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6M47

X-ray structure of a Drosophila dopamine transporter with NET-like mutations (D121G/S426M/F471L) in tramadol bound form

Summary for 6M47
Entry DOI10.2210/pdb6m47/pdb
Related6M0F 6M0Z 6M2R 6M38 6M3Z
Related PRD IDPRD_900001
DescriptorSodium-dependent dopamine transporter, DECANE, Antibody fragment 9D5 light chain, ... (11 entities in total)
Functional Keywordsneurotransmitter transporter, antibody fragment, membrane protein
Biological sourceDrosophila melanogaster (Fruit fly)
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Total number of polymer chains3
Total formula weight108815.43
Authors
Shabareesh, P.,Mallela, A.K.,Joseph, D.,Penmatsa, A. (deposition date: 2020-03-05, release date: 2021-02-17, Last modification date: 2024-10-30)
Primary citationPidathala, 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: 33850134
DOI: 10.1038/s41467-021-22385-9
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (3.252 Å)
Structure validation

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