Any feedback?
Please rate this page
(literature.php)
(0/150)

BRENDA support

Literature summary extracted from

  • Amer, A.O.; Valvano, M.A.
    Conserved amino acid residues found in a predicted cytosolic domain of the lipopolysaccharide biosynthetic protein WecA are implicated in the recognition of UDP-N-acetylglucosamine (2001), Microbiology, 147, 3015-3025.
    View publication on PubMed

Cloned(Commentary)

EC Number Cloned (Comment) Organism
2.7.8.33 design of a vector system to generate C-terminal protein fusions to the FLAG epitope, which is used to find conditions to monitor WecA by immunoblot analysis with anti-FLAG antibodies, to determine the correct site for initiation of translation, and to investigate the localization of hybrid proteins in the cytoplasmic membrane Escherichia coli
2.7.8.33 detailed examination of the role of a conserved motif within the predicted large cytosolic loop Escherichia coli

Localization

EC Number Localization Comment Organism GeneOntology No. Textmining
2.7.8.33 membrane design of a vector system to generate C-terminal protein fusions to the FLAG epitope, which is used to find conditions to monitor WecA by immunoblot analysis with anti-FLAG antibodies, to determine the correct site for initiation of translation, and to investigate the localization of hybrid proteins in the cytoplasmic membrane Escherichia coli 16020
-
2.7.8.33 membrane modelling of the topology of WecA taking into account the available experimental data from the topological analysis of MraY Escherichia coli 16020
-

Organism

EC Number Organism UniProt Comment Textmining
2.7.8.33 Escherichia coli P0AC78
-
-

Synonyms

EC Number Synonyms Comment Organism
2.7.8.33 GlcNAc:undecaprenyl-phosphate GlcNAc-1-phosphate transferase
-
 Escherichia coli
2.7.8.33 Rfe
-
 Escherichia coli
2.7.8.33 UDP-N-acetylglucosamine:undecaprenyl-phosphate GlcNAc-1-phosphate transferase
-
 Escherichia coli
2.7.8.33 WecA
-
 Escherichia coli