about
Biogenesis and transmembrane topology of the CHIP28 water channel at the endoplasmic reticulumProcessing of yellow fever virus polyprotein: role of cellular proteases in maturation of the structural proteinsMembrane topology and insertion of membrane proteins: search for topogenic signalsComplementation of formyl peptide receptor-mediated signal transduction in Xenopus laevis oocytes.The cytoplasmic domain of Escherichia coli leader peptidase is a "translocation poison" sequence.The amplified H circle of methotrexate-resistant leishmania tarentolae contains a novel P-glycoprotein geneTopology analysis of the SecY protein, an integral membrane protein involved in protein export in Escherichia coli.Physiological basis for conservation of the signal recognition particle targeting pathway in Escherichia coli.Co-translational targeting and translocation of the amino terminus of opsin across the endoplasmic membrane requires GTP but not ATP.Positively charged amino acid residues can act as topogenic determinants in membrane proteinsMultiple topogenic sequences in bovine opsin.Determinants of membrane protein topologyIn vivo assembly of rhodopsin from expressed polypeptide fragmentsIntracellular traffic of newly synthesized proteins. Current understanding and future prospectsSoluble factors stimulating secretory protein translocation in bacteria and yeast can substitute for each other.Protein-Trap Insertional Mutagenesis Uncovers New Genes Involved in Zebrafish Skin Development, Including a Neuregulin 2a-Based ErbB Signaling Pathway Required during Median Fin Fold MorphogenesisPartial deletion of membrane-bound domain of 3-hydroxy-3-methylglutaryl coenzyme A reductase eliminates sterol-enhanced degradation and prevents formation of crystalloid endoplasmic reticulumThe influenza hemagglutinin insertion signal is not cleaved and does not halt translocation when presented to the endoplasmic reticulum membrane as part of a translocating polypeptide.Cell surface expression of membrane-anchored v-sis gene products: glycosylation is not required for cell surface transportProtein translocation across the yeast microsomal membrane is stimulated by a soluble factorA specific transmembrane domain of a coronavirus E1 glycoprotein is required for its retention in the Golgi region.Signals for the incorporation and orientation of cytochrome P450 in the endoplasmic reticulum membrane.Topogenesis of mitochondrial inner membrane uncoupling protein. Rerouting transmembrane segments to the soluble matrix compartment.Molecular dissection of the NH2-terminal signal/anchor sequence of rat dipeptidyl peptidase IVTopology and phosphorylation of soybean nodulin-26, an intrinsic protein of the peribacteroid membraneProtein translocation across the rough endoplasmic reticulum.Nuclear export signal-interacting protein forms complexes with lamin A/C-Nups to mediate the CRM1-independent nuclear export of large hepatitis delta antigen.In vivo topological analysis of Ste2, a yeast plasma membrane protein, by using beta-lactamase gene fusionsGenetic and biochemical evaluation of eucaryotic membrane protein topology: multiple transmembrane domains of Saccharomyces cerevisiae 3-hydroxy-3-methylglutaryl coenzyme A reductaseBiogenesis and transmembrane orientation of the cellular isoform of the scrapie prion protein [published errratum appears in Mol Cell Biol 1987 May;7(5):2035]Determination of the orientation of an integral membrane protein and sites of glycosylation by oligonucleotide-directed mutagenesis: influenza B virus NB glycoprotein lacks a cleavable signal sequence and has an extracellular NH2-terminal region.Coupled translocation events generate topological heterogeneity at the endoplasmic reticulum membrane.The yeast acid phosphatase can enter the secretory pathway without its N-terminal signal sequence.The N-terminal 22 amino acid residues in the lactose permease of Escherichia coli are not obligatory for membrane insertion or transport activity.Insertion of proteins into bacterial membranes: mechanism, characteristics, and comparisons with the eucaryotic process.Molecular chaperones and photoreceptor function.Sequence requirements for membrane assembly of polytopic membrane proteins: molecular dissection of the membrane insertion process and topogenesis of the human MDR3 P-glycoprotein.Determinant of the extracellular location of the N-terminus of human multidrug-resistance-associated protein.The accessibility of yeast ribosomal protein L1 as probed by proteolysis and site-directed mutagenesis is different in intact 60 and 80 S ribosome.Transcriptional regulation of secretory capacity by bZip transcription factors.
P2860
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P2860
description
1985 nî lūn-bûn
@nan
1985年の論文
@ja
1985年学术文章
@wuu
1985年学术文章
@zh
1985年学术文章
@zh-cn
1985年学术文章
@zh-hans
1985年学术文章
@zh-my
1985年学术文章
@zh-sg
1985年學術文章
@yue
1985年學術文章
@zh-hant
name
Bovine opsin has more than one signal sequence.
@en
Bovine opsin has more than one signal sequence.
@nl
type
label
Bovine opsin has more than one signal sequence.
@en
Bovine opsin has more than one signal sequence.
@nl
prefLabel
Bovine opsin has more than one signal sequence.
@en
Bovine opsin has more than one signal sequence.
@nl
P356
P1433
P1476
Bovine opsin has more than one signal sequence.
@en
P2093
Friedlander M
P2888
P304
P356
10.1038/318338A0
P407
P577
1985-11-01T00:00:00Z
P6179
1006173890