone and cohumulone biosynthesis
-
-
PWY-5133
complex N-linked glycan biosynthesis (plants)
-
-
PWY-7920
complex N-linked glycan biosynthesis (vertebrates)
-
-
PWY-7426
coumarin biosynthesis (via 2-coumarate)
-
-
PWY-5176
coumarins biosynthesis (engineered)
-
-
PWY-7398
creatine phosphate biosynthesis
-
-
PWY-6158
cremeomycin biosynthesis
-
-
PWY-8296
crepenynate biosynthesis
-
-
PWY-6013
crotonate fermentation (to acetate and cyclohexane carboxylate)
-
-
PWY-7401
crotonyl-CoA/ethylmalonyl-CoA/hydroxybutyryl-CoA cycle (engineered)
-
-
PWY-7854
curacin A biosynthesis
-
-
PWY-8358
curcuminoid biosynthesis
-
-
PWY-6432
cutin biosynthesis
-
-
PWY-321
Cutin, suberine and wax biosynthesis
-
-
cyanide degradation
-
-
P401-PWY
cyanide detoxification I
-
-
ASPSYNII-PWY
Cyanoamino acid metabolism
-
-
cyclic electron flow
-
-
PWY-8270
cyclobis-(1rarr6)-alpha-nigerosyl biosynthesis
-
-
PWY-8317
Cysteine and methionine metabolism
-
-
cytosolic NADPH production (yeast)
-
-
PWY-7268
D-Amino acid metabolism
-
-
D-arabinose degradation V
-
-
PWY-8334
D-galactonate degradation
-
-
GALACTCAT-PWY
D-galactosamine and N-acetyl-D-galactosamine degradation
-
-
PWY-7395
D-galactose degradation I (Leloir pathway)
-
-
PWY-6317
D-galactose degradation IV
-
-
PWY-6693
D-galactose detoxification
-
-
PWY-3821
D-galacturonate degradation II
-
-
PWY-6486
D-galacturonate degradation III
-
-
PWY-8391
D-galacturonate degradation IV
-
-
PWY-6491
D-glucuronate degradation II
-
-
PWY-6501
D-glucuronate degradation III
-
-
PWY-8390
d-mannose degradation
-
-
D-mannose degradation I
-
-
MANNCAT-PWY
D-mannose degradation II
-
-
PWY3O-1743
D-myo-inositol (1,3,4)-trisphosphate biosynthesis
-
-
PWY-6364
D-myo-inositol (1,4,5)-trisphosphate biosynthesis
-
-
PWY-6351
D-myo-inositol (1,4,5)-trisphosphate degradation
-
-
PWY-6363
D-myo-inositol (1,4,5,6)-tetrakisphosphate biosynthesis
-
-
PWY-6366
D-myo-inositol-5-phosphate metabolism
-
-
PWY-6367
D-phenylglycine degradation
-
-
PWY-8161
D-sorbitol biosynthesis I
-
-
PWY-5054
D-sorbitol degradation I
-
-
PWY-4101
D-sorbitol degradation II
-
-
SORBDEG-PWY
D-xylose degradation I
-
-
XYLCAT-PWY
D-xylose degradation IV
-
-
PWY-7294
D-xylose degradation to ethylene glycol (engineered)
-
-
PWY-7178
daphnetin modification
-
-
PWY-7055
degradation of aromatic, nitrogen containing compounds
-
-
degradation of hexoses
-
-
degradation of pentoses
-
-
degradation of sugar acids
-
-
degradation of sugar alcohols
-
-
dehydroabietic acid biosynthesis
-
-
PWY-5421
desferrioxamine B biosynthesis
-
-
PWY-6376
desferrioxamine E biosynthesis
-
-
PWY-6375
detoxification of reactive carbonyls in chloroplasts
-
-
PWY-6786
di-homo-gamma-linolenate metabolites biosynthesis
-
-
PWY-8396
di-myo-inositol phosphate biosynthesis
-
-
PWY-6664
diacylglycerol and triacylglycerol biosynthesis
-
-
TRIGLSYN-PWY
diethylphosphate degradation
-
-
PWY-5491
digitoxigenin biosynthesis
-
-
PWY-6032
DIMBOA-glucoside biosynthesis
-
-
PWY-6950
dimethylsulfoniopropanoate biosynthesis I (Wollastonia)
-
-
PWY-6054
dimethylsulfoniopropanoate biosynthesis II (Spartina)
-
-
PWY-6055
dimethylsulfoniopropanoate degradation I (cleavage)
-
-
PWY-6046
dimorphecolate biosynthesis
-
-
PWY-5368
diphenyl ethers degradation
-
-
PWY-7747
dipicolinate biosynthesis
-
-
PWY-8088
dissimilatory sulfate reduction I (to hydrogen sufide))
-
-
DISSULFRED-PWY
diterpene phytoalexins precursors biosynthesis
Diterpenoid biosynthesis
-
-
divinyl ether biosynthesis I
-
-
PWY-5406
divinyl ether biosynthesis II
-
-
PWY-5409
docosahexaenoate biosynthesis I (lower eukaryotes)
-
-
PWY-7053
docosahexaenoate biosynthesis III (6-desaturase, mammals)
-
-
PWY-7606
docosahexaenoate biosynthesis IV (4-desaturase, mammals)
-
-
PWY-7727
docosahexaenoate metabolites biosynthesis
-
-
PWY-8400
dolabralexins biosynthesis
-
-
PWY-7994
dolichol and dolichyl phosphate biosynthesis
dopamine degradation
-
-
PWY6666-2
drosopterin and aurodrosopterin biosynthesis
-
-
PWY-7442
Drug metabolism - cytochrome P450
-
-
Drug metabolism - other enzymes
-
-
dTDP-beta-L-rhamnose biosynthesis
-
-
DTDPRHAMSYN-PWY
dTMP de novo biosynthesis (mitochondrial)
-
-
PWY66-385
dZTP biosynthesis
-
-
PWY-8289
echinatin biosynthesis
-
-
PWY-6325
ectoine biosynthesis
-
-
P101-PWY
ent-kaurene biosynthesis I
-
-
PWY-5032
enterobactin biosynthesis
Entner Doudoroff pathway
-
-
Entner-Doudoroff pathway I
-
-
PWY-8004
Entner-Doudoroff pathway II (non-phosphorylative)
-
-
NPGLUCAT-PWY
Entner-Doudoroff pathway III (semi-phosphorylative)
-
-
PWY-2221
Entner-Doudoroff shunt
-
-
ENTNER-DOUDOROFF-PWY
ephedrine biosynthesis
-
-
PWY-5883
epoxysqualene biosynthesis
-
-
PWY-5670
ergosterol biosynthesis I
-
-
PWY-6075
ergosterol biosynthesis II
-
-
PWY-7154
ergothioneine biosynthesis I (bacteria)
-
-
PWY-7255
erythritol biosynthesis I
-
-
PWY-8372
erythritol biosynthesis II
-
-
PWY-8373
erythro-tetrahydrobiopterin biosynthesis I
-
-
PWY-5663
erythromycin D biosynthesis
-
-
PWY-7106
Escherichia coli serotype O:127 O antigen biosynthesis
-
-
PWY-8231
Escherichia coli serotype O:1B/Salmonella enterica serotype O:42 O antigen biosynthesis
-
-
PWY-8237
Escherichia coli serotype O:85/Salmonella enterica serotype O:17 O antigen biosynthesis
-
-
PWY-8207
Escherichia coli serotype O:86 O antigen biosynthesis
-
-
PWY-7290
esculetin modification
-
-
PWY-7058
ethanol degradation I
-
-
ETOH-ACETYLCOA-ANA-PWY
ethanol degradation II
-
-
PWY66-21
ethanol degradation III
-
-
PWY66-161
ethanol degradation IV
-
-
PWY66-162
ethanolamine utilization
-
-
PWY0-1477
ethene biosynthesis I (plants)
-
-
ETHYL-PWY
ethene biosynthesis II (microbes)
-
-
PWY-6853
ethene biosynthesis III (microbes)
-
-
PWY-6854
ethene biosynthesis IV (engineered)
-
-
PWY-7126
ethene biosynthesis V (engineered)
-
-
PWY-7124
Ether lipid metabolism
-
-
ethiin metabolism
-
-
PWY-5708
Ethylbenzene degradation
-
-
ethylbenzene degradation (anaerobic)
-
-
PWY-481
ethylmalonyl-CoA pathway
-
-
PWY-5741
eugenol and isoeugenol biosynthesis
-
-
PWY-5859
eumelanin biosynthesis
-
-
PWY-6498
even iso-branched-chain fatty acid biosynthesis
-
-
PWY-8175
extended VTC2 cycle
-
-
PWY4FS-13
farnesene biosynthesis
-
-
PWY-5725
farnesylcysteine salvage pathway
-
-
PWY-6577
fatty acid alpha-oxidation I (plants)
-
-
PWY-2501
fatty acid beta-oxidation I (generic)
-
-
FAO-PWY
fatty acid beta-oxidation II (plant peroxisome)
-
-
PWY-5136
fatty acid beta-oxidation IV (unsaturated, even number)
-
-
PWY-5138
fatty acid beta-oxidation V (unsaturated, odd number, di-isomerase-dependent)
-
-
PWY-6837
fatty acid beta-oxidation VI (mammalian peroxisome)
-
-
PWY66-391
fatty acid beta-oxidation VII (yeast peroxisome)
-
-
PWY-7288
Fatty acid biosynthesis
-
-
fatty acid biosynthesis initiation (mitochondria)
-
-
PWY66-429
fatty acid biosynthesis initiation (plant mitochondria)
-
-
PWY-6799
fatty acid biosynthesis initiation (type I)
-
-
PWY-5966-1
fatty acid biosynthesis initiation (type II)
-
-
PWY-4381
Fatty acid degradation
-
-
Fatty acid elongation
-
-
fatty acid elongation -- saturated
-
-
FASYN-ELONG-PWY
fatty acid salvage
-
-
PWY-7094
Fe(II) oxidation
-
-
PWY-6692
FeMo cofactor biosynthesis
-
-
PWY-7710
ferrichrome A biosynthesis
-
-
PWY-7571
ferulate and sinapate biosynthesis
-
-
PWY-5168
firefly bioluminescence
-
-
PWY-7913
flavin biosynthesis I (bacteria and plants)
-
-
RIBOSYN2-PWY
flavin biosynthesis II (archaea)
-
-
PWY-6167
flavin biosynthesis III (fungi)
-
-
PWY-6168
Flavone and flavonol biosynthesis
-
-
flavonoid biosynthesis
-
-
PWY1F-FLAVSYN
Flavonoid biosynthesis
-
-
flavonoid biosynthesis (in equisetum)
-
-
PWY-6787
flavonoid di-C-glucosylation
-
-
PWY-7897
flavonol acylglucoside biosynthesis I - kaempferol derivatives
-
-
PWY-7168
flavonol acylglucoside biosynthesis III - quercetin derivatives
-
-
PWY-7172
flavonol biosynthesis
-
-
PWY-3101
flexixanthin biosynthesis
-
-
PWY-7947
fluoroacetate degradation
-
-
PWY-6646
folate transformations I
-
-
PWY-2201
folate transformations II (plants)
-
-
PWY-3841
folate transformations III (E. coli)
-
-
1CMET2-PWY
formaldehyde assimilation I (serine pathway)
-
-
PWY-1622
formaldehyde assimilation II (assimilatory RuMP Cycle)
-
-
PWY-1861
formaldehyde assimilation III (dihydroxyacetone cycle)
-
-
P185-PWY
formaldehyde oxidation
-
-
formaldehyde oxidation I
-
-
RUMP-PWY
formaldehyde oxidation II (glutathione-dependent)
-
-
PWY-1801
formaldehyde oxidation VII (THF pathway)
-
-
PWY-7909
formate assimilation into 5,10-methylenetetrahydrofolate
-
-
PWY-1722
formate oxidation to CO2
-
-
PWY-1881
formate to nitrite electron transfer
-
-
PWY0-1585
free phenylpropanoid acid biosynthesis
-
-
PWY-2181
fructan biosynthesis
-
-
PWY-822
fructan degradation
-
-
PWY-862
fructose 2,6-bisphosphate biosynthesis
-
-
PWY66-423
Fructose and mannose metabolism
-
-
furaneol and mesifurane biosynthesis
-
-
PWY-5975
fusicoccin A biosynthesis
-
-
PWY-6659
GABA shunt I
-
-
GLUDEG-I-PWY
GABA shunt II
-
-
PWY-8346
galactolipid biosynthesis I
-
-
PWY-401
gallate biosynthesis
-
-
PWY-6707
gallate degradation III (anaerobic)
-
-
P3-PWY
gamma-glutamyl cycle
-
-
PWY-4041
gamma-linolenate biosynthesis II (animals)
-
-
PWY-6000
ganglio-series glycosphingolipids biosynthesis
-
-
PWY-7836
GDP-alpha-D-glucose biosynthesis
-
-
PWY-5661
GDP-L-galactose biosynthesis
-
-
PWY-5115
GDP-mannose biosynthesis
-
-
PWY-5659
gentisate degradation I
-
-
PWY-6223
geraniol and geranial biosynthesis
-
-
PWY-5829
geranyl acetate biosynthesis
-
-
PWY-5835
geranyl diphosphate biosynthesis
-
-
PWY-5122
geranylgeranyl diphosphate biosynthesis
-
-
PWY-5120
germacrene biosynthesis
-
-
PWY-5733
gibberellin biosynthesis III (early C-13 hydroxylation)
-
-
PWY-5035
gibberellin inactivation I (2beta-hydroxylation)
-
-
PWY-102
gibberellin inactivation II (methylation)
-
-
PWY-6477
ginsenoside metabolism
-
-
ginsenosides biosynthesis
-
-
PWY-5672
gliotoxin biosynthesis
-
-
PWY-7533
globo-series glycosphingolipids biosynthesis
-
-
PWY-7838
gluconeogenesis I
-
-
GLUCONEO-PWY
gluconeogenesis II (Methanobacterium thermoautotrophicum)
-
-
PWY-6142
gluconeogenesis III
-
-
PWY66-399
glucose and glucose-1-phosphate degradation
-
-
GLUCOSE1PMETAB-PWY
glucose degradation (oxidative)
-
-
DHGLUCONATE-PYR-CAT-PWY
glucosinolate activation
-
-
PWY-5267
Glucosinolate biosynthesis
-
-
glucosinolate biosynthesis from dihomomethionine
-
-
PWYQT-4471
glucosinolate biosynthesis from hexahomomethionine
-
-
PWYQT-4475
glucosinolate biosynthesis from homomethionine
-
-
PWY-1187
glucosinolate biosynthesis from pentahomomethionine
-
-
PWYQT-4474
glucosinolate biosynthesis from phenylalanine
-
-
PWY-2821
glucosinolate biosynthesis from tetrahomomethionine
-
-
PWYQT-4473
glucosinolate biosynthesis from trihomomethionine
-
-
PWYQT-4472
glucosinolate biosynthesis from tryptophan
-
-
PWY-601
glucosinolate biosynthesis from tyrosine
-
-
PWY-7901
glucosylglycerol biosynthesis
-
-
PWY-7902
glutamate and glutamine metabolism
-
-
glutamate removal from folates
-
-
PWY-2161B
glutaminyl-tRNAgln biosynthesis via transamidation
-
-
PWY-5921
glutaryl-CoA degradation
-
-
PWY-5177
glutathione biosynthesis
-
-
GLUTATHIONESYN-PWY
Glutathione metabolism
-
-
glutathione metabolism
-
-
glutathione-mediated detoxification I
-
-
PWY-4061
glutathione-mediated detoxification II
-
-
PWY-6842
glutathione-peroxide redox reactions
-
-
PWY-4081
glycerol degradation I
-
-
PWY-4261
glycerol degradation to butanol
-
-
PWY-7003
glycerol-3-phosphate to fumarate electron transfer
-
-
PWY0-1582
Glycerolipid metabolism
-
-
Glycerophospholipid metabolism
-
-
glycine betaine biosynthesis
-
-
glycine betaine biosynthesis I (Gram-negative bacteria)
-
-
BETSYN-PWY
glycine betaine biosynthesis II (Gram-positive bacteria)
-
-
PWY-3722
glycine betaine biosynthesis III (plants)
-
-
PWY1F-353
glycine betaine degradation I
-
-
PWY-3661
glycine betaine degradation II (mammalian)
-
-
PWY-3661-1
glycine betaine degradation III
-
-
PWY-8325
glycine biosynthesis I
-
-
GLYSYN-PWY
glycine biosynthesis II
-
-
GLYCINE-SYN2-PWY
glycine cleavage
-
-
GLYCLEAV-PWY
glycine degradation (reductive Stickland reaction)
-
-
PWY-8015
Glycine, serine and threonine metabolism
-
-
glycogen biosynthesis
-
-
glycogen biosynthesis I (from ADP-D-Glucose)
-
-
GLYCOGENSYNTH-PWY
glycogen biosynthesis II (from UDP-D-Glucose)
-
-
PWY-5067
glycogen biosynthesis III (from alpha-maltose 1-phosphate)
-
-
PWY-7900
glycogen degradation I
-
-
GLYCOCAT-PWY
glycogen degradation II
-
-
PWY-5941
glycolate and glyoxylate degradation II
-
-
GLYOXDEG-PWY
glycolipid desaturation
-
-
PWY-782
Glycolysis / Gluconeogenesis
-
-
glycolysis I (from glucose 6-phosphate)
-
-
GLYCOLYSIS
glycolysis II (from fructose 6-phosphate)
-
-
PWY-5484
glycolysis III (from glucose)
-
-
ANAGLYCOLYSIS-PWY
glycolysis IV
-
-
PWY-1042
glycolysis V (Pyrococcus)
-
-
P341-PWY
Glycosaminoglycan biosynthesis - chondroitin sulfate / dermatan sulfate
-
-
Glycosaminoglycan biosynthesis - heparan sulfate / heparin
-
-
Glycosaminoglycan biosynthesis - keratan sulfate
-
-
Glycosaminoglycan degradation
-
-
glycosaminoglycan-protein linkage region biosynthesis
-
-
PWY-6557
Glycosphingolipid biosynthesis - ganglio series
-
-
Glycosphingolipid biosynthesis - globo and isoglobo series
-
-
Glycosphingolipid biosynthesis - lacto and neolacto series
-
-
glycyrrhetinate biosynthesis
-
-
PWY-7066
Glyoxylate and dicarboxylate metabolism
-
-
glyoxylate assimilation
-
-
PWY-5744
glyoxylate cycle
-
-
GLYOXYLATE-BYPASS
glyphosate degradation I
-
-
PWY-7804
glyphosate degradation III
-
-
PWY-7807
gondoate biosynthesis (anaerobic)
-
-
PWY-7663
gossypol biosynthesis
-
-
PWY-5773
grixazone biosynthesis
-
-
PWY-7153
guaiacol biosynthesis
-
-
PWY18C3-23
guanosine deoxyribonucleotides de novo biosynthesis I
-
-
PWY-7226
guanosine deoxyribonucleotides de novo biosynthesis II
-
-
PWY-7222
guanosine nucleotides degradation I
-
-
PWY-6607
guanosine nucleotides degradation II
-
-
PWY-6606
guanosine nucleotides degradation III
-
-
PWY-6608
guanosine ribonucleotides de novo biosynthesis
-
-
PWY-7221
H. pylori 26695 O-antigen biosynthesis
-
-
PWY2DNV-5
heme b biosynthesis I (aerobic)
-
-
HEME-BIOSYNTHESIS-II
heme b biosynthesis II (oxygen-independent)
-
-
HEMESYN2-PWY
heme b biosynthesis V (aerobic)
-
-
HEME-BIOSYNTHESIS-II-1
heme degradation I
-
-
PWY-5874
heparin degradation
-
-
PWY-7644
heterolactic fermentation
-
-
P122-PWY
histamine biosynthesis
-
-
PWY-6173
histamine degradation
-
-
PWY-6181
homocysteine and cysteine interconversion
-
-
PWY-801
homofuraneol biosynthesis
-
-
PWY-7910
homoglutathione biosynthesis
-
-
PWY-6840
homospermidine biosynthesis I
-
-
PWY-5907
homospermidine biosynthesis II
-
-
PWY-8149
hydrogen sulfide biosynthesis II (mammalian)
-
-
PWY66-426
hydrogen to fumarate electron transfer
-
-
PWY0-1576
hydroxycinnamic acid serotonin amides biosynthesis
-
-
PWY-5473
hydroxycinnamic acid tyramine amides biosynthesis
-
-
PWY-5474
hydroxylated fatty acid biosynthesis (plants)
-
-
PWY-6433
hypoglycin biosynthesis
-
-
PWY-5826
hypotaurine degradation
-
-
PWY-7387
i antigen and I antigen biosynthesis
-
-
PWY-7837
icosapentaenoate biosynthesis I (lower eukaryotes)
-
-
PWY-6958
icosapentaenoate biosynthesis II (6-desaturase, mammals)
-
-
PWY-7049
icosapentaenoate biosynthesis III (8-desaturase, mammals)
-
-
PWY-7724
icosapentaenoate biosynthesis V (8-desaturase, lower eukaryotes)
-
-
PWY-7602
icosapentaenoate biosynthesis VI (fungi)
-
-
PWY-6940
icosapentaenoate metabolites biosynthesis
-
-
PWY-8399
incomplete reductive TCA cycle
-
-
P42-PWY
Indole alkaloid biosynthesis
-
-
indole glucosinolate activation (herbivore attack)
-
-
PWYQT-4476
indole glucosinolate activation (intact plant cell)
-
-
PWYQT-4477
indole-3-acetate biosynthesis I
-
-
PWYDQC-4
indole-3-acetate biosynthesis II
-
-
PWY-581
indole-3-acetate biosynthesis III (bacteria)
-
-
PWY-3161
indole-3-acetate biosynthesis IV (bacteria)
-
-
PWY-5025
indole-3-acetate biosynthesis V (bacteria and fungi)
-
-
PWY-5026
indole-3-acetate biosynthesis VI (bacteria)
-
-
TRPIAACAT-PWY
indole-3-acetate degradation II
-
-
PWY-8087
inosine 5'-phosphate degradation
-
-
PWY-5695
Inositol phosphate metabolism
-
-
Insect hormone biosynthesis
-
-
inulin degradation
-
-
PWY-8314
ipsdienol biosynthesis
-
-
PWY-7410
iron reduction and absorption
-
-
PWY-5934
Isoflavonoid biosynthesis
-
-
isoflavonoid biosynthesis I
-
-
PWY-2002
isoflavonoid biosynthesis II
-
-
PWY-2083
isoleucine metabolism
-
-
isopimaric acid biosynthesis
-
-
PWY-5422
isoprene biosynthesis I
-
-
PWY-6270
isoprene biosynthesis II (engineered)
-
-
PWY-7391
isoprenoid biosynthesis
-
-
isopropanol biosynthesis (engineered)
-
-
PWY-6876
Isoquinoline alkaloid biosynthesis
-
-
isorenieratene biosynthesis I (actinobacteria)
-
-
PWY-7938
itaconate degradation
-
-
PWY-5749
jadomycin biosynthesis
-
-
PWY-6679
jasmonic acid biosynthesis
-
-
PWY-735
jasmonoyl-amino acid conjugates biosynthesis I
-
-
PWY-6220
jasmonoyl-amino acid conjugates biosynthesis II
-
-
PWY-6233
juniperonate biosynthesis
-
-
PWY-7619
justicidin B biosynthesis
-
-
PWY-6824
juvenile hormone III biosynthesis I
-
-
PWY-6575
juvenile hormone III biosynthesis II
-
-
PWY-6650
kaempferol diglycoside biosynthesis (pollen-specific)
-
-
PWY-7191
kaempferol gentiobioside biosynthesis
-
-
PWY-7143
kaempferol glycoside biosynthesis (Arabidopsis)
-
-
PWY-5320
kaempferol triglucoside biosynthesis
-
-
PWY-5348
kauralexin biosynthesis
-
-
PWY-6887
ketogenesis
-
-
PWY66-367
L-alanine biosynthesis I
-
-
ALANINE-VALINESYN-PWY
L-alanine biosynthesis II
-
-
ALANINE-SYN2-PWY
L-alanine degradation II (to D-lactate)
-
-
ALACAT2-PWY
L-alanine degradation III
-
-
ALANINE-DEG3-PWY
L-alanine degradation IV
-
-
PWY1-2
L-alanine degradation V (oxidative Stickland reaction)
-
-
PWY-8189
L-alanine degradation VI (reductive Stickland reaction)
-
-
PWY-8188
L-arabinose degradation II
-
-
PWY-5515
L-arabinose degradation IV
-
-
PWY-7295
L-arginine biosynthesis I (via L-ornithine)
-
-
ARGSYN-PWY
L-arginine biosynthesis II (acetyl cycle)
-
-
ARGSYNBSUB-PWY
L-arginine biosynthesis III (via N-acetyl-L-citrulline)
-
-
PWY-5154
L-arginine biosynthesis IV (archaea)
-
-
PWY-7400
L-arginine degradation I (arginase pathway)
-
-
ARGASEDEG-PWY
L-arginine degradation II (AST pathway)
-
-
AST-PWY
L-arginine degradation III (arginine decarboxylase/agmatinase pathway)
-
-
PWY0-823
L-arginine degradation IV (arginine decarboxylase/agmatine deiminase pathway)
-
-
ARGDEG-III-PWY
L-arginine degradation V (arginine deiminase pathway)
-
-
ARGDEGRAD-PWY
L-arginine degradation VI (arginase 2 pathway)
-
-
ARG-PRO-PWY
L-arginine degradation VII (arginase 3 pathway)
-
-
ARG-GLU-PWY
L-arginine degradation X (arginine monooxygenase pathway)
-
-
ARGDEG-V-PWY
L-arginine degradation XIII (reductive Stickland reaction)
-
-
PWY-8187
L-arginine degradation XIV (oxidative Stickland reaction)
-
-
PWY-6344
L-ascorbate biosynthesis I (plants, L-galactose pathway)
-
-
PWY-882
L-ascorbate biosynthesis II (plants, L-gulose pathway)
-
-
PWY4FS-11
L-ascorbate biosynthesis IV (animals, D-glucuronate pathway)
-
-
PWY3DJ-35471
L-ascorbate biosynthesis V (euglena, D-galacturonate pathway)
-
-
PWY-6415
L-ascorbate biosynthesis VI (plants, myo-inositol pathway)
-
-
PWY-8142
L-ascorbate biosynthesis VII (plants, D-galacturonate pathway)
-
-
PWY-8143
L-ascorbate biosynthesis VIII (engineered pathway)
-
-
PWY-7165
L-ascorbate degradation II (bacterial, aerobic)
-
-
PWY-6961
L-ascorbate degradation III
-
-
PWY-6960
L-asparagine biosynthesis I
-
-
ASPARAGINE-BIOSYNTHESIS
L-asparagine biosynthesis II
-
-
ASPARAGINESYN-PWY
L-asparagine biosynthesis III (tRNA-dependent)
-
-
PWY490-4
L-asparagine degradation I
-
-
ASPARAGINE-DEG1-PWY
L-asparagine degradation II
-
-
PWY-4002
L-asparagine degradation III (mammalian)
-
-
ASPARAGINE-DEG1-PWY-1
L-aspartate biosynthesis
-
-
ASPARTATESYN-PWY
L-aspartate degradation I
-
-
ASPARTATE-DEG1-PWY
L-aspartate degradation II (aerobic)
-
-
PWY-8291
L-aspartate degradation III (anaerobic)
-
-
PWY-8294
L-carnitine degradation II
-
-
PWY-3641
L-citrulline biosynthesis
-
-
CITRULBIO-PWY
L-citrulline degradation
-
-
CITRULLINE-DEG-PWY
L-cysteine biosynthesis I
-
-
CYSTSYN-PWY
L-cysteine biosynthesis III (from L-homocysteine)
-
-
HOMOCYSDEGR-PWY
L-cysteine biosynthesis IX (Trichomonas vaginalis)
-
-
PWY-8010
L-cysteine biosynthesis VI (reverse transsulfuration)
-
-
PWY-I9
L-dopa and L-dopachrome biosynthesis
-
-
PWY-6481
L-dopa degradation I (mammalian)
-
-
PWY-6334
L-dopa degradation II (bacterial)
-
-
PWY-8110
L-glutamate biosynthesis I
-
-
GLUTSYN-PWY
L-glutamate biosynthesis II
-
-
GLUTAMATE-SYN2-PWY
L-glutamate biosynthesis IV
-
-
GLUGLNSYN-PWY
L-glutamate biosynthesis V
-
-
PWY-4341
L-glutamate degradation I
-
-
GLUTAMATE-DEG1-PWY
L-glutamate degradation II
-
-
GLUTDEG-PWY
L-glutamate degradation IX (via 4-aminobutanoate)
-
-
PWY0-1305
L-glutamate degradation V (via hydroxyglutarate)
-
-
P162-PWY
L-glutamate degradation VI (to pyruvate)
-
-
PWY-5087
L-glutamate degradation X
-
-
PWY-5766
L-glutamate degradation XI (reductive Stickland reaction)
-
-
PWY-8190
L-glutamine biosynthesis I
-
-
GLNSYN-PWY
L-glutamine degradation I
-
-
GLUTAMINDEG-PWY
L-glutamine degradation II
-
-
GLUTAMINEFUM-PWY
L-histidine degradation I
-
-
HISDEG-PWY
L-histidine degradation II
-
-
PWY-5028
L-histidine degradation III
-
-
PWY-5030
L-histidine degradation V
-
-
PWY-5031
L-histidine degradation VI
-
-
HISHP-PWY
L-homocysteine biosynthesis
-
-
PWY-5344
L-homoserine biosynthesis
-
-
HOMOSERSYN-PWY
L-isoleucine biosynthesis I (from threonine)
-
-
ILEUSYN-PWY
L-isoleucine biosynthesis II
-
-
PWY-5101
L-isoleucine biosynthesis III
-
-
PWY-5103
L-isoleucine biosynthesis IV
-
-
PWY-5104
L-isoleucine biosynthesis V
-
-
PWY-5108
L-isoleucine degradation I
-
-
ILEUDEG-PWY
L-isoleucine degradation II
-
-
PWY-5078
L-isoleucine degradation III (oxidative Stickland reaction)
-
-
PWY-8184
L-lactaldehyde degradation
-
-
L-leucine biosynthesis
-
-
LEUSYN-PWY
L-leucine degradation I
-
-
LEU-DEG2-PWY
L-leucine degradation III
-
-
PWY-5076
L-leucine degradation IV (reductive Stickland reaction)
-
-
PWY-7767
L-leucine degradation V (oxidative Stickland reaction)
-
-
PWY-8185
L-lysine biosynthesis I
-
-
DAPLYSINESYN-PWY
L-lysine biosynthesis II
-
-
PWY-2941
L-lysine biosynthesis III
-
-
PWY-2942
L-lysine biosynthesis IV
-
-
LYSINE-AMINOAD-PWY
L-lysine biosynthesis V
-
-
PWY-3081
L-lysine biosynthesis VI
-
-
PWY-5097
L-lysine degradation I
-
-
PWY0-461
L-lysine degradation X
-
-
PWY-6328
L-lysine degradation XI
-
-
LYSINE-DEG1-PWY
L-lysine fermentation to acetate and butanoate
-
-
P163-PWY
L-malate degradation II
-
-
PWY-7686
L-methionine biosynthesis I
-
-
HOMOSER-METSYN-PWY
L-methionine biosynthesis II
-
-
PWY-702
L-methionine biosynthesis III
-
-
HSERMETANA-PWY
L-methionine biosynthesis IV
-
-
PWY-7977
L-methionine degradation I (to L-homocysteine)
-
-
METHIONINE-DEG1-PWY
L-methionine degradation III
-
-
PWY-5082
L-methionine salvage cycle II (plants)
-
-
PWY-7270
L-methionine salvage from L-homocysteine
-
-
ADENOSYLHOMOCYSCAT-PWY
L-Ndelta-acetylornithine biosynthesis
-
-
PWY-6922
L-nicotianamine biosynthesis
-
-
PWY-5957
L-ornithine biosynthesis I
-
-
GLUTORN-PWY
L-ornithine biosynthesis II
-
-
ARGININE-SYN4-PWY
L-ornithine degradation I (L-proline biosynthesis)
-
-
ORN-AMINOPENTANOATE-CAT-PWY
L-phenylalanine biosynthesis I
-
-
PHESYN
L-phenylalanine biosynthesis II
-
-
PWY-3462
L-phenylalanine degradation II (anaerobic)
-
-
ANAPHENOXI-PWY
L-phenylalanine degradation III
-
-
PWY-5079
L-phenylalanine degradation IV (mammalian, via side chain)
-
-
PWY-6318
L-phenylalanine degradation VI (reductive Stickland reaction)
-
-
PWY-8014
L-proline biosynthesis I (from L-glutamate)
-
-
PROSYN-PWY
L-proline biosynthesis II (from arginine)
-
-
PWY-4981
L-proline biosynthesis III (from L-ornithine)
-
-
PWY-3341
L-proline degradation I
-
-
PROUT-PWY
L-selenocysteine biosynthesis I (bacteria)
-
-
PWY0-901
L-selenocysteine biosynthesis II (archaea and eukaryotes)
-
-
PWY-6281
L-serine biosynthesis I
-
-
SERSYN-PWY
L-serine biosynthesis II
-
-
PWY-8011
L-sorbose degradation
-
-
P302-PWY
L-threonine biosynthesis
-
-
HOMOSER-THRESYN-PWY
L-threonine degradation I
-
-
PWY-5437
L-threonine degradation III (to methylglyoxal)
-
-
THRDLCTCAT-PWY
L-threonine degradation V
-
-
PWY66-428
L-tryptophan biosynthesis
-
-
TRPSYN-PWY
L-tryptophan degradation I (via anthranilate)
-
-
TRPCAT-PWY
L-tryptophan degradation IV (via indole-3-lactate)
-
-
TRPKYNCAT-PWY
L-tryptophan degradation to 2-amino-3-carboxymuconate semialdehyde
-
-
PWY-5651
L-tryptophan degradation V (side chain pathway)
-
-
PWY-3162
L-tryptophan degradation VI (via tryptamine)
-
-
PWY-3181
L-tryptophan degradation VIII (to tryptophol)
-
-
PWY-5081
L-tryptophan degradation X (mammalian, via tryptamine)
-
-
PWY-6307
L-tryptophan degradation XI (mammalian, via kynurenine)
-
-
PWY-6309
L-tryptophan degradation XIII (reductive Stickland reaction)
-
-
PWY-8017
L-tyrosine biosynthesis I
-
-
TYRSYN
L-tyrosine biosynthesis II
-
-
PWY-3461
L-tyrosine biosynthesis III
-
-
PWY-6120
L-tyrosine degradation I
-
-
TYRFUMCAT-PWY
L-tyrosine degradation II
-
-
PWY-5151
L-tyrosine degradation III
-
-
PWY3O-4108
L-tyrosine degradation IV (to 4-methylphenol)
-
-
PWY-7514
L-tyrosine degradation V (reductive Stickland reaction)
-
-
PWY-8016
L-valine biosynthesis
-
-
VALSYN-PWY
L-valine degradation I
-
-
VALDEG-PWY
L-valine degradation II
-
-
PWY-5057
L-valine degradation III (oxidative Stickland reaction)
-
-
PWY-8183
labdane-type diterpenes biosynthesis
-
-
PWY-6645
lacinilene C biosynthesis
-
-
PWY-5828
lactate fermentation to acetate, CO2 and hydrogen (Desulfovibrionales)
-
-
PWY-8377
lacto-series glycosphingolipids biosynthesis
-
-
PWY-7839
lactucaxanthin biosynthesis
-
-
PWY-5175
lanosterol biosynthesis
-
-
PWY-6132
leucodelphinidin biosynthesis
-
-
PWY-5152
leucopelargonidin and leucocyanidin biosynthesis
-
-
PWY1F-823
leukotriene biosynthesis
-
-
PWY66-375
levopimaric acid biosynthesis
-
-
PWY-5412
Limonene and pinene degradation
-
-
limonene degradation IV (anaerobic)
-
-
PWY-8029
linalool biosynthesis I
-
-
PWY-7182
linamarin degradation
-
-
PWY-3121
linoleate biosynthesis I (plants)
-
-
PWY-5995
linoleate biosynthesis II (animals)
-
-
PWY-6001
linoleate metabolites biosynthesis
-
-
PWY-8395
Linoleic acid metabolism
-
-
linustatin bioactivation
-
-
PWY-7091
lipid A-core biosynthesis (E. coli K-12)
-
-
LIPA-CORESYN-PWY
lipid A-core biosynthesis (Salmonella)
-
-
PWY1R65-1
lipid IVA biosynthesis (2,3-diamino-2,3-dideoxy-D-glucopyranose-containing)
-
-
PWY2B4Q-4
lipid IVA biosynthesis (E. coli)
-
-
NAGLIPASYN-PWY
lipid IVA biosynthesis (generic)
-
-
PWY-8283
lipid IVA biosynthesis (H. pylori)
-
-
PWYI-14
lipid IVA biosynthesis (P. gingivalis)
-
-
PWY-8245
lipid IVA biosynthesis (P. putida)
-
-
PWY-8073
lipid IVA biosynthesis (Vibrio cholerae serogroup O1 El Tor)
-
-
PWY2G6Z-2
lipoate biosynthesis and incorporation I
-
-
PWY0-501
lipoate biosynthesis and incorporation II
-
-
PWY0-1275
lipoate biosynthesis and incorporation III (Bacillus)
-
-
PWY-6987
lipoate biosynthesis and incorporation IV (yeast)
-
-
PWY-7382
lipoate biosynthesis and incorporation V (mammals)
-
-
PWY0-501-1
Lipoic acid metabolism
-
-
Lipopolysaccharide biosynthesis
-
-
lipoxin biosynthesis
-
-
PWY66-392
long chain fatty acid ester synthesis (engineered)
-
-
PWY-6873
long-chain fatty acid activation
-
-
PWY-5143
lotaustralin degradation
-
-
PWY-6002
lupanine biosynthesis
-
-
PWY-5468
lupulone and humulone biosynthesis
-
-
PWY-5132
lutein biosynthesis
-
-
PWY-5947
luteolin biosynthesis
-
-
PWY-5060
luteolin triglucuronide degradation
-
-
PWY-7445
lychnose and isolychnose biosynthesis
-
-
PWY-6524
macrolide antibiotic biosynthesis
-
-
malate/L-aspartate shuttle pathway
-
-
MALATE-ASPARTATE-SHUTTLE-PWY
mandelate degradation I
-
-
PWY-1501
manganese oxidation I
-
-
PWY-6591
mangrove triterpenoid biosynthesis
-
-
PWY-6109
mannitol biosynthesis
-
-
PWY-3881
mannitol cycle
-
-
PWY-6531
mannitol degradation I
-
-
MANNIDEG-PWY
mannitol degradation II
-
-
PWY-3861
maresin biosynthesis
-
-
PWY-8356
matairesinol biosynthesis
-
-
PWY-5466
melatonin degradation I
-
-
PWY-6398
melatonin degradation II
-
-
PWY-6399
melibiose degradation
-
-
PWY0-1301
menaquinol-4 biosynthesis II
-
-
PWY-7998
metabolism of amino sugars and derivatives
-
-
metabolism of disaccharids
-
-
Metabolism of xenobiotics by cytochrome P450
-
-
Methanobacterium thermoautotrophicum biosynthetic metabolism
-
-
PWY-6146
methanofuran biosynthesis
-
-
PWY-5254
methanogenesis from acetate
-
-
METH-ACETATE-PWY
methanol oxidation to formaldehyde IV
-
-
PWY-5506
methiin metabolism
-
-
PWY-7614
methionine metabolism
-
-
methyl indole-3-acetate interconversion
-
-
PWY-6303
methyl ketone biosynthesis (engineered)
-
-
PWY-7007
methyl parathion degradation
-
-
PWY-5489
methyl phomopsenoate biosynthesis
-
-
PWY-7721
methyl tert-butyl ether degradation
-
-
PWY-7779
methylerythritol phosphate pathway I
-
-
NONMEVIPP-PWY
methylerythritol phosphate pathway II
-
-
PWY-7560
methylglyoxal degradation
-
-
methylglyoxal degradation I
-
-
PWY-5386
methylglyoxal degradation III
-
-
PWY-5453
methylglyoxal degradation VIII
-
-
PWY-5386-1
methylquercetin biosynthesis
-
-
PWY-6064
methylsalicylate biosynthesis
-
-
PWY18C3-22
methylsalicylate degradation
-
-
PWY-6184, PWY18C3-24
mevalonate degradation
-
-
PWY-5074
mevalonate metabolism
-
-
mevalonate pathway I (eukaryotes and bacteria)
-
-
PWY-922
mevalonate pathway II (haloarchaea)
-
-
PWY-6174
mevalonate pathway III (Thermoplasma)
-
-
PWY-7524
mevalonate pathway IV (archaea)
-
-
PWY-8125
Microbial metabolism in diverse environments
-
-
mitochondrial L-carnitine shuttle
-
-
PWY-6111
mitochondrial NADPH production (yeast)
-
-
PWY-7269
mixed acid fermentation
-
-
FERMENTATION-PWY
molybdenum cofactor biosynthesis
-
-
molybdenum cofactor sulfulylation (eukaryotes)
-
-
PWY-5963
momilactone A biosynthesis
-
-
PWY-7477
mono-trans, poly-cis decaprenyl phosphate biosynthesis
-
-
PWY-6383
Monobactam biosynthesis
-
-
Monoterpenoid biosynthesis
-
-
mRNA capping I
-
-
PWY-7375
mRNA capping II
-
-
PWY-7379
mucin core 1 and core 2 O-glycosylation
-
-
PWY-7433
mucin core 3 and core 4 O-glycosylation
-
-
PWY-7435
Mucin type O-glycan biosynthesis
-
-
mupirocin biosynthesis
-
-
PWY-8012
mycobacterial sulfolipid biosynthesis
-
-
PWY-7746
mycobactin biosynthesis
-
-
PWY185E-1
mycolate biosynthesis
-
-
PWYG-321
mycolyl-arabinogalactan-peptidoglycan complex biosynthesis
-
-
PWY-6397
mycothiol biosynthesis
-
-
PWY1G-0
myo-inositol biosynthesis
myricetin gentiobioside biosynthesis
-
-
PWY-7140
myxol-2' fucoside biosynthesis
-
-
PWY-6279
N-acetyl-D-galactosamine degradation
-
-
PWY-7077
N-acetylglucosamine degradation I
-
-
GLUAMCAT-PWY
N-Glycan biosynthesis
-
-
NAD biosynthesis from 2-amino-3-carboxymuconate semialdehyde
-
-
PWY-5653
NAD biosynthesis from nicotinamide
-
-
NAD-BIOSYNTHESIS-III
NAD de novo biosynthesis I
-
-
PYRIDNUCSYN-PWY
NAD de novo biosynthesis III
-
-
PWY-8352
NAD de novo biosynthesis IV (anaerobic)
-
-
PWY-8277
NAD phosphorylation and dephosphorylation
-
-
NADPHOS-DEPHOS-PWY
NAD phosphorylation and transhydrogenation
-
-
NADPHOS-DEPHOS-PWY-1
NAD salvage (plants)
-
-
PWY-5381
NAD salvage pathway I (PNC VI cycle)
-
-
PYRIDNUCSAL-PWY
NAD salvage pathway II (PNC IV cycle)
-
-
PWY-7761
NAD salvage pathway III (to nicotinamide riboside)
-
-
NAD-BIOSYNTHESIS-II
NAD salvage pathway V (PNC V cycle)
-
-
PWY3O-4107
NAD(P)/NADPH interconversion
-
-
PWY-5083
NADH to cytochrome bd oxidase electron transfer I
-
-
PWY0-1334
NADH to cytochrome bd oxidase electron transfer II
-
-
PWY0-1568
NADH to cytochrome bo oxidase electron transfer I
-
-
PWY0-1335
NADH to cytochrome bo oxidase electron transfer II
-
-
PWY0-1567
NADH to fumarate electron transfer
-
-
PWY0-1336
NADP biosynthesis
-
-
PWY-8148
NADPH to cytochrome c oxidase via plastocyanin
-
-
PWY-8271
Naphthalene degradation
-
-
naringenin biosynthesis (engineered)
-
-
PWY-7397
neoabietic acid biosynthesis
-
-
PWY-5413
neolacto-series glycosphingolipids biosynthesis
-
-
PWY-7841
neolinustatin bioactivation
-
-
PWY-7092
Neomycin, kanamycin and gentamicin biosynthesis
-
-
neoxanthin biosynthesis
-
-
PWY-6809
nepetalactone biosynthesis
-
-
PWY-8069
nerol biosynthesis
-
-
PWY-8177
neurosporaxanthin biosynthesis
-
-
PWY-6681
Nicotinate and nicotinamide metabolism
-
-
nicotine biosynthesis
-
-
PWY-5316
nicotine degradation I (pyridine pathway)
-
-
P181-PWY
nicotine degradation IV
-
-
PWY66-201
nicotine degradation V
-
-
PWY66-221
nitrate reduction I (denitrification)
-
-
DENITRIFICATION-PWY
nitrate reduction II (assimilatory)
-
-
PWY-381
nitrate reduction V (assimilatory)
-
-
PWY-5675
nitrate reduction VI (assimilatory)
-
-
PWY490-3
nitrate reduction VII (denitrification)
-
-
PWY-6748
nitrate reduction VIIIb (dissimilatory)
-
-
PWY0-1573
nitrate reduction X (dissimilatory, periplasmic)
-
-
PWY0-1584
nitric oxide biosynthesis II (mammals)
-
-
PWY-4983
nitrifier denitrification
-
-
PWY-7084
nitrite-dependent anaerobic methane oxidation
-
-
PWY-6523
nitrogen fixation I (ferredoxin)
-
-
N2FIX-PWY
nitrogen remobilization from senescing leaves
-
-
PWY-6549
Nitrotoluene degradation
-
-
nocardicin A biosynthesis
-
-
PWY-7797
nonaprenyl diphosphate biosynthesis II
-
-
PWY-6520
noradrenaline and adrenaline degradation
-
-
PWY-6342
norspermidine biosynthesis
-
-
PWY-6562
Novobiocin biosynthesis
-
-
nucleoside and nucleotide degradation (archaea)
-
-
PWY-5532
O-antigen biosynthesis
-
-
O-Antigen nucleotide sugar biosynthesis
-
-
o-diquinones biosynthesis
-
-
PWY-6752
octanoyl-[acyl-carrier protein] biosynthesis (mitochondria, yeast)
-
-
PWY-7388
octopamine biosynthesis
-
-
PWY-7297
odd iso-branched-chain fatty acid biosynthesis
-
-
PWY-8174
okenone biosynthesis
-
-
PWY-7591
oleandomycin activation/inactivation
-
-
PWY-6972
oleanolate biosynthesis
-
-
PWY-7069
oleate beta-oxidation
-
-
PWY0-1337
oleate beta-oxidation (isomerase-dependent, yeast)
-
-
PWY-7291
oleate biosynthesis I (plants)
-
-
PWY-5147
oleate biosynthesis II (animals and fungi)
-
-
PWY-5996
oleate biosynthesis III (cyanobacteria)
-
-
PWY-7587
oleate biosynthesis IV (anaerobic)
-
-
PWY-7664
oleoresin monoterpene volatiles biosynthesis
-
-
PWY-5423
oleoresin sesquiterpene volatiles biosynthesis
-
-
PWY-5425
One carbon pool by folate
-
-
ophiobolin F biosynthesis
-
-
PWY-7720
ophthalmate biosynthesis
-
-
PWY-8043
oryzalide A biosynthesis
-
-
PWY-7481
Other glycan degradation
-
-
Other types of O-glycan biosynthesis
-
-
oxalate degradation III
-
-
PWY-6696
oxalate degradation IV
-
-
PWY-6697
oxalate degradation V
-
-
PWY-6698
oxalate degradation VI
-
-
PWY-7985
oxidative decarboxylation of pyruvate
-
-
Oxidative phosphorylation
-
-
oxidative phosphorylation
-
-
palmitate biosynthesis
-
-
palmitate biosynthesis I (type I fatty acid synthase)
-
-
PWY-5994
palmitate biosynthesis II (type II fatty acid synthase)
-
-
PWY-5971
palmitate biosynthesis III
-
-
PWY-8279
palmitoleate biosynthesis I (from (5Z)-dodec-5-enoate)
-
-
PWY-6282
palmitoleate biosynthesis II (plants and bacteria)
-
-
PWY-5366
palmitoleate biosynthesis IV (fungi and animals)
-
-
PWY3O-1801
palmitoyl ethanolamide biosynthesis
-
-
PWY-8055
palustric acid biosynthesis
-
-
PWY-5414
Pantothenate and CoA biosynthesis
-
-
pantothenate biosynthesis
-
-
paraoxon degradation
-
-
PWY-5490
parathion degradation
-
-
PARATHION-DEGRADATION-PWY
partial TCA cycle (obligate autotrophs)
-
-
PWY-5913
paspaline biosynthesis
-
-
PWY-7492
patulin biosynthesis
-
-
PWY-7490
pectin degradation I
-
-
PWY-7246
pectin degradation II
-
-
PWY-7248
pederin biosynthesis
-
-
PWY-8049
Penicillin and cephalosporin biosynthesis
-
-
pentachlorophenol degradation
-
-
PCPDEG-PWY
pentacyclic triterpene biosynthesis
-
-
PWY-7251
Pentose and glucuronate interconversions
-
-
Pentose phosphate pathway
-
-
pentose phosphate pathway
-
-
pentose phosphate pathway (non-oxidative branch) I
-
-
NONOXIPENT-PWY
pentose phosphate pathway (non-oxidative branch) II
-
-
PWY-8178
pentose phosphate pathway (oxidative branch) I
-
-
OXIDATIVEPENT-PWY
pentose phosphate pathway (partial)
-
-
P21-PWY
peptido-conjugates in tissue regeneration biosynthesis
-
-
PWY-8355
Peptidoglycan biosynthesis
-
-
peptidoglycan biosynthesis
-
-
peptidoglycan biosynthesis II (staphylococci)
-
-
PWY-5265
peptidoglycan biosynthesis IV (Enterococcus faecium)
-
-
PWY-6471
peptidoglycan maturation (meso-diaminopimelate containing)
-
-
PWY0-1586
peptidoglycan recycling I
-
-
PWY0-1261
peptidoglycan recycling II
-
-
PWY-7883
petrobactin biosynthesis
-
-
PWY-6289
petroselinate biosynthesis
-
-
PWY-5367
phaselate biosynthesis
-
-
PWY-6320
Phenazine biosynthesis
-
-
phenolic malonylglucosides biosynthesis
-
-
PWY-6930
phenylacetate degradation (aerobic)
-
-
phenylacetate degradation I (aerobic)
-
-
PWY0-321
Phenylalanine metabolism
-
-
phenylalanine metabolism
-
-
Phenylalanine, tyrosine and tryptophan biosynthesis
-
-
phenylethanol biosynthesis
-
-
PWY-5751
phenylethylamine degradation I
-
-
2PHENDEG-PWY
phenylmercury acetate degradation
phenylpropanoid biosynthesis
-
-
PWY-361
Phenylpropanoid biosynthesis
-
-
phenylpropanoid biosynthesis
-
-
phenylpropanoid biosynthesis, initial reactions
-
-
PWY1F-467
phenylpropanoids methylation (ice plant)
-
-
PWY-7498
pheomelanin biosynthesis
-
-
PWY-7917
phloridzin biosynthesis
-
-
PWY-6515
phosalacine biosynthesis
-
-
PWY-7769
phosphate acquisition
-
-
PWY-6348
phosphatidate biosynthesis (yeast)
-
-
PWY-7411
phosphatidate metabolism, as a signaling molecule
-
-
PWY-7039
phosphatidylcholine acyl editing
-
-
PWY-6803
phosphatidylcholine biosynthesis I
-
-
PWY3O-450
phosphatidylcholine biosynthesis VI
-
-
PWY-6826
phosphatidylcholine biosynthesis VII
-
-
PWY-7470
phosphatidylcholine resynthesis via glycerophosphocholine
-
-
PWY-7367
phosphatidylethanolamine biosynthesis II
-
-
PWY4FS-6
phosphatidylethanolamine bioynthesis
-
-
phosphatidylglycerol biosynthesis I
-
-
PWY4FS-7
phosphatidylglycerol biosynthesis II
-
-
PWY4FS-8
phosphatidylinositol biosynthesis I (bacteria)
-
-
PWY-6580
phosphatidylserine and phosphatidylethanolamine biosynthesis I
-
-
PWY-5669
phosphinothricin tripeptide biosynthesis
-
-
PWY-6322
phospholipases
-
-
LIPASYN-PWY
phospholipid desaturation
-
-
PWY-762
phospholipid remodeling (phosphatidate, yeast)
-
-
PWY-7417
phospholipid remodeling (phosphatidylcholine, yeast)
-
-
PWY-7416
phospholipid remodeling (phosphatidylethanolamine, yeast)
-
-
PWY-7409
Phosphonate and phosphinate metabolism
-
-
phosphopantothenate biosynthesis I
-
-
PANTO-PWY
photorespiration I
-
-
PWY-181
photorespiration II
-
-
PWY-8362
photorespiration III
-
-
PWY-8363
photosynthesis light reactions
-
-
PWY-101
photosynthetic 3-hydroxybutanoate biosynthesis (engineered)
-
-
PWY-7218
phycoerythrobilin biosynthesis I
-
-
PWY-5915
phycourobilin biosynthesis
-
-
PWY-7579
phytate degradation I
-
-
PWY-4702
phytochelatins biosynthesis
-
-
PWY-6745
phytochromobilin biosynthesis
-
-
PWY-7170
phytol degradation
-
-
PWY66-389
phytol salvage pathway
-
-
PWY-5107
phytosterol biosynthesis (plants)
-
-
PWY-2541
pinitol biosynthesis I
-
-
PWY-6738
pinobanksin biosynthesis
-
-
PWY-5059
plasmalogen biosynthesis I (aerobic)
-
-
PWY-7782
plasmalogen degradation
-
-
PWY-7783
plastoquinol-9 biosynthesis I
-
-
PWY-1581
platensimycin biosynthesis
-
-
PWY-8179
plaunotol biosynthesis
-
-
PWY-6691
poly(3-O-beta-D-glucopyranosyl-N-acetylgalactosamine 1-phosphate) wall teichoic acid biosynthesis
-
-
PWY-7819
poly(glycerol phosphate) wall teichoic acid biosynthesis
-
-
TEICHOICACID-PWY
poly(ribitol phosphate) wall teichoic acid biosynthesis I (B. subtilis)
-
-
PWY-7815
poly(ribitol phosphate) wall teichoic acid biosynthesis II (S. aureus)
-
-
PWY-7816
poly-hydroxy fatty acids biosynthesis
-
-
PWY-6710
Polycyclic aromatic hydrocarbon degradation
-
-
polyhydroxybutanoate biosynthesis
-
-
PWY1-3
polymethylated myricetin biosynthesis (tomato)
-
-
PWY-7160
polymethylated quercetin biosynthesis
-
-
PWY-7161
Porphyrin and chlorophyll metabolism
-
-
ppGpp metabolism
-
-
PPGPPMET-PWY
preQ0 biosynthesis
-
-
PWY-6703
Primary bile acid biosynthesis
-
-
proanthocyanidins biosynthesis from flavanols
-
-
PWY-641
procollagen hydroxylation and glycosylation
-
-
PWY-7894
progesterone biosynthesis
-
-
PWY-7299
proline to cytochrome bo oxidase electron transfer
-
-
PWY0-1544
propanethial S-oxide biosynthesis
-
-
PWY-5707
propanoate fermentation to 2-methylbutanoate
-
-
PWY-5109
Propanoate metabolism
-
-
propanoyl-CoA degradation II
-
-
PWY-7574
propionate fermentation
-
-
protectin biosynthesis
-
-
PWY-8357
protective electron sinks in the thylakoid membrane (PSII to PTOX)
-
-
PWY1YI0-7
protein N-glycosylation initial phase (eukaryotic)
-
-
MANNOSYL-CHITO-DOLICHOL-BIOSYNTHESIS
protein N-glycosylation processing phase (plants and animals)
-
-
PWY-7919
protein S-nitrosylation and denitrosylation
-
-
PWY-7798
protein ubiquitination
-
-
PWY-7511
protocatechuate degradation II (ortho-cleavage pathway)
-
-
PROTOCATECHUATE-ORTHO-CLEAVAGE-PWY
psilocybin biosynthesis
-
-
PWY-7936
purine deoxyribonucleosides degradation I
-
-
PWY-7179
purine deoxyribonucleosides degradation II
-
-
PWY-7179-1
purine deoxyribonucleosides salvage
-
-
PWY-7224
purine nucleobases degradation I (anaerobic)
-
-
P164-PWY
purine nucleobases degradation II (anaerobic)
-
-
PWY-5497
purine ribonucleosides degradation
-
-
PWY0-1296
putrescine biosynthesis I
-
-
PWY-40
putrescine biosynthesis II
-
-
PWY-43
putrescine biosynthesis III
-
-
PWY-46
putrescine degradation I
-
-
PUTDEG-PWY
putrescine degradation III
-
-
PWY-0
putrescine degradation IV
-
-
PWY-2
putrescine degradation V
-
-
PWY-3
pyrethrin I biosynthesis
-
-
PWY-6926
pyridoxal 5'-phosphate biosynthesis I
-
-
PYRIDOXSYN-PWY
pyrimidine deoxyribonucleosides degradation
-
-
PWY-7181
pyrimidine deoxyribonucleosides salvage
-
-
PWY-7199
pyrimidine deoxyribonucleotide phosphorylation
-
-
PWY-7197
pyrimidine deoxyribonucleotides biosynthesis from CTP
-
-
PWY-7210
pyrimidine deoxyribonucleotides de novo biosynthesis I
-
-
PWY-7184
pyrimidine deoxyribonucleotides de novo biosynthesis II
-
-
PWY-7187
pyrimidine deoxyribonucleotides de novo biosynthesis III
-
-
PWY-6545
pyrimidine deoxyribonucleotides de novo biosynthesis IV
-
-
PWY-7198
pyrimidine deoxyribonucleotides dephosphorylation
-
-
PWY-7206
Pyrimidine metabolism
-
-
pyrimidine metabolism
-
-
pyrimidine nucleobases salvage I
-
-
PWY-7183
pyrimidine ribonucleosides degradation
-
-
PWY0-1295
pyrimidine ribonucleosides salvage I
-
-
PWY-7193
pyrimidine ribonucleosides salvage II
-
-
PWY-6556
pyrrolnitrin biosynthesis
-
-
PWY-6831
pyruvate decarboxylation to acetyl CoA I
-
-
PYRUVDEHYD-PWY
pyruvate decarboxylation to acetyl CoA II
-
-
PWY-6970
pyruvate fermentation to (R)-acetoin I
-
-
PWY-5938
pyruvate fermentation to (R)-acetoin II
-
-
PWY-5939
pyruvate fermentation to (R)-lactate
-
-
PWY-8274
pyruvate fermentation to (S)-acetoin
-
-
PWY-6389
pyruvate fermentation to (S)-lactate
-
-
PWY-5481
pyruvate fermentation to acetate II
-
-
PWY-5482
pyruvate fermentation to acetate IV
-
-
PWY-5485
pyruvate fermentation to acetate VIII
-
-
PWY-5768
pyruvate fermentation to acetoin III
-
-
PWY3O-440
pyruvate fermentation to acetone
-
-
PWY-6588
pyruvate fermentation to butanoate
-
-
CENTFERM-PWY
pyruvate fermentation to butanol I
-
-
PWY-6583
pyruvate fermentation to butanol II (engineered)
-
-
PWY-6883
pyruvate fermentation to ethanol I
-
-
PWY-5480
pyruvate fermentation to ethanol II
-
-
PWY-5486
pyruvate fermentation to ethanol III
-
-
PWY-6587
pyruvate fermentation to hexanol (engineered)
-
-
PWY-6863
pyruvate fermentation to isobutanol (engineered)
-
-
PWY-7111
pyruvate fermentation to propanoate I
-
-
P108-PWY
quercetin diglycoside biosynthesis (pollen-specific)
-
-
PWY-7192
quercetin gentiotetraside biosynthesis
-
-
PWY-7137
quercetin glucoside biosynthesis (Allium)
-
-
PWY-7129
quercetin glycoside biosynthesis (Arabidopsis)
-
-
PWY-5321
quercetin sulfate biosynthesis
-
-
PWY-6199
quercetin triglucoside biosynthesis
-
-
PWY-7173
quinate degradation I
-
-
QUINATEDEG-PWY
quinate degradation II
-
-
PWY-6416
reactive oxygen species degradation
-
-
DETOX1-PWY-1
rebeccamycin biosynthesis
-
-
PWY-6324
reductive acetyl coenzyme A pathway
-
-
reductive acetyl coenzyme A pathway I (homoacetogenic bacteria)
-
-
CODH-PWY
reductive glycine pathway of autotrophic CO2 fixation
-
-
PWY-8303
reductive TCA cycle I
-
-
P23-PWY
reductive TCA cycle II
-
-
PWY-5392
resolvin D biosynthesis
-
-
PWY66-397
resveratrol biosynthesis
-
-
PWY-84
retinol biosynthesis
-
-
PWY-6857
rhamnogalacturonan type I degradation II (bacteria)
-
-
PWY-6771
Riboflavin metabolism
-
-
ricinoleate biosynthesis
-
-
PWY-7618
rosmarinic acid biosynthesis I
-
-
PWY-5048
rosmarinic acid biosynthesis II
-
-
PWY-5049
rubber biosynthesis
-
-
PWY-5815
Rubisco shunt
-
-
PWY-5723
rutin biosynthesis
-
-
PWY-5390
rutin degradation
-
-
PWY-6848
S-(6-hydroxy-4-methylhexan-4-yl)-L-cysteinylglycine degradation
-
-
PWY-8302
S-adenosyl-L-methionine biosynthesis
-
-
SAM-PWY
S-adenosyl-L-methionine salvage I
-
-
PWY-6151
S-adenosyl-L-methionine salvage II
-
-
PWY-5041
S-methyl-5'-thioadenosine degradation I
-
-
PWY-6754
S-methyl-5'-thioadenosine degradation IV
-
-
PWY0-1391
S-methyl-5-thio-alpha-D-ribose 1-phosphate degradation I
-
-
PWY-4361
S-methyl-5-thio-alpha-D-ribose 1-phosphate degradation II
-
-
PWY-7174
S-methyl-5-thio-alpha-D-ribose 1-phosphate degradation III
-
-
PWY-8132
saframycin A biosynthesis
-
-
PWY-7671
sakuranetin biosynthesis
-
-
PWY-5116
salicortin biosynthesis
-
-
PWY-6763
salicylate biosynthesis I
-
-
PWY-6406
salicylate biosynthesis II
-
-
PWY-8321
salicylate degradation I
-
-
PWY-6183
salidroside biosynthesis
-
-
PWY-6802
salinosporamide A biosynthesis
-
-
PWY-6627
Salmonella enterica serotype O:13 O antigen biosynthesis
-
-
PWY-8230
Salmonella enterica serotype O:54 O antigen biosynthesis
-
-
PWY-8204
salvigenin biosynthesis
-
-
PWY-7325
santalene biosynthesis II
-
-
PWY-6836
saponin biosynthesis II
-
-
PWY-5756
sciadonate biosynthesis
-
-
PWY-6598
scopoletin biosynthesis
-
-
PWY-6792
secologanin and strictosidine biosynthesis
-
-
PWY-5290
sedoheptulose bisphosphate bypass
-
-
PWY0-1517
selenate reduction
-
-
PWY-6932
seleno-amino acid biosynthesis (plants)
-
-
PWY-6936
seleno-amino acid detoxification and volatilization III
-
-
PWY-6933
Selenocompound metabolism
-
-
selenocysteine biosynthesis
-
-
serine racemization
-
-
PWY-8140
serotonin and melatonin biosynthesis
-
-
PWY-6030
serotonin degradation
-
-
PWY-6313
sesamin biosynthesis
-
-
PWY-5469
Sesquiterpenoid and triterpenoid biosynthesis
-
-
sinapate ester biosynthesis
-
-
PWY-3301
sitosterol degradation to androstenedione
-
-
PWY-6948
solasodine glycosylation
-
-
PWY18C3-4
sophorolipid biosynthesis
-
-
SOPHOROSYLOXYDOCOSANOATE-SYN-PWY
sophorosyloxydocosanoate deacetylation
-
-
SOPHOROSYLOXYDOCOSANOATE-DEG-PWY
sorbitol biosynthesis II
-
-
PWY-5530
sorgoleone biosynthesis
-
-
PWY-5987
soybean saponin I biosynthesis
-
-
PWY-5203
spermidine biosynthesis I
-
-
BSUBPOLYAMSYN-PWY
spermidine biosynthesis II
-
-
PWY-6559
spermidine biosynthesis III
-
-
PWY-6834
spermine and spermidine degradation I
-
-
PWY-6117
spermine biosynthesis
-
-
ARGSPECAT-PWY
sphingolipid biosynthesis (mammals)
-
-
PWY-7277
sphingolipid biosynthesis (plants)
-
-
PWY-5129
sphingolipid biosynthesis (yeast)
-
-
SPHINGOLIPID-SYN-PWY
Sphingolipid metabolism
-
-
sphingomyelin metabolism
-
-
PWY3DJ-11281
sphingosine and sphingosine-1-phosphate metabolism
-
-
PWY3DJ-11470
sphingosine metabolism
-
-
Spodoptera littoralis pheromone biosynthesis
-
-
PWY-7656
sporopollenin precursors biosynthesis
-
-
PWY-6733
stachyose biosynthesis
-
-
PWY-5337
stachyose degradation
-
-
PWY-6527
Starch and sucrose metabolism
-
-
starch biosynthesis
-
-
PWY-622
starch degradation I
-
-
PWY-842
starch degradation II
-
-
PWY-6724
starch degradation III
-
-
PWY-6731
starch degradation V
-
-
PWY-6737
Staurosporine biosynthesis
-
-
stearate biosynthesis I (animals)
-
-
PWY-5972
stearate biosynthesis II (bacteria and plants)
-
-
PWY-5989
stearate biosynthesis III (fungi)
-
-
PWY3O-355
stearate biosynthesis IV
-
-
PWY-8280
stellariose and mediose biosynthesis
-
-
PWY-6525
stellatic acid biosynthesis
-
-
PWY-7736
Steroid hormone biosynthesis
-
-
sterol biosynthesis (methylotrophs)
-
-
PWY-8026
sterol:steryl ester interconversion (yeast)
-
-
PWY-7424
stigma estolide biosynthesis
-
-
PWY-6453
Stilbenoid, diarylheptanoid and gingerol biosynthesis
-
-
streptomycin biosynthesis
-
-
PWY-5940
Streptomycin biosynthesis
-
-
streptorubin B biosynthesis
-
-
PWY1A0-6120
strychnine biosynthesis
-
-
PWY-8216
suberin monomers biosynthesis
succinate to chytochrome c oxidase via cytochrome c6
-
-
PWY1YI0-2
succinate to cytochrome bd oxidase electron transfer
-
-
PWY0-1353
succinate to cytochrome bo oxidase electron transfer
-
-
PWY0-1329
succinate to cytochrome c oxidase via plastocyanin
-
-
PWY1YI0-3
succinate to plastoquinol oxidase
-
-
PWY1YI0-8
sucrose biosynthesis I (from photosynthesis)
-
-
SUCSYN-PWY
sucrose biosynthesis II
-
-
PWY-7238
sucrose biosynthesis III
-
-
PWY-7347
sucrose degradation I (sucrose phosphotransferase)
-
-
SUCUTIL-PWY
sucrose degradation II (sucrose synthase)
-
-
PWY-3801
sucrose degradation III (sucrose invertase)
-
-
PWY-621
sucrose degradation IV (sucrose phosphorylase)
-
-
PWY-5384
sucrose degradation V (sucrose alpha-glucosidase)
-
-
PWY66-373
sucrose degradation VII (sucrose 3-dehydrogenase)
-
-
SUCROSEUTIL2-PWY
sulfate activation for sulfonation
-
-
PWY-5340
sulfated glycosaminoglycan metabolism
-
-
sulfide oxidation IV (mitochondria)
-
-
PWY-7927
sulfite oxidation II
-
-
PWY-5279
sulfite oxidation III
-
-
PWY-5278
sulfite oxidation IV (sulfite oxidase)
-
-
PWY-5326
sulfolactate degradation III
-
-
PWY-6638
sulfolipid biosynthesis
-
-
sulfopterin metabolism
-
-
sulfoquinovosyl diacylglycerol biosynthesis
-
-
PWYQT-4427
sulfur volatiles biosynthesis
-
-
PWY-6736
superoxide radicals degradation
-
-
DETOX1-PWY
superpathway of C28 brassinosteroid biosynthesis
-
-
PWY-6544
superpathway of dimethylsulfoniopropanoate degradation
-
-
PWY-6049
superpathway of fatty acid biosynthesis initiation
-
-
FASYN-INITIAL-PWY
superpathway of fermentation (Chlamydomonas reinhardtii)
-
-
PWY4LZ-257
superpathway of glucose and xylose degradation
-
-
PWY-6901
superpathway of glycolysis and the Entner-Doudoroff pathway
-
-
GLYCOLYSIS-E-D
superpathway of glyoxylate cycle and fatty acid degradation
-
-
PWY-561
superpathway of hyoscyamine (atropine) and scopolamine biosynthesis
-
-
PWY-7341
superpathway of L-aspartate and L-asparagine biosynthesis
-
-
ASPASN-PWY
superpathway of methylsalicylate metabolism
-
-
PWY18C3-25
superpathway of nicotine biosynthesis
-
-
PWY-7342
superpathway of ornithine degradation
-
-
ORNDEG-PWY
superpathway of photosynthetic hydrogen production
-
-
PWY-7731
superpathway of polyamine biosynthesis II
-
-
POLYAMINSYN3-PWY
superpathway of pyrimidine deoxyribonucleotides de novo biosynthesis (E. coli)
-
-
PWY0-166
superpathway of scopolin and esculin biosynthesis
-
-
PWY-7186
superpathway of UDP-glucose-derived O-antigen building blocks biosynthesis
-
-
PWY-7328
syringetin biosynthesis
-
-
PWY-5391
Taurine and hypotaurine metabolism
-
-
taurine biosynthesis III
-
-
PWY-8359
taxadiene biosynthesis (engineered)
-
-
PWY-7392
TCA cycle I (prokaryotic)
-
-
TCA
TCA cycle II (plants and fungi)
-
-
PWY-5690
TCA cycle III (animals)
-
-
PWY66-398
TCA cycle IV (2-oxoglutarate decarboxylase)
-
-
P105-PWY
TCA cycle V (2-oxoglutarate synthase)
-
-
PWY-6969
TCA cycle VI (Helicobacter)
-
-
REDCITCYC
TCA cycle VII (acetate-producers)
-
-
PWY-7254
TCA cycle VIII (Chlamydia)
-
-
TCA-1
teichuronic acid biosynthesis (B. subtilis 168)
-
-
PWY-7820
terminal O-glycans residues modification (via type 2 precursor disaccharide)
-
-
PWY-7434
Terpenoid backbone biosynthesis
-
-
testosterone and androsterone degradation to androstendione (aerobic)
-
-
PWY-6943
tetradecanoate biosynthesis (mitochondria)
-
-
PWY66-430
tetrahydrofolate biosynthesis I
-
-
PWY-6614
tetrahydrofolate biosynthesis II
-
-
PWY2DNV-11
tetrahydrofolate metabolism
-
-
tetrahydrofolate salvage from 5,10-methenyltetrahydrofolate
-
-
PWY-6613
tetrahydromethanopterin biosynthesis
-
-
PWY-6148
tetrahydromonapterin biosynthesis
-
-
PWY0-1433
tetrapyrrole biosynthesis I (from glutamate)
-
-
PWY-5188
tetrapyrrole biosynthesis II (from glycine)
-
-
PWY-5189
theophylline degradation
-
-
PWY-6999
thiazole component of thiamine diphosphate biosynthesis I
-
-
PWY-6892
thiazole component of thiamine diphosphate biosynthesis II
-
-
PWY-6891
thioredoxin pathway
-
-
THIOREDOX-PWY
threo-tetrahydrobiopterin biosynthesis
-
-
PWY-6983
thymine degradation
-
-
PWY-6430
thyroid hormone metabolism II (via conjugation and/or degradation)
-
-
PWY-6261
toluene degradation II (aerobic) (via 4-methylcatechol)
-
-
TOLUENE-DEG-3-OH-PWY
toluene degradation to 2-hydroxypentadienoate (via toluene-cis-diol)
-
-
TOLUENE-DEG-DIOL-PWY
toluene degradation to 2-hydroxypentadienoate I (via o-cresol)
-
-
TOLUENE-DEG-2-OH-PWY
toxoflavin biosynthesis
-
-
PWY-7991
trans, trans-farnesyl diphosphate biosynthesis
-
-
PWY-5123
trans-caffeate degradation (aerobic)
-
-
PWY-8003
trans-lycopene biosynthesis II (oxygenic phototrophs and green sulfur bacteria)
-
-
PWY-6475
trans-zeatin biosynthesis
-
-
PWY-2681
traumatin and (Z)-3-hexen-1-yl acetate biosynthesis
-
-
PWY-5410
trehalose biosynthesis I
-
-
TRESYN-PWY
trehalose biosynthesis II
-
-
PWY-881
trehalose biosynthesis III
-
-
TREHALOSESYN-PWY
trehalose biosynthesis IV
-
-
PWY-2622
trehalose biosynthesis V
-
-
PWY-2661
trehalose degradation I (low osmolarity)
-
-
TREDEGLOW-PWY
trehalose degradation II (cytosolic)
-
-
PWY0-1182
trehalose degradation IV
-
-
PWY-2722
trehalose degradation V
-
-
PWY-2723
trehalose degradation VI (periplasmic)
-
-
PWY0-1466
triacylglycerol degradation
-
-
LIPAS-PWY
trichome monoterpenes biosynthesis
-
-
PWY-6447
tricin biosynthesis
-
-
PWY-7995
tRNA charging
-
-
TRNA-CHARGING-PWY
tRNA processing
-
-
PWY0-1479
tRNA splicing I
-
-
PWY-6689
tRNA splicing II
-
-
PWY-7803
tropane alkaloids biosynthesis
-
-
PWY-5317
Tropane, piperidine and pyridine alkaloid biosynthesis
-
-
Tryptophan metabolism
-
-
tryptophan metabolism
-
-
tunicamycin biosynthesis
-
-
PWY-7821
tylosin biosynthesis
-
-
PWY-7415
type I lipoteichoic acid biosynthesis (S. aureus)
-
-
PWY-7817
type IV lipoteichoic acid biosynthesis (S. pneumoniae)
-
-
PWY-7818
ubiquinol-10 biosynthesis (late decarboxylation)
-
-
PWY-5872
Ubiquinone and other terpenoid-quinone biosynthesis
-
-
UDP-alpha-D-galactose biosynthesis
-
-
PWY-7344
UDP-alpha-D-galacturonate biosynthesis I (from UDP-D-glucuronate)
-
-
PWY-4861
UDP-alpha-D-glucose biosynthesis
-
-
PWY-7343
UDP-alpha-D-glucuronate biosynthesis (from myo-inositol)
-
-
PWY-4841
UDP-alpha-D-glucuronate biosynthesis (from UDP-glucose)
-
-
PWY-7346
UDP-GlcNAc biosynthesis
-
-
UDP-N-acetyl-alpha-D-mannosaminouronate biosynthesis
-
-
PWY-7335
UDP-N-acetyl-D-galactosamine biosynthesis I
-
-
PWY-5512
UDP-N-acetyl-D-galactosamine biosynthesis II
-
-
PWY-5514
UDP-N-acetyl-D-galactosamine biosynthesis III
-
-
PWY-8013
UDP-N-acetyl-D-glucosamine biosynthesis I
-
-
UDPNAGSYN-PWY
UDP-N-acetyl-D-glucosamine biosynthesis II
-
-
UDPNACETYLGALSYN-PWY
UDP-N-acetylmuramoyl-pentapeptide biosynthesis I (meso-diaminopimelate containing)
-
-
PWY-6387
UDP-N-acetylmuramoyl-pentapeptide biosynthesis II (lysine-containing)
-
-
PWY-6386
ultra-long-chain fatty acid biosynthesis
-
-
PWY-8041
umbelliferone biosynthesis
-
-
PWY-6982
UMP biosynthesis I
-
-
PWY-5686
UMP biosynthesis II
-
-
PWY-7790
UMP biosynthesis III
-
-
PWY-7791
uracil degradation I (reductive)
-
-
PWY-3982
urate conversion to allantoin I
-
-
PWY-5691
urea degradation II
-
-
PWY-5704
UTP and CTP de novo biosynthesis
-
-
PWY-7176
UTP and CTP dephosphorylation I
-
-
PWY-7185
UTP and CTP dephosphorylation II
-
-
PWY-7177
Valine, leucine and isoleucine biosynthesis
-
-
Valine, leucine and isoleucine degradation
-
-
valproate beta-oxidation
-
-
PWY-8182
vancomycin resistance I
-
-
PWY-6454
vancomycin resistance II
-
-
PWY-6455
vanillin biosynthesis I
-
-
PWY-5665
Various types of N-glycan biosynthesis
-
-
vernolate biosynthesis III
-
-
PWY-6917
very long chain fatty acid biosynthesis I
-
-
PWY-5080
very long chain fatty acid biosynthesis II
-
-
PWY-7036
vindoline, vindorosine and vinblastine biosynthesis
-
-
PWY-5292
viridicatumtoxin biosynthesis
-
-
PWY-7659
vitamin B1 metabolism
-
-
Vitamin B6 metabolism
-
-
vitamin B6 metabolism
-
-
vitamin E biosynthesis (tocopherols)
-
-
PWY-1422
vitamin E biosynthesis (tocotrienols)
-
-
PWY-7436
volatile benzenoid biosynthesis I (ester formation)
-
-
PWY-4203
volatile esters biosynthesis (during fruit ripening)
-
-
PWY-6801
wax esters biosynthesis I
-
-
PWY-5884
wax esters biosynthesis II
-
-
PWY-5885
xanthohumol biosynthesis
-
-
PWY-5135
xanthommatin biosynthesis
-
-
PWY-8249
xylitol degradation I
-
-
LARABITOLUTIL-PWY
xyloglucan degradation II (exoglucanase)
-
-
PWY-6807
zealexin biosynthesis
-
-
PWY-6888
zerumbone biosynthesis
-
-
PWY-6265
zymosterol biosynthesis
-
-
PWY-6074
(5R)-carbapenem carboxylate biosynthesis
-
-
PWY-5737
(5R)-carbapenem carboxylate biosynthesis
-
-
4-hydroxymandelate degradation
-
-
4-HYDROXYMANDELATE-DEGRADATION-PWY
4-hydroxymandelate degradation
-
-
4-hydroxyphenylacetate degradation
-
-
3-HYDROXYPHENYLACETATE-DEGRADATION-PWY
4-hydroxyphenylacetate degradation
-
-
adipate degradation
-
-
PWY-8354
bile acid biosynthesis, neutral pathway
-
-
PWY-6061
bile acid biosynthesis, neutral pathway
-
-
catecholamine biosynthesis
-
-
PWY66-301
catecholamine biosynthesis
-
-
cis-vaccenate biosynthesis
-
-
PWY-5973
cis-vaccenate biosynthesis
-
-
cyanate degradation
-
-
CYANCAT-PWY
diterpene phytoalexins precursors biosynthesis
-
-
PWY-2981
diterpene phytoalexins precursors biosynthesis
-
-
dolichol and dolichyl phosphate biosynthesis
-
-
PWY-6129
dolichol and dolichyl phosphate biosynthesis
-
-
enterobactin biosynthesis
-
-
ENTBACSYN-PWY
enterobactin biosynthesis
-
-
folate polyglutamylation
-
-
PWY-2161
folate polyglutamylation
-
-
methylaspartate cycle
-
-
PWY-6728
methylaspartate cycle
-
-
morphine biosynthesis
-
-
PWY-5270
morphine biosynthesis
-
-
myo-inositol biosynthesis
-
-
PWY-2301
myo-inositol biosynthesis
-
-
octane oxidation
-
-
P221-PWY
phenylmercury acetate degradation
-
-
P641-PWY
phenylmercury acetate degradation
-
-
suberin monomers biosynthesis
-
-
PWY-1121
suberin monomers biosynthesis
-
-
taxol biosynthesis
-
-
PWY-5660
urea cycle
-
-
PWY-4984
vitamin K-epoxide cycle
-
-
PWY-7999
vitamin K-epoxide cycle
-
-
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.
vascular tissues in the pedicel, the main expression site of LeACO1 is in cell layers just outside the flower pedicel abscission zone in its proximal and distal part
brenda
-
brenda
significantly negative regulation of GSNOR on the fifth axillary buds outgrowth
brenda
-
-
brenda
-
brenda
constitutive
brenda
-
brenda
-
-
brenda
-
-
brenda
-
brenda
-
-
brenda
-
gametophytically-expressed F3GalTase
brenda
-
brenda
-
the highest activities are found in the youngest parts of the plant: apical buds, flowers and leaf blades
brenda
-
brenda
-
uninuclear microspores
brenda
specific
brenda
-
-
brenda
-
brenda
-
brenda
after abscission induction, ACO1 protein is synthesized in phloem companion cells, in which it is localized mainly in the cytoplasm
brenda
-
brenda
-
brenda
-
-
brenda
-
brenda
high level
brenda
-
-
brenda
LeGOLS-1 mRNA is most abundant in radicle tips
brenda
-
brenda
main and lateral roots
brenda
type VI glandular trichome, highly expressed
brenda
-
brenda
-
brenda
-
brenda
-
brenda
-
preferentially accumulated in phloem and sieve cells
brenda
-
brenda
-
-
brenda
-
-
brenda
the ethylene biosynthesis genes LeACO4 is preferentially expressed in vascular tissues
brenda
-
high activity
brenda
high level
brenda
-
the highest activities are found in the youngest parts of the plant: apical buds, flowers and leaf blades
brenda
-
brenda
SlFRK3 is expressed mainly in the cambium and newly differentiating xylem cells
brenda
-
brenda
-
phosphate-starved
brenda
-
-
brenda
-
expression of LePLDbeta1 is increased upon treatment with xylanase
brenda
-
LePLDalpha1, is transcriptionally up-regulated and activated in cell suspension cultures treated with salt
brenda
-
phosphate-starved
brenda
-
phosphate-starved cells
brenda
-
brenda
-
high expression level
brenda
-
NiR 1 occurs in etiolated cotyledons, NiR2 is predominant in seedlings grown in light
brenda
-
-
brenda
-
from phosphate-starved cells
brenda
-
-
brenda
-
after germination, exclusively in micropylar region, after wounding, also in lateral endosperm
brenda
LeGOLS-1 mRNA is present in endosperm caps
brenda
micropylar and lateral
brenda
A0A2D1N4Z8, A0A3Q7H2B2, A0A3Q7IET9, A0ZS62, A0ZS63, A5JV19, A9LRT7, B6ECN9, C4NFG1, C6K2K9, C6K2L0, C7U110, D2Y3F4, E7AIM3, H6WYS2, H9D2D6, K4BE78, K4BS77, K4BTE6, K4C3H8, P05116, P24157, P28554, P51107, P93199, Q1XBU5, Q43503, Q4U1I4, Q4U1I5, Q8L4N2, Q8L5J1, Q8LP11
-
137660, 390314, 655562, 657099, 675132, 682392, 685648, 689544, 689590, 702104, 704876, 706249, 716504, 716556, 716562, 719900, 723052, 724489, 726172, 726232, 728449, 730122, 742854, 743489, 745005, 746107, 757823, 758411, 759277, 762145, 762186
brenda
-
co-expression of isozyme CWI with endogenous proteinous inhibitor VIF in flowers
brenda
exclusive expresion of CYP716A46 in flowers
brenda
-
high activity
brenda
high expression
brenda
high expression level
brenda
high transcription rate
brenda
highest expression
brenda
isoform GME2 transcript content is high in flowers
brenda
-
low expression level
brenda
lower enzyme level, constitutive
brenda
main expression
brenda
moderate expression
brenda
predominantly isozyme GGPS2
brenda
-
the enzyme shows highly increased activity about 35 days after flowering
brenda
-
the highest activities are found in the youngest parts of the plant: apical buds, flowers and leaf blades
brenda
very low expresion level
brenda
A0A2D1N4Z8, A0A3Q7H2B2, A0A3Q7I0S2, A0A3Q7IET9, A4ZYQ6, A9LRT7, A9QNE7, B6ECN9, C4NFG1, C6K2K9, C6K2L0, C7U110, D0QU16, D2Y3F4, E7DN63, G3JX11, H6WYS2, H9D2D6, K4BS77, K4BTE6, K4C3H8, K7W9N9, O04924, P05116, P08196, P09607, P18485, P24157, P29000, P54153, P93199, P93229, P93230, P93541, Q09Y74, Q09Y76, Q09Y77, Q09Y78, Q15I66, Q1KSC5, Q1KSC6, Q1PA40, Q3I5C3, Q3I5C4, Q3SC88, Q40144, Q42882, Q43503, Q43527, Q43528, Q4VDN6, Q54K39, Q6RHX7, Q6RHX8, Q6RHX9, Q6RHY0, Q6RHY1, Q84P52, Q84P53, Q84P54, Q8L4N2, Q8L5J1, Q8LP11, Q94LA1, Q9FR51, Q9FXK8, Q9FZ05, Q9SDX0, Q9SLN9, Q9ZWP2
-
2938, 2941, 3204, 34574, 34575, 34578, 34594, 135811, 135844, 136074, 136776, 171690, 286387, 286663, 286737, 389602, 390314, 487783, 487785, 489001, 636400, 636720, 637870, 637875, 637881, 637885, 637887, 639510, 640273, 640436, 641505, 641506, 641510, 641511, 643153, 650703, 653576, 655453, 656621, 656947, 659618, 666551, 666678, 666992, 670560, 674092, 674094, 674118, 675655, 676544, 676639, 676648, 679554, 680286, 682538, 683975, 689590, 689673, 694758, 696485, 696847, 699806, 700220, 701078, 702104, 704876, 704882, 706249, 706376, 710300, 713081, 715755, 716286, 716504, 716539, 716556, 716562, 716571, 716616, 719759, 721522, 722429, 723052, 723434, 723462, 723654, 725121, 726130, 726138, 726172, 726224, 726232, 726435, 728203, 728241, 729774, 730122, 730611, 730754, 734014, 734385, 736597, 736689, 736999, 739152, 739463, 740956, 742854, 742998, 745005, 746465, 748483, 748953, 751887, 757823, 758037, 758411, 759277, 762145, 762186, 763324, 764896
brenda
-
activity is highest at early stages of development
brenda
almost exclusively expressed in red fruit and root
brenda
and all other organs
brenda
at different stages of ripening
brenda
collected at the breaker stage, which is defined as the stage where first spot of pink/red color appears at the blossom end
brenda
-
decreased activity approximately 10fold between young and mature green fruits, increased activity during fruit development in red ripe fruit
brenda
-
decreases during fruit growth and ripening
brenda
-
during early seed development
brenda
expression in green immature fruit
brenda
-
expression of Endo-LE mRNA does not vary significantly with the tomato ripening process
brenda
expression of SlSGT3 is clearly different from other isozymes since its mRNA levels are low in developing fruits (small green and mature green stages) but increase sharply when fruits start to ripe and remain at similar high levels until the red mature stage
brenda
-
fruits exhibit ACC deaminase activity during ripening
brenda
GABA-T1 is the predominant isoform in stamens and maturing fruit tissue
brenda
GCHI mRNA level is highest in unripe fruit
brenda
-
GDH activity increases during the fruit ripening along with the content of free glutamate, the most abundant amino acid of ripe fruit involved in conferring the genuine tomato flavour. Only the active homohexamer of GDH beta-subunits is detected in roots while heterohexamers of GDH alpha- and beta-subunits are found in fruits. alpha-Subunit Slgdh-NAD;A1-3 transcripts are detected in all tomato tissues examined, showing the highest levels in mature green fruits, contrasting with beta-subunit Slgdh-NAD;B1 transcripts which are detected mainly in roots or in mature fruits when treated with glutamate, NaCl or salicylic acid
brenda
-
gene NXS is expressed at relatively lower level at breaker and red-ripe stages in genotype EC-521086
brenda
generally, highest transglucosylase activities (gene SIXTH1 - EC 2.4.1.207) during fruit growth, decrease during ripening, accordingly hydrolase activity decrease during ripening as indicated by xyloglucan viscosity decrease, expression of 10 different XTH genes in Solanum lycopersicum: SIXTH12 (group 2) highly expressed during fruit growth, decrease during ripening
brenda
generally, highest transglucosylase activities (gene SIXTH1 - EC 2.4.1.207) during fruit growth, decrease during ripening, accordingly hydrolase activity decrease during ripening as indicated by xyloglucan viscosity decrease, expression of 10 different XTH genes in Solanum lycopersicum: SIXTH3 (group 2) with generally low expression and no strong phase-dependent expression pattern
brenda
generally, highest transglucosylase activities (gene SIXTH1 - EC 2.4.1.207) during fruit growth, decrease during ripening, accordingly hydrolase activity decrease during ripening as indicated by xyloglucan viscosity decrease, expression of 10 different XTH genes in Solanum lycopersicum: SIXTH4 (group 1) highly expressed during fruit growth, decrease during ripening
brenda
generally, highest transglucosylase activities (gene SIXTH1 - EC 2.4.1.207) during fruit growth, decrease during ripening, accordingly hydrolase activity decrease during ripening as indicated by xyloglucan viscosity decrease, expression of 10 different XTH genes in Solanum lycopersicum: SIXTH6 (group 3) highly expressed during fruit growth, decrease during ripening
brenda
generally, highest transglucosylase activities (gene SIXTH1 - EC 2.4.1.207) during fruit growth, decrease during ripening, accordingly hydrolase activity decrease during ripening as indicated by xyloglucan viscosity decrease, expression of 10 different XTH genes in Solanum lycopersicum: SIXTH7 (group 1) highly expressed during fruit growth, decrease during ripening
brenda
generally, highest transglucosylase activities (gene SIXTH1 - EC 2.4.1.207) during fruit growth, decrease during ripening, accordingly hydrolase activity decrease during ripening as indicated by xyloglucan viscosity decrease, expression of 10 different XTH genes in Solanum lycopersicum: SIXTH8 (group 3) mainly expressed during ripening
brenda
generally, highest transglucosylase activities (gene SIXTH1 - EC 2.4.1.207) during fruit growth, decrease during ripening, accordingly hydrolase activity decrease during ripening as indicated by xyloglucan viscosity decrease, expression of 10 different XTH genes in Solanum lycopersicum: SIXTH9 (group 2) with generally low expression and no strong phase-dependent expression pattern
brenda
generally, highest transglucosylase activities (gene SIXTH1 - EC 2.4.1.207) during fruit growth, decrease during ripening, accordingly hydrolase activity decrease during ripening as indicated by xyloglucan viscosity decrease, expression of 10 different XTH genes in Solanum lycopersicum: SlXTH2 (group 2) with generally low expression and no strong phase-dependent expression pattern
brenda
generally, highest transglucosylase activities (gene SIXTH1 - EC 2.4.1.207) during fruit growth, decrease during ripening, accordingly hydrolase activity decrease during ripening as indicated by xyloglucan viscosity decrease, expression of 10 different XTH genes in Solanum lycopersicum: SlXTH5 (group 3) mainly expressed during ripening
brenda
green and red
brenda
green and ripening
brenda
-
GS2 is only detected in green fruits, not detected in red, mature fruits
brenda
-
high activity of PG2 in ripe tomato fruit pericarp tissue
brenda
-
high expression
brenda
high expression in mature fruit
brenda
-
high expression in red mature fruits
brenda
-
highest activity at the breaker stage
brenda
highest expression in ripe fruit leaf at day 92
brenda
highest expression of in ripe fruit leaf at day 92
brenda
highest level of transcripts is found in the later stages of fruit development
brenda
immature fruit, minor expression
brenda
immature green, mature green, turning, pink, red, full ripe
brenda
in green fruit, isoform Sus4 is expressed at nearly 200fold lower levels than isoform Sus3. Elevated level of expression in ripening fruit for isoform Sus3
brenda
in green fruit, isoform Sus4 is expressed at nearly 200fold lower levels than sioform Sus3
brenda
in small green, mature green, and mature red fruits. SlSGT1 mRNA levels decrease when fruits start to ripe (breaker and orange stages) but increase again in red ripe fruits
brenda
in small green, mature green, and mature red fruits. SlSGT2 mRNA levels decrease when fruits start to ripe (breaker and orange stages) but increase again in red ripe fruits
brenda
-
in wild-type fruit, the mRNA levels of CRTISO increase 10fold during the breaker stage of fruit ripening. Expression of CRTISO in fruit of the mutant tangerine(mic) is similar to that in the wild type
brenda
increase in CCT activity is observed during ripening, reaching a maximum in the peel of red fruit
brenda
-
intact and wounded fruits of different ripening stages
brenda
-
isoenzyme A is the predominant enzyme form
brenda
isoform GME2 transcript content is low in differential stages of fruits
brenda
isoform Man4a is expressed in the fruit cell wall at all ripening stages, but it is not active during the initial green stage. This is not due to the presence of inhibitors of its activity, nor due to changes in its mRNA sequence
brenda
LekdsA mRNAs are preferentially expressed in dividing tissues during fruit development
brenda
-
level of mRNA increases greatly during fruit ripening, highest level detectable in orange fruit, predominantly in the outer cell-layers of the pericarp
brenda
-
low enzyme activity levels in green and red fruits
brenda
-
low expression level
brenda
low transcription rate
brenda
lower enzyme level, constitutive
brenda
-
mature green
brenda
mature green and ripe
brenda
-
mature green fruit
brenda
mature green tomato fruits
brenda
Q9LWA6
mature green, pink and red
brenda
preferential expression
brenda
red fruit, not during early stages of ripening
brenda
-
red ripe tomatoes
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-
ripe fruit flesh, the enzyme is located in skin, flesh, locular gel and columella of tomato fruits. Its abundance does not increase during ripening, but decreases during senescence
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ripe ftuit
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-
ripe tomato
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-
ripe tomato. Varieties Galeon and Soto have about 50% of each enzyme, whereas Malpica and Perfectpeel contain more PG1 than PG2
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ripening, predominantly isozyme GGPS2
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-
specific activity of beta-acetylhexosaminidase increases during ripening with a peak at the climacteric stage, isoenzyme I
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-
specific activity of beta-acetylhexosaminidase increases during ripening with a peak at the climacteric stage, isoenzyme II
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the enzyme is highly expressed in the pistil and stamens and in fruits during ripening
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transcript in mature fruit and in immature fruit
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transcript in mature fruit, no transcript detected in immature fruit
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-
tXET-B1 is most abundant in pink fruit pericarp
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vascular tissue
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-
wounded fruits
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young developing, isozyme profile, expression analysis, overview
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-
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-
isoenzyme B and C in comparable amounts
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LeEXT gene is expressed in outer cell layers of the hypocotyl, after auxin treatment overlapping spatial distribution in the epidermis and outer cortical cell layers
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-
-
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-
RNA blot hybridization
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A0A0C5AJS1, A0A2D1N4Z8, A0A3Q7E952, A0A3Q7FJ72, A0A3Q7H2B2, A0A3Q7IET9, A0A3Q7IJD4, A5H1Q7, A5JV19, A8IFQ7, B3EYD3, B5B3R3, B9TU32, C0LIR3, C1K5M3, C4NFG1, C5IU71, C6K2K9, C6K2L0, C7U110, D2Y3F4, D2Y3T9, G3JX11, H6WYS2, H9D2D6, K4BS77, K4BTE6, K4BW79, K4C3H8, O04924, P18485, P25306, P28554, P35511, P43280, P54153, P83379, P83380, P93229, P93230, Q09Y74, Q09Y76, Q09Y77, Q09Y78, Q1PA40, Q1XBU5, Q2KTH4, Q3I5C3, Q3I5C4, Q3SC88, Q42882, Q43503, Q4U1I4, Q4U1I5, Q4VDN6, Q4W5U8, Q54K39, Q6RFY3, Q84P52, Q84P53, Q84P54, Q8LP11, Q8VYU3, Q9ZR58
-
4477, 4488, 30844, 34354, 81108, 94289, 286507, 390314, 390330, 392005, 392011, 392891, 438117, 438157, 485615, 485935, 636362, 636810, 643144, 643153, 643167, 653576, 657105, 660407, 663150, 664746, 665076, 675132, 675250, 675655, 676354, 676544, 676651, 676709, 681238, 682331, 682392, 682413, 682451, 683975, 683987, 689397, 689400, 689544, 689590, 689614, 689673, 689687, 693181, 693853, 694612, 694666, 694686, 694766, 694777, 699399, 700220, 700810, 702104, 704876, 704882, 705354, 706130, 706239, 713076, 713081, 713223, 713238, 713266, 716357, 716497, 716504, 716556, 716616, 723052, 723462, 724489, 725121, 725140, 725797, 726130, 726138, 726144, 726172, 726182, 726230, 726232, 726244, 726435, 734385, 734429, 736696, 738766, 739268, 739385, 739463, 740956, 743489, 743565, 746178, 746465, 747657, 748483, 750865, 751852, 751887, 757491, 757823, 758411, 759277, 759800, 761187, 761622, 762145, 762159, 762186, 763128, 763391, 763562, 763605, 764807, 764896, 765341, 765597, 765847
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-
35 kDa isozyme CKX35 in chlorotic leaves associated with a reduction in representative cytokinin levels and high H2O2 concentrations, and 37 kDa isozyme CKX37 in green leaves associated with representative CKs and H2O2 at normal levels
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-
apoplastic fluid
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apoplastic space of tomato leaves
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cDNA clone of the tomato IPI gene is amplified using cDNA from young leaves as template
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-
co-expression of isozyme CWI with endogenous proteinous inhibitor VIF in green leaves
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collected at the mature green stage
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constitutive expression, higher in young leaves compared to old ones
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-
drought stress does not cause an increase of zeaxanthin epoxidase mRNA. Strong diurnal expression pattern for zeaxanthin epoxidase, oscillation with a phase very similar to light-harvesting complex II mRNA, oscillation continues in a 48 h dark period
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-
during drought stress, NCED mRNA increrases. NCED mRNA has a diurnal cycle coincident with the light/dark transition
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-
enzyme accumulation in wounded leaves
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-
enzyme activity in wild-type, no activity in Moco sulfurase mutant flacca
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expression in vascular tissues of the leaves and stems
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expression is higher in young leaves compared to old ones
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expression of isoform LIN6 in sink tissues, such as pollen grains and vascular tissues of leaves and stems
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BT012891
expression of LeLUT1 is the highest in the leaves in tomato
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-
form Lf
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-
high expression
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high level
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-
higher enzyme expression level in leaves compared to stems
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higher levels
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highest expression levels are observed in leaves and roots
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in fulla differentiated leaves the basal activity is 1.5fold lower than in immature leAVES
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induction of isoform LeARG2 upon wounding and treatment with jasmonic acid
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isoform GME2 transcript content is high in leaves
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-
isoleucine-sensitive enzyme form occurs predominantly in younger leaves, isoleucine-insensitive enzyme form occurs predominantly in older leaves
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isozyme profile, expression analysis, overview
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-
leaf blade, high activity
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leaf inoculated with potato spindle tuber viroid. In viroid-infected tomato leaf the activity of the host-encoded RdRP is significantly increased. Viroids are not translated into proteins so that they cannot code for a viroid-specific RNA replicase
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-
low activity
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-
low activity in young leaf
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low expression
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-
low level
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mature and senescent
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-
mild reductions in mitochondrial citrate synthase activity results in a compromised nitrate assimilation and reduced leaf pigmentation but have no effect on photosynthetic performance or growth
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minor expression
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KJ755870
not expressed under normal growth but induced by alamethicin and methyl jasmonate treatments
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predominantly isozyme GGPS1
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-
senescent, expression of both RNases Le and LX
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-
the content of PPDK g/fresh weight increases in tomato leaves as they mature until the mid-stage of development, and declines during their senescence
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-
the enzyme is not only present in senescent leaves but also at other stages of leaf development
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-
upregulation in leaves infected by the bacterial pathogen Pseudomonas syringae, high activity in phloem cells of the main vascular bundles and in secondary veins of the leaf blade
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vascular tissue
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young
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young leaf, high transcription rate
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-
young, developing and fully expanded leaves, RNA blot hybridisation
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-
34565, 34567, 34569, 34571, 34573, 34578, 34584, 114114, 641502, 641510, 641511, 674118, 694758, 729774, 730754, 734014
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-
2 isoforms I and II
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-
enzyme appears at the stage in which many ripening-related changes start, and remains present throughout fruit ripening
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low level
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-
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LeETR2 mRNA expression is down-regulated in senescing leaf petioles
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vascular tissue
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-
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expressed in phloem companion cells of both internal and external phloem
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phloem campanion cells
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-
preferentially accumulated in phloem and sieve cells
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RNaseLE transcript accumulation occurs preferentially upon wounding
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-
this zone contains several layers of small and regular cells with dense cytoplasm, enzyme expression at proximal and distal sides
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vascular tissues in the pedicel, the main expression site of LeACO1 is in cell layers just outside the flower pedicel abscission zone in its proximal and distal part
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binuclear pollen
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expression of isoform LIN6 in sink tissues, such as pollen grains and vascular tissues of leaves and stems
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in vitro germination at 25°C for 8 h (to 50% impaired in absence of functional GWD, starch accumulation and reduction in level of soluble sugars)
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-
lower F3GalTase activity than in Petunia hybrida pollen
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SlFRK4 is expressed only in pollen
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A0A0C5AJS1, A0A2D1N4Z8, A0A3Q7H2B2, A0A3Q7IET9, B6ECN9, C4NFG1, C6K2K9, C6K2L0, C7U110, D2Y3F4, E7AIM3, G1JUH1, H6WYS2, H9D2D6, K4BE78, K4BS77, K4BTE6, K4C3H8, K7W9N9, O04924, O49187, P22180, P28554, P29000, P43280, P83379, P83380, P93229, P93230, Q09Y74, Q09Y76, Q09Y77, Q09Y78, Q0GGX1, Q10712, Q1PA40, Q2KTH4, Q3I5C3, Q3I5C4, Q3SC88, Q41342, Q42882, Q54K39, Q5K2N1, Q69F00, Q6EMC0, Q84P52, Q84P53, Q84P54, Q8GZD8, Q8LP11, Q96578, Q9SPD5, Q9XHH3
-
4076, 137660, 391539, 392011, 438034, 441679, 487895, 637520, 643153, 663112, 675685, 676557, 676651, 682331, 689590, 689673, 689687, 690052, 695412, 699808, 700220, 700824, 702104, 704875, 704876, 704882, 706130, 706264, 713445, 716357, 716504, 716562, 716971, 718235, 718249, 719900, 720788, 723434, 724489, 726232, 728066, 729321, 736999, 739268, 739463, 741621, 742854, 743489, 746107, 751852, 751887, 757491, 758411, 759277, 759800, 760796, 761616, 762145, 762186, 762617, 763391, 763592, 764896
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-
abundant
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adventitious roots on stems, primordia
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almost exclusively expressed in red fruit and root
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-
colonized by Glomus mosseae or Glomus intraradices
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-
drought stress causes an increase of zeaxanthin epoxidase mRNA
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-
during drought stress, NCED mRNA increrases
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-
enzyme activity in wild-type, no activity in Moco sulfurase mutant flacca
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-
greatest abundance
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high enzyme level
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-
high enzyme level, several fold higher than in leaves
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highest expression level
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highest expression levels are observed in leaves and roots
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-
isoenzyme C is the predominant enzyme form
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isoform GME2 transcript content is low in leaves
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isoform sus4 is expressed at nearly 200fold lower levels than sioform Sus3
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LeDES transcripts are most abundant in roots. A low level of LeDES mRNA is observed in stem tissue, but no accumulation is detected in flower buds, petioles, cotyledons, or leaves. Extracts from roots of young plants, but not extracts from stem or leaf tissue, catalyze efficient formation of colneleate from the hydroperoxide precursor
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-
low expression
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low transcription rate
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lower enzyme level, constitutive
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meristematic zone at root tip and elongation zone at root tip
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minor expression
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moderate expression
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-
no increase of activity during hypoxia
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-
only the active homohexamer of GDH beta-subunits is detected in roots while heterohexamers of GDH alpha- and beta-subunits are found in fruits. alpha-Subunit Slgdh-NAD;A1-3 transcripts are detected in all tomato tissues examined, showing the highest levels in mature green fruits, contrasting with beta-subunit Slgdh-NAD;B1 transcripts which are detected mainly in roots or in mature fruits when treated with glutamate, NaCl or salicylic acid
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-
revealed the presence of LePT1 transcript in the root cap and in the external layers of the root
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specifically expressed in root
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-
two forms, R1 and R2
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-
upregulation in nematode-infected roots
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vascular tissue
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-
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-
activity increases in the micropylar and lateral endosperm during and following germination
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embryo, micropylar and lateral endosperm, during and following germination
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expression in germinating seed and seedling
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-
germinated
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-
high increase in enzyme expression during germination
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-
increase in activity following germination
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LeETR2 mRNA is expressed at low levels throughout the plant but is induced in imbibing seeds prior to germination
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low expression
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A0A2D1N4Z8, A0A3Q7E952, A0ZS62, A0ZS63, D2Y3F4, D2Y3T9, E7AIM3, K4BS77, K4BTE6, K4C3H8, P35511, P83379, P83380, Q9LWA6, Q9XHH3
-
391537, 636810, 650806, 653605, 661624, 666992, 676651, 682331, 685648, 694744, 695412, 710285, 714099, 719900, 725140, 726182, 736696, 736999, 743539, 746051, 748872, 757491, 759277, 760796, 763128, 763592, 764896
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expression in germinating seed and seedling
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LeETR2 mRNA expression is down-regulated in elongating seedlings
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low expression
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-
maximum activity 4 days after germination
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-
source for isolating RNA
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-
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-
highest expression
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-
in the anthesis stage, gene SlUPB1 expression in heat-tolerant tomato variant CL5915 stamens, growing at 35/30°C (day/night), is 2.16 and 2.93times greater than that in a heat-sensitive tomato variant L4783 cultivated at 30/25°C or 25/20°C, respectively
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A0A3Q7E952, A0A3Q7IJD4, A9LRT7, B6ECN9, C4NFG1, C6K2K9, C6K2L0, D2Y3F4, E7AIM3, G1JUH1, H6WYS2, K4BE78, K4C627, K4CJ56, O04924, P29000, P83379, P83380, P93229, P93230, Q09Y74, Q09Y76, Q09Y77, Q09Y78, Q1PA40, Q1XBU5, Q2KTH4, Q3I5C3, Q3I5C4, Q3SC88, Q40144, Q42882, Q4U1I4, Q4U1I5, Q54K39, Q5K2N1, Q84P52, Q84P53, Q84P54, Q8LP11
-
393486, 487895, 636810, 636837, 643153, 675132, 675685, 682331, 682392, 689590, 689673, 700220, 704876, 704882, 706130, 706249, 713081, 716504, 716562, 718235, 719900, 724489, 726105, 726232, 729321, 737033, 739463, 742854, 746107, 751887, 755052, 759800, 763128, 763592, 764896, 765597
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constitutive
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elevated expression of isoform Sus4 in the higher, less mature portions of stem
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expression in vascular tissues of the leaves and stems
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expression of isoform LIN6 in sink tissues, such as pollen grains and vascular tissues of leaves and stems
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green
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-
high activity in tissues from young plants
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high transcription rate
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-
internode
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isoform GME2 transcript content is moderate in leaves
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isoform SUS3 expression is not significantly altered throughout the internodes
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LeDES transcripts are most abundant in roots. A low level of LeDES mRNA is observed in stem tissue, but no accumulation is detected in flower buds, petioles, cotyledons, or leaves. Extracts from roots of young plants, but not extracts from stem or leaf tissue, catalyze efficient formation of colneleate from the hydroperoxide precursor
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low expression
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-
low level
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minor expression
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-
RNA blot hybridization
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-
tXET-B1 is detected in stems
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vascular tissue
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very low expresion level
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-
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glandular trichome
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-
stem trichome, highest expression
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trichomes of leaf but not of stem
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type VI trichomes of leaves and stems, high expression level of SlCPT1
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-
brenda
expressed in phloem companion cells of both internal and external phloem
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SlFRK3 is expressed mainly in the cambium and newly differentiating xylem cells
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additional information
alpha-DOX1 transcripts are detected in the roots and absent in all other organs
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additional information
-
analysis of tissue and cellular localization of the enzyme, detailed overview
brenda
additional information
CrtR-b2 transcript levels are absent in leaves and sepals
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additional information
CYP75A31 real-time PCR expression analysis in the vegetative tomato plant parts
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additional information
differential expression patterns of the three GABA-T isoforms in reproductive tissues, but not vegetative tissues, overview
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additional information
-
enzyme activity is present in all organs tested, with quantitative differences. In youngest parts of the plant, both endo N-acetyl-beta-D-glucosaminidase and N4-N-acetyl-beta-D-glucosaminidase activity are detected, associated with high levels of proteins and protease activities
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additional information
KJ755870
enzyme is not expressed in any tissue under normal growth
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additional information
enzyme SlCPT6 is exclusively expressed in red fruit and roots
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additional information
expressed in all organs examined
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additional information
-
expression in all cell types and plant organs, with preferential accumulation in lignified tissues
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additional information
expression is higher in roots and stems compared to leaves of young plants
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additional information
BT012891
expression pattern in various tomato organs, quantitative expression analysis, overview
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additional information
-
gene NXS expression analysis in different genotypes, overview
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additional information
GSNOR expression and activity during development of Solanum spp. genotypes. Highest expression level in stems, high expression in roots and senescent leaves, moderate expression in mature leaves and apex, low in seedlings, overview. GSNOR localizes mainly in the vascular tissue and epidermal cells of the leaf sections
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additional information
GSNOR is thought to be localized in the phloem and xylem parenchyma cells of the vasculature
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additional information
high level in plant placenta
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additional information
highest expression levels are observed at 10 and 20 days after anthesis
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additional information
highest levels of enzyme activity in reproductive tissues
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additional information
immunolocalization study and and expression pattern analysis
brenda
additional information
immunolocalization study and expression pattern analysis
brenda
additional information
isoform PE2 expression is not detected in tissues surrounding seeds, such as locular tissue, seed, placenta, and core
brenda
additional information
-
isoform ToTal1, present in all tissues examined
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additional information
isozyme tissue distribution, overview
brenda
additional information
LeETR1 is expressed constitutively in all plant tissues examined
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additional information
Lip1 is widely expressed, particularly in reproductive organs
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additional information
Lip1p is widely expressed, particularly in reproductive organs
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additional information
low RNaseLER transcript abundances in almost all parts of tomato plants
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additional information
mRNA is constitutively expressed in vegetative and reproductive tissues
brenda
additional information
-
mRNA not detectable in root
brenda
additional information
no enzyme expression in leaves
brenda
additional information
no enzyme expression in leaves, roots, and stems
brenda
additional information
-
no enzyme expression in root
brenda
additional information
no expression in leaf
brenda
additional information
no expression of SlCPT1 in leaves, flowers, roots, and fruits
brenda
additional information
-
no significant difference in enzyme activity between dark-grown and light-grown seedlings
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additional information
-
not detected in microspore mother cells or mature pollen grains
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additional information
-
not detected in roots
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additional information
-
not expressed in bald stems
brenda
additional information
not in leaf
brenda
additional information
-
PPDK polypeptide abundance and not PPDK activity is determined, because in the darkened leaves of C3 plants, PPDK is present largely as an inactive phosphorylated form
brenda
additional information
-
present in all types of cells and tissues
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additional information
PT4 expression analysis, no expression in non-mycorrhizal roots, shoots, and leaves
brenda
additional information
-
real-time quantitative RT-PCR expression analysis
brenda
additional information
SlGMP3 transcript levels are high in stems, flowers, and young leaves, whereas low in roots, and fruits at breaker and red ripe stages, expression patterns, overview
brenda
additional information
-
subunit distributin and expression patterns in tissues of tomato, overview. The level of GDH alpha- and beta-subunits in tomato plants is regulated differently in each tomato organ
brenda
additional information
the gene for the NAD+-dependent enzyme shows higher expression in the roots in the later stages of Solanum lycopersicum fruit development and especially during fruit ripening. Unique expression profiles imply that QDH genes for NAD+- and NADP+-specific enzymes, gene expression analysis
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additional information
-
the highest PME activity is detected in samples isolated from green fruits, whereas soluble proteins isolated from green and red fruit possess the lowest PMEI inhibitor activity. Root and stems possess high PME activities, while low activities are detected in leaf tissues, suggesting that vegetative tissues also undergo dynamic pectin modification
brenda
additional information
the NADP+-specific enzyme shows higher expression levels in green tissues, including leaves, green stems and flowers and during the early stages of fruit development, gene expression analysis. The unique expression profiles imply that QDH genes for NAD+- and NADP+-specific enzymes are likely to have distinct physiological roles
brenda
additional information
-
the OMT gene shows patterns strongly correlating with both accumulation of anthocyanins and expression of anthocyanin biosynthesis genes
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additional information
the SlSGT isozyme encoding genes have specialized but still largely overlapping expression patterns in different organs of tomato plants and throughout the different stages of fruit development and ripening
brenda
additional information
the SlSGT isozyme encoding genes have specialized but still largely overlapping expression patterns in different organs of tomato plants and throughout the different stages of fruit development and ripening. SlSGT1 is the most intensely expressed in root, leaf, and flower tissues, being roots and leaves the tissues where the highest levels of SlSGT1 mRNA are detected. SlSGT1 is again the most actively expressed SlSGT gene in both developing (small green and mature green stages) and mature red fruits
brenda
additional information
the SlSGT isozyme encoding genes have specialized but still largely overlapping expression patterns in different organs of tomato plants and throughout the different stages of fruit development and ripening. SlSGT4 transcripts are barely detectable in all samples analyzed.
brenda
additional information
tissue expression pattern, overview. Transcripts of SlCGT, enzyme activity, and caffeoylglucarate accumulate preferentially in tomato leaves and flowers
brenda
additional information
-
tomato lines with strongly reduced source leaf cell wall-bound invertase activity by RNAi inhibition, 10-15% source leaf activity, while sink leaves and petioles still have 40-60% of wild-type activity, no alterations in other organs and tissue: Lin8-RNAi line 33, line 50, line 57, gene-silencing
brenda
additional information
transcript levels of SlSA1H are highest in stems and its expression is correlated with the formation of the methylated catechol derivatives guaiacol and veratrole
brenda
additional information
-
transcript profiling of isozymes ADK1 and ADK2, during desiccation the enzyme expression level remains constant up to 27 days after pollination, then decreases, and peaking again at day 43, then decreases again, overview
brenda
additional information
-
transcripts of the catalytic subunit FTR-c are detected in all tissues examined, including roots, leaves, flowers, fruits, and seeds
brenda
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