4XPG
X-ray structure of Drosophila dopamine transporter with subsiteB mutations (D121G/S426M) bound to beta-CFT or Win35428
Summary for 4XPG
| Entry DOI | 10.2210/pdb4xpg/pdb |
| Descriptor | Dopamine transporter, antibody fragment light chain, antibody fragment heavy chain, ... (7 entities in total) |
| Functional Keywords | all alpha-helical integral membrane protein, transport protein-inhibitor complex, transport protein/inhibitor |
| Biological source | Drosophila melanogaster More |
| Total number of polymer chains | 3 |
| Total formula weight | 113904.73 |
| Authors | Penmatsa, A.,Wang, K.H.,Gouaux, E. (deposition date: 2015-01-16, release date: 2015-05-06, Last modification date: 2024-10-16) |
| Primary citation | Wang, K.H.,Penmatsa, A.,Gouaux, E. Neurotransmitter and psychostimulant recognition by the dopamine transporter. Nature, 521:322-327, 2015 Cited by PubMed Abstract: Na(+)/Cl(-)-coupled biogenic amine transporters are the primary targets of therapeutic and abused drugs, ranging from antidepressants to the psychostimulants cocaine and amphetamines, and to their cognate substrates. Here we determine X-ray crystal structures of the Drosophila melanogaster dopamine transporter (dDAT) bound to its substrate dopamine, a substrate analogue 3,4-dichlorophenethylamine, the psychostimulants d-amphetamine and methamphetamine, or to cocaine and cocaine analogues. All ligands bind to the central binding site, located approximately halfway across the membrane bilayer, in close proximity to bound sodium and chloride ions. The central binding site recognizes three chemically distinct classes of ligands via conformational changes that accommodate varying sizes and shapes, thus illustrating molecular principles that distinguish substrates from inhibitors in biogenic amine transporters. PubMed: 25970245DOI: 10.1038/nature14431 PDB entries with the same primary citation |
| Experimental method | X-RAY DIFFRACTION (3.21 Å) |
Structure validation
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