Enzymes
| UniProtKB help_outline | 1 proteins |
Reaction participants Show >> << Hide
- Name help_outline petunidin Identifier CHEBI:193101 Charge -1 Formula C16H11O7 InChIKeyhelp_outline AFOLOMGWVXKIQL-UHFFFAOYSA-M SMILEShelp_outline C1=2C([O+]=C(C3=CC(=C(C(=C3)OC)O)O)C(=C1)[O-])=CC(=CC2[O-])O 2D coordinates Mol file for the small molecule Search links Involved in 2 reaction(s) Find molecules that contain or resemble this structure Find proteins in UniProtKB for this molecule
- Name help_outline UDP-α-D-glucose Identifier CHEBI:58885 (Beilstein: 3827329) help_outline Charge -2 Formula C15H22N2O17P2 InChIKeyhelp_outline HSCJRCZFDFQWRP-JZMIEXBBSA-L SMILEShelp_outline OC[C@H]1O[C@H](OP([O-])(=O)OP([O-])(=O)OC[C@H]2O[C@H]([C@H](O)[C@@H]2O)n2ccc(=O)[nH]c2=O)[C@H](O)[C@@H](O)[C@@H]1O 2D coordinates Mol file for the small molecule Search links Involved in 231 reaction(s) Find molecules that contain or resemble this structure Find proteins in UniProtKB for this molecule
- Name help_outline petunidin 3-O-beta-D-glucoside Identifier CHEBI:193103 Charge 0 Formula C22H22O12 InChIKeyhelp_outline CCQDWIRWKWIUKK-QKYBYQKWSA-N SMILEShelp_outline C1(=C(O[C@@H]2O[C@@H]([C@@H](O)[C@H](O)[C@H]2O)CO)C=C3C(=[O+]1)C=C(O)C=C3[O-])C4=CC(=C(O)C(=C4)OC)O 2D coordinates Mol file for the small molecule Search links Involved in 1 reaction(s) Find molecules that contain or resemble this structure Find proteins in UniProtKB for this molecule
- Name help_outline UDP Identifier CHEBI:58223 Charge -3 Formula C9H11N2O12P2 InChIKeyhelp_outline XCCTYIAWTASOJW-XVFCMESISA-K SMILEShelp_outline O[C@@H]1[C@@H](COP([O-])(=O)OP([O-])([O-])=O)O[C@H]([C@@H]1O)n1ccc(=O)[nH]c1=O 2D coordinates Mol file for the small molecule Search links Involved in 576 reaction(s) Find molecules that contain or resemble this structure Find proteins in UniProtKB for this molecule
Cross-references
| RHEA:74139 | RHEA:74140 | RHEA:74141 | RHEA:74142 | |
|---|---|---|---|---|
| Reaction direction help_outline | undefined | left-to-right | right-to-left | bidirectional |
| UniProtKB help_outline |
|
Related reactions help_outline
More general form(s) of this reaction
Publications
-
Characterization of two key flavonoid 3-O-glycosyltransferases involved in the formation of flower color in Rhododendron delavayi.
Sun W., Sun S., Xu H., Wang Y., Chen Y., Xu X., Yi Y., Ju Z.
Flower color, largely determined by anthocyanin, is one of the most important ornamental values of <i>Rhododendron delavayi</i>. However, scant information of anthocyanin biosynthesis has been reported in <i>R. delavayi</i>. We found that anthocyanidin 3-<i>O</i>-glycosides were the predominant an ... >> More
Flower color, largely determined by anthocyanin, is one of the most important ornamental values of <i>Rhododendron delavayi</i>. However, scant information of anthocyanin biosynthesis has been reported in <i>R. delavayi</i>. We found that anthocyanidin 3-<i>O</i>-glycosides were the predominant anthocyanins detected in <i>R. delavayi</i> flowers accounting for 93.68-96.31% of the total anthocyanins during its development, which indicated the key role of flavonoid 3-<i>O</i>-glycosyltransferase (3GT) on <i>R. delavayi</i> flower color formation. Subsequently, based on correlation analysis between anthocyanins accumulation and <i>Rd3GTs</i> expressions during flower development, <i>Rd3GT1</i> and <i>Rd3GT6</i> were preliminarily identified as the pivotal <i>3GT</i> genes involved in the formation of color of <i>R. delavayi</i> flower. Tissue-specific expressions of <i>Rd3GT1</i> and <i>Rd3GT6</i> were examined, and their function as 3GT <i>in vivo</i> was confirmed through introducing into <i>Arabidopsis UGT78D2</i> mutant and <i>Nicotiana tabacum</i> plants. Furthermore, biochemical characterizations showed that both <i>Rd3GT1</i> and <i>Rd3GT6</i> could catalyze the addition of UDP-sugar to the 3-OH of anthocyanidin, and preferred UDP-Gal as their sugar donor and cyanidin as the most efficient substrate. This study not only provides insights into the biosynthesis of anthocyanin in <i>R. delavayi</i>, but also makes contribution to understand the mechanisms of its flower color formation. << Less
Front. Plant Sci. 13:863482-863482(2022) [PubMed] [EuropePMC]
This publication is cited by 10 other entries.