Engineering and characterization of a superfolder green fluorescent protein. - Wikidata - wikimedia - TriplyDB

Engineering and characterization of a superfolder green fluorescent protein.

Engineering and characterization of a superfolder green fluorescent protein.

http://www.wikidata.org/entity/Q34478574

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Quantitative in vivo solubility and reconstitution of truncated circular permutants of green fluorescent protein B4GAT1 is the priming enzyme for the LARGE-dependent functional glycosylation of α-dystroglycan Human liver cell trafficking mutants: characterization and whole exome sequencing Imaging proteins inside cells with fluorescent tags Translational control and target recognition by Escherichia coli small RNAs in vivo Mutations conferring a noncytotoxic phenotype on chikungunya virus replicons compromise enzymatic properties of nonstructural protein 2 Advanced Fluorescence Protein-Based Synapse-Detectors Design and development of genetically encoded fluorescent sensors to monitor intracellular chemical and physical parameters Specific in vivo knockdown of protein function by intrabodies Topological mapping methods for α-helical bacterial membrane proteins--an update and a guide Recent advances in live cell imaging of hepatoma cells Development of cysteine-free fluorescent proteins for the oxidative environment Centromere protein F includes two sites that couple efficiently to depolymerizing microtubules Melanoma cells break down LPA to establish local gradients that drive chemotactic dispersal Positive feedback of NDT80 expression ensures irreversible meiotic commitment in budding yeast Visualization of Periplasmic and Cytoplasmic Proteins with a Self-Labeling Protein Tag.Simultaneous characterization of cellular RNA structure and function with in-cell SHAPE-Seq Nano-scale alignment of proteins on a flexible DNA backbone Translation dynamics of single mRNAs in live cells and neurons.The novel 2Fe–2S outer mitochondrial protein mitoNEET displays conformational flexibility in its N-terminal cytoplasmic tethering domain Synthetic Biology of Proteins: Tuning GFPs Folding and Stability with Fluoroproline Applicability of superfolder YFP bimolecular fluorescence complementation in vitro Circular Permutation of Red Fluorescent Proteins Mutation of the His ligand in mitoNEET stabilizes the 2Fe–2S cluster despite conformational heterogeneity in the ligand environment Optimization of a GCaMP Calcium Indicator for Neural Activity Imaging Visualization of Synaptic Inhibition with an Optogenetic Sensor Developed by Cell-Free Protein Engineering Automation Enzymatic Basis for N-Glycan Sialylation: STRUCTURE OF RAT 2,6-SIALYLTRANSFERASE (ST6GAL1) REVEALS CONSERVED AND UNIQUE FEATURES FOR GLYCAN SIALYLATION Split green fluorescent protein as a modular binding partner for protein crystallization The Designability of Protein Switches by Chemical Rescue of Structure: Mechanisms of Inactivation and Reactivation Green-lighting green fluorescent protein: Faster and more efficient folding by eliminating acis-transpeptide isomerization event Random Single Amino Acid Deletion Sampling Unveils Structural Tolerance and the Benefits of Helical Registry Shift on GFP Folding and Structure Different photochemical events of a genetically encoded phenyl azide define and modulate GFP fluorescence Replacement of highly conserved E222 by the photostable non-photoconvertible histidine in GFP Rational Structure-Based Design of Bright GFP-Based Complexes with Tunable Dimerization Functional and structural characterization of a potent GH74 endo-xyloglucanase from the soil saprophyte Cellvibrio japonicus unravels the first step of xyloglucan degradation Architecture of the type IVa pilus machine Impact of the crystallization condition on importin-β conformation ER cargo properties specify a requirement for COPII coat rigidity mediated by Sec13p.Targeting of Nbp1 to the inner nuclear membrane is essential for spindle pole body duplication.The GCKIII kinase Sps1 and the 14-3-3 isoforms, Bmh1 and Bmh2, cooperate to ensure proper sporulation in Saccharomyces cerevisiae.

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P2860

Engineering and characterization of a superfolder green fluorescent protein.

http://www.wikidata.org/entity/Q34478574

description

2005 nî lūn-bûn

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2005 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած

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2005 թվականի դեկտեմբերին հրատարակված գիտական հոդված

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2005年の論文

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2005年論文

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2005年論文

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2005年論文

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2005年論文

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2005年論文

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2005年论文

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name

Engineering and characterization of a superfolder green fluorescent protein.

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Engineering and characterization of a superfolder green fluorescent protein.

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Engineering and characterization of a superfolder green fluorescent protein.

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type

label

Engineering and characterization of a superfolder green fluorescent protein.

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Engineering and characterization of a superfolder green fluorescent protein.

@en

Engineering and characterization of a superfolder green fluorescent protein.

@nl

prefLabel

Engineering and characterization of a superfolder green fluorescent protein.

@ast

Engineering and characterization of a superfolder green fluorescent protein.

@en

Engineering and characterization of a superfolder green fluorescent protein.

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Nature Biotechnology

P1476

Engineering and characterization of a superfolder green fluorescent protein.

@en

P2093

Geoffrey S Waldo

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

Jean-Denis Pédelacq

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Stéphanie Cabantous

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Timothy Tran

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P2860

Circularly permuted variants of the green fluorescent protein

Circular permutation and receptor insertion within green fluorescent proteins

Homo-FRET microscopy in living cells to measure monomer-dimer transition of GFP-tagged proteins.

The C-terminal domain of TAP interacts with the nuclear pore complex and promotes export of specific CTE-bearing RNA substrates

DNA shuffling by random fragmentation and reassembly: in vitro recombination for molecular evolution

Crystallography & NMR System: A New Software Suite for Macromolecular Structure Determination

Crystal structure and refolding properties of the mutant F99S/M153T/V163A of the green fluorescent protein

The structure of Pyrococcus furiosus glutamate dehydrogenase reveals a key role for ion-pair networks in maintaining enzyme stability at extreme temperatures

Crystal structure of the Aequorea victoria green fluorescent protein

The green fluorescent protein

P2888

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79-88

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scholarly article

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10.1038/NBT1172

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1

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24

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Thomas C. Terwilliger

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2005-12-20T00:00:00Z

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7400495

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1046582276

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16369541

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