AsCYP76AD1 |
CYP450 |
Amaranthus tricolor |
Amaranthaceae |
Yes |
Linoleic Acid,Palmitic Acid,Linolenic Acid,Arachic Acid,Spinasterol |
-- |
|
NC_080047.1 |
-- |
Wang H,Xu D,Wang S, et al. Chromosome-scale Amaranthus tricolor genome provides insights into the evolution of the genus Amaranthus and the mechanism of betalain biosynthesis. DNA Res. 2023;30 (1):. doi:10.1093/dnares/dsac050 |
LsCYP |
CYP450 |
Lactuca sativa |
Asteraceae |
Yes |
Flavonoids,Ascorbic Acid,Tocopherols,Sesquiterpenoids |
cytochrome P450 CYP72A219 |
|
LOC111884384 |
https://www.ncbi.nlm.nih.gov/gene/111884384 |
-- |
LsCYP |
CYP450 |
Lactuca sativa |
Asteraceae |
Yes |
Flavonoids,Ascorbic Acid,Tocopherols,Sesquiterpenoids |
flavonoid 3',5'-hydroxylase 1 |
|
LOC111887493 |
https://www.ncbi.nlm.nih.gov/gene/111887493 |
-- |
PdCYP |
CYP450 |
Phoenix dactylifera |
Arecaceae |
Yes |
Jujube Glycoside,Chrysoeriol-7-glucoside,Pheflolic Acid,Gallic Acid,Ferulic Acid |
cytochrome P450 72A15 |
|
LOC103696920 |
https://www.ncbi.nlm.nih.gov/gene/103696920 |
-- |
PdCYP |
CYP450 |
Phoenix dactylifera |
Arecaceae |
Yes |
Jujube Glycoside,Chrysoeriol-7-glucoside,Pheflolic Acid,Gallic Acid,Ferulic Acid |
cytochrome P450 72A15 |
|
LOC103696921 |
https://www.ncbi.nlm.nih.gov/gene/103696921 |
-- |
PdCYP |
CYP450 |
Phoenix dactylifera |
Arecaceae |
Yes |
Jujube Glycoside,Chrysoeriol-7-glucoside,Pheflolic Acid,Gallic Acid,Ferulic Acid |
alpha-humulene 10-hydroxylase-like |
|
LOC103698752 |
https://www.ncbi.nlm.nih.gov/gene/103698752 |
-- |
PdCYP |
CYP450 |
Phoenix dactylifera |
Arecaceae |
Yes |
Jujube Glycoside,Chrysoeriol-7-glucoside,Pheflolic Acid,Gallic Acid,Ferulic Acid |
cytochrome P450 CYP72A219 |
|
LOC103703363 |
https://www.ncbi.nlm.nih.gov/gene/103703363 |
-- |
PdCYP |
CYP450 |
Phoenix dactylifera |
Arecaceae |
Yes |
Jujube Glycoside,Chrysoeriol-7-glucoside,Pheflolic Acid,Gallic Acid,Ferulic Acid |
cytokinin hydroxylase |
|
LOC103705582 |
https://www.ncbi.nlm.nih.gov/gene/103705582 |
-- |
PdCYP |
CYP450 |
Phoenix dactylifera |
Arecaceae |
Yes |
Jujube Glycoside,Chrysoeriol-7-glucoside,Pheflolic Acid,Gallic Acid,Ferulic Acid |
cytochrome P450 734A1 |
|
LOC103716275 |
https://www.ncbi.nlm.nih.gov/gene/103716275 |
-- |
PdCYP |
CYP450 |
Phoenix dactylifera |
Arecaceae |
Yes |
Jujube Glycoside,Chrysoeriol-7-glucoside,Pheflolic Acid,Gallic Acid,Ferulic Acid |
cytochrome P450 704C1 |
|
LOC103721382 |
https://www.ncbi.nlm.nih.gov/gene/103721382 |
-- |
PdCYP709B2 |
CYP450 |
Phoenix dactylifera |
Arecaceae |
Yes |
Jujube Glycoside,Chrysoeriol-7-glucoside,Pheflolic Acid,Gallic Acid,Ferulic Acid |
cytochrome P450 709B2-like |
|
LOC103696907 |
https://www.ncbi.nlm.nih.gov/gene/103696907 |
-- |
PdCYP709B2-like |
CYP450 |
Phoenix dactylifera |
Arecaceae |
Yes |
Jujube Glycoside,Chrysoeriol-7-glucoside,Pheflolic Acid,Gallic Acid,Ferulic Acid |
cytochrome P450 709B2-like |
|
LOC103698412 |
https://www.ncbi.nlm.nih.gov/gene/103698412 |
-- |
PdCYP711A1 |
CYP450 |
Phoenix dactylifera |
Arecaceae |
Yes |
Jujube Glycoside,Chrysoeriol-7-glucoside,Pheflolic Acid,Gallic Acid,Ferulic Acid |
cytochrome P450 711A1 |
|
LOC103709562 |
https://www.ncbi.nlm.nih.gov/gene/103709562 |
-- |
PdCYP714C2 |
CYP450 |
Phoenix dactylifera |
Arecaceae |
Yes |
Jujube Glycoside,Chrysoeriol-7-glucoside,Pheflolic Acid,Gallic Acid,Ferulic Acid |
cytochrome P450 714C2-like |
|
LOC103697824 |
https://www.ncbi.nlm.nih.gov/gene/103697824 |
-- |
PdCYP714C2 |
CYP450 |
Phoenix dactylifera |
Arecaceae |
Yes |
Jujube Glycoside,Chrysoeriol-7-glucoside,Pheflolic Acid,Gallic Acid,Ferulic Acid |
cytochrome P450 714C2-like |
|
LOC103712265 |
https://www.ncbi.nlm.nih.gov/gene/103712265 |
-- |
PdCYP72A15 |
CYP450 |
Phoenix dactylifera |
Arecaceae |
Yes |
Jujube Glycoside,Chrysoeriol-7-glucoside,Pheflolic Acid,Gallic Acid,Ferulic Acid |
cytochrome P450 72A15-like |
|
LOC103697368 |
https://www.ncbi.nlm.nih.gov/gene/103697368 |
-- |
PdCYP72A15 |
CYP450 |
Phoenix dactylifera |
Arecaceae |
Yes |
Jujube Glycoside,Chrysoeriol-7-glucoside,Pheflolic Acid,Gallic Acid,Ferulic Acid |
cytochrome P450 72A15-like |
|
LOC103698045 |
https://www.ncbi.nlm.nih.gov/gene/103698045 |
-- |
PdCYP734A1 |
CYP450 |
Phoenix dactylifera |
Arecaceae |
Yes |
Jujube Glycoside,Chrysoeriol-7-glucoside,Pheflolic Acid,Gallic Acid,Ferulic Acid |
cytochrome P450 734A1 |
|
LOC103710957 |
https://www.ncbi.nlm.nih.gov/gene/103710957 |
-- |
PdCYP75B137 |
CYP450 |
Phoenix dactylifera |
Arecaceae |
Yes |
Jujube Glycoside,Chrysoeriol-7-glucoside,Pheflolic Acid,Gallic Acid,Ferulic Acid |
flavonoid 3'-monooxygenase CYP75B137-like |
|
LOC103702901 |
https://www.ncbi.nlm.nih.gov/gene/103702901 |
-- |
PdCYP78A3 |
CYP450 |
Phoenix dactylifera |
Arecaceae |
Yes |
Jujube Glycoside,Chrysoeriol-7-glucoside,Pheflolic Acid,Gallic Acid,Ferulic Acid |
cytochrome P450 78A3-like |
|
LOC103708728 |
https://www.ncbi.nlm.nih.gov/gene/103708728 |
-- |
PdCYP78A5 |
CYP450 |
Phoenix dactylifera |
Arecaceae |
Yes |
Jujube Glycoside,Chrysoeriol-7-glucoside,Pheflolic Acid,Gallic Acid,Ferulic Acid |
cytochrome P450 78A5-like |
|
LOC103715852 |
https://www.ncbi.nlm.nih.gov/gene/103715852 |
-- |
PdCYP78A9 |
CYP450 |
Phoenix dactylifera |
Arecaceae |
Yes |
Jujube Glycoside,Chrysoeriol-7-glucoside,Pheflolic Acid,Gallic Acid,Ferulic Acid |
cytochrome P450 78A9-like |
|
LOC103699197 |
https://www.ncbi.nlm.nih.gov/gene/103699197 |
-- |
PdCYP79A68 |
CYP450 |
Phoenix dactylifera |
Arecaceae |
Yes |
Jujube Glycoside,Chrysoeriol-7-glucoside,Pheflolic Acid,Gallic Acid,Ferulic Acid |
tryptophan N-monooxygenase CYP79A68-like |
|
LOC103720455 |
https://www.ncbi.nlm.nih.gov/gene/103720455 |
-- |
PdCYP81Q32 |
CYP450 |
Phoenix dactylifera |
Arecaceae |
Yes |
Jujube Glycoside,Chrysoeriol-7-glucoside,Pheflolic Acid,Gallic Acid,Ferulic Acid |
cytochrome P450 81Q32-like
|
|
LOC103700914 |
https://www.ncbi.nlm.nih.gov/gene/103700914 |
-- |
PdCYP |
CYP450 |
Phoenix dactylifera |
Arecaceae |
Yes |
Jujube Glycoside,Chrysoeriol-7-glucoside,Pheflolic Acid,Gallic Acid,Ferulic Acid |
cytochrome P450 704C1 |
|
LOC120108100 |
https://www.ncbi.nlm.nih.gov/gene/120108100 |
-- |
PdCYP |
CYP450 |
Phoenix dactylifera |
Arecaceae |
Yes |
Jujube Glycoside,Chrysoeriol-7-glucoside,Pheflolic Acid,Gallic Acid,Ferulic Acid |
abscisic acid 8'-hydroxylase 2 |
|
LOC120110976 |
https://www.ncbi.nlm.nih.gov/gene/120110976 |
-- |
PdCYP |
CYP450 |
Phoenix dactylifera |
Arecaceae |
Yes |
Jujube Glycoside,Chrysoeriol-7-glucoside,Pheflolic Acid,Gallic Acid,Ferulic Acid |
cytochrome P450 709B2 |
|
LOC120112175 |
https://www.ncbi.nlm.nih.gov/gene/120112175 |
-- |
HaCYP |
CYP450 |
Helianthus annuus |
Asteraceae |
Yes |
Sesquiterpene Lactones,Sesquiterpenes,Steroids,Polyphenols,Aromatics |
cytochrome P450 76T24 |
|
LOC110879566 |
https://www.ncbi.nlm.nih.gov/gene/110879566 |
-- |
HaCYP |
CYP450 |
Helianthus annuus |
Asteraceae |
Yes |
Sesquiterpene Lactones,Sesquiterpenes,Steroids,Polyphenols,Aromatics |
cytochrome P450 93A3 |
|
LOC110942908 |
https://www.ncbi.nlm.nih.gov/gene/110942908 |
-- |
HaCYP |
CYP450 |
Helianthus annuus |
Asteraceae |
Yes |
Sesquiterpene Lactones,Sesquiterpenes,Steroids,Polyphenols,Aromatics |
cytochrome P450 CYP72A219 |
|
LOC110895002 |
https://www.ncbi.nlm.nih.gov/gene/110895002 |
-- |
HaCYP |
CYP450 |
Helianthus annuus |
Asteraceae |
Yes |
Sesquiterpene Lactones,Sesquiterpenes,Steroids,Polyphenols,Aromatics |
cytochrome P450 CYP749A22 |
|
LOC110918705 |
https://www.ncbi.nlm.nih.gov/gene/110918705 |
-- |
HaCYP |
CYP450 |
Helianthus annuus |
Asteraceae |
Yes |
Sesquiterpene Lactones,Sesquiterpenes,Steroids,Polyphenols,Aromatics |
cytochrome P450 CYP82D47 |
|
LOC110923440 |
https://www.ncbi.nlm.nih.gov/gene/110923440 |
-- |
HaCYP |
CYP450 |
Helianthus annuus |
Asteraceae |
Yes |
Sesquiterpene Lactones,Sesquiterpenes,Steroids,Polyphenols,Aromatics |
eupatolide synthase |
|
LOC110929409 |
https://www.ncbi.nlm.nih.gov/gene/110929409 |
-- |
HaCYP |
CYP450 |
Helianthus annuus |
Asteraceae |
Yes |
Sesquiterpene Lactones,Sesquiterpenes,Steroids,Polyphenols,Aromatics |
labd-13Z-ene-9,15,16-triol synthase, chloroplastic |
|
LOC110941556 |
https://www.ncbi.nlm.nih.gov/gene/110941556 |
-- |
HaCYP |
CYP450 |
Helianthus annuus |
Asteraceae |
Yes |
Sesquiterpene Lactones,Sesquiterpenes,Steroids,Polyphenols,Aromatics |
probable (S)-N-methylcoclaurine 3'-hydroxylase isozyme 2 |
|
LOC110897567 |
https://www.ncbi.nlm.nih.gov/gene/110897567 |
-- |
HaCYP |
CYP450 |
Helianthus annuus |
Asteraceae |
Yes |
Sesquiterpene Lactones,Sesquiterpenes,Steroids,Polyphenols,Aromatics |
-- |
|
LOC110941831 |
https://www.ncbi.nlm.nih.gov/gene/110941831 |
-- |
BrCYP |
CYP450 |
Brassica rapa |
Brassicaceae |
Yes |
Flavonoids,Phenolic Acids,Triterpenes,Polysaccharides |
cytochrome P450 709B1 |
|
LOC103852728 |
https://www.ncbi.nlm.nih.gov/gene/103852728 |
-- |
BrCYP |
CYP450 |
Brassica rapa |
Brassicaceae |
Yes |
Flavonoids,Phenolic Acids,Triterpenes,Polysaccharides |
cytochrome P450 71A14 |
|
LOC103874339 |
https://www.ncbi.nlm.nih.gov/gene/103874339 |
-- |
BrCYP |
CYP450 |
Brassica rapa |
Brassicaceae |
Yes |
Flavonoids,Phenolic Acids,Triterpenes,Polysaccharides |
cytochrome P450 72A13 |
|
LOC103841893 |
https://www.ncbi.nlm.nih.gov/gene/103841893 |
-- |
BrCYP |
CYP450 |
Brassica rapa |
Brassicaceae |
Yes |
Flavonoids,Phenolic Acids,Triterpenes,Polysaccharides |
cytochrome P450 81D11 |
|
LOC103854185 |
https://www.ncbi.nlm.nih.gov/gene/103854185 |
-- |
BrCYP18-3 |
CYP450 |
Brassica rapa |
Brassicaceae |
Yes |
Flavonoids,Phenolic Acids,Triterpenes,Polysaccharides |
peptidyl-prolyl cis-trans isomerase CYP18-3 |
|
LOC100777759 |
https://www.ncbi.nlm.nih.gov/gene/100777759 |
-- |
AtCYP1 |
CYP450 |
Arabidopsis thaliana |
Brassicaceae |
Yes |
Indole-3-acetic Acid |
rotamase CYP 1 |
|
AT4G38740 |
https://www.ncbi.nlm.nih.gov/gene/830029 |
Kosmacz M, Gorka M, Schmidt S, et al. Protein and metabolite composition of Arabidopsis stress granules. New Phytol. 2019;222(3):1420-1433. doi:10.1111/nph.15690 |
AtCYP3 |
CYP450 |
Arabidopsis thaliana |
Brassicaceae |
Yes |
Indole-3-acetic Acid |
rotamase CYP 3 |
|
AT2G16600 |
https://www.ncbi.nlm.nih.gov/gene/816161 |
Mair A, Xu SL, Branon TC, Ting AY, Bergmann DC. Proximity labeling of protein complexes and cell-type-specific organellar proteomes in Arabidopsis enabled by TurboID. Elife. 2019;8:e47864. doi:10.7554/eLife.47864 |
AtCYP3 |
CYP450 |
Arabidopsis thaliana |
Brassicaceae |
Yes |
Indole-3-acetic Acid |
rotamase CYP 3 |
|
AT2G16600 |
https://www.ncbi.nlm.nih.gov/gene/816161 |
Mair A, Xu SL, Branon TC, Ting AY, Bergmann DC. Proximity labeling of protein complexes and cell-type-specific organellar proteomes in Arabidopsis enabled by TurboID. Elife. 2019;8:e47864. doi:10.7554/eLife.47864 |
AtCYP4 |
CYP450 |
Arabidopsis thaliana |
Brassicaceae |
Yes |
Indole-3-acetic Acid |
rotamase CYP 4 |
|
LOC825376 |
https://www.ncbi.nlm.nih.gov/gene/825376 |
Liebthal M, Strüve M, Li X, et al. Redox-Dependent Conformational Dynamics of Decameric 2-Cysteine Peroxiredoxin and its Interaction with Cyclophilin 20-3. Plant Cell Physiol. 2016;57(7):1415-1425. doi:10.1093/pcp/pcw031 |
AtCYP4 |
CYP450 |
Arabidopsis thaliana |
Brassicaceae |
Yes |
Indole-3-acetic Acid |
rotamase CYP 4 |
|
LOC825376 |
https://www.ncbi.nlm.nih.gov/gene/825376 |
Liebthal M, Strüve M, Li X, et al. Redox-Dependent Conformational Dynamics of Decameric 2-Cysteine Peroxiredoxin and its Interaction with Cyclophilin 20-3. Plant Cell Physiol. 2016;57(7):1415-1425. doi:10.1093/pcp/pcw031 |
AtCYP |
CYP450 |
Arabidopsis thaliana |
Brassicaceae |
Yes |
Indole-3-acetic Acid |
cytochrome P450 |
|
AT3G44970 |
https://www.ncbi.nlm.nih.gov/gene/823632 |
-- |
AtCYP |
CYP450 |
Arabidopsis thaliana |
Brassicaceae |
Yes |
Indole-3-acetic Acid |
cytochrome P450 |
|
CYP71B30P |
https://www.ncbi.nlm.nih.gov/gene/824496 |
-- |
AtCYP |
CYP450 |
Arabidopsis thaliana |
Brassicaceae |
Yes |
Indole-3-acetic Acid |
cytochrome P450 |
|
CYP79A3P |
https://www.ncbi.nlm.nih.gov/gene/833580 |
-- |
AtCYP |
CYP450 |
Arabidopsis thaliana |
Brassicaceae |
Yes |
Indole-3-acetic Acid |
cytochrome P450 |
|
CYP716A1 |
https://www.ncbi.nlm.nih.gov/gene/833607 |
-- |
AtCYP |
CYP450 |
Arabidopsis thaliana |
Brassicaceae |
Yes |
Indole-3-acetic Acid |
cytochrome P450 |
|
AT5G36130 |
https://www.ncbi.nlm.nih.gov/gene/833610 |
-- |
AtCYP |
CYP450 |
Arabidopsis thaliana |
Brassicaceae |
Yes |
Indole-3-acetic Acid |
cytochrome P450 |
|
CYP708A3 |
https://www.ncbi.nlm.nih.gov/gene/844185 |
-- |
AtCYP1 |
CYP450 |
Arabidopsis thaliana |
Brassicaceae |
Yes |
Indole-3-acetic Acid |
rotamase CYP 1 |
|
AT4G38740 |
https://www.ncbi.nlm.nih.gov/gene/830029 |
Kosmacz M, Gorka M, Schmidt S, et al. Protein and metabolite composition of Arabidopsis stress granules. New Phytol. 2019;222(3):1420-1433. doi:10.1111/nph.15690 |
BnCYP |
CYP450 |
Brassica napus |
Brassicaceae |
No |
Isothiocyanate,Indole Compounds,Carotene |
cytochrome P450 72C1 |
|
LOC106414937 |
https://www.ncbi.nlm.nih.gov/gene/106414937 |
-- |
BnCYP |
CYP450 |
Brassica napus |
Brassicaceae |
No |
Isothiocyanate,Indole Compounds,Carotene |
cytochrome P450 98A8 |
|
LOC106405584 |
https://www.ncbi.nlm.nih.gov/gene/106405584 |
-- |
BnCYP |
CYP450 |
Brassica napus |
Brassicaceae |
No |
Isothiocyanate,Indole Compounds,Carotene |
peptidyl-prolyl cis-trans isomerase |
|
LOC106347045 |
https://www.ncbi.nlm.nih.gov/gene/106347045 |
-- |
TwCYP |
CYP450 |
Tripterygium wilfordii |
Celastraceae |
Yes |
Triptolide,Triptolide A,Triptolide B,Triptolide B |
cytochrome P450 711A1 |
|
LOC119997666 |
https://www.ncbi.nlm.nih.gov/gene/119997666 |
-- |
TwCYP |
CYP450 |
Tripterygium wilfordii |
Celastraceae |
Yes |
Triptolide,Triptolide A,Triptolide B,Triptolide B |
cytochrome P450 714A1 |
|
LOC119996206 |
https://www.ncbi.nlm.nih.gov/gene/119996206 |
-- |
TwCYP |
CYP450 |
Tripterygium wilfordii |
Celastraceae |
Yes |
Triptolide,Triptolide A,Triptolide B,Triptolide B |
cytochrome P450 71D10 |
|
LOC119986046 |
https://www.ncbi.nlm.nih.gov/gene/119986046 |
-- |
TwCYP |
CYP450 |
Tripterygium wilfordii |
Celastraceae |
Yes |
Triptolide,Triptolide A,Triptolide B,Triptolide B |
cytochrome P450 734A1 |
|
LOC120009369 |
https://www.ncbi.nlm.nih.gov/gene/120009369 |
-- |
TwCYP |
CYP450 |
Tripterygium wilfordii |
Celastraceae |
Yes |
Triptolide,Triptolide A,Triptolide B,Triptolide B |
cytochrome P450 87A3 |
|
LOC119990223 |
https://www.ncbi.nlm.nih.gov/gene/119990223 |
-- |
TwCYP |
CYP450 |
Tripterygium wilfordii |
Celastraceae |
Yes |
Triptolide,Triptolide A,Triptolide B,Triptolide B |
cytochrome P450 CYP749A22 |
|
LOC120015502 |
https://www.ncbi.nlm.nih.gov/gene/120015502 |
-- |
TwCYP |
CYP450 |
Tripterygium wilfordii |
Celastraceae |
Yes |
Triptolide,Triptolide A,Triptolide B,Triptolide B |
cytokinin hydroxylase |
|
LOC119989676 |
https://www.ncbi.nlm.nih.gov/gene/119989676 |
-- |
TwCYP |
CYP450 |
Tripterygium wilfordii |
Celastraceae |
Yes |
Triptolide,Triptolide A,Triptolide B,Triptolide B |
-- |
|
LOC120005313 |
https://www.ncbi.nlm.nih.gov/gene/120005313 |
-- |
BvCYP76AD1 |
CYP450 |
Beta vulgaris |
Chenopodiaceae |
No |
Anthocyanins,Tannins |
-- |
|
HQ656023 |
https://www.ncbi.nlm.nih.gov/gene/?term=HQ656023 |
Hatlestad, G.J., Sunnadeniya, R.M., Akhavan, N.A., Gonzalez, A., Goldman, I.L., McGrath,J.M., Lloyd, A.M., 2012. The beet R locus encodes a new cytochrome P450 required for red betalain production. Nat. Genet. 44, 816–820. |
GsCYP75A110 |
CYP450 |
Gloriosa superba |
Colchicaceae |
Yes |
Colchicine |
cytochrome P450 |
|
QLI49056.1 |
https://www.ncbi.nlm.nih.gov/protein/QLI49056.1 |
Bhambhani S,Kondhare KR,Giri AP. Diversity in Chemical Structures and Biological Properties of Plant Alkaloids. Molecules. 2021;26 (11):null. doi:10.3390/molecules26113374 |
GsCYP75A109 |
CYP450 |
Gloriosa superba |
Colchicaceae |
Yes |
Colchicine |
-- |
|
QLI49053.1 |
https://www.ncbi.nlm.nih.gov/protein/QLI49053.1 |
Huang W,Wang Y,Tian W, et al. Biosynthesis Investigations of Terpenoid, Alkaloid, and Flavonoid Antimicrobial Agents Derived from Medicinal Plants. Antibiotics (Basel). 2022;11 (10):. doi:10.3390/antibiotics11101380 |
McCYP |
CYP450 |
Momordica charantia |
Cucurbitaceae |
Yes |
Bitter Gourd Extract,Peptide-P |
peptidyl-prolyl cis-trans isomerase |
|
LOC111007901 |
https://www.ncbi.nlm.nih.gov/gene/111007901 |
-- |
CsCYP72A219 |
CYP450 |
Cucumis sativus |
Cucurbitaceae |
Yes |
Carbohydrates,Carotene,Niacin,Calcium,Phosphorus |
cytochrome P450 CYP72A219 |
|
LOC101213974 |
https://www.ncbi.nlm.nih.gov/gene/101213974 |
-- |
RvCYP |
CYP450 |
Rhododendron vialii |
Ericaceae |
Yes |
Lignan |
assisting alcohol dehydrogenase |
|
LOC131301494 |
https://www.ncbi.nlm.nih.gov/gene/131301494 |
-- |
RcCYP |
CYP450 |
Ricinus communis |
Euphorbiaceae |
Yes |
Triacylglycerol,Castor Alkaloid |
p-coumarate 3-hydroxylase |
|
LOC8277408 |
https://www.ncbi.nlm.nih.gov/gene/8277408 |
-- |
GmCYP |
CYP450 |
Glycine max |
Papilionaceae |
No |
Calcium,Phosphorus |
peptidyl-prolyl cis-trans isomerase 1 |
|
LOC100777759 |
https://www.ncbi.nlm.nih.gov/gene/100777759 |
-- |
LjCYP |
CYP450 |
Lotus japonicus |
Fabaceae |
Yes |
Corniculatusin |
assisting alcohol dehydrogenase |
|
LOC130747806 |
https://www.ncbi.nlm.nih.gov/gene/130747806 |
-- |
CaCYP |
CYP450 |
Cicer arietinum |
Fabaceae |
Yes |
Polysaccharides,Phospholipids,Phenols,Isoflavones |
cytochrome P450 monooxygenase |
|
LOC101501904 |
https://www.ncbi.nlm.nih.gov/gene/101501904 |
-- |
VaCYP |
CYP450 |
Vigna angularis |
Fabaceae |
Yes |
Triterpenoidsaponin |
cytochrome P450 714C2 |
|
LOC108341189 |
https://www.ncbi.nlm.nih.gov/gene/108341189 |
-- |
MsCYP |
CYP450 |
Magnolia sinica |
Magnoliaceae |
Yes |
Phenols,Magnolia Alkaloids |
assisting alcohol dehydrogenase |
|
LOC131232841 |
https://www.ncbi.nlm.nih.gov/gene/131232841 |
-- |
GhCYP |
CYP450 |
Gossypium hirsutum |
Malvaceae |
Yes |
Cellulose |
cytochrome P450 86A1 |
|
LOC107917892 |
https://www.ncbi.nlm.nih.gov/gene/107917892 |
-- |
VcCYP90B27 |
CYP450 |
Veratrum californicum |
Melanthiaceae |
Yes |
Colchicine,β-Sitosterol |
-- |
|
KJ869252 |
https://www.ncbi.nlm.nih.gov/nuccore/KJ869252 |
Augustin MM,Ruzicka DR,Shukla AK, et al. Elucidating steroid alkaloid biosynthesis in Veratrum californicum: production of verazine in Sf9 cells. Plant J. 2015;82 (6):991-1003. doi:10.1111/tpj.12871 |
VcCYP90G1 |
CYP450 |
Veratrum californicum |
Melanthiaceae |
Yes |
Colchicine,β-Sitosterol |
-- |
|
KJ869260.1 |
https://www.ncbi.nlm.nih.gov/nuccore/KJ869260.1 |
Augustin MM,Ruzicka DR,Shukla AK, et al. Elucidating steroid alkaloid biosynthesis in Veratrum californicum: production of verazine in Sf9 cells. Plant J. 2015;82 (6):991-1003. doi:10.1111/tpj.12871 |
VcCYP94N1 |
CYP450 |
Veratrum californicum |
Melanthiaceae |
Yes |
Colchicine,β-Sitosterol |
-- |
|
KJ869255.1 |
https://www.ncbi.nlm.nih.gov/nuccore/KJ869255.1 |
Augustin MM,Ruzicka DR,Shukla AK, et al. Elucidating steroid alkaloid biosynthesis in Veratrum californicum: production of verazine in Sf9 cells. Plant J. 2015;82 (6):991-1003. doi:10.1111/tpj.12871 |
EgCYP |
CYP450 |
Eucalyptus grandis |
Myrtaceae |
Yes |
Eucalyptus Oil,Organic Acids,Tannins |
-- |
|
LOC104417598 |
https://www.ncbi.nlm.nih.gov/gene/104417598 |
-- |
EgCYP |
CYP450 |
Eucalyptus grandis |
Myrtaceae |
Yes |
Eucalyptus Oil,Organic Acids,Tannins |
cucurbitadienol 11-hydroxylase |
|
LOC104417599 |
https://www.ncbi.nlm.nih.gov/gene/104417599 |
-- |
EgCYP71AP13 |
CYP450 |
Eucalyptus grandis |
Myrtaceae |
Yes |
Eucalyptus Oil,Organic Acids,Tannins |
cytochrome P450 71AP13 |
|
LOC104417541 |
https://www.ncbi.nlm.nih.gov/gene/104417541 |
-- |
EgCYP71D95 |
CYP450 |
Eucalyptus grandis |
Myrtaceae |
Yes |
Eucalyptus Oil,Organic Acids,Tannins |
cytochrome P450 71D95 |
|
LOC104417833 |
https://www.ncbi.nlm.nih.gov/gene/104417833 |
-- |
EgCYP81E8-like |
CYP450 |
Eucalyptus grandis |
Myrtaceae |
Yes |
Eucalyptus Oil,Organic Acids,Tannins |
cytochrome P450 81E8-like |
|
LOC104420374 |
https://www.ncbi.nlm.nih.gov/gene/104420374 |
-- |
EgCYP93A3-like |
CYP450 |
Eucalyptus grandis |
Myrtaceae |
Yes |
Eucalyptus Oil,Organic Acids,Tannins |
cytochrome P450 93A3-like |
|
LOC104420553 |
https://www.ncbi.nlm.nih.gov/gene/104420553 |
-- |
EgCYP71D312 |
CYP450 |
Eucalyptus grandis |
Myrtaceae |
Yes |
Eucalyptus Oil,Organic Acids,Tannins |
cytochrome P450 CYP71D312 |
|
LOC104417836 |
https://www.ncbi.nlm.nih.gov/gene/104417836 |
-- |
EgCYP |
CYP450 |
Eucalyptus grandis |
Myrtaceae |
Yes |
Eucalyptus Oil,Organic Acids,Tannins |
premnaspirodiene oxygenase |
|
LOC104420602 |
https://www.ncbi.nlm.nih.gov/gene/104420602 |
-- |
EgCYP |
CYP450 |
Eucalyptus grandis |
Myrtaceae |
Yes |
Eucalyptus Oil,Organic Acids,Tannins |
tyrosine N-monooxygenase |
|
LOC104417845 |
https://www.ncbi.nlm.nih.gov/gene/104417845 |
-- |
EgCYP |
CYP450 |
Eucalyptus grandis |
Myrtaceae |
Yes |
Eucalyptus Oil,Organic Acids,Tannins |
valine N-monooxygenase 1 |
|
LOC104420178 |
https://www.ncbi.nlm.nih.gov/gene/104420178 |
-- |
EgCYP714C2 |
CYP450 |
Eucalyptus grandis |
Myrtaceae |
Yes |
Eucalyptus Oil,Organic Acids,Tannins |
cytochrome P450 |
|
LOC104421742 |
https://www.ncbi.nlm.nih.gov/gene/104421742 |
-- |
NnCYP719A22 |
CYP450 |
Nelumbo nucifera |
Nymphaeaceae |
Yes |
Roemerine |
methylenedioxy bridge synthase |
|
OP795716 |
https://www.ncbi.nlm.nih.gov/gene/?term=OP795716 |
Menéndez-Perdomo IM,Facchini PJ. Elucidation of the (R)-enantiospecific benzylisoquinoline alkaloid biosynthetic pathways in sacred lotus (Nelumbo nucifera). Sci Rep. 2023;13 (1):2955. doi:10.1038/s41598-023-29415-0 |
NnCYP80Q1 |
CYP450 |
Nelumbo nucifera |
Nymphaeaceae |
Yes |
Roemerine |
proaporphine synthase |
|
OP795717 |
https://www.ncbi.nlm.nih.gov/gene/?term=OP795717 |
Menéndez-Perdomo IM,Facchini PJ. Elucidation of the (R)-enantiospecific benzylisoquinoline alkaloid biosynthetic pathways in sacred lotus (Nelumbo nucifera). Sci Rep. 2023;13 (1):2955. doi:10.1038/s41598-023-29415-0 |
NnCYP80Q2 |
CYP450 |
Nelumbo nucifera |
Nymphaeaceae |
Yes |
Roemerine |
bisbenzylisoquinoline synthase |
|
OP795718 |
https://www.ncbi.nlm.nih.gov/gene/?term=OP795718 |
Menéndez-Perdomo IM,Facchini PJ. Elucidation of the (R)-enantiospecific benzylisoquinoline alkaloid biosynthetic pathways in sacred lotus (Nelumbo nucifera). Sci Rep. 2023;13 (1):2955. doi:10.1038/s41598-023-29415-0 |
EcCYP82B1 |
CYP450 |
Eschscholzia californica |
Papaveraceae |
Yes |
Chelirubine,Sanguinarine,Macarpine |
protopine 6-hydroxylase |
|
BAK20464.1 |
https://www.ncbi.nlm.nih.gov/protein/BAK20464.1 |
Hori K,Yamada Y,Purwanto R, et al. Mining of the Uncharacterized Cytochrome P450 Genes Involved in Alkaloid Biosynthesis in California Poppy Using a Draft Genome Sequence. Plant Cell Physiol. 2018;59 (2):222-233. doi:10.1093/pcp/pcx210 |
EcCYP82N5 |
CYP450 |
Eschscholzia californica |
Papaveraceae |
Yes |
Chelirubine,Sanguinarine,Macarpine |
(S)-N-methylcoclaurine 3'-hydroxylase |
|
AAC39454.1 |
https://www.ncbi.nlm.nih.gov/protein/AAC39454.1 |
Hori K,Yamada Y,Purwanto R, et al. Mining of the Uncharacterized Cytochrome P450 Genes Involved in Alkaloid Biosynthesis in California Poppy Using a Draft Genome Sequence. Plant Cell Physiol. 2018;59 (2):222-233. doi:10.1093/pcp/pcx210 |
EcCYP80B1 |
CYP450 |
Eschscholzia californica |
Papaveraceae |
Yes |
Chelirubine,Sanguinarine,Macarpine |
(S)-N-methylcoclaurine 3'-hydroxylase |
|
AF014801 |
https://www.ncbi.nlm.nih.gov/nuccore/AF014801 |
Pauli HH,Kutchan TM. Molecular cloning and functional heterologous expression of two alleles encoding (S)-N-methylcoclaurine 3'-hydroxylase (CYP80B1), a new methyl jasmonate-inducible cytochrome P-450-dependent mono-oxygenase of benzylisoquinoline alkaloid biosynthesis. Plant J. 1998;13 (6):793-801. doi:10.1046/j.1365-313x.1998.00085.x |
EcCYP82N2v2 |
CYP450 |
Eschscholzia californica |
Papaveraceae |
Yes |
Chelirubine,Sanguinarine,Macarpine |
protopine 6-hydroxylase |
|
AB598834 |
https://www.ncbi.nlm.nih.gov/nuccore/AB598834 |
Takemura T,Ikezawa N,Iwasa K, et al. Molecular cloning and characterization of a cytochrome P450 in sanguinarine biosynthesis from Eschscholzia californica cells. Phytochemistry. 2013;91:100-8. doi:10.1016/j.phytochem.2012.02.013 |
PsCYP82Y1 |
CYP450 |
Papaver somniferum |
Papaveraceae |
Yes |
Isoquinolinetype Alkaloids,Protopine,Isocorydine,Papaverine,Morphine,Codeine,Sangulnarine,Chelerythrine,Bocconine,Narcotine,Rhoeadane |
cytochrome P451 |
|
JQ659005 |
https://www.ncbi.nlm.nih.gov/nuccore/JQ659005 |
Dang TT,Facchini PJ. CYP82Y1 is N-methylcanadine 1-hydroxylase, a key noscapine biosynthetic enzyme in opium poppy. J Biol Chem. 2014;289 (4):2013-26. doi:10.1074/jbc.M113.505099 |
PsCYP82X1 |
CYP450 |
Papaver somniferum |
Papaveraceae |
Yes |
Isoquinolinetype Alkaloids,Protopine,Isocorydine,Papaverine,Morphine,Codeine,Sangulnarine,Chelerythrine,Bocconine,Narcotine,Rhoeadane |
cytochrome P450 |
|
JQ659002 |
https://www.ncbi.nlm.nih.gov/nuccore/JQ659002 |
Dang TT,Facchini PJ. CYP82Y1 is N-methylcanadine 1-hydroxylase, a key noscapine biosynthetic enzyme in opium poppy. J Biol Chem. 2014;289 (4):2013-26. doi:10.1074/jbc.M113.505100 |
PsCYP82X2 |
CYP450 |
Papaver somniferum |
Papaveraceae |
Yes |
Isoquinolinetype Alkaloids,Protopine,Isocorydine,Papaverine,Morphine,Codeine,Sangulnarine,Chelerythrine,Bocconine,Narcotine,Rhoeadane |
cytochrome P450 |
|
JQ659004 |
https://www.ncbi.nlm.nih.gov/nuccore/JQ659004 |
Dang TT,Facchini PJ. CYP82Y1 is N-methylcanadine 1-hydroxylase, a key noscapine biosynthetic enzyme in opium poppy. J Biol Chem. 2014;289 (4):2013-26. doi:10.1074/jbc.M113.505101 |
CjCYP82R1 |
CYP450 |
Papaver somniferum |
Papaveraceae |
Yes |
Isoquinolinetype Alkaloids,Protopine,Isocorydine,Papaverine,Morphine,Codeine,Sangulnarine,Chelerythrine,Bocconine,Narcotine,Rhoeadane |
cytochrome P450 |
|
BAF98472 |
https://www.ncbi.nlm.nih.gov/protein/BAF98472 |
Dang TT,Facchini PJ. CYP82Y1 is N-methylcanadine 1-hydroxylase, a key noscapine biosynthetic enzyme in opium poppy. J Biol Chem. 2014;289 (4):2013-26. doi:10.1074/jbc.M113.505102 |
PsCYP82N3 |
CYP450 |
Papaver somniferum |
Papaveraceae |
Yes |
Isoquinolinetype Alkaloids,Protopine,Isocorydine,Papaverine,Morphine,Codeine,Sangulnarine,Chelerythrine,Bocconine,Narcotine,Rhoeadane |
protopine 6-hydroxylase |
|
KC154002 |
https://www.ncbi.nlm.nih.gov/nuccore/KC154002 |
Dang TT,Facchini PJ. CYP82Y1 is N-methylcanadine 1-hydroxylase, a key noscapine biosynthetic enzyme in opium poppy. J Biol Chem. 2014;289 (4):2013-26. doi:10.1074/jbc.M113.505103 |
PsCYP719A21 |
CYP450 |
Papaver somniferum |
Papaveraceae |
Yes |
Isoquinolinetype Alkaloids,Protopine,Isocorydine,Papaverine,Morphine,Codeine,Sangulnarine,Chelerythrine,Bocconine,Narcotine,Rhoeadane |
cytochrome P450 |
|
JQ659003 |
https://www.ncbi.nlm.nih.gov/nuccore/JQ659003 |
Dang TT,Facchini PJ. CYP82Y1 is N-methylcanadine 1-hydroxylase, a key noscapine biosynthetic enzyme in opium poppy. J Biol Chem. 2014;289 (4):2013-26. doi:10.1074/jbc.M113.505105 |
PsCYP719B1 |
CYP450 |
Papaver somniferum |
Papaveraceae |
Yes |
Isoquinolinetype Alkaloids,Protopine,Isocorydine,Papaverine,Morphine,Codeine,Sangulnarine,Chelerythrine,Bocconine,Narcotine,Rhoeadane |
salutaridine synthase |
|
ABR14720 |
https://www.ncbi.nlm.nih.gov/protein/ABR14720 |
Dang TT,Facchini PJ. CYP82Y1 is N-methylcanadine 1-hydroxylase, a key noscapine biosynthetic enzyme in opium poppy. J Biol Chem. 2014;289 (4):2013-26. doi:10.1074/jbc.M113.505106 |
PsCYP719A25 |
CYP450 |
Papaver somniferum |
Papaveraceae |
Yes |
Isoquinolinetype Alkaloids,Protopine,Isocorydine,Papaverine,Morphine,Codeine,Sangulnarine,Chelerythrine,Bocconine,Narcotine,Rhoeadane |
cheilanthifoline synthase |
|
GU325749 |
https://www.ncbi.nlm.nih.gov/nuccore/GU325749 |
Dang TT,Facchini PJ. CYP82Y1 is N-methylcanadine 1-hydroxylase, a key noscapine biosynthetic enzyme in opium poppy. J Biol Chem. 2014;289 (4):2013-26. doi:10.1074/jbc.M113.505107 |
CjCYP80G2 |
CYP450 |
Papaver somniferum |
Papaveraceae |
Yes |
Isoquinolinetype Alkaloids,Protopine,Isocorydine,Papaverine,Morphine,Codeine,Sangulnarine,Chelerythrine,Bocconine,Narcotine,Rhoeadane |
corytuberine synthase |
|
AB288053 |
https://www.ncbi.nlm.nih.gov/nuccore/AB288053 |
Dang TT,Facchini PJ. CYP82Y1 is N-methylcanadine 1-hydroxylase, a key noscapine biosynthetic enzyme in opium poppy. J Biol Chem. 2014;289 (4):2013-26. doi:10.1074/jbc.M113.505110 |
AtCYP82C2 |
CYP450 |
Papaver somniferum |
Papaveraceae |
Yes |
Isoquinolinetype Alkaloids,Protopine,Isocorydine,Papaverine,Morphine,Codeine,Sangulnarine,Chelerythrine,Bocconine,Narcotine,Rhoeadane |
Indole-3-carbonyl nitrile 4-hydroxylase |
|
O49394 |
https://www.ncbi.nlm.nih.gov/protein/O49394 |
Dang TT,Facchini PJ. CYP82Y1 is N-methylcanadine 1-hydroxylase, a key noscapine biosynthetic enzyme in opium poppy. J Biol Chem. 2014;289 (4):2013-26. doi:10.1074/jbc.M113.505111 |
NtCYP82E4v1 |
CYP450 |
Papaver somniferum |
Papaveraceae |
Yes |
Isoquinolinetype Alkaloids,Protopine,Isocorydine,Papaverine,Morphine,Codeine,Sangulnarine,Chelerythrine,Bocconine,Narcotine,Rhoeadane |
cytochrome P450 monooxygenase |
|
DQ131886 |
https://www.ncbi.nlm.nih.gov/nuccore/DQ131886 |
Dang TT,Facchini PJ. CYP82Y1 is N-methylcanadine 1-hydroxylase, a key noscapine biosynthetic enzyme in opium poppy. J Biol Chem. 2014;289 (4):2013-26. doi:10.1074/jbc.M113.505112 |
VvCYP82C4 |
CYP450 |
Papaver somniferum |
Papaveraceae |
Yes |
Isoquinolinetype Alkaloids,Protopine,Isocorydine,Papaverine,Morphine,Codeine,Sangulnarine,Chelerythrine,Bocconine,Narcotine,Rhoeadane |
cytochrome P452 |
|
XP_02284810 |
https://www.ncbi.nlm.nih.gov/nuccore/?term=XP_02284810 |
Dang TT,Facchini PJ. CYP82Y1 is N-methylcanadine 1-hydroxylase, a key noscapine biosynthetic enzyme in opium poppy. J Biol Chem. 2014;289 (4):2013-26. doi:10.1074/jbc.M113.505114 |
GmCYP82G4 |
CYP450 |
Papaver somniferum |
Papaveraceae |
Yes |
Isoquinolinetype Alkaloids,Protopine,Isocorydine,Papaverine,Morphine,Codeine,Sangulnarine,Chelerythrine,Bocconine,Narcotine,Rhoeadane |
xanthotoxin 5-hydroxylase |
|
XP_003523888 |
https://www.ncbi.nlm.nih.gov/protein/XP_003523888 |
Dang TT,Facchini PJ. CYP82Y1 is N-methylcanadine 1-hydroxylase, a key noscapine biosynthetic enzyme in opium poppy. J Biol Chem. 2014;289 (4):2013-26. doi:10.1074/jbc.M113.505115 |
CjCYP719A1 |
CYP450 |
Coptis chinensis |
Ranunculaceae |
Yes |
Berberine,Berberine,Isoberberine,Rutin |
methylenedioxy bridge-forming enzyme |
|
AB026122.1 |
https://www.ncbi.nlm.nih.gov/gene/?term=AB026122.1 |
Liu Y,Wang B,Shu S, et al. Analysis of the Coptis chinensis genome reveals the diversification of protoberberine-type alkaloids. Nat Commun. 2021;12 (1):3276. doi:10.1038/s41467-021-23611-0 |
CjCYP719A18 |
CYP450 |
Coptis chinensis |
Ranunculaceae |
Yes |
Berberine,Berberine,Isoberberine,Rutin |
protoberberine-type alkaloids |
|
ANY58145.1 |
https://www.ncbi.nlm.nih.gov/gene/?term=ANY58145.1 |
Liu Y,Wang B,Shu S, et al. Analysis of the Coptis chinensis genome reveals the diversification of protoberberine-type alkaloids. Nat Commun. 2021;12 (1):3276. doi:10.1038/s41467-021-23611-1 |
CjCYP719A19 |
CYP450 |
Coptis chinensis |
Ranunculaceae |
Yes |
Berberine,Berberine,Isoberberine,Rutin |
protoberberine-type alkaloids |
|
ANY58146.1 |
https://www.ncbi.nlm.nih.gov/gene/?term=ANY58146.1 |
Liu Y,Wang B,Shu S, et al. Analysis of the Coptis chinensis genome reveals the diversification of protoberberine-type alkaloids. Nat Commun. 2021;12 (1):3276. doi:10.1038/s41467-021-23611-2 |
EcCYP719A2 |
CYP450 |
Coptis chinensis |
Ranunculaceae |
Yes |
Berberine,Berberine,Isoberberine,Rutin |
protoberberine-type alkaloids |
|
AB126257.1 |
https://www.ncbi.nlm.nih.gov/gene/?term=AB126257.1 |
Liu Y,Wang B,Shu S, et al. Analysis of the Coptis chinensis genome reveals the diversification of protoberberine-type alkaloids. Nat Commun. 2021;12 (1):3276. doi:10.1038/s41467-021-23611-3 |
EcCYP719A5 |
CYP450 |
Coptis chinensis |
Ranunculaceae |
Yes |
Berberine,Berberine,Isoberberine,Rutin |
protoberberine-type alkaloids |
|
AB434654.1 |
https://www.ncbi.nlm.nih.gov/gene/?term=AB434654.1 |
Liu Y,Wang B,Shu S, et al. Analysis of the Coptis chinensis genome reveals the diversification of protoberberine-type alkaloids. Nat Commun. 2021;12 (1):3276. doi:10.1038/s41467-021-23611-4 |
ZjCYP |
CYP450 |
Ziziphus jujuba |
Rhamnaceae |
Yes |
Phenols,Flavonoids,Polysaccharides,Vitamin C,Pentacyclic Triterpenoids,Saponins,Lauric Acid,β-Carotene |
assisting alcohol dehydrogenase |
|
LOC107414727 |
https://www.ncbi.nlm.nih.gov/gene/107414727 |
-- |
ZjCYP |
CYP450 |
Ziziphus jujuba |
Rhamnaceae |
Yes |
Phenols,Flavonoids,Polysaccharides,Vitamin C,Pentacyclic Triterpenoids,Saponins,Lauric Acid,β-Carotene |
peptidyl-prolyl cis-trans isomerase CYP19-3 |
|
LOC107412176 |
https://www.ncbi.nlm.nih.gov/gene/107412176 |
-- |
RcCYP |
CYP450 |
Rosa chinensis |
Rosaceae |
Yes |
Flavonoids,Phenolic Acids,Pentacyclic Triterpenes,Steroids |
labd-13Z-ene-9,15,16-triol synthase |
|
LOC112178526 |
https://www.ncbi.nlm.nih.gov/gene/112178526 |
-- |
RcCYP |
CYP450 |
Rosa chinensis |
Rosaceae |
Yes |
Flavonoids,Phenolic Acids,Pentacyclic Triterpenes,Steroids |
protein DETOXIFICATION 45 |
|
LOC112172234 |
https://www.ncbi.nlm.nih.gov/gene/112172234 |
-- |
PdCYP |
CYP450 |
Prunus dulcis |
Rosaceae |
Yes |
Sterols,Methylsterols,Triterpenols,Hydrocarbons |
alpha-humulene 10-hydroxylase |
|
LOC117618671 |
https://www.ncbi.nlm.nih.gov/gene/117618671 |
-- |
PdCYP |
CYP450 |
Prunus dulcis |
Rosaceae |
Yes |
Sterols,Methylsterols,Triterpenols,Hydrocarbons |
cytochrome P450 CYP749A22 |
|
LOC117637521 |
https://www.ncbi.nlm.nih.gov/gene/117637521 |
-- |
CsCYP |
CYP450 |
Citrus sinensis |
Rutaceae |
Yes |
Decanal,Citral,Limonene,Octanol |
assisting alcohol dehydrogenase |
|
LOC102623660 |
https://www.ncbi.nlm.nih.gov/gene/102623660 |
-- |
CsCYP |
CYP450 |
Citrus sinensis |
Rutaceae |
Yes |
Decanal,Citral,Limonene,Octanol |
assisting alcohol dehydrogenase |
|
LOC115716320 |
https://www.ncbi.nlm.nih.gov/gene/115716320 |
-- |
CsCYP |
CYP450 |
Citrus sinensis |
Rutaceae |
Yes |
Decanal,Citral,Limonene,Octanol |
peptidyl-prolyl cis-trans isomerase |
|
LOC101501904 |
https://www.ncbi.nlm.nih.gov/gene/101501904 |
-- |
CaCYP |
CYP450 |
Capsicum annuum |
Solanaceae |
Yes |
Capsaicin |
cysteine proteinase 3 |
|
LOC107877862 |
https://www.ncbi.nlm.nih.gov/gene/107877862 |
-- |
StCYP |
CYP450 |
Solanum tuberosum |
Solanaceae |
Yes |
Carbohydrates,Cellulose |
low-temperature-induced cysteine proteinase |
|
LOC102582822 |
https://www.ncbi.nlm.nih.gov/gene/102582822 |
-- |
SlCYP |
CYP450 |
Solanum lycopersicum |
Solanaceae |
Yes |
Carotenoids |
-- |
|
LOC100736432 |
https://www.ncbi.nlm.nih.gov/gene/100736432 |
-- |
SlCYP |
CYP450 |
Solanum lycopersicum |
Solanaceae |
Yes |
Carotenoids |
Cyp-3 cysteine proteinase |
|
LOC101252505 |
https://www.ncbi.nlm.nih.gov/gene/101252505 |
-- |
AbCYP82M3 |
CYP450 |
Atropa belladonna |
Solanaceae |
Yes |
Hyoscyamine,Atropine,Scopolamine,Belladonin |
tropinone synthase |
|
MH292964 |
https://www.ncbi.nlm.nih.gov/nuccore/MH292964.1/ |
Bedewitz MA,Jones AD,D'Auria JC, et al. Tropinone synthesis via an atypical polyketide synthase and P450-mediated cyclization. Nat Commun. 2018;9 (1):5281. doi:10.1038/s41467-018-07671-3 |
NtCYP |
CYP450 |
Nicotiana tomentosiformis |
Solanaceae |
Yes |
L-nicotine,Quinine,Dehydrotoxine,Nicotine |
(S)-N-methylcoclaurine 3'-hydroxylase isozyme 2 |
|
LOC104102595 |
https://www.ncbi.nlm.nih.gov/gene/104102595 |
-- |
NtCYP |
CYP450 |
Nicotiana tomentosiformis |
Solanaceae |
Yes |
L-nicotine,Quinine,Dehydrotoxine,Nicotine |
3,9-dihydroxypterocarpan 6A-monooxygenase-like |
|
LOC104096160 |
https://www.ncbi.nlm.nih.gov/gene/104096160 |
-- |
NtCYP |
CYP450 |
Nicotiana tomentosiformis |
Solanaceae |
Yes |
L-nicotine,Quinine,Dehydrotoxine,Nicotine |
alkane hydroxylase MAH1 |
|
LOC104100153 |
https://www.ncbi.nlm.nih.gov/gene/104100153 |
-- |
NtCYP |
CYP450 |
Nicotiana tomentosiformis |
Solanaceae |
Yes |
L-nicotine,Quinine,Dehydrotoxine,Nicotine |
cytochrome P450 714B1-like |
|
LOC104113159 |
https://www.ncbi.nlm.nih.gov/gene/104113159 |
-- |
NtCYP |
CYP450 |
Nicotiana tomentosiformis |
Solanaceae |
Yes |
L-nicotine,Quinine,Dehydrotoxine,Nicotine |
cytochrome P450 714C2-like |
|
LOC104121060 |
https://www.ncbi.nlm.nih.gov/gene/104121060 |
-- |
NtCYP |
CYP450 |
Nicotiana tomentosiformis |
Solanaceae |
Yes |
L-nicotine,Quinine,Dehydrotoxine,Nicotine |
cytochrome P450 734A1-like |
|
LOC104085859 |
https://www.ncbi.nlm.nih.gov/gene/104085859 |
-- |
NtCYP |
CYP450 |
Nicotiana tomentosiformis |
Solanaceae |
Yes |
L-nicotine,Quinine,Dehydrotoxine,Nicotine |
cytochrome P450 89A2-like |
|
LOC104118408 |
https://www.ncbi.nlm.nih.gov/gene/104118408 |
-- |
NtCYP |
CYP450 |
Nicotiana tomentosiformis |
Solanaceae |
Yes |
L-nicotine,Quinine,Dehydrotoxine,Nicotine |
cytochrome P450 93A3-like |
|
LOC104097413 |
https://www.ncbi.nlm.nih.gov/gene/104097413 |
-- |
NtCYP |
CYP450 |
Nicotiana tomentosiformis |
Solanaceae |
Yes |
L-nicotine,Quinine,Dehydrotoxine,Nicotine |
geraniol 8-hydroxylase-like |
|
LOC104120481 |
https://www.ncbi.nlm.nih.gov/gene/104120481 |
-- |
NtCYP |
CYP450 |
Nicotiana tomentosiformis |
Solanaceae |
Yes |
L-nicotine,Quinine,Dehydrotoxine,Nicotine |
isoleucine N-monooxygenase |
|
LOC104095765 |
https://www.ncbi.nlm.nih.gov/gene/104095765 |
-- |
NtCYP |
CYP450 |
Nicotiana tomentosiformis |
Solanaceae |
Yes |
L-nicotine,Quinine,Dehydrotoxine,Nicotine |
isoleucine N-monooxygenase 1-like |
|
LOC104097091 |
https://www.ncbi.nlm.nih.gov/gene/104097091 |
-- |
NtCYP |
CYP450 |
Nicotiana tomentosiformis |
Solanaceae |
Yes |
L-nicotine,Quinine,Dehydrotoxine,Nicotine |
premnaspirodiene oxygenase |
|
LOC104103514 |
https://www.ncbi.nlm.nih.gov/gene/104103514 |
-- |
NtCYP |
CYP450 |
Nicotiana tomentosiformis |
Solanaceae |
Yes |
L-nicotine,Quinine,Dehydrotoxine,Nicotine |
premnaspirodiene oxygenase-like |
|
LOC104103395 |
https://www.ncbi.nlm.nih.gov/gene/104103395 |
-- |
NtCYP |
CYP450 |
Nicotiana tomentosiformis |
Solanaceae |
Yes |
L-nicotine,Quinine,Dehydrotoxine,Nicotine |
-- |
|
LOC104093267 |
https://www.ncbi.nlm.nih.gov/gene/104093267 |
-- |
LrOMT |
OMT |
Lycoris radiata |
Amaryllidaceae |
Yes |
Lycine,Homolycorine,Pseudolycorine,Alicin,Demethyl Allicin,Demethyl Homolycorine,Allicin,Narcissus,Allicin |
O-methyltransferase |
|
MK805029.1 |
https://www.ncbi.nlm.nih.gov/nuccore/MK805029.1 |
Li W, Qiao C, Pang J, Zhang G, Luo Y. The versatile O-methyltransferase LrOMT catalyzes multiple O-methylation reactions in amaryllidaceae alkaloids biosynthesis. Int J Biol Macromol. 2019;141:680-692. doi:10.1016/j.ijbiomac.2019.09.011 |
RsOMT |
OMT |
Rauvolfia serpentina |
Apocynaceae |
Yes |
γ-Linoleic Acid,Fatty Acids,Carotenoids |
caffeic acid O-methyltransferase |
|
KX687825.1 |
https://www.ncbi.nlm.nih.gov/nuccore/KX687825.1 |
Wiens B, De Luca V. Molecular and biochemical characterization of a benzenoid/phenylpropanoid meta/para-O-methyltransferase from Rauwolfia serpentina roots. Phytochemistry. 2016;132:5-15. doi:10.1016/j.phytochem.2016.10.004 |
ACOMT |
OMT |
Acorus calamus |
Araceae |
Yes |
β- Asarone,α-Asarum Ether |
-- |
|
CM060867.1 |
https://www.ncbi.nlm.nih.gov/nuccore/CM060867.1 |
Givnish TJ, et al. Monocot plastid phylogenomics, timeline, net rates of species diversification, the power of multi-gene analyses, and a functional model for the origin of monocots. Am. J. Bot. 2018;105:1888–1910. |
ACOMT |
OMT |
Acorus calamus |
Araceae |
Yes |
β- Asarone,α-Asarum Ether |
-- |
|
CM060868.1 |
https://www.ncbi.nlm.nih.gov/nuccore/CM060868.1 |
Givnish TJ, et al. Monocot plastid phylogenomics, timeline, net rates of species diversification, the power of multi-gene analyses, and a functional model for the origin of monocots. Am. J. Bot. 2018;105:1888–1910. |
ACOMT |
OMT |
Acorus calamus |
Araceae |
Yes |
β- Asarone,α-Asarum Ether |
-- |
|
CM060877.1 |
https://www.ncbi.nlm.nih.gov/nuccore/CM060877.1 |
Givnish TJ, et al. Monocot plastid phylogenomics, timeline, net rates of species diversification, the power of multi-gene analyses, and a functional model for the origin of monocots. Am. J. Bot. 2018;105:1888–1910. |
ACOMT |
OMT |
Acorus calamus |
Araceae |
Yes |
β- Asarone,α-Asarum Ether |
-- |
|
CM060879.1 |
https://www.ncbi.nlm.nih.gov/nuccore/CM060879.1 |
Givnish TJ, et al. Monocot plastid phylogenomics, timeline, net rates of species diversification, the power of multi-gene analyses, and a functional model for the origin of monocots. Am. J. Bot. 2018;105:1888–1910. |
ACOMT |
OMT |
Acorus calamus |
Araceae |
Yes |
β- Asarone,α-Asarum Ether |
-- |
|
JAUJYO000000000.1 |
https://www.ncbi.nlm.nih.gov/nuccore/JAUJYO000000000.1 |
Givnish TJ, et al. Monocot plastid phylogenomics, timeline, net rates of species diversification, the power of multi-gene analyses, and a functional model for the origin of monocots. Am. J. Bot. 2018;105:1888–1910. |
ACOMT |
OMT |
Acorus calamus |
Araceae |
Yes |
β- Asarone,α-Asarum Ether |
-- |
|
JAUJYO010000010.1 |
https://www.ncbi.nlm.nih.gov/nuccore/JAUJYO010000010.1 |
Givnish TJ, et al. Monocot plastid phylogenomics, timeline, net rates of species diversification, the power of multi-gene analyses, and a functional model for the origin of monocots. Am. J. Bot. 2018;105:1888–1910. |
ACOMT |
OMT |
Acorus calamus |
Araceae |
Yes |
β- Asarone,α-Asarum Ether |
-- |
|
JAUJYO010000011.1 |
https://www.ncbi.nlm.nih.gov/nuccore/JAUJYO010000011.1 |
Givnish TJ, et al. Monocot plastid phylogenomics, timeline, net rates of species diversification, the power of multi-gene analyses, and a functional model for the origin of monocots. Am. J. Bot. 2018;105:1888–1910. |
ACOMT |
OMT |
Acorus calamus |
Araceae |
Yes |
β- Asarone,α-Asarum Ether |
-- |
|
JAUJYO010000020.1 |
https://www.ncbi.nlm.nih.gov/nuccore/JAUJYO010000020.1 |
Givnish TJ, et al. Monocot plastid phylogenomics, timeline, net rates of species diversification, the power of multi-gene analyses, and a functional model for the origin of monocots. Am. J. Bot. 2018;105:1888–1910. |
ACOMT |
OMT |
Acorus calamus |
Araceae |
Yes |
β- Asarone,α-Asarum Ether |
-- |
|
JAUJYO010000022.1 |
https://www.ncbi.nlm.nih.gov/nuccore/JAUJYO010000022.1 |
Givnish TJ, et al. Monocot plastid phylogenomics, timeline, net rates of species diversification, the power of multi-gene analyses, and a functional model for the origin of monocots. Am. J. Bot. 2018;105:1888–1910. |
EgOMT |
OMT |
Elaeis guineensis |
Arecaceae |
Yes |
Carotenoids |
trans-resveratrol di-O-methyltransferase |
|
JN003483.1 |
https://www.ncbi.nlm.nih.gov/nuccore/JN003483.1 |
-- |
N7OMT |
OMT |
Berberis koreana |
Berberidaceae |
Yes |
Berberine,Oxyacanthine,Jatrorrhizine,Magnoflorine,Berbamine |
-- |
|
-- |
-- |
Roy NS,Choi IY,Um T, et al. Gene Expression and Isoform Identification of PacBio Full-Length cDNA Sequences for Berberine Biosynthesis in Berberis koreana. Plants (Basel). 2021;10 (7):null. doi:10.3390/plants10071314 |
SOMT |
OMT |
Berberis koreana |
Berberidaceae |
Yes |
Berberine,Oxyacanthine,Jatrorrhizine,Magnoflorine,Berbamine |
-- |
|
-- |
-- |
Roy NS,Choi IY,Um T, et al. Gene Expression and Isoform Identification of PacBio Full-Length cDNA Sequences for Berberine Biosynthesis in Berberis koreana. Plants (Basel). 2021;10 (7):null. doi:10.3390/plants10071315 |
HNMC4’OMT |
OMT |
Sinopodophyllum hexandrum |
Berberidaceae |
Yes |
Cardiac Glycosides,Steroidal Saponins |
3'-hydroxy-N-methyl-(S)-coclaurine 4'-O-methyltransferase |
|
KJ786960 |
https://www.ncbi.nlm.nih.gov/nuccore/KJ786960 |
Yu X, Liu Z, Sun X. Single-cell and spatial multi-omics in the plant sciences: Technical advances, applications, and perspectives. Plant Commun. 2023;4(3):100508. doi:10.1016/j.xplc.2022.100508 |
ShCCoA-OMT |
OMT |
Sinopodophyllum hexandrum |
Berberidaceae |
Yes |
Cardiac Glycosides,Steroidal Saponins |
caffeoyl CoA O-methyltransferase |
|
MW531750.1 |
https://www.ncbi.nlm.nih.gov/nuccore/MW531750.1 |
-- |
ShOMT |
OMT |
Sinopodophyllum hexandrum |
Berberidaceae |
Yes |
Cardiac Glycosides,Steroidal Saponins |
catechol O-methyltransferase |
|
FK934374.1 |
https://www.ncbi.nlm.nih.gov/nuccore/FK934374.1 |
-- |
BnOMT |
OMT |
Brassica napus |
Brassicaceae |
No |
Isothiocyanate,Indole Compounds,Carotene |
O-methyltransferase |
|
JX258816.1 |
https://www.ncbi.nlm.nih.gov/nuccore/JX258816.1 |
-- |
BnOMT |
OMT |
Brassica napus |
Brassicaceae |
No |
Isothiocyanate,Indole Compounds,Carotene |
O-methyltransferase |
|
JX258815.1 |
https://www.ncbi.nlm.nih.gov/nuccore/JX258815.1 |
-- |
BnOMT |
OMT |
Brassica napus |
Brassicaceae |
No |
Isothiocyanate,Indole Compounds,Carotene |
O-methyltransferase |
|
JX258814.1 |
https://www.ncbi.nlm.nih.gov/nuccore/JX258814.1 |
-- |
BnOMT |
OMT |
Brassica napus |
Brassicaceae |
No |
Isothiocyanate,Indole Compounds,Carotene |
O-methyltransferase |
|
KJ914580.1 |
https://www.ncbi.nlm.nih.gov/nuccore/KJ914580.1 |
-- |
BnOMT |
OMT |
Brassica napus |
Brassicaceae |
No |
Isothiocyanate,Indole Compounds,Carotene |
O-methyltransferase |
|
KJ914579.1 |
https://www.ncbi.nlm.nih.gov/nuccore/KJ914579.1 |
-- |
BjSadmt |
OMT |
Brassica juncea |
Brassicaceae |
Yes |
Thioglucoside |
S-adenosylmethionine-dependent methyltransferase |
|
HM627211.1 |
https://www.ncbi.nlm.nih.gov/nuccore/HM627211.1 |
-- |
GsOMT1 |
OMT |
Gloriosa superba |
Colchicaceae |
Yes |
Colchicine |
O-methyltransferase |
|
MT512039 |
https://www.ncbi.nlm.nih.gov/nuccore/MT512039) |
Huang W,Wang Y,Tian W, et al. Biosynthesis Investigations of Terpenoid, Alkaloid, and Flavonoid Antimicrobial Agents Derived from Medicinal Plants. Antibiotics (Basel). 2022;11(10):1380. doi:10.3390/antibiotics11101380 |
GsNMT1 |
OMT |
Gloriosa superba |
Colchicaceae |
Yes |
Colchicine |
-- |
|
-- |
-- |
Huang W,Wang Y,Tian W, et al. Biosynthesis Investigations of Terpenoid, Alkaloid, and Flavonoid Antimicrobial Agents Derived from Medicinal Plants. Antibiotics (Basel). 2022;11(10):1380. doi:10.3390/antibiotics11101380 |
GsOMT2 |
OMT |
Gloriosa superba |
Colchicaceae |
Yes |
Colchicine |
O-methyltransferase |
|
MT512043 |
https://www.ncbi.nlm.nih.gov/nuccore/MT512043 |
Huang W,Wang Y,Tian W, et al. Biosynthesis Investigations of Terpenoid, Alkaloid, and Flavonoid Antimicrobial Agents Derived from Medicinal Plants. Antibiotics (Basel). 2022;11(10):1380. doi:10.3390/antibiotics11101380 |
GsOMT3 |
OMT |
Gloriosa superba |
Colchicaceae |
Yes |
Colchicine |
O-methyltransferase |
|
MT512044 |
https://www.ncbi.nlm.nih.gov/nuccore/MT512044 |
Huang W,Wang Y,Tian W, et al. Biosynthesis Investigations of Terpenoid, Alkaloid, and Flavonoid Antimicrobial Agents Derived from Medicinal Plants. Antibiotics (Basel). 2022;11(10):1380. doi:10.3390/antibiotics11101380 |
GsOMT4 |
OMT |
Gloriosa superba |
Colchicaceae |
Yes |
Colchicine |
O-methyltransferase |
|
MT512046 |
https://www.ncbi.nlm.nih.gov/nuccore/MT512046 |
Huang W,Wang Y,Tian W, et al. Biosynthesis Investigations of Terpenoid, Alkaloid, and Flavonoid Antimicrobial Agents Derived from Medicinal Plants. Antibiotics (Basel). 2022;11(10):1380. doi:10.3390/antibiotics11101380 |
VcOMT |
OMT |
Vaccinium corymbosum |
Ericaceae |
Yes |
Anthocyanin |
O-methyltransferase |
|
KJ830748.1 |
https://www.ncbi.nlm.nih.gov/nuccore/KJ830748.1 |
-- |
NtPMT |
OMT |
Caragana korshinskii kom |
Fabaceae |
Yes |
Anthocyanidin,Hemicellulose |
Putrescine N-Methyltransferase |
|
DD093782.1 |
https://www.ncbi.nlm.nih.gov/nuccore/DD093782.1 |
Xia K,Liu X,Zhang Q, et al. Promoting scopolamine biosynthesis in transgenic Atropa belladonna plants with pmt and h6h overexpression under field conditions. Plant Physiol Biochem. 2016;106:46-53. doi:10.1016/j.plaphy.2016.04.034 |
Ps2OMT |
OMT |
Pisum sativum |
Papilionaceae |
Yes |
Carotenoids |
plastidic 2-oxoglutarate |
|
FN297817.1 |
https://www.ncbi.nlm.nih.gov/nuccore/FN297817.1 |
Riebeseel E, Häusler RE, Radchuk R, et al. The 2-oxoglutarate/malate translocator mediates amino acid and storage protein biosynthesis in pea embryos. Plant J. 2010;61(2):350-363. doi:10.1111/j.1365-313X.2009.04058.x |
LuOMT |
OMT |
Lotus uliginosus |
Fabaceae |
Yes |
Corniculatusin,Corniculatusin-3-O-β-D-galactoside |
O-methyltransferase |
|
EH380094.1 |
https://www.ncbi.nlm.nih.gov/nuccore/EH380094.1 |
-- |
MtOMT1 |
OMT |
Medicago truncatula |
Fabaceae |
Yes |
Coumarins,Polysaccharides,Saponins |
-- |
|
BV165455.1 |
https://www.ncbi.nlm.nih.gov/nuccore/BV165455.1 |
Choi HK, Luckow MA, Doyle J, Cook DR. Development of nuclear gene-derived molecular markers linked to legume genetic maps. Mol Genet Genomics. 2006;276(1):56-70. doi:10.1007/s00438-006-0118-8 |
MtOMT2 |
OMT |
Medicago truncatula |
Fabaceae |
Yes |
Coumarins,Polysaccharides,Saponins |
-- |
|
BV165456.1 |
https://www.ncbi.nlm.nih.gov/nuccore/BV165456.1 |
Choi HK, Luckow MA, Doyle J, Cook DR. Development of nuclear gene-derived molecular markers linked to legume genetic maps. Mol Genet Genomics. 2006;276(1):56-70. doi:10.1007/s00438-006-0118-8 |
VaOMT |
OMT |
Vigna angularis |
Fabaceae |
Yes |
Triterpenoidsaponin |
-- |
|
CM003374.1 |
https://www.ncbi.nlm.nih.gov/nuccore/CM003374.1 |
-- |
TaOMT1 |
OMT |
Triticum aestivum |
Gramineae |
Yes |
Albumin,Globulin,Gliadin,Glutenin |
1 caffeoyl-CoA O-methyltransferase 1 |
|
MG979066.1 |
https://www.ncbi.nlm.nih.gov/nuccore/MG979066.1 |
Li X, Qian X, Lǚ X, et al. Upregulated structural and regulatory genes involved in anthocyanin biosynthesis for coloration of purple grains during the middle and late grain-filling stages. Plant Physiol Biochem. 2018;130:235-247. doi:10.1016/j.plaphy.2018.07.011 |
TaOMT |
OMT |
Triticum aestivum |
Gramineae |
Yes |
Albumin,Globulin,Gliadin,Glutenin |
O-methyltransferase |
|
EC907558.1 |
https://www.ncbi.nlm.nih.gov/nuccore/EC907558.1 |
-- |
OsOMT |
OMT |
Oryza sativa |
Gramineae |
Yes |
Anthocyanidin,Hemicellulose |
-- |
|
AP014965.1 |
https://www.ncbi.nlm.nih.gov/nuccore/AP014965.1 |
Kawahara Y, de la Bastide M, Hamilton JP, et al. Improvement of the Oryza sativa Nipponbare reference genome using next generation sequence and optical map data. Rice (N Y). 2013;6(1):4. doi:10.1186/1939-8433-6-4 |
OsOMT |
OMT |
Oryza sativa |
Gramineae |
Yes |
Anthocyanidin,Hemicellulose |
-- |
|
AP014961.1 |
https://www.ncbi.nlm.nih.gov/nuccore/AP014961.1 |
Kawahara Y, de la Bastide M, Hamilton JP, et al. Improvement of the Oryza sativa Nipponbare reference genome using next generation sequence and optical map data. Rice (N Y). 2013;6(1):4. doi:10.1186/1939-8433-6-4 |
OsOMT |
OMT |
Oryza sativa |
Gramineae |
Yes |
Anthocyanidin,Hemicellulose |
-- |
|
AP008212.2 |
https://www.ncbi.nlm.nih.gov/nuccore/AP008212.2 |
Ohyanagi H, Tanaka T, Sakai H, et al. The Rice Annotation Project Database (RAP-DB): hub for Oryza sativa ssp. japonica genome information. Nucleic Acids Res. 2006;34(Database issue):D741-D744. doi:10.1093/nar/gkj094 |
OsOMT |
OMT |
Oryza sativa |
Gramineae |
Yes |
Anthocyanidin,Hemicellulose |
-- |
|
AP008218.2 |
https://www.ncbi.nlm.nih.gov/nuccore/AP008218.2 |
Ohyanagi H, Tanaka T, Sakai H, et al. The Rice Annotation Project Database (RAP-DB): hub for Oryza sativa ssp. japonica genome information. Nucleic Acids Res. 2006;34(Database issue):D741-D744. doi:10.1093/nar/gkj094 |
OsOMT |
OMT |
Oryza sativa |
Gramineae |
Yes |
Anthocyanidin,Hemicellulose |
-- |
|
AP008215.2 |
https://www.ncbi.nlm.nih.gov/nuccore/AP008215.2 |
Ohyanagi H, Tanaka T, Sakai H, et al. The Rice Annotation Project Database (RAP-DB): hub for Oryza sativa ssp. japonica genome information. Nucleic Acids Res. 2006;34(Database issue):D741-D744. doi:10.1093/nar/gkj094 |
OsOMT |
OMT |
Oryza sativa |
Gramineae |
Yes |
Anthocyanidin,Hemicellulose |
-- |
|
AP008211.2 |
https://www.ncbi.nlm.nih.gov/nuccore/AP008211.2 |
Ohyanagi H, Tanaka T, Sakai H, et al. The Rice Annotation Project Database (RAP-DB): hub for Oryza sativa ssp. japonica genome information. Nucleic Acids Res. 2006;34(Database issue):D741-D744. doi:10.1093/nar/gkj094 |
OsOMT |
OMT |
Oryza sativa |
Gramineae |
Yes |
Anthocyanidin,Hemicellulose |
-- |
|
AP008216.2 |
https://www.ncbi.nlm.nih.gov/nuccore/AP008216.2 |
Ohyanagi H, Tanaka T, Sakai H, et al. The Rice Annotation Project Database (RAP-DB): hub for Oryza sativa ssp. japonica genome information. Nucleic Acids Res. 2006;34(Database issue):D741-D744. doi:10.1093/nar/gkj094 |
OsOMT |
OMT |
Oryza sativa |
Gramineae |
Yes |
Anthocyanidin,Hemicellulose |
-- |
|
EU882982.1 |
https://www.ncbi.nlm.nih.gov/nuccore/AK072740.1 |
Rice Full-Length cDNA Consortium; National Institute of Agrobiological Sciences Rice Full-Length cDNA Project Team, Kikuchi S, et al. Collection, mapping, and annotation of over 28,000 cDNA clones from japonica rice. Science. 2003;301(5631):376-379. doi:10.1126/science.1081288 |
OsOMT |
OMT |
Oryza sativa |
Gramineae |
Yes |
Anthocyanidin,Hemicellulose |
-- |
|
AK069721.1 |
https://www.ncbi.nlm.nih.gov/nuccore/AK069721.1 |
Rice Full-Length cDNA Consortium; National Institute of Agrobiological Sciences Rice Full-Length cDNA Project Team, Kikuchi S, et al. Collection, mapping, and annotation of over 28,000 cDNA clones from japonica rice. Science. 2003;301(5631):376-379. doi:10.1126/science.1081288 |
OsOMT |
OMT |
Oryza sativa |
Gramineae |
Yes |
Anthocyanidin,Hemicellulose |
-- |
|
AK069308.1 |
https://www.ncbi.nlm.nih.gov/nuccore/AK069308.1 |
Rice Full-Length cDNA Consortium; National Institute of Agrobiological Sciences Rice Full-Length cDNA Project Team, Kikuchi S, et al. Collection, mapping, and annotation of over 28,000 cDNA clones from japonica rice. Science. 2003;301(5631):376-379. doi:10.1126/science.1081288 |
OsOMT |
OMT |
Oryza sativa |
Gramineae |
Yes |
Anthocyanidin,Hemicellulose |
-- |
|
AK068905.1 |
https://www.ncbi.nlm.nih.gov/nuccore/AK068905.1 |
Rice Full-Length cDNA Consortium; National Institute of Agrobiological Sciences Rice Full-Length cDNA Project Team, Kikuchi S, et al. Collection, mapping, and annotation of over 28,000 cDNA clones from japonica rice. Science. 2003;301(5631):376-379. doi:10.1126/science.1081288 |
OsOMT |
OMT |
Oryza sativa |
Gramineae |
Yes |
Anthocyanidin,Hemicellulose |
O-methyltransferase |
|
CB096268.1 |
https://www.ncbi.nlm.nih.gov/nuccore/CB096268.1 |
-- |
OsOMT |
OMT |
Oryza sativa |
Gramineae |
Yes |
Anthocyanidin,Hemicellulose |
O-methyltransferase |
|
CA764922.1 |
https://www.ncbi.nlm.nih.gov/nuccore/CA764922.1 |
-- |
Id6OMT |
OMT |
Iris dichotoma |
Iridaceae |
Yes |
Volatile Oils |
O-methyltransferase |
|
MW525205.1 |
https://www.ncbi.nlm.nih.gov/nuccore/MW525205.1 |
-- |
MXvOdOMT |
OMT |
Medicago sativa subsp. X varia |
Fabaceae |
Yes |
Alfalfa Polysaccharides,Alfalfa Saponins |
O-diphenol-O-methyl transferase |
|
AJ248322.1 |
https://www.ncbi.nlm.nih.gov/nuccore/AJ248322.1 |
Jiménez-Zurdo JI, Frugier F, Crespi MD, Kondorosi A. Expression profiles of 22 novel molecular markers for organogenetic pathways acting in alfalfa nodule development. Mol Plant Microbe Interact. 2000;13(1):96-106. doi:10.1094/MPMI.2000.13.1.96 |
GaOMT |
OMT |
Genlisea aurea |
Lentibulariaceae |
No |
γ-Linoleic Acid,Fatty Acids,Carotenoids |
-- |
|
KE535343.1 |
https://www.ncbi.nlm.nih.gov/nuccore/KE535343.1 |
Leushkin EV, Sutormin RA, Nabieva ER, Penin AA, Kondrashov AS, Logacheva MD. The miniature genome of a carnivorous plant Genlisea aurea contains a low number of genes and short non-coding sequences. BMC Genomics. 2013;14:476. doi:10.1186/1471-2164-14-476 |
GaOMT |
OMT |
Genlisea aurea |
Lentibulariaceae |
No |
γ-Linoleic Acid,Fatty Acids,Carotenoids |
-- |
|
KE537233.1 |
https://www.ncbi.nlm.nih.gov/nuccore/KE537233.1 |
Leushkin EV, Sutormin RA, Nabieva ER, Penin AA, Kondrashov AS, Logacheva MD. The miniature genome of a carnivorous plant Genlisea aurea contains a low number of genes and short non-coding sequences. BMC Genomics. 2013;14:476. doi:10.1186/1471-2164-14-476 |
GaOMT |
OMT |
Genlisea aurea |
Lentibulariaceae |
No |
γ-Linoleic Acid,Fatty Acids,Carotenoids |
-- |
|
AUSU01008715.1 |
https://www.ncbi.nlm.nih.gov/nuccore/AUSU01008715.1 |
Leushkin EV, Sutormin RA, Nabieva ER, Penin AA, Kondrashov AS, Logacheva MD. The miniature genome of a carnivorous plant Genlisea aurea contains a low number of genes and short non-coding sequences. BMC Genomics. 2013;14:476. doi:10.1186/1471-2164-14-476 |
GaOMT |
OMT |
Genlisea aurea |
Lentibulariaceae |
No |
γ-Linoleic Acid,Fatty Acids,Carotenoids |
-- |
|
AUSU01010609.1 |
https://www.ncbi.nlm.nih.gov/nuccore/AUSU01010609.1 |
Leushkin EV, Sutormin RA, Nabieva ER, Penin AA, Kondrashov AS, Logacheva MD. The miniature genome of a carnivorous plant Genlisea aurea contains a low number of genes and short non-coding sequences. BMC Genomics. 2013;14:476. doi:10.1186/1471-2164-14-476 |
LtOMT |
OMT |
Linum tenue |
Linaceae |
Yes |
Tocopherol,Lignans,Cyanide |
-- |
|
CAMGYJ010000004.1 |
https://www.ncbi.nlm.nih.gov/nuccore/CAMGYJ010000004.1 |
-- |
GaOMT |
OMT |
Gossypium arboreum |
Malvaceae |
Yes |
Palmitic Acid |
-- |
|
KN399258.1 |
https://www.ncbi.nlm.nih.gov/nuccore/KN399258.1 |
-- |
GaOMT |
OMT |
Gossypium arboreum |
Malvaceae |
Yes |
Palmitic Acid |
-- |
|
KN400214.1 |
https://www.ncbi.nlm.nih.gov/nuccore/KN400214.1 |
-- |
GaOMT |
OMT |
Gossypium anomalum |
Malvaceae |
Yes |
Polyester |
-- |
|
CM033491.1 |
https://www.ncbi.nlm.nih.gov/nuccore/CM033491.1 |
Grover CE, Yuan D, Arick MA, et al. The Gossypium anomalum genome as a resource for cotton improvement and evolutionary analysis of hybrid incompatibility. G3 (Bethesda). 2021;11(11):jkab319. doi:10.1093/g3journal/jkab319 |
GaOMT |
OMT |
Gossypium anomalum |
Malvaceae |
Yes |
Polyester |
-- |
|
JAHUZN010000008.1 |
https://www.ncbi.nlm.nih.gov/nuccore/JAHUZN010000008.1 |
Grover CE, Yuan D, Arick MA, et al. The Gossypium anomalum genome as a resource for cotton improvement and evolutionary analysis of hybrid incompatibility. G3 (Bethesda). 2021;11(11):jkab319. doi:10.1093/g3journal/jkab319 |
GaOMT |
OMT |
Gossypium anomalum |
Malvaceae |
Yes |
Polyester |
-- |
|
CM033495.1 |
https://www.ncbi.nlm.nih.gov/nuccore/CM033495.1 |
Grover CE, Yuan D, Arick MA, et al. The Gossypium anomalum genome as a resource for cotton improvement and evolutionary analysis of hybrid incompatibility. G3 (Bethesda). 2021;11(11):jkab319. doi:10.1093/g3journal/jkab319 |
GaOMT |
OMT |
Gossypium anomalum |
Malvaceae |
Yes |
Polyester |
-- |
|
JAHUZN010000012.1 |
https://www.ncbi.nlm.nih.gov/nuccore/JAHUZN010000012.1 |
Grover CE, Yuan D, Arick MA, et al. The Gossypium anomalum genome as a resource for cotton improvement and evolutionary analysis of hybrid incompatibility. G3 (Bethesda). 2021;11(11):jkab319. doi:10.1093/g3journal/jkab319 |
MaMT1 |
OMT |
Morus alba |
Moraceae |
Yes |
Flavonoids,Phenols,Quinones,Triterpenes,Coumarins,Polyhydroxyalkaloids |
serine hydroxymethyltransferase |
|
OM140666 |
https://www.ncbi.nlm.nih.gov/nuccore/OM140666 |
Wan J,Liao Y,Liu J, et al. Screening, cloning and functional characterization of key methyltransferase genes involved in the methylation step of 1-deoxynojirimycin alkaloids biosynthesis in mulberry leaves. Planta. 2022;255 (6):121. doi:10.1007/s00425-022-03901-7 |
MaOMT |
OMT |
Morus alba |
Moraceae |
Yes |
Flavonoids,Phenols,Quinones,Triterpenes,Coumarins,Polyhydroxyalkaloids |
-- |
|
MN937270.1 |
https://www.ncbi.nlm.nih.gov/nuccore/MN937270.1 |
-- |
MaOMT |
OMT |
Morus alba |
Moraceae |
Yes |
Flavonoids,Phenols,Quinones,Triterpenes,Coumarins,Polyhydroxyalkaloids |
-- |
|
MN937269.1 |
https://www.ncbi.nlm.nih.gov/nuccore/MN937269.1 |
-- |
MaOMT |
OMT |
Morus alba |
Moraceae |
Yes |
Flavonoids,Phenols,Quinones,Triterpenes,Coumarins,Polyhydroxyalkaloids |
-- |
|
MN937268.1 |
https://www.ncbi.nlm.nih.gov/nuccore/MN937268.1 |
-- |
MaOMT |
OMT |
Morus alba |
Moraceae |
Yes |
Flavonoids,Phenols,Quinones,Triterpenes,Coumarins,Polyhydroxyalkaloids |
-- |
|
MN937267.1 |
https://www.ncbi.nlm.nih.gov/nuccore/MN937267.1 |
-- |
EgOMT |
OMT |
Eucalyptus gunnii |
Myrtaceae |
Yes |
Eucalyptus Oil,Organic Acids,Tannins |
O-Methyltransferase |
|
X74814.1 |
https://www.ncbi.nlm.nih.gov/nuccore/X74814.1 |
Poeydomenge O, Boudet AM, Grima-Pettenati J. A cDNA encoding S-adenosyl-L-methionine:caffeic acid 3-O-methyltransferase from Eucalyptus. Plant Physiol. 1994;105(2):749-750. doi:10.1104/pp.105.2.749 |
NnOMT5 |
OMT |
Nelumbo nucifera |
Nymphaeaceae |
Yes |
Roemerine |
7-O-methyltransferase |
|
OP795722 |
https://www.ncbi.nlm.nih.gov/nuccore/OP795722 |
Menéndez-Perdomo IM,Facchini PJ. Elucidation of the (R)-enantiospecific benzylisoquinoline alkaloid biosynthetic pathways in sacred lotus (Nelumbo nucifera). Sci Rep. 2023;13 (1):2955. doi:10.1038/s41598-023-29415-0 |
NnOMT7 |
OMT |
Nelumbo nucifera |
Nymphaeaceae |
Yes |
Roemerine |
7-O-methyltransferase |
|
OP795724 |
https://www.ncbi.nlm.nih.gov/nuccore/OP795724 |
Menéndez-Perdomo IM,Facchini PJ. Elucidation of the (R)-enantiospecific benzylisoquinoline alkaloid biosynthetic pathways in sacred lotus (Nelumbo nucifera). Sci Rep. 2023;13 (1):2955. doi:10.1038/s41598-023-29415-0 |
NnOMT1 |
OMT |
Nelumbo nucifera |
Nymphaeaceae |
Yes |
Roemerine |
-- |
|
OP795721 |
https://www.ncbi.nlm.nih.gov/nuccore/OP795721 |
Menéndez-Perdomo IM,Facchini PJ. Elucidation of the (R)-enantiospecific benzylisoquinoline alkaloid biosynthetic pathways in sacred lotus (Nelumbo nucifera). Sci Rep. 2023;13 (1):2955. doi:10.1038/s41598-023-29415-0 |
NnOMT1 |
OMT |
Nelumbo nucifera |
Nymphaeaceae |
Yes |
Roemerine |
6-O-methyltransferase |
|
XM_010245752 |
https://www.ncbi.nlm.nih.gov/nuccore/XM_010245752 |
Menéndez-Perdomo IM,Facchini PJ. Isolation and characterization of two O -methyltransferases involved in benzylisoquinoline alkaloid biosynthesis in sacred lotus ( Nelumbo nucifera ). J Biol Chem. 2020;295 (6):1598-1612. doi:10.1074/jbc.RA119.011547 |
NnOMT5 |
OMT |
Nelumbo nucifera |
Nymphaeaceae |
Yes |
Roemerine |
6-O-methyltransferase |
|
XM_010277761 |
https://www.ncbi.nlm.nih.gov/nuccore/XM_010277761 |
Menéndez-Perdomo IM,Facchini PJ. Isolation and characterization of two O -methyltransferases involved in benzylisoquinoline alkaloid biosynthesis in sacred lotus ( Nelumbo nucifera ). J Biol Chem. 2020;295 (6):1598-1612. doi:10.1074/jbc.RA119.011548 |
NnCNMT |
OMT |
Nelumbo nucifera |
Nymphaeaceae |
Yes |
Roemerine |
-- |
|
-- |
-- |
Pyne ME,Gold ND,Martin VJJ. Pathway elucidation and microbial synthesis of proaporphine and bis-benzylisoquinoline alkaloids from sacred lotus (Nelumbo nucifera). Metab Eng. 2023;77:162-173. doi:10.1016/j.ymben.2023.03.010 |
Nn6OMT |
OMT |
Nelumbo nucifera |
Nymphaeaceae |
Yes |
Roemerine |
-- |
|
-- |
-- |
Pyne ME,Gold ND,Martin VJJ. Pathway elucidation and microbial synthesis of proaporphine and bis-benzylisoquinoline alkaloids from sacred lotus (Nelumbo nucifera). Metab Eng. 2023;77:162-173. doi:10.1016/j.ymben.2023.03.010 |
NnNCS |
OMT |
Nelumbo nucifera |
Nymphaeaceae |
Yes |
Roemerine |
-- |
|
-- |
-- |
Pyne ME,Gold ND,Martin VJJ. Pathway elucidation and microbial synthesis of proaporphine and bis-benzylisoquinoline alkaloids from sacred lotus (Nelumbo nucifera). Metab Eng. 2023;77:162-173. doi:10.1016/j.ymben.2023.03.010 |
DoOMT |
OMT |
Dendrobium officinale |
Orchidaceae |
Yes |
Dendrobine |
caffeoyl CoA O-methyltransferase |
|
KF876839.1 |
https://www.ncbi.nlm.nih.gov/nuccore/KF876839.1 |
Gang Z, Ben-Xiang HU , Da-Wei Z, et al. Isolation and expression analysis of caffeoyl CoA O-methyltransferase gene in Dendrobium officinale[J]. Chinese Traditional and Herbal Drugs. 2014;45(8):1143-1149. doi:10.7501/j.issn.0253-2670.2014.08.019. |
GeCCoA-OMT |
OMT |
Gastrodia elata |
Orchidaceae |
Yes |
Phenylacetic Acid Compounds,Terpenoids |
-- |
|
MW041608.1 |
https://www.ncbi.nlm.nih.gov/nuccore/MW041608.1 |
-- |
GflOMT1 |
OMT |
Glaucium flavum |
Papaveraceae |
Yes |
Blood Root Alkaloids |
O-methyltransferase |
|
KP176693 |
https://www.ncbi.nlm.nih.gov/nuccore/KP176693 |
Chang L, Hagel JM, Facchini PJ. Isolation and Characterization of O-methyltransferases Involved in the Biosynthesis of Glaucine in Glaucium flavum. Plant Physiol. 2015;169 (2):1127-40. doi:10.1104/pp.15.01240 |
GflOMT2 |
OMT |
Glaucium flavum |
Papaveraceae |
Yes |
Blood Root Alkaloids |
O-methyltransferase |
|
KP176694 |
https://www.ncbi.nlm.nih.gov/nuccore/KP176694 |
Chang L, Hagel JM, Facchini PJ. Isolation and Characterization of O-methyltransferases Involved in the Biosynthesis of Glaucine in Glaucium flavum. Plant Physiol. 2015;169 (2):1127-40. doi:10.1104/pp.15.01241 |
GflOMT6 |
OMT |
Glaucium flavum |
Papaveraceae |
Yes |
Blood Root Alkaloids |
O-methyltransferase |
|
KP176698 |
https://www.ncbi.nlm.nih.gov/nuccore/KP176698 |
Chang L, Hagel JM, Facchini PJ. Isolation and Characterization of O-methyltransferases Involved in the Biosynthesis of Glaucine in Glaucium flavum. Plant Physiol. 2015;169 (2):1127-40. doi:10.1104/pp.15.01242 |
GflOMT7 |
OMT |
Glaucium flavum |
Papaveraceae |
Yes |
Blood Root Alkaloids |
O-methyltransferase |
|
KP176699 |
https://www.ncbi.nlm.nih.gov/nuccore/KP176699 |
Chang L, Hagel JM, Facchini PJ. Isolation and Characterization of O-methyltransferases Involved in the Biosynthesis of Glaucine in Glaucium flavum. Plant Physiol. 2015;169 (2):1127-40. doi:10.1104/pp.15.01243 |
EcOMT |
OMT |
Eschscholzia californica |
Papaveraceae |
Yes |
Chelirubine,Sanguinarine,Macarpine |
O-methyltransferase |
|
AB745042.1 |
https://www.ncbi.nlm.nih.gov/nuccore/AB745042.1 |
Becker A, Yamada Y, Sato F. California poppy (Eschscholzia californica), the Papaveraceae golden girl model organism for evodevo and specialized metabolism. Front Plant Sci. 2023;14:1084358. doi:10.3389/fpls.2023.1084358 |
EcOMT |
OMT |
Eschscholzia californica |
Papaveraceae |
Yes |
Chelirubine,Sanguinarine,Macarpine |
O-methyltransferase |
|
EU882970.1 |
https://www.ncbi.nlm.nih.gov/nuccore/EU882970.1 |
Becker A, Yamada Y, Sato F. California poppy (Eschscholzia californica), the Papaveraceae golden girl model organism for evodevo and specialized metabolism. Front Plant Sci. 2023;14:1084358. doi:10.3389/fpls.2023.1084358 |
EcOMT |
OMT |
Eschscholzia californica |
Papaveraceae |
Yes |
Chelirubine,Sanguinarine,Macarpine |
O-methyltransferase |
|
LC171866.1 |
https://www.ncbi.nlm.nih.gov/nuccore/LC171866.1 |
Becker A, Yamada Y, Sato F. California poppy (Eschscholzia californica), the Papaveraceae golden girl model organism for evodevo and specialized metabolism. Front Plant Sci. 2023;14:1084358. doi:10.3389/fpls.2023.1084358 |
EcOMT |
OMT |
Eschscholzia californica |
Papaveraceae |
Yes |
Chelirubine,Sanguinarine,Macarpine |
scoulerine/reticuline O-methyltransferase |
|
LC171865.1 |
https://www.ncbi.nlm.nih.gov/nuccore/LC171865.1 |
Becker A, Yamada Y, Sato F. California poppy (Eschscholzia californica), the Papaveraceae golden girl model organism for evodevo and specialized metabolism. Front Plant Sci. 2023;14:1084358. doi:10.3389/fpls.2023.1084358 |
Ec4’OMT |
OMT |
Eschscholzia californica |
Papaveraceae |
Yes |
Chelirubine,Sanguinarine,Macarpine |
3'-hydroxy-N-methylcoclaurine-4'-O-methyltransferase |
|
AB745041 |
https://www.ncbi.nlm.nih.gov/nuccore/AB745041 |
Bu J, Zhang X, Li Q, et al. Catalytic promiscuity of O-methyltransferases from Corydalis yanhusuo leading to the structural diversity of benzylisoquinoline alkaloids. Hortic Res. 2022;9:uhac152. doi:10.1093/hr/uhac152 |
PsSOMT1 |
OMT |
Papaver somniferum |
Papaveraceae |
Yes |
Isoquinolinetype Alkaloids,Protopine,Isocorydine,Papaverine,Morphine,Codeine,Sangulnarine,Chelerythrine,Bocconine,Narcotine,Rhoeadane |
scoulerine-9-O-methyltransferase |
|
JN185323 |
https://www.ncbi.nlm.nih.gov/nuccore/JN185323 |
Ozber N, Facchini PJ. Phloem-specific localization of benzylisoquinoline alkaloid metabolism in opium poppy. J Plant Physiol. 2022;271:153641. doi:10.1016/j.jplph.2022.153641 |
Ps6OMT |
OMT |
Papaver somniferum |
Papaveraceae |
Yes |
Isoquinolinetype Alkaloids,Protopine,Isocorydine,Papaverine,Morphine,Codeine,Sangulnarine,Chelerythrine,Bocconine,Narcotine,Rhoeadane |
-- |
|
-- |
-- |
Pyne ME,Gold ND,Martin VJJ. Pathway elucidation and microbial synthesis of proaporphine and bis-benzylisoquinoline alkaloids from sacred lotus (Nelumbo nucifera). Metab Eng. 2023;77:162-173. doi:10.1016/j.ymben.2023.03.010 |
Ps6OMT |
OMT |
Papaver somniferum |
Papaveraceae |
Yes |
Isoquinolinetype Alkaloids,Protopine,Isocorydine,Papaverine,Morphine,Codeine,Sangulnarine,Chelerythrine,Bocconine,Narcotine,Rhoeadane |
norcoclaurine 6-O-methyltransferase |
|
AY217335 |
https://www.ncbi.nlm.nih.gov/nuccore/AY217335 |
Winzer T,Gazda V,He Z, et al. A Papaver somniferum 10-gene cluster for synthesis of the anticancer alkaloid noscapine. Science. 2012;336 (6089):1704-8. doi:10.1126/science.1220757 |
Ps7OMT |
OMT |
Papaver somniferum |
Papaveraceae |
Yes |
Isoquinolinetype Alkaloids,Protopine,Isocorydine,Papaverine,Morphine,Codeine,Sangulnarine,Chelerythrine,Bocconine,Narcotine,Rhoeadane |
(R,S)-reticuline 7-O-methyltransferase |
|
AY268893 |
https://www.ncbi.nlm.nih.gov/nuccore/AY268893 |
Winzer T,Gazda V,He Z, et al. A Papaver somniferum 10-gene cluster for synthesis of the anticancer alkaloid noscapine. Science. 2012;336 (6089):1704-8. doi:10.1126/science.1220758 |
Ps4’OMT |
OMT |
Papaver somniferum |
Papaveraceae |
Yes |
Isoquinolinetype Alkaloids,Protopine,Isocorydine,Papaverine,Morphine,Codeine,Sangulnarine,Chelerythrine,Bocconine,Narcotine,Rhoeadane |
3'-hydroxy-N-methylcoclaurine 4'-O-methyltransferase |
|
AY217333 |
https://www.ncbi.nlm.nih.gov/nuccore/AY217333 |
Winzer T,Gazda V,He Z, et al. A Papaver somniferum 10-gene cluster for synthesis of the anticancer alkaloid noscapine. Science. 2012;336 (6089):1704-8. doi:10.1126/science.1220759 |
Ps4’OMT2 |
OMT |
Papaver somniferum |
Papaveraceae |
Yes |
Isoquinolinetype Alkaloids,Protopine,Isocorydine,Papaverine,Morphine,Codeine,Sangulnarine,Chelerythrine,Bocconine,Narcotine,Rhoeadane |
3'-hydroxy-N-methylcoclaurine 4'-O-methyltransferase |
|
AY217334 |
https://www.ncbi.nlm.nih.gov/nuccore/AY217334 |
Winzer T,Gazda V,He Z, et al. A Papaver somniferum 10-gene cluster for synthesis of the anticancer alkaloid noscapine. Science. 2012;336 (6089):1704-8. doi:10.1126/science.1220760 |
PsN7OMT |
OMT |
Papaver somniferum |
Papaveraceae |
Yes |
Isoquinolinetype Alkaloids,Protopine,Isocorydine,Papaverine,Morphine,Codeine,Sangulnarine,Chelerythrine,Bocconine,Narcotine,Rhoeadane |
norreticuline-7-O-methyltransferase |
|
FJ156103 |
https://www.ncbi.nlm.nih.gov/nuccore/FJ156103 |
Winzer T,Gazda V,He Z, et al. A Papaver somniferum 10-gene cluster for synthesis of the anticancer alkaloid noscapine. Science. 2012;336 (6089):1704-8. doi:10.1126/science.1220761 |
CyOMT2 |
OMT |
Corydalis yanhusuo |
Papaveraceae |
Yes |
Tetrahydropalmatine |
-- |
|
-- |
-- |
Bu J, Zhang X, Li Q, et al. Catalytic promiscuity of O-methyltransferases from Corydalis yanhusuo leading to the structural diversity of benzylisoquinoline alkaloids. Hortic Res. 2022;9:uhac152. doi:10.1093/hr/uhac152 |
CyOMT5 |
OMT |
Corydalis yanhusuo |
Papaveraceae |
Yes |
Tetrahydropalmatine |
-- |
|
-- |
-- |
Bu J,Zhang X,Li Q, et al. Catalytic promiscuity of O -methyltransferases from Corydalis yanhusuo leading to the structural diversity of benzylisoquinoline alkaloids. Hortic Res. 2022;9:uhac152. doi:10.1093/hr/uhac152 |
CyOMT7 |
OMT |
Corydalis yanhusuo |
Papaveraceae |
Yes |
Tetrahydropalmatine |
-- |
|
-- |
-- |
Bu J,Zhang X,Li Q, et al. Catalytic promiscuity of O -methyltransferases from Corydalis yanhusuo leading to the structural diversity of benzylisoquinoline alkaloids. Hortic Res. 2022;9:uhac152. doi:10.1093/hr/uhac152 |
PsOMT |
OMT |
Pinus sylvestris |
Pinaceae |
Yes |
Ginsenosides,Polysaccharides |
-- |
|
KX545295.1 |
https://www.ncbi.nlm.nih.gov/nuccore/KX545295.1 |
Paasela T, Lim KJ, Pietiäinen M, Teeri TH. The O-methyltransferase PMT2 mediates methylation of pinosylvin in Scots pine. New Phytol. 2017;214(4):1537-1550. doi:10.1111/nph.14480 |
PrOMT |
OMT |
Pinus radiata |
Pinoideae |
No |
Uranium,Cobalt,Radium |
O-methyltransferase |
|
U70873.1 |
https://www.ncbi.nlm.nih.gov/nuccore/U70873.1 |
-- |
ZmOMT |
OMT |
Zea mays |
Poaceae |
Yes |
Flavonoids,Polysaccharides,Saponins,Alkaloids,Tannic Acid,Chlorogenic Acid,Volatile Oils,Steroids |
O-methyltransferase |
|
M73235.1 |
https://www.ncbi.nlm.nih.gov/nuccore/M73235.1 |
Collazo P, Montoliu L, Puigdomènech P, Rigau J. Structure and expression of the lignin O-methyltransferase gene from Zea mays L. Plant Mol Biol. 1992;20(5):857-867. doi:10.1007/BF00027157 |
ZmCOMT |
OMT |
Zea mays |
Poaceae |
Yes |
Flavonoids,Polysaccharides,Saponins,Alkaloids,Tannic Acid,Chlorogenic Acid,Volatile Oils,Steroids |
caffeic acid 3-O-methyltransferase |
|
NP_001106047 |
https://www.ncbi.nlm.nih.gov/protein/NP_001106047 |
Meng Y, Li J, Liu J, et al. Ploidy effect and genetic architecture exploration of stalk traits using DH and its corresponding haploid populations in maize. BMC Plant Biol. 2016;16:50. doi:10.1186/s12870-016-0742-3 |
ZmcOmT |
OMT |
Zea mays |
Poaceae |
Yes |
Flavonoids,Polysaccharides,Saponins,Alkaloids,Tannic Acid,Chlorogenic Acid,Volatile Oils,Steroids |
-- |
|
-- |
-- |
Meng Y, Li J, Liu J, et al. Ploidy effect and genetic architecture exploration of stalk traits using DH and its corresponding haploid populations in maize. BMC Plant Biol. 2016;16:50. doi:10.1186/s12870-016-0742-3 |
ZmOMT |
OMT |
Zea mays |
Poaceae |
Yes |
Flavonoids,Polysaccharides,Saponins,Alkaloids,Tannic Acid,Chlorogenic Acid,Volatile Oils,Steroids |
O-methyltransferase |
|
BQ619438.1 |
https://www.ncbi.nlm.nih.gov/nuccore/BQ619438.1 |
-- |
ZmOMT |
OMT |
Zea mays |
Poaceae |
Yes |
Flavonoids,Polysaccharides,Saponins,Alkaloids,Tannic Acid,Chlorogenic Acid,Volatile Oils,Steroids |
-- |
|
HB859164.1 |
https://www.ncbi.nlm.nih.gov/nuccore/HB859164.1 |
-- |
ZmOMT |
OMT |
Zea mays |
Poaceae |
Yes |
Flavonoids,Polysaccharides,Saponins,Alkaloids,Tannic Acid,Chlorogenic Acid,Volatile Oils,Steroids |
-- |
|
HB859162.1 |
https://www.ncbi.nlm.nih.gov/nuccore/HB859162.1 |
-- |
ZmOMT |
OMT |
Zea mays |
Poaceae |
Yes |
Flavonoids,Polysaccharides,Saponins,Alkaloids,Tannic Acid,Chlorogenic Acid,Volatile Oils,Steroids |
-- |
|
HB859161.1 |
https://www.ncbi.nlm.nih.gov/nuccore/HB859161.1 |
-- |
ZmOMT |
OMT |
Zea mays |
Poaceae |
Yes |
Flavonoids,Polysaccharides,Saponins,Alkaloids,Tannic Acid,Chlorogenic Acid,Volatile Oils,Steroids |
-- |
|
HB859160.1 |
https://www.ncbi.nlm.nih.gov/nuccore/HB859160.1 |
-- |
ZmOMT |
OMT |
Zea mays |
Poaceae |
Yes |
Flavonoids,Polysaccharides,Saponins,Alkaloids,Tannic Acid,Chlorogenic Acid,Volatile Oils,Steroids |
-- |
|
HB859159.1 |
https://www.ncbi.nlm.nih.gov/nuccore/HB859159.1 |
-- |
ZmOMT |
OMT |
Zea mays |
Poaceae |
Yes |
Flavonoids,Polysaccharides,Saponins,Alkaloids,Tannic Acid,Chlorogenic Acid,Volatile Oils,Steroids |
-- |
|
HB859158.1 |
https://www.ncbi.nlm.nih.gov/nuccore/HB859158.1 |
-- |
ZmOMT |
OMT |
Zea mays |
Poaceae |
Yes |
Flavonoids,Polysaccharides,Saponins,Alkaloids,Tannic Acid,Chlorogenic Acid,Volatile Oils,Steroids |
-- |
|
HB859157.1 |
https://www.ncbi.nlm.nih.gov/nuccore/HB859157.1 |
-- |
SsOMT |
OMT |
Saccharum spontaneum |
Poaceae |
Yes |
Glycyrrhetinic Acid,Glycyrrhetinic Acid |
O-methyltransferase |
|
KU314758.1 |
https://www.ncbi.nlm.nih.gov/nuccore/KU314758.1 |
-- |
SsOMT |
OMT |
Saccharum spontaneum |
Poaceae |
Yes |
Glycyrrhetinic Acid,Glycyrrhetinic Acid |
-- |
|
KU314757.1 |
https://www.ncbi.nlm.nih.gov/nuccore/KU314757.1 |
-- |
SsOMT |
OMT |
Saccharum spontaneum |
Poaceae |
Yes |
Glycyrrhetinic Acid,Glycyrrhetinic Acid |
-- |
|
KU314756.1 |
https://www.ncbi.nlm.nih.gov/nuccore/KU314756.1 |
-- |
SsOMT |
OMT |
Saccharum spontaneum |
Poaceae |
Yes |
Glycyrrhetinic Acid,Glycyrrhetinic Acid |
-- |
|
KU314755.1 |
https://www.ncbi.nlm.nih.gov/nuccore/KU314755.1 |
-- |
SsOMT |
OMT |
Saccharum spontaneum |
Poaceae |
Yes |
Glycyrrhetinic Acid,Glycyrrhetinic Acid |
-- |
|
KU314754.1 |
https://www.ncbi.nlm.nih.gov/nuccore/KU314754.1 |
-- |
ShOMT |
OMT |
Saccharum hybrid |
Poaceae |
Yes |
Organic Acids,Calcium |
O-methyltransferase |
|
OL350832.1 |
https://www.ncbi.nlm.nih.gov/nuccore/OL350832.1 |
-- |
AjOMT |
OMT |
Ardisia japonica |
Primulaceae |
Yes |
1,4-Benzoquinone,Hydroxyethyl Cellulose,Ethanol Extract of Rosa japonica Leaves |
O-methyltransferases |
|
OR267196.1 |
https://www.ncbi.nlm.nih.gov/nuccore/OR267196.1 |
-- |
Tf4’OMT |
OMT |
Thalictrum flavum |
Ranunculaceae |
Yes |
Berberin,β-Sitosterol,N-desmethylthalistyline,5-O-demethylthalistyline |
3'-hydroxy-N-methyl-(S)-coclaurine 4'-O-methyltransferase |
|
AY610510 |
https://www.ncbi.nlm.nih.gov/nuccore/AY610510 |
Becker A, Yamada Y, Sato F. California poppy (Eschscholzia californica), the Papaveraceae golden girl model organism for evodevo and specialized metabolism. Front Plant Sci. 2023;14:1084358. doi:10.3389/fpls.2023.1084358 |
Tf6OMT |
OMT |
Thalictrum flavum |
Ranunculaceae |
Yes |
Berberin,β-Sitosterol,N-desmethylthalistyline,5-O-demethylthalistyline |
glaucum (S)-norcoclaurine 6-O-methyltransferase |
|
AY610507 |
https://www.ncbi.nlm.nih.gov/nuccore/AY610507 |
Menéndez-Perdomo IM, Facchini PJ. Elucidation of the (R)-enantiospecific benzylisoquinoline alkaloid biosynthetic pathways in sacred lotus (Nelumbo nucifera). Sci Rep. 2023;13(1):2955. doi:10.1038/s41598-023-29415-0 |
TfSOMT |
OMT |
Thalictrum flavum |
Ranunculaceae |
Yes |
Berberin,β-Sitosterol,N-desmethylthalistyline,5-O-demethylthalistyline |
glaucum (S)-norcoclaurine 7-O-methyltransferase |
|
AY610512 |
https://www.ncbi.nlm.nih.gov/nuccore/AY610512 |
Menéndez-Perdomo IM, Facchini PJ. Elucidation of the (R)-enantiospecific benzylisoquinoline alkaloid biosynthetic pathways in sacred lotus (Nelumbo nucifera). Sci Rep. 2023;13(1):2955. doi:10.1038/s41598-023-29415-0 |
Cc6OMT2 |
OMT |
Coptis chinensis |
Ranunculaceae |
Yes |
Berberine,Berberine,Isoberberine,Rutin |
6-O-methyltransferase |
|
MH165876 |
https://www.ncbi.nlm.nih.gov/nuccore/MH165876 |
He SM,Liang YL,Cong K, et al. Identification and Characterization of Genes Involved in Benzylisoquinoline Alkaloid Biosynthesis in Coptis Species. Front Plant Sci. 2018;9:731. doi:10.3389/fpls.2018.00732 |
Ct7OMT |
OMT |
Coptis chinensis |
Ranunculaceae |
Yes |
Berberine,Berberine,Isoberberine,Rutin |
norcoclaurine-7OMT |
|
MH165877 |
https://www.ncbi.nlm.nih.gov/nuccore/MH165877 |
He SM,Liang YL,Cong K, et al. Identification and Characterization of Genes Involved in Benzylisoquinoline Alkaloid Biosynthesis in Coptis Species. Front Plant Sci. 2018;9:731. doi:10.3389/fpls.2018.00733 |
CtSOMT |
OMT |
Coptis chinensis |
Ranunculaceae |
Yes |
Berberine,Berberine,Isoberberine,Rutin |
scoulerine 9-OMT |
|
MH165874 |
https://www.ncbi.nlm.nih.gov/nuccore/MH165874 |
He SM,Liang YL,Cong K, et al. Identification and Characterization of Genes Involved in Benzylisoquinoline Alkaloid Biosynthesis in Coptis Species. Front Plant Sci. 2018;9:731. doi:10.3389/fpls.2018.00734 |
Cj4’OMT |
OMT |
Coptis japonica |
Ranunculaceae |
Yes |
Berberine,Berberine,Isoberberine,Rutin |
3'-hydroxy-N-methy lcoclaurine 4'-O-methyltransferase |
|
D29812 |
https://www.ncbi.nlm.nih.gov/nuccore/D29812 |
Inui T,Kawano N,Shitan N, et al. Improvement of benzylisoquinoline alkaloid productivity by overexpression of 3'-hydroxy-N-methylcoclaurine 4'-O-methyltransferase in transgenic Coptis japonica plants. Biol Pharm Bull. 2012;35 (5):650-9. doi:10.1248/bpb.35.651 |
Cj6OMT |
OMT |
Coptis japonica |
Ranunculaceae |
Yes |
Berberine,Berberine,Isoberberine,Rutin |
S-adenosyl-L-methionine:norcoclaurine 6-O-methyltransferase |
|
D29811 |
https://www.ncbi.nlm.nih.gov/nuccore/D29811 |
Inui T,Kawano N,Shitan N, et al. Improvement of benzylisoquinoline alkaloid productivity by overexpression of 3'-hydroxy-N-methylcoclaurine 4'-O-methyltransferase in transgenic Coptis japonica plants. Biol Pharm Bull. 2012;35 (5):650-9. doi:10.1248/bpb.35.650 |
CjCoOMT |
OMT |
Coptis japonica |
Ranunculaceae |
Yes |
Berberine,Berberine,Isoberberine,Rutin |
columbamine O-methyltransferase |
|
AB073908 |
https://www.ncbi.nlm.nih.gov/nuccore/AB073908 |
Inui T,Kawano N,Shitan N, et al. Improvement of benzylisoquinoline alkaloid productivity by overexpression of 3'-hydroxy-N-methylcoclaurine 4'-O-methyltransferase in transgenic Coptis japonica plants. Biol Pharm Bull. 2012;35 (5):650-9. doi:10.1248/bpb.35.652 |
CjSOMT |
OMT |
Coptis japonica |
Ranunculaceae |
Yes |
Berberine,Berberine,Isoberberine,Rutin |
scoulerine 9-O-methyltransferase |
|
D29809 |
https://www.ncbi.nlm.nih.gov/nuccore/D29809 |
Inui T,Kawano N,Shitan N, et al. Improvement of benzylisoquinoline alkaloid productivity by overexpression of 3'-hydroxy-N-methylcoclaurine 4'-O-methyltransferase in transgenic Coptis japonica plants. Biol Pharm Bull. 2012;35 (5):650-9. doi:10.1248/bpb.35.653 |
TtOMT |
OMT |
Thalictrum tuberosum |
Ranunculaceae |
Yes |
Thalidasine Ⅰ,Thalifoetidine Ⅱ |
catechol O-methyltransferase |
|
AF064696.2 |
https://www.ncbi.nlm.nih.gov/nuccore/AF064696.2 |
Frick S, Kutchan TM. Molecular cloning and functional expression of O-methyltransferases common to isoquinoline alkaloid and phenylpropanoid biosynthesis. Plant J. 1999;17(4):329-339. doi:10.1046/j.1365-313x.1999.00379.x |
TtOMT |
OMT |
Thalictrum tuberosum |
Ranunculaceae |
Yes |
Thalidasine Ⅰ,Thalifoetidine Ⅱ |
O-methyltransferase |
|
AF064697.1 |
https://www.ncbi.nlm.nih.gov/nuccore/AF064697.1 |
Frick S, Kutchan TM. Molecular cloning and functional expression of O-methyltransferases common to isoquinoline alkaloid and phenylpropanoid biosynthesis. Plant J. 1999;17(4):329-339. doi:10.1046/j.1365-313x.1999.00379.x |
TtOMT |
OMT |
Thalictrum tuberosum |
Ranunculaceae |
Yes |
Thalidasine Ⅰ,Thalifoetidine Ⅱ |
catechol O-methyltransferase |
|
AF064695.1 |
https://www.ncbi.nlm.nih.gov/nuccore/AF064695.1 |
Frick S, Kutchan TM. Molecular cloning and functional expression of O-methyltransferases common to isoquinoline alkaloid and phenylpropanoid biosynthesis. Plant J. 1999;17(4):329-339. doi:10.1046/j.1365-313x.1999.00379.x |
TtOMT |
OMT |
Thalictrum tuberosum |
Ranunculaceae |
Yes |
Thalidasine Ⅰ,Thalifoetidine Ⅱ |
catechol O-methyltransferase |
|
AF064694.1 |
https://www.ncbi.nlm.nih.gov/nuccore/AF064694.1 |
Frick S, Kutchan TM. Molecular cloning and functional expression of O-methyltransferases common to isoquinoline alkaloid and phenylpropanoid biosynthesis. Plant J. 1999;17(4):329-339. doi:10.1046/j.1365-313x.1999.00379.x |
TtOMT |
OMT |
Thalictrum tuberosum |
Ranunculaceae |
Yes |
Thalidasine Ⅰ,Thalifoetidine Ⅱ |
catechol O-methyltransferase |
|
AF064693.1 |
https://www.ncbi.nlm.nih.gov/nuccore/AF064693.1 |
Frick S, Kutchan TM. Molecular cloning and functional expression of O-methyltransferases common to isoquinoline alkaloid and phenylpropanoid biosynthesis. Plant J. 1999;17(4):329-339. doi:10.1046/j.1365-313x.1999.00379.x |
FXaOMT |
OMT |
Fragaria ananassa |
Rosaceae |
Yes |
Carotenoids,Calcium,Coumarins,Saponins,Organic Acids |
O-methyltransferase |
|
KX450222.1 |
https://www.ncbi.nlm.nih.gov/nuccore/KX450222.1 |
Fu X, Cheng S, Zhang Y, et al. Differential responses of four biosynthetic pathways of aroma compounds in postharvest strawberry (Fragaria×ananassa Duch.) under interaction of light and temperature. Food Chem. 2017;221:356-364. doi:10.1016/j.foodchem.2016.10.082 |
FXaOMT |
OMT |
Fragaria ananassa |
Rosaceae |
Yes |
Carotenoids,Calcium,Coumarins,Saponins,Organic Acids |
O-methyltransferase |
|
JQ322659.1 |
https://www.ncbi.nlm.nih.gov/nuccore/JQ322659.1 |
Zorrilla-Fontanesi Y, Rambla JL, Cabeza A, et al. Genetic analysis of strawberry fruit aroma and identification of O-methyltransferase FaOMT as the locus controlling natural variation in mesifurane content. Plant Physiol. 2012;159(2):851-870. doi:10.1104/pp.111.188318 |
FXaOMT |
OMT |
Fragaria ananassa |
Rosaceae |
Yes |
Carotenoids,Calcium,Coumarins,Saponins,Organic Acids |
O-methyltransferase |
|
JQ322657.1 |
https://www.ncbi.nlm.nih.gov/nuccore/JQ322657.1 |
Zorrilla-Fontanesi Y, Rambla JL, Cabeza A, et al. Genetic analysis of strawberry fruit aroma and identification of O-methyltransferase FaOMT as the locus controlling natural variation in mesifurane content. Plant Physiol. 2012;159(2):851-870. doi:10.1104/pp.111.188318 |
FXaOMT |
OMT |
Fragaria ananassa |
Rosaceae |
Yes |
Carotenoids,Calcium,Coumarins,Saponins,Organic Acids |
O-methyltransferase |
|
JQ322656.1 |
https://www.ncbi.nlm.nih.gov/nuccore/JQ322656.1 |
Zorrilla-Fontanesi Y, Rambla JL, Cabeza A, et al. Genetic analysis of strawberry fruit aroma and identification of O-methyltransferase FaOMT as the locus controlling natural variation in mesifurane content. Plant Physiol. 2012;159(2):851-870. doi:10.1104/pp.111.188318 |
FXaOMT |
OMT |
Fragaria ananassa |
Rosaceae |
Yes |
Carotenoids,Calcium,Coumarins,Saponins,Organic Acids |
O-methyltransferase |
|
JQ322655.1 |
https://www.ncbi.nlm.nih.gov/nuccore/JQ322655.1 |
Zorrilla-Fontanesi Y, Rambla JL, Cabeza A, et al. Genetic analysis of strawberry fruit aroma and identification of O-methyltransferase FaOMT as the locus controlling natural variation in mesifurane content. Plant Physiol. 2012;159(2):851-870. doi:10.1104/pp.111.188318 |
FXaOMT |
OMT |
Fragaria ananassa |
Rosaceae |
Yes |
Carotenoids,Calcium,Coumarins,Saponins,Organic Acids |
O-methyltransferase |
|
JQ322654.1 |
https://www.ncbi.nlm.nih.gov/nuccore/JQ322654.1 |
Zorrilla-Fontanesi Y, Rambla JL, Cabeza A, et al. Genetic analysis of strawberry fruit aroma and identification of O-methyltransferase FaOMT as the locus controlling natural variation in mesifurane content. Plant Physiol. 2012;159(2):851-870. doi:10.1104/pp.111.188318 |
FXaOMT |
OMT |
Fragaria ananassa |
Rosaceae |
Yes |
Carotenoids,Calcium,Coumarins,Saponins,Organic Acids |
O-methyltransferase |
|
JQ322653.1 |
https://www.ncbi.nlm.nih.gov/nuccore/JQ322653.1 |
Zorrilla-Fontanesi Y, Rambla JL, Cabeza A, et al. Genetic analysis of strawberry fruit aroma and identification of O-methyltransferase FaOMT as the locus controlling natural variation in mesifurane content. Plant Physiol. 2012;159(2):851-870. doi:10.1104/pp.111.188318 |
FXaOMT |
OMT |
Fragaria ananassa |
Rosaceae |
Yes |
Carotenoids,Calcium,Coumarins,Saponins,Organic Acids |
O-methyltransferase |
|
JQ322652.1 |
https://www.ncbi.nlm.nih.gov/nuccore/JQ322652.1 |
Zorrilla-Fontanesi Y, Rambla JL, Cabeza A, et al. Genetic analysis of strawberry fruit aroma and identification of O-methyltransferase FaOMT as the locus controlling natural variation in mesifurane content. Plant Physiol. 2012;159(2):851-870. doi:10.1104/pp.111.188318 |
FXaOMT |
OMT |
Fragaria ananassa |
Rosaceae |
Yes |
Carotenoids,Calcium,Coumarins,Saponins,Organic Acids |
O-methyltransferase |
|
JQ322651.1 |
https://www.ncbi.nlm.nih.gov/nuccore/JQ322651.1 |
Zorrilla-Fontanesi Y, Rambla JL, Cabeza A, et al. Genetic analysis of strawberry fruit aroma and identification of O-methyltransferase FaOMT as the locus controlling natural variation in mesifurane content. Plant Physiol. 2012;159(2):851-870. doi:10.1104/pp.111.188318 |
FXaOMT |
OMT |
Fragaria ananassa |
Rosaceae |
Yes |
Carotenoids,Calcium,Coumarins,Saponins,Organic Acids |
O-methyltransferase |
|
JQ322658.1 |
https://www.ncbi.nlm.nih.gov/nuccore/JQ322658.1 |
Zorrilla-Fontanesi Y, Rambla JL, Cabeza A, et al. Genetic analysis of strawberry fruit aroma and identification of O-methyltransferase FaOMT as the locus controlling natural variation in mesifurane content. Plant Physiol. 2012;159(2):851-870. doi:10.1104/pp.111.188318 |
MtOMT |
OMT |
Macromeles tschonoskii |
Rosaceae |
Yes |
Saponins |
-- |
|
LC437822.1 |
https://www.ncbi.nlm.nih.gov/nuccore/LC437822.1 |
Aizawa M. An Overlooked Tree Species, Micromeles calocarpa (Rehder) M. Aizawa (Rosaceae), from Central Japan[J]. Acta phytotaxonomica et geobotanica: APG, 2021;72(1). doi:10.18942/apg.202007. |
MtOMT |
OMT |
Macromeles tschonoskii |
Rosaceae |
Yes |
Saponins |
-- |
|
LC437874.1 |
https://www.ncbi.nlm.nih.gov/nuccore/LC437874.1 |
-- |
MtOMT |
OMT |
Macromeles tschonoskii |
Rosaceae |
Yes |
Saponins |
ribulose-1,5-bisphosphate carboxylase |
|
LC437831.1 |
https://www.ncbi.nlm.nih.gov/nuccore/LC437831.1 |
-- |
PmOMT1 |
OMT |
Prunus mume |
Rosaceae |
Yes |
Chlorogenic Acid,Isoquercitrin,Hyperoside |
O-methyltransferase |
|
GU339212.1 |
https://www.ncbi.nlm.nih.gov/nuccore/GU339212.1 |
-- |
PtOMT1 |
OMT |
Populus tremuloides |
Salicaceae |
Yes |
Lignin |
caffeic acid/5-hydroxyferulic acid O-methyltransferase |
|
U13171.1 |
https://www.ncbi.nlm.nih.gov/nuccore/U13171.1 |
Tsai CJ, Podila GK, Chiang VL. Nucleotide sequence of a Populus tremuloides gene encoding bispecific caffeic acid/5-hydroxyferulic acid O-methyltransferase. Plant Physiol. 1995;107(4):1459. doi:10.1104/pp.107.4.1459 |
BpOMT |
OMT |
Bergenia purpurascens |
Saxifragaceae |
Yes |
Condensed Tannins of Bergenin,Catechins,Arbutin Glycosides |
O-methyltransferases |
|
OR267195.1 |
https://www.ncbi.nlm.nih.gov/nuccore/OR267195.1 |
-- |
StOMT |
OMT |
Solanum tuberosum |
Solanaceae |
Yes |
Carbohydrates,Cellulose |
-- |
|
X99853.1 |
https://www.ncbi.nlm.nih.gov/nuccore/X99853.1 |
-- |
AbPMT |
OMT |
Atropa belladonna |
Solanaceae |
Yes |
Hyoscyamine,Atropine,Scopolamine,Belladonin |
putrescine methyltransferase |
|
ON647441.1 |
https://www.ncbi.nlm.nih.gov/nuccore/ON647441.1 |
Xia K,Liu X,Zhang Q, et al. Promoting scopolamine biosynthesis in transgenic Atropa belladonna plants with pmt and h6h overexpression under field conditions. Plant Physiol Biochem. 2016;106:46-53. doi:10.1016/j.plaphy.2016.04.034 |
NtOMT1 |
OMT |
Nicotiana tabacum |
Solanaceae |
Yes |
Nicotine |
O-methyltransferase |
|
M84411.1 |
https://www.ncbi.nlm.nih.gov/nuccore/M84411.1 |
Jaeck E, Dumas B, Geoffroy P, et al. Regulation of enzymes involved in lignin biosynthesis: induction of O-methyltransferase mRNAs during the hypersensitive reaction of tobacco to tobacco mosaic virus. Mol Plant Microbe Interact. 1992;5(4):294-300. doi:10.1094/mpmi-5-294 |
NtOMT |
OMT |
Nicotiana tabacum |
Solanaceae |
Yes |
Nicotine |
O-methyltransferase |
|
X74453.1 |
https://www.ncbi.nlm.nih.gov/nuccore/X74453.1 |
Jaeck E, Martz F, Stiefel V, Fritig B, Legrand M. Expression of class I O-methyltransferase in healthy and TMV-infected tobacco. Mol Plant Microbe Interact. 1996;9(8):681-688. doi:10.1094/mpmi-9-0681 |
NtOMT |
OMT |
Nicotiana tabacum |
Solanaceae |
Yes |
Nicotine |
O-methyltransferase |
|
X74452.1 |
https://www.ncbi.nlm.nih.gov/nuccore/X74452.1 |
Jaeck E, Martz F, Stiefel V, Fritig B, Legrand M. Expression of class I O-methyltransferase in healthy and TMV-infected tobacco. Mol Plant Microbe Interact. 1996;9(8):681-688. doi:10.1094/mpmi-9-0681 |
NtOdOMT |
OMT |
Nicotiana tabacum |
Solanaceae |
Yes |
Nicotine |
o-diphenol-O-methyltransferase |
|
X71430.1 |
https://www.ncbi.nlm.nih.gov/nuccore/X71430.1 |
Pellegrini L, Geoffroy P, Fritig B, Legrand M. Molecular cloning and expression of a new class of ortho-diphenol-O-methyltransferases induced in tobacco (Nicotiana tabacum L.) leaves by infection or elicitor treatment. Plant Physiol. 1993;103(2):509-517. doi:10.1104/pp.103.2.509 |
NtOMT1 |
OMT |
Nicotiana tabacum |
Solanaceae |
Yes |
Nicotine |
orthomethyl transferase |
|
AJ937843.1 |
https://www.ncbi.nlm.nih.gov/nuccore/AJ937843.1 |
Szatmari A, Ott PG, Varga GJ, et al. Characterisation of basal resistance (BR) by expression patterns of newly isolated representative genes in tobacco. Plant Cell Rep. 2006;25(7):728-740. doi:10.1007/s00299-005-0110-5 |
Nt3OMT |
OMT |
Nicotiana tabacum |
Solanaceae |
Yes |
Nicotine |
-- |
|
-- |
-- |
Szatmari A, Ott PG, Varga GJ, et al. Characterisation of basal resistance (BR) by expression patterns of newly isolated representative genes in tobacco. Plant Cell Rep. 2006;25(7):728-740. doi:10.1007/s00299-005-0110-5 |
VaAOMT |
OMT |
Vitis amurensis |
Vitaceae |
Yes |
Ampelopsin B,Myricetin,Kaempferol,Luteolin |
anthocyanin-O-methyltransferase |
|
GU237132.1 |
https://www.ncbi.nlm.nih.gov/nuccore/GU237132.1 |
-- |
S9OMT |
OMT |
Thalictrum flavum |
Ranunculaceae |
-- |
-- |
-- |
|
-- |
-- |
Li Y,Li S,Thodey K, et al. Complete biosynthesis of noscapine and halogenated alkaloids in yeast. Proc Natl Acad Sci U S A. 2018;115 (17):E3922-E3931. doi:10.1073/pnas.1721469115 |
4'OMT |
OMT |
Papaver somniferum |
Papaveraceae |
Yes |
-- |
-- |
|
-- |
-- |
Li Y,Li S,Thodey K, et al. Complete biosynthesis of noscapine and halogenated alkaloids in yeast. Proc Natl Acad Sci U S A. 2018;115 (17):E3922-E3931. doi:10.1073/pnas.1721469116 |
CNMT |
OMT |
-- |
-- |
-- |
-- |
-- |
|
-- |
-- |
Li Y,Li S,Thodey K, et al. Complete biosynthesis of noscapine and halogenated alkaloids in yeast. Proc Natl Acad Sci U S A. 2018;115 (17):E3922-E3931. doi:10.1073/pnas.1721469117 |
EnMT4 |
OMT |
-- |
-- |
-- |
-- |
-- |
|
-- |
-- |
Wang YJ,Huang JP,Tian T, et al. Discovery and Engineering of the Cocaine Biosynthetic Pathway. J Am Chem Soc. 2022;144 (48):22000-22007. doi:10.1021/jacs.2c09091 |
MhrOMT |
OMT |
Malus hybrid rootstock |
-- |
-- |
-- |
O-methyltransferase |
|
GO502189.1 |
https://www.ncbi.nlm.nih.gov/nuccore/GO502189.1 |
-- |