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Yorodumi- EMDB-38396: The Cryo-EM structure of MPXV E5 C-terminal in complex with DNA -
+Open data
-Basic information
Entry | Database: EMDB / ID: EMD-38396 | |||||||||
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Title | The Cryo-EM structure of MPXV E5 C-terminal in complex with DNA | |||||||||
Map data | ||||||||||
Sample |
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Keywords | helicase / REPLICATION | |||||||||
Function / homology | Function and homology information helicase activity / Hydrolases; Acting on acid anhydrides; Acting on acid anhydrides to facilitate cellular and subcellular movement / host cell cytoplasm / hydrolase activity / ATP binding Similarity search - Function | |||||||||
Biological species | Monkeypox virus | |||||||||
Method | single particle reconstruction / cryo EM / Resolution: 2.67 Å | |||||||||
Authors | Zhang W / Liu Y / Gao H / Gan J | |||||||||
Funding support | China, 1 items
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Citation | Journal: Cell Discov / Year: 2024 Title: Structural and functional insights into the helicase protein E5 of Mpox virus. Authors: Weizhen Zhang / Yusong Liu / Mengquan Yang / Jie Yang / Zhiwei Shao / Yanqing Gao / Xinran Jiang / Ruixue Cui / Yixi Zhang / Xin Zhao / Qiyuan Shao / Chulei Cao / Huili Li / Linxi Li / Hehua ...Authors: Weizhen Zhang / Yusong Liu / Mengquan Yang / Jie Yang / Zhiwei Shao / Yanqing Gao / Xinran Jiang / Ruixue Cui / Yixi Zhang / Xin Zhao / Qiyuan Shao / Chulei Cao / Huili Li / Linxi Li / Hehua Liu / Haishan Gao / Jianhua Gan / Abstract: Mpox virus (MPXV) can cause mpox in humans. Due to its quick and wide spread in the past two years, mpox has turned into a significant public health concern. Helicase E5 is a multi-domain protein; ...Mpox virus (MPXV) can cause mpox in humans. Due to its quick and wide spread in the past two years, mpox has turned into a significant public health concern. Helicase E5 is a multi-domain protein; its primer synthesis and DNA unwinding activity are required for genome uncoating and DNA replication of MPXV. However, the in vitro DNA unwinding activity has never been demonstrated. Here, we report the structural and biochemical studies of MPXV E5, showing that the full-length protein adopts an auto-inhibited conformation. Truncation of the N-terminus can recover the in vitro unwinding activity of E5 towards the forked DNA. Further structural analysis reveals that MPXV E5 shares a conserved mechanism in DNA unwinding and primer synthesis with the homologous proteins. These findings not only advance our understanding on the function of MPXV E5, but also provide a solid basis for the development of anti-poxvirus drugs. | |||||||||
History |
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-Structure visualization
Supplemental images |
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-Downloads & links
-EMDB archive
Map data | emd_38396.map.gz | 79 MB | EMDB map data format | |
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Header (meta data) | emd-38396-v30.xml emd-38396.xml | 15.5 KB 15.5 KB | Display Display | EMDB header |
FSC (resolution estimation) | emd_38396_fsc.xml | 9.2 KB | Display | FSC data file |
Images | emd_38396.png | 26.3 KB | ||
Filedesc metadata | emd-38396.cif.gz | 5.8 KB | ||
Others | emd_38396_half_map_1.map.gz emd_38396_half_map_2.map.gz | 77.6 MB 77.6 MB | ||
Archive directory | http://ftp.pdbj.org/pub/emdb/structures/EMD-38396 ftp://ftp.pdbj.org/pub/emdb/structures/EMD-38396 | HTTPS FTP |
-Validation report
Summary document | emd_38396_validation.pdf.gz | 919 KB | Display | EMDB validaton report |
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Full document | emd_38396_full_validation.pdf.gz | 918.6 KB | Display | |
Data in XML | emd_38396_validation.xml.gz | 17.5 KB | Display | |
Data in CIF | emd_38396_validation.cif.gz | 22.4 KB | Display | |
Arichive directory | https://ftp.pdbj.org/pub/emdb/validation_reports/EMD-38396 ftp://ftp.pdbj.org/pub/emdb/validation_reports/EMD-38396 | HTTPS FTP |
-Related structure data
Related structure data | 8xj8MC 8xifC 8xigC 8xj6C 8xj7C 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_38396.map.gz / Format: CCP4 / Size: 83.7 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: 1.081 Å | ||||||||||||||||||||||||||||||||||||
Density |
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Symmetry | Space group: 1 | ||||||||||||||||||||||||||||||||||||
Details | EMDB XML:
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-Supplemental data
-Half map: #2
File | emd_38396_half_map_1.map | ||||||||||||
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Projections & Slices |
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Density Histograms |
-Half map: #1
File | emd_38396_half_map_2.map | ||||||||||||
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Projections & Slices |
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Density Histograms |
-Sample components
-Entire : Monkeypox virus
Entire | Name: Monkeypox virus |
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Components |
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-Supramolecule #1: Monkeypox virus
Supramolecule | Name: Monkeypox virus / type: virus / ID: 1 / Parent: 0 / Macromolecule list: #1-#2 / NCBI-ID: 10244 / Sci species name: Monkeypox virus / Virus type: VIRION / Virus isolate: SPECIES / Virus enveloped: Yes / Virus empty: Yes |
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-Macromolecule #1: DNA (70-MER)
Macromolecule | Name: DNA (70-MER) / type: dna / ID: 1 / Number of copies: 1 / Classification: DNA |
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Source (natural) | Organism: Monkeypox virus |
Molecular weight | Theoretical: 21.440668 KDa |
Sequence | String: (DA)(DA)(DC)(DG)(DA)(DG)(DT)(DC)(DA)(DA) (DG)(DC)(DG)(DC)(DA)(DT)(DC)(DC)(DC)(DG) (DT)(DT)(DT)(DT)(DT)(DT)(DT)(DT)(DT) (DT)(DT)(DT)(DT)(DT)(DT)(DT)(DT)(DT)(DT) (DT) (DT)(DT)(DT)(DT)(DT)(DT) ...String: (DA)(DA)(DC)(DG)(DA)(DG)(DT)(DC)(DA)(DA) (DG)(DC)(DG)(DC)(DA)(DT)(DC)(DC)(DC)(DG) (DT)(DT)(DT)(DT)(DT)(DT)(DT)(DT)(DT) (DT)(DT)(DT)(DT)(DT)(DT)(DT)(DT)(DT)(DT) (DT) (DT)(DT)(DT)(DT)(DT)(DT)(DT)(DT) (DT)(DT)(DC)(DG)(DG)(DG)(DA)(DT)(DG)(DC) (DG)(DC) (DT)(DT)(DG)(DA)(DC)(DT)(DC) (DG)(DT)(DT) |
-Macromolecule #2: Monkeypox virus E5
Macromolecule | Name: Monkeypox virus E5 / type: protein_or_peptide / ID: 2 / Number of copies: 6 / Enantiomer: LEVO EC number: Hydrolases; Acting on acid anhydrides; Acting on acid anhydrides to facilitate cellular and subcellular movement |
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Source (natural) | Organism: Monkeypox virus |
Molecular weight | Theoretical: 53.282012 KDa |
Recombinant expression | Organism: Escherichia coli (E. coli) |
Sequence | String: GNKLFNIAQR ILDTNSVLLT ERGDHIVWIN NSWKFNSEEP LITKLILSIR HQLPKEYSSE LLCPRKRKTV EANIRDMLVD SVETDTYPD KLPFKNGVLD LVDGMFYSGD DAKKYTCTVS TGFKFDDTKF VEDSPEMEEL MNIINDIQPL TDENKKNREL Y EKTLSSCL ...String: GNKLFNIAQR ILDTNSVLLT ERGDHIVWIN NSWKFNSEEP LITKLILSIR HQLPKEYSSE LLCPRKRKTV EANIRDMLVD SVETDTYPD KLPFKNGVLD LVDGMFYSGD DAKKYTCTVS TGFKFDDTKF VEDSPEMEEL MNIINDIQPL TDENKKNREL Y EKTLSSCL CGATKGCLTF FFGETATGKS TTKRLLKSAI GDLFVETGQT ILTDVLDKGP NPFIANMHLK RSVFCSELPD FA CSGSKKI RSDNIKKLTE PCVIGRPCFS NKINNRNHAT IIIDTNYKPV FDRIDNALMR RIAVVRFRTH FSQPSGREAA ENN DAYDKV KLLDEGLDGK IQNNRYRFAF LYLLVKWYKK YHIPIMKLYP TPEEIPDFAF YLKIGTLLVS SSVKHIPLMT DLSK KGYIL YDNVVTLPLT TFQQKISKYF NSRLFGHDIE SFINRHKKFA NVSDEYLQYI FIEDISSP UniProtKB: Uncoating factor OPG117 |
-Macromolecule #3: PHOSPHOAMINOPHOSPHONIC ACID-ADENYLATE ESTER
Macromolecule | Name: PHOSPHOAMINOPHOSPHONIC ACID-ADENYLATE ESTER / type: ligand / ID: 3 / Number of copies: 3 / Formula: ANP |
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Molecular weight | Theoretical: 506.196 Da |
Chemical component information | ChemComp-ANP: |
-Macromolecule #4: MAGNESIUM ION
Macromolecule | Name: MAGNESIUM ION / type: ligand / ID: 4 / Number of copies: 3 / Formula: MG |
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Molecular weight | Theoretical: 24.305 Da |
-Experimental details
-Structure determination
Method | cryo EM |
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Processing | single particle reconstruction |
Aggregation state | particle |
-Sample preparation
Buffer | pH: 8 |
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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 (6k x 4k) / Average electron dose: 50.0 e/Å2 |
Electron beam | Acceleration voltage: 300 kV / Electron source: FIELD EMISSION GUN |
Electron optics | Illumination mode: FLOOD BEAM / Imaging mode: BRIGHT FIELD / Nominal defocus max: 2.0 µm / Nominal defocus min: 1.0 µm |
Experimental equipment | Model: Titan Krios / Image courtesy: FEI Company |