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Name ^help_outline an α-L-Fuc-(1→2)-β-D-Gal-(1→3)-β-D-GalNAc derivative Identifier CHEBI:233970 Charge 0 Formula C20H34NO15R SMILES^help_outline *OC1OC(CO)C(O)C(OC2OC(CO)C(O)C(O)C2OC3OC(C)C(O)C(O)C3O)C1NC(=O)C 2D coordinates Mol file for the small molecule Search links Involved in 3 reaction(s) Find molecules that contain or resemble this structure Find proteins in UniProtKB for this molecule
Name ^help_outline UDP-N-acetyl-α-D-galactosamine Identifier CHEBI:67138 Charge -2 Formula C17H25N3O17P2 InChIKey^help_outline LFTYTUAZOPRMMI-NESSUJCYSA-L SMILES^help_outline CC(=O)N[C@@H]1[C@@H](O)[C@@H](O)[C@@H](CO)O[C@@H]1OP([O-])(=O)OP([O-])(=O)OC[C@H]1O[C@H]([C@H](O)[C@@H]1O)n1ccc(=O)[nH]c1=O 2D coordinates Mol file for the small molecule Search links Involved in 61 reaction(s) Find molecules that contain or resemble this structure Find proteins in UniProtKB for this molecule
Name ^help_outline an α-D-GalNAc-(1→3)-[α-L-Fuc-(1→2)]-β-D-Gal-(1→3)-β-D-GalNAc derivative Identifier CHEBI:233968 Charge 0 Formula C28H47N2O20R SMILES^help_outline *OC1OC(CO)C(O)C(OC2OC(CO)C(O)C(OC3OC(CO)C(O)C(O)C3NC(=O)C)C2OC4OC(C)C(O)C(O)C4O)C1NC(=O)C 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 InChIKey^help_outline XCCTYIAWTASOJW-XVFCMESISA-K SMILES^help_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 711 reaction(s) Find molecules that contain or resemble this structure Find proteins in UniProtKB for this molecule
Name ^help_outline H⁺ Identifier CHEBI:15378 Charge 1 Formula H InChIKey^help_outline GPRLSGONYQIRFK-UHFFFAOYSA-N SMILES^help_outline [H+] 2D coordinates Mol file for the small molecule Search links Involved in 10,232 reaction(s) Find molecules that contain or resemble this structure Find proteins in UniProtKB for this molecule

Cross-references

	RHEA:84539	RHEA:84540	RHEA:84541	RHEA:84542
Reaction direction	undefined	left-to-right	right-to-left	bidirectional
UniProtKB ^help_outline

Related reactions ^help_outline

More general form(s) of this reaction

RHEA:19021
an α-L-fucosyl-(1→2)-β-D-galactosyl derivative + UDP-N-acetyl-α-D-galactosamine = an N-acetyl-α-D-galactosaminyl-(1→3)-[α-L-fucosyl-(1→2)]-β-D-galactosyl derivative + UDP + H⁺

Publications

Bacterial homologue of human blood group A transferase.

Yi W., Shen J., Zhou G., Li J., Wang P.G.

A bacterial version of human blood group A transferase was identified and found to be able to accept five naturally existing H-antigen core structures as good substrates, demonstrating its versatility for synthesis of blood group A antigens. Furthermore, this enzyme was applied in the engineering ... >> More

A bacterial version of human blood group A transferase was identified and found to be able to accept five naturally existing H-antigen core structures as good substrates, demonstrating its versatility for synthesis of blood group A antigens. Furthermore, this enzyme was applied in the engineering of bacterial cell surface polysaccharides by remodeling blood group B mimicry into blood group A mimicry. << Less

J Am Chem Soc 130:14420-14421(2008) [PubMed] [EuropePMC]

This publication is cited by 4 other entries.

Comments

Citation (not indexed by PubMed): DOI: 10.1021/acscatal.6b02755 J Ye, X Liu, P Peng, W Yi, X Chen, F Wang, H Cao (2016) Diversity-oriented enzymatic modular assembly of ABO histo-blood group antigens. ACS Catalysis, 6, 12, 8140-8144