+Open data
-Basic information
Entry | Database: EMDB / ID: EMD-41099 | |||||||||
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Title | Quis-bound intermediate mGlu5 | |||||||||
Map data | QUIS bound active mGlu5 in complex with Nb43 | |||||||||
Sample |
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Keywords | GPCR / SIGNALING PROTEIN | |||||||||
Function / homology | Function and homology information A2A adenosine receptor binding / regulation of translational elongation / phospholipase C-activating G protein-coupled glutamate receptor signaling pathway / G protein-coupled receptor activity involved in regulation of postsynaptic membrane potential / trans-synaptic signaling by endocannabinoid, modulating synaptic transmission / adenylate cyclase inhibiting G protein-coupled glutamate receptor activity / positive regulation of long-term neuronal synaptic plasticity / : / desensitization of G protein-coupled receptor signaling pathway / G protein-coupled glutamate receptor signaling pathway ...A2A adenosine receptor binding / regulation of translational elongation / phospholipase C-activating G protein-coupled glutamate receptor signaling pathway / G protein-coupled receptor activity involved in regulation of postsynaptic membrane potential / trans-synaptic signaling by endocannabinoid, modulating synaptic transmission / adenylate cyclase inhibiting G protein-coupled glutamate receptor activity / positive regulation of long-term neuronal synaptic plasticity / : / desensitization of G protein-coupled receptor signaling pathway / G protein-coupled glutamate receptor signaling pathway / neurotransmitter receptor activity involved in regulation of postsynaptic cytosolic calcium ion concentration / astrocyte projection / Class C/3 (Metabotropic glutamate/pheromone receptors) / protein kinase C-activating G protein-coupled receptor signaling pathway / glutamate receptor activity / Neurexins and neuroligins / protein tyrosine kinase activator activity / : / positive regulation of protein tyrosine kinase activity / regulation of synaptic transmission, glutamatergic / protein tyrosine kinase binding / dendritic shaft / locomotory behavior / learning / G protein-coupled receptor activity / postsynaptic density membrane / synapse organization / regulation of protein phosphorylation / Schaffer collateral - CA1 synapse / cognition / cellular response to amyloid-beta / regulation of translation / chemical synaptic transmission / G alpha (q) signalling events / dendritic spine / positive regulation of MAPK cascade / learning or memory / glutamatergic synapse / regulation of DNA-templated transcription / identical protein binding / plasma membrane / cytoplasm Similarity search - Function | |||||||||
Biological species | Homo sapiens (human) / Lama glama (llama) | |||||||||
Method | single particle reconstruction / cryo EM / Resolution: 3.0 Å | |||||||||
Authors | Krishna Kumar K / Wang H / Kobilka BK | |||||||||
Funding support | United States, 1 items
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Citation | Journal: bioRxiv / Year: 2023 Title: Step-wise activation of a Family C GPCR. Authors: Kaavya Krishna Kumar / Haoqing Wang / Chris Habrian / Naomi R Latorraca / Jun Xu / Evan S O'Brien / Chensong Zhang / Elizabeth Montabana / Antoine Koehl / Susan Marqusee / Ehud Y Isacoff / Brian K Kobilka / Abstract: Metabotropic glutamate receptors belong to a family of G protein-coupled receptors that are obligate dimers and possess a large extracellular ligand-binding domain (ECD) that is linked via a cysteine- ...Metabotropic glutamate receptors belong to a family of G protein-coupled receptors that are obligate dimers and possess a large extracellular ligand-binding domain (ECD) that is linked via a cysteine-rich domain (CRDs) to their 7-transmembrane (TM) domain. Upon activation, these receptors undergo a large conformational change to transmit the ligand binding signal from the ECD to the G protein-coupling TM. In this manuscript, we propose a model for a sequential, multistep activation mechanism of metabotropic glutamate receptor subtype 5. We present a series of structures in lipid nanodiscs, from inactive to fully active, including agonist-bound intermediate states. Further, using bulk and single-molecule fluorescence imaging we reveal distinct receptor conformations upon allosteric modulator and G protein binding. | |||||||||
History |
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-Structure visualization
Supplemental images |
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-Downloads & links
-EMDB archive
Map data | emd_41099.map.gz | 128.5 MB | EMDB map data format | |
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Header (meta data) | emd-41099-v30.xml emd-41099.xml | 12 KB 12 KB | Display Display | EMDB header |
Images | emd_41099.png | 51.2 KB | ||
Filedesc metadata | emd-41099.cif.gz | 6.1 KB | ||
Archive directory | http://ftp.pdbj.org/pub/emdb/structures/EMD-41099 ftp://ftp.pdbj.org/pub/emdb/structures/EMD-41099 | HTTPS FTP |
-Related structure data
Related structure data | 8t8mMC 8t6jC 8t7hC 8taoC 41803 41804 M: atomic model generated by this map C: citing same article (ref.) |
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Similar structure data | Similarity search - Function & homologyF&H Search |
-Links
EMDB pages | EMDB (EBI/PDBe) / EMDataResource |
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Related items in Molecule of the Month |
-Map
File | Download / File: emd_41099.map.gz / Format: CCP4 / Size: 149.9 MB / Type: IMAGE STORED AS FLOATING POINT NUMBER (4 BYTES) | ||||||||||||||||||||
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Annotation | QUIS bound active mGlu5 in complex with Nb43 | ||||||||||||||||||||
Voxel size | X=Y=Z: 1.111 Å | ||||||||||||||||||||
Density |
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Symmetry | Space group: 1 | ||||||||||||||||||||
Details | EMDB XML:
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-Supplemental data
-Sample components
-Entire : Metabotropic glutamate receptor 5 in complex with Quis
Entire | Name: Metabotropic glutamate receptor 5 in complex with Quis |
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Components |
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-Supramolecule #1: Metabotropic glutamate receptor 5 in complex with Quis
Supramolecule | Name: Metabotropic glutamate receptor 5 in complex with Quis type: organelle_or_cellular_component / ID: 1 / Parent: 0 / Macromolecule list: #1-#2 |
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Source (natural) | Organism: Homo sapiens (human) |
-Macromolecule #1: Metabotropic glutamate receptor 5
Macromolecule | Name: Metabotropic glutamate receptor 5 / type: protein_or_peptide / ID: 1 / Number of copies: 2 / Enantiomer: LEVO |
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Source (natural) | Organism: Homo sapiens (human) |
Molecular weight | Theoretical: 98.868297 KDa |
Recombinant expression | Organism: Spodoptera frugiperda (fall armyworm) |
Sequence | String: MKTIIALSYI FCLVFADYKD DDDAAQSSER RVVAHMPGDI IIGALFSVHH QPTVDKVHER KCGAVREQYG IQRVEAMLHT LERINSDPT LLPNITLGCE IRDSCWHSAV ALEQSIEFIR DSLISSEEEE GLVRCVDGSS SSFRSKKPIV GVIGPGSSSV A IQVQNLLQ ...String: MKTIIALSYI FCLVFADYKD DDDAAQSSER RVVAHMPGDI IIGALFSVHH QPTVDKVHER KCGAVREQYG IQRVEAMLHT LERINSDPT LLPNITLGCE IRDSCWHSAV ALEQSIEFIR DSLISSEEEE GLVRCVDGSS SSFRSKKPIV GVIGPGSSSV A IQVQNLLQ LFNIPQIAYS ATSMDLSDKT LFKYFMRVVP SDAQQARAMV DIVKRYNWTY VSAVHTEGNY GESGMEAFKD MS AKEGICI AHSYKIYSNA GEQSFDKLLK KLTSHLPKAR VVACFCEGMT VRGLLMAMRR LGLAGEFLLL GSDGWADRYD VTD GYQREA VGGITIKLQS PDVKWFDDYY LKLRPETNHR NPWFQEFWQH RFQCRLEGFP QENSKYNKTC NSSLTLKTHH VQDS KMGFV INAIYSMAYG LHNMQMSLCP GYAGLCDAMK PIDGRKLLES LMKTNFTGVS GDTILFDENG DSPGRYEIMN FKEMG KDYF DYINVGSWDN GELKMDDDEV WSKKSNIIRS VCSEPCEKGQ IKVIRKGEVS CCWTCTPCKE NEYVFDEYTC KACQLG SWP TDDLTGCDLI PVQYLRWGDP EPIAAVVFAC LGLLATLFVT VVFIIYRDTP VVKSSSRELC YIILAGICLG YLCTFCL IA KPKQIYCYLQ RIGIGLSPAM SYSALVTKTN RIARILAGSK KKICTKKPRF MSACAQLVIA FILICIQLGI IVALFIME P PDIMHDYPSI REVYLICNTT NLGVVTPLGY NGLLILSCTF YAFKTRNVPA NFNEAKYIAF TMYTTCIIWL AFVPIYFGS NYKIITMCFS VSLSATVALG CMFVPKVYII LAKPERNVRS AFTTSTVVRM HVGDGKSSSA ASRSSSLVNL WKRRGSSGET L UniProtKB: Metabotropic glutamate receptor 5 |
-Macromolecule #2: Nb43
Macromolecule | Name: Nb43 / type: protein_or_peptide / ID: 2 / Number of copies: 2 / Enantiomer: LEVO |
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Source (natural) | Organism: Lama glama (llama) |
Molecular weight | Theoretical: 13.354672 KDa |
Recombinant expression | Organism: Escherichia coli BL21(DE3) (bacteria) |
Sequence | String: QVQLVESGGG LVQAGGSLRL SCAASGRTFT SYAMGWFRQA PGKERESVAA ISSSGGSTHY ADSVKGRFTI SRDNSKNTVY LQMNSLKPE DTAVYYCAAA MYGSRWPDWE YDYWGQGTQV TVSS |
-Macromolecule #3: (S)-2-AMINO-3-(3,5-DIOXO-[1,2,4]OXADIAZOLIDIN-2-YL)-PROPIONIC ACID
Macromolecule | Name: (S)-2-AMINO-3-(3,5-DIOXO-[1,2,4]OXADIAZOLIDIN-2-YL)-PROPIONIC ACID type: ligand / ID: 3 / Number of copies: 2 / Formula: QUS |
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Molecular weight | Theoretical: 189.126 Da |
Chemical component information | ChemComp-QUS: |
-Experimental details
-Structure determination
Method | cryo EM |
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Processing | single particle reconstruction |
Aggregation state | particle |
-Sample preparation
Buffer | pH: 7.4 |
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Vitrification | Cryogen name: ETHANE |
-Electron microscopy
Microscope | FEI TITAN KRIOS |
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Electron beam | Acceleration voltage: 300 kV / Electron source: FIELD EMISSION GUN |
Electron optics | Illumination mode: FLOOD BEAM / Imaging mode: BRIGHT FIELDBright-field microscopy / Nominal defocus max: 2.0 µm / Nominal defocus min: 0.7000000000000001 µm |
Image recording | Film or detector model: GATAN K3 BIOQUANTUM (6k x 4k) / Average electron dose: 50.0 e/Å2 |
Experimental equipment | Model: Titan Krios / Image courtesy: FEI Company |
-Image processing
Startup model | Type of model: EMDB MAP EMDB ID: |
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Initial angle assignment | Type: MAXIMUM LIKELIHOOD |
Final angle assignment | Type: MAXIMUM LIKELIHOOD |
Final reconstruction | Resolution.type: BY AUTHOR / Resolution: 3.0 Å / Resolution method: FSC 0.143 CUT-OFF / Number images used: 183295 |