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Literature summary extracted from

  • Siarheyeva, A.; Sharom, F.J.
    The ABC transporter MsbA interacts with lipid A and amphipathic drugs at different sites (2009), Biochem. J., 419, 317-328 .
    View publication on PubMedView publication on EuropePMC

Cloned(Commentary)

EC Number Cloned (Comment) Organism
7.5.2.6 gene msbA, recombinant expression of His-tagged wild-type and mutant C88S/C135S enzymes in Escherichia coli strain BL21-Codonplus(DE3)-RIL in cytoplasmic membrane vesicles Salmonella enterica subsp. enterica serovar Typhimurium

Protein Variants

EC Number Protein Variants Comment Organism
7.5.2.6 C315S site-directed mutagenesis, the mutant ATPase activity of the C88S and C315S mutants does not differ substantially from that of wild-type MsbA Salmonella enterica subsp. enterica serovar Typhimurium
7.5.2.6 C88S site-directed mutagenesis, the mutant ATPase activity of the C88S and C315S mutants does not differ substantially from that of wild-type MsbA Salmonella enterica subsp. enterica serovar Typhimurium
7.5.2.6 C88S/C315S site-directed mutagenesis Salmonella enterica subsp. enterica serovar Typhimurium
7.5.2.6 additional information the mutant enzymes are T561C and E506Q/T561C are labeled with MIANS fluorescent probes Salmonella enterica subsp. enterica serovar Typhimurium

KM Value [mM]

EC Number KM Value [mM] KM Value Maximum [mM] Substrate Comment Organism Structure
7.5.2.6 0.52
-
ATP recombinant His-tagged wild-type enzyme, ATPase activity, pH 7.5, 37°C Salmonella enterica subsp. enterica serovar Typhimurium

Localization

EC Number Localization Comment Organism GeneOntology No. Textmining
7.5.2.6 inner membrane topological model of the MsbA protein, the six transmembrane helices in each MsbA monomer extend into the cytosol, forming an intracellular domain that may play a role in coupling ATP hydrolysis to substrate transport, overview Salmonella enterica subsp. enterica serovar Typhimurium
-
-

Metals/Ions

EC Number Metals/Ions Comment Organism Structure
7.5.2.6 Mg2+ required Salmonella enterica subsp. enterica serovar Typhimurium

Natural Substrates/ Products (Substrates)

EC Number Natural Substrates Organism Comment (Nat. Sub.) Natural Products Comment (Nat. Pro.) Rev. Reac.
7.5.2.6 ATP + H2O + lipid A-core oligosaccharide[side 1] Salmonella enterica subsp. enterica serovar Typhimurium
-
ADP + phosphate + lipid A-core oligosaccharide[side 2]
-
?

Organism

EC Number Organism UniProt Comment Textmining
7.5.2.6 Salmonella enterica subsp. enterica serovar Typhimurium P63359
-
-

Purification (Commentary)

EC Number Purification (Comment) Organism
7.5.2.6 recombinant N-terminally His6-tagged wild-type and mutant C88S/C135S enzymes from Escherichia coli strain BL21-Codonplus(DE3)-RIL by n-dodecyl-beta-D-maltopyranoside solubilization from membranes, nickel affinity chromatography, and ultrafiltration Salmonella enterica subsp. enterica serovar Typhimurium

Specific Activity [micromol/min/mg]

EC Number Specific Activity Minimum [µmol/min/mg] Specific Activity Maximum [µmol/min/mg] Comment Organism
7.5.2.6 0.4
-
purified recombinant His-tagged wild-type enzyme, ATPase activity, pH 7.5, 37°C Salmonella enterica subsp. enterica serovar Typhimurium

Substrates and Products (Substrate)

EC Number Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
7.5.2.6 ATP + H2O + daunorubicin[side 1]
-
Salmonella enterica subsp. enterica serovar Typhimurium ADP + phosphate + daunorubicin[side 2]
-
?
7.5.2.6 ATP + H2O + lipid A-core oligosaccharide[side 1]
-
Salmonella enterica subsp. enterica serovar Typhimurium ADP + phosphate + lipid A-core oligosaccharide[side 2]
-
?
7.5.2.6 additional information simultaneous high affinity binding to MsbA of lipid A (the putative physiological substrate) and daunorubicin, which suggests that the protein has separate binding sites for these two compounds. The effects of nucleotide and lipid A/daunorubicin binding to MsbA are additive, and binding could occur in any order. The two substrate-binding sites appear to communicate with each other, and also with the nucleotide-binding site in the nucleotide-binding domains, NBDs. The two monomers function independently, and do not interact co-operatively with each other, analysis using MIANS-labeled enzyme, MIANS, i.e. 2-(4-maleimidylanilino)naphthalene-6-sulfonic acid, is a cysteine-reactive fluorescent probe for soluble and membrane-bound proteins, fluorescence quenching studies. The percentage quenching values observed for lipid A and daunorubicin are also similar regardless of the order of titration. The binding affinity for lipid A is reduced about 5fold at 23°C and about 7fold at 10°C when the daunorubicin-binding site is occupied first Salmonella enterica subsp. enterica serovar Typhimurium ?
-
?

Subunits

EC Number Subunits Comment Organism
7.5.2.6 homodimer the two monomers function independently, and do not interact co-operatively with each other Salmonella enterica subsp. enterica serovar Typhimurium
7.5.2.6 More secondary structure analysis of MsbA Salmonella enterica subsp. enterica serovar Typhimurium

Synonyms

EC Number Synonyms Comment Organism
7.5.2.6 MsbA
-
Salmonella enterica subsp. enterica serovar Typhimurium

Temperature Optimum [°C]

EC Number Temperature Optimum [°C] Temperature Optimum Maximum [°C] Comment Organism
7.5.2.6 37
-
assay at Salmonella enterica subsp. enterica serovar Typhimurium

pH Optimum

EC Number pH Optimum Minimum pH Optimum Maximum Comment Organism
7.5.2.6 7.5
-
assay at Salmonella enterica subsp. enterica serovar Typhimurium

Cofactor

EC Number Cofactor Comment Organism Structure
7.5.2.6 ATP
-
Salmonella enterica subsp. enterica serovar Typhimurium