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Yorodumi- EMDB-0388: Structure of bacteriophage T7 lagging-strand DNA polymerase (D5A/... -
+Open data
-Basic information
Entry | Database: EMDB / ID: EMD-0388 | |||||||||
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Title | Structure of bacteriophage T7 lagging-strand DNA polymerase (D5A/E7A)/Trx interacting with primase domains of two gp4 subunits (C and D), with gp4 helicase bound to a DNA fork and dTTP (LagL2) | |||||||||
Map data | T7 DNA polymerase/Trx interacting with two primase domains (C and D) of T7 helicase (gp4) in complex with a fork DNA substrate and dTTP (from gp4-gp5 lagging-strand complex LagL2) | |||||||||
Sample |
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Biological species | Enterobacteria phage T7 (virus) / Escherichia coli (E. coli) | |||||||||
Method | single particle reconstruction / cryo EM / Resolution: 7.1 Å | |||||||||
Authors | Gao Y / Fox T / Val N / Yang W | |||||||||
Citation | Journal: Science / Year: 2019 Title: Structures and operating principles of the replisome. Authors: Yang Gao / Yanxiang Cui / Tara Fox / Shiqiang Lin / Huaibin Wang / Natalia de Val / Z Hong Zhou / Wei Yang / Abstract: Visualization in atomic detail of the replisome that performs concerted leading- and lagging-DNA strand synthesis at a replication fork has not been reported. Using bacteriophage T7 as a model ...Visualization in atomic detail of the replisome that performs concerted leading- and lagging-DNA strand synthesis at a replication fork has not been reported. Using bacteriophage T7 as a model system, we determined cryo-electron microscopy structures up to 3.2-angstroms resolution of helicase translocating along DNA and of helicase-polymerase-primase complexes engaging in synthesis of both DNA strands. Each domain of the spiral-shaped hexameric helicase translocates sequentially hand-over-hand along a single-stranded DNA coil, akin to the way AAA+ ATPases (adenosine triphosphatases) unfold peptides. Two lagging-strand polymerases are attached to the primase, ready for Okazaki fragment synthesis in tandem. A β hairpin from the leading-strand polymerase separates two parental DNA strands into a T-shaped fork, thus enabling the closely coupled helicase to advance perpendicular to the downstream DNA duplex. These structures reveal the molecular organization and operating principles of a replisome. | |||||||||
History |
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-Structure visualization
Movie |
Movie viewer |
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Structure viewer | EM map: SurfViewMolmilJmol/JSmol |
Supplemental images |
-Downloads & links
-EMDB archive
Map data | emd_0388.map.gz | 4.1 MB | EMDB map data format | |
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Header (meta data) | emd-0388-v30.xml emd-0388.xml | 18 KB 18 KB | Display Display | EMDB header |
FSC (resolution estimation) | emd_0388_fsc.xml | 8.6 KB | Display | FSC data file |
Images | emd_0388.png | 116.1 KB | ||
Archive directory | http://ftp.pdbj.org/pub/emdb/structures/EMD-0388 ftp://ftp.pdbj.org/pub/emdb/structures/EMD-0388 | HTTPS FTP |
-Validation report
Summary document | emd_0388_validation.pdf.gz | 78.3 KB | Display | EMDB validaton report |
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Full document | emd_0388_full_validation.pdf.gz | 77.4 KB | Display | |
Data in XML | emd_0388_validation.xml.gz | 493 B | Display | |
Arichive directory | https://ftp.pdbj.org/pub/emdb/validation_reports/EMD-0388 ftp://ftp.pdbj.org/pub/emdb/validation_reports/EMD-0388 | HTTPS FTP |
-Related structure data
Related structure data | 0357C 0359C 0362C 0363C 0364C 0365C 0379C 0380C 0381C 0382C 0386C 0387C 0389C 0390C 0391C 0392C 0393C 0394C 0395C 6n7iC 6n7nC 6n7sC 6n7tC 6n7vC 6n7wC 6n9uC 6n9vC 6n9wC 6n9xC C: citing same article (ref.) |
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Similar structure data |
-Links
EMDB pages | EMDB (EBI/PDBe) / EMDataResource |
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-Map
File | Download / File: emd_0388.map.gz / Format: CCP4 / Size: 52.7 MB / Type: IMAGE STORED AS FLOATING POINT NUMBER (4 BYTES) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Annotation | T7 DNA polymerase/Trx interacting with two primase domains (C and D) of T7 helicase (gp4) in complex with a fork DNA substrate and dTTP (from gp4-gp5 lagging-strand complex LagL2) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Projections & slices | Image control
Images are generated by Spider. | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Voxel size | X=Y=Z: 1.72 Å | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Density |
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Symmetry | Space group: 1 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Details | EMDB XML:
CCP4 map header:
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-Supplemental data
-Sample components
-Entire : T7 DNA polymerase/Trx interacting with two primase domains (C and...
Entire | Name: T7 DNA polymerase/Trx interacting with two primase domains (C and D) of T7 helicase (gp4) in complex with a fork DNA substrate and dTTP (from gp4-gp5 lagging-strand complex LagL2) |
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Components |
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-Supramolecule #1: T7 DNA polymerase/Trx interacting with two primase domains (C and...
Supramolecule | Name: T7 DNA polymerase/Trx interacting with two primase domains (C and D) of T7 helicase (gp4) in complex with a fork DNA substrate and dTTP (from gp4-gp5 lagging-strand complex LagL2) type: complex / ID: 1 / Parent: 0 / Macromolecule list: all |
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Source (natural) | Organism: Enterobacteria phage T7 (virus) |
Recombinant expression | Organism: Escherichia coli (E. coli) |
-Macromolecule #1: gene product 4 helicase-primase
Macromolecule | Name: gene product 4 helicase-primase / type: protein_or_peptide / ID: 1 / Enantiomer: LEVO |
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Source (natural) | Organism: Enterobacteria phage T7 (virus) |
Sequence | String: MDNSHDSDSV FLYHIPCDNC GSSDGNSLFS DGHTFCYVCE KWTAGNEDTK ERASKRKPSG GKPMTYNVW NFGESNGRYS ALTARGISKE TCQKAGYWIA KVDGVMYQVA DYRDQNGNIV S QKVRDKDK NFKTTGSHKS DALFGKHLWN GGKKIVVTEG EIDMLTVMEL ...String: MDNSHDSDSV FLYHIPCDNC GSSDGNSLFS DGHTFCYVCE KWTAGNEDTK ERASKRKPSG GKPMTYNVW NFGESNGRYS ALTARGISKE TCQKAGYWIA KVDGVMYQVA DYRDQNGNIV S QKVRDKDK NFKTTGSHKS DALFGKHLWN GGKKIVVTEG EIDMLTVMEL QDCKYPVVSL GH GASAAKK TCAANYEYFD QFEQIILMFD MDEAGRKAVE EAAQVLPAGK VRVAVLPCKD ANE CHLNGH DREIMEQVWN AGPWIPDGVV SALSLRERIR EHLSSEESVG LLFSGCTGIN DKTL GARGG EVIMVTSGSG MGKSTFVRQQ ALQWGTAMGK KVGLAMLQES VEETAEDLIG LHNRV RLRQ SDSLKREIIE NGKFDQWFDE LFGNDTFHLY DSFAEAETDR LLAKLAYMRS GLGCDV IIL DHISIVVSAS GESDERKMID NLMTKLKGFA KSTGVVLVVI CHLKNPDKGK AHEEGRP VS ITDLRGSGAL RQLSDTIIAL ERNQQGDMPN LVLVRILKCR FTGDTGIAGY MEYNKETG W LEPSSYSGEE ESHSESTDWS NDTDF |
-Macromolecule #2: gene product 5 DNA polymerase
Macromolecule | Name: gene product 5 DNA polymerase / type: protein_or_peptide / ID: 2 / Enantiomer: LEVO |
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Source (natural) | Organism: Enterobacteria phage T7 (virus) |
Sequence | String: MIVSAIAANA LLESVTKFHC GVIYDYSTAE YVSYRPSDFG AYLDALEAEV ARGGLIVFHN GHKYDVPAL TKLAKLQLNR EFHLPRENCI DTLVLSRLIH SNLKDTDMGL LRSGKLPGKR F GSHALEAW GYRLGEMKGE YKDDFKRMLE EQGEEYVDGM EWWNFNEEMM ...String: MIVSAIAANA LLESVTKFHC GVIYDYSTAE YVSYRPSDFG AYLDALEAEV ARGGLIVFHN GHKYDVPAL TKLAKLQLNR EFHLPRENCI DTLVLSRLIH SNLKDTDMGL LRSGKLPGKR F GSHALEAW GYRLGEMKGE YKDDFKRMLE EQGEEYVDGM EWWNFNEEMM DYNVQDVVVT KA LLEKLLS DKHYFPPEID FTDVGYTTFW SESLEAVDIE HRAAWLLAKQ ERNGFPFDTK AIE ELYVEL AARRSELLRK LTETFGSWYQ PKGGTEMFCH PRTGKPLPKY PRIKTPKVGG IFKK PKNKA QREGREPCEL DTREYVAGAP YTPVEHVVFN PSSRDHIQKK LQEAGWVPTK YTDKG APVV DDEVLEGVRV DDPEKQAAID LIKEYLMIQK RIGQSAEGDK AWLRYVAEDG KIHGSV NPN GAVTGRATHA FPNLAQIPGV RSPYGEQCRA AFGAEHHLDG ITGKPWVQAG IDASGLE LR CLAHFMARFD NGEYAHEILN GDIHTKNQIA AELPTRDNAK TFIYGFLYGA GDEKIGQI V GAGKERGKEL KKKFLENTPA IAALRESIQQ TLVESSQWVA GEQQVKWKRR WIKGLDGRK VHVRSPHAAL NTLLQSAGAL ICKLWIIKTE EMLVEKGLKH GWDGDFAYMA WVHDEIQVGC RTEEIAQVV IETAQEAMRW VGDHWNFRCL LDTEGKMGPN WAICH |
-Macromolecule #3: Thioredoxin
Macromolecule | Name: Thioredoxin / type: protein_or_peptide / ID: 3 / Enantiomer: LEVO |
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Source (natural) | Organism: Escherichia coli (E. coli) |
Sequence | String: MSDKIIHLTD DSFDTDVLKA DGAILVDFWA EWCGPCKMIA PILDEIADEY QGKLTVAKLN IDQNPGTAP KYGIRGIPTL LLFKNGEVAA TKVGALSKGQ LKEFLDANLA |
-Macromolecule #4: Primer
Macromolecule | Name: Primer / type: dna / ID: 4 / Classification: DNA |
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Source (natural) | Organism: Enterobacteria phage T7 (virus) |
Sequence | String: (DG)(DG)(DT)(DA)(DC)(DA)(DA)(DC)(DT)(DT) (DG)(DA)(DC)(DG)(DA)(DC)(DA)(DT)(DA)(DG) (DC)(DG)(DT)(DG)(DOA) |
-Macromolecule #5: Template
Macromolecule | Name: Template / type: dna / ID: 5 / Classification: DNA |
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Source (natural) | Organism: Enterobacteria phage T7 (virus) |
Sequence | String: (DT)(DT)(DT)(DG)(DG)(DT)(DC)(DA)(DT)(DT) (DT)(DT)(DT)(DT)(DT)(DT)(DT)(DT)(DT)(DT) (DT)(DT)(DT)(DT)(DT)(DT)(DT)(DT)(DA)(DC) (DG)(DG)(DA)(DG)(DT)(DC)(DG)(DT)(DT)(DT) (DC)(DG)(DA)(DC)(DT)(DC)(DC) ...String: (DT)(DT)(DT)(DG)(DG)(DT)(DC)(DA)(DT)(DT) (DT)(DT)(DT)(DT)(DT)(DT)(DT)(DT)(DT)(DT) (DT)(DT)(DT)(DT)(DT)(DT)(DT)(DT)(DA)(DC) (DG)(DG)(DA)(DG)(DT)(DC)(DG)(DT)(DT)(DT) (DC)(DG)(DA)(DC)(DT)(DC)(DC)(DG)(DT)(DT) (DA)(DT)(DC)(DA)(DC)(DG)(DC)(DT)(DA)(DT) (DG)(DT)(DC)(DG)(DT)(DC)(DA)(DA)(DG)(DT) (DT)(DG)(DT)(DA)(DC)(DC) |
-Experimental details
-Structure determination
Method | cryo EM |
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Processing | single particle reconstruction |
Aggregation state | particle |
-Sample preparation
Buffer | pH: 7.5 Component:
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Grid | Details: unspecified | ||||||||||||
Vitrification | Cryogen name: ETHANE / Chamber humidity: 100 % / Chamber temperature: 295 K / Instrument: FEI VITROBOT MARK I |
-Electron microscopy
Microscope | FEI TITAN KRIOS |
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Image recording | Film or detector model: GATAN K2 SUMMIT (4k x 4k) / Detector mode: COUNTING / Average electron dose: 40.0 e/Å2 |
Electron beam | Acceleration voltage: 300 kV / Electron source: FIELD EMISSION GUN |
Electron optics | Illumination mode: FLOOD BEAM / Imaging mode: BRIGHT FIELD |
Experimental equipment | Model: Titan Krios / Image courtesy: FEI Company |
+Image processing
-Atomic model buiding 1
Initial model | PDB ID: |
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Refinement | Space: REAL / Protocol: FLEXIBLE FIT |