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Yorodumi- EMDB-33108: Cryo-EM structure of the human chemokine receptor CX3CR1 in compl... -
+Open data
-Basic information
Entry | Database: EMDB / ID: EMD-33108 | ||||||||||||
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Title | Cryo-EM structure of the human chemokine receptor CX3CR1 in complex with CX3CL1 and Gi1 | ||||||||||||
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Sample |
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Keywords | G protein-coupled receptor / chemokine receptor / CX3CR1 / CX3CL1 / SIGNALING PROTEIN | ||||||||||||
Function / homology | Function and homology information C-X3-C chemokine receptor activity / dendritic tree / multiple spine synapse organization, single dendrite / negative regulation of microglial cell mediated cytotoxicity / macropinosome membrane / C-X3-C chemokine binding / regulation of microglial cell migration / CXCR1 chemokine receptor binding / positive regulation of calcium-independent cell-cell adhesion / negative regulation of glutamate receptor signaling pathway ...C-X3-C chemokine receptor activity / dendritic tree / multiple spine synapse organization, single dendrite / negative regulation of microglial cell mediated cytotoxicity / macropinosome membrane / C-X3-C chemokine binding / regulation of microglial cell migration / CXCR1 chemokine receptor binding / positive regulation of calcium-independent cell-cell adhesion / negative regulation of glutamate receptor signaling pathway / negative regulation of interleukin-1 alpha production / leukocyte adhesive activation / CX3C chemokine receptor binding / negative regulation of hippocampal neuron apoptotic process / microglial cell activation involved in immune response / host-mediated regulation of intestinal microbiota composition / autocrine signaling / lymphocyte chemotaxis / synapse pruning / central nervous system maturation / positive regulation of microglial cell migration / negative regulation of neuron migration / synapse maturation / negative regulation of microglial cell activation / regulation of lipopolysaccharide-mediated signaling pathway / antifungal innate immune response / positive regulation of transforming growth factor beta1 production / chemokine receptor activity / positive regulation of I-kappaB phosphorylation / microglial cell proliferation / CCR chemokine receptor binding / positive regulation of actin filament bundle assembly / leukocyte migration involved in inflammatory response / C-C chemokine receptor activity / C-C chemokine binding / leukocyte tethering or rolling / integrin activation / angiogenesis involved in wound healing / regulation of tumor necrosis factor production / eosinophil chemotaxis / G protein-coupled peptide receptor activity / positive regulation of monocyte chemotaxis / chemokine-mediated signaling pathway / regulation of nitric oxide biosynthetic process / leukocyte chemotaxis / Chemokine receptors bind chemokines / chemokine activity / negative regulation of cell-substrate adhesion / negative regulation of interleukin-1 beta production / positive regulation of neurogenesis / positive regulation of cell-matrix adhesion / neuron remodeling / positive chemotaxis / positive regulation of neuroblast proliferation / neuronal cell body membrane / RSV-host interactions / chemoattractant activity / negative regulation of interleukin-6 production / Respiratory syncytial virus (RSV) attachment and entry / social behavior / negative regulation of apoptotic signaling pathway / negative regulation of tumor necrosis factor production / regulation of neurogenesis / negative regulation of long-term synaptic potentiation / negative regulation of extrinsic apoptotic signaling pathway in absence of ligand / T cell migration / D2 dopamine receptor binding / Adenylate cyclase inhibitory pathway / positive regulation of protein localization to cell cortex / cellular defense response / regulation of cAMP-mediated signaling / G protein-coupled serotonin receptor binding / extrinsic apoptotic signaling pathway in absence of ligand / cellular response to forskolin / cellular response to transforming growth factor beta stimulus / regulation of mitotic spindle organization / neutrophil chemotaxis / adenylate cyclase-inhibiting G protein-coupled receptor signaling pathway / cell chemotaxis / positive regulation of release of sequestered calcium ion into cytosol / negative regulation of cell migration / cell projection / response to ischemia / Regulation of insulin secretion / G protein-coupled receptor binding / G protein-coupled receptor activity / positive regulation of smooth muscle cell proliferation / calcium-mediated signaling / microglial cell activation / brain development / modulation of chemical synaptic transmission / G-protein beta/gamma-subunit complex binding / Olfactory Signaling Pathway / regulation of synaptic plasticity / adenylate cyclase-modulating G protein-coupled receptor signaling pathway / Activation of the phototransduction cascade / G beta:gamma signalling through PLC beta / Presynaptic function of Kainate receptors / Thromboxane signalling through TP receptor / G protein-coupled acetylcholine receptor signaling pathway Similarity search - Function | ||||||||||||
Biological species | Homo sapiens (human) | ||||||||||||
Method | single particle reconstruction / cryo EM / Resolution: 3.4 Å | ||||||||||||
Authors | Lu M / Zhao W / Han S / Zhu Y / Wu B / Zhao Q | ||||||||||||
Funding support | China, 3 items
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Citation | Journal: Sci Adv / Year: 2022 Title: Activation of the human chemokine receptor CX3CR1 regulated by cholesterol. Authors: Minmin Lu / Wenli Zhao / Shuo Han / Xiaowen Lin / Tingyu Xu / Qiuxiang Tan / Mu Wang / Cuiying Yi / Xiaojing Chu / Weibo Yang / Ya Zhu / Beili Wu / Qiang Zhao / Abstract: As the only member of the CX3C chemokine receptor subfamily, CX3CR1 binds to its sole endogenous ligand CX3CL1, which shows notable potential as a therapeutic target in atherosclerosis, cancer, and ...As the only member of the CX3C chemokine receptor subfamily, CX3CR1 binds to its sole endogenous ligand CX3CL1, which shows notable potential as a therapeutic target in atherosclerosis, cancer, and neuropathy. However, the drug development of CX3CR1 is hampered partially by the lack of structural information. Here, we present two cryo-electron microscopy structures of CX3CR1-G complexes in ligand-free and CX3CL1-bound states at 2.8- and 3.4-Å resolution, respectively. Together with functional data, the structures reveal the key factors that govern the recognition of CX3CL1 by both CX3CR1 and US28. A much smaller conformational change of helix VI upon activation than previously solved class A GPCR-G complex structures is observed in CX3CR1, which may correlate with three cholesterol molecules that play essential roles in conformation stabilization and signaling transduction. Thus, our data deepen the understanding of cholesterol modulation in GPCR (G protein-coupled receptor) signaling and provide insights into the diversity of G protein coupling. | ||||||||||||
History |
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-Structure visualization
Supplemental images |
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-Downloads & links
-EMDB archive
Map data | emd_33108.map.gz | 59.9 MB | EMDB map data format | |
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Header (meta data) | emd-33108-v30.xml emd-33108.xml | 18.8 KB 18.8 KB | Display Display | EMDB header |
Images | emd_33108.png | 95.3 KB | ||
Filedesc metadata | emd-33108.cif.gz | 6.3 KB | ||
Others | emd_33108_half_map_1.map.gz emd_33108_half_map_2.map.gz | 49.6 MB 49.6 MB | ||
Archive directory | http://ftp.pdbj.org/pub/emdb/structures/EMD-33108 ftp://ftp.pdbj.org/pub/emdb/structures/EMD-33108 | HTTPS FTP |
-Validation report
Summary document | emd_33108_validation.pdf.gz | 810.9 KB | Display | EMDB validaton report |
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Full document | emd_33108_full_validation.pdf.gz | 810.4 KB | Display | |
Data in XML | emd_33108_validation.xml.gz | 12 KB | Display | |
Data in CIF | emd_33108_validation.cif.gz | 14.2 KB | Display | |
Arichive directory | https://ftp.pdbj.org/pub/emdb/validation_reports/EMD-33108 ftp://ftp.pdbj.org/pub/emdb/validation_reports/EMD-33108 | HTTPS FTP |
-Related structure data
Related structure data | 7xbxMC 7xbwC 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_33108.map.gz / Format: CCP4 / Size: 64 MB / Type: IMAGE STORED AS FLOATING POINT NUMBER (4 BYTES) | ||||||||||||||||||||||||||||||||||||
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Projections & slices | Image control
Images are generated by Spider. | ||||||||||||||||||||||||||||||||||||
Voxel size | X=Y=Z: 1.045 Å | ||||||||||||||||||||||||||||||||||||
Density |
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Symmetry | Space group: 1 | ||||||||||||||||||||||||||||||||||||
Details | EMDB XML:
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-Supplemental data
-Half map: #1
File | emd_33108_half_map_1.map | ||||||||||||
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Projections & Slices |
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Density Histograms |
-Half map: #2
File | emd_33108_half_map_2.map | ||||||||||||
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Projections & Slices |
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Density Histograms |
-Sample components
-Entire : Chemokine receptor CX3CR1 in complex with CX3CL1 Gi1
Entire | Name: Chemokine receptor CX3CR1 in complex with CX3CL1 Gi1 |
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Components |
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-Supramolecule #1: Chemokine receptor CX3CR1 in complex with CX3CL1 Gi1
Supramolecule | Name: Chemokine receptor CX3CR1 in complex with CX3CL1 Gi1 / type: complex / ID: 1 / Parent: 0 / Macromolecule list: #1-#4 |
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Source (natural) | Organism: Homo sapiens (human) |
-Macromolecule #1: Guanine nucleotide-binding protein G(i) subunit alpha-1
Macromolecule | Name: Guanine nucleotide-binding protein G(i) subunit alpha-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: 40.447141 KDa |
Recombinant expression | Organism: Spodoptera frugiperda (fall armyworm) |
Sequence | String: MGCTLSAEDK AAVERSKMID RNLREDGEKA AREVKLLLLG AGESGKCTIV KQMKIIHEAG YSEEECKQYK AVVYSNTIQS IIAIIRAMG RLKIDFGDSA RADDARQLFV LAGAAEEGFM TAELAGVIKR LWKDSGVQAC FNRSREYQLN DSAAYYLNDL D RIAQPNYI ...String: MGCTLSAEDK AAVERSKMID RNLREDGEKA AREVKLLLLG AGESGKCTIV KQMKIIHEAG YSEEECKQYK AVVYSNTIQS IIAIIRAMG RLKIDFGDSA RADDARQLFV LAGAAEEGFM TAELAGVIKR LWKDSGVQAC FNRSREYQLN DSAAYYLNDL D RIAQPNYI PTQQDVLRTR VKTTGIVETH FTFKDLHFKM FDVTAQRSER KKWIHCFEGV TAIIFCVALS DYDLVLAEDE EM NRMHASM KLFDSICNNK WFTDTSIILF LNKKDLFEEK IKKSPLTICY PEYAGSNTYE EAAAYIQCQF EDLNKRKDTK EIY THFTCS TDTKNVQFVF DAVTDVIIKN NLKDCGLF UniProtKB: Guanine nucleotide-binding protein G(i) subunit alpha-1 |
-Macromolecule #2: Guanine nucleotide-binding protein G(I)/G(S)/G(T) subunit beta-1
Macromolecule | Name: Guanine nucleotide-binding protein G(I)/G(S)/G(T) subunit beta-1 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: 38.245805 KDa |
Recombinant expression | Organism: Spodoptera frugiperda (fall armyworm) |
Sequence | String: HHHHHHMSEL DQLRQEAEQL KNQIRDARKA CADATLSQIT NNIDPVGRIQ MRTRRTLRGH LAKIYAMHWG TDSRLLVSAS QDGKLIIWD SYTTNKVHAI PLRSSWVMTC AYAPSGNYVA CGGLDNICSI YNLKTREGNV RVSRELAGHT GYLSCCRFLD D NQIVTSSG ...String: HHHHHHMSEL DQLRQEAEQL KNQIRDARKA CADATLSQIT NNIDPVGRIQ MRTRRTLRGH LAKIYAMHWG TDSRLLVSAS QDGKLIIWD SYTTNKVHAI PLRSSWVMTC AYAPSGNYVA CGGLDNICSI YNLKTREGNV RVSRELAGHT GYLSCCRFLD D NQIVTSSG DTTCALWDIE TGQQTTTFTG HTGDVMSLSL APDTRLFVSG ACDASAKLWD VREGMCRQTF TGHESDINAI CF FPNGNAF ATGSDDATCR LFDLRADQEL MTYSHDNIIC GITSVSFSKS GRLLLAGYDD FNCNVWDALK ADRAGVLAGH DNR VSCLGV TDDGMAVATG SWDSFLKIWN UniProtKB: Guanine nucleotide-binding protein G(I)/G(S)/G(T) subunit beta-1 |
-Macromolecule #3: Guanine nucleotide-binding protein G(I)/G(S)/G(O) subunit gamma-2
Macromolecule | Name: Guanine nucleotide-binding protein G(I)/G(S)/G(O) subunit gamma-2 type: protein_or_peptide / ID: 3 / Number of copies: 1 / Enantiomer: LEVO |
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Source (natural) | Organism: Homo sapiens (human) |
Molecular weight | Theoretical: 7.861143 KDa |
Recombinant expression | Organism: Spodoptera frugiperda (fall armyworm) |
Sequence | String: MASNNTASIA QARKLVEQLK MEANIDRIKV SKAAADLMAY CEAHAKEDPL LTPVPASENP FREKKFFCAI L UniProtKB: Guanine nucleotide-binding protein G(I)/G(S)/G(O) subunit gamma-2 |
-Macromolecule #4: Processed fractalkine,CX3C chemokine receptor 1
Macromolecule | Name: Processed fractalkine,CX3C chemokine receptor 1 / type: protein_or_peptide / ID: 4 / Number of copies: 1 / Enantiomer: LEVO |
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Source (natural) | Organism: Homo sapiens (human) |
Molecular weight | Theoretical: 51.55825 KDa |
Recombinant expression | Organism: Spodoptera frugiperda (fall armyworm) |
Sequence | String: (PCA)HHGVTKCNI TCSKMTSKIP VALLIHYQQN QASCCKRAII LETRQHRLFC ADPKEQWVKD AMQHLDRQAA ALTRNG SGS GSGSGSGSGS GSGSGSGSGS GSGSDQFPES VTENFEYDDL AEACYIGDIV VFGTVFLSIF YSVIFAIGLV GNLLVVF AL TNSKKPKSVT ...String: (PCA)HHGVTKCNI TCSKMTSKIP VALLIHYQQN QASCCKRAII LETRQHRLFC ADPKEQWVKD AMQHLDRQAA ALTRNG SGS GSGSGSGSGS GSGSGSGSGS GSGSDQFPES VTENFEYDDL AEACYIGDIV VFGTVFLSIF YSVIFAIGLV GNLLVVF AL TNSKKPKSVT DIYLLNLALS DLLFVATLPF WTHYLINEKG LHNAMCKFTT AFFFIGFFGS IFFLTVISID RYLAIVLA A NSMNNRTVQH GVTISLGVWA AAILVAAPQF MFTKQKENEC CGDYPEVLQE IWPVLRNVET NFLGFLLPLL IMSYCYFRI IQTLFSSKNH KKAKAIKLIL LVVIVFFLFW TPYNVVIFLE TLKLYDFFPS CDMRKDLRLA LSVTETVAFS HCCLNPLIYA FAGEKFRRY LYHLYGKCLA VLEFLEVLFQ GPWSHPQFEK GGGSGGGSGG SAWSHPQFEK DYKDDDDK UniProtKB: Fractalkine, CX3C chemokine receptor 1 |
-Macromolecule #5: CHOLESTEROL
Macromolecule | Name: CHOLESTEROL / type: ligand / ID: 5 / Number of copies: 2 / Formula: CLR |
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Molecular weight | Theoretical: 386.654 Da |
Chemical component information | ChemComp-CLR: |
-Experimental details
-Structure determination
Method | cryo EM |
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Processing | single particle reconstruction |
Aggregation state | particle |
-Sample preparation
Buffer | pH: 7.5 |
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Vitrification | Cryogen name: ETHANE |
-Electron microscopy
Microscope | FEI TITAN KRIOS |
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Image recording | Film or detector model: GATAN K3 BIOQUANTUM (6k x 4k) / Average electron dose: 2.1875 e/Å2 |
Electron beam | Acceleration voltage: 300 kV / Electron source: FIELD EMISSION GUN |
Electron optics | Illumination mode: SPOT SCAN / Imaging mode: BRIGHT FIELD / Nominal defocus max: 1.5 µm / Nominal defocus min: 0.8 µm |
Experimental equipment | Model: Titan Krios / Image courtesy: FEI Company |
-Image processing
Startup model | Type of model: INSILICO MODEL |
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Final reconstruction | Resolution.type: BY AUTHOR / Resolution: 3.4 Å / Resolution method: FSC 0.143 CUT-OFF / Number images used: 490779 |
Initial angle assignment | Type: MAXIMUM LIKELIHOOD |
Final angle assignment | Type: MAXIMUM LIKELIHOOD |