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Literature summary for 4.2.1.115 extracted from

  • Rosey, E.L.; Kennedy, M.J.; Petrella, D.K.; Ulrich, R.G.; Yancey, R.J.
    Inactivation of Serpulina hyodysenteriae flaA1 and flaB1 periplasmic flagellar genes by electroporation-mediated allelic exchange (1995), J. Bacteriol., 177, 5959-5970.
    View publication on PubMedView publication on EuropePMC

Cloned(Commentary)

Cloned (Comment) Organism
gene flaA1, DNA and amino acid sequence determination and analysis Brachyspira hyodysenteriae

Protein Variants

Protein Variants Comment Organism
additional information disruption of flaA1 and flaB1 genes by replacement of internal fragments with chloramphenicol and/or kanamycin gene cassettes. Both mutations selectively abolish expression of the targeted gene without affecting synthesis of the other flagellar polypeptide. flaA1 and flaB1 mutant strains exhibit altered motility in vitro and are less efficient in movement through a liquid medium. Paradoxically, isogenic strains containing specifically disrupted flaA1 or flaB1 alleles are capable of assembling periplasmic flagella that are morphologically wild-type, phenotype, detailed overview Brachyspira hyodysenteriae

Localization

Localization Comment Organism GeneOntology No. Textmining
flagellum
-
Brachyspira hyodysenteriae
-
-
periplasm
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Brachyspira hyodysenteriae
-
-

Organism

Organism UniProt Comment Textmining
Brachyspira hyodysenteriae
-
gene flaA1
-
Brachyspira hyodysenteriae B204
-
gene flaA1
-

Synonyms

Synonyms Comment Organism
FlaA1
-
Brachyspira hyodysenteriae