EC Number   |
Recommended Name |
Source Tissue |
Reference |
|---|
    1.1.1.1 | alcohol dehydrogenase |
seed |
- |
285559, 285561, 285562, 285628, 285629, 285634 |
| 1.1.1.100 | 3-oxoacyl-[acyl-carrier-protein] reductase |
seed |
- |
285669, 285675, 285679 |
| 1.1.1.14 | L-iditol 2-dehydrogenase |
seed |
activity is higher than in cortex per mg and fresh weight, and contributes significantly to whole fruit activity during weeks 2-5 after bloom. Isoforms SDH1 and SDH3 are expressed in both seed and cortex tissue. Isoforms SDH6 and SDH9 are expressed in seed tissues only |
688074 |
| 1.1.1.191 | indole-3-acetaldehyde reductase (NADPH) |
seed |
- |
286152, 286154, 286155 |
| 1.1.1.191 | indole-3-acetaldehyde reductase (NADPH) |
seed |
two isoenzymes, TH and TL |
286153 |
| 1.1.1.195 | cinnamyl-alcohol dehydrogenase |
seed |
developing |
347818 |
| 1.1.1.195 | cinnamyl-alcohol dehydrogenase |
seed |
quantitative realtime PCR enzyme expression analysis during seed development, overview. CAD2 shows the highest expression level of all three CAD isozymes in Carthamus tinctorius |
741132 |
| 1.1.1.205 | IMP dehydrogenase |
seed |
- |
347943 |
| 1.1.1.21 | aldose reductase |
seed |
- |
700796 |
| 1.1.1.219 | dihydroflavonol 4-reductase |
seed |
- |
657067 |
| 1.1.1.219 | dihydroflavonol 4-reductase |
seed |
preferential expression in root and seed |
760791 |
| 1.1.1.224 | mannose-6-phosphate 6-reductase |
seed |
- |
348008 |
| 1.1.1.25 | shikimate dehydrogenase (NADP+) |
seed |
- |
740821 |
| 1.1.1.25 | shikimate dehydrogenase (NADP+) |
seed |
determination of the variability in flowering phenology of Scots pine (Pinus sylvestris L.) clones in a seed orchard, genetic structure and genetic markers (13 isozyme loci and 5 chloroplast and 3 nuclear DNA microsatellite loci) among groups of clones that are differentisated by flowering phenology, overview. The frequency of allele 2 at the shikimate dehydrogenase A locus (ShDH A 2) differs significantly between the groups of early- and late-flowering trees and between the groups of intermediate- and late-flowering trees. In addition, a significant difference in the frequencies of the genotype ShDH A 11 is observed between the intermediate- and late-flowering groups, the ShDH A locus might be considered as isoenzymatic marker that differentiates these flowering groups of Scots pine clones |
740347 |
| 1.1.1.25 | shikimate dehydrogenase (NADP+) |
seed |
immature, highest expression level of VvSDH3 |
740821 |
| 1.1.1.263 | 1,5-anhydro-D-fructose reductase |
seed |
- |
207966 |
| 1.1.1.267 | 1-deoxy-D-xylulose-5-phosphate reductoisomerase |
seed |
- |
762871 |
| 1.1.1.284 | S-(hydroxymethyl)glutathione dehydrogenase |
seed |
- |
726241, 80983 |
| 1.1.1.284 | S-(hydroxymethyl)glutathione dehydrogenase |
seed |
dried seeds |
706210 |
| 1.1.1.294 | chlorophyll(ide) b reductase |
seed |
innercellular structures of the enzyme wild-type and mutant seeds |
726228 |
| 1.1.1.3 | homoserine dehydrogenase |
seed |
- |
689647 |
| 1.1.1.318 | eugenol synthase |
seed |
- |
763553 |
| 1.1.1.319 | isoeugenol synthase |
seed |
- |
763553 |
| 1.1.1.330 | very-long-chain 3-oxoacyl-CoA reductase |
seed |
- |
741241 |
| 1.1.1.334 | methylecgonone reductase |
seed |
- |
718331 |
| 1.1.1.34 | hydroxymethylglutaryl-CoA reductase (NADPH) |
seed |
- |
722329, 740956 |
| 1.1.1.34 | hydroxymethylglutaryl-CoA reductase (NADPH) |
seed |
developing |
740956 |
| 1.1.1.35 | 3-hydroxyacyl-CoA dehydrogenase |
seed |
- |
672317 |
| 1.1.1.37 | malate dehydrogenase |
seed |
- |
286649, 669675, 723710 |
| 1.1.1.37 | malate dehydrogenase |
seed |
PM-associated MDH isozyme |
-, 723059 |
| 1.1.1.40 | malate dehydrogenase (oxaloacetate-decarboxylating) (NADP+) |
seed |
- |
654369, 713212, 739251, 761181, 762132 |
| 1.1.1.41 | isocitrate dehydrogenase (NAD+) |
seed |
- |
670547 |
| 1.1.1.42 | isocitrate dehydrogenase (NADP+) |
seed |
- |
286782 |
| 1.1.1.42 | isocitrate dehydrogenase (NADP+) |
seed |
high expression level |
-, 722338 |
| 1.1.1.44 | phosphogluconate dehydrogenase (NADP+-dependent, decarboxylating) |
seed |
- |
286857, 286859, 286864, 286877 |
| 1.1.1.44 | phosphogluconate dehydrogenase (NADP+-dependent, decarboxylating) |
seed |
low expression |
762190 |
| 1.1.1.49 | glucose-6-phosphate dehydrogenase (NADP+) |
seed |
- |
700801 |
| 1.1.1.8 | glycerol-3-phosphate dehydrogenase (NAD+) |
seed |
high level of transcripts accumulation in roots and early stage developing seeds |
762241 |
| 1.1.3.15 | (S)-2-hydroxy-acid oxidase |
seed |
germinated seed, expression level is similar to ubiquitin |
763602 |
| 1.1.3.9 | galactose oxidase |
seed |
seed coat epidermis |
763560 |
| 1.1.5.3 | glycerol-3-phosphate dehydrogenase |
seed |
high level of transcripts accumulation in roots and early stage developing seeds |
762241 |
| 1.10.3.1 | catechol oxidase |
seed |
- |
671857, 686666 |
| 1.10.3.3 | L-ascorbate oxidase |
seed |
- |
439905, 439908 |
| 1.11.1.11 | L-ascorbate peroxidase |
seed |
- |
439861, 765656 |
| 1.11.1.11 | L-ascorbate peroxidase |
seed |
germinating |
654378 |
| 1.11.1.24 | thioredoxin-dependent peroxiredoxin |
seed |
- |
686691 |
| 1.11.1.24 | thioredoxin-dependent peroxiredoxin |
seed |
transcript is not detected in the seeds, but its expression level increases at germination and is maintained thereafter |
725978 |
| 1.11.1.24 | thioredoxin-dependent peroxiredoxin |
seed |
transcript level is abundant at the seed stage, but rapidly decreases after imbibitions |
725978 |
| 1.11.1.24 | thioredoxin-dependent peroxiredoxin |
seed |
transcript level is low at the seed stage, rapidly increases for 10 days after imbibitions, and gradually disappears thereafter |
725978 |
| 1.11.1.6 | catalase |
seed |
- |
439781 |
| 1.11.1.6 | catalase |
seed |
developing, expression and activity increase in non hydrated seeds and during desiccation on the mother plant and after artificial drying on the flowerhead |
656410 |
| 1.11.1.7 | peroxidase |
seed |
- |
673542 |
| 1.11.1.7 | peroxidase |
seed |
isoenzyme POX I |
676374 |
| 1.11.1.7 | peroxidase |
seed |
isoenzyme POX II |
676374 |
| 1.11.1.7 | peroxidase |
seed |
peroxidase activity in mature seed is very low. Peroxidase activity is gradually increased at 1 to 2 days after germination. The peroxidase activity reaches a peak at 3 days after germination, and then decreases from 4 to 5 day after germination |
675644 |
| 1.11.1.7 | peroxidase |
seed |
seed coat |
659637 |
| 1.11.1.9 | glutathione peroxidase |
seed |
moderate mRNA level in immature seed |
758029 |
| 1.11.2.3 | plant seed peroxygenase |
seed |
- |
711060, 711277, 712255, 712256, 712329, 712357, 712359, 712776, 713275, 713303, 765579, 765627, 765649 |
| 1.11.2.3 | plant seed peroxygenase |
seed |
isoform Clo-1 |
713295 |
| 1.13.11.12 | linoleate 13S-lipoxygenase |
seed |
- |
706122 |
| 1.13.11.12 | linoleate 13S-lipoxygenase |
seed |
low abundance in immature seeds |
706252 |
| 1.13.11.12 | linoleate 13S-lipoxygenase |
seed |
Oep2LOX2 during development and ripening of Picual and Arbequina olive fruit |
704142 |
| 1.13.11.18 | persulfide dioxygenase |
seed |
- |
764794 |
| 1.13.11.18 | persulfide dioxygenase |
seed |
strong ETHE1 expression occurs in the peripheral and chalazal endosperm of wild-type seeds prior to cellularization |
726227 |
| 1.13.11.27 | 4-hydroxyphenylpyruvate dioxygenase |
seed |
- |
743829 |
| 1.13.11.33 | arachidonate 15-lipoxygenase |
seed |
- |
702247 |
| 1.13.11.34 | arachidonate 5-lipoxygenase |
seed |
ungerminated |
688512 |
| 1.13.11.51 | 9-cis-epoxycarotenoid dioxygenase |
seed |
- |
-, 689602, 726372, 746158 |
| 1.13.11.51 | 9-cis-epoxycarotenoid dioxygenase |
seed |
imbibed. NCED2 plays a minor role in high temperature-induced abscisic acid synthesis and germination inhibition |
689601 |
| 1.13.11.51 | 9-cis-epoxycarotenoid dioxygenase |
seed |
imbibed. NCED5 plays a minor role in high temperature-induced abscisic acid synthesis and germination inhibition |
689601 |
| 1.13.11.51 | 9-cis-epoxycarotenoid dioxygenase |
seed |
imbibed. NCED9 plays a major role in high temperature-induced abscisic acid synthesis and germination inhibition |
689601 |
| 1.13.11.51 | 9-cis-epoxycarotenoid dioxygenase |
seed |
levels of abscisic acid are controlled by phytochrome through down-regulation of LsNCED2 and LsNCED4 expression |
689602 |
| 1.13.11.51 | 9-cis-epoxycarotenoid dioxygenase |
seed |
NCED4 expression is elevated during late seed development but is not required for seed maturation |
-, 726168 |
| 1.13.11.58 | linoleate 9S-lipoxygenase |
seed |
- |
742051 |
| 1.13.11.58 | linoleate 9S-lipoxygenase |
seed |
embryo |
396147 |
| 1.13.11.58 | linoleate 9S-lipoxygenase |
seed |
expressed early in seed development |
-, 703536 |
| 1.13.11.58 | linoleate 9S-lipoxygenase |
seed |
the expression level of the r9-LOX1 gene is higher in imbibed seeds rather than developing seeds |
706170 |
| 1.13.11.68 | 9-cis-beta-carotene 9',10'-cleaving dioxygenase |
seed |
low expression level of CCD8 |
746148 |
| 1.13.11.70 | all-trans-10'-apo-beta-carotenal 13,14-cleaving dioxygenase |
seed |
low expression level of CCD8 |
746148 |
| 1.13.11.92 | fatty acid alpha-dioxygenase |
seed |
germinating and developing plant |
761741 |
| 1.13.11.B6 | linoleate 9/13-lipoxygenase |
seed |
- |
396184, 706122, 706645 |
| 1.13.11.B6 | linoleate 9/13-lipoxygenase |
seed |
constitutively expressed in cotyledons and embryos of immature seeds |
706250 |
| 1.13.11.B6 | linoleate 9/13-lipoxygenase |
seed |
detected in all developmental stages, negligible activity in mature seed |
703538 |
| 1.13.11.B6 | linoleate 9/13-lipoxygenase |
seed |
OsLOX1 transcripts are detected at low abundance in immature seeds and newly germinated seedlings, but accumulate rapidly and transiently in response to wounding or brown planthopper attack, reaching a peak 3 h after wounding and 6 h after insect feeding |
706252 |
| 1.14.11.13 | gibberellin 2beta-dioxygenase |
seed |
- |
439269, 439271, 439273, 439274, 689497 |
| 1.14.11.13 | gibberellin 2beta-dioxygenase |
seed |
dry seed: GA2ox1 and GA2ox4 not expressed, high levels of GA2ox2 and GA2ox3, GA2ox6 dominant, 24 h inhibited seed: low expression of GA2ox1 and GA2ox4, highest expression of GA2ox2 and GA2ox6, expression of GA2ox3 |
700733 |
| 1.14.11.13 | gibberellin 2beta-dioxygenase |
seed |
from day 10-12 PsGA2ox1 levels increase dramatically and remain elevated through day 20 after anthesis, high levels of PsGA2ox1 mRNA are found in testa compared with the cotyledons at day 26 after anthesis |
700830 |
| 1.14.11.13 | gibberellin 2beta-dioxygenase |
seed |
in the suspensor neck region from the late globular stage up to the heart stage |
676453 |
| 1.14.11.13 | gibberellin 2beta-dioxygenase |
seed |
mature and immature seeds |
439270 |
| 1.14.11.13 | gibberellin 2beta-dioxygenase |
seed |
mature seeds |
439271, 439272 |
| 1.14.11.13 | gibberellin 2beta-dioxygenase |
seed |
presence of seeds is required for normal development of fruit from pericarp, removal of seeds leads to slowing of pericarp growth and subsequent abscission, the seed is the terminal nutrient sink when the development of the pea embryo begins |
700830 |
| 1.14.11.13 | gibberellin 2beta-dioxygenase |
seed |
relatively strong expression in immature and low expression in mature seeds |
700768 |
| 1.14.11.13 | gibberellin 2beta-dioxygenase |
seed |
the enzyme (CuGA2ox2/3) is highly expressed |
764817 |
| 1.14.11.13 | gibberellin 2beta-dioxygenase |
seed |
the transcript of CuGA2ox8 accumulates mainly in new leaves and flower buds in the adult phase |
764817 |
| 1.14.11.15 | gibberellin 3beta-dioxygenase |
seed |
- |
676398, 676453 |
| 1.14.11.15 | gibberellin 3beta-dioxygenase |
seed |
endosperm |
439266 |
| 1.14.11.15 | gibberellin 3beta-dioxygenase |
seed |
expressed predominantly during seed germination |
439265 |
| 1.14.11.15 | gibberellin 3beta-dioxygenase |
seed |
immature |
439261, 439262, 439263 |
| 1.14.11.15 | gibberellin 3beta-dioxygenase |
seed |
mRNA level increases at day 4 after anthesis and again 8 to 12 days after anthesis, when seed development is rapid |
660218 |
| 1.14.11.2 | procollagen-proline 4-dioxygenase |
seed |
- |
439244 |
