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Insights into the mechanism and pharmacology of neurotransmitter sodium symporters.
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2
SLC6 neurotransmitter transporters: structure, function, and regulation.
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Chloride binding site of neurotransmitter sodium symporters.
Proc Natl Acad Sci U S A. 2013 May 21;110(21):8489-94. doi: 10.1073/pnas.1221279110. Epub 2013 May 2.
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Mechanism of chloride interaction with neurotransmitter:sodium symporters.
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The use of LeuT as a model in elucidating binding sites for substrates and inhibitors in neurotransmitter transporters.
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Is protein structure enough? A review of the role of lipids in SLC6 transporter function.
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The allosteric mechanism of substrate-specific transport in SLC6 is mediated by a volumetric sensor.
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Biophysical Approaches to the Study of LeuT, a Prokaryotic Homolog of Neurotransmitter Sodium Symporters.
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Structures of LeuT in bicelles define conformation and substrate binding in a membrane-like context.
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Unifying perspectives on the activity and genotypic targeting of pharmacological chaperones.
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Molecular basis of human GABA transporter 3 inhibition.
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Balancing Therapeutic Efficacy and Safety of MDMA and Novel MDXX Analogues as Novel Treatments for Autism Spectrum Disorder.
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Molecular basis of inhibition of the amino acid transporter BAT1 (SLC6A19).
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Dimerization and antidepressant recognition at noradrenaline transporter.
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Computation-guided analysis of paroxetine binding to hSERT reveals functionally important structural elements and dynamics.
Neuropharmacology. 2019 Dec 15;161:107411. doi: 10.1016/j.neuropharm.2018.10.040. Epub 2018 Nov 1.
2
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Substrate-modulated unwinding of transmembrane helices in the NSS transporter LeuT.
Sci Adv. 2018 May 11;4(5):eaar6179. doi: 10.1126/sciadv.aar6179. eCollection 2018 May.
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Structural biology of solute carrier (SLC) membrane transport proteins.
Mol Membr Biol. 2017 Feb-Mar;34(1-2):1-32. doi: 10.1080/09687688.2018.1448123. Epub 2018 Apr 13.
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Structural basis for recognition of diverse antidepressants by the human serotonin transporter.
Nat Struct Mol Biol. 2018 Feb;25(2):170-175. doi: 10.1038/s41594-018-0026-8. Epub 2018 Jan 29.
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A direct interaction of cholesterol with the dopamine transporter prevents its out-to-inward transition.
PLoS Comput Biol. 2018 Jan 12;14(1):e1005907. doi: 10.1371/journal.pcbi.1005907. eCollection 2018 Jan.
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Mapping the Binding Site for Escitalopram and Paroxetine in the Human Serotonin Transporter Using Genetically Encoded Photo-Cross-Linkers.
ACS Chem Biol. 2017 Oct 20;12(10):2558-2562. doi: 10.1021/acschembio.7b00338. Epub 2017 Sep 26.

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