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Open data
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Basic information
| Entry | Database: PDB / ID: 6x3e | |||||||||||||||||||||||||||
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| Title | hEAAT3-Asymmetric-1o2i | |||||||||||||||||||||||||||
Components | Excitatory amino acid transporter 3 | |||||||||||||||||||||||||||
Keywords | TRANSPORT PROTEIN / Asymmetric / Outward-facing bound / Inward-facing open | |||||||||||||||||||||||||||
| Function / homology | Function and homology informationD-aspartate transmembrane transport / regulation of protein targeting to membrane / D-aspartate transmembrane transporter activity / Defective SLC1A1 is implicated in schizophrenia 18 (SCZD18) and dicarboxylic aminoaciduria (DCBXA) / distal dendrite / cysteine transport / cysteine transmembrane transporter activity / neurotransmitter receptor transport to plasma membrane / high-affinity L-glutamate transmembrane transporter activity / glutamate:sodium symporter activity ...D-aspartate transmembrane transport / regulation of protein targeting to membrane / D-aspartate transmembrane transporter activity / Defective SLC1A1 is implicated in schizophrenia 18 (SCZD18) and dicarboxylic aminoaciduria (DCBXA) / distal dendrite / cysteine transport / cysteine transmembrane transporter activity / neurotransmitter receptor transport to plasma membrane / high-affinity L-glutamate transmembrane transporter activity / glutamate:sodium symporter activity / L-glutamate import / response to decreased oxygen levels / cellular response to mercury ion / : / L-glutamate transmembrane transporter activity / retina layer formation / L-glutamate transmembrane transport / glutathione biosynthetic process / D-aspartate import across plasma membrane / L-aspartate transmembrane transport / cellular response to ammonium ion / righting reflex / zinc ion transmembrane transport / L-aspartate transmembrane transporter activity / cellular response to bisphenol A / intracellular glutamate homeostasis / grooming behavior / L-aspartate import across plasma membrane / Glutamate Neurotransmitter Release Cycle / monoatomic anion channel activity / L-glutamate import across plasma membrane / proximal dendrite / transepithelial transport / apical dendrite / intracellular zinc ion homeostasis / blood vessel morphogenesis / cellular response to cocaine / chloride transmembrane transporter activity / motor neuron apoptotic process / G protein-coupled dopamine receptor signaling pathway / response to anesthetic / response to morphine / glutamate receptor signaling pathway / superoxide metabolic process / neurotransmitter transport / heart contraction / perisynaptic space / maintenance of blood-brain barrier / dopamine metabolic process / adult behavior / motor behavior / asymmetric synapse / conditioned place preference / glial cell projection / synaptic cleft / behavioral fear response / postsynaptic modulation of chemical synaptic transmission / response to axon injury / positive regulation of heart rate / transport across blood-brain barrier / monoatomic ion transport / neurogenesis / axon terminus / chloride transmembrane transport / response to amphetamine / dendritic shaft / cell periphery / locomotory behavior / synapse organization / brain development / Schaffer collateral - CA1 synapse / memory / long-term synaptic potentiation / recycling endosome membrane / cytokine-mediated signaling pathway / late endosome membrane / presynapse / cellular response to oxidative stress / early endosome membrane / perikaryon / chemical synaptic transmission / gene expression / dendritic spine / negative regulation of neuron apoptotic process / apical plasma membrane / membrane raft / response to xenobiotic stimulus / axon / neuronal cell body / dendrite / cell surface / extracellular exosome / metal ion binding / identical protein binding / membrane / plasma membrane Similarity search - Function | |||||||||||||||||||||||||||
| Biological species | Homo sapiens (human) | |||||||||||||||||||||||||||
| Method | ELECTRON MICROSCOPY / single particle reconstruction / cryo EM / Resolution: 3.42 Å | |||||||||||||||||||||||||||
Authors | Qiu, B. / Matthies, D. / Boudker, O. | |||||||||||||||||||||||||||
| Funding support | United States, 1items
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Citation | Journal: Sci Adv / Year: 2021Title: Cryo-EM structures of excitatory amino acid transporter 3 visualize coupled substrate, sodium, and proton binding and transport. Authors: Biao Qiu / Doreen Matthies / Eva Fortea / Zhiheng Yu / Olga Boudker / ![]() Abstract: Human excitatory amino acid transporter 3 (hEAAT3) mediates glutamate uptake in neurons, intestine, and kidney. Here, we report cryo-EM structures of hEAAT3 in several functional states where the ...Human excitatory amino acid transporter 3 (hEAAT3) mediates glutamate uptake in neurons, intestine, and kidney. Here, we report cryo-EM structures of hEAAT3 in several functional states where the transporter is empty, bound to coupled sodium ions only, or fully loaded with three sodium ions, a proton, and the substrate aspartate. The structures suggest that hEAAT3 operates by an elevator mechanism involving three functionally independent subunits. When the substrate-binding site is near the cytoplasm, it has a remarkably low affinity for the substrate, perhaps facilitating its release and allowing the rapid transport turnover. The mechanism of the coupled uptake of the sodium ions and the substrate is conserved across evolutionarily distant families and is augmented by coupling to protons in EAATs. The structures further suggest a mechanism by which a conserved glutamate residue mediates proton symport. | |||||||||||||||||||||||||||
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Structure visualization
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| Structure viewer | Molecule: Molmil Jmol/JSmol |
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Downloads & links
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Download
| PDBx/mmCIF format | 6x3e.cif.gz | 219 KB | Display | PDBx/mmCIF format |
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| PDB format | pdb6x3e.ent.gz | 173.5 KB | Display | PDB format |
| PDBx/mmJSON format | 6x3e.json.gz | Tree view | PDBx/mmJSON format | |
| Others | Other downloads |
-Validation report
| Summary document | 6x3e_validation.pdf.gz | 992 KB | Display | wwPDB validaton report |
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| Full document | 6x3e_full_validation.pdf.gz | 998.2 KB | Display | |
| Data in XML | 6x3e_validation.xml.gz | 40.6 KB | Display | |
| Data in CIF | 6x3e_validation.cif.gz | 63.9 KB | Display | |
| Arichive directory | https://data.pdbj.org/pub/pdb/validation_reports/x3/6x3e ftp://data.pdbj.org/pub/pdb/validation_reports/x3/6x3e | HTTPS FTP |
-Related structure data
| Related structure data | ![]() 22020MC ![]() 6x2lC ![]() 6x2zC ![]() 6x3fC M: map data used to model this data C: citing same article ( |
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| Similar structure data |
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Assembly
| Deposited unit | ![]()
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Components
| #1: Protein | Mass: 57301.168 Da / Num. of mol.: 3 Source method: isolated from a genetically manipulated source Details: The Glycine and Proline at the N terminal are the residues left after PreScission Protease treatment Source: (gene. exp.) Homo sapiens (human) / Gene: SLC1A1, EAAC1, EAAT3 / Production host: Homo sapiens (human) / References: UniProt: P43005#2: Chemical | ChemComp-ASP / | #3: Chemical | Has ligand of interest | Y | Has protein modification | N | |
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-Experimental details
-Experiment
| Experiment | Method: ELECTRON MICROSCOPY |
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| EM experiment | Aggregation state: PARTICLE / 3D reconstruction method: single particle reconstruction |
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Sample preparation
| Component | Name: Asymmetric hEAAT3 trimer / Type: COMPLEX / Entity ID: #1 / Source: RECOMBINANT | ||||||||||||||||||||||||||||||
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| Source (natural) | Organism: Homo sapiens (human) | ||||||||||||||||||||||||||||||
| Source (recombinant) | Organism: Homo sapiens (human) | ||||||||||||||||||||||||||||||
| Buffer solution | pH: 8 | ||||||||||||||||||||||||||||||
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| Specimen | Conc.: 6 mg/ml / Embedding applied: NO / Shadowing applied: NO / Staining applied: NO / Vitrification applied: YES / Details: This sample was mono disperse | ||||||||||||||||||||||||||||||
| Specimen support | Grid material: COPPER / Grid mesh size: 400 divisions/in. / Grid type: Quantifoil R1.2/1.3 | ||||||||||||||||||||||||||||||
| Vitrification | Instrument: FEI VITROBOT MARK IV / Cryogen name: ETHANE / Humidity: 100 % / Chamber temperature: 277 K / Details: blot 3s |
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Electron microscopy imaging
| Experimental equipment | ![]() Model: Titan Krios / Image courtesy: FEI Company |
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| Microscopy | Model: FEI TITAN KRIOS |
| Electron gun | Electron source: FIELD EMISSION GUN / Accelerating voltage: 300 kV / Illumination mode: FLOOD BEAM |
| Electron lens | Mode: BRIGHT FIELD / Nominal magnification: 105000 X / Nominal defocus max: 1500 nm / Nominal defocus min: 500 nm / Cs: 2.7 mm / C2 aperture diameter: 100 µm |
| Specimen holder | Cryogen: NITROGEN / Specimen holder model: FEI TITAN KRIOS AUTOGRID HOLDER |
| Image recording | Electron dose: 60 e/Å2 / Film or detector model: GATAN K3 BIOQUANTUM (6k x 4k) |
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Processing
| Software | Name: PHENIX / Version: 1.18rc1_3769: / Classification: refinement | ||||||||||||||||||||||||||||||||
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| EM software |
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| CTF correction | Type: PHASE FLIPPING AND AMPLITUDE CORRECTION | ||||||||||||||||||||||||||||||||
| Particle selection | Num. of particles selected: 190599 | ||||||||||||||||||||||||||||||||
| Symmetry | Point symmetry: C1 (asymmetric) | ||||||||||||||||||||||||||||||||
| 3D reconstruction | Resolution: 3.42 Å / Resolution method: FSC 0.143 CUT-OFF / Num. of particles: 158349 / Symmetry type: POINT | ||||||||||||||||||||||||||||||||
| Refine LS restraints |
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About Yorodumi




Homo sapiens (human)
United States, 1items
Citation
UCSF Chimera



















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