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8WVG

Transporter bound with inhibitor

Summary for 8WVG
Entry DOI10.2210/pdb8wvg/pdb
Related8WRD 8WRE
EMDB information37867
DescriptorFabH, FabL, Synaptic vesicular amine transporter, ... (5 entities in total)
Functional Keywordstransporter, membrane protein
Biological sourceHomo sapiens (human)
More
Total number of polymer chains3
Total formula weight116910.48
Authors
Im, D.,Iwata, S. (deposition date: 2023-10-23, release date: 2024-09-25, Last modification date: 2024-10-02)
Primary citationIm, D.,Jormakka, M.,Juge, N.,Kishikawa, J.I.,Kato, T.,Sugita, Y.,Noda, T.,Uemura, T.,Shiimura, Y.,Miyaji, T.,Asada, H.,Iwata, S.
Neurotransmitter recognition by human vesicular monoamine transporter 2.
Nat Commun, 15:7661-7661, 2024
Cited by
PubMed Abstract: Human vesicular monoamine transporter 2 (VMAT2), a member of the SLC18 family, plays a crucial role in regulating neurotransmitters in the brain by facilitating their uptake and storage within vesicles, preparing them for exocytotic release. Because of its central role in neurotransmitter signalling and neuroprotection, VMAT2 is a target for neurodegenerative diseases and movement disorders, with its inhibitor being used as therapeutics. Despite the importance of VMAT2 in pharmacophysiology, the molecular basis of VMAT2-mediated neurotransmitter transport and its inhibition remains unclear. Here we show the cryo-electron microscopy structure of VMAT2 in the substrate-free state, in complex with the neurotransmitter dopamine, and in complex with the inhibitor tetrabenazine. In addition to these structural determinations, monoamine uptake assays, mutational studies, and pKa value predictions were performed to characterize the dynamic changes in VMAT2 structure. These results provide a structural basis for understanding VMAT2-mediated vesicular transport of neurotransmitters and a platform for modulation of current inhibitor design.
PubMed: 39284862
DOI: 10.1038/s41467-024-51960-z
PDB entries with the same primary citation
Experimental method
ELECTRON MICROSCOPY (3.18 Å)
Structure validation

227111

數據於2024-11-06公開中

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