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Yorodumi- EMDB-31768: Cryo-EM structure of SARS-CoV-2 S-Kappa variant (B.1.617.1), one ... -
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Open data
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Basic information
| Entry | Database: EMDB / ID: EMD-31768 | |||||||||||||||
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| Title | Cryo-EM structure of SARS-CoV-2 S-Kappa variant (B.1.617.1), one RBD-up conformation 1 | |||||||||||||||
Map data | SARS-CoV-2 S-Kappa variant, one RBD-up (conformation 1), unsharpened map | |||||||||||||||
Sample |
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Keywords | SARS-CoV-2 / Spike protein / VIRAL PROTEIN | |||||||||||||||
| Function / homology | Function and homology informationsymbiont-mediated disruption of host tissue / Maturation of spike protein / Translation of Structural Proteins / Virion Assembly and Release / host cell surface / host extracellular space / viral translation / symbiont-mediated-mediated suppression of host tetherin activity / Induction of Cell-Cell Fusion / structural constituent of virion ...symbiont-mediated disruption of host tissue / Maturation of spike protein / Translation of Structural Proteins / Virion Assembly and Release / host cell surface / host extracellular space / viral translation / symbiont-mediated-mediated suppression of host tetherin activity / Induction of Cell-Cell Fusion / structural constituent of virion / entry receptor-mediated virion attachment to host cell / membrane fusion / Attachment and Entry / host cell endoplasmic reticulum-Golgi intermediate compartment membrane / positive regulation of viral entry into host cell / receptor-mediated virion attachment to host cell / host cell surface receptor binding / symbiont-mediated suppression of host innate immune response / receptor ligand activity / endocytosis involved in viral entry into host cell / fusion of virus membrane with host plasma membrane / fusion of virus membrane with host endosome membrane / viral envelope / symbiont entry into host cell / virion attachment to host cell / SARS-CoV-2 activates/modulates innate and adaptive immune responses / host cell plasma membrane / virion membrane / identical protein binding / membrane / plasma membrane Similarity search - Function | |||||||||||||||
| Biological species | ![]() | |||||||||||||||
| Method | single particle reconstruction / cryo EM / Resolution: 2.9 Å | |||||||||||||||
Authors | Yang TJ / Yu PY | |||||||||||||||
| Funding support | Taiwan, 4 items
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Citation | Journal: To Be PublishedTitle: Cryo-EM structure of SARS-CoV-2 S-Kappa variant (B.1.617.1), one RBD-up conformation 1 Authors: Yang TJ / Yu PY / Chang YC / Hsu STD | |||||||||||||||
| History |
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Structure visualization
| Movie |
Movie viewer |
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| Structure viewer | EM map: SurfView Molmil Jmol/JSmol |
| Supplemental images |
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Downloads & links
-EMDB archive
| Map data | emd_31768.map.gz | 108.5 MB | EMDB map data format | |
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| Header (meta data) | emd-31768-v30.xml emd-31768.xml | 15 KB 15 KB | Display Display | EMDB header |
| Images | emd_31768.png | 53.2 KB | ||
| Filedesc metadata | emd-31768.cif.gz | 6.2 KB | ||
| Others | emd_31768_additional_1.map.gz | 204 MB | ||
| Archive directory | http://ftp.pdbj.org/pub/emdb/structures/EMD-31768 ftp://ftp.pdbj.org/pub/emdb/structures/EMD-31768 | HTTPS FTP |
-Validation report
| Summary document | emd_31768_validation.pdf.gz | 508.4 KB | Display | EMDB validaton report |
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| Full document | emd_31768_full_validation.pdf.gz | 508 KB | Display | |
| Data in XML | emd_31768_validation.xml.gz | 7.1 KB | Display | |
| Data in CIF | emd_31768_validation.cif.gz | 8.3 KB | Display | |
| Arichive directory | https://ftp.pdbj.org/pub/emdb/validation_reports/EMD-31768 ftp://ftp.pdbj.org/pub/emdb/validation_reports/EMD-31768 | HTTPS FTP |
-Related structure data
| Related structure data | ![]() 7v7eMC ![]() 7v76C ![]() 7v77C ![]() 7v78C ![]() 7v79C ![]() 7v7aC ![]() 7v7dC ![]() 7v7fC ![]() 7v7gC ![]() 7v7hC ![]() 7v7iC ![]() 7v7jC ![]() 7v7nC ![]() 7v7oC ![]() 7v7pC ![]() 7v7qC ![]() 7v7rC ![]() 7v7sC ![]() 7v7tC ![]() 7v7uC ![]() 7v7vC ![]() 7v7zC ![]() 7v80C ![]() 7v81C ![]() 7v82C ![]() 7v83C ![]() 7v84C ![]() 7v85C ![]() 7v86C ![]() 7v87C ![]() 7v88C ![]() 7v89C ![]() 7v8aC ![]() 7v8bC ![]() 7v8cC M: atomic model generated by this map C: citing same article ( |
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| Similar structure data |
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Links
| EMDB pages | EMDB (EBI/PDBe) / EMDataResource |
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| Related items in Molecule of the Month |
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Map
| File | Download / File: emd_31768.map.gz / Format: CCP4 / Size: 216 MB / Type: IMAGE STORED AS FLOATING POINT NUMBER (4 BYTES) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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| Annotation | SARS-CoV-2 S-Kappa variant, one RBD-up (conformation 1), unsharpened map | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Projections & slices | Image control
Images are generated by Spider. | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Voxel size | X=Y=Z: 1.1 Å | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Density |
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| Symmetry | Space group: 1 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Details | EMDB XML:
CCP4 map header:
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-Supplemental data
-Additional map: SARS-CoV-2 S-Kappa variant, one RBD-up (conformation 1), sharpened...
| File | emd_31768_additional_1.map | ||||||||||||
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| Annotation | SARS-CoV-2 S-Kappa variant, one RBD-up (conformation 1), sharpened map | ||||||||||||
| Projections & Slices |
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| Density Histograms |
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Sample components
-Entire : SARS-CoV-2 spike glycoprotein
| Entire | Name: SARS-CoV-2 spike glycoprotein |
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| Components |
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-Supramolecule #1: SARS-CoV-2 spike glycoprotein
| Supramolecule | Name: SARS-CoV-2 spike glycoprotein / type: organelle_or_cellular_component / ID: 1 / Parent: 0 / Macromolecule list: #1 Details: Kappa variant (B.1.617.1), one RBD-up conformation 1 |
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| Source (natural) | Organism: ![]() |
| Molecular weight | Theoretical: 540 KDa |
-Macromolecule #1: Spike glycoprotein
| Macromolecule | Name: Spike glycoprotein / type: protein_or_peptide / ID: 1 / Details: Kappa variant (B.1.617.1) / Number of copies: 3 / Enantiomer: LEVO |
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| Source (natural) | Organism: ![]() |
| Molecular weight | Theoretical: 142.266422 KDa |
| Recombinant expression | Organism: Homo sapiens (human) |
| Sequence | String: MFVFLVLLPL VSSQCVNLTT RTQLPPAYTN SFTRGVYYPD KVFRSSVLHS TQDLFLPFFS NVTWFHAIHV SGTNGTKRFD NPVLPFNDG VYFASTEKSN IIRGWIFGTT LDSKTQSLLI VNNATNVVIK VCEFQFCNDP FLDVYYHKNN KSWMKSEFRV Y SSANNCTF ...String: MFVFLVLLPL VSSQCVNLTT RTQLPPAYTN SFTRGVYYPD KVFRSSVLHS TQDLFLPFFS NVTWFHAIHV SGTNGTKRFD NPVLPFNDG VYFASTEKSN IIRGWIFGTT LDSKTQSLLI VNNATNVVIK VCEFQFCNDP FLDVYYHKNN KSWMKSEFRV Y SSANNCTF EYVSQPFLMD LEGKQGNFKN LREFVFKNID GYFKIYSKHT PINLVRDLPQ GFSALEPLVD LPIGINITRF QT LLALHRS YLTPGDSSSG WTAGAAAYYV GYLQPRTFLL KYNENGTITD AVDCALDPLS ETKCTLKSFT VEKGIYQTSN FRV QPTESI VRFPNITNLC PFGEVFNATR FASVYAWNRK RISNCVADYS VLYNSASFST FKCYGVSPTK LNDLCFTNVY ADSF VIRGD EVRQIAPGQT GKIADYNYKL PDDFTGCVIA WNSNNLDSKV GGNYNYRYRL FRKSNLKPFE RDISTEIYQA GSTPC NGVQ GFNCYFPLQS YGFQPTNGVG YQPYRVVVLS FELLHAPATV CGPKKSTNLV KNKCVNFNFN GLTGTGVLTE SNKKFL PFQ QFGRDIADTT DAVRDPQTLE ILDITPCSFG GVSVITPGTN TSNQVAVLYQ GVNCTEVPVA IHADQLTPTW RVYSTGS NV FQTRAGCLIG AEHVNNSYEC DIPIGAGICA SYQTQTNSPG SASSVASQSI IAYTMSLGAE NSVAYSNNSI AIPTNFTI S VTTEILPVSM TKTSVDCTMY ICGDSTECSN LLLQYGSFCT QLNRALTGIA VEQDKNTQEV FAQVKQIYKT PPIKDFGGF NFSQILPDPS KPSKRSFIED LLFNKVTLAD AGFIKQYGDC LGDIAARDLI CAQKFNGLTV LPPLLTDEMI AQYTSALLAG TITSGWTFG AGAALQIPFA MQMAYRFNGI GVTQNVLYEN QKLIANQFNS AIGKIQDSLS STASALGKLQ DVVNQNAQAL N TLVKQLSS NFGAISSVLN DILSRLDPPE AEVQIDRLIT GRLQSLQTYV TQQLIRAAEI RASANLAATK MSECVLGQSK RV DFCGKGY HLMSFPQSAP HGVVFLHVTY VPAHEKNFTT APAICHDGKA HFPREGVFVS NGTDWFVTQR NFYEPQIITT DNT FVSGNC DVVIGIVNNT VYDPLQPELD SFKEELDKYF KNHTSPDVDL GDISGINASV VNIQKEIDRL NEVAKNLNES LIDL QELGK YEQEFGSGGY IPEAPRDGQA YVRKDGEWVL LSTFLKGQDN SADIQHSGRP LESRGPFEQK LISEEDLNMH TGHHH HHH UniProtKB: Spike glycoprotein |
-Macromolecule #3: 2-acetamido-2-deoxy-beta-D-glucopyranose
| Macromolecule | Name: 2-acetamido-2-deoxy-beta-D-glucopyranose / type: ligand / ID: 3 / Number of copies: 14 / 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 |
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Sample preparation
| Concentration | 1 mg/mL | ||||||||||||
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| Buffer | pH: 7.6 Component:
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| Vitrification | Cryogen name: ETHANE / Chamber humidity: 100 % / Chamber temperature: 277 K / Instrument: FEI VITROBOT MARK IV Details: blot for 2.5 seconds before plunging; blot force: 0; waiting time: 30s. |
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Electron microscopy
| Microscope | FEI TITAN KRIOS |
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| Image recording | Film or detector model: GATAN K3 (6k x 4k) / Average electron dose: 1.0 e/Å2 |
| Electron beam | Acceleration voltage: 300 kV / Electron source: FIELD EMISSION GUN |
| Electron optics | Illumination mode: FLOOD BEAM / Imaging mode: BRIGHT FIELD / Cs: 2.7 mm |
| Sample stage | Cooling holder cryogen: NITROGEN |
| Experimental equipment | ![]() Model: Titan Krios / Image courtesy: FEI Company |
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Image processing
| Startup model | Type of model: INSILICO MODEL Details: generated by ab-initio reconstruction in cryoSparc v2 |
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| Final reconstruction | Applied symmetry - Point group: C1 (asymmetric) / Resolution.type: BY AUTHOR / Resolution: 2.9 Å / Resolution method: FSC 0.143 CUT-OFF / Software - Name: cryoSPARC / Number images used: 160584 |
| Initial angle assignment | Type: RANDOM ASSIGNMENT / Software - Name: cryoSPARC |
| Final angle assignment | Type: ANGULAR RECONSTITUTION / Software - Name: cryoSPARC |
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Keywords
Authors
Taiwan, 4 items
Citation
UCSF Chimera




















































































Z (Sec.)
Y (Row.)
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Homo sapiens (human)

