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Open data
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Basic information
Entry | ![]() | |||||||||
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Title | MPXV DNA polymerase complex in editing state 2 | |||||||||
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![]() | complex / replicate / DNA / mpox / polymerase / REPLICATION/DNA / REPLICATION-DNA complex | |||||||||
Function / homology | ![]() uracil DNA N-glycosylase activity / viral DNA genome replication / DNA recombination / DNA-directed DNA polymerase / DNA-directed DNA polymerase activity / DNA replication / hydrolase activity / DNA repair / nucleotide binding / DNA binding Similarity search - Function | |||||||||
Biological species | ![]() | |||||||||
Method | single particle reconstruction / cryo EM / Resolution: 3.0 Å | |||||||||
![]() | Xie YF / Kuai L / Peng Q / Wang Q / Wang H / Li XM / Qi JX / Ding Q / Shi Y / Gao F | |||||||||
Funding support | ![]()
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![]() | ![]() Title: Structural basis of DNA replication fidelity of the Mpox virus. Authors: Yufeng Xie / Lu Kuai / Qi Peng / Qian Wang / Han Wang / Xiaomei Li / Jianxun Qi / Qiang Ding / Yi Shi / George F Gao / ![]() Abstract: The Mpox virus (MPXV) is an orthopoxvirus that caused a global outbreak in 2022. The poxvirus DNA polymerase complex is responsible for the replication and integrity of the viral genome; however, the ...The Mpox virus (MPXV) is an orthopoxvirus that caused a global outbreak in 2022. The poxvirus DNA polymerase complex is responsible for the replication and integrity of the viral genome; however, the molecular mechanisms underlying DNA replication fidelity are still unclear. In this study, we determined the cryoelectron microscopy (cryo-EM) structures of the MPXV F8-A22-E4 polymerase holoenzyme in its editing state, in complex with mismatched primer-template DNA and DNA containing uracil deoxynucleotide. We showed that the MPXV polymerase has a similar replication-to-edit transition mechanism to proofread the mismatched nucleotides like the B-family DNA polymerases of other species. The unique processivity cofactor A22-E4 undergoes conformational changes in different working states and might affect the proofreading process. Moreover, we elucidated the base excision repair (BER) function of E4 as a uracil-DNA glycosylase and the coupling mechanism of genome replication and BER, characteristic of poxviruses. Our findings greatly enhance our molecular understanding of DNA replication fidelity of orthopoxviruses and will stimulate the development of broad-spectrum antiviral drugs. | |||||||||
History |
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Structure visualization
Supplemental images |
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Downloads & links
-EMDB archive
Map data | ![]() | 110.7 MB | ![]() | |
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Header (meta data) | ![]() ![]() | 23.4 KB 23.4 KB | Display Display | ![]() |
Images | ![]() | 70 KB | ||
Filedesc metadata | ![]() | 7.8 KB | ||
Others | ![]() ![]() | 116.2 MB 116.2 MB | ||
Archive directory | ![]() ![]() | HTTPS FTP |
-Validation report
Summary document | ![]() | 725.5 KB | Display | ![]() |
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Full document | ![]() | 725 KB | Display | |
Data in XML | ![]() | 13.6 KB | Display | |
Data in CIF | ![]() | 16.2 KB | Display | |
Arichive directory | ![]() ![]() | HTTPS FTP |
-Related structure data
Related structure data | ![]() 9k9vMC ![]() 9k9rC ![]() 9k9sC ![]() 9k9tC ![]() 9k9uC 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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Related items in Molecule of the Month |
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Map
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Projections & slices | Image control
Images are generated by Spider. | ||||||||||||||||||||||||||||||||||||
Voxel size | X=Y=Z: 0.85 Å | ||||||||||||||||||||||||||||||||||||
Density |
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Symmetry | Space group: 1 | ||||||||||||||||||||||||||||||||||||
Details | EMDB XML:
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-Supplemental data
-Half map: #2
File | emd_62200_half_map_1.map | ||||||||||||
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Projections & Slices |
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Density Histograms |
-Half map: #1
File | emd_62200_half_map_2.map | ||||||||||||
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Density Histograms |
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Sample components
-Entire : MPXV DNA polymerase in complex with primer/4U template DNA
Entire | Name: MPXV DNA polymerase in complex with primer/4U template DNA |
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Components |
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-Supramolecule #1: MPXV DNA polymerase in complex with primer/4U template DNA
Supramolecule | Name: MPXV DNA polymerase in complex with primer/4U template DNA type: complex / ID: 1 / Parent: 0 / Macromolecule list: all |
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Source (natural) | Organism: ![]() |
-Macromolecule #1: DNA polymerase
Macromolecule | Name: DNA polymerase / type: protein_or_peptide / ID: 1 / Number of copies: 1 / Enantiomer: LEVO / EC number: DNA-directed DNA polymerase |
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Source (natural) | Organism: ![]() |
Molecular weight | Theoretical: 119.837016 KDa |
Recombinant expression | Organism: ![]() |
Sequence | String: MWSHPQFEKG SGSWSHPQFE KGSGSMDVRC INWFESHGEN RFLYLKSRCR NGETVFIRFP HYFYYVVTDE IYQSLSPPPF NARPMGKMR TIDIDETISY NLDIKDRKCS VADMWLIEEP KKRSIQNATM DEFFNISWFY ISNGISPDGC YSLDEQYLTK I NNGCYHCD ...String: MWSHPQFEKG SGSWSHPQFE KGSGSMDVRC INWFESHGEN RFLYLKSRCR NGETVFIRFP HYFYYVVTDE IYQSLSPPPF NARPMGKMR TIDIDETISY NLDIKDRKCS VADMWLIEEP KKRSIQNATM DEFFNISWFY ISNGISPDGC YSLDEQYLTK I NNGCYHCD DPRNCFAKEI PRFDIPRSYL FLAIACHFDK KFPSVFINPI SHTSYCYIDL SGKRLLFTLI NEEMLTEQEI QE AVDRGCL RIQSLMEMDY ERELVLCSEI VLLRIAKQLL ELTFDYVVTF NGHNFDLRYI TNRLELLTGE KIIFRSPDKK EAV HLCIYE RNQSSHKGVC GMANTTFHVN NNNGTIFFDL YSFIQKSEKL DSYKLDSISK NAFSCMGKVL NRGVREMTFI GDDT TDAKG KADTFAKVLT TGNYVTVDED IICKVIRKDI LENGFKVVLS CPTLPNDIYK LSFGKDDIDL AQMYKDYNLN IALDM ARYC IHDACLCQYL WEYYGVETKT DAGAATYVLP QSMVFEYRAS TIIKGPLLKL LLETKTILVR SETKQKFPYE GGKVFA PKQ KMFSNNVLIF DYNSLYPNVC IFGNLSPETL VGVVVSTNRL EEEINNQLLL QKYPPPRYIT VHCEPRLPNL ISEIAIF DR SIEGTIPRLL RTFLAERARY KKMLKQATSS TEKAIYDSMQ YTYKIVANSV YGLMGFRNSA LYSYASAKSC TSIGRRMI L YLESVLNGAE LSNGMLRFAN TLSNPFYMDD RDINPIVKTS LPIDYRFRFR SVYGDTDSVF TEIDSQDVDK SIEIAKELE RLINSRVLFN NFKIEFEAVY KNLIMQSKKK YTTMKYSASS NSKSVPERIN KGTSETRRDV SKFHKNMIKT YKTRLSEMLS EGRMNSNQV CIDILRSLET DLRSEFDSRS SPLELFMLSR MHHSNYKSAD NPNMYLVTEY NKNNPETIEL GERYYFAYIC P ANVPWTKK LVNIKTYETI IDRSFKLGSN QRIFYEVYFK RLTSEIVNLL DNKVLCISFF QRMFGSRPTF YEA UniProtKB: DNA polymerase |
-Macromolecule #2: Uracil-DNA glycosylase
Macromolecule | Name: Uracil-DNA glycosylase / type: protein_or_peptide / ID: 2 / Number of copies: 1 / Enantiomer: LEVO |
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Source (natural) | Organism: ![]() |
Molecular weight | Theoretical: 25.107742 KDa |
Recombinant expression | Organism: ![]() |
Sequence | String: MNSVTISHAP YTITYHDDWE PVMSQLVEFY NEVASWLLRD ETSPIPDKFF IQLKQPLRNK RVCVCGIDPY PKDGTGVPFE SPNFTKKSI KEIASSISRL TGVIDYKGYN LNIIDGVIPW NYYLSCKLGE TKSHAIYWDK ISKLLLQHIT KHVSVLYCLG K TDFSNIRA ...String: MNSVTISHAP YTITYHDDWE PVMSQLVEFY NEVASWLLRD ETSPIPDKFF IQLKQPLRNK RVCVCGIDPY PKDGTGVPFE SPNFTKKSI KEIASSISRL TGVIDYKGYN LNIIDGVIPW NYYLSCKLGE TKSHAIYWDK ISKLLLQHIT KHVSVLYCLG K TDFSNIRA KLESPVTTIV GYHPAARDHQ FEKDRSFEII NVLLELDNKT PINWAQGFIY UniProtKB: Uracil-DNA glycosylase |
-Macromolecule #3: DNA polymerase processivity factor
Macromolecule | Name: DNA polymerase processivity factor / type: protein_or_peptide / ID: 3 / Number of copies: 1 / Enantiomer: LEVO |
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Source (natural) | Organism: ![]() |
Molecular weight | Theoretical: 49.203926 KDa |
Recombinant expression | Organism: ![]() |
Sequence | String: MTSSADLTNL KELLSLYKSL RFSDSVAIEK YNSLVEWGTS TYWKIGVQKV TNVETSISDY YDEVKNKPFN IDPGYYIFLP VYFGSVFIY SKGKNMVELG SGNSFQIPDE IRSACNKVLD SDNGIDFLRF VLLNNRWIME DAISKYQSPV NIFKLASEYG L NIPNYLEI ...String: MTSSADLTNL KELLSLYKSL RFSDSVAIEK YNSLVEWGTS TYWKIGVQKV TNVETSISDY YDEVKNKPFN IDPGYYIFLP VYFGSVFIY SKGKNMVELG SGNSFQIPDE IRSACNKVLD SDNGIDFLRF VLLNNRWIME DAISKYQSPV NIFKLASEYG L NIPNYLEI EIEEDTLFDD ELYSIMERSF DDTFPKISIS YIKLGELKRQ VVDFFKFSFM YIESIKVDRI GDNIFIPSVI TK SGKKILV KDVDHLIRSK VREHTFVKVK KKNTFSILYD YDGNGTETRG EVIKRIIDTI GRDYYVNGKY FSKVGIAGLK QLT NKLDIN ECATVDELVD EINKSGTVKR KIKNQSVFDL SRECLGYPEA DFITLVNNMR FKIENCKVVN FNIENTNCLN NPSI ETIYG NFNQFVSIFN TVTDVKKRLF E UniProtKB: DNA polymerase processivity factor |
-Macromolecule #4: DNA (25-MER)
Macromolecule | Name: DNA (25-MER) / type: dna / ID: 4 / Number of copies: 1 / Classification: DNA |
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Source (natural) | Organism: ![]() |
Molecular weight | Theoretical: 7.696997 KDa |
Sequence | String: (DA)(DG)(DC)(DT)(DA)(DT)(DG)(DA)(DC)(DC) (DA)(DT)(DG)(DA)(DT)(DT)(DA)(DC)(DG)(DA) (DA)(DT)(DT)(DG)(DT) |
-Macromolecule #5: DNA (38-MER)
Macromolecule | Name: DNA (38-MER) / type: dna / ID: 5 / Number of copies: 1 / Classification: DNA |
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Source (natural) | Organism: ![]() |
Molecular weight | Theoretical: 11.677539 KDa |
Sequence | String: (DC)(DT)(DG)(DC)(DA)(DC)(DG)(DA)(DA)(DT) (DT)(DA)(DA)(DG)(DC)(DA)(DA)(DT)(DT)(DC) (DG)(DT)(DA)(DA)(DT)(DC)(DA)(DT)(DG) (DG)(DT)(DC)(DA)(DT)(DA)(DG)(DC)(DT) |
-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: 8 |
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Vitrification | Cryogen name: ETHANE |
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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: 50.0 e/Å2 |
Electron beam | Acceleration voltage: 300 kV / Electron source: ![]() |
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 |