CSDB glycosyltransferase search

1 glycosyltransferase activity has been found.
Please note that CSDB GT database covers only a few species: Arabidopsis thaliana, Escherichia coli, Saccharomyces cerevisiae, Acinetobacter baumannii.

Enzyme / Gene	Activity	Object	References
Enzyme name: 73B2 UniProt ID: Q94C57.1 CAZy family: GT1 Gene name: UGT73B2 / At4g34135 Gene GenBank ID: 829560	Synthesized dimer: DGlcp(1-7)Subst // Subst = isorhamnetin = SMILES O{3}C1=C(C2=CC={54}C(O)C(OC)=C2)OC3=C({5}C(O)=C{7}C(O)=C3)C1=O Donor (ID 34839): ?DGlcp(1-P-P-5)xXnucU Acceptor (ID 34965): Subst // Subst = isorhamnetin = SMILES O{3}C1=C(C2=CC={54}C(O)C(OC)=C2)OC3=C({5}C(O)=C{7}C(O)=C3)C1=O Status: evidence in vitro Confirmation methods: in vitro (purified protein) ID: 1168 Notes: Although the predominant activity was specific for the C-7 position, a 15-fold lower activity could also be identified for the C-3 position.	Organism (ID 12415): Arabidopsis thaliana Organ/tissue: leaf,root, flower ,seedling Full structure (ID 34966):	Langlois-Meurinne et al. 2005 DOI: 10.1104/pp.105.067223 Lim et al. 2006a DOI: 10.1007/BF03031161 Kim et al. 2006b DOI: 10.1016/j.plantsci.2005.12.013 Willits et al. 2004 DOI: 10.1016/j.phytochem.2003.10.005

#GTR ID	Enzyme name	Enzyme group	Enzyme Genbank ID	Derived ID mark	Enzyme Uniprot ID	Derived ID mark	CAZY family	Gene name	Gene Genbank ID	Derived ID mark	Gene cluster	Full structure CSDB structure ID	Side product CSDB structure ID	Full structure	Full structure is fragment (0|1)	Synthesized bond	Synthesized bond location (from root ~ subst position)	Donor structure ID	Substrate structure	Confirmation status	Methods used	Notes	Molecule role	Molecule is a model of role (0|1)	Molecule is a precursor of role (0|1)	Main CSDB record ID	Additional CSDB record IDs	CSDB organism IDs	Organism names	Organs and tissues	References (;-separated)
1168	73B2				Q94C57.1		GT1	UGT73B2 / At4g34135	829560			34966		?DGlcp(1-7)Subst // Subst = isorhamnetin = SMILES O{3}C1=C(C2=CC={54}C(O)C(OC)=C2)OC3=C({5}C(O)=C{7}C(O)=C3)C1=O	0	?DGlcp(1-7)Subst // Subst = isorhamnetin = SMILES O{3}C1=C(C2=CC={54}C(O)C(OC)=C2)OC3=C({5}C(O)=C{7}C(O)=C3)C1=O	1~7	?DGlcp(1-P-P-5)xXnucU	Subst // Subst = isorhamnetin = SMILES O{3}C1=C(C2=CC={54}C(O)C(OC)=C2)OC3=C({5}C(O)=C{7}C(O)=C3)C1=O	in vitro	in vitro (purified protein)	Although the predominant activity was specific for the C-7 position, a 15-fold lower activity could also be identified for the C-3 position.		0	0			12415	Arabidopsis thaliana 	leaf,root, flower ,seedling	Langlois-Meurinne et al. 2005 (doi: 10.1104/pp.105.067223); Lim et al. 2006a (doi: 10.1007/BF03031161); Kim et al. 2006b (doi: 10.1016/j.plantsci.2005.12.013); Willits et al. 2004 (doi: 10.1016/j.phytochem.2003.10.005)