A mechanism for intracellular release of Na+ by neurotransmitter/sodium symporters. - Wikidata - awgldk - TriplyDB

A mechanism for intracellular release of Na+ by neurotransmitter/sodium symporters.

A mechanism for intracellular release of Na+ by neurotransmitter/sodium symporters.

http://www.wikidata.org/entity/Q30623808

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Monoamine transporters: insights from molecular dynamics simulations Spontaneous inward opening of the dopamine transporter is triggered by PIP2-regulated dynamics of the N-terminus A conserved leucine occupies the empty substrate site of LeuT in the Na(+)-free return state.Neurotransmitter and psychostimulant recognition by the dopamine transporter.Unveiling the Mechanism of Arginine Transport through AdiC with Molecular Dynamics Simulations: The Guiding Role of Aromatic Residues Direct assessment of substrate binding to the Neurotransmitter:Sodium Symporter LeuT by solid state NMR Exploring the Inhibitory Mechanism of Approved Selective Norepinephrine Reuptake Inhibitors and Reboxetine Enantiomers by Molecular Dynamics Study A comprehensive review of the lipid cubic phase or in meso method for crystallizing membrane and soluble proteins and complexes.COMSAT: Residue contact prediction of transmembrane proteins based on support vector machines and mixed integer linear programming.Structural and mechanistic basis of proton-coupled metal ion transport in the SLC11/NRAMP family.Identification of a second substrate-binding site in solute-sodium symporters.Interaction of α-Lipoic Acid with the Human Na+/Multivitamin Transporter (hSMVT).Functional mechanisms of neurotransmitter transporters regulated by lipid-protein interactions of their terminal loops.Family resemblances: A common fold for some dimeric ion-coupled secondary transporters Substrate-induced unlocking of the inner gate determines the catalytic efficiency of a neurotransmitter:sodium symporter.Energy landscape of LeuT from molecular simulations Two Na+ Sites Control Conformational Change in a Neurotransmitter Transporter Homolog Genetically encoded photocrosslinkers locate the high-affinity binding site of antidepressant drugs in the human serotonin transporter.Control of serotonin transporter phosphorylation by conformational state.Na+ coordination at the Na2 site of the Na+/I- symporter.Transition metal ion FRET uncovers K(+) regulation of a neurotransmitter/sodium symporter.A Markov State-based Quantitative Kinetic Model of Sodium Release from the Dopamine Transporter.Convergent evolution of the arginine deiminase pathway: the ArcD and ArcE arginine/ornithine exchangers Structure-activity relationship studies of citalopram derivatives: examining substituents conferring selectivity for the allosteric site in the 5-HT transporter Crystallization of Membrane Proteins: An Overview.Membrane Protein Crystallisation: Current Trends and Future Perspectives.Alternating access mechanisms of LeuT-fold transporters: trailblazing towards the promised energy landscapes.Electrogenic Binding of Intracellular Cations Defines a Kinetic Decision Point in the Transport Cycle of the Human Serotonin Transporter.A generic protocol for protein crystal dehydration using the HC1b humidity controller.Biophysical Approaches to the Study of LeuT, a Prokaryotic Homolog of Neurotransmitter Sodium Symporters.Raoult's law revisited: accurately predicting equilibrium relative humidity points for humidity control experiments.Binding site residues control inhibitor selectivity in the human norepinephrine transporter but not in the human dopamine transporter Molecular Mechanism of Dopamine Transport by Human Dopamine Transporter.Importance of the Extracellular Loop 4 in the Human Serotonin Transporter for Inhibitor Binding and Substrate Translocation.Outer membrane phospholipase A's roles in Helicobacter pylori acid adaptation.A dualistic conformational response to substrate binding in the human serotonin transporter reveals a high affinity state for serotonin.Core Transmembrane Domain 6 Plays a Pivotal Role in the Transport Cycle of the Sodium/Proline Symporter PutP.Thermodynamic Coupling Function Analysis of Allosteric Mechanisms in the Human Dopamine Transporter.Cholesterol binding to a conserved site modulates conformation, pharmacology and transport kinetics of the human serotonin transporter.The role of transmembrane segment 5 (TM5) in Na2 release and the conformational transition of neurotransmitter:sodium symporters toward the inward-open state.

P2860

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P2860

A mechanism for intracellular release of Na+ by neurotransmitter/sodium symporters.

http://www.wikidata.org/entity/Q30623808

description

2014 nî lūn-bûn

@nan

2014 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած

@hyw

2014 թվականի հոտեմբերին հրատարակված գիտական հոդված

@hy

2014年の論文

@ja

2014年論文

@yue

2014年論文

@zh-hant

2014年論文

@zh-hk

2014年論文

@zh-mo

2014年論文

@zh-tw

2014年论文

@wuu

name

A mechanism for intracellular release of Na+ by neurotransmitter/sodium symporters.

@ast

A mechanism for intracellular release of Na+ by neurotransmitter/sodium symporters.

@en

type

label

A mechanism for intracellular release of Na+ by neurotransmitter/sodium symporters.

@ast

A mechanism for intracellular release of Na+ by neurotransmitter/sodium symporters.

@en

prefLabel

A mechanism for intracellular release of Na+ by neurotransmitter/sodium symporters.

@ast

A mechanism for intracellular release of Na+ by neurotransmitter/sodium symporters.

@en

P1433

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P1433

Nature Structural & Molecular Biology

P1476

A mechanism for intracellular release of Na+ by neurotransmitter/sodium symporters.

@en

P2093

Lina Malinauskaite

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

Linda Reinhard

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

Matthias Quick

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

P2860

Plasma membrane monoamine transporters: structure, regulation and function

Electrostatics of nanosystems: application to microtubules and the ribosome

X-ray structure of dopamine transporter elucidates antidepressant mechanism

MUSCLE: multiple sequence alignment with high accuracy and high throughput

PHENIX: a comprehensive Python-based system for macromolecular structure solution

Jalview Version 2--a multiple sequence alignment editor and analysis workbench

Structure of a prokaryotic virtual proton pump at 3.2 Å resolution

The Crystal Structure of a Sodium Galactose Transporter Reveals Mechanistic Insights into Na+/Sugar Symport

Structure and Molecular Mechanism of a Nucleobase-Cation-Symport-1 Family Transporter

A competitive inhibitor traps LeuT in an open-to-out conformation.

P2888

P304

1006-1012

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

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scholarly article

P356

10.1038/NSMB.2894

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11

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P478

21

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P50

Jonathan Javitch

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2014-10-05T00:00:00Z

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25282149

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P921

neurotransmitter

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4346222

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