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(4Z,7Z,10Z,13Z,16Z)-docosapentaenoate biosynthesis (6-desaturase)
-
-
PWY-7726
(5Z)-dodecenoate biosynthesis II
-
-
PWY-7858
(7Z,10Z,13Z)-hexadecatrienoate biosynthesis
-
-
PWY-7590
(aminomethyl)phosphonate degradation
-
-
PWY-7805
(S)-reticuline biosynthesis I
-
-
PWY-3581
1,3-beta-D-glucan biosynthesis
-
-
PWY-6773
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
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
3,8-divinyl-chlorophyllide a biosynthesis I (aerobic, light-dependent)
-
-
CHLOROPHYLL-SYN
3,8-divinyl-chlorophyllide a biosynthesis III (aerobic, light independent)
-
-
PWY-7159
3-(4-hydroxyphenyl)pyruvate biosynthesis
-
-
PWY-5886
4-aminobutanoate degradation IV
-
-
PWY-6473
4-hydroxybenzoate biosynthesis I (eukaryotes)
-
-
PWY-5754
6-gingerol analog biosynthesis (engineered)
-
-
PWY-6920
9-cis, 11-trans-octadecadienoyl-CoA degradation (isomerase-dependent, yeast)
-
-
PWY-7340
9-lipoxygenase and 9-allene oxide synthase pathway
-
-
PWY-5407
abscisic acid biosynthesis
-
-
PWY-695
abscisic acid degradation by glucosylation
-
-
PWY-5272
acetaldehyde biosynthesis II
-
-
PWY-6330
acrylonitrile degradation I
-
-
PWY-7308
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
Alanine, aspartate and glutamate metabolism
-
-
allantoin degradation
-
-
allantoin degradation to ureidoglycolate I (urea producing)
-
-
PWY-5697
allantoin degradation to ureidoglycolate II (ammonia producing)
-
-
PWY-5698
alpha-linolenate biosynthesis I (plants and red algae)
-
-
PWY-5997
alpha-linolenate biosynthesis II (cyanobacteria)
-
-
PWY-7598
alpha-Linolenic acid metabolism
-
-
Amino sugar and nucleotide sugar metabolism
-
-
Aminobenzoate degradation
-
-
anaerobic energy metabolism (invertebrates, cytosol)
-
-
PWY-7383
anandamide biosynthesis I
-
-
PWY-8051
anandamide biosynthesis II
-
-
PWY-8053
androstenedione degradation I (aerobic)
-
-
PWY-6944
androstenedione degradation II (anaerobic)
-
-
PWY-8152
arachidonate biosynthesis IV (8-detaturase, lower eukaryotes)
-
-
PWY-7601
Arginine and proline metabolism
-
-
Arginine biosynthesis
-
-
arginine dependent acid resistance
-
-
PWY0-1299
aromatic glucosinolate activation
-
-
PWY-6684
arsenate detoxification I
-
-
PWY-8264
Ascorbate and aldarate metabolism
-
-
ascorbate glutathione cycle
-
-
PWY-2261
ascorbate recycling (cytosolic)
-
-
PWY-6370
aspartate and asparagine metabolism
-
-
assimilatory sulfate reduction II
-
-
SULFMETII-PWY
assimilatory sulfate reduction III
-
-
PWY-6683
assimilatory sulfate reduction IV
-
-
PWY1ZNC-1
atromentin biosynthesis
-
-
PWY-7518
avenanthramide biosynthesis
-
-
PWY-8157
beta-alanine biosynthesis IV
-
-
PWY-5760
beta-Alanine metabolism
-
-
Bifidobacterium shunt
-
-
P124-PWY
Biosynthesis of secondary metabolites
-
-
Biosynthesis of siderophore group nonribosomal peptides
-
-
Biosynthesis of unsaturated fatty acids
-
-
brassicicene C biosynthesis
-
-
PWY-7517
butanol and isobutanol biosynthesis (engineered)
-
-
PWY-7396
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
caffeine degradation III (bacteria, via demethylation)
-
-
PWY-6538
capsaicin biosynthesis
-
-
PWY-5710
capsiconiate biosynthesis
-
-
PWY-6027
Carbon fixation in photosynthetic organisms
-
-
Carbon fixation pathways in prokaryotes
-
-
cardenolide glucosides biosynthesis
-
-
PWY-6036
Carotenoid biosynthesis
-
-
CDP-diacylglycerol biosynthesis
-
-
CDP-diacylglycerol biosynthesis I
-
-
PWY-5667
CDP-diacylglycerol biosynthesis II
-
-
PWY0-1319
cell-surface glycoconjugate-linked phosphocholine biosynthesis
-
-
PWY-7886
ceramide and sphingolipid recycling and degradation (yeast)
-
-
PWY-7119
ceramide degradation (generic)
-
-
PWY-6483
ceramide degradation by alpha-oxidation
-
-
PWY66-388
chlorogenic acid biosynthesis I
-
-
PWY-6039
chlorophyll a degradation I
-
-
PWY-5098
chlorophyll a degradation II
-
-
PWY-6927
chlorophyll a degradation III
-
-
PWY-7164
chlorophyll metabolism
-
-
chlorosalicylate degradation
-
-
PWY-6107
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
Citrate cycle (TCA cycle)
-
-
CMP phosphorylation
-
-
PWY-7205
colanic acid building blocks biosynthesis
-
-
COLANSYN-PWY
coumarins biosynthesis (engineered)
-
-
PWY-7398
crotonyl-CoA/ethylmalonyl-CoA/hydroxybutyryl-CoA cycle (engineered)
-
-
PWY-7854
curcuminoid biosynthesis
-
-
PWY-6432
Cutin, suberine and wax biosynthesis
-
-
cyclic electron flow
-
-
PWY-8270
Cysteine and methionine metabolism
-
-
cytokinin-O-glucosides biosynthesis
-
-
PWY-2902
cytosolic NADPH production (yeast)
-
-
PWY-7268
D-Amino acid metabolism
-
-
D-galactose degradation I (Leloir pathway)
-
-
PWY-6317
D-galactose detoxification
-
-
PWY-3821
d-mannose degradation
-
-
D-myo-inositol (1,4,5,6)-tetrakisphosphate biosynthesis
-
-
PWY-6366
D-myo-inositol (3,4,5,6)-tetrakisphosphate biosynthesis
-
-
PWY-6365
degradation of aromatic, nitrogen containing compounds
-
-
degradation of hexoses
-
-
diacylglycerol and triacylglycerol biosynthesis
-
-
TRIGLSYN-PWY
dissimilatory sulfate reduction I (to hydrogen sufide))
-
-
DISSULFRED-PWY
Diterpenoid biosynthesis
-
-
docosahexaenoate biosynthesis III (6-desaturase, mammals)
-
-
PWY-7606
Drug metabolism - other enzymes
-
-
dZTP biosynthesis
-
-
PWY-8289
enterobactin biosynthesis
-
-
Entner Doudoroff pathway
-
-
Entner-Doudoroff pathway I
-
-
PWY-8004
ethanol degradation IV
-
-
PWY66-162
ethene biosynthesis I (plants)
-
-
ETHYL-PWY
ethene biosynthesis V (engineered)
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-
PWY-7124
Ether lipid metabolism
-
-
farnesylcysteine salvage pathway
-
-
PWY-6577
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 degradation
-
-
flavin biosynthesis I (bacteria and plants)
-
-
RIBOSYN2-PWY
flavin biosynthesis II (archaea)
-
-
PWY-6167
flavin biosynthesis III (fungi)
-
-
PWY-6168
Flavonoid biosynthesis
-
-
formaldehyde assimilation I (serine pathway)
-
-
PWY-1622
formaldehyde assimilation III (dihydroxyacetone cycle)
-
-
P185-PWY
formaldehyde oxidation
-
-
formaldehyde oxidation II (glutathione-dependent)
-
-
PWY-1801
Fructose and mannose metabolism
-
-
fusicoccin A biosynthesis
-
-
PWY-6659
GDP-mannose biosynthesis
-
-
PWY-5659
geranylgeranyl diphosphate biosynthesis
-
-
PWY-5120
gibberellin biosynthesis III (early C-13 hydroxylation)
-
-
PWY-5035
gibberellin inactivation I (2beta-hydroxylation)
-
-
PWY-102
gluconeogenesis I
-
-
GLUCONEO-PWY
gluconeogenesis III
-
-
PWY66-399
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
Glutathione metabolism
-
-
glycerol degradation to butanol
-
-
PWY-7003
Glycerolipid metabolism
-
-
Glycerophospholipid metabolism
-
-
Glycine, serine and threonine metabolism
-
-
glycogen biosynthesis
-
-
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
Glyoxylate and dicarboxylate metabolism
-
-
glyphosate degradation III
-
-
PWY-7807
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
heme b biosynthesis I (aerobic)
-
-
HEME-BIOSYNTHESIS-II
heme b biosynthesis V (aerobic)
-
-
HEME-BIOSYNTHESIS-II-1
heterolactic fermentation
-
-
P122-PWY
homocysteine and cysteine interconversion
-
-
PWY-801
hydrogen sulfide biosynthesis II (mammalian)
-
-
PWY66-426
hydroxylated fatty acid biosynthesis (plants)
-
-
PWY-6433
icosapentaenoate biosynthesis V (8-desaturase, lower eukaryotes)
-
-
PWY-7602
icosapentaenoate biosynthesis VI (fungi)
-
-
PWY-6940
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 VI (bacteria)
-
-
TRPIAACAT-PWY
indolmycin biosynthesis
-
-
PWY-7770
inosine 5'-phosphate degradation
-
-
PWY-5695
inositol diphosphates biosynthesis
-
-
PWY-6369
Inositol phosphate metabolism
-
-
isoprenoid biosynthesis
-
-
jasmonic acid biosynthesis
-
-
PWY-735
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 V (oxidative Stickland reaction)
-
-
PWY-8189
L-alanine degradation VI (reductive Stickland reaction)
-
-
PWY-8188
L-arginine biosynthesis III (via N-acetyl-L-citrulline)
-
-
PWY-5154
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 X (arginine monooxygenase pathway)
-
-
ARGDEG-V-PWY
L-ascorbate biosynthesis I (plants, L-galactose pathway)
-
-
PWY-882
L-ascorbate biosynthesis VI (plants, myo-inositol pathway)
-
-
PWY-8142
L-ascorbate biosynthesis VII (plants, D-galacturonate pathway)
-
-
PWY-8143
L-ascorbate degradation II (bacterial, aerobic)
-
-
PWY-6961
L-ascorbate degradation III
-
-
PWY-6960
L-asparagine biosynthesis I
-
-
ASPARAGINE-BIOSYNTHESIS
L-cysteine biosynthesis III (from L-homocysteine)
-
-
HOMOCYSDEGR-PWY
L-cysteine biosynthesis VI (reverse transsulfuration)
-
-
PWY-I9
L-leucine degradation I
-
-
LEU-DEG2-PWY
L-lysine biosynthesis VI
-
-
PWY-5097
L-methionine degradation III
-
-
PWY-5082
L-nicotianamine biosynthesis
-
-
PWY-5957
L-ornithine biosynthesis I
-
-
GLUTORN-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-serine biosynthesis II
-
-
PWY-8011
L-tryptophan degradation IV (via indole-3-lactate)
-
-
TRPKYNCAT-PWY
L-tryptophan degradation VIII (to tryptophol)
-
-
PWY-5081
L-tryptophan degradation XIII (reductive Stickland reaction)
-
-
PWY-8017
L-tyrosine biosynthesis I
-
-
TYRSYN
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
Linoleic acid metabolism
-
-
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 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
-
-
long chain fatty acid ester synthesis (engineered)
-
-
PWY-6873
lychnose and isolychnose biosynthesis
-
-
PWY-6524
metabolism of disaccharids
-
-
methanol oxidation to formaldehyde IV
-
-
PWY-5506
methionine metabolism
-
-
methyl indole-3-acetate interconversion
-
-
PWY-6303
methyl ketone biosynthesis (engineered)
-
-
PWY-7007
methyl phomopsenoate biosynthesis
-
-
PWY-7721
methylglyoxal degradation
-
-
methylsalicylate biosynthesis
-
-
PWY18C3-22
methylsalicylate degradation
-
-
PWY-6184
Microbial metabolism in diverse environments
-
-
mixed acid fermentation
-
-
FERMENTATION-PWY
molybdenum cofactor biosynthesis
-
-
molybdopterin biosynthesis
-
-
PWY-6823
Monobactam biosynthesis
-
-
mycolyl-arabinogalactan-peptidoglycan complex biosynthesis
-
-
PWY-6397
NADH repair (eukaryotes)
-
-
PWY-6938
NADPH repair (eukaryotes)
-
-
PWY-8137
Naphthalene degradation
-
-
nitrogen remobilization from senescing leaves
-
-
PWY-6549
nonaprenyl diphosphate biosynthesis II
-
-
PWY-6520
O-Antigen nucleotide sugar biosynthesis
-
-
oleate beta-oxidation (isomerase-dependent, yeast)
-
-
PWY-7291
oleate biosynthesis III (cyanobacteria)
-
-
PWY-7587
ophiobolin F biosynthesis
-
-
PWY-7720
Oxidative phosphorylation
-
-
palmitoyl ethanolamide biosynthesis
-
-
PWY-8055
Pantothenate and CoA biosynthesis
-
-
partial TCA cycle (obligate autotrophs)
-
-
PWY-5913
paspaline biosynthesis
-
-
PWY-7492
pectin degradation I
-
-
PWY-7246
pectin degradation II
-
-
PWY-7248
Pentose and glucuronate interconversions
-
-
Pentose phosphate pathway
-
-
pentose phosphate pathway (non-oxidative branch) II
-
-
PWY-8178
Phenylalanine metabolism
-
-
phenylalanine metabolism
-
-
Phenylalanine, tyrosine and tryptophan biosynthesis
-
-
phenylpropanoid biosynthesis
-
-
PWY-361
Phenylpropanoid biosynthesis
-
-
phenylpropanoid biosynthesis
-
-
phenylpropanoids methylation (ice plant)
-
-
PWY-7498
phosphatidate biosynthesis (yeast)
-
-
PWY-7411
phosphatidylcholine biosynthesis I
-
-
PWY3O-450
phosphatidylethanolamine bioynthesis
-
-
phospholipases
-
-
LIPASYN-PWY
phospholipid desaturation
-
-
PWY-762
photorespiration I
-
-
PWY-181
photorespiration II
-
-
PWY-8362
photorespiration III
-
-
PWY-8363
photosynthesis light reactions
-
-
PWY-101
phytochelatins biosynthesis
-
-
PWY-6745
plasmalogen biosynthesis I (aerobic)
-
-
PWY-7782
plasmalogen degradation
-
-
PWY-7783
plaunotol biosynthesis
-
-
PWY-6691
Polycyclic aromatic hydrocarbon degradation
-
-
polyhydroxydecanoate biosynthesis
-
-
PWY-6657
Porphyrin and chlorophyll metabolism
-
-
ppGpp metabolism
-
-
PPGPPMET-PWY
Propanoate metabolism
-
-
propanoyl-CoA degradation II
-
-
PWY-7574
protective electron sinks in the thylakoid membrane (PSII to PTOX)
-
-
PWY1YI0-7
protein S-nitrosylation and denitrosylation
-
-
PWY-7798
purine deoxyribonucleosides salvage
-
-
PWY-7224
purine nucleobases degradation II (anaerobic)
-
-
PWY-5497
putrescine biosynthesis I
-
-
PWY-40
putrescine biosynthesis II
-
-
PWY-43
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 metabolism
-
-
pyrimidine metabolism
-
-
pyruvate fermentation to acetate VIII
-
-
PWY-5768
pyruvate fermentation to acetoin III
-
-
PWY3O-440
pyruvate fermentation to ethanol II
-
-
PWY-5486
reactive oxygen species degradation
-
-
DETOX1-PWY-1
reductive TCA cycle I
-
-
P23-PWY
retinol biosynthesis
-
-
PWY-6857
Riboflavin metabolism
-
-
rosmarinic acid biosynthesis I
-
-
PWY-5048
rosmarinic acid biosynthesis II
-
-
PWY-5049
salicylate biosynthesis I
-
-
PWY-6406
salicylate biosynthesis II
-
-
PWY-8321
salicylate degradation I
-
-
PWY-6183
scopoletin biosynthesis
-
-
PWY-6792
selenate reduction
-
-
PWY-6932
Selenocompound metabolism
-
-
serotonin and melatonin biosynthesis
-
-
PWY-6030
solasodine glycosylation
-
-
PWY18C3-4
sophorosyloxydocosanoate deacetylation
-
-
SOPHOROSYLOXYDOCOSANOATE-DEG-PWY
spermidine biosynthesis III
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PWY-6834
spermine and spermidine degradation I
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PWY-6117
spermine and spermidine degradation III
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PWY-6441
Sphingolipid metabolism
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sphingosine and sphingosine-1-phosphate metabolism
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PWY3DJ-11470
sphingosine metabolism
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stachyose biosynthesis
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PWY-5337
stachyose degradation
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PWY-6527
Starch and sucrose metabolism
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starch biosynthesis
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PWY-622
starch degradation II
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PWY-6724
stearate biosynthesis I (animals)
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PWY-5972
stearidonate biosynthesis (cyanobacteria)
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PWY-7595
stellariose and mediose biosynthesis
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PWY-6525
stellatic acid biosynthesis
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PWY-7736
sterol biosynthesis (methylotrophs)
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PWY-8026
stigma estolide biosynthesis
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PWY-6453
Stilbenoid, diarylheptanoid and gingerol biosynthesis
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suberin monomers biosynthesis
sucrose biosynthesis I (from photosynthesis)
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SUCSYN-PWY
sucrose biosynthesis II
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PWY-7238
sucrose biosynthesis III
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PWY-7347
sucrose degradation II (sucrose synthase)
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PWY-3801
sulfate activation for sulfonation
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PWY-5340
sulfite oxidation III
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PWY-5278
superoxide radicals degradation
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DETOX1-PWY
superpathway of glucose and xylose degradation
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PWY-6901
superpathway of pyrimidine deoxyribonucleotides de novo biosynthesis (E. coli)
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PWY0-166
superpathway of UDP-glucose-derived O-antigen building blocks biosynthesis
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PWY-7328
TCA cycle I (prokaryotic)
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TCA
TCA cycle IV (2-oxoglutarate decarboxylase)
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P105-PWY
TCA cycle V (2-oxoglutarate synthase)
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PWY-6969
TCA cycle VI (Helicobacter)
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REDCITCYC
TCA cycle VII (acetate-producers)
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PWY-7254
Terpenoid backbone biosynthesis
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theophylline degradation
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PWY-6999
trehalose biosynthesis I
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TRESYN-PWY
trehalose biosynthesis V
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PWY-2661
triacylglycerol degradation
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LIPAS-PWY
Tropane, piperidine and pyridine alkaloid biosynthesis
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Tryptophan metabolism
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tryptophan metabolism
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type I lipoteichoic acid biosynthesis (S. aureus)
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PWY-7817
type IV lipoteichoic acid biosynthesis (S. pneumoniae)
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PWY-7818
Ubiquinone and other terpenoid-quinone biosynthesis
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UDP-alpha-D-galactose biosynthesis
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PWY-7344
UDP-alpha-D-glucose biosynthesis
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PWY-7343
UDP-alpha-D-glucuronate biosynthesis (from myo-inositol)
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PWY-4841
UTP and CTP de novo biosynthesis
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PWY-7176
Valine, leucine and isoleucine biosynthesis
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Valine, leucine and isoleucine degradation
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volatile benzenoid biosynthesis I (ester formation)
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PWY-4203
xyloglucan degradation II (exoglucanase)
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PWY-6807
folate polyglutamylation
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PWY-2161
folate polyglutamylation
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methylaspartate cycle
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PWY-6728
methylaspartate cycle
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suberin monomers biosynthesis
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PWY-1121
suberin monomers biosynthesis
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XDH1 is expressed in epidermal cells albeit at relatively lower levels compared with mesophyll cells
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AtGlcAK is highly expressed in flowers
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floral organs
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in anthers and in particular in anther tapetal cells, localized in the anther-filament junction site, localized in sepals, petals and pistils, but not in pollen grains
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lower expression level
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moderate to lower expression of PME31
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present in very young flower buds, later during flower development in pistils and anthers, especially in pistil walls and septum of young flowers. Anther filaments, pollen grains, nectar andguard cells of sepals are stained too, pollen staining persists during pollination and pollen tube growth
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CCR1 is expressed basipetally in the leaf, CCR1 expression is developmentally regulated in leaves,overview. Leaves on day 9 show CCR1 expression strongly at the tip, mildly in the middle, and no expression at the proximal regions
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cytosolic DHAR1 and chloroplastic DHAR3 contribute approximately equally and constitute almost all the leaf DHAR activity, while DHAR2 makes a minor contribution
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enzyme levels increase during growth and maturation at 15-26°C
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four of the GFDP synthases are targeted to the plastoglobules of the chloroplast and one is targeted to the mitochondria
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fully expanded rosette leaves
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high expression level of SAV3
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mature
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PDC2 appears to be leaf-specific
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rosette and cauline leaves, weak expression
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rosette leaves, of 35-day-old plants
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ubiquitously expressed in Arabidopsis tissues and organs
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very low expression of PME31
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isozyme SUS1
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isozyme SUS4
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in mature pollen grains during pollination and pollen tube growth
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MIOX4 is highly expressed in pollen
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MIOX5 is highly expressed in pollen
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only isozyme PPRD2
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AHK5 is most highly expressed in roots
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AtGlcAK is highly expressed in roots
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CEK1 is highly expressed in the root tips of germinating seedlings at days 1-4
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lower expression level
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PDC1 is predominantly present in roots
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Pht1;9 is highly expressed in phosphate-starved roots
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predominantly
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the enzyme is expressed specifically in roots
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ubiquitously expressed in Arabidopsis tissues and organs
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weak expression
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dry, main expression
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enzyme PME31 is highly expressed in dry seeds
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isozyme RS4 is seed-specific
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NNRD is restricted to seeds but appears to be dispensable during the normal Arabidopsis life cycle, NNRD accumulates in seeds
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the enzyme is expressed mainly in seeds
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CEK1 is highly expressed in the root tips of germinating seedlings at days 1-4
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MIOX1 is expressed preferentially in seedlings
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MIOX2 is expressed preferentially in seedlings
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Raf11 promoter activity is observed in embryos and most of the seedling tissues, except emerging leaves and root tips, Raf11 expression patterns, overview
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ubiquitously expressed in Arabidopsis tissues and organs
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UGT85A1 is mainly expressed in the early seedlings, spatial-temporal expression patterns, overview
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weak expression
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apical meristem cells
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abscission zones
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fourth siliques numbered from the top of 35-day-old plants
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green
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low expression of PME31
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moderate expression level
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high expression
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low expression of PME31
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moderate expression level
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ubiquitously expressed in Arabidopsis tissues and organs
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vegetative shoot meristem
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weak expression
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high MIOX1 expression level in syncytia, induced in roots by attack through the beet cyst nematode Heterodera schachtii, metabolome analysis of syncytium, overview
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high MIOX2 expression level in syncytia, induced in roots by attack through the beet cyst nematode Heterodera schachtii, metabolome analysis of syncytium, overview
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high MIOX4 expression level in syncytia, induced in roots by attack through the beet cyst nematode Heterodera schachtii, metabolome analysis of syncytium, overview
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high MIOX5 expression level in syncytia, induced in roots by attack through the beet cyst nematode Heterodera schachtii, metabolome analysis of syncytium, overview
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isozyme FPGS1 is preferentially expressed in vascular tissues
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transgenic ProMKK3:GUS lines show basal expression that is strongly induced by Pseudomonas syringae pv tomato strain DC3000 infection but not by abiotic stresses
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additional information
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CCR1 is a developmentally regulated gene, whose basipetally ordered expression pattern perfectly matches that of exit from the cell proliferation phase during leaf development
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additional information
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CEK1 is preferentially expressed in vegetative tissue, with roots as the primary tissue for the expression
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additional information
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enzyme expression analysis in wild-type and mutant plant organs, overview
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additional information
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expression of gene JMJ15 is relatively low and is limited to a number of tissues during vegetative growth but is higher in young floral organs. JMJ15 displays a highly tissue-specific expression pattern
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additional information
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expression of isozyme AtSLD2 is limited to flowers and siliques. AtSLD1 contributes to DELTA8 LCB desaturation in stems, flowers, leaves, siliques and roots, while isozyme AtSLD2 has a small effect on desaturation in every tissue, even in flowers and siliques, where AtSLD2 is highly expressed
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additional information
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expression pattern of AtPAO2 during seedling and flower growth and development through analysis of promoter activity in AtPAO::GUS transgenic Arabidopsis thaliana plants. AtPAO2 is mostly expressed in the quiescent center, columella initials and pollen
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expression pattern of AtPAO3 during seedling and flower growth and development through analysis of promoter activity in AtPAO::GUS transgenic Arabidopsis thaliana plants. AtPAO3 is mostly expressed in columella, guard cells and pollen
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expression pattern of AtPAO5 during seedling and flower growth and development through analysis of promoter activity in AtPAO::GUS transgenic Arabidopsis thaliana plants. AtPAO5 is mostly expressed in the vascular system of roots and hypocotyls
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additional information
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gene AtTPS1 is widely expressed throughout the plant
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high overall expression in seedling
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in non-infected wild-type plants, isozyme ADC2 expression is much higher than ADC1 expression. ADC2 expression is strongly associated with seed germination, root and leaf development
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additional information
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isozyme AtSLD1 is broadly expressed in all tissues. AtSLD1 contributes to DELTA8 LCB desaturation in stems, flowers, leaves, siliques and roots, while isozyme AtSLD2 has a small effect on desaturation in every tissue, even in flowers and siliques, where AtSLD2 is highly expressed
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isozyme TGG1 is expressed in guard cells and phloem cells and and isozyme TGG1 protein is highly abundant in guard cells. In contrast, TGG2 is only expressed in phloem-associated cells
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no expression in root hair zone
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no expression of CKI1 in seedling, roots, stem, and leaves
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additional information
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no expression of Pht1;9 in shoots
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additional information
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not in seeds, expression analysis, overview
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additional information
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PARG1 is induced primarily in mitotically active cells
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additional information
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plant growth conditions and phenotypic analysis of wild-type and mutant plants, overview
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additional information
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polyprenol reductases are expressed in a tissue-specific manner in Arabidopsis thaliana. Isozyme PPRD1 is expressed in young seedlings, while in older plants, it is mainly expressed in the roots and flowers. Expression of PPRD1 increases in the roots and decreases in the leaves. Isozyme expression analysis, overview
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polyprenol reductases are expressed in a tissue-specific manner in Arabidopsis thaliana. Isozyme PRD2 is expressed in all organs analyzed in young seedlings and older plants. With age, expression of PPRD2 is fairly constant in the roots and decreases in the leaves. Isozyme expression analysis, overview
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quantitative reverse transcription PCR enzyme expression analysis
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quantitative RT-PCR enzyme expression analysis in leaves and roots, overview
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RNR2Tso2 is more prevalent than RNR2A throughout development and in most organs, suggesting that RNR2Tso2 is the predominant RNR2 in Arabidopsis thaliana. RNR2Tso2 levels are more varied than RNR2A levels in response to environmental changes and exposure to chemicals
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RT-PCR enzyme expression analysis, overview
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SAV3 has a localized and dynamic expression pattern
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spatial distribution of endoplasmic reticulum-localized CKI1 in the syncytial embryo sac is mediated by nuclear position and migration, overview
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temporal expression pattern of DGAT1, overview. DGAT1 expression is upregulated from 3 to 96 h upon cold exposure, with levels increasing 197 and 43fold in the shoots and the roots, respectively, at 96 h
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the ADC1 promoter activity is low during vegetative development. In non-infected wild-type plants, isozyme ADC2 expression is much higher than ADC1 expression
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the AtALN promoter activity is present in specific plant tissues during plant development and is strongly repressed by salt stress
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the enzyme expression is mainly localized to unfertilized ovules present in flowers after anthesis and in green siliques, no enzyme expression in vegetative organs, e.g. root and leaf, quantitative reverse transcription-PCR expression analysis. The highest expression is detected in green siliques, tissue- and development-specific expression pattern, overview
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the enzyme expression levels gradually increase in an age-dependent manner, expression profiling, overview
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the enzyme expression levels gradually increases in an age-dependent manner, expression profiling, overview
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the enzyme is expressed in all Arabidopsis organs
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the enzyme is ubiquitously expressed in Arabidopsis tissues and organs
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the transcripts abundance of isozyme AtGALK2 is much less than that of isozyme AtGlcAK in all analyzed tissues. Except for the transcripts in seed, the expression abundance of AtGALK2 in the rest of detected tissues is always less than half the level of AtGlcAK
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tissue-specific expression, overview
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while AtTSB1 is the predominantly expressed isoform in vegetative tissues, AtTSB1 and AtTSBtype2 reach similar transcript levels in seeds, tissue-specific expression pattern, overview
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XTH30 is highly expressed in the root, flower, stem, and etiolated hypocotyl. XTH30 accumulates at high levels in root, stem, and flower but at low levels in rosette leaves and cauline leaves, real-time PCR enzyme expression analysis, expression pattern, overview
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