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- EMDB-29744: local refinement of the primase/DNA/primer region in mutant T4 pr... -
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Open data
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Basic information
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Title | local refinement of the primase/DNA/primer region in mutant T4 primosome | |||||||||
![]() | focus refinement of the primase/DNA-RNA region | |||||||||
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![]() | phage / complex / helicase / REPLICATION | |||||||||
Biological species | ![]() | |||||||||
Method | single particle reconstruction / cryo EM / Resolution: 4.1 Å | |||||||||
![]() | Feng X / Li H | |||||||||
Funding support | ![]()
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![]() | ![]() Title: Structural basis of the T4 bacteriophage primosome assembly and primer synthesis. Authors: Xiang Feng / Michelle M Spiering / Ruda de Luna Almeida Santos / Stephen J Benkovic / Huilin Li / ![]() Abstract: The T4 bacteriophage gp41 helicase and gp61 primase assemble into a primosome to couple DNA unwinding with RNA primer synthesis for DNA replication. How the primosome is assembled and how the primer ...The T4 bacteriophage gp41 helicase and gp61 primase assemble into a primosome to couple DNA unwinding with RNA primer synthesis for DNA replication. How the primosome is assembled and how the primer length is defined are unclear. Here we report a series of cryo-EM structures of T4 primosome assembly intermediates. We show that gp41 alone is an open spiral, and ssDNA binding triggers a large-scale scissor-like conformational change that drives the ring closure and activates the helicase. Helicase activation exposes a cryptic hydrophobic surface to recruit the gp61 primase. The primase binds the helicase in a bipartite mode in which the N-terminal Zn-binding domain and the C-terminal RNA polymerase domain each contain a helicase-interacting motif that bind to separate gp41 N-terminal hairpin dimers, leading to the assembly of one primase on the helicase hexamer. Our study reveals the T4 primosome assembly process and sheds light on the RNA primer synthesis mechanism. | |||||||||
History |
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Structure visualization
Supplemental images |
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Downloads & links
-EMDB archive
Map data | ![]() | 63.3 MB | ![]() | |
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Header (meta data) | ![]() ![]() | 17.2 KB 17.2 KB | Display Display | ![]() |
FSC (resolution estimation) | ![]() | 14.6 KB | Display | ![]() |
Images | ![]() | 44.1 KB | ||
Others | ![]() ![]() | 115.8 MB 115.8 MB | ||
Archive directory | ![]() ![]() | HTTPS FTP |
-Validation report
Summary document | ![]() | 725.8 KB | Display | ![]() |
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Full document | ![]() | 725.4 KB | Display | |
Data in XML | ![]() | 18.1 KB | Display | |
Data in CIF | ![]() | 23.7 KB | Display | |
Arichive directory | ![]() ![]() | HTTPS FTP |
-Related structure data
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Links
EMDB pages | ![]() ![]() |
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Map
File | ![]() | ||||||||||||||||||||||||||||||||||||
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Annotation | focus refinement of the primase/DNA-RNA region | ||||||||||||||||||||||||||||||||||||
Projections & slices | Image control
Images are generated by Spider. | ||||||||||||||||||||||||||||||||||||
Voxel size | X=Y=Z: 1.029 Å | ||||||||||||||||||||||||||||||||||||
Density |
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Symmetry | Space group: 1 | ||||||||||||||||||||||||||||||||||||
Details | EMDB XML:
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-Supplemental data
-Half map: #1
File | emd_29744_half_map_1.map | ||||||||||||
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Projections & Slices |
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Density Histograms |
-Half map: #2
File | emd_29744_half_map_2.map | ||||||||||||
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Projections & Slices |
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Density Histograms |
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Sample components
-Entire : Complex of mutated T4 bacteriophage helicase gp41 with ssDNA/RNA ...
Entire | Name: Complex of mutated T4 bacteriophage helicase gp41 with ssDNA/RNA hybrid |
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Components |
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-Supramolecule #1: Complex of mutated T4 bacteriophage helicase gp41 with ssDNA/RNA ...
Supramolecule | Name: Complex of mutated T4 bacteriophage helicase gp41 with ssDNA/RNA hybrid type: complex / ID: 1 / Parent: 0 / Macromolecule list: all |
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Source (natural) | Organism: ![]() |
-Macromolecule #1: Bacteriophage T4 DNA primase
Macromolecule | Name: Bacteriophage T4 DNA primase / type: protein_or_peptide / ID: 1 / Enantiomer: LEVO EC number: Transferases; Transferring phosphorus-containing groups; Nucleotidyltransferases |
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Source (natural) | Organism: ![]() |
Recombinant expression | Organism: ![]() ![]() |
Sequence | String: MSSIPWIDNE FAYRALAHLP KFTQVNNSST FKLRFRCPVC GDSKTDQNKA RGWYYGDNNE GNIHCYNCN YHAPIGIYLK EFEPDLYREY IFEIRKEKGK SRPIEKPKEL PKQPEKKIIK S LPSCVRLD KLAEDHPIIK YVKARCIPKD KWKYLWFTTE WPKLVNSIAP ...String: MSSIPWIDNE FAYRALAHLP KFTQVNNSST FKLRFRCPVC GDSKTDQNKA RGWYYGDNNE GNIHCYNCN YHAPIGIYLK EFEPDLYREY IFEIRKEKGK SRPIEKPKEL PKQPEKKIIK S LPSCVRLD KLAEDHPIIK YVKARCIPKD KWKYLWFTTE WPKLVNSIAP GTYKKEISEP RL VIPIYNA NGKAESFQGR ALKKDAPQKY ITIEAYPEAT KIYGVERVKD GDVYVLEGPI DSL FIENGI AITGGQLDLE VVPFKDRRVW VLDNEPRHPD TIKRMTKLVD AGERVMFWDK SPWK SKDVN DMIRKEGATP EQIMEYMKNN IAQGLMAKMR LSKYAKI |
-Macromolecule #2: DNA (70-mer)
Macromolecule | Name: DNA (70-mer) / type: dna / ID: 2 / Classification: DNA |
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Source (natural) | Organism: ![]() |
Sequence | String: (DG)(DA)(DA)(DT)(DG)(DA)(DG)(DG)(DA)(DG) (DT)(DA)(DG)(DT)(DA)(DG)(DT)(DG)(DA)(DA) (DT)(DG)(DT)(DA)(DG)(DT)(DG)(DA)(DG) (DG)(DT)(DA)(DA)(DT)(DA)(DT)(DC)(DG)(DG) (DC) (DT)(DG)(DG)(DT)(DC)(DT) ...String: (DG)(DA)(DA)(DT)(DG)(DA)(DG)(DG)(DA)(DG) (DT)(DA)(DG)(DT)(DA)(DG)(DT)(DG)(DA)(DA) (DT)(DG)(DT)(DA)(DG)(DT)(DG)(DA)(DG) (DG)(DT)(DA)(DA)(DT)(DA)(DT)(DC)(DG)(DG) (DC) (DT)(DG)(DG)(DT)(DC)(DT)(DG)(DG) (DT)(DC)(DT)(DG)(DT)(DG)(DC)(DC)(DA)(DA) (DG)(DT) (DT)(DG)(DC)(DT)(DG)(DC)(DA) (DA)(DA)(DA) |
-Macromolecule #3: RNA (5'-R(*(GTP)P*CP*CP*GP*A)-3')
Macromolecule | Name: RNA (5'-R(*(GTP)P*CP*CP*GP*A)-3') / type: rna / ID: 3 |
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Source (natural) | Organism: ![]() |
Sequence | String: (GTP)CCGA |
-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: 7.8 Component:
Details: 20 mM HEPES pH 7.8, 100 mM NaCl, 10 mM MgCl2 and 2 mM DTT | |||||||||||||||
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Vitrification | Cryogen name: ETHANE |
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Electron microscopy
Microscope | FEI TITAN KRIOS |
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Image recording | Film or detector model: GATAN K3 (6k x 4k) / Average electron dose: 66.0 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 |
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Image processing
-Atomic model buiding 1
Refinement | Space: REAL / Protocol: OTHER |
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