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(5R)-carbapenem carboxylate biosynthesis
(7Z,10Z,13Z)-hexadecatrienoate biosynthesis
-
-
PWY-7590
(9Z)-tricosene biosynthesis
-
-
PWY-7035
(S)-propane-1,2-diol degradation
-
-
PWY-7013
(S)-reticuline biosynthesis
-
-
(S)-reticuline biosynthesis I
-
-
PWY-3581
(S)-reticuline biosynthesis II
-
-
PWY-6133
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
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-arachidonoylglycerol biosynthesis
-
-
PWY-8052
2-oxoglutarate decarboxylation to succinyl-CoA
-
-
PWY-5084
3,8-divinyl-chlorophyllide a biosynthesis I (aerobic, light-dependent)
-
-
CHLOROPHYLL-SYN
3-(4-hydroxyphenyl)pyruvate biosynthesis
-
-
PWY-5886
3-dehydroquinate biosynthesis II (archaea)
-
-
PWY-6160
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
4-aminobutanoate degradation V
-
-
PWY-5022
4-coumarate degradation (aerobic)
-
-
PWY-8002
4-coumarate degradation (anaerobic)
-
-
PWY-7046
4-hydroxy-2-nonenal detoxification
-
-
PWY-7112
4-hydroxybenzoate biosynthesis I (eukaryotes)
-
-
PWY-5754
4-hydroxybenzoate biosynthesis III (plants)
-
-
PWY-6435
5-deoxystrigol biosynthesis
-
-
PWY-7101
6-gingerol analog biosynthesis (engineered)
-
-
PWY-6920
9-lipoxygenase and 9-allene oxide synthase pathway
-
-
PWY-5407
9-lipoxygenase and 9-hydroperoxide lyase pathway
-
-
PWY-5408
abscisic acid biosynthesis
-
-
PWY-695
acetaldehyde biosynthesis I
-
-
PWY-6333
acetone degradation I (to methylglyoxal)
-
-
PWY-5451
acetone degradation III (to propane-1,2-diol)
-
-
PWY-7466
acetyl CoA biosynthesis
-
-
acetyl-CoA biosynthesis from citrate
-
-
PWY-5172
acetylene degradation (anaerobic)
-
-
P161-PWY
adenosine deoxyribonucleotides de novo biosynthesis I
-
-
PWY-7227
adenosine deoxyribonucleotides de novo biosynthesis II
-
-
PWY-7220
adenosine ribonucleotides de novo biosynthesis
-
-
PWY-7219
Alanine, aspartate and glutamate metabolism
-
-
alkane oxidation
-
-
PWY-2724
allantoin degradation
-
-
allantoin degradation to glyoxylate II
-
-
PWY-5692
allantoin degradation to ureidoglycolate I (urea producing)
-
-
PWY-5697
allantoin degradation to ureidoglycolate II (ammonia producing)
-
-
PWY-5698
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
-
-
Amaryllidacea alkaloids biosynthesis
-
-
PWY-7826
Amino sugar and nucleotide sugar metabolism
-
-
Aminoacyl-tRNA biosynthesis
-
-
Aminobenzoate degradation
-
-
ammonia assimilation cycle I
-
-
PWY-6963
ammonia assimilation cycle II
-
-
PWY-6964
ammonia assimilation cycle III
-
-
AMMASSIM-PWY
ammonia oxidation II (anaerobic)
-
-
P303-PWY
anaerobic energy metabolism (invertebrates, cytosol)
-
-
PWY-7383
anandamide biosynthesis I
-
-
PWY-8051
anandamide biosynthesis II
-
-
PWY-8053
apigenin glycosides biosynthesis
-
-
PWY-6010
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
-
-
aromatic biogenic amine degradation (bacteria)
-
-
PWY-7431
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
ATP biosynthesis
-
-
PWY-7980
atrazine degradation I (aerobic)
-
-
P141-PWY
atrazine degradation III
-
-
PWY-5731
atromentin biosynthesis
-
-
PWY-7518
avenanthramide biosynthesis
-
-
PWY-8157
baicalein degradation (hydrogen peroxide detoxification)
-
-
PWY-7214
benzoate biosynthesis II (CoA-independent, non-beta-oxidative)
-
-
PWY-6444
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-D-glucuronide and D-glucuronate degradation
-
-
PWY-7247
Betalain biosynthesis
-
-
betanidin degradation
-
-
PWY-5461
betaxanthin biosynthesis
-
-
PWY-5426
betaxanthin biosynthesis (via dopamine)
-
-
PWY-5403
Bifidobacterium shunt
-
-
P124-PWY
Biosynthesis of enediyne antibiotics
-
-
Biosynthesis of secondary metabolites
-
-
Biosynthesis of unsaturated fatty acids
-
-
Bisphenol degradation
-
-
Brassinosteroid biosynthesis
-
-
bupropion degradation
-
-
PWY66-241
butanol and isobutanol biosynthesis (engineered)
-
-
PWY-7396
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
-
-
caffeoylglucarate biosynthesis
-
-
PWY-6673
Calvin-Benson-Bassham cycle
-
-
CALVIN-PWY
camalexin biosynthesis
-
-
CAMALEXIN-SYN
capsiconiate biosynthesis
-
-
PWY-6027
Carbon fixation in photosynthetic organisms
-
-
Carbon fixation pathways in prokaryotes
-
-
cardenolide glucosides biosynthesis
-
-
PWY-6036
Carotenoid biosynthesis
-
-
carotenoid biosynthesis
-
-
catecholamine biosynthesis
cellulose biosynthesis
-
-
PWY-1001
ceramide and sphingolipid recycling and degradation (yeast)
-
-
PWY-7119
ceramide degradation by alpha-oxidation
-
-
PWY66-388
chitin degradation I (archaea)
-
-
PWY-6855
chitin degradation II (Vibrio)
-
-
PWY-6902
chitin degradation III (Serratia)
-
-
PWY-7822
Chloroalkane and chloroalkene degradation
-
-
chlorobactene biosynthesis
-
-
PWY-7939
chlorogenic acid biosynthesis I
-
-
PWY-6039
chlorogenic acid biosynthesis II
-
-
PWY-6040
chlorophyll a degradation I
-
-
PWY-5098
chlorophyll a degradation II
-
-
PWY-6927
chlorophyll a degradation III
-
-
PWY-7164
chlorophyll metabolism
-
-
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
choline degradation I
-
-
CHOLINE-BETAINE-ANA-PWY
choline degradation IV
-
-
PWY-7494
cinnamoyl-CoA biosynthesis
-
-
PWY-6457
Citrate cycle (TCA cycle)
-
-
CMP phosphorylation
-
-
PWY-7205
CO2 fixation into oxaloacetate (anaplerotic)
-
-
PWYQT-4429
colanic acid building blocks biosynthesis
-
-
COLANSYN-PWY
complex N-linked glycan biosynthesis (plants)
-
-
PWY-7920
coniferin metabolism
-
-
PWY-116
coumarins biosynthesis (engineered)
-
-
PWY-7398
creatine phosphate biosynthesis
-
-
PWY-6158
cremeomycin biosynthesis
-
-
PWY-8296
curcuminoid biosynthesis
-
-
PWY-6432
Cyanoamino acid metabolism
-
-
cyclic electron flow
-
-
PWY-8270
Cysteine and methionine metabolism
-
-
cytokinin-O-glucosides biosynthesis
-
-
PWY-2902
cytosolic NADPH production (yeast)
-
-
PWY-7268
D-galactose degradation I (Leloir pathway)
-
-
PWY-6317
D-galactose detoxification
-
-
PWY-3821
d-mannose degradation
-
-
D-mannose degradation I
-
-
MANNCAT-PWY
D-mannose degradation II
-
-
PWY3O-1743
D-myo-inositol (1,4,5)-trisphosphate biosynthesis
-
-
PWY-6351
D-myo-inositol (1,4,5,6)-tetrakisphosphate biosynthesis
-
-
PWY-6366
D-myo-inositol (3,4,5,6)-tetrakisphosphate biosynthesis
-
-
PWY-6365
D-myo-inositol-5-phosphate metabolism
-
-
PWY-6367
degradation of aromatic, nitrogen containing compounds
-
-
degradation of hexoses
-
-
degradation of pentoses
-
-
degradation of sugar acids
-
-
di-homo-gamma-linolenate metabolites biosynthesis
-
-
PWY-8396
dimethylsulfoniopropanoate biosynthesis I (Wollastonia)
-
-
PWY-6054
dimethylsulfoniopropanoate biosynthesis II (Spartina)
-
-
PWY-6055
dipicolinate biosynthesis
-
-
PWY-8088
diterpene phytoalexins precursors biosynthesis
Diterpenoid biosynthesis
-
-
divinyl ether biosynthesis I
-
-
PWY-5406
divinyl ether biosynthesis II
-
-
PWY-5409
docosahexaenoate metabolites biosynthesis
-
-
PWY-8400
dopamine degradation
-
-
PWY6666-2
Drug metabolism - cytochrome P450
-
-
Drug metabolism - other enzymes
-
-
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
Entner Doudoroff pathway
-
-
Entner-Doudoroff pathway I
-
-
PWY-8004
ephedrine biosynthesis
-
-
PWY-5883
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 III (microbes)
-
-
PWY-6854
ethene biosynthesis IV (engineered)
-
-
PWY-7126
ethene biosynthesis V (engineered)
-
-
PWY-7124
Ether lipid metabolism
-
-
extended VTC2 cycle
-
-
PWY4FS-13
fatty acid alpha-oxidation I (plants)
-
-
PWY-2501
Fatty acid degradation
-
-
Fatty acid elongation
-
-
ferulate and sinapate biosynthesis
-
-
PWY-5168
Flavone and flavonol biosynthesis
-
-
flavonoid biosynthesis
-
-
PWY1F-FLAVSYN
Flavonoid biosynthesis
-
-
flavonoid biosynthesis (in equisetum)
-
-
PWY-6787
flavonoid di-C-glucosylation
-
-
PWY-7897
flavonol biosynthesis
-
-
PWY-3101
flexixanthin biosynthesis
-
-
PWY-7947
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 III (dihydroxyacetone cycle)
-
-
P185-PWY
formaldehyde oxidation
-
-
formaldehyde oxidation II (glutathione-dependent)
-
-
PWY-1801
free phenylpropanoid acid biosynthesis
-
-
PWY-2181
Fructose and mannose metabolism
-
-
GABA shunt I
-
-
GLUDEG-I-PWY
GABA shunt II
-
-
PWY-8346
galactolipid biosynthesis I
-
-
PWY-401
GDP-alpha-D-glucose biosynthesis
-
-
PWY-5661
GDP-L-galactose biosynthesis
-
-
PWY-5115
GDP-mannose biosynthesis
-
-
PWY-5659
gibberellin biosynthesis III (early C-13 hydroxylation)
-
-
PWY-5035
gibberellin inactivation I (2beta-hydroxylation)
-
-
PWY-102
ginsenoside metabolism
-
-
ginsenosides biosynthesis
-
-
PWY-5672
gliotoxin biosynthesis
-
-
PWY-7533
gluconeogenesis I
-
-
GLUCONEO-PWY
gluconeogenesis II (Methanobacterium thermoautotrophicum)
-
-
PWY-6142
gluconeogenesis III
-
-
PWY66-399
glucose and glucose-1-phosphate degradation
-
-
GLUCOSE1PMETAB-PWY
glucosylglycerol biosynthesis
-
-
PWY-7902
glutamate and glutamine metabolism
-
-
Glutathione metabolism
-
-
glutathione metabolism
-
-
glutathione-mediated detoxification I
-
-
PWY-4061
glutathione-mediated detoxification II
-
-
PWY-6842
glutathione-peroxide redox reactions
-
-
PWY-4081
glycerol degradation to butanol
-
-
PWY-7003
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, 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
-
-
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
Glycosaminoglycan degradation
-
-
Glycosphingolipid biosynthesis - ganglio series
-
-
Glyoxylate and dicarboxylate metabolism
-
-
glyoxylate assimilation
-
-
PWY-5744
grixazone biosynthesis
-
-
PWY-7153
guanosine deoxyribonucleotides de novo biosynthesis I
-
-
PWY-7226
guanosine deoxyribonucleotides de novo biosynthesis II
-
-
PWY-7222
guanosine ribonucleotides de novo biosynthesis
-
-
PWY-7221
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
heterolactic fermentation
-
-
P122-PWY
histamine degradation
-
-
PWY-6181
hydroxycinnamic acid serotonin amides biosynthesis
-
-
PWY-5473
hydroxycinnamic acid tyramine amides biosynthesis
-
-
PWY-5474
hydroxylated fatty acid biosynthesis (plants)
-
-
PWY-6433
hypotaurine degradation
-
-
PWY-7387
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
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 VI (bacteria)
-
-
TRPIAACAT-PWY
indole-3-acetate inactivation IX
-
-
PWY-1741
indolmycin biosynthesis
-
-
PWY-7770
Inositol phosphate metabolism
-
-
Insect hormone biosynthesis
-
-
inulin degradation
-
-
PWY-8314
isoleucine metabolism
-
-
isopenicillin N biosynthesis
-
-
PWY-5629
isoprenoid biosynthesis
-
-
Isoquinoline alkaloid biosynthesis
-
-
isorenieratene biosynthesis I (actinobacteria)
-
-
PWY-7938
jasmonic acid biosynthesis
-
-
PWY-735
juniperonate biosynthesis
-
-
PWY-7619
justicidin B biosynthesis
-
-
PWY-6824
kauralexin biosynthesis
-
-
PWY-6887
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 degradation I (arginase pathway)
-
-
ARGASEDEG-PWY
L-arginine degradation II (AST pathway)
-
-
AST-PWY
L-arginine degradation VI (arginase 2 pathway)
-
-
ARG-PRO-PWY
L-arginine degradation XIII (reductive Stickland reaction)
-
-
PWY-8187
L-ascorbate biosynthesis I (plants, L-galactose pathway)
-
-
PWY-882
L-ascorbate biosynthesis II (plants, L-gulose pathway)
-
-
PWY4FS-11
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-aspartate degradation II (aerobic)
-
-
PWY-8291
L-aspartate degradation III (anaerobic)
-
-
PWY-8294
L-citrulline biosynthesis
-
-
CITRULBIO-PWY
L-cysteine biosynthesis I
-
-
CYSTSYN-PWY
L-dopa degradation II (bacterial)
-
-
PWY-8110
L-glutamate biosynthesis IV
-
-
GLUGLNSYN-PWY
L-glutamate biosynthesis V
-
-
PWY-4341
L-glutamate degradation I
-
-
GLUTAMATE-DEG1-PWY
L-glutamate degradation IX (via 4-aminobutanoate)
-
-
PWY0-1305
L-glutamate degradation V (via hydroxyglutarate)
-
-
P162-PWY
L-glutamate degradation XI (reductive Stickland reaction)
-
-
PWY-8190
L-glutamine biosynthesis I
-
-
GLNSYN-PWY
L-glutamine degradation II
-
-
GLUTAMINEFUM-PWY
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 degradation II
-
-
PWY-5078
L-leucine biosynthesis
-
-
LEUSYN-PWY
L-leucine degradation I
-
-
LEU-DEG2-PWY
L-leucine degradation III
-
-
PWY-5076
L-lysine biosynthesis I
-
-
DAPLYSINESYN-PWY
L-lysine biosynthesis II
-
-
PWY-2941
L-lysine biosynthesis III
-
-
PWY-2942
L-lysine biosynthesis VI
-
-
PWY-5097
L-lysine degradation I
-
-
PWY0-461
L-lysine degradation X
-
-
PWY-6328
L-methionine biosynthesis IV
-
-
PWY-7977
L-methionine degradation III
-
-
PWY-5082
L-Ndelta-acetylornithine biosynthesis
-
-
PWY-6922
L-nicotianamine biosynthesis
-
-
PWY-5957
L-ornithine biosynthesis II
-
-
ARGININE-SYN4-PWY
L-phenylalanine biosynthesis I
-
-
PHESYN
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 III (from L-ornithine)
-
-
PWY-3341
L-proline degradation I
-
-
PROUT-PWY
L-serine biosynthesis II
-
-
PWY-8011
L-tryptophan degradation IV (via indole-3-lactate)
-
-
TRPKYNCAT-PWY
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 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
L-valine biosynthesis
-
-
VALSYN-PWY
L-valine degradation II
-
-
PWY-5057
lanosterol biosynthesis
-
-
PWY-6132
leucodelphinidin biosynthesis
-
-
PWY-5152
leucopelargonidin and leucocyanidin biosynthesis
-
-
PWY1F-823
Limonene and pinene degradation
-
-
limonene degradation IV (anaerobic)
-
-
PWY-8029
linoleate metabolites biosynthesis
-
-
PWY-8395
Linoleic acid metabolism
-
-
lipid A-core biosynthesis (E. coli K-12)
-
-
LIPA-CORESYN-PWY
lipoate biosynthesis and incorporation II
-
-
PWY0-1275
Lipoic acid metabolism
-
-
lutein biosynthesis
-
-
PWY-5947
luteolin biosynthesis
-
-
PWY-5060
luteolin glycosides biosynthesis
-
-
PWY-6239
luteolin triglucuronide degradation
-
-
PWY-7445
lychnose and isolychnose biosynthesis
-
-
PWY-6524
mannitol biosynthesis
-
-
PWY-3881
mannitol degradation II
-
-
PWY-3861
maresin biosynthesis
-
-
PWY-8356
matairesinol biosynthesis
-
-
PWY-5466
melatonin degradation I
-
-
PWY-6398
metabolism of disaccharids
-
-
Metabolism of xenobiotics by cytochrome P450
-
-
Methanobacterium thermoautotrophicum biosynthetic metabolism
-
-
PWY-6146
methanofuran biosynthesis
-
-
PWY-5254
methanol oxidation to formaldehyde IV
-
-
PWY-5506
methionine metabolism
-
-
methyl indole-3-acetate interconversion
-
-
PWY-6303
methylerythritol phosphate pathway I
-
-
NONMEVIPP-PWY
methylerythritol phosphate pathway II
-
-
PWY-7560
methylglyoxal degradation
-
-
methylglyoxal degradation I
-
-
PWY-5386
methylglyoxal degradation VIII
-
-
PWY-5386-1
methylsalicylate degradation
-
-
PWY18C3-24
Microbial metabolism in diverse environments
-
-
mitochondrial NADPH production (yeast)
-
-
PWY-7269
mixed acid fermentation
-
-
FERMENTATION-PWY
momilactone A biosynthesis
-
-
PWY-7477
Monobactam biosynthesis
-
-
mRNA capping I
-
-
PWY-7375
mycolate biosynthesis
-
-
PWYG-321
mycolyl-arabinogalactan-peptidoglycan complex biosynthesis
-
-
PWY-6397
myxol-2' fucoside biosynthesis
-
-
PWY-6279
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 V (PNC V cycle)
-
-
PWY3O-4107
NAD(P)/NADPH interconversion
-
-
PWY-5083
NADP biosynthesis
-
-
PWY-8148
NADPH to cytochrome c oxidase via plastocyanin
-
-
PWY-8271
Naphthalene degradation
-
-
naringenin biosynthesis (engineered)
-
-
PWY-7397
naringenin C-glucosylation
-
-
PWY-6602
Neomycin, kanamycin and gentamicin biosynthesis
-
-
Nicotinate and nicotinamide metabolism
-
-
nicotine degradation IV
-
-
PWY66-201
nicotine degradation V
-
-
PWY66-221
nitrate reduction I (denitrification)
-
-
DENITRIFICATION-PWY
nitrate reduction II (assimilatory)
-
-
PWY-381
nitrate reduction VII (denitrification)
-
-
PWY-6748
nitric oxide biosynthesis II (mammals)
-
-
PWY-4983
nitrifier denitrification
-
-
PWY-7084
nitrite-dependent anaerobic methane oxidation
-
-
PWY-6523
nitrogen remobilization from senescing leaves
-
-
PWY-6549
nocardicin A biosynthesis
-
-
PWY-7797
noradrenaline and adrenaline degradation
-
-
PWY-6342
norspermidine biosynthesis
-
-
PWY-6562
nucleoside and nucleotide degradation (archaea)
-
-
PWY-5532
O-Antigen nucleotide sugar biosynthesis
-
-
o-diquinones biosynthesis
-
-
PWY-6752
octopamine biosynthesis
-
-
PWY-7297
okenone biosynthesis
-
-
PWY-7591
oleandomycin activation/inactivation
-
-
PWY-6972
One carbon pool by folate
-
-
orientin and isoorientin biosynthesis I
-
-
PWY-7188
oryzalide A biosynthesis
-
-
PWY-7481
Other glycan degradation
-
-
oxidative decarboxylation of pyruvate
-
-
Oxidative phosphorylation
-
-
oxidative phosphorylation
-
-
Pantothenate and CoA biosynthesis
-
-
pantothenate biosynthesis
-
-
parkeol biosynthesis
-
-
PWY-8027
partial TCA cycle (obligate autotrophs)
-
-
PWY-5913
Penicillin and cephalosporin biosynthesis
-
-
pentachlorophenol degradation
-
-
PCPDEG-PWY
Pentose and glucuronate interconversions
-
-
Pentose phosphate pathway
-
-
pentose phosphate pathway
-
-
pentose phosphate pathway (oxidative branch) I
-
-
OXIDATIVEPENT-PWY
peptido-conjugates in tissue regeneration biosynthesis
-
-
PWY-8355
peptidoglycan recycling I
-
-
PWY0-1261
phaselate biosynthesis
-
-
PWY-6320
Phenylalanine metabolism
-
-
phenylalanine metabolism
-
-
phenylethanol biosynthesis
-
-
PWY-5751
phenylpropanoid biosynthesis
-
-
PWY-361
Phenylpropanoid biosynthesis
-
-
phenylpropanoid biosynthesis
-
-
phenylpropanoid biosynthesis, initial reactions
-
-
PWY1F-467
phenylpropanoids methylation (ice plant)
-
-
PWY-7498
phosalacine biosynthesis
-
-
PWY-7769
phosphatidate metabolism, as a signaling molecule
-
-
PWY-7039
phosphatidylcholine acyl editing
-
-
PWY-6803
phosphatidylethanolamine bioynthesis
-
-
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
phytate degradation I
-
-
PWY-4702
phytochelatins biosynthesis
-
-
PWY-6745
phytol degradation
-
-
PWY66-389
pinocembrin C-glucosylation
-
-
PWY-7189
plasmalogen degradation
-
-
PWY-7783
plastoquinol-9 biosynthesis I
-
-
PWY-1581
platensimycin biosynthesis
-
-
PWY-8179
polyphosphate metabolism
-
-
PWY-8138
Porphyrin and chlorophyll metabolism
-
-
ppGpp metabolism
-
-
PPGPPMET-PWY
proline to cytochrome bo oxidase electron transfer
-
-
PWY0-1544
protectin biosynthesis
-
-
PWY-8357
protective electron sinks in the thylakoid membrane (PSII to PTOX)
-
-
PWY1YI0-7
protein S-nitrosylation and denitrosylation
-
-
PWY-7798
protein ubiquitination
-
-
PWY-7511
psilocybin biosynthesis
-
-
PWY-7936
purine deoxyribonucleosides salvage
-
-
PWY-7224
purine nucleobases degradation II (anaerobic)
-
-
PWY-5497
putrescine degradation I
-
-
PUTDEG-PWY
putrescine degradation III
-
-
PWY-0
putrescine degradation IV
-
-
PWY-2
putrescine degradation V
-
-
PWY-3
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 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 (S)-acetoin
-
-
PWY-6389
pyruvate fermentation to ethanol I
-
-
PWY-5480
pyruvate fermentation to ethanol II
-
-
PWY-5486
pyruvate fermentation to ethanol III
-
-
PWY-6587
pyruvate fermentation to isobutanol (engineered)
-
-
PWY-7111
reactive oxygen species degradation
-
-
DETOX1-PWY-1
reductive TCA cycle I
-
-
P23-PWY
resolvin D biosynthesis
-
-
PWY66-397
resveratrol biosynthesis
-
-
PWY-84
retinol biosynthesis
-
-
PWY-6857
rosmarinic acid biosynthesis I
-
-
PWY-5048
Rubisco shunt
-
-
PWY-5723
S-methyl-5-thio-alpha-D-ribose 1-phosphate degradation I
-
-
PWY-4361
salidroside biosynthesis
-
-
PWY-6802
saponin biosynthesis II
-
-
PWY-5756
sciadonate biosynthesis
-
-
PWY-6598
secologanin and strictosidine biosynthesis
-
-
PWY-5290
seleno-amino acid biosynthesis (plants)
-
-
PWY-6936
serotonin and melatonin biosynthesis
-
-
PWY-6030
serotonin degradation
-
-
PWY-6313
sesamin biosynthesis
-
-
PWY-5469
Sesquiterpenoid and triterpenoid biosynthesis
-
-
solasodine glycosylation
-
-
PWY18C3-4
spermidine biosynthesis I
-
-
BSUBPOLYAMSYN-PWY
spermidine biosynthesis II
-
-
PWY-6559
spermidine biosynthesis III
-
-
PWY-6834
spermine and spermidine degradation I
-
-
PWY-6117
spermine and spermidine degradation III
-
-
PWY-6441
spermine biosynthesis
-
-
ARGSPECAT-PWY
Sphingolipid metabolism
-
-
sphingosine and sphingosine-1-phosphate metabolism
-
-
PWY3DJ-11470
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
stearate biosynthesis I (animals)
-
-
PWY-5972
stellariose and mediose biosynthesis
-
-
PWY-6525
Steroid hormone biosynthesis
-
-
sterol biosynthesis (methylotrophs)
-
-
PWY-8026
Stilbenoid, diarylheptanoid and gingerol biosynthesis
-
-
Streptomycin biosynthesis
-
-
suberin monomers biosynthesis
sucrose biosynthesis I (from photosynthesis)
-
-
SUCSYN-PWY
sucrose biosynthesis II
-
-
PWY-7238
sucrose biosynthesis III
-
-
PWY-7347
sucrose degradation II (sucrose synthase)
-
-
PWY-3801
sucrose degradation III (sucrose invertase)
-
-
PWY-621
sucrose degradation V (sucrose alpha-glucosidase)
-
-
PWY66-373
superoxide radicals degradation
-
-
DETOX1-PWY
superpathway of fermentation (Chlamydomonas reinhardtii)
-
-
PWY4LZ-257
superpathway of glucose and xylose degradation
-
-
PWY-6901
superpathway of indole-3-acetate conjugate biosynthesis
-
-
PWY-1782
superpathway of methylsalicylate metabolism
-
-
PWY18C3-25
superpathway of phospholipid biosynthesis II (plants)
-
-
PHOSLIPSYN2-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
-
-
TCA cycle II (plants and fungi)
-
-
PWY-5690
TCA cycle III (animals)
-
-
PWY66-398
Terpenoid backbone biosynthesis
-
-
tetrahydrofolate biosynthesis I
-
-
PWY-6614
tetrahydrofolate metabolism
-
-
thyroid hormone metabolism II (via conjugation and/or degradation)
-
-
PWY-6261
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
triacylglycerol degradation
-
-
LIPAS-PWY
tricin biosynthesis
-
-
PWY-7995
tRNA charging
-
-
TRNA-CHARGING-PWY
tRNA processing
-
-
PWY0-1479
Tryptophan metabolism
-
-
tryptophan metabolism
-
-
type I lipoteichoic acid biosynthesis (S. aureus)
-
-
PWY-7817
Ubiquinone and other terpenoid-quinone biosynthesis
-
-
UDP-alpha-D-galactose biosynthesis
-
-
PWY-7344
UDP-alpha-D-glucose biosynthesis
-
-
PWY-7343
UDP-GlcNAc biosynthesis
-
-
UDP-N-acetyl-D-galactosamine biosynthesis II
-
-
PWY-5514
UDP-N-acetyl-D-glucosamine biosynthesis I
-
-
UDPNAGSYN-PWY
UDP-N-acetyl-D-glucosamine biosynthesis II
-
-
UDPNACETYLGALSYN-PWY
ultra-long-chain fatty acid biosynthesis
-
-
PWY-8041
umbelliferone biosynthesis
-
-
PWY-6982
urea degradation II
-
-
PWY-5704
UTP and CTP de novo biosynthesis
-
-
PWY-7176
Valine, leucine and isoleucine biosynthesis
-
-
Valine, leucine and isoleucine degradation
-
-
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
Vitamin B6 metabolism
-
-
vitamin E biosynthesis (tocopherols)
-
-
PWY-1422
vitamin E biosynthesis (tocotrienols)
-
-
PWY-7436
xanthohumol biosynthesis
-
-
PWY-5135
xanthommatin biosynthesis
-
-
PWY-8249
xyloglucan degradation II (exoglucanase)
-
-
PWY-6807
(5R)-carbapenem carboxylate biosynthesis
-
-
PWY-5737
(5R)-carbapenem carboxylate biosynthesis
-
-
catecholamine biosynthesis
-
-
PWY66-301
catecholamine biosynthesis
-
-
cyanate degradation
-
-
CYANCAT-PWY
diterpene phytoalexins precursors biosynthesis
-
-
PWY-2981
diterpene phytoalexins precursors biosynthesis
-
-
folate polyglutamylation
-
-
PWY-2161
folate polyglutamylation
-
-
methylaspartate cycle
-
-
PWY-6728
methylaspartate cycle
-
-
octane oxidation
-
-
P221-PWY
suberin monomers biosynthesis
-
-
PWY-1121
suberin monomers biosynthesis
-
-
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.
high expression level
brenda
-
brenda
-
brenda
isoform AO1 is expressed in the developing rice grains at 1, 7, and 21 days after flowering
brenda
PGL, encoding chlorophyllide a oxygenase 1, is mainly expressed in the chlorenchyma
brenda
-
-
brenda
-
brenda
-
brenda
-
brenda
-
-
brenda
moderate expression level
brenda
-
brenda
high expression
brenda
highest expression in the leaf, followed by the pod and the panicle
brenda
-
brenda
-
brenda
-
-
brenda
-
brenda
-
brenda
-
brenda
and endosperm, main expression site
brenda
OsGA3ox1 is specifically expressed in the late developmental stages of anthers
brenda
the enzyme is specifically expressed in the tapetum of anthers
brenda
-
brenda
lowest expression
brenda
-
brenda
and anther, main expression site
brenda
constitutively expressed with a high expression in developing endosperm
brenda
moderate expression
brenda
OsGLN1,1, under nitrogen-limited condition
brenda
OsGLN1,2, under nitrogen-sufficient condition
brenda
OsGLN1,1, under nitrogen-limited condition
brenda
OsGLN1,2, under nitrogen-sufficient condition
brenda
-
brenda
high expression level
brenda
-
highest expression
brenda
-
brenda
moderate expression
brenda
especially the uppermost
brenda
high expression level
brenda
isozyme OsPSS-1 gene is expressed predominantly in elongating cells
brenda
-
brenda
grain tocotrienol and HGGT levels increase in the early stage and then reach a plateau
brenda
A0A0P0W2E0, A0A0P0X1V6, A0A0P0XHN6, A4KAG8, B7F7B9, B9FLJ1, O24174, P0C0L0, P0C0L1, P14656, Q0DF89, Q0DWQ1, Q0DWY3, Q0IMS5, Q0JA75, Q0JC10, Q0JEQ2, Q0JGK4, Q0JKD0, Q0JR55, Q10L32, Q10M74, Q10N21, Q10PV5, Q10RT5, Q2QPW1, Q2QQJ5, Q2QWM9, Q2QWU2, Q2QXY1, Q2RAP0, Q53JI9, Q53WJ1, Q5JK52, Q5VP94, Q5Z8T8, Q65XA0, Q67WN8, Q68YV7, Q68YV9, Q69RJ0, Q69SV0, Q6BDZ9, Q6F6A2, Q6GZ42, Q6YV04, Q6Z2T6, Q6Z5J6, Q6Z9A3, Q6ZD89, Q6ZFJ3, Q6ZHS4, Q6ZHZ1, Q6ZJ97, Q6ZJJ1, Q7XJ02, Q7XWU3, Q7XXN4, Q84JH5, Q84LK3, Q84NP3, Q941T9, Q948T6, Q9FE01, Q9FTU1, Q9LI00, Q9SDJ2
-
676582, 694574, 694713, 706253, 711072, 720763, 726482, 728470, 728501, 728513, 730617, 736578, 738614, 738765, 738913, 739330, 739446, 741174, 742734, 743294, 745635, 746126, 746218, 746502, 746596, 746981, 748914, 755243, 756811, 757363, 757484, 758040, 758975, 759938, 759948, 760794, 760795, 761175, 761209, 761954, 762190, 762849, 763103, 764578, 764775, 764795, 765156, 765584, 765632, 765656
brenda
expressed at high levels in developing leaves, expression decreases dramatically in fully mature leaves
brenda
expression is high in leaf
brenda
expression is relatively constant throughout leaf development
brenda
FC1 is expressed slightly more at the seedling stage than at the heading stage
brenda
high light-induced expression level
brenda
highe transcript level was observed in the leaf blade and leaf sheath during the different developmental stages
brenda
highest expression among the tissues tested. In plants carrying the Zebra leaf mutation, yellow and green striped leaves appear at the seedling stage and gradually turn pale green towards the end of the tillering stage
brenda
highest expression in mature leaves
brenda
highest expression of isoform VTC1-1
brenda
highly expressed
brenda
highly expressed in leaf and leaf sheath
brenda
in 15 DAG seedlings, mature full-length OsGolS1 is expressed only in leaf sheath of etiolated plants. In contrast, the q-PCR indicative of pre-mRNA accumulation relative to actin (housekeeping gene) expression shows a strikingly different profile. The pre-mRNA of OsGolS1 is accumulated in the leaf tissue of etiolated plants at a high level, about fourfold to the accumulation of actin. In one-month-old plants, mature OsGolS1 is found only in leaf sheath
brenda
in one-month-old plants mature OsGolS1 is found only in leaf sheath, OsGolS2 shows both mature and pre-mRNA in sheath. OsGolS2 pre-mRNA is expressed 25fold in leaf sheath
brenda
leaf and sheath, predominant expression
brenda
leaf sheath
brenda
low expression level
brenda
low expression level at blade sheath, high expression level at blade ear
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of seedling
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OsAS2 mRNA is abundant in leaf blades and sheathes of rice
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OsDXR is strongly expressed in the leaves of both developmental stages, high overall expression level in leaves
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-
predominant expression
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predominant expression, abundantly expressed in leaves and leaf sheaths
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preferential expression in the leaf sheath
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produced at high levels in leaf mesophyll cells
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KY366226
young leaves
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-
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high expression
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highe transcript level was observed in the leaf blade and leaf sheath during the different developmental stages
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highest activity in outer leaf sheaths and lowest in inner leaf sheaths
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highly expressed in leaf and leaf sheath
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-
-
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expressed at the reproductive stage
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high expression in nodes
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A0A5S6R7K3, P0C0L0, P0C0L1, Q0DWY3, Q0JA75, Q0JEQ2, Q0JR55, Q10N21, Q40710, Q5JK52, Q69SV0, Q6ZHS4, Q6ZJJ1, Q7XJ02, Q7XWU3, Q851K9, Q8S7E1, Q9FE01
-
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highest expression in the leaf, followed by the pod and the panicle
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-
highest expression of isoform CCR19
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-
young panicle
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-
-
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OsUAM1 and OsUAM2 are expressed ubiquitously throughout plant development, but OsUAM3 is expressed primarily in reproductive tissue, particularly at the pollen cell wall formation developmental stage
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A0A0F7QZZ2, A0A1Q2SVY7, A0A5S6R7K3, A3BE68, B7F7B9, B9FDB8, P0C0L0, P0C0L1, P14654, P14656, Q0DI55, Q0DWH1, Q0IMS5, Q0JA75, Q0JEQ2, Q0JGK4, Q0JR55, Q10CE4, Q10L32, Q10N21, Q10PV5, Q40710, Q4W8D0, Q53JI9, Q5JK52, Q5MBR3, Q5Z8T8, Q67WN8, Q69SV0, Q6H5L4, Q6Z9A3, Q6ZHS4, Q6ZHZ1, Q6ZJJ1, Q7FAS1, Q7XJ02, Q7XWU3, Q84JH5, Q8H3I4, Q8LNZ3, Q8W250, Q941T9, Q9FE01, Q9FWQ2, Q9LI00
-
679760, 720763, 728465, 728470, 739330, 739446, 746968, 748914, 749149, 751680, 756836, 757362, 758040, 758975, 759634, 759938, 760001, 761209, 761954, 761983, 762190, 762869, 762871, 763328, 764578, 764775, 765616, 765632, 765656
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expressed in roots at the vegetative growth stage, expressed in the outer cortex and the vascular cylinder in the root mature zone
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expression is high in root
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FC1 is expressed slightly more at the seedling stage than at the heading stage
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gene OsEGL1 is expressed in seedling, and young and adult plant roots
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high dark-induced expression level
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-
high expression
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high expression level
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-
highest expression of isoform CCR20 and CCR21
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highest expression of isoform VTC1-3
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isoform DGK1 is highly expressed in roots
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low expression level
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NADH-GOGAT is primarily located in plastids of non-photosynthetic tissues such as roots
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OsAS2 mRNA is detectable in the roots, its content decreases when NH+4 is supplied
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OscZOG1 is highly expressed in primary root meristem and lateral root primordia in rice
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OsGLN1,1 is expressed in epidermis and exodermis under nitrogen-limited condition. Within the central cylinder of the elongating zone the enzyme is induced by ammonium
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OsGLN1,2 is expressed in epidermis and exodermis under nitrogen-sufficient condition. Within the central cylinder of the elongating zone the enzyme is induced by ammonium
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OsGS1;2 gene is mainly expressed in surface cells of roots
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root surface cell-specific expression of OsAS1 gene. OsAS1 is mainly expressed in the roots, with in situ hybridization showing that the corresponding mRNA is specifically accumulated in the three cell layers of the root surface (epidermis, exodermis and sclerenchyma) in an NH4+-dependent manner
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very low enzyme content
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weakly expressed
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A0A1Q2SVY7, A0A224ASC9, B7EJX7, B7F7B9, D6QSX9, O24174, P0C0L0, P0C0L1, Q0DI55, Q0JEQ2, Q0JGK4, Q10L32, Q10N21, Q2QWU2, Q2QXY1, Q2QXY9, Q2RAP0, Q2RAP8, Q53JI9, Q5VP94, Q5VRI1, Q67WN8, Q69SV0, Q6YV04, Q6ZHZ1, Q6ZJJ1, Q76I22, Q7XJ02, Q84LK3, Q8W250, Q9FE01
-
711072, 716618, 720763, 742051, 745635, 748914, 757670, 757963, 759935, 759962, 762849, 762871, 764578, 765656
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expressed predominantly in the developing seeds of black rice and not in those of white and red rice
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highest expression
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low expression
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predominantly expressed in developing seeds during active starch synthesis
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quantitative RT-PCR enzyme expression analysis shows that the expression of OsIAGLU is relatively higher in the late developing and the early germinating seeds
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A0A0P0W2E0, A0A1Q2SVY7, A0A224ASC9, A0A5S6R7K3, B7EJX7, B9EZV5, P0C0L0, P0C0L1, P14656, Q0DI55, Q0DWY3, Q0JB48, Q0JEQ2, Q0JR55, Q10L32, Q10MX3, Q10N21, Q2QWM9, Q2QWU2, Q40710, Q43011, Q53WJ1, Q5JNT6, Q5UAW3, Q5VP94, Q5VRI1, Q5Z8T8, Q69SV0, Q6H5L4, Q6YV04, Q6Z2T6, Q6ZJ97, Q6ZJJ1, Q76I22, Q7XJ02, Q7XQT2, Q7XSZ0, Q7XU02, Q7XU03, Q851G2, Q851K9, Q8LNZ3, Q9FE01, Q9FTU1, Q9SDJ2, U5LY03
-
709317, 709698, 711072, 723476, 728470, 736599, 738765, 739446, 741174, 743320, 743426, 746041, 746112, 746144, 746218, 746244, 746502, 748914, 749149, 751680, 755243, 758063, 759634, 759935, 759938, 759948, 759954, 760001, 761175, 762025, 764578, 765584, 765656
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highest expression in aerial part of 2-week-old seedlings
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A0A5S6R7K3, B7F7B9, B9FDB8, Q0JA75, Q0JGK4, Q2QWU2, Q40710, Q53JI9, Q5VP94, Q67WN8, Q6YV04, Q6ZHS4, Q6ZHZ1, Q7XSZ0, Q7XWU3, Q8LNZ3, Q9FWQ2
-
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-
highest expression of isoform CCR17
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-
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low expression level
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P14656, Q0JA75, Q10CE4, Q10PV5, Q5MBR3, Q5Z8T8, Q6ZHS4, Q7FAS1, Q7XWU3, Q8H3I4, Q9SDJ2
-
728470, 746218, 757362, 758040, 759938, 761954, 762869, 763103, 764775, 764795, 765616
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FC1 is expressed slightly more at the seedling stage than at the heading stage. At the heading stage, a strong FC1 expression level in the first internode
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high expression
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low expression level
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moderate expression level
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very low content
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additional information
-
(R)-beta-tyrosine occurs in the seeds, leaves, roots, and root exudates of the Nipponbare cultivar. Dry rice seeds from plants that have not been elicited with jasmonic acid also contain significant amounts of beta-tyrosine. When rice seedlings are grown hydroponically, beta-tyrosine is secreted into the medium
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additional information
-
BC12 is mainly expressed in tissues undergoing cell division and secondary wall thickening
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additional information
cultivar/tissue specific expression of r9-LOX1, the expression is generally much higher in active bran/seed than in stabilized bran, mature seeds, and regenerated plants
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additional information
eight APX isozymes are expressed differently in root, leaf, panicle, anther, pistil and seed
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additional information
eight APX isozymes are expressed differently in root, leaf, panicle, anther, pistil and seed. High expression level of isozyme OsAPX1
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additional information
eight APX isozymes are expressed differently in root, leaf, panicle, anther, pistil and seed. High expression level of isozyme OsAPX2
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additional information
Q10RT5
enzyme expression analysis in different tissues of rice
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additional information
enzyme expression analysis in in leaves and roots of the vegetative stage and in leaves, roots, florets, and seeds of the reproductive stage, expression patterns, overview
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additional information
enzyme expression in relation to N levels in roots and shoots, overview
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additional information
enzyme is constitutively expressed in all tested tissues under normal growth conditions
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additional information
expressed in all tested tissues and organs, with the highest expression in the leaf, followed by the pod and the panicle. Lowest expression in stem and the root
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additional information
expression pattern of OsIAGLU in various developmental and germination stages in rice using quantitative RT-PCR approach
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additional information
gene is expressed at a low level in all of the examined tissues
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additional information
gene OsCRD1 is mainly expressed in green tissues, including stem, leaf, tassel and sheath, but not in root
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additional information
increase in OsTPP7 expression between 2 and 4 days of growth in the dark under submergence, elevated expression under submergence and an absence of OsTPP7 expression in leaves. Anaerobic germination is tolerated through the presence of a functional OsTPP7 gene
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additional information
isozyme OsAS1 mRNA is the major species in rice roots when the seedlings are hydroponically grown for 18 d after germination with water
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additional information
KAO is broadly expressed in many organs and tissues
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additional information
low constitutive expression of Osr9-LOX1 in rice leaves, stems, and spikelets, but high constitutive expression in roots, expression analysis
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additional information
main expression in sclerenchyma cell of secondary cell wall and vascular bundle region. Panicle, at the heading stage, show strong FC1 expression level
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additional information
mRNA and protein contents of GS isoforms, overview
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additional information
OsAS1 mRNA is the major species in rice roots when the seedlings are hydroponically grown for 18 d after germination with water
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additional information
OscZOG1 is preferentially expressed in shoot and root meristematic tissues and nascent organs
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additional information
OsMSRB5 is mainly expressed in leaves, with low transcriptional levels of OsMSRB5 observed in seeds, stems, and roots
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additional information
OsNADK1 functions in the whole plant and in all developmental stages
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additional information
OsUAM3 coexpression networks include pectin catabolic enzymes. Co-expression network in silico analysis, quantitative RT-PCR analysis of OsUAM isozymes gene expression in various organs at different developmental stages, overview
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additional information
OsVTC1-8 transcript level is low in both leaves and roots
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additional information
plant-wide developmental and tissue-specific profile of isozymes OsGolS1 and OsGolS2 functional expression, overview. In 3-month-old plants, mature OsGolS1 is found in late panicle, shoot, and also in root tissue with a precursor
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additional information
plant-wide developmental and tissue-specific profile of isozymes OsGolS1 and OsGolS2 functional expression, overview. OsGolS2 pre-mRNA is expressed in all light-grown tissue, ranging from 25fold in leaf sheath to twofold in the root compared to actin. The etiolated plants also show high accumulation of pre-mRNA in roots. In one-month-old plants mature OsGolS1 is found only in leaf sheath, OsGolS2 shows both mature and pre-mRNA in sheath. OsGolS2 is not found in 3-month-old plants
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additional information
predominantly expressed in elongating cells
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additional information
quantitative reverse transcription polymerase chain reaction (qRT-PCR) analyses of wild-type plants reveals that OsPSS-1 is expressed in various organs, including roots, culms, and leaves, with the highest expression in panicles
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additional information
the enzyme is ubiquitously distributed in the plant. Relatively higher expression of OsMKK4/SMG1 is detected in younger organs than in older ones
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additional information
the expression level of isozyyme OsPCS2 is higher than that of isozyme OsPCS1 in the shoots and roots of rice plants
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additional information
the expression level of isozyyme OsPCS2 is higher than that of isozyme OsPCS1 in the shoots and roots of rice plants. The expression pattern of OsPCS1 splice variants is not changed by Cd or As stress in both shoots and roots
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additional information
tissue specificity and diurnal change in gene expression of the sucrose phosphate synthase gene family, overview. Isozyme comparison: gene SPS1 is preferentially expressed in source tissues, whereas genes SPS2, SPS6, and SPS8 are expressed equally in source and sink tissues, mRNA levels of SPS1, SPS8, and SPS11 are considerably higher in seeds than in shoots and roots
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additional information
YSL1 is expressed mainly in photosynthetic tissues and organs, almost no expression is detected in root, and its encoded protein is transported into the chloroplast with a signal peptide
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