+Open data
-Basic information
Entry | Database: EMDB / ID: EMD-0993 | ||||||||||||||||||
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Title | Cryo-EM map of PAC1 receptor bound to PACAP38 and Gs protein | ||||||||||||||||||
Map data | Sharpened map of PAC1 receptor bound to PACAP38 and Gs protein | ||||||||||||||||||
Sample |
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Function / homology | Function and homology information negative regulation of response to reactive oxygen species / development of primary female sexual characteristics / vasoactive intestinal polypeptide receptor activity / positive regulation of cAMP-mediated signaling / NGF-independant TRKA activation / G protein-coupled peptide receptor activity / positive regulation of small GTPase mediated signal transduction / neuropeptide binding / positive regulation of inositol phosphate biosynthetic process / positive regulation of calcium ion transport into cytosol ...negative regulation of response to reactive oxygen species / development of primary female sexual characteristics / vasoactive intestinal polypeptide receptor activity / positive regulation of cAMP-mediated signaling / NGF-independant TRKA activation / G protein-coupled peptide receptor activity / positive regulation of small GTPase mediated signal transduction / neuropeptide binding / positive regulation of inositol phosphate biosynthetic process / positive regulation of calcium ion transport into cytosol / PKA activation in glucagon signalling / peptide hormone binding / adenylate cyclase binding / hair follicle placode formation / developmental growth / D1 dopamine receptor binding / bicellular tight junction / multicellular organismal response to stress / intracellular transport / renal water homeostasis / Hedgehog 'off' state / adenylate cyclase-activating adrenergic receptor signaling pathway / activation of adenylate cyclase activity / cellular response to glucagon stimulus / cAMP-mediated signaling / adenylate cyclase activator activity / regulation of insulin secretion / trans-Golgi network membrane / negative regulation of inflammatory response to antigenic stimulus / bone development / G-protein beta/gamma-subunit complex binding / Olfactory Signaling Pathway / caveola / adenylate cyclase-modulating G protein-coupled receptor signaling pathway / Activation of the phototransduction cascade / adenylate cyclase-activating G protein-coupled receptor signaling pathway / G beta:gamma signalling through PLC beta / Presynaptic function of Kainate receptors / Thromboxane signalling through TP receptor / G protein-coupled acetylcholine receptor signaling pathway / G protein activity / G-protein activation / platelet aggregation / Activation of G protein gated Potassium channels / Inhibition of voltage gated Ca2+ channels via Gbeta/gamma subunits / Prostacyclin signalling through prostacyclin receptor / Glucagon signaling in metabolic regulation / G beta:gamma signalling through CDC42 / cognition / G beta:gamma signalling through BTK / ADP signalling through P2Y purinoceptor 12 / small GTPase binding / Sensory perception of sweet, bitter, and umami (glutamate) taste / Synthesis, secretion, and inactivation of Glucagon-like Peptide-1 (GLP-1) / photoreceptor disc membrane / Glucagon-type ligand receptors / Adrenaline,noradrenaline inhibits insulin secretion / Vasopressin regulates renal water homeostasis via Aquaporins / G alpha (z) signalling events / Glucagon-like Peptide-1 (GLP1) regulates insulin secretion / cellular response to catecholamine stimulus / ADORA2B mediated anti-inflammatory cytokines production / sensory perception of taste / ADP signalling through P2Y purinoceptor 1 / G beta:gamma signalling through PI3Kgamma / adenylate cyclase-activating dopamine receptor signaling pathway / Cooperation of PDCL (PhLP1) and TRiC/CCT in G-protein beta folding / GPER1 signaling / cellular response to prostaglandin E stimulus / Inactivation, recovery and regulation of the phototransduction cascade / G-protein beta-subunit binding / heterotrimeric G-protein complex / sensory perception of smell / G alpha (12/13) signalling events / extracellular vesicle / signaling receptor complex adaptor activity / Thrombin signalling through proteinase activated receptors (PARs) / GTPase binding / response to estradiol / positive regulation of cold-induced thermogenesis / retina development in camera-type eye / signaling receptor activity / Ca2+ pathway / phospholipase C-activating G protein-coupled receptor signaling pathway / G alpha (i) signalling events / fibroblast proliferation / spermatogenesis / G alpha (s) signalling events / Hydrolases; Acting on acid anhydrides; Acting on GTP to facilitate cellular and subcellular movement / G alpha (q) signalling events / response to ethanol / Ras protein signal transduction / cell population proliferation / Extra-nuclear estrogen signaling / cell differentiation / receptor complex / cell surface receptor signaling pathway / endosome / response to xenobiotic stimulus / G protein-coupled receptor signaling pathway Similarity search - Function | ||||||||||||||||||
Biological species | Homo sapiens (human) | ||||||||||||||||||
Method | single particle reconstruction / cryo EM / Resolution: 2.65 Å | ||||||||||||||||||
Authors | Liang YL / Belousoff MJ / Zhao P / Danev R / Sexton PM / Wootten D | ||||||||||||||||||
Funding support | Australia, Japan, 5 items
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Citation | Journal: Mol Cell / Year: 2020 Title: Toward a Structural Understanding of Class B GPCR Peptide Binding and Activation. Authors: Yi-Lynn Liang / Matthew J Belousoff / Peishen Zhao / Cassandra Koole / Madeleine M Fletcher / Tin T Truong / Villy Julita / George Christopoulos / H Eric Xu / Yan Zhang / Maryam Khoshouei / ...Authors: Yi-Lynn Liang / Matthew J Belousoff / Peishen Zhao / Cassandra Koole / Madeleine M Fletcher / Tin T Truong / Villy Julita / George Christopoulos / H Eric Xu / Yan Zhang / Maryam Khoshouei / Arthur Christopoulos / Radostin Danev / Patrick M Sexton / Denise Wootten / Abstract: Class B G protein-coupled receptors (GPCRs) are important therapeutic targets for major diseases. Here, we present structures of peptide and Gs-bound pituitary adenylate cyclase-activating peptide, ...Class B G protein-coupled receptors (GPCRs) are important therapeutic targets for major diseases. Here, we present structures of peptide and Gs-bound pituitary adenylate cyclase-activating peptide, PAC1 receptor, and corticotropin-releasing factor (CRF), (CRF1) receptor. Together with recently solved structures, these provide coverage of the major class B GPCR subfamilies. Diverse orientations of the extracellular domain to the receptor core in different receptors are at least partially dependent on evolutionary conservation in the structure and nature of peptide interactions. Differences in peptide interactions to the receptor core also influence the interlinked TM2-TM1-TM6/ECL3/TM7 domain, and this is likely important in their diverse signaling. However, common conformational reorganization of ECL2, linked to reorganization of ICL2, modulates G protein contacts. Comparison between receptors reveals ICL2 as a key domain forming dynamic G protein interactions in a receptor- and ligand-specific manner. This work advances our understanding of class B GPCR activation and Gs coupling. | ||||||||||||||||||
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_0993.map.gz | 19.5 MB | EMDB map data format | |
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Header (meta data) | emd-0993-v30.xml emd-0993.xml | 20.4 KB 20.4 KB | Display Display | EMDB header |
Images | emd_0993.png | 121.4 KB | ||
Masks | emd_0993_msk_1.map | 20.8 MB | Mask map | |
Others | emd_0993_additional.map.gz emd_0993_additional_1.map.gz emd_0993_half_map_1.map.gz emd_0993_half_map_2.map.gz | 15.8 MB 15.8 MB 15.8 MB 15.8 MB | ||
Archive directory | http://ftp.pdbj.org/pub/emdb/structures/EMD-0993 ftp://ftp.pdbj.org/pub/emdb/structures/EMD-0993 | HTTPS FTP |
-Validation report
Summary document | emd_0993_validation.pdf.gz | 79.8 KB | Display | EMDB validaton report |
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Full document | emd_0993_full_validation.pdf.gz | 78.9 KB | Display | |
Data in XML | emd_0993_validation.xml.gz | 492 B | Display | |
Arichive directory | https://ftp.pdbj.org/pub/emdb/validation_reports/EMD-0993 ftp://ftp.pdbj.org/pub/emdb/validation_reports/EMD-0993 | HTTPS FTP |
-Related structure data
Related structure data | 6p9xC 6p9yC C: citing same article (ref.) |
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Similar structure data | |
EM raw data | EMPIAR-10359 (Title: Cryo-EM of PAC1 receptor bound to PACAP38 and Gs protein Data size: 4.8 TB Data #1: Unaligned multi-frame gain-normalized movies in LZW compressed TIFF format [micrographs - multiframe]) |
-Links
EMDB pages | EMDB (EBI/PDBe) / EMDataResource |
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Related items in Molecule of the Month |
-Map
File | Download / File: emd_0993.map.gz / Format: CCP4 / Size: 20.8 MB / Type: IMAGE STORED AS FLOATING POINT NUMBER (4 BYTES) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Annotation | Sharpened map of PAC1 receptor bound to PACAP38 and Gs protein | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Projections & slices | Image control
Images are generated by Spider. | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Voxel size | X=Y=Z: 1.207 Å | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Density |
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Symmetry | Space group: 1 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Details | EMDB XML:
CCP4 map header:
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-Supplemental data
-Mask #1
File | emd_0993_msk_1.map | ||||||||||||
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Projections & Slices |
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Density Histograms |
-Additional map: Unprocessed map of PAC1 receptor bound to PACAP38 and Gs protein
File | emd_0993_additional.map | ||||||||||||
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Annotation | Unprocessed map of PAC1 receptor bound to PACAP38 and Gs protein | ||||||||||||
Projections & Slices |
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Density Histograms |
-Additional map: Unprocessed map of PAC1 receptor bound to PACAP38 and Gs protein
File | emd_0993_additional_1.map | ||||||||||||
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Annotation | Unprocessed map of PAC1 receptor bound to PACAP38 and Gs protein | ||||||||||||
Projections & Slices |
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Density Histograms |
-Half map: Unprocessed half-map of PAC1 receptor bound to PACAP38 and Gs protein
File | emd_0993_half_map_1.map | ||||||||||||
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Annotation | Unprocessed half-map of PAC1 receptor bound to PACAP38 and Gs protein | ||||||||||||
Projections & Slices |
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Density Histograms |
-Half map: Unprocessed half-map of PAC1 receptor bound to PACAP38 and Gs protein
File | emd_0993_half_map_2.map | ||||||||||||
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Annotation | Unprocessed half-map of PAC1 receptor bound to PACAP38 and Gs protein | ||||||||||||
Projections & Slices |
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Density Histograms |
-Sample components
-Entire : PAC1 receptor bound to PACAP38 and Gs protein
Entire | Name: PAC1 receptor bound to PACAP38 and Gs protein |
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Components |
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-Supramolecule #1: PAC1 receptor bound to PACAP38 and Gs protein
Supramolecule | Name: PAC1 receptor bound to PACAP38 and Gs protein / type: complex / ID: 1 / Parent: 0 |
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Source (natural) | Organism: Homo sapiens (human) |
Recombinant expression | Organism: Trichoplusia ni (cabbage looper) |
Molecular weight | Theoretical: 150 kDa/nm |
-Experimental details
-Structure determination
Method | cryo EM |
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Processing | single particle reconstruction |
Aggregation state | particle |
-Sample preparation
Concentration | 4.35 mg/mL |
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Buffer | pH: 7.4 |
Grid | Model: Quantifoil R1.2/1.3 / Material: COPPER/RHODIUM / Mesh: 200 / Pretreatment - Type: GLOW DISCHARGE / Pretreatment - Atmosphere: AIR |
Vitrification | Cryogen name: ETHANE / Chamber humidity: 100 % / Chamber temperature: 277 K / Instrument: FEI VITROBOT MARK IV / Details: blot time 10 s. |
-Electron microscopy
Microscope | FEI TITAN KRIOS |
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Specialist optics | Phase plate: VOLTA PHASE PLATE / Energy filter - Name: GIF Quantum LS / Energy filter - Slit width: 25 eV |
Image recording | Film or detector model: GATAN K3 BIOQUANTUM (6k x 4k) / Number grids imaged: 1 / Number real images: 7650 / Average exposure time: 3.715 sec. / Average electron dose: 64.0 e/Å2 Details: Volta phase plate images: 4032; Conventional defocus images: 3618 |
Electron beam | Acceleration voltage: 300 kV / Electron source: FIELD EMISSION GUN |
Electron optics | C2 aperture diameter: 50.0 µm / Calibrated defocus max: 1.6 µm / Calibrated defocus min: 0.4 µm / Illumination mode: FLOOD BEAM / Imaging mode: BRIGHT FIELD / Cs: 2.7 mm / Nominal defocus max: 1.6 µm / Nominal defocus min: 0.4 µm / Nominal magnification: 105000 |
Sample stage | Specimen holder model: FEI TITAN KRIOS AUTOGRID HOLDER / Cooling holder cryogen: NITROGEN |
Experimental equipment | Model: Titan Krios / Image courtesy: FEI Company |