Identification of a chloride ion binding site in Na+/Cl -dependent transporters.
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LeuT-desipramine structure reveals how antidepressants block neurotransmitter reuptakeX-ray structure of dopamine transporter elucidates antidepressant mechanismSynaptic Vesicle Protein NTT4/XT1 (SLC6A17) Catalyzes Na+-coupled Neutral Amino Acid TransportAntidepressant specificity of serotonin transporter suggested by three LeuT-SSRI structuresMonoamine transporters: insights from molecular dynamics simulationsInsights to ligand binding to the monoamine transporters-from homology modeling to LeuBAT and dDATDesigning modulators of monoamine transporters using virtual screening techniquesHow LeuT shapes our understanding of the mechanisms of sodium-coupled neurotransmitter transportersA conserved leucine occupies the empty substrate site of LeuT in the Na(+)-free return state.Complete mapping of substrate translocation highlights the role of LeuT N-terminal segment in regulating transport cycleModeling and dynamics of the inward-facing state of a Na+/Cl- dependent neurotransmitter transporter homologueStructural basis for action by diverse antidepressants on biogenic amine transportersThe atypical stimulant and nootropic modafinil interacts with the dopamine transporter in a different manner than classical cocaine-like inhibitorsLigand binding in the conserved interhelical loop of CorA, a magnesium transporter from Mycobacterium tuberculosisOutcome of a workshop on applications of protein models in biomedical researchMutations in the GlyT2 gene (SLC6A5) are a second major cause of startle disease.Molecular architecture and the structural basis for anion interaction in prestin and SLC26 transporters.Substrate-dependent proton antiport in neurotransmitter:sodium symporters.Expression, purification and structural analysis of functional GABA transporter 1 using the baculovirus expression system.Binding and orientation of tricyclic antidepressants within the central substrate site of the human serotonin transporter.The N terminus of monoamine transporters is a lever required for the action of amphetaminesThe substrate-driven transition to an inward-facing conformation in the functional mechanism of the dopamine transporter.Comparison of human solute carriersConformational flexibility of transmembrane helix VII of the human serotonin transporter impacts ion dependence and transport.The high-affinity binding site for tricyclic antidepressants resides in the outer vestibule of the serotonin transporter.Reconstructing a chloride-binding site in a bacterial neurotransmitter transporter homologue.Kinase-dependent Regulation of Monoamine Neurotransmitter Transporters.The second sodium site in the dopamine transporter controls cation permeation and is regulated by chloride.Cytoplasmic permeation pathway of neurotransmitter transporters.GATMD: γ-aminobutyric acid transporter mutagenesis database.Computational and biochemical docking of the irreversible cocaine analog RTI 82 directly demonstrates ligand positioning in the dopamine transporter central substrate-binding site.X-ray structures and mechanism of the human serotonin transporter.Halorhodopsin pumps Cl- and bacteriorhodopsin pumps protons by a common mechanism that uses conserved electrostatic interactions.Mutational analysis of the high-affinity zinc binding site validates a refined human dopamine transporter homology modelSLC6 transporters: structure, function, regulation, disease association and therapeuticsThe mechanistic basis for noncompetitive ibogaine inhibition of serotonin and dopamine transportersHomology modeling of human γ-butyric acid transporters and the binding of pro-drugs 5-aminolevulinic acid and methyl aminolevulinic acid used in photodynamic therapy.Microseconds simulations reveal a new sodium-binding site and the mechanism of sodium-coupled substrate uptake by LeuTInteraction of cocaine-, benztropine-, and GBR12909-like compounds with wild-type and mutant human dopamine transporters: molecular features that differentially determine antagonist-binding properties.Location of the antidepressant binding site in the serotonin transporter: importance of Ser-438 in recognition of citalopram and tricyclic antidepressants.
P2860
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P2860
Identification of a chloride ion binding site in Na+/Cl -dependent transporters.
description
2007 nî lūn-bûn
@nan
2007年の論文
@ja
2007年論文
@yue
2007年論文
@zh-hant
2007年論文
@zh-hk
2007年論文
@zh-mo
2007年論文
@zh-tw
2007年论文
@wuu
2007年论文
@zh
2007年论文
@zh-cn
name
Identification of a chloride ion binding site in Na+/Cl -dependent transporters.
@ast
Identification of a chloride ion binding site in Na+/Cl -dependent transporters.
@en
type
label
Identification of a chloride ion binding site in Na+/Cl -dependent transporters.
@ast
Identification of a chloride ion binding site in Na+/Cl -dependent transporters.
@en
prefLabel
Identification of a chloride ion binding site in Na+/Cl -dependent transporters.
@ast
Identification of a chloride ion binding site in Na+/Cl -dependent transporters.
@en
P2093
P2860
P356
P1476
Identification of a chloride ion binding site in Na+/Cl -dependent transporters
@en
P2093
Barry Honig
Gary Rudnick
Sotiria Tavoulari
Yuan-Wei Zhang
P2860
P304
12761-12766
P356
10.1073/PNAS.0705600104
P407
P577
2007-07-24T00:00:00Z