EC Number |
Substrates |
Organism |
Products |
Reversibility |
---|
2.4.1.289 | dTDP-6-deoxy-beta-L-mannose + N-acetyl-alpha-D-glucosaminyl-diphospho-trans,octacis-decaprenol |
- |
Mycobacterium tuberculosis |
dTDP + alpha-L-rhamnopyranosyl-(1->3)-N-acetyl-alpha-D-glucosaminyl-diphospho-trans,octacis-decaprenol |
- |
? |
2.4.1.289 | dTDP-6-deoxy-beta-L-mannose + N-acetyl-alpha-D-glucosaminyl-diphospho-trans,octacis-decaprenol |
- |
Campylobacter jejuni |
dTDP + alpha-L-rhamnopyranosyl-(1->3)-N-acetyl-alpha-D-glucosaminyl-diphospho-trans,octacis-decaprenol |
- |
? |
2.4.1.289 | dTDP-6-deoxy-beta-L-mannose + N-acetyl-alpha-D-glucosaminyl-diphospho-trans,octacis-decaprenol |
natural acceptor substrate GlcNAc-P-P-decaprenyl |
Mycobacterium tuberculosis |
dTDP + alpha-L-rhamnopyranosyl-(1->3)-N-acetyl-alpha-D-glucosaminyl-diphospho-trans,octacis-decaprenol |
- |
? |
2.4.1.289 | dTDP-6-deoxy-beta-L-mannose + N-acetyl-alpha-D-glucosaminyl-diphospho-trans,octacis-decaprenol |
- |
Campylobacter jejuni NCTC 11168 |
dTDP + alpha-L-rhamnopyranosyl-(1->3)-N-acetyl-alpha-D-glucosaminyl-diphospho-trans,octacis-decaprenol |
- |
? |
2.4.1.289 | dTDP-6-deoxy-beta-L-mannose + N-acetyl-alpha-D-glucosaminyl-diphospho-trans,octacis-decaprenol |
- |
Mycobacterium tuberculosis H37Rv |
dTDP + alpha-L-rhamnopyranosyl-(1->3)-N-acetyl-alpha-D-glucosaminyl-diphospho-trans,octacis-decaprenol |
- |
? |
2.4.1.289 | dTDP-6-deoxy-beta-L-mannose + N-acetyl-alpha-D-glucosaminyl-diphospho-trans,octacis-decaprenol |
natural acceptor substrate GlcNAc-P-P-decaprenyl |
Mycobacterium tuberculosis H37Rv |
dTDP + alpha-L-rhamnopyranosyl-(1->3)-N-acetyl-alpha-D-glucosaminyl-diphospho-trans,octacis-decaprenol |
- |
? |
2.4.1.289 | dTDP-beta-L-rhamnose + GlcNAc-diphospho-trans,octacis-decaprenol |
- |
Mycobacterium tuberculosis |
? |
- |
? |
2.4.1.289 | dTDP-beta-L-rhamnose + GlcNAc-diphospho-trans,octacis-decaprenol |
- |
Mycobacterium tuberculosis H37Rv |
? |
- |
? |
2.4.1.289 | more |
in vitro transfer of N,N'-diacetylbacillosamine phosphate onto Und-P and the in vitro enzymatic synthesis of the heptasacccharide using a chemically synthesized undecaprenyl diphosphate-linked N,N'-diacetylbacillosamine. The reactions of PglC, PglA, PglH, PglJ and PglI are coupled in a single reaction vessel, NMR spectrometric product analysis |
Campylobacter jejuni |
? |
- |
? |
2.4.1.289 | more |
in vitro, trisaccharide is prepared by using PglA and PglJ and then reacts singly with PglH |
Campylobacter jejuni |
? |
- |
? |