Rapid purification of native SecA fromEscherichia coli: Development of a new affinity chromatography procedure

No abstract is available for this paper.

• Publication year

  1994

• Venue

  Current Microbiology

• Publication date

  1994-12-01

• Fields of study

  Biology, Medicine, Chemistry

• Identifiers
  DOI 10.1007/BF01570224PMID 7765521
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

• SecA is plastid-encoded in a red alga: implications for the evolution of plastid genomes and the thylakoid protein import apparatus

  2004cited by this paper
• The complete general secretory pathway in gram-negative bacteria.

  1993cited by this paper
• Characterization of a Bacillus subtilis SecA mutant protein deficient in translocation ATPase and release from the membrane

  1993cited by this paper
• SecY, SecE, and band 1 form the membrane-embedded domain of Escherichia coli preprotein translocase.

  1992cited by this paper
• Identification of a chloroplast-encoded secA gene homologue in a chromophytic alga: possible role in chloroplast protein translocation

  1992cited by this paper
• SecA protein needs both acidic phospholipids and SecY/E protein for functional high-affinity binding to the Escherichia coli plasma membrane.

  1991cited by this paper
• ΔμH+ and ATP function at different steps of the catalytic cycle of preprotein translocase

  1991cited by this paper
• Sequencing reveals similarity of the wild-type div+ gene of Bacillus subtilis to the Escherichia coli secA gene.

  1991cited by this paper
• Sequencing reveals similarity of the wild-type div+ gene of Bacillus subtilis to the Escherichia coli secA gene.

  1991cited by this paper
• Reconstitution of a protein translocation system containing purified SecY, SecE, and SecA from Escherichia coli.

  1991cited by this paper
• Regulation of Escherichia coli secA mRNA translation by a secretion-responsive element

  1991cited by this paper
• Conservation of components of the Escherichia coli export machinery in prokaryotes.

  1991cited by this paper
• Characterization of Escherichia coli SecA protein binding to a site on its mRNA involved in autoregulation.

  1991cited by this paper
• Conservation of components of the export machinery in prokaryotes

  1991cited by this paper
• SecA protein: Autoregulated initiator of secretory precursor protein translocation across theE. coli plasma membrane

  1990cited by this paper
• Reconstitution of translocation activity for secretory proteins from solubilized components of Escherichia coli.

  1990cited by this paper
• Complementation of two overlapping fragments of SecA, a protein translocation ATPase of Escherichia coli, allows ATP binding to its amino-terminal region.

  1990cited by this paper
• SecA protein autogenously represses its own translation during normal protein secretion in Escherichia coli

  1989cited by this paper
• SecA protein, a peripheral protein of the Escherichia coli plasma membrane, is essential for the functional binding and translocation of proOmpA.

  1989cited by this paper
• SecA protein hydrolyzes ATP and is an essential component of the protein translocation ATPase of Escherichia coli.

  1989influential reference
• Nucleotide sequence of the secA gene and secA(Ts) mutations preventing protein export in Escherichia coli

  1988cited by this paper
• Sequence of the lon gene in Escherichia coli. A heat-shock gene which encodes the ATP-dependent protease La.

  1988cited by this paper
• SecA protein is required for secretory protein translocation into E. coli membrane vesicles.

  1988cited by this paper
• Alkaline phosphatase and OmpA protein can be translocated posttranslationally into membrane vesicles of Escherichia coli

  1985cited by this paper
• Energy-requiring translocation of the OmpA protein and alkaline phosphatase of Escherichia coli into inner membrane vesicles

  1984cited by this paper
• The effect of nucleotide presaturation on the chromatographic behaviour of 6-phosphogluconate dehydrogenase from Bacillus stearothermophilus on immobilized triazine dyes.

  1981cited by this paper
• Affinity chromatography on immobilised triazine dyes. Studies on the interaction with multinucleotide-dependent enzymes.

  1981cited by this paper
• The purification of isocitrate dehydrogenase from Escherichia coli using immobilized dyes [proceedings].

  1980cited by this paper
• An improved assay for nanomole amounts of inorganic phosphate.

  1979cited by this paper
• The purification of nucleotide-dependent enzymes with dye-polysaccharide resins.

  1978cited by this paper
• A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding.

  1976cited by this paper
• High resolution two-dimensional electrophoresis of proteins.

  1975cited by this paper

• Expression, purification, and characterization of Pseudomonas aeruginosa SecA.

  2006cites this paper
• Regulation of the Escherichia coli secA Gene Is Mediated by Two Distinct RNA Structural Conformations

  1999cites this paper