6M0F
X-ray structure of Drosophila dopamine transporter with subsiteB mutations (D121G/S426M) in substrate-free form
Summary for 6M0F
Entry DOI | 10.2210/pdb6m0f/pdb |
Related | 4M48 4XNX 4XP1 4XPH |
Descriptor | Sodium-dependent dopamine transporter, Antibody fragment (9D5) Light chain, Antibody fragment (9D5) heavy chain, ... (8 entities in total) |
Functional Keywords | neurotransmitter transporter, antibody fragment, membrane protein |
Biological source | Drosophila melanogaster (Fruit fly) More |
Total number of polymer chains | 3 |
Total formula weight | 107821.35 |
Authors | Shabareesh, P.,Mallela, A.K.,Joseph, D.,Penmatsa, A. (deposition date: 2020-02-21, release date: 2021-02-17, Last modification date: 2023-11-29) |
Primary citation | Pidathala, S.,Mallela, A.K.,Joseph, D.,Penmatsa, A. Structural basis of norepinephrine recognition and transport inhibition in neurotransmitter transporters. Nat Commun, 12:2199-2199, 2021 Cited by PubMed Abstract: Norepinephrine is a biogenic amine neurotransmitter that has widespread effects on alertness, arousal and pain sensation. Consequently, blockers of norepinephrine uptake have served as vital tools to treat depression and chronic pain. Here, we employ the Drosophila melanogaster dopamine transporter as a surrogate for the norepinephrine transporter and determine X-ray structures of the transporter in its substrate-free and norepinephrine-bound forms. We also report structures of the transporter in complex with inhibitors of chronic pain including duloxetine, milnacipran and a synthetic opioid, tramadol. When compared to dopamine, we observe that norepinephrine binds in a different pose, in the vicinity of subsite C within the primary binding site. Our experiments reveal that this region is the binding site for chronic pain inhibitors and a determinant for norepinephrine-specific reuptake inhibition, thereby providing a paradigm for the design of specific inhibitors for catecholamine neurotransmitter transporters. PubMed: 33850134DOI: 10.1038/s41467-021-22385-9 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (3.3 Å) |
Structure validation
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