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Open data
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Basic information
Entry | ![]() | |||||||||
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Title | Sarbecovirus GX2013 Spike Trimer in a Locked Conformation | |||||||||
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![]() | spike protein / VIRAL PROTEIN | |||||||||
Function / homology | ![]() host cell endoplasmic reticulum-Golgi intermediate compartment membrane / receptor-mediated virion attachment to host cell / 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 / host cell plasma membrane / virion membrane / membrane Similarity search - Function | |||||||||
Biological species | ![]() | |||||||||
Method | single particle reconstruction / cryo EM / Resolution: 3.3 Å | |||||||||
![]() | Wang J / Xiong X | |||||||||
Funding support | 2 items
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![]() | ![]() Title: SARS-related coronavirus S-protein structures reveal synergistic RBM interactions underpinning high-affinity human ACE2 binding. Authors: Jingjing Wang / Yong Ma / Zimu Li / Hang Yuan / Banghui Liu / Zexuan Li / Mengzhen Su / Gul Habib / Yutong Liu / Lutang Fu / Peiyi Wang / Mei Li / Jun He / Jing Chen / Peng Zhou / Zhengli ...Authors: Jingjing Wang / Yong Ma / Zimu Li / Hang Yuan / Banghui Liu / Zexuan Li / Mengzhen Su / Gul Habib / Yutong Liu / Lutang Fu / Peiyi Wang / Mei Li / Jun He / Jing Chen / Peng Zhou / Zhengli Shi / Xinwen Chen / Xiaoli Xiong / ![]() Abstract: High-affinity and specific binding toward the human angiotensin-converting enzyme 2 (hACE2) receptor by severe acute respiratory syndrome coronavirus (SARS)-related coronaviruses (SARSr-CoVs) remains ...High-affinity and specific binding toward the human angiotensin-converting enzyme 2 (hACE2) receptor by severe acute respiratory syndrome coronavirus (SARS)-related coronaviruses (SARSr-CoVs) remains incompletely understood. We report cryo-electron microscopy structures of eight different S-proteins from SARSr-CoVs found across Asia, Europe, and Africa. These S-proteins all adopt tightly packed, locked, prefusion conformations. These structures enable the classification of SARSr-CoV S-proteins into three types, based on their receptor-binding motif (RBM) structures and ACE2 binding characteristics. Type-2 S-proteins often preferentially bind bat ACE2 (bACE2) over hACE2. We report a structure of a type-2 BtKY72-RBD in complex with bACE2 to understand ACE2 specificity. Structure-guided mutagenesis of BtKY72-RBD reveals that multiple synergistic mutations in four different regions of RBM are required to achieve high-affinity hACE2 binding. Similar RBM changes can also confer hACE2 binding to another type-2 BM48-31 S-protein, which is primarily non-ACE2 binding. These results provide an understanding of how high-affinity hACE2 binding may be acquired by SARSr-CoV S-proteins. | |||||||||
History |
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Structure visualization
Supplemental images |
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Downloads & links
-EMDB archive
Map data | ![]() | 62.9 MB | ![]() | |
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Header (meta data) | ![]() ![]() | 20.2 KB 20.2 KB | Display Display | ![]() |
Images | ![]() | 67.9 KB | ||
Filedesc metadata | ![]() | 7.1 KB | ||
Others | ![]() ![]() | 116.2 MB 116.2 MB | ||
Archive directory | ![]() ![]() | HTTPS FTP |
-Related structure data
Related structure data | ![]() 8zy6MC ![]() 8zy0C ![]() 8zy1C ![]() 8zy2C ![]() 8zy3C ![]() 8zy4C ![]() 8zy5C ![]() 8zy7C ![]() 8zy9C ![]() 8zyaC M: atomic model generated by this map C: citing same article ( |
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Similar structure data | Similarity search - Function & homology ![]() |
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Links
EMDB pages | ![]() ![]() |
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Map
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Projections & slices | Image control
Images are generated by Spider. | ||||||||||||||||||||||||||||||||||||
Voxel size | X=Y=Z: 1.314 Å | ||||||||||||||||||||||||||||||||||||
Density |
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Symmetry | Space group: 1 | ||||||||||||||||||||||||||||||||||||
Details | EMDB XML:
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-Supplemental data
-Half map: #2
File | emd_60557_half_map_1.map | ||||||||||||
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Projections & Slices |
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Density Histograms |
-Half map: #1
File | emd_60557_half_map_2.map | ||||||||||||
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Projections & Slices |
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Density Histograms |
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Sample components
-Entire : the spike protein of GX2013
Entire | Name: the spike protein of GX2013 |
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Components |
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-Supramolecule #1: the spike protein of GX2013
Supramolecule | Name: the spike protein of GX2013 / type: organelle_or_cellular_component / ID: 1 / Parent: 0 / Macromolecule list: #1 |
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Source (natural) | Organism: ![]() |
-Macromolecule #1: Spike glycoprotein
Macromolecule | Name: Spike glycoprotein / type: protein_or_peptide / ID: 1 / Number of copies: 3 / Enantiomer: LEVO |
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Source (natural) | Organism: ![]() |
Molecular weight | Theoretical: 139.117812 KDa |
Recombinant expression | Organism: ![]() |
Sequence | String: MKILILAFLA SLAKAQEGCG IISRKPQPKM AQVSSSRRGV YYNDDIFRSD VLHLTQDYFL PFDSNLTQYF SLNVDSDRYT YFDNPILDF GDGVYFAATE KSNVIRGWIF GSSFDNTTQS AVIVNNSTHI IIRVCNFNLC KEPMYTVSRG TQQNSWVYQS A FNCTYDRV ...String: MKILILAFLA SLAKAQEGCG IISRKPQPKM AQVSSSRRGV YYNDDIFRSD VLHLTQDYFL PFDSNLTQYF SLNVDSDRYT YFDNPILDF GDGVYFAATE KSNVIRGWIF GSSFDNTTQS AVIVNNSTHI IIRVCNFNLC KEPMYTVSRG TQQNSWVYQS A FNCTYDRV EKSFQLDTAP KTGNFKDLRE YVFKNRDGFL SVYQTYTAVN LPRGLPQGFS VLRPILKLPF GINITSYRVV MA MFSQSTS NFLPESAAYY VGNLKYSTFM LSFNENGTIT DAIDCSQNPL AELKCTIKNF NVNKGIYQTS NFRVSPTQEV VRF PNITNR CPFDKVFNAT RFPNVYAWER TKISDCVADY TVLYNSTSFS TFKCYGVSPS KLIDLCFTSV YADTFLIRSS EVRQ VAPGE TGVIADYNYK LPDDFTGCVI AWNTAKQDTG NYYYRSHRKT KLKPFERDLS SDDGNGVYTL STYDFNPNVP VAYQA TRVV VLSFELLNAP ATVCGPKLST QLVKNQCVNF NFNGLKGTGV LTPSLKRFQS FQQFGRDTSD FTDSVRDPQT LEILDI SPC SFGGVSVITP GTNASSEVAV LYQDVNCTDV PTAIRADQLT PAWRVYSTGL NVFQTQAGCL IGAEHVNASY ECDIPIG AG ICASYHTASV LRSTGQKSIV AYTMSLGAEN SIAYANNSIA IPTNFSISVT TEVMPVSMAK TSVDCTMYIC GDSLECSN L LLQYGSFCTQ LNRALTGIAI EQDKNTQEVF AQVKQMYKTP AIKDFGGFNF SQILPDPSKP TKRSFIEDLL FNKVTLADA GFMKQYGECL GDISARDLIC AQKFNGLTVL PPLLTDEMIA AYTAALVSGT ATAGWTFGAG AALQIPFAMQ MAYRFNGIGV TQNVLYENQ KQIANQFNKA ISQIQESLTT TSTALGKLQD VVNQNAQALN TLVKQLSSNF GAISSVLNDI LSRLDKVEAE V QIDRLITG RLQSLQTYVT QQLIRAAEIR ASANLAATKM SECVLGQSKR VDFCGKGYHL MSFPQAAPHG VVFLHVTYVP SQ ERNFTTA PAICHEGKAY FPREGVFVSN GTSWFITQRN FYSPQLITTD NTFVSGNCDV VIGIINNTVY DPLQPELDSF KDE LDKYFK NHTSPDVDLG DISGINASVV NIQKEIDRLN EVAKNLNESL IDLQELGKYE QGSGYIPEAP RDGQAYVRKD GEWV LLSTF LLEVLFQGPG HHHHHHHHSA WSHPQFEKGG GSGGGGSGGS AWSHPQFEKS A 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: 39 / 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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![]() | single particle reconstruction |
Aggregation state | particle |
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Sample preparation
Buffer | pH: 7.4 Component:
Details: 137 mM NaCl, 2.7 mM KCl, 10 mM Na2HPO4, and 1.8 mM KH2PO4. | |||||||||||||||
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Vitrification | Cryogen name: ETHANE |
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Electron microscopy
Microscope | FEI TALOS ARCTICA |
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Image recording | Film or detector model: GATAN K3 (6k x 4k) / Average electron dose: 60.0 e/Å2 |
Electron beam | Acceleration voltage: 200 kV / Electron source: ![]() |
Electron optics | Illumination mode: FLOOD BEAM / Imaging mode: OTHER / Nominal defocus max: 2.5 µm / Nominal defocus min: 0.8 µm |
Experimental equipment | ![]() Model: Talos Arctica / Image courtesy: FEI Company |