Superfolder GFP is fluorescent in oxidizing environments when targeted via the Sec translocon - Wikidata - awgldk - TriplyDB

Superfolder GFP is fluorescent in oxidizing environments when targeted via the Sec translocon

Superfolder GFP is fluorescent in oxidizing environments when targeted via the Sec translocon

http://www.wikidata.org/entity/Q34816912

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Topological mapping methods for α-helical bacterial membrane proteins--an update and a guide Development of cysteine-free fluorescent proteins for the oxidative environment Integrity of Narrow Epithelial Tubes in the C. elegans Excretory System Requires a Transient Luminal Matrix Visualization of Periplasmic and Cytoplasmic Proteins with a Self-Labeling Protein Tag.Futile protein folding cycles in the ER are terminated by the unfolded protein O-mannosylation pathway.Defining hepatic dysfunction parameters in two models of fatty liver disease in zebrafish larvae A cationic lumen in the Wzx flippase mediates anionic O-antigen subunit translocation in Pseudomonas aeruginosa PAO1 Occurrence and subcellular distribution of the NADPHX repair system in mammals ERdj4 protein is a soluble endoplasmic reticulum (ER) DnaJ family protein that interacts with ER-associated degradation machinery A palette of fluorescent proteins optimized for diverse cellular environments Imaging the alphavirus exit pathway.The nematode homologue of Mediator complex subunit 28, F28F8.5, is a critical regulator of C. elegans development.Nonmigraine-associated TRESK K+ channel variant C110R does not increase the excitability of trigeminal ganglion neurons.Biochemical and cellular analysis of human variants of the DYT1 dystonia protein, TorsinA/TOR1A Bacterial cytoplasm as an effective cell compartment for producing functional VHH-based affinity reagents and Camelidae IgG-like recombinant antibodies Secretion of a foreign protein from budding yeasts is enhanced by cotranslational translocation and by suppression of vacuolar targeting.Deglycosylation-dependent fluorescent proteins provide unique tools for the study of ER-associated degradation.Approaches to imaging unfolded secretory protein stress in living cells.Photobleaching methods to study Golgi complex dynamics in living cells.Engineering and exploitation of a fluorescent HIV-1 gp120 for live cell CD4 binding assays Using superfolder green fluorescent protein for periplasmic protein localization studies.Kar2p availability defines distinct forms of endoplasmic reticulum stress in living cells.Mini-Tn7 Insertion in an Artificial attTn7 Site Enables Depletion of the Essential Master Regulator CtrA in the Phytopathogen Agrobacterium tumefaciens A Bystander Mechanism Explains the Specific Phenotype of a Broadly Expressed Misfolded Protein.The Regulatory Domain of Squalene Monooxygenase Contains a Re-entrant Loop and Senses Cholesterol via a Conformational Change.Rational design of ultrastable and reversibly photoswitchable fluorescent proteins for super-resolution imaging of the bacterial periplasm.Proinsulin intermolecular interactions during secretory trafficking in pancreatic β cells Cysteineless non-glycosylated monomeric blue fluorescent protein, secBFP2, for studies in the eukaryotic secretory pathway.ERdj3 regulates BiP occupancy in living cells.The effects of ER morphology on synaptic structure and function in Drosophila melanogaster.Molecular Pharmacology of δ-Opioid Receptors.Fluorescent proteins in cellular organelles: serious pitfalls and some solutions.Exploring cells with targeted biosensors Probing endoplasmic reticulum dynamics using fluorescence imaging and photobleaching techniques.Molecular dissection of phage endolysin: an interdomain interaction confers host specificity in Lysin A of Mycobacterium phage D29.Perspectives for using genetically encoded fluorescent biosensors in plants Engineered fluorescent proteins illuminate the bacterial periplasm Subcellular functions of proteins under fluorescence single-cell microscopy.Glycosylation-directed quality control of protein folding.Measuring the Uptake and Transactivation Function of HIV-1 Tat Protein in a Trans-cellular Cocultivation Setup.

P2860

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P2860

Superfolder GFP is fluorescent in oxidizing environments when targeted via the Sec translocon

http://www.wikidata.org/entity/Q34816912

description

2011 nî lūn-bûn

@nan

2011 թուականի Փետրուարին հրատարակուած գիտական յօդուած

@hyw

2011 թվականի փետրվարին հրատարակված գիտական հոդված

@hy

2011年の論文

@ja

2011年論文

@yue

2011年論文

@zh-hant

2011年論文

@zh-hk

2011年論文

@zh-mo

2011年論文

@zh-tw

2011年论文

@wuu

name

Superfolder GFP is fluorescent ...... argeted via the Sec translocon

@ast

Superfolder GFP is fluorescent ...... argeted via the Sec translocon

@en

Superfolder GFP is fluorescent ...... argeted via the Sec translocon

@nl

type

label

Superfolder GFP is fluorescent ...... argeted via the Sec translocon

@ast

Superfolder GFP is fluorescent ...... argeted via the Sec translocon

@en

Superfolder GFP is fluorescent ...... argeted via the Sec translocon

@nl

prefLabel

Superfolder GFP is fluorescent ...... argeted via the Sec translocon

@ast

Superfolder GFP is fluorescent ...... argeted via the Sec translocon

@en

Superfolder GFP is fluorescent ...... argeted via the Sec translocon

@nl

P1433

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P2860

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P356

J.1600-0854.2011.01168.X

P1433

P1476

Superfolder GFP is fluorescent ...... argeted via the Sec translocon

@en

P2093

Deborah E Aronson

http://www.w3.org/2001/XMLSchema#string

Lindsey M Costantini

http://www.w3.org/2001/XMLSchema#string

P2860

Protein quality control in the bacterial periplasm

Crystal structure of the Aequorea victoria green fluorescent protein

The green fluorescent protein

Green fluorescent protein as a marker for gene expression

Extraction, purification and properties of aequorin, a bioluminescent protein from the luminous hydromedusan, Aequorea

Oligomerization of green fluorescent protein in the secretory pathway of endocrine cells

Partitioning of lipid-modified monomeric GFPs into membrane microdomains of live cells

Diffusion of green fluorescent protein in the aqueous-phase lumen of endoplasmic reticulum.

Formation of stacked ER cisternae by low affinity protein interactions.

Export of active green fluorescent protein to the periplasm by the twin-arginine translocase (Tat) pathway in Escherichia coli.

P304

543-548

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.1111/J.1600-0854.2011.01168.X

http://www.w3.org/2001/XMLSchema#string

P433

5

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P478

12

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P50

P577

2011-02-25T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

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49774594

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21255213

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P932

3079558

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