2.4.1.B69: N,N'-diacetylbacillosaminyl-diphospho-undecaprenol alpha-1,3-glucosyltransferase
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For detailed information about N,N'-diacetylbacillosaminyl-diphospho-undecaprenol alpha-1,3-glucosyltransferase, go to the full flat file.
Reaction
Synonyms
pglG, PglH
ECTree
2.4.1.B69 N,N'-diacetylbacillosaminyl-diphospho-undecaprenol alpha-1,3-glucosyltransferaseAdvanced search results
results (
results (| Results | in table |
|---|---|
| 1 | AA Sequence |
| 2 | Cloned(Commentary) |
| 9 | General Information |
| 4 | Organism |
| 1 | Protein Variants |
| 1 | Reaction |
| 3 | Reference |
| 5 | Substrates and Products (Substrate) |
| 4 | Synonyms |
| 1 | Systematic Name |
Cloned
Cloned on EC 2.4.1.B69 - N,N'-diacetylbacillosaminyl-diphospho-undecaprenol alpha-1,3-glucosyltransferase
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CLONED (Commentary) 
ORGANISM
UNIPROT
LITERATURE
gene pglG, genotyping, overview. The variable presence of two open reading frames (ORFs) in the pgl locus includes a putative glycosyltransferase gene, pglG, in addition to a glucosyltransferase-expressing gene, pglH. Strains lacking these two ORFs retain the first 40 bp of pglG and the last 100 bp of pglH. Homologous recombination within the pgl loci through genomic analysis of 100 African serogroup A isolates is detected representing the clonal replacement of hypervirulent meningococcal clone sequence type 7 (ST-7) by the ST-2859 descendant clone
gene pglH, genotyping, overview. The variable presence of two open reading frames (ORFs) in the pgl locus includes a putative glycosyltransferase gene, pglG, in addition to a glucosyltransferase-expressing gene, pglH. One subcluster has pglH while the other has the pglH2 variant allele. Strains lacking these two ORFs retain the first 40 bp of pglG and the last 100 bp of pglH. Homologous recombination within the pgl loci through genomic analysis of 100 African serogroup A isolates is detected representing the clonal replacement of hypervirulent meningococcal clone sequence type 7 (ST-7) by the ST-2859 descendant clone. Polymorphisms exist at the gene level described for pglH and pglH2, where only one nonsynonymous mutation is accountable for the glycoform switch from Glc to GlcNAc. One subcluster has pglH while the other has the pglH2 variant allele. The pglH locus shows polymorphisms between STs along the whole gene. A 5' point mutation (guanosine to cytosine) adjacent to the polycytosine [poly(C)] tract is found in individuals 20, 22, and 33 carrying ST-192 isolates
