CSDB glycosyltransferase search

5 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: 74B1 UniProt ID: O48676 CAZy family: GT1 Gene name: UGT74B1 / AT1G24100 Gene GenBank ID: 839022	Synthesized dimer: DGlcp(1-1')Subst // Subst = phenylacetothiohydroximate = SMILES {151}O/N=C({51}S)/CC1=CC=CC=C1 Donor (ID 33557): ?DGlcp(1-P-P-5)xXnucU Acceptor (ID 33753): Subst // Subst = phenylacetothiohydroximate = SMILES {151}O/N=C({51}S)/CC1=CC=CC=C1 Status: direct evidence in vivo Confirmation methods: in vitro (purified protein), in vitro (crude extract), mutation, mutation (in vitro) ID: 1290 Notes: Glc C1 is linked to S atom at -C(=NOH)S.	Organism (ID 9805): Arabidopsis thaliana Organ/tissue: leaf, silique, stem, root Full structure (ID 28231): CSDB ID(s): 60826	Grubb et al. 2004 DOI: 10.1111/j.1365-313X.2004.02261.x Grubb et al. 2014 DOI: 10.1111/tpj.12541 Kopycki et al. 2013 DOI: 10.1042/BJ20121403 Latife et al. 2019 DOI: 10.1016/j.mcat.2019.110631
Enzyme name: 74C1 UniProt ID: Q9SKC1.1 CAZy family: GT1 Gene name: AT2G31790 Gene GenBank ID: 817736	Synthesized dimer: DGlcp(1-1')Subst // Subst = phenylacetothiohydroximate = SMILES {151}O/N=C({51}S)/CC1=CC=CC=C1 Donor (ID 33557): ?DGlcp(1-P-P-5)xXnucU Acceptor (ID 33753): Subst // Subst = phenylacetothiohydroximate = SMILES {151}O/N=C({51}S)/CC1=CC=CC=C1 Status: evidence in vitro Confirmation methods: in vitro (purified protein) ID: 1295 Notes: Glc C1 is linked to S atom at -C(=NOH)S.	Organism (ID 9805): Arabidopsis thaliana Full structure (ID 28231): CSDB ID(s): 60826	Grubb et al. 2014 DOI: 10.1111/tpj.12541
Enzyme name: 74D1 UniProt ID: Q9SKC5.1 CAZy family: GT1 Gene name: UGT74D1 / AT2G31750 Gene GenBank ID: 817732	Synthesized dimer: DGlcp(1-1')Subst // Subst = phenylacetothiohydroximate = SMILES {151}O/N=C({51}S)/CC1=CC=CC=C1 Donor (ID 33557): ?DGlcp(1-P-P-5)xXnucU Acceptor (ID 33753): Subst // Subst = phenylacetothiohydroximate = SMILES {151}O/N=C({51}S)/CC1=CC=CC=C1 Status: evidence in vitro Confirmation methods: in vitro (purified protein) ID: 1296 Notes: Glc C1 is linked to S atom at -C(=NOH)S.	Organism (ID 9805): Arabidopsis thaliana Organ/tissue: leaf Full structure (ID 28231): CSDB ID(s): 60826	Song et al. 2005 DOI: 10.1007/BF03030584 Grubb et al. 2014 DOI: 10.1111/tpj.12541
Enzyme name: 74E2 UniProt ID: Q9SYK9.1 CAZy family: GT1 Gene name: UGT74E2 / AT1G05680 Gene GenBank ID: 837075	Synthesized dimer: DGlcp(1-1')Subst // Subst = phenylacetothiohydroximate = SMILES {151}O/N=C({51}S)/CC1=CC=CC=C1 Donor (ID 33557): ?DGlcp(1-P-P-5)xXnucU Acceptor (ID 33753): Subst // Subst = phenylacetothiohydroximate = SMILES {151}O/N=C({51}S)/CC1=CC=CC=C1 Status: evidence in vitro Confirmation methods: in vitro (purified protein) ID: 1313 Notes: Glc C1 is linked to S atom at -C(=NOH)S.	Organism (ID 9805): Arabidopsis thaliana Organ/tissue: leaf, root Full structure (ID 28231): CSDB ID(s): 60826	Grubb et al. 2014 DOI: 10.1111/tpj.12541 Tognetti et al. 2010 DOI: 10.1105/tpc.109.071316
Enzyme name: 74F1 UniProt ID: O22820.1 CAZy family: GT1 Gene name: UGT74F1 / AT2G43840 Gene GenBank ID: 818988	Synthesized dimer: DGlcp(1-1')Subst // Subst = phenylacetothiohydroximate = SMILES {151}O/N=C({51}S)/CC1=CC=CC=C1 Donor (ID 33557): ?DGlcp(1-P-P-5)xXnucU Acceptor (ID 33753): Subst // Subst = phenylacetothiohydroximate = SMILES {151}O/N=C({51}S)/CC1=CC=CC=C1 Status: evidence in vitro Confirmation methods: in vitro (purified protein) ID: 1324 Notes: Glc C1 is linked to S atom at -C(=NOH)S.	Organism (ID 9805): Arabidopsis thaliana Full structure (ID 28231): CSDB ID(s): 60826	Grubb et al. 2014 DOI: 10.1111/tpj.12541

#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)
1290	74B1				O48676		GT1	UGT74B1 / AT1G24100 	839022			28231		?DGlcp(1-1')Subst // Subst = phenylacetothiohydroximate = SMILES {151}O/N=C({51}S)/CC1=CC=CC=C1	0	?DGlcp(1-1')Subst // Subst = phenylacetothiohydroximate = SMILES {151}O/N=C({51}S)/CC1=CC=CC=C1	1~51	?DGlcp(1-P-P-5)xXnucU	Subst // Subst = phenylacetothiohydroximate = SMILES {151}O/N=C({51}S)/CC1=CC=CC=C1	in vivo	in vitro (purified protein), in vitro (crude extract), mutation, mutation (in vitro)	Glc C1 is linked to S atom at -C(=NOH)S.		0	0	60826		9805	Arabidopsis thaliana 	leaf, silique, stem, root	Grubb et al. 2004 (doi: 10.1111/j.1365-313X.2004.02261.x); Grubb et al. 2014 (doi: 10.1111/tpj.12541); Kopycki et al. 2013 (doi: 10.1042/BJ20121403); Latife et al. 2019 (doi: 10.1016/j.mcat.2019.110631)	
1295	74C1				Q9SKC1.1		GT1	AT2G31790 	817736			28231		?DGlcp(1-1')Subst // Subst = phenylacetothiohydroximate = SMILES {151}O/N=C({51}S)/CC1=CC=CC=C1	0	?DGlcp(1-1')Subst // Subst = phenylacetothiohydroximate = SMILES {151}O/N=C({51}S)/CC1=CC=CC=C1	1~51	?DGlcp(1-P-P-5)xXnucU	Subst // Subst = phenylacetothiohydroximate = SMILES {151}O/N=C({51}S)/CC1=CC=CC=C1	in vitro	in vitro (purified protein)	Glc C1 is linked to S atom at -C(=NOH)S.		0	0		60826	9805	Arabidopsis thaliana 		Grubb et al. 2014 (doi: 10.1111/tpj.12541)	
1296	74D1				Q9SKC5.1		GT1	UGT74D1 / AT2G31750 	817732			28231		?DGlcp(1-1')Subst // Subst = phenylacetothiohydroximate = SMILES {151}O/N=C({51}S)/CC1=CC=CC=C1	0	?DGlcp(1-1')Subst // Subst = phenylacetothiohydroximate = SMILES {151}O/N=C({51}S)/CC1=CC=CC=C1	1~51	?DGlcp(1-P-P-5)xXnucU	Subst // Subst = phenylacetothiohydroximate = SMILES {151}O/N=C({51}S)/CC1=CC=CC=C1	in vitro	in vitro (purified protein)	Glc C1 is linked to S atom at -C(=NOH)S.		0	0		60826	9805	Arabidopsis thaliana 	leaf	Song et al. 2005 (doi: 10.1007/BF03030584); Grubb et al. 2014 (doi: 10.1111/tpj.12541)	
1313	74E2				Q9SYK9.1		GT1	UGT74E2 / AT1G05680 	837075			28231		?DGlcp(1-1')Subst // Subst = phenylacetothiohydroximate = SMILES {151}O/N=C({51}S)/CC1=CC=CC=C1	0	?DGlcp(1-1')Subst // Subst = phenylacetothiohydroximate = SMILES {151}O/N=C({51}S)/CC1=CC=CC=C1	1~51	?DGlcp(1-P-P-5)xXnucU	Subst // Subst = phenylacetothiohydroximate = SMILES {151}O/N=C({51}S)/CC1=CC=CC=C1	in vitro	in vitro (purified protein)	Glc C1 is linked to S atom at -C(=NOH)S.		0	0		60826	9805	Arabidopsis thaliana 	leaf, root	Grubb et al. 2014 (doi: 10.1111/tpj.12541); Tognetti et al. 2010 (doi: 10.1105/tpc.109.071316)	
1324	74F1				O22820.1		GT1	UGT74F1 / AT2G43840 	818988			28231		?DGlcp(1-1')Subst // Subst = phenylacetothiohydroximate = SMILES {151}O/N=C({51}S)/CC1=CC=CC=C1	0	?DGlcp(1-1')Subst // Subst = phenylacetothiohydroximate = SMILES {151}O/N=C({51}S)/CC1=CC=CC=C1	1~51	?DGlcp(1-P-P-5)xXnucU	Subst // Subst = phenylacetothiohydroximate = SMILES {151}O/N=C({51}S)/CC1=CC=CC=C1	in vitro	in vitro (purified protein)	Glc C1 is linked to S atom at -C(=NOH)S.		0	0		60826	9805	Arabidopsis thaliana 		Grubb et al. 2014 (doi: 10.1111/tpj.12541)