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Open data
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Basic information
| Entry | Database: PDB / ID: 6rax | ||||||
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| Title | D. melanogaster CMG-DNA, State 1B | ||||||
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Keywords | HYDOLASE / Helicase / ATPase / AAA+ / DNA unwinding / HYDROLASE | ||||||
| Function / homology | Function and homology informationUnwinding of DNA / Assembly of the pre-replicative complex / Switching of origins to a post-replicative state / DNA endoreduplication / Activation of ATR in response to replication stress / Activation of the pre-replicative complex / eggshell chorion gene amplification / Orc1 removal from chromatin / DNA amplification / DNA strand elongation involved in mitotic DNA replication ...Unwinding of DNA / Assembly of the pre-replicative complex / Switching of origins to a post-replicative state / DNA endoreduplication / Activation of ATR in response to replication stress / Activation of the pre-replicative complex / eggshell chorion gene amplification / Orc1 removal from chromatin / DNA amplification / DNA strand elongation involved in mitotic DNA replication / GINS complex / mitotic DNA replication preinitiation complex assembly / resolution of meiotic recombination intermediates / premeiotic DNA replication / mitotic DNA replication / CMG complex / DNA replication preinitiation complex / MCM complex / double-strand break repair via break-induced replication / mitotic DNA replication initiation / chromosome condensation / DNA strand elongation involved in DNA replication / DNA replication origin binding / DNA replication initiation / DNA helicase activity / regulation of DNA-templated transcription elongation / mitotic spindle organization / meiotic cell cycle / helicase activity / mitotic cell cycle / single-stranded DNA binding / DNA helicase / DNA replication / cell division / chromatin binding / ATP hydrolysis activity / zinc ion binding / ATP binding / nucleus / cytoplasm / cytosol Similarity search - Function | ||||||
| Biological species | ![]() | ||||||
| Method | ELECTRON MICROSCOPY / single particle reconstruction / cryo EM / Resolution: 3.99 Å | ||||||
Authors | Eickhoff, P. / Martino, F. / Costa, A. | ||||||
Citation | Journal: Cell Rep / Year: 2019Title: Molecular Basis for ATP-Hydrolysis-Driven DNA Translocation by the CMG Helicase of the Eukaryotic Replisome. Authors: Patrik Eickhoff / Hazal B Kose / Fabrizio Martino / Tatjana Petojevic / Ferdos Abid Ali / Julia Locke / Nele Tamberg / Andrea Nans / James M Berger / Michael R Botchan / Hasan Yardimci / Alessandro Costa / ![]() Abstract: In the eukaryotic replisome, DNA unwinding by the Cdc45-MCM-Go-Ichi-Ni-San (GINS) (CMG) helicase requires a hexameric ring-shaped ATPase named minichromosome maintenance (MCM), which spools single- ...In the eukaryotic replisome, DNA unwinding by the Cdc45-MCM-Go-Ichi-Ni-San (GINS) (CMG) helicase requires a hexameric ring-shaped ATPase named minichromosome maintenance (MCM), which spools single-stranded DNA through its central channel. Not all six ATPase sites are required for unwinding; however, the helicase mechanism is unknown. We imaged ATP-hydrolysis-driven translocation of the CMG using cryo-electron microscopy (cryo-EM) and found that the six MCM subunits engage DNA using four neighboring protomers at a time, with ATP binding promoting DNA engagement. Morphing between different helicase states leads us to suggest a non-symmetric hand-over-hand rotary mechanism, explaining the asymmetric requirements of ATPase function around the MCM ring of the CMG. By imaging of a higher-order replisome assembly, we find that the Mrc1-Csm3-Tof1 fork-stabilization complex strengthens the interaction between parental duplex DNA and the CMG at the fork, which might support the coupling between DNA translocation and fork unwinding. | ||||||
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Structure visualization
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| Structure viewer | Molecule: Molmil Jmol/JSmol |
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Downloads & links
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Download
| PDBx/mmCIF format | 6rax.cif.gz | 935.4 KB | Display | PDBx/mmCIF format |
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| PDB format | pdb6rax.ent.gz | 746.9 KB | Display | PDB format |
| PDBx/mmJSON format | 6rax.json.gz | Tree view | PDBx/mmJSON format | |
| Others | Other downloads |
-Validation report
| Summary document | 6rax_validation.pdf.gz | 1.7 MB | Display | wwPDB validaton report |
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| Full document | 6rax_full_validation.pdf.gz | 1.9 MB | Display | |
| Data in XML | 6rax_validation.xml.gz | 170.6 KB | Display | |
| Data in CIF | 6rax_validation.cif.gz | 251.2 KB | Display | |
| Arichive directory | https://data.pdbj.org/pub/pdb/validation_reports/ra/6rax ftp://data.pdbj.org/pub/pdb/validation_reports/ra/6rax | HTTPS FTP |
-Related structure data
| Related structure data | ![]() 4786MC ![]() 4785C ![]() 4787C ![]() 4788C ![]() 6rawC ![]() 6rayC ![]() 6razC M: map data used to model this data C: citing same article ( |
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| Similar structure data |
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Assembly
| Deposited unit | ![]()
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Components
-DNA replication licensing factor ... , 6 types, 6 molecules 234567
| #1: Protein | Mass: 100537.438 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Source: (gene. exp.) ![]() Trichoplusia ni (cabbage looper) / References: UniProt: P49735, DNA helicase |
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| #2: Protein | Mass: 91045.164 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Source: (gene. exp.) ![]() Trichoplusia ni (cabbage looper) / References: UniProt: Q9XYU1, DNA helicase |
| #3: Protein | Mass: 96735.094 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Source: (gene. exp.) ![]() Trichoplusia ni (cabbage looper) / References: UniProt: Q26454, DNA helicase |
| #4: Protein | Mass: 82375.320 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Source: (gene. exp.) ![]() Trichoplusia ni (cabbage looper) / References: UniProt: Q9VGW6, DNA helicase |
| #5: Protein | Mass: 92467.820 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Source: (gene. exp.) ![]() Trichoplusia ni (cabbage looper) / References: UniProt: Q9V461, DNA helicase |
| #6: Protein | Mass: 81399.352 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Source: (gene. exp.) ![]() Trichoplusia ni (cabbage looper) / References: UniProt: Q9XYU0, DNA helicase |
-DNA chain , 2 types, 2 molecules XY
| #7: DNA chain | Mass: 6381.123 Da / Num. of mol.: 1 / Source method: obtained synthetically / Source: (synth.) ![]() |
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| #8: DNA chain | Mass: 2426.617 Da / Num. of mol.: 1 / Source method: obtained synthetically / Source: (synth.) ![]() |
-Protein , 5 types, 5 molecules AHLMN
| #9: Protein | Mass: 65968.789 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Source: (gene. exp.) ![]() Gene: CDC45L, anon-1Ec, CDC45, Cdc45, cdc45, D, dCDC45, dCDC45L, DmCdc45, Dmel\CG3658, EG:BACR7A4.11, CG3658, Dmel_CG3658 Production host: Trichoplusia ni (cabbage looper) / References: UniProt: O96989 |
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| #10: Protein | Mass: 23333.693 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Source: (gene. exp.) ![]() Gene: Psf1, CG9187-PA, Dmel\CG9187, psf1, CG9187, Dmel_CG9187 Production host: Trichoplusia ni (cabbage looper) / References: UniProt: Q9W0I7 |
| #11: Protein | Mass: 23141.781 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Source: (gene. exp.) ![]() Trichoplusia ni (cabbage looper) / References: UniProt: Q9VQY9 |
| #12: Protein | Mass: 24829.984 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Source: (gene. exp.) ![]() Trichoplusia ni (cabbage looper) / References: UniProt: Q9W2V7 |
| #13: Protein | Mass: 26148.234 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Source: (gene. exp.) ![]() Gene: Sld5, anon-WO0172774.61, Dmel\CG14549, CG14549, Dmel_CG14549 Production host: Trichoplusia ni (cabbage looper) / References: UniProt: Q9VBI1 |
-Non-polymers , 2 types, 6 molecules 


| #14: Chemical | | #15: Chemical | |
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-Details
| Has ligand of interest | Y |
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| Has protein modification | Y |
-Experimental details
-Experiment
| Experiment | Method: ELECTRON MICROSCOPY |
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| EM experiment | Aggregation state: PARTICLE / 3D reconstruction method: single particle reconstruction |
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Sample preparation
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| Buffer solution | pH: 7.6 | ||||||||||||||||||||||||
| Specimen | Embedding applied: NO / Shadowing applied: NO / Staining applied: NO / Vitrification applied: YES | ||||||||||||||||||||||||
| Vitrification | Cryogen name: ETHANE |
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Electron microscopy imaging
| Experimental equipment | ![]() Model: Titan Krios / Image courtesy: FEI Company |
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| Microscopy | Model: FEI TITAN KRIOS |
| Electron gun | Electron source: FIELD EMISSION GUN / Accelerating voltage: 300 kV / Illumination mode: OTHER |
| Electron lens | Mode: BRIGHT FIELD |
| Image recording | Electron dose: 50 e/Å2 / Film or detector model: GATAN K2 SUMMIT (4k x 4k) |
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Processing
| CTF correction | Type: PHASE FLIPPING AND AMPLITUDE CORRECTION |
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| 3D reconstruction | Resolution: 3.99 Å / Resolution method: FSC 0.143 CUT-OFF / Num. of particles: 92754 / Symmetry type: POINT |
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