CSDB glycosyltransferase search

3 glycosyltransferase activities have 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: YjiC UniProt ID: Q65JC2 CAZy family: GT1 Gene name: TRNA_RS31140 Gene GenBank ID: 3031168	Synthesized dimer: bDGlcp(1-4')Subst // Subst = naringenin = SMILES O=C1CC(C2=CC={54}C(O)C=C2)OC3=C{7}C(O)={6}C{5}C(O)=C13 Donor (ID 34898): aDGlcp(1-P-P-5)xXnucU Acceptor (ID 34954): Subst // Subst = naringenin = SMILES O=C1CC(C2=CC={54}C(O)C=C2)OC3=C{7}C(O)={6}C{5}C(O)=C13 Status: evidence in vitro Confirmation methods: in vitro (purified protein) ID: 3021	Organism (ID 17063): Bacillus licheniformis DSM 13 Full structure (ID 21847): CSDB ID(s): 50166, 66758	Thapa et al. 2019 DOI: 10.1007/s00253-019-10060-5
Synthesized dimer: bDGlcp(1-4')Subst // Subst = naringenin = SMILES O=C1CC(C2=CC={54}C(O)C=C2)OC3=C{7}C(O)={6}C{5}C(O)=C13 Donor (ID 34898): aDGlcp(1-P-P-5)xXnucU Acceptor (ID 34954): Subst // Subst = naringenin = SMILES O=C1CC(C2=CC={54}C(O)C=C2)OC3=C{7}C(O)={6}C{5}C(O)=C13 Status: evidence in vitro Confirmation methods: in vitro (purified protein) ID: 3022	Organism (ID 17063): Bacillus licheniformis DSM 13 Full structure (ID 36545):
Synthesized dimer: bDGlcp(1-4')Subst // Subst = naringenin = SMILES O=C1CC(C2=CC={54}C(O)C=C2)OC3=C{7}C(O)={6}C{5}C(O)=C13 Donor (ID 34898): aDGlcp(1-P-P-5)xXnucU Acceptor (ID 34954): Subst // Subst = naringenin = SMILES O=C1CC(C2=CC={54}C(O)C=C2)OC3=C{7}C(O)={6}C{5}C(O)=C13 Status: evidence in vitro Confirmation methods: in vitro (purified protein) ID: 3024	Organism (ID 17063): Bacillus licheniformis DSM 13 Full structure (ID 36545):

#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)
3021	YjiC				Q65JC2		GT1	TRNA_RS31140	3031168			21847		bDGlcp(1-4')Subst // Subst = naringenin = SMILES O=C1CC(C2=CC={54}C(O)C=C2)OC3=C{7}C(O)={6}C{5}C(O)=C13	0	bDGlcp(1-4')Subst // Subst = naringenin = SMILES O=C1CC(C2=CC={54}C(O)C=C2)OC3=C{7}C(O)={6}C{5}C(O)=C13	1~54	aDGlcp(1-P-P-5)xXnucU	Subst // Subst = naringenin = SMILES O=C1CC(C2=CC={54}C(O)C=C2)OC3=C{7}C(O)={6}C{5}C(O)=C13	in vitro	in vitro (purified protein)			0	0		50166,66758	17063	Bacillus licheniformis DSM 13		Thapa et al. 2019 (doi: 10.1007/s00253-019-10060-5)	
3022	YjiC				Q65JC2		GT1	TRNA_RS31140	3031168			36545		bDGlcp(1-7)[bDGlcp(1-4')]Subst // Subst = naringenin = SMILES O=C1CC(C2=CC={54}C(O)C=C2)OC3=C{7}C(O)={6}C{5}C(O)=C13	0	bDGlcp(1-4')Subst // Subst = naringenin = SMILES O=C1CC(C2=CC={54}C(O)C=C2)OC3=C{7}C(O)={6}C{5}C(O)=C13	1~54	aDGlcp(1-P-P-5)xXnucU	Subst // Subst = naringenin = SMILES O=C1CC(C2=CC={54}C(O)C=C2)OC3=C{7}C(O)={6}C{5}C(O)=C13	in vitro	in vitro (purified protein)			0	0			17063	Bacillus licheniformis DSM 13		Thapa et al. 2019 (doi: 10.1007/s00253-019-10060-5)	
3024	YjiC				Q65JC2		GT1	TRNA_RS31140	3031168			36545		bDGlcp(1-7)[bDGlcp(1-4')]Subst // Subst = naringenin = SMILES O=C1CC(C2=CC={54}C(O)C=C2)OC3=C{7}C(O)={6}C{5}C(O)=C13	0	bDGlcp(1-4')Subst // Subst = naringenin = SMILES O=C1CC(C2=CC={54}C(O)C=C2)OC3=C{7}C(O)={6}C{5}C(O)=C13	1~54	aDGlcp(1-P-P-5)xXnucU	Subst // Subst = naringenin = SMILES O=C1CC(C2=CC={54}C(O)C=C2)OC3=C{7}C(O)={6}C{5}C(O)=C13	in vitro	in vitro (purified protein)			0	0			17063	Bacillus licheniformis DSM 13		Thapa et al. 2019 (doi: 10.1007/s00253-019-10060-5)