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Open data
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Basic information
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| Title | MERSmut-CoV M protein dimer in complex with FAb B | |||||||||
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Sample |
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Keywords | M protein / SARS-CoV-2 / inhibitor bound complex / viral protein / MEMBRANE PROTEIN-IMMUNE SYSTEM-INHIBITOR complex | |||||||||
| Function / homology | Function and homology informationhost cell Golgi membrane / structural constituent of virion / viral envelope / virion membrane / membrane Similarity search - Function | |||||||||
| Biological species | Homo sapiens (human) / ![]() | |||||||||
| Method | single particle reconstruction / cryo EM / Resolution: 3.15 Å | |||||||||
Authors | Mann MK / Abeywickrema P | |||||||||
| Funding support | United States, 1 items
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Citation | Journal: Commun Biol / Year: 2025Title: Structural insights into MERS and SARS coronavirus membrane proteins. Authors: Mandeep Kaur Mann / Yanting Yin / Simone Marsili / Jiexiong Xie / Jordi Doijen / Robyn Miller / Madison Piassek / Nick van den Broeck / Christopher Kinyanjui Kariuki / Heidi L M de Gruyter / ...Authors: Mandeep Kaur Mann / Yanting Yin / Simone Marsili / Jiexiong Xie / Jordi Doijen / Robyn Miller / Madison Piassek / Nick van den Broeck / Christopher Kinyanjui Kariuki / Heidi L M de Gruyter / Anouk A Leijs / Eric J Snijder / Martijn J van Hemert / Ken Keustermans / Michiel Van Gool / Xiaodi Yu / Marnix van Loock / Anil Koul / Sujata Sharma / Ellen Van Damme / Pravien Abeywickrema / ![]() Abstract: The membrane (M) protein of coronaviruses is essential for maintaining structural integrity during membrane virion budding and viral pathogenesis. Given its high conservation in lineages within the ...The membrane (M) protein of coronaviruses is essential for maintaining structural integrity during membrane virion budding and viral pathogenesis. Given its high conservation in lineages within the betacoronavirus genus, such as sarbecoviruses, the M protein presents as an attractive therapeutic target; however, developing broad-spectrum antivirals targeting coronaviruses such as MERS-CoV is challenging due to lower sequence conservation and limited structural information available beyond that of the SARS-CoV-2 M protein. In this study, we report 3-3.2 Å resolution structures of MERS-CoV M protein, engineered with a SARS-CoV-2-like antibody interface, representing the first human merbecovirus M protein structure, and SARS-CoV M protein structures, with and without a previously identified SARS-CoV-2 M protein inhibitor, JNJ-9676. We highlight the structural differences between the MERS-CoV, SARS-CoV and SARS-CoV-2 M proteins, and present insights into the conservation of the JNJ-9676 binding pocket as well as key differences that could be targeted to accelerate the design of specific MERS-CoV and broad-spectrum antivirals targeting coronavirus M proteins. | |||||||||
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Structure visualization
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Downloads & links
-EMDB archive
| Map data | emd_49951.map.gz | 85.7 MB | EMDB map data format | |
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| Header (meta data) | emd-49951-v30.xml emd-49951.xml | 20.3 KB 20.3 KB | Display Display | EMDB header |
| Images | emd_49951.png | 44.5 KB | ||
| Filedesc metadata | emd-49951.cif.gz | 6.3 KB | ||
| Others | emd_49951_half_map_1.map.gz emd_49951_half_map_2.map.gz | 84.6 MB 84.6 MB | ||
| Archive directory | http://ftp.pdbj.org/pub/emdb/structures/EMD-49951 ftp://ftp.pdbj.org/pub/emdb/structures/EMD-49951 | HTTPS FTP |
-Related structure data
| Related structure data | ![]() 9nz5MC ![]() 9nz3C ![]() 9nz4C M: atomic model generated by this map C: citing same article ( |
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| Similar structure data | Similarity search - Function & homology F&H Search |
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Links
| EMDB pages | EMDB (EBI/PDBe) / EMDataResource |
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Map
| File | Download / File: emd_49951.map.gz / Format: CCP4 / Size: 91.1 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: 0.837 Å | ||||||||||||||||||||||||||||||||||||
| Density |
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| Symmetry | Space group: 1 | ||||||||||||||||||||||||||||||||||||
| Details | EMDB XML:
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-Supplemental data
-Half map: #2
| File | emd_49951_half_map_1.map | ||||||||||||
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| Projections & Slices |
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| Density Histograms |
-Half map: #1
| File | emd_49951_half_map_2.map | ||||||||||||
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| Projections & Slices |
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| Density Histograms |
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Sample components
-Entire : MERSmut-CoV M protein dimer in complex with FAb B
| Entire | Name: MERSmut-CoV M protein dimer in complex with FAb B |
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| Components |
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-Supramolecule #1: MERSmut-CoV M protein dimer in complex with FAb B
| Supramolecule | Name: MERSmut-CoV M protein dimer in complex with FAb B / type: complex / ID: 1 / Parent: 0 / Macromolecule list: all |
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| Source (natural) | Organism: Homo sapiens (human) |
-Macromolecule #1: Membrane protein
| Macromolecule | Name: Membrane protein / type: protein_or_peptide / ID: 1 / Number of copies: 2 / Enantiomer: LEVO |
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| Source (natural) | Organism: ![]() |
| Molecular weight | Theoretical: 29.542191 KDa |
| Recombinant expression | Organism: Mammalian expression vector Flag-MCS-pcDNA3.1 (others) |
| Sequence | String: MSNMTQLTEA QIIAIIKDWN FAWSLIFLLI TIVLQYGYPS RSMTVYVFKM FVLWLLWPSS MALSIFSAVY PIDLASQIIS GIVAAVSAM MWISYFVQSI RLFMRTGSWW SFNPETNCLL NVPFGGTIVV RPLVEDSTSV TAVVTRGHLK MAGMHFGACD Y DRLPKEVT ...String: MSNMTQLTEA QIIAIIKDWN FAWSLIFLLI TIVLQYGYPS RSMTVYVFKM FVLWLLWPSS MALSIFSAVY PIDLASQIIS GIVAAVSAM MWISYFVQSI RLFMRTGSWW SFNPETNCLL NVPFGGTIVV RPLVEDSTSV TAVVTRGHLK MAGMHFGACD Y DRLPKEVT VAKPNVLIYL KMVKRQSYGT NSGVAIYSRY RIGNYRSPPI TADIELALLR ASNSLEVLFQ GPSRGGSGAA AG SGSGSGS PSRLEEELRR RLTEGSEPEA UniProtKB: Membrane protein |
-Macromolecule #2: FAb B light chain
| Macromolecule | Name: FAb B light chain / type: protein_or_peptide / ID: 2 / Number of copies: 2 / Enantiomer: LEVO |
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| Source (natural) | Organism: Homo sapiens (human) |
| Molecular weight | Theoretical: 24.157424 KDa |
| Recombinant expression | Organism: Mammalian expression vector Flag-MCS-pcDNA3.1 (others) |
| Sequence | String: ASDIVMTQSP ASLAVSLGQR ATISCKASQS IDYDGDNYMN WYQQKPGQPP KLLIYTTSNL ESGIPARFSG SGSGTDFTLN IHPVEEGDA ATYYCQQNNE DPYTFGGGTK LEIKRADAAP TVSIFPPSSE QLTSGGASVV CFLNNFYPKD INVKWKIDGS E RQNGVLNS ...String: ASDIVMTQSP ASLAVSLGQR ATISCKASQS IDYDGDNYMN WYQQKPGQPP KLLIYTTSNL ESGIPARFSG SGSGTDFTLN IHPVEEGDA ATYYCQQNNE DPYTFGGGTK LEIKRADAAP TVSIFPPSSE QLTSGGASVV CFLNNFYPKD INVKWKIDGS E RQNGVLNS WTDQDSKDST YSMSSTLTLT KDEYERHNSY TCEATHKTST SPIVKSFNRN EC |
-Macromolecule #3: FAb B heavy chain
| Macromolecule | Name: FAb B heavy chain / type: protein_or_peptide / ID: 3 / Number of copies: 2 / Enantiomer: LEVO |
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| Source (natural) | Organism: Homo sapiens (human) |
| Molecular weight | Theoretical: 24.211092 KDa |
| Recombinant expression | Organism: Mammalian expression vector Flag-MCS-pcDNA3.1 (others) |
| Sequence | String: EVQLQQSGPE LVKPGASMKI SCKTSGYSFT GYTMNWVKQS HGKNLEWIGL INPYNGDTSY NQKFKGKATL TVDKSSSTAY MELLSLTSE DSAVYYCEVI NTYWGQGTLV TVSAAKTTPP SVYPLAPGSA AQTNSMVTLG CLVKGYFPEP VTVTWNSGSL S SGVHTFPA ...String: EVQLQQSGPE LVKPGASMKI SCKTSGYSFT GYTMNWVKQS HGKNLEWIGL INPYNGDTSY NQKFKGKATL TVDKSSSTAY MELLSLTSE DSAVYYCEVI NTYWGQGTLV TVSAAKTTPP SVYPLAPGSA AQTNSMVTLG CLVKGYFPEP VTVTWNSGSL S SGVHTFPA VLQSDLYTLS SSVTVPSSTW PSETVTCNVA HPASSTKVDK KIVPRDCGSG SHHHHHH |
-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: NITROGEN |
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Electron microscopy
| Microscope | TFS KRIOS |
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| Image recording | Film or detector model: GATAN K3 (6k x 4k) / Average electron dose: 51.96 e/Å2 |
| Electron beam | Acceleration voltage: 300 kV / Electron source: FIELD EMISSION GUN |
| Electron optics | Illumination mode: FLOOD BEAM / Imaging mode: DIFFRACTION / Nominal defocus max: 2.3000000000000003 µm / Nominal defocus min: 1.4000000000000001 µm |
| Experimental equipment | ![]() Model: Titan Krios / Image courtesy: FEI Company |
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About Yorodumi




Keywords
Homo sapiens (human)
Authors
United States, 1 items
Citation






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Y (Row.)
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Processing
FIELD EMISSION GUN

