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Yorodumi- EMDB-20824: Human metabotropic GABA(B) receptor in its intermediate state 1. -
+Open data
-Basic information
Entry | Database: EMDB / ID: EMD-20824 | |||||||||
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Title | Human metabotropic GABA(B) receptor in its intermediate state 1. | |||||||||
Map data | Sharpened map of GABAB heterodimer intermediate 1 in complex with agonist (SKF97541). | |||||||||
Sample |
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Keywords | G protein-coupled receptor / GABA / GABAB / Neurotransmitter / MEMBRANE PROTEIN | |||||||||
Function / homology | Function and homology information G protein-coupled neurotransmitter receptor activity involved in regulation of postsynaptic membrane potential / GABA B receptor activation / G protein-coupled neurotransmitter receptor activity involved in regulation of presynaptic membrane potential / G protein-coupled GABA receptor complex / negative regulation of gamma-aminobutyric acid secretion / neuron-glial cell signaling / G protein-coupled GABA receptor activity / G protein-coupled receptor heterodimeric complex / negative regulation of epinephrine secretion / negative regulation of dopamine secretion ...G protein-coupled neurotransmitter receptor activity involved in regulation of postsynaptic membrane potential / GABA B receptor activation / G protein-coupled neurotransmitter receptor activity involved in regulation of presynaptic membrane potential / G protein-coupled GABA receptor complex / negative regulation of gamma-aminobutyric acid secretion / neuron-glial cell signaling / G protein-coupled GABA receptor activity / G protein-coupled receptor heterodimeric complex / negative regulation of epinephrine secretion / negative regulation of dopamine secretion / positive regulation of growth hormone secretion / extracellular matrix protein binding / GABA receptor complex / negative regulation of adenylate cyclase activity / positive regulation of glutamate secretion / Class C/3 (Metabotropic glutamate/pheromone receptors) / synaptic transmission, GABAergic / gamma-aminobutyric acid signaling pathway / negative regulation of synaptic transmission / axolemma / GABA-ergic synapse / adenylate cyclase-inhibiting G protein-coupled receptor signaling pathway / dendritic shaft / response to nicotine / mitochondrial membrane / Schaffer collateral - CA1 synapse / Activation of G protein gated Potassium channels / Inhibition of voltage gated Ca2+ channels via Gbeta/gamma subunits / osteoblast differentiation / transmembrane signaling receptor activity / synaptic vesicle / presynaptic membrane / G alpha (i) signalling events / chemical synaptic transmission / postsynaptic membrane / response to ethanol / dendritic spine / neuron projection / protein heterodimerization activity / G protein-coupled receptor signaling pathway / negative regulation of cell population proliferation / neuronal cell body / glutamatergic synapse / endoplasmic reticulum membrane / extracellular space / plasma membrane / cytoplasm Similarity search - Function | |||||||||
Biological species | Homo sapiens (human) | |||||||||
Method | single particle reconstruction / cryo EM / Resolution: 6.3 Å | |||||||||
Authors | Shaye H / Han GW | |||||||||
Funding support | United States, 2 items
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Citation | Journal: Nature / Year: 2020 Title: Structural basis of the activation of a metabotropic GABA receptor. Authors: Hamidreza Shaye / Andrii Ishchenko / Jordy Homing Lam / Gye Won Han / Li Xue / Philippe Rondard / Jean-Philippe Pin / Vsevolod Katritch / Cornelius Gati / Vadim Cherezov / Abstract: Metabotropic γ-aminobutyric acid receptors (GABA) are involved in the modulation of synaptic responses in the central nervous system and have been implicated in neuropsychological conditions that ...Metabotropic γ-aminobutyric acid receptors (GABA) are involved in the modulation of synaptic responses in the central nervous system and have been implicated in neuropsychological conditions that range from addiction to psychosis. GABA belongs to class C of the G-protein-coupled receptors, and its functional entity comprises an obligate heterodimer that is composed of the GB1 and GB2 subunits. Each subunit possesses an extracellular Venus flytrap domain, which is connected to a canonical seven-transmembrane domain. Here we present four cryo-electron microscopy structures of the human full-length GB1-GB2 heterodimer: one structure of its inactive apo state, two intermediate agonist-bound forms and an active form in which the heterodimer is bound to an agonist and a positive allosteric modulator. The structures reveal substantial differences, which shed light on the complex motions that underlie the unique activation mechanism of GABA. Our results show that agonist binding leads to the closure of the Venus flytrap domain of GB1, triggering a series of transitions, first rearranging and bringing the two transmembrane domains into close contact along transmembrane helix 6 and ultimately inducing conformational rearrangements in the GB2 transmembrane domain via a lever-like mechanism to initiate downstream signalling. This active state is stabilized by a positive allosteric modulator binding at the transmembrane dimerization interface. | |||||||||
History |
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-Structure visualization
Movie |
Movie viewer |
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Structure viewer | EM map: SurfViewMolmilJmol/JSmol |
Supplemental images |
-Downloads & links
-EMDB archive
Map data | emd_20824.map.gz | 128.4 MB | EMDB map data format | |
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Header (meta data) | emd-20824-v30.xml emd-20824.xml | 18.3 KB 18.3 KB | Display Display | EMDB header |
Images | emd_20824.png | 82.8 KB | ||
Filedesc metadata | emd-20824.cif.gz | 6.9 KB | ||
Others | emd_20824_additional.map.gz | 67.3 MB | ||
Archive directory | http://ftp.pdbj.org/pub/emdb/structures/EMD-20824 ftp://ftp.pdbj.org/pub/emdb/structures/EMD-20824 | HTTPS FTP |
-Validation report
Summary document | emd_20824_validation.pdf.gz | 476.4 KB | Display | EMDB validaton report |
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Full document | emd_20824_full_validation.pdf.gz | 476 KB | Display | |
Data in XML | emd_20824_validation.xml.gz | 6.7 KB | Display | |
Data in CIF | emd_20824_validation.cif.gz | 7.7 KB | Display | |
Arichive directory | https://ftp.pdbj.org/pub/emdb/validation_reports/EMD-20824 ftp://ftp.pdbj.org/pub/emdb/validation_reports/EMD-20824 | HTTPS FTP |
-Related structure data
Related structure data | 6uoaMC 6uo8C 6uo9C 6vjmC M: atomic model generated by this map C: citing same article (ref.) |
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Similar structure data |
-Links
EMDB pages | EMDB (EBI/PDBe) / EMDataResource |
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Related items in Molecule of the Month |
-Map
File | Download / File: emd_20824.map.gz / Format: CCP4 / Size: 137.1 MB / Type: IMAGE STORED AS FLOATING POINT NUMBER (4 BYTES) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Annotation | Sharpened map of GABAB heterodimer intermediate 1 in complex with agonist (SKF97541). | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Projections & slices | Image control
Images are generated by Spider. | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Voxel size | X=Y=Z: 0.8521 Å | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Density |
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Symmetry | Space group: 1 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Details | EMDB XML:
CCP4 map header:
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-Supplemental data
-Additional map: Unfiltered map of GABAB heterodimer intermediate 1 in...
File | emd_20824_additional.map | ||||||||||||
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Annotation | Unfiltered map of GABAB heterodimer intermediate 1 in complex with agonist (SKF97541). | ||||||||||||
Projections & Slices |
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Density Histograms |
-Sample components
-Entire : Human metabotropic GABA(B) receptor in intermediate state 1
Entire | Name: Human metabotropic GABA(B) receptor in intermediate state 1 |
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Components |
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-Supramolecule #1: Human metabotropic GABA(B) receptor in intermediate state 1
Supramolecule | Name: Human metabotropic GABA(B) receptor in intermediate state 1 type: complex / ID: 1 / Parent: 0 / Macromolecule list: #1-#2 |
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Source (natural) | Organism: Homo sapiens (human) |
Molecular weight | Theoretical: 174 KDa |
-Macromolecule #1: Gamma-aminobutyric acid type B receptor subunit 1
Macromolecule | Name: Gamma-aminobutyric acid type B receptor subunit 1 / type: protein_or_peptide / ID: 1 / Number of copies: 1 / Enantiomer: LEVO |
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Source (natural) | Organism: Homo sapiens (human) |
Molecular weight | Theoretical: 86.450977 KDa |
Recombinant expression | Organism: Spodoptera frugiperda (fall armyworm) |
Sequence | String: GSERRAVYIG ALFPMSGGWP GGQACQPAVE MALEDVNSRR DILPDYELKL IHHDSKCDPG QATKYLYELL YNDPIKIILM PGCSSVSTL VAEAARMWNL IVLSYGSSSP ALSNRQRFPT FFRTHPSATL HNPTRVKLFE KWGWKKIATI QQTTEVFTST L DDLEERVK ...String: GSERRAVYIG ALFPMSGGWP GGQACQPAVE MALEDVNSRR DILPDYELKL IHHDSKCDPG QATKYLYELL YNDPIKIILM PGCSSVSTL VAEAARMWNL IVLSYGSSSP ALSNRQRFPT FFRTHPSATL HNPTRVKLFE KWGWKKIATI QQTTEVFTST L DDLEERVK EAGIEITFRQ SFFSDPAVPV KNLKRQDARI IVGLFYETEA RKVFCEVYKE RLFGKKYVWF LIGWYADNWF KI YDPSINC TVDEMTEAVE GHITTEIVML NPANTRSISN MTSQEFVEKL TKRLKRHPEE TGGFQEAPLA YDAIWALALA LNK TSGGGG RSGVRLEDFN YNNQTITDQI YRAMNSSSFE GVSGHVVFDA SGSRMAWTLI EQLQGGSYKK IGYYDSTKDD LSWS KTDKW IGGSPPADQT LVIKTFRFLS QKLFISVSVL SSLGIVLAVV CLSFNIYNSH VRYIQNSQPN LNNLTAVGCS LALAA VFPL GLDGYHIGRN QFPFVCQARL WLLGLGFSLG YGSMFTKIWW VHTVFTKKEE KKEWRKTLEP WKLYATVGLL VGMDVL TLA IWQIVDPLHR TIETFAKEEP KEDIDVSILP QLEHCSSRKM NTWLGIFYGY KGLLLLLGIF LAYETKSVST EKINDHR AV GMAIYNVAVL CLITAPVTMI LSSQQDAAFA FASLAIVFSS YITLVVLFVP KMRRLITRGE WQSEAQDTMK TGSSTNNN E EEKSRLLEKE NRELEKIIAE KEERVSELRH QLQSRLEVLF Q UniProtKB: Gamma-aminobutyric acid type B receptor subunit 1 |
-Macromolecule #2: Gamma-aminobutyric acid type B receptor subunit 2
Macromolecule | Name: Gamma-aminobutyric acid type B receptor subunit 2 / type: protein_or_peptide / ID: 2 / Number of copies: 1 / Enantiomer: LEVO |
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Source (natural) | Organism: Homo sapiens (human) |
Molecular weight | Theoretical: 88.200844 KDa |
Recombinant expression | Organism: Spodoptera frugiperda (fall armyworm) |
Sequence | String: GWARGAPRPP PSSPPLSIMG LMPLTKEVAK GSIGRGVLPA VELAIEQIRN ESLLRPYFLD LRLYDTECDN AKGLKAFYDA IKYGPNHLM VFGGVCPSVT SIIAESLQGW NLVQLSFAAT TPVLADKKKY PYFFRTVPSD NAVNPAILKL LKHYQWKRVG T LTQDVQRF ...String: GWARGAPRPP PSSPPLSIMG LMPLTKEVAK GSIGRGVLPA VELAIEQIRN ESLLRPYFLD LRLYDTECDN AKGLKAFYDA IKYGPNHLM VFGGVCPSVT SIIAESLQGW NLVQLSFAAT TPVLADKKKY PYFFRTVPSD NAVNPAILKL LKHYQWKRVG T LTQDVQRF SEVRNDLTGV LYGEDIEISD TESFSNDPCT SVKKLKGNDV RIILGQFDQN MAAKVFCCAY EENMYGSKYQ WI IPGWYEP SWWEQVHTEA NSSRCLRKNL LAAMEGYIGV DFEPLSSKQI KTISGKTPQQ YEREYNNKRS GVGPSKFHGY AYD GIWVIA KTLQRAMETL HASSRHQRIQ DFNYTDHTLG RIILNAMNET NFFGVTGQVV FRNGERMGTI KFTQFQDSRE VKVG EYNAV ADTLEIINDT IRFQGSEPPK DKTIILEQLR KISLPLYSIL SALTILGMIM ASAFLFFNIK NRNQKLIKMS SPYMN NLII LGGMLSYASI FLFGLDGSFV SEKTFETLCT VRTWILTVGY TTAFGAMFAK TWRVHAIFKN VKMKKKIIKD QKLLVI VGG MLLIDLCILI CWQAVDPLRR TVEKYSMEPD PAGRDISIRP LLEHCENTHM TIWLGIVYAY KGLLMLFGCF LAWETRN VS IPALNDSKYI GMSVYNVGIM CIIGAAVSFL TRDQPNVQFC IVALVIIFCS TITLCLVFVP KLITLRTNPD AATQNRRF Q FTQNQKKEDS KTSTSVTSVN QASTSRLEGL QSENHRLRMK ITELDKDLEE VTMQLQDT UniProtKB: Gamma-aminobutyric acid type B receptor subunit 2 |
-Macromolecule #4: 2-acetamido-2-deoxy-beta-D-glucopyranose
Macromolecule | Name: 2-acetamido-2-deoxy-beta-D-glucopyranose / type: ligand / ID: 4 / Number of copies: 1 / Formula: NAG |
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Molecular weight | Theoretical: 221.208 Da |
Chemical component information | ChemComp-NAG: |
-Experimental details
-Structure determination
Method | cryo EM |
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Processing | single particle reconstruction |
Aggregation state | particle |
-Sample preparation
Concentration | 10 mg/mL |
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Buffer | pH: 7.5 |
Grid | Model: Quantifoil R1.2/1.3 / Material: GOLD / Mesh: 200 / Pretreatment - Type: GLOW DISCHARGE |
Vitrification | Cryogen name: ETHANE / Chamber humidity: 95 % / Chamber temperature: 293.15 K / Instrument: LEICA EM GP |
-Electron microscopy
Microscope | FEI TITAN KRIOS |
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Image recording | Film or detector model: GATAN K3 (6k x 4k) / Number grids imaged: 1 / Number real images: 14271 / Average exposure time: 0.07 sec. / Average electron dose: 1.2 e/Å2 |
Electron beam | Acceleration voltage: 300 kV / Electron source: FIELD EMISSION GUN |
Electron optics | C2 aperture diameter: 70.0 µm / Calibrated magnification: 29000 / Illumination mode: OTHER / Imaging mode: BRIGHT FIELD / Cs: 2.7 mm / Nominal defocus max: -3.0 µm / Nominal defocus min: -1.5 µm / Nominal magnification: 29000 |
Sample stage | Specimen holder model: FEI TITAN KRIOS AUTOGRID HOLDER / Cooling holder cryogen: NITROGEN |
Experimental equipment | Model: Titan Krios / Image courtesy: FEI Company |