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Yorodumi- EMDB-20382: CryoEM structure of zebra fish alpha-1 glycine receptor bound wit... -
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Open data
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Basic information
| Entry | Database: EMDB / ID: EMD-20382 | |||||||||
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| Title | CryoEM structure of zebra fish alpha-1 glycine receptor bound with Taurine in SMA, super-open state | |||||||||
Map data | unsharpened map | |||||||||
Sample |
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Keywords | glycine receptor / SMA / CryoEM / MEMBRANE PROTEIN | |||||||||
| Function / homology | Function and homology informationNeurotransmitter receptors and postsynaptic signal transmission / extracellularly glycine-gated ion channel activity / extracellularly glycine-gated chloride channel activity / transmitter-gated monoatomic ion channel activity / regulation of neuron differentiation / ligand-gated monoatomic ion channel activity / glycine binding / cellular response to zinc ion / cellular response to ethanol / response to amino acid ...Neurotransmitter receptors and postsynaptic signal transmission / extracellularly glycine-gated ion channel activity / extracellularly glycine-gated chloride channel activity / transmitter-gated monoatomic ion channel activity / regulation of neuron differentiation / ligand-gated monoatomic ion channel activity / glycine binding / cellular response to zinc ion / cellular response to ethanol / response to amino acid / chloride channel complex / monoatomic ion transport / chloride transmembrane transport / central nervous system development / cellular response to amino acid stimulus / transmembrane signaling receptor activity / perikaryon / postsynaptic membrane / dendrite / zinc ion binding / membrane / plasma membrane Similarity search - Function | |||||||||
| Biological species | ![]() | |||||||||
| Method | single particle reconstruction / cryo EM / Resolution: 3.1 Å | |||||||||
Authors | Yu J / Zhu H | |||||||||
| Funding support | United States, 1 items
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Citation | Journal: Cell / Year: 2021Title: Mechanism of gating and partial agonist action in the glycine receptor. Authors: Jie Yu / Hongtao Zhu / Remigijus Lape / Timo Greiner / Juan Du / Wei Lü / Lucia Sivilotti / Eric Gouaux / ![]() Abstract: Ligand-gated ion channels mediate signal transduction at chemical synapses and transition between resting, open, and desensitized states in response to neurotransmitter binding. Neurotransmitters ...Ligand-gated ion channels mediate signal transduction at chemical synapses and transition between resting, open, and desensitized states in response to neurotransmitter binding. Neurotransmitters that produce maximum open channel probabilities (Po) are full agonists, whereas those that yield lower than maximum Po are partial agonists. Cys-loop receptors are an important class of neurotransmitter receptors, yet a structure-based understanding of the mechanism of partial agonist action has proven elusive. Here, we study the glycine receptor with the full agonist glycine and the partial agonists taurine and γ-amino butyric acid (GABA). We use electrophysiology to show how partial agonists populate agonist-bound, closed channel states and cryo-EM reconstructions to illuminate the structures of intermediate, pre-open states, providing insights into previously unseen conformational states along the receptor reaction pathway. We further correlate agonist-induced conformational changes to Po across members of the receptor family, providing a hypothetical mechanism for partial and full agonist action at Cys-loop receptors. | |||||||||
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Structure visualization
| Movie |
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| Structure viewer | EM map: SurfView Molmil Jmol/JSmol |
| Supplemental images |
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Downloads & links
-EMDB archive
| Map data | emd_20382.map.gz | 97.9 MB | EMDB map data format | |
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| Header (meta data) | emd-20382-v30.xml emd-20382.xml | 9.8 KB 9.8 KB | Display Display | EMDB header |
| FSC (resolution estimation) | emd_20382_fsc.xml | 11.4 KB | Display | FSC data file |
| Images | emd_20382.png | 75.5 KB | ||
| Filedesc metadata | emd-20382.cif.gz | 5.5 KB | ||
| Archive directory | http://ftp.pdbj.org/pub/emdb/structures/EMD-20382 ftp://ftp.pdbj.org/pub/emdb/structures/EMD-20382 | HTTPS FTP |
-Validation report
| Summary document | emd_20382_validation.pdf.gz | 568.6 KB | Display | EMDB validaton report |
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| Full document | emd_20382_full_validation.pdf.gz | 568.1 KB | Display | |
| Data in XML | emd_20382_validation.xml.gz | 12.3 KB | Display | |
| Data in CIF | emd_20382_validation.cif.gz | 16.4 KB | Display | |
| Arichive directory | https://ftp.pdbj.org/pub/emdb/validation_reports/EMD-20382 ftp://ftp.pdbj.org/pub/emdb/validation_reports/EMD-20382 | HTTPS FTP |
-Related structure data
| Related structure data | ![]() 6pm0MC ![]() 6ploC ![]() 6plpC ![]() 6plqC ![]() 6plrC ![]() 6plsC ![]() 6pltC ![]() 6pluC ![]() 6plvC ![]() 6plwC ![]() 6plxC ![]() 6plyC ![]() 6plzC ![]() 6pm1C ![]() 6pm2C ![]() 6pm3C ![]() 6pm4C ![]() 6pm5C ![]() 6pm6C ![]() 6pxdC M: atomic model generated by this map C: citing same article ( |
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| Similar structure data |
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Links
| EMDB pages | EMDB (EBI/PDBe) / EMDataResource |
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| Related items in Molecule of the Month |
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Map
| File | Download / File: emd_20382.map.gz / Format: CCP4 / Size: 125 MB / Type: IMAGE STORED AS FLOATING POINT NUMBER (4 BYTES) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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| Annotation | unsharpened map | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Projections & slices | Image control
Images are generated by Spider. | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Voxel size | X=Y=Z: 0.823 Å | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Density |
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| Symmetry | Space group: 1 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Details | EMDB XML:
CCP4 map header:
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-Supplemental data
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Sample components
-Entire : glycine receptor in complex with Taurine
| Entire | Name: glycine receptor in complex with Taurine |
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| Components |
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-Supramolecule #1: glycine receptor in complex with Taurine
| Supramolecule | Name: glycine receptor in complex with Taurine / type: complex / ID: 1 / Parent: 0 / Macromolecule list: #1 |
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| Source (natural) | Organism: ![]() |
| Molecular weight | Theoretical: 250 kDa/nm |
-Macromolecule #1: Glycine receptor subunit alphaZ1
| Macromolecule | Name: Glycine receptor subunit alphaZ1 / type: protein_or_peptide / ID: 1 / Number of copies: 5 / Enantiomer: LEVO |
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| Source (natural) | Organism: ![]() |
| Molecular weight | Theoretical: 52.537598 KDa |
| Recombinant expression | Organism: ![]() |
| Sequence | String: MFALGIYLWE TIVFFSLAAS QQAAARKAAS PMPPSEFLDK LMGKVSGYDA RIRPNFKGPP VNVTCNIFIN SFGSIAETTM DYRVNIFLR QQWNDPRLAY SEYPDDSLDL DPSMLDSIWK PDLFFANEKG ANFHEVTTDN KLLRISKNGN VLYSIRITLV L ACPMDLKN ...String: MFALGIYLWE TIVFFSLAAS QQAAARKAAS PMPPSEFLDK LMGKVSGYDA RIRPNFKGPP VNVTCNIFIN SFGSIAETTM DYRVNIFLR QQWNDPRLAY SEYPDDSLDL DPSMLDSIWK PDLFFANEKG ANFHEVTTDN KLLRISKNGN VLYSIRITLV L ACPMDLKN FPMDVQTCIM QLESFGYTMN DLIFEWDEKG AVQVADGLTL PQFILKEEKD LRYCTKHYNT GKFTCIEARF HL ERQMGYY LIQMYIPSLL IVILSWVSFW INMDAAPARV GLGITTVLTM TTQSSGSRAS LPKVSYVKAI DIWMAVCLLF VFS ALLEYA AVNFIARQHK ELLRFQRRRR HLKEDEAGDG RFSFAAYGMG PACLQAKDGM AIKGNNNNAP TSTNPPEKTV EEMR KLFIS RAKRIDTVSR VAFPLVFLIF NIFYWITYKI IRSEDIHKQL VPRGSHHHHH HHH UniProtKB: Glycine receptor subunit alphaZ1 |
-Macromolecule #3: 2-AMINOETHANESULFONIC ACID
| Macromolecule | Name: 2-AMINOETHANESULFONIC ACID / type: ligand / ID: 3 / Number of copies: 5 / Formula: TAU |
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| Molecular weight | Theoretical: 125.147 Da |
| Chemical component information | ![]() ChemComp-TAU: |
-Experimental details
-Structure determination
| Method | cryo EM |
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Processing | single particle reconstruction |
| Aggregation state | particle |
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Sample preparation
| Buffer | pH: 8 |
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| Vitrification | Cryogen name: ETHANE |
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Electron microscopy
| Microscope | FEI TITAN KRIOS |
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| Image recording | Film or detector model: GATAN K2 SUMMIT (4k x 4k) / Average electron dose: 40.8 e/Å2 |
| Electron beam | Acceleration voltage: 300 kV / Electron source: FIELD EMISSION GUN |
| Electron optics | Illumination mode: FLOOD BEAM / Imaging mode: BRIGHT FIELD / Cs: 2.7 mm |
| Experimental equipment | ![]() Model: Titan Krios / Image courtesy: FEI Company |
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United States, 1 items
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