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Yorodumi- PDB-7wvv: Cryo-EM structure of the human formyl peptide receptor 2 in compl... -
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Basic information
| Entry | Database: PDB / ID: 7wvv | ||||||||||||
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| Title | Cryo-EM structure of the human formyl peptide receptor 2 in complex with fMLFII and Gi2 | ||||||||||||
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Keywords | SIGNALING PROTEIN / G protein-coupled receptor / formyl peptide receptor / FPR2 / fMLFII | ||||||||||||
| Function / homology | Function and homology informationN-formyl peptide receptor activity / complement receptor activity / dentinogenesis / immune response-regulating cell surface receptor signaling pathway / negative regulation of adenylate cyclase-activating adrenergic receptor signaling pathway / scavenger receptor binding / negative regulation of calcium ion-dependent exocytosis / RAGE receptor binding / G protein-coupled adenosine receptor signaling pathway / negative regulation of adenylate cyclase activity ...N-formyl peptide receptor activity / complement receptor activity / dentinogenesis / immune response-regulating cell surface receptor signaling pathway / negative regulation of adenylate cyclase-activating adrenergic receptor signaling pathway / scavenger receptor binding / negative regulation of calcium ion-dependent exocytosis / RAGE receptor binding / G protein-coupled adenosine receptor signaling pathway / negative regulation of adenylate cyclase activity / complement receptor mediated signaling pathway / positive regulation of neural precursor cell proliferation / positive regulation of innate immune response / positive regulation of monocyte chemotaxis / Formyl peptide receptors bind formyl peptides and many other ligands / negative regulation of synaptic transmission / positive regulation of urine volume / cargo receptor activity / positive chemotaxis / gamma-aminobutyric acid signaling pathway / regulation of calcium ion transport / tertiary granule membrane / negative regulation of apoptotic signaling pathway / ficolin-1-rich granule membrane / neuronal dense core vesicle / specific granule membrane / positive regulation of vascular associated smooth muscle cell proliferation / positive regulation of superoxide anion generation / Adenylate cyclase inhibitory pathway / response to nutrient / astrocyte activation / positive regulation of phagocytosis / receptor-mediated endocytosis / hippocampal mossy fiber to CA3 synapse / Regulation of insulin secretion / calcium-mediated signaling / microglial cell activation / electron transport chain / G protein-coupled receptor binding / negative regulation of inflammatory response / G protein-coupled receptor activity / cellular response to amyloid-beta / G-protein beta/gamma-subunit complex binding / chemotaxis / adenylate cyclase-inhibiting G protein-coupled receptor signaling pathway / Olfactory Signaling Pathway / Activation of the phototransduction cascade / G protein-coupled acetylcholine receptor signaling pathway / G beta:gamma signalling through PLC beta / Presynaptic function of Kainate receptors / Thromboxane signalling through TP receptor / Activation of G protein gated Potassium channels / Inhibition of voltage gated Ca2+ channels via Gbeta/gamma subunits / G-protein activation / Glucagon signaling in metabolic regulation / G beta:gamma signalling through CDC42 / Prostacyclin signalling through prostacyclin receptor / G beta:gamma signalling through BTK / Synthesis, secretion, and inactivation of Glucagon-like Peptide-1 (GLP-1) / photoreceptor disc membrane / ADP signalling through P2Y purinoceptor 12 / Sensory perception of sweet, bitter, and umami (glutamate) taste / Glucagon-type ligand receptors / Adrenaline,noradrenaline inhibits insulin secretion / Vasopressin regulates renal water homeostasis via Aquaporins / Glucagon-like Peptide-1 (GLP1) regulates insulin secretion / G alpha (z) signalling events / cellular response to catecholamine stimulus / ADP signalling through P2Y purinoceptor 1 / ADORA2B mediated anti-inflammatory cytokines production / 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 / G alpha (12/13) signalling events / heterotrimeric G-protein complex / Inactivation, recovery and regulation of the phototransduction cascade / G-protein beta-subunit binding / amyloid-beta binding / extracellular vesicle / sensory perception of taste / adenylate cyclase-activating G protein-coupled receptor signaling pathway / Thrombin signalling through proteinase activated receptors (PARs) / signaling receptor complex adaptor activity / positive regulation of cytosolic calcium ion concentration / signaling receptor activity / retina development in camera-type eye / GTPase binding / cell body / fibroblast proliferation / Ca2+ pathway / midbody / High laminar flow shear stress activates signaling by PIEZO1 and PECAM1:CDH5:KDR in endothelial cells / G alpha (i) signalling events / G alpha (s) signalling events / phospholipase C-activating G protein-coupled receptor signaling pathway / G alpha (q) signalling events / Hydrolases; Acting on acid anhydrides; Acting on GTP to facilitate cellular and subcellular movement / negative regulation of neuron apoptotic process Similarity search - Function | ||||||||||||
| Biological species | Homo sapiens (human) | ||||||||||||
| Method | ELECTRON MICROSCOPY / single particle reconstruction / cryo EM / Resolution: 2.9 Å | ||||||||||||
Authors | Zhu, Y. / Lin, X. / Zong, X. / Han, S. / Zhao, Q. / Wu, B. | ||||||||||||
| Funding support | China, 3items
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Citation | Journal: Nat Commun / Year: 2022Title: Structural basis of FPR2 in recognition of Aβ and neuroprotection by humanin. Authors: Ya Zhu / Xiaowen Lin / Xin Zong / Shuo Han / Mu Wang / Yuxuan Su / Limin Ma / Xiaojing Chu / Cuiying Yi / Qiang Zhao / Beili Wu / ![]() Abstract: Formyl peptide receptor 2 (FPR2) has been shown to mediate the cytotoxic effects of the β amyloid peptide Aβ and serves as a receptor for humanin, a peptide that protects neuronal cells from damage ...Formyl peptide receptor 2 (FPR2) has been shown to mediate the cytotoxic effects of the β amyloid peptide Aβ and serves as a receptor for humanin, a peptide that protects neuronal cells from damage by Aβ, implying its involvement in the pathogenesis of Alzheimer's disease (AD). However, the interaction pattern between FPR2 and Aβ or humanin remains unknown. Here we report the structures of FPR2 bound to G and Aβ or N-formyl humanin (fHN). Combined with functional data, the structures reveal two critical regions that govern recognition and activity of Aβ and fHN, including a polar binding cavity within the receptor helical bundle and a hydrophobic binding groove in the extracellular region. In addition, the structures of FPR2 and FPR1 in complex with different formyl peptides were determined, providing insights into ligand recognition and selectivity of the FPR family. These findings uncover key factors that define the functionality of FPR2 in AD and other inflammatory diseases and would enable drug development. | ||||||||||||
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Structure visualization
| Structure viewer | Molecule: Molmil Jmol/JSmol |
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Downloads & links
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Download
| PDBx/mmCIF format | 7wvv.cif.gz | 183.7 KB | Display | PDBx/mmCIF format |
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| PDB format | pdb7wvv.ent.gz | 132.5 KB | Display | PDB format |
| PDBx/mmJSON format | 7wvv.json.gz | Tree view | PDBx/mmJSON format | |
| Others | Other downloads |
-Validation report
| Arichive directory | https://data.pdbj.org/pub/pdb/validation_reports/wv/7wvv ftp://data.pdbj.org/pub/pdb/validation_reports/wv/7wvv | HTTPS FTP |
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-Related structure data
| Related structure data | ![]() 32859MC ![]() 7wvuC ![]() 7wvwC ![]() 7wvxC ![]() 7wvyC M: map data used to model this data C: citing same article ( |
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| Similar structure data | Similarity search - Function & homology F&H Search |
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Links
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Assembly
| Deposited unit | ![]()
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Components
| #1: Protein/peptide | Mass: 663.868 Da / Num. of mol.: 1 / Source method: obtained synthetically / Source: (synth.) Homo sapiens (human) |
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| #2: Protein | Mass: 56710.328 Da / Num. of mol.: 1 / Mutation: S211L Source method: isolated from a genetically manipulated source Source: (gene. exp.) Homo sapiens (human) / Gene: cybC, FPR2, FPRH1, FPRL1, LXA4R / Production host: ![]() |
| #3: Protein | Mass: 40502.863 Da / Num. of mol.: 1 / Mutation: S47N, G204A, A327S, E246A Source method: isolated from a genetically manipulated source Source: (gene. exp.) Homo sapiens (human) / Gene: GNAI2, GNAI2B / Production host: ![]() |
| #4: Protein | Mass: 38744.371 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Source: (gene. exp.) Homo sapiens (human) / Gene: GNB1 / Production host: ![]() |
| #5: Protein | Mass: 7861.143 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Source: (gene. exp.) Homo sapiens (human) / Gene: GNG2 / Production host: ![]() |
| Has ligand of interest | N |
| Has protein modification | Y |
-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: Formyl peptide receptor 2 in complex with fMLFII and Gi2 Type: COMPLEX / Entity ID: all / Source: RECOMBINANT |
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| Source (natural) | Organism: Homo sapiens (human) |
| Source (recombinant) | Organism: ![]() |
| Buffer solution | pH: 7.5 |
| Specimen | Embedding applied: NO / Shadowing applied: NO / Staining applied: NO / Vitrification applied: YES |
| Vitrification | Cryogen name: ETHANE |
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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: SPOT SCAN |
| Electron lens | Mode: BRIGHT FIELD / Nominal defocus max: 1500 nm / Nominal defocus min: 800 nm |
| Image recording | Electron dose: 2.1875 e/Å2 / Film or detector model: GATAN K3 BIOQUANTUM (6k x 4k) |
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Processing
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| CTF correction | Type: NONE | ||||||||||||||||||||||||
| 3D reconstruction | Resolution: 2.9 Å / Resolution method: FSC 0.143 CUT-OFF / Num. of particles: 1216356 / Symmetry type: POINT | ||||||||||||||||||||||||
| Refinement | Cross valid method: NONE Stereochemistry target values: GeoStd + Monomer Library + CDL v1.2 | ||||||||||||||||||||||||
| Displacement parameters | Biso mean: 46.44 Å2 | ||||||||||||||||||||||||
| Refine LS restraints |
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About Yorodumi



Homo sapiens (human)
China, 3items
Citation








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FIELD EMISSION GUN