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Open data
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Basic information
| Entry | Database: EMDB / ID: EMD-31546 | |||||||||
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| Title | SARS-COV-2 Spike RBDMACSp36 binding to mACE2 | |||||||||
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Keywords | SARS-COV-2 Spike / mACE2 / VIRAL PROTEIN | |||||||||
| Function / homology | Function and homology informationMetabolism of Angiotensinogen to Angiotensins / angiotensin-converting enzyme 2 / positive regulation of L-proline import across plasma membrane / Hydrolases; Acting on peptide bonds (peptidases); Metallocarboxypeptidases / angiotensin-mediated drinking behavior / positive regulation of gap junction assembly / tryptophan transport / regulation of cardiac conduction / maternal process involved in female pregnancy / peptidyl-dipeptidase activity ...Metabolism of Angiotensinogen to Angiotensins / angiotensin-converting enzyme 2 / positive regulation of L-proline import across plasma membrane / Hydrolases; Acting on peptide bonds (peptidases); Metallocarboxypeptidases / angiotensin-mediated drinking behavior / positive regulation of gap junction assembly / tryptophan transport / regulation of cardiac conduction / maternal process involved in female pregnancy / peptidyl-dipeptidase activity / transporter activator activity / carboxypeptidase activity / angiotensin maturation / metallocarboxypeptidase activity / positive regulation of cardiac muscle contraction / negative regulation of smooth muscle cell proliferation / brush border membrane / negative regulation of ERK1 and ERK2 cascade / virus receptor activity / endopeptidase activity / symbiont-mediated disruption of host tissue / Maturation of spike protein / Translation of Structural Proteins / Virion Assembly and Release / host cell surface / viral translation / host extracellular space / symbiont-mediated-mediated suppression of host tetherin activity / Induction of Cell-Cell Fusion / structural constituent of virion / membrane fusion / entry receptor-mediated virion attachment to host cell / 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 / cilium / symbiont-mediated suppression of host innate immune response / apical plasma membrane / 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 / cell surface / extracellular space / extracellular region / metal ion binding / identical protein binding / membrane / plasma membrane / cytoplasm Similarity search - Function | |||||||||
| Biological species | ![]() ![]() | |||||||||
| Method | single particle reconstruction / cryo EM / Resolution: 3.69 Å | |||||||||
Authors | Wang X / Cao L | |||||||||
Citation | Journal: Nat Commun / Year: 2021Title: Characterization and structural basis of a lethal mouse-adapted SARS-CoV-2. Authors: Shihui Sun / Hongjing Gu / Lei Cao / Qi Chen / Qing Ye / Guan Yang / Rui-Ting Li / Hang Fan / Yong-Qiang Deng / Xiaopeng Song / Yini Qi / Min Li / Jun Lan / Rui Feng / Yan Guo / Na Zhu / Si ...Authors: Shihui Sun / Hongjing Gu / Lei Cao / Qi Chen / Qing Ye / Guan Yang / Rui-Ting Li / Hang Fan / Yong-Qiang Deng / Xiaopeng Song / Yini Qi / Min Li / Jun Lan / Rui Feng / Yan Guo / Na Zhu / Si Qin / Lei Wang / Yi-Fei Zhang / Chao Zhou / Lingna Zhao / Yuehong Chen / Meng Shen / Yujun Cui / Xiao Yang / Xinquan Wang / Wenjie Tan / Hui Wang / Xiangxi Wang / Cheng-Feng Qin / ![]() Abstract: There is an urgent need for animal models to study SARS-CoV-2 pathogenicity. Here, we generate and characterize a novel mouse-adapted SARS-CoV-2 strain, MASCp36, that causes severe respiratory ...There is an urgent need for animal models to study SARS-CoV-2 pathogenicity. Here, we generate and characterize a novel mouse-adapted SARS-CoV-2 strain, MASCp36, that causes severe respiratory symptoms, and mortality. Our model exhibits age- and gender-related mortality akin to severe COVID-19. Deep sequencing identified three amino acid substitutions, N501Y, Q493H, and K417N, at the receptor binding domain (RBD) of MASCp36, during in vivo passaging. All three RBD mutations significantly enhance binding affinity to its endogenous receptor, ACE2. Cryo-electron microscopy analysis of human ACE2 (hACE2), or mouse ACE2 (mACE2), in complex with the RBD of MASCp36, at 3.1 to 3.7 Å resolution, reveals the molecular basis for the receptor-binding switch. N501Y and Q493H enhance the binding affinity to hACE2, whereas triple mutations at N501Y/Q493H/K417N decrease affinity and reduce infectivity of MASCp36. Our study provides a platform for studying SARS-CoV-2 pathogenesis, and unveils the molecular mechanism for its rapid adaptation and evolution. | |||||||||
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Structure visualization
| Movie |
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| Structure viewer | EM map: SurfView Molmil Jmol/JSmol |
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Downloads & links
-EMDB archive
| Map data | emd_31546.map.gz | 37.8 MB | EMDB map data format | |
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| Header (meta data) | emd-31546-v30.xml emd-31546.xml | 12 KB 12 KB | Display Display | EMDB header |
| Images | emd_31546.png | 55.5 KB | ||
| Filedesc metadata | emd-31546.cif.gz | 5.7 KB | ||
| Archive directory | http://ftp.pdbj.org/pub/emdb/structures/EMD-31546 ftp://ftp.pdbj.org/pub/emdb/structures/EMD-31546 | HTTPS FTP |
-Validation report
| Summary document | emd_31546_validation.pdf.gz | 538.6 KB | Display | EMDB validaton report |
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| Full document | emd_31546_full_validation.pdf.gz | 538.2 KB | Display | |
| Data in XML | emd_31546_validation.xml.gz | 5.7 KB | Display | |
| Data in CIF | emd_31546_validation.cif.gz | 6.6 KB | Display | |
| Arichive directory | https://ftp.pdbj.org/pub/emdb/validation_reports/EMD-31546 ftp://ftp.pdbj.org/pub/emdb/validation_reports/EMD-31546 | HTTPS FTP |
-Related structure data
| Related structure data | ![]() 7fdkMC ![]() 7fdgC ![]() 7fdhC ![]() 7fdiC 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_31546.map.gz / Format: CCP4 / Size: 40.6 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: 1.04 Å | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Density |
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| Symmetry | Space group: 1 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Details | EMDB XML:
CCP4 map header:
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-Supplemental data
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Sample components
-Entire : SARS-COV-2 Spike RBDMACSp36-mACE2
| Entire | Name: SARS-COV-2 Spike RBDMACSp36-mACE2 |
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| Components |
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-Supramolecule #1: SARS-COV-2 Spike RBDMACSp36-mACE2
| Supramolecule | Name: SARS-COV-2 Spike RBDMACSp36-mACE2 / type: complex / ID: 1 / Parent: 0 / Macromolecule list: #1-#2 |
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| Source (natural) | Organism: ![]() |
-Macromolecule #1: Angiotensin-converting enzyme 2
| Macromolecule | Name: Angiotensin-converting enzyme 2 / type: protein_or_peptide / ID: 1 / Number of copies: 1 / Enantiomer: LEVO / EC number: angiotensin-converting enzyme 2 |
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| Source (natural) | Organism: ![]() |
| Molecular weight | Theoretical: 71.70843 KDa |
| Recombinant expression | Organism: Homo sapiens (human) |
| Sequence | String: MSSSSWLLLS LVAVTAAQSL TEENAKTFLN NFNQEAEDLS YQSSLASWNY NTNITEENAQ KMSEAAAKWS AFYEEQSKTA QSFSLQEIQ TPIIKRQLQA LQQSGSSALS ADKNKQLNTI LNTMSTIYST GKVCNPKNPQ ECLLLEPGLD EIMATSTDYN S RLWAWEGW ...String: MSSSSWLLLS LVAVTAAQSL TEENAKTFLN NFNQEAEDLS YQSSLASWNY NTNITEENAQ KMSEAAAKWS AFYEEQSKTA QSFSLQEIQ TPIIKRQLQA LQQSGSSALS ADKNKQLNTI LNTMSTIYST GKVCNPKNPQ ECLLLEPGLD EIMATSTDYN S RLWAWEGW RAEVGKQLRP LYEEYVVLKN EMARANNYND YGDYWRGDYE AEGADGYNYN RGQLIEDVEH TFAEIKPLYE HL HAYVRRK LMDTYPSYIS PTGCLPAHLL GDMWGRFWTN LYPLTVPFAQ KPNIDVTDAM MNQGWDAERI FKEAEKFFVS VGL PHMTQG FWANSMLTDE ADGRKVVCHP TAWDLGHGDF RIKMCTKVTM DNFLTAHHEM GHIQYDMAYA RQPFLLRNGA NEGF HEAVG EIMSLSAATP KHLKSIGLLP SDFQEDSETE INFLLKQALT IVGTLPFTYM LEKWRWMVFR GEIPKEQWMK KWWEM KREI VGVVEPLPHD ETYCDPASLF HVSNDYSFIR YYTRTIYQFQ FQEALCQAAK YNGSLHKCDI SNSTEAGQKL LKMLSL GNS EPWTKALENV VGARNMDVKP LLNYFQPLFD WLKEQNRNSF VGWNTEWSPY ADHHHHHH UniProtKB: Angiotensin-converting enzyme 2 |
-Macromolecule #2: Spike protein S1
| Macromolecule | Name: Spike protein S1 / type: protein_or_peptide / ID: 2 / Number of copies: 1 / Enantiomer: LEVO |
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| Source (natural) | Organism: ![]() |
| Molecular weight | Theoretical: 24.096109 KDa |
| Recombinant expression | Organism: Homo sapiens (human) |
| Sequence | String: MFVFLVLLPL VSSTNLCPFG EVFNATRFAS VYAWNRKRIS NCVADYSVLY NSASFSTFKC YGVSPTKLND LCFTNVYADS FVIRGDEVR QIAPGQTGNI ADYNYKLPDD FTGCVIAWNS NNLDSKVGGN YNYLYRLFRK SNLKPFERDI STEIYQAGST P CNGVEGFN ...String: MFVFLVLLPL VSSTNLCPFG EVFNATRFAS VYAWNRKRIS NCVADYSVLY NSASFSTFKC YGVSPTKLND LCFTNVYADS FVIRGDEVR QIAPGQTGNI ADYNYKLPDD FTGCVIAWNS NNLDSKVGGN YNYLYRLFRK SNLKPFERDI STEIYQAGST P CNGVEGFN CYFPLHSYGF QPTYGVGYQP YRVVVLSFEL LHAPATVCGH HHHHH 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: 3 / 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
| Buffer | pH: 7.5 |
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| Vitrification | Cryogen name: ETHANE |
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Electron microscopy
| Microscope | FEI TITAN |
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| Image recording | Film or detector model: GATAN K2 BASE (4k x 4k) / Average electron dose: 60.0 e/Å2 |
| Electron beam | Acceleration voltage: 300 kV / Electron source: FIELD EMISSION GUN |
| Electron optics | Illumination mode: FLOOD BEAM / Imaging mode: BRIGHT FIELD |
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Image processing
| Startup model | Type of model: RANDOM CONICAL TILT |
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| Final reconstruction | Resolution.type: BY AUTHOR / Resolution: 3.69 Å / Resolution method: FSC 0.143 CUT-OFF / Number images used: 162615 |
| Initial angle assignment | Type: ANGULAR RECONSTITUTION |
| Final angle assignment | Type: RANDOM ASSIGNMENT |
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Homo sapiens (human)
