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(S)-reticuline biosynthesis
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(S)-reticuline biosynthesis I
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PWY-3581
2,3-cis-flavanols biosynthesis
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PWY-6035
2,3-trans-flavanols biosynthesis
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PWY-6029
4-hydroxy-2-nonenal detoxification
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PWY-7112
adenosine ribonucleotides de novo biosynthesis
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PWY-7219
Arginine and proline metabolism
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Arginine biosynthesis
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Ascorbate and aldarate metabolism
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avenanthramide biosynthesis
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PWY-8157
bacterial bioluminescence
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PWY-7723
baicalein degradation (hydrogen peroxide detoxification)
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PWY-7214
benzoate biosynthesis II (CoA-independent, non-beta-oxidative)
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PWY-6444
betanidin degradation
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PWY-5461
Biosynthesis of secondary metabolites
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camalexin biosynthesis
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CAMALEXIN-SYN
Carbon fixation in photosynthetic organisms
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chlorogenic acid biosynthesis I
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PWY-6039
chlorogenic acid biosynthesis II
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PWY-6040
cinnamoyl-CoA biosynthesis
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PWY-6457
creatine phosphate biosynthesis
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PWY-6158
Cysteine and methionine metabolism
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Drug metabolism - cytochrome P450
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Drug metabolism - other enzymes
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ephedrine biosynthesis
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PWY-5883
ethanol degradation IV
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PWY66-162
ethene biosynthesis III (microbes)
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PWY-6854
Flavonoid biosynthesis
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flavonoid biosynthesis (in equisetum)
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PWY-6787
flavonol biosynthesis
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PWY-3101
gliotoxin biosynthesis
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PWY-7533
glutathione biosynthesis
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GLUTATHIONESYN-PWY
Glutathione metabolism
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glutathione metabolism
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glutathione-mediated detoxification I
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PWY-4061
glutathione-mediated detoxification II
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PWY-6842
glutathione-peroxide redox reactions
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PWY-4081
Glycine, serine and threonine metabolism
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Glycolysis / Gluconeogenesis
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Glyoxylate and dicarboxylate metabolism
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homocysteine and cysteine interconversion
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PWY-801
hydrogen sulfide biosynthesis II (mammalian)
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PWY66-426
indole glucosinolate activation (intact plant cell)
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PWYQT-4477
Isoquinoline alkaloid biosynthesis
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justicidin B biosynthesis
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PWY-6824
L-ascorbate degradation II (bacterial, aerobic)
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PWY-6961
L-ascorbate degradation III
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PWY-6960
L-cysteine biosynthesis III (from L-homocysteine)
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HOMOCYSDEGR-PWY
leucodelphinidin biosynthesis
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PWY-5152
leucopelargonidin and leucocyanidin biosynthesis
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PWY1F-823
luteolin triglucuronide degradation
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PWY-7445
matairesinol biosynthesis
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PWY-5466
Metabolism of xenobiotics by cytochrome P450
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methanol oxidation to formaldehyde IV
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PWY-5506
Microbial metabolism in diverse environments
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nitric oxide biosynthesis II (mammals)
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PWY-4983
nocardicin A biosynthesis
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PWY-7797
ophthalmate biosynthesis
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PWY-8043
pentachlorophenol degradation
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PCPDEG-PWY
phaselate biosynthesis
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PWY-6320
Phenylalanine metabolism
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phenylpropanoid biosynthesis
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PWY-361
Phenylpropanoid biosynthesis
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phenylpropanoid biosynthesis
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phenylpropanoid biosynthesis, initial reactions
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PWY1F-467
phosphate acquisition
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PWY-6348
proanthocyanidins biosynthesis from flavanols
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PWY-641
reactive oxygen species degradation
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DETOX1-PWY-1
Riboflavin metabolism
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rosmarinic acid biosynthesis I
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PWY-5048
rutin biosynthesis
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PWY-5390
sesamin biosynthesis
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PWY-5469
Starch and sucrose metabolism
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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
superoxide radicals degradation
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DETOX1-PWY
syringetin biosynthesis
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PWY-5391
taurine biosynthesis III
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PWY-8359
Tryptophan metabolism
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vitamin B1 metabolism
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xanthommatin biosynthesis
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PWY-8249
suberin monomers biosynthesis
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PWY-1121
suberin monomers biosynthesis
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brenda
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brenda
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brenda
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brenda
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brenda
grown under light or dark condition
brenda
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brenda
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brenda
highest enzyme expression, especially high at initial bloom
brenda
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brenda
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testa
brenda
additional information
differential expression of isozymes FLS1 and FLS2 in different organs, flowering stages and maturing seeds of tartary buckwheat cultivars Hokkai T8 and Hokkai T10, overview
brenda
additional information
gene expression of FtLAR during sprout development under dark and light conditions in cvs. T8 and T10, determination of catechin and epicatechin contents in sprouts, the expression pattern of anthocyanidin reductase (ANR) and leucoanthocyanidin reductase (LAR) do not match the accumulation pattern of proanthocyanidins in different organs of the two cultivars Hokkai T8 and Hokkai T10. FtANR expression levels are higher in T8 than T10 under both conditions. Specifically, transcript level in T8 under dark condition is higher than that under light condition, although fluctuation pattern is observed in light condition. FtANR expression is increased from 0 to 3 days-after-sowing for T8 cultivar under dark condition and remained relatively constant on 6, 9, and 12 days-after-sowing. The catechin content is correlated with color pigment. Epicatechin content is affected by light in T8 only, whereas T10 remains unaffected by light. Flowers of T8 and T10 contain the highest levels of epicatechin, whereas the lowest amount of epicatechin is in the seeds at stage 3 in T8
brenda
additional information
gene expression of FtLAR during sprout development under dark and light conditions in cvs. T8 and T10, determination of catechin and epicatechin contents in sprouts, the expression pattern of anthocyanidin reductase (ANR) and leucoanthocyanidin reductase (LAR) do not match the accumulation pattern of proanthocyanidins in different organs of the two cultivars Hokkai T8 and Hokkai T10. FtLAR does not show large variations in its expression patterns among all the organs in cultivars Hokkai T8 and T10. Epicatechin content is higher than the catechin content in both T8 and T10. In T10, catechin is found mostly in the flowers and roots, whereas in T8, higher amounts are found in leaves and seeds at stage 1. Catechin content in T10 is highest in roots. Hokkai T10 wild roots in the soil and hairy roots are red in color. The catechin content is correlated with color pigment
brenda
additional information
the overall expression levels are the highest in leaves and flowers, the enzyme shows a moderate level in stems, and lower expression in flower buds and immature seeds
brenda
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