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IUBMB Comments The enzyme has been characterized from the saponin-producing crucifer plant Barbarea vulgaris .
The enzyme appears in viruses and cellular organisms
Synonyms ugt73c11, ugt73c10, more
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cellulose synthase-like glycosyltransferase
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glucuronosyltransferase
AIE12488.1, AKA44603.1
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UDP-glycosyltransferase
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UDP-glycosyltransferase
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UGT73C10
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UGT73C11
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UDP-alpha-D-glucose + oleanolate = UDP + oleanolate 3-O-beta-D-glucoside
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transfer of glycosyl group
transfer of glycosyl group
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transfer of glycosyl group
AKA44603.1, AIE12488.1
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MetaCyc
ginsenosides biosynthesis
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UDP-alpha-D-glucose:oleanolate 3-O-glucosyltransferase
The enzyme has been characterized from the saponin-producing crucifer plant Barbarea vulgaris.
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apigenin + UDP-Glc
apigenin-7-glucoside + UDP
Calenduloside E
Chikusetsusaponin IVa +UDP
AKA44603.1, AIE12488.1
Substrates: oleanane-type ginsenoside biosynthesis in P. ginseng callus Products: -
ir
calenduloside E + UDP-Glc
chikusetsusaponin IVa + UDP
AKA44603.1, AIE12488.1
Substrates: high catalytic efficiency E Products: -
ir
calenduloside E + UDP-Glc
zingibroside R1 + UDP
AKA44603.1, AIE12488.1
Substrates: - Products: -
ir
chikusetsusaponin IVa + UDP-Glc
ginsenoside Ro + UDP
luteolin
luteolin glucosides
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Substrates: flavonoid patway Products: -
ir
luteolin + UDP-Glc
luteolin-7-glucoside + UDP
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Substrates: flavonoid patway Products: -
ir
luteolin + UDP-Glc
multiple products + UDP
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Substrates: - Products: -
ir
oleanolic acid + UDP-Glc
?
AKA44603.1, AIE12488.1
Substrates: - Products: -
ir
oleanolic acid + UDP-Glc
oleanolic acid 28-O-glucopyranosyl ester + UDP
AKA44603.1, AIE12488.1
Substrates: - Products: -
ir
oleanolic acid +UDP-GlcA
calenduloside E +UDP
oleanolic acid 28-O-glucopyranosyl ester
?
AKA44603.1, AIE12488.1
Substrates: - Products: -
?
protopanaxadiol
?
AKA44603.1, AIE12488.1
Substrates: - Products: -
?
quercetin
quercetin glucosides
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Substrates: flavonoid patway Products: -
ir
quercetin + UDP-Glc
multiple products + UDP
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Substrates: - Products: -
ir
quercetin + UDP-Glc
quercetin-7-glucoside + UDP
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Substrates: flavonoid patway Products: -
ir
UDP-alpha-D-glucose + glycyrrhetinic acid
UDP + glycyrrhetinic acid 3-O-beta-monoglucose
Substrates: the highest conversion is found at the substrate molar ratio UDP-alpha-D-glucose/glycyrrhetinate of 5:1 with 98% conversion after 6 h Products: -
ir
UDP-alpha-D-glucose + oleanolate
UDP + oleanolate 3-O-beta-D-glucoside
Substrates: the enzyme specifically glucosylates oleanoate at the C3 position Products: -
?
Zingibroside R1
Ginsenoside Ro +UDP
AKA44603.1, AIE12488.1
Substrates: oleanane-type ginsenoside biosynthesis in P. ginseng callus Products: -
ir
zingibroside R1 + UDP-Glc
ginsenoside Ro + UDP
AKA44603.1, AIE12488.1
Substrates: high affinity Products: -
ir
additional information
?
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apigenin + UDP-Glc
apigenin-7-glucoside + UDP
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Substrates: flavonoid patway Products: -
ir
apigenin + UDP-Glc
apigenin-7-glucoside + UDP
-
Substrates: - Products: -
ir
chikusetsusaponin IVa + UDP-Glc
ginsenoside Ro + UDP
AKA44603.1, AIE12488.1
Substrates: - Products: -
ir
chikusetsusaponin IVa + UDP-Glc
ginsenoside Ro + UDP
AKA44603.1, AIE12488.1
Substrates: high affinity and catalytic efficiency Products: -
ir
oleanolic acid +UDP-GlcA
calenduloside E +UDP
AKA44603.1, AIE12488.1
Substrates: the studies revealed that PgCSyGT1 is the key GT in ginseng responsible for calenduloside E biosynthesis via transfer of the glucuronosyl moiety of UDP-glucuronic acid to the C3 position of oleanolic acid Products: -
?
oleanolic acid +UDP-GlcA
calenduloside E +UDP
AKA44603.1, AIE12488.1
Substrates: - Products: -
?
additional information
?
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Substrates: the enzyme shows weak activity toward quercetin and kaempferol at 0.1 mM concentration, while at 0.01 mM no activity detected Products: -
?
additional information
?
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Substrates: the enzyme shows weak activity toward quercetin and kaempferol at 0.1 mM concentration, while at 0.01 mM no activity detected Products: -
?
additional information
?
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Substrates: no activity with UDP-glucuronic acid Products: -
?
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apigenin + UDP-Glc
apigenin-7-glucoside + UDP
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Substrates: flavonoid patway Products: -
ir
Calenduloside E
Chikusetsusaponin IVa +UDP
AKA44603.1, AIE12488.1
Substrates: oleanane-type ginsenoside biosynthesis in P. ginseng callus Products: -
ir
calenduloside E + UDP-Glc
zingibroside R1 + UDP
AKA44603.1, AIE12488.1
Substrates: - Products: -
ir
chikusetsusaponin IVa + UDP-Glc
ginsenoside Ro + UDP
AKA44603.1, AIE12488.1
Substrates: - Products: -
ir
luteolin
luteolin glucosides
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Substrates: flavonoid patway Products: -
ir
luteolin + UDP-Glc
luteolin-7-glucoside + UDP
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Substrates: flavonoid patway Products: -
ir
oleanolic acid + UDP-Glc
?
AKA44603.1, AIE12488.1
Substrates: - Products: -
ir
oleanolic acid +UDP-GlcA
calenduloside E +UDP
AKA44603.1, AIE12488.1
Substrates: the studies revealed that PgCSyGT1 is the key GT in ginseng responsible for calenduloside E biosynthesis via transfer of the glucuronosyl moiety of UDP-glucuronic acid to the C3 position of oleanolic acid Products: -
?
quercetin
quercetin glucosides
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Substrates: flavonoid patway Products: -
ir
quercetin + UDP-Glc
quercetin-7-glucoside + UDP
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Substrates: flavonoid patway Products: -
ir
UDP-alpha-D-glucose + oleanolate
UDP + oleanolate 3-O-beta-D-glucoside
Substrates: the enzyme specifically glucosylates oleanoate at the C3 position Products: -
?
Zingibroside R1
Ginsenoside Ro +UDP
AKA44603.1, AIE12488.1
Substrates: oleanane-type ginsenoside biosynthesis in P. ginseng callus Products: -
ir
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Mg2+
about 110% activity at 5 mM
additional information
not influenced by Ba2+, Ni2+, Mn2+, and Ca2+
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Co2+
about 68% residual activity at 5 mM
Cu2+
complete inhibition at 5 mM
Fe2+
about 85% residual activity at 5 mM
Zn2+
about 22% residual activity at 5 mM
additional information
not inhibited by EDTA
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0.097 - 0.691
calenduloside E
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0.304
chikusetsusaponin IVa
AKA44603.1, AIE12488.1
pH 7.0, 30 °C, 12h
0.104
glycyrrhetinic acid
at pH 7.4 and 37°C
0.041
luteolin
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pH 8.0, Temp 37 °C, 30 min
0.853
oleanolic acid
AKA44603.1, AIE12488.1
pH 7.0, 30 °C, 12h
0.036
quercetin
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pH 8.0, Temp 37 °C, 30 min
0.486
UDP-alpha-D-glucose
at pH 7.4 and 37°C
0.28
zingibroside R1
AKA44603.1, AIE12488.1
pH 7.0, 30 °C, 12h
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0.097
calenduloside E
AKA44603.1, AIE12488.1
pH 7.0, 30 °C, 12h
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0.691
calenduloside E
AKA44603.1, AIE12488.1
pH 7.0, 30 °C, 12h
-
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0.001 - 0.025
calenduloside E
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0.002
chikusetsusaponin IVa
AKA44603.1, AIE12488.1
pH 7.0, 30 °C, 12h
0.091
glycyrrhetinic acid
at pH 7.4 and 37°C
1.16
luteolin
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pH 8.0, Temp 37 °C, 30 min
0.034
oleanolic acid
AKA44603.1, AIE12488.1
pH 7.0, 30 °C, 12h
5.93
quercetin
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pH 8.0, Temp 37 °C, 30 min
0.102
UDP-alpha-D-glucose
at pH 7.4 and 37°C
0.054
zingibroside R1
AKA44603.1, AIE12488.1
pH 7.0, 30 °C, 12h
-
0.001
calenduloside E
AKA44603.1, AIE12488.1
pH 7.0, 30 °C, 12h
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0.025
calenduloside E
AKA44603.1, AIE12488.1
pH 7.0, 30 °C, 12h
-
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0.001 - 0.257
calenduloside E
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0.006
chikusetsusaponin IVa
AKA44603.1, AIE12488.1
pH 7.0, 30 °C, 12h
0.873
glycyrrhetinic acid
at pH 7.4 and 37°C
28.5
luteolin
-
pH 8.0, Temp 37 °C, 30 min
0.04
oleanolic acid
AKA44603.1, AIE12488.1
pH 7.0, 30 °C, 12h
165.69
quercetin
-
pH 8.0, Temp 37 °C, 30 min
0.215
UDP-alpha-D-glucose
at pH 7.4 and 37°C
0.194
zingibroside R1
AKA44603.1, AIE12488.1
pH 7.0, 30 °C, 12h
-
0.001
calenduloside E
AKA44603.1, AIE12488.1
pH 7.0, 30 °C, 12h
-
0.257
calenduloside E
AKA44603.1, AIE12488.1
pH 7.0, 30 °C, 12h
-
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6 - 8
more than 60% activity between pH 6.0 and 8.0
7
AKA44603.1, AIE12488.1
Tris-HCl 50 mM
8
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Tris-HCl 50 mM
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25 - 45
more than 50% activity between 25 and 45°C
30
AKA44603.1, AIE12488.1
Incubation temperature for enzymatic activity and kinetic assays for 1-12 h under standard conditions
37
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Incubations carried out for 30 min - 6 h
37
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Incubations carried out for 30 min â 6 h
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brenda
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UniProt
brenda
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brenda
Barbarea vulgaris subsp. arcuata
UniProt
brenda
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brenda
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AIE12488.1, AKA44603.1
GenBank
brenda
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brenda
AKA44603.1, AIE12488.1
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brenda
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brenda
Highest Expressing Human Cell Lines
Filter by:
Cell Line Links
Gene Links
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metabolism
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the enzyme is involved in saponin biosynthesis
metabolism
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EpUGT95 is a key player in facilitating the di-glucosylation processes of luteolin and quercetin
metabolism
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EpUGT73 facilitates glucose glycosylation at the C7 position of apigenin, luteolin and quercetin, exhibiting a remarkable substrate heterogeneity and catalytic site specificity
metabolism
AKA44603.1, AIE12488.1
biosynthesis of diverse oleanane-type ginsenosides
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73C13_BARVU
495
0
55427
Swiss-Prot
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73C11_BARVU
495
0
55613
Swiss-Prot
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73C12_BARVU
495
0
55576
Swiss-Prot
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UGT1_BARVU
495
0
55599
Swiss-Prot
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73C10_BARVU
495
0
55486
Swiss-Prot
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Ni-NTA column chromatography
purified from the cell extracts using glutathione agarose affinity chromatography
AKA44603.1, AIE12488.1
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cloned from E. phaseoloides into pMal-C2X vector
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expressed in Escherichia coli BL21(DE3) cells
expressed in Escherichia coli XJb(DE3) cells
expressed in Nicotiana benthamiana
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expression in E. coli BL21(DE3)
AKA44603.1, AIE12488.1
expression in Escherichia coli BL21(DE3)
AKA44603.1, AIE12488.1
from E. phaseoloides into pMal-C2X vector; expression in E. coli BL21(DE3)
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biotechnology
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the research integrated metabolomics and transcriptomics enabling identification of key enzymes in triterpenoid and flavonoid biosynthesis
biotechnology
AKA44603.1, AIE12488.1
Oleanane-type saponins have the potential to treat many diseases. The research studies showed that oleanane-type ginsenosides with structures similar to that of ginsenoside Ro also had high biological activity
biotechnology
AKA44603.1, AIE12488.1
Oleanane-type saponins have the potential to treat many diseases.The research studies showed that oleanane-type ginsenosides with structures similar to that of ginsenoside Ro also had high biological activity
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Liu, X.; Zhang, L.; Feng, X.; Lv, B.; Li, C.
Biosynthesis of glycyrrhetinic acid-3-O-monoglucose using glycosyltransferase UGT73C11 from Barbarea vulgaris
Ind. Eng. Chem. Res.
56
14949-14958
2017
Barbarea vulgaris (K4GGT4)
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brenda
Erthmann, P.O.; Agerbirk, N.; Bak, S.
A tandem array of UDP-glycosyltransferases from the UGT73C subfamily glycosylate sapogenins, forming a spectrum of mono- and bisdesmosidic saponins
Plant Mol. Biol.
97
37-55
2018
Barbarea vulgaris
brenda
Augustin, J.M.; Drok, S.; Shinoda, T.; Sanmiya, K.; Nielsen, J.K.; Khakimov, B.; Olsen, C.E.; Hansen, E.H.; Kuzina, V.; Ekstrom, C.T.; Hauser, T.; Bak, S.
UDP-glycosyltransferases from the UGT73C subfamily in Barbarea vulgaris catalyze sapogenin 3-O-glucosylation in saponin-mediated insect resistance
Plant Physiol.
160
1881-1895
2012
Barbarea vulgaris (K4GKX2), Barbarea vulgaris
brenda
Xu, X.; Tang, R.; Liu, L.; Zhang, Q.; Xiong, H.; Mei, Z.; Liu, Y.
Comparative transcriptome-metabolome study reveals the functions of pentacyclic triterpene synthase and flavonoid glycosyltransferases in Entada phaseoloides
Int. J. Biol. Macromol.
318
145278
2025
Entada phaseoloides
brenda
Zhang, H.; Hua, X.; Zheng, D.; Wu, H.; Li, C.; Rao, P.; Wen, M.; Choi, Y.E.; Xue, Z.; Wang, Y.; Li, Y.
De Novo Biosynthesis of Oleanane-Type Ginsenosides in Saccharomyces cerevisiae Using Two Types of Glycosyltransferases from Panax ginseng
J. Agric. Food Chem.
70
2231-2240
2022
Panax ginseng, Panax ginseng (AKA44603.1), Panax ginseng (AIE12488.1)
brenda
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