Positively charged amino acid residues can act as topogenic determinants in membrane proteins
about
Two cysteines in each periplasmic domain of the membrane protein DsbB are required for its function in protein disulfide bond formationNovel topology of BfpE, a cytoplasmic membrane protein required for type IV fimbrial biogenesis in enteropathogenic Escherichia coliThe complete general secretory pathway in gram-negative bacteriaExport of maltose-binding protein species with altered charge distribution surrounding the signal peptide hydrophobic core in Escherichia coli cells harboring prl suppressor mutations.Topological organization of the hyaluronan synthase from Streptococcus pyogenes.lac permease of Escherichia coli: topology and sequence elements promoting membrane insertionGenetic analysis of membrane protein topology by a sandwich gene fusion approach.Topology of RbsC, a membrane component of the ribose transporter, belonging to the AraH superfamilySec dependent and sec independent assembly of E. coli inner membrane proteins: the topological rules depend on chain lengthA signal sequence is not required for protein export in prlA mutants of Escherichia coliUnbalanced charge distribution as a determinant for dependence of a subset of Escherichia coli membrane proteins on the membrane insertase YidC.Escherichia coli alkaline phosphatase localized to the cytoplasm slowly acquires enzymatic activity in cells whose growth has been suspended: a caution for gene fusion studies.Characterization of transmembrane domains 6, 7, and 8 of MalF by mutational analysisBiotinylation in vivo as a sensitive indicator of protein secretion and membrane protein insertionDomain-swapping analysis of FtsI, FtsL, and FtsQ, bitopic membrane proteins essential for cell division in Escherichia coliDecoding signals for membrane protein assembly using alkaline phosphatase fusions.Gene fusion analysis of membrane protein topology: a direct comparison of alkaline phosphatase and beta-lactamase fusionsStructural analysis of a mouse mammary tumor virus superantigen.Membrane topology of the high-affinity L-glutamate transporter (GLAST-1) of the central nervous system.Cloning a plant amino acid transporter by functional complementation of a yeast amino acid transport mutant.Charge composition features of model single-span membrane proteins that determine selection of YidC and SecYEG translocase pathways in Escherichia coli.In vivo topological analysis of Ste2, a yeast plasma membrane protein, by using beta-lactamase gene fusionsNeisseria gonorrhoeae PilC expression provides a selective mechanism for structural diversity of pili.Molecular simulations of aromatase reveal new insights into the mechanism of ligand binding.A 30-residue-long "export initiation domain" adjacent to the signal sequence is critical for protein translocation across the inner membrane of Escherichia coliTranslocation of N-terminal tails across the plasma membraneThe translocation of negatively charged residues across the membrane is driven by the electrochemical potential: evidence for an electrophoresis-like membrane transfer mechanism.Subunit interactions in ABC transporters: a conserved sequence in hydrophobic membrane proteins of periplasmic permeases defines an important site of interaction with the ATPase subunits.Structure-function study of MalF protein by random mutagenesis.Membrane topology of the NixA nickel transporter of Helicobacter pylori: two nickel transport-specific motifs within transmembrane helices II and III.Signal sequence mutations as tools for the characterization of LamB folding intermediates.Membrane topology analysis of Escherichia coli K-12 Mtr permease by alkaline phosphatase and beta-galactosidase fusions.Topological analysis of the Rhodobacter capsulatus PucC protein and effects of C-terminal deletions on light-harvesting complex II.The oxygen sensor FixL of Rhizobium meliloti is a membrane protein containing four possible transmembrane segments.Membrane topology analysis of cyclic glucan synthase, a virulence determinant of Brucella abortus.C-terminal sequences can inhibit the insertion of membrane proteins into the endoplasmic reticulum of Saccharomyces cerevisiae.Characterization of CetA and CetB, a bipartite energy taxis system in Campylobacter jejuni.The 'positive-inside rule' applies to thylakoid membrane proteins.Putative membrane components of signal transduction pathways for ambient pH regulation in Aspergillus and meiosis in saccharomyces are homologous.A topological model for the high-affinity nickel transporter of Alcaligenes eutrophus.
P2860
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P2860
Positively charged amino acid residues can act as topogenic determinants in membrane proteins
description
1989 nî lūn-bûn
@nan
1989 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
1989 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
1989年の論文
@ja
1989年論文
@yue
1989年論文
@zh-hant
1989年論文
@zh-hk
1989年論文
@zh-mo
1989年論文
@zh-tw
1989年论文
@wuu
name
Positively charged amino acid ...... erminants in membrane proteins
@ast
Positively charged amino acid ...... erminants in membrane proteins
@en
Positively charged amino acid ...... erminants in membrane proteins
@nl
type
label
Positively charged amino acid ...... erminants in membrane proteins
@ast
Positively charged amino acid ...... erminants in membrane proteins
@en
Positively charged amino acid ...... erminants in membrane proteins
@nl
prefLabel
Positively charged amino acid ...... erminants in membrane proteins
@ast
Positively charged amino acid ...... erminants in membrane proteins
@en
Positively charged amino acid ...... erminants in membrane proteins
@nl
P2860
P356
P1476
Positively charged amino acid ...... erminants in membrane proteins
@en
P2093
P2860
P304
P356
10.1073/PNAS.86.23.9446
P407
P577
1989-12-01T00:00:00Z