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Yorodumi- PDB-8twa: Cryo-EM structure of S. cerevisiae Ctf18-RFC-PCNA-PolE-DNA complex -
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Open data
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Basic information
| Entry | Database: PDB / ID: 8twa | ||||||||||||
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| Title | Cryo-EM structure of S. cerevisiae Ctf18-RFC-PCNA-PolE-DNA complex | ||||||||||||
Components |
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Keywords | DNA BINDING PROTEIN/DNA / Ctf18 / RFC2-5 / PCNA / Pol2 / DNA / DNA BINDING PROTEIN-DNA complex | ||||||||||||
| Function / homology | Function and homology informationmaintenance of mitotic sister chromatid cohesion / gene conversion / DNA replication initiation / positive regulation of DNA metabolic process / Mismatch repair (MMR) directed by MSH2:MSH6 (MutSalpha) / meiotic mismatch repair / Rad17 RFC-like complex / Gap-filling DNA repair synthesis and ligation in GG-NER / Processive synthesis on the lagging strand / epsilon DNA polymerase complex ...maintenance of mitotic sister chromatid cohesion / gene conversion / DNA replication initiation / positive regulation of DNA metabolic process / Mismatch repair (MMR) directed by MSH2:MSH6 (MutSalpha) / meiotic mismatch repair / Rad17 RFC-like complex / Gap-filling DNA repair synthesis and ligation in GG-NER / Processive synthesis on the lagging strand / epsilon DNA polymerase complex / Removal of the Flap Intermediate / telomere tethering at nuclear periphery / Elg1 RFC-like complex / DNA replication factor C complex / Ctf18 RFC-like complex / E3 ubiquitin ligases ubiquitinate target proteins / Polymerase switching / maintenance of DNA trinucleotide repeats / SUMO binding / SUMOylation of DNA replication proteins / nucleotide-excision repair, DNA gap filling / Translesion synthesis by REV1 / Translesion synthesis by POLK / Translesion synthesis by POLI / Activation of the pre-replicative complex / Translesion Synthesis by POLH / DNA replication checkpoint signaling / establishment of mitotic sister chromatid cohesion / DNA replication proofreading / PCNA complex / Termination of translesion DNA synthesis / Activation of ATR in response to replication stress / single-stranded DNA 3'-5' DNA exonuclease activity / lagging strand elongation / mitotic DNA replication checkpoint signaling / DNA damage tolerance / mitotic intra-S DNA damage checkpoint signaling / silent mating-type cassette heterochromatin formation / Hydrolases; Acting on ester bonds; Exodeoxyribonucleases producing 5'-phosphomonoesters / sister chromatid cohesion / mitotic sister chromatid cohesion / error-free translesion synthesis / DNA polymerase processivity factor activity / leading strand elongation / nuclear replication fork / Gap-filling DNA repair synthesis and ligation in TC-NER / Dual incision in TC-NER / chromosome, centromeric region / DNA replication initiation / error-prone translesion synthesis / translesion synthesis / subtelomeric heterochromatin formation / mismatch repair / base-excision repair, gap-filling / positive regulation of DNA repair / DNA damage checkpoint signaling / positive regulation of DNA replication / replication fork / nucleotide-excision repair / double-strand break repair via homologous recombination / base-excision repair / double-strand break repair via nonhomologous end joining / DNA-templated DNA replication / double-strand break repair / mitotic cell cycle / single-stranded DNA binding / 4 iron, 4 sulfur cluster binding / double-stranded DNA binding / DNA-directed DNA polymerase / DNA-directed DNA polymerase activity / chromosome, telomeric region / DNA replication / DNA repair / nucleotide binding / mRNA binding / chromatin / ATP hydrolysis activity / mitochondrion / DNA binding / zinc ion binding / ATP binding / identical protein binding / nucleus / cytosol Similarity search - Function | ||||||||||||
| Biological species | ![]() synthetic construct (others) | ||||||||||||
| Method | ELECTRON MICROSCOPY / single particle reconstruction / cryo EM / Resolution: 4.1 Å | ||||||||||||
Authors | Yuan, Z. / Georgescu, R. / O'Donnell, M. / Li, H. | ||||||||||||
| Funding support | United States, 3items
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Citation | Journal: Science / Year: 2024Title: Mechanism of PCNA loading by Ctf18-RFC for leading-strand DNA synthesis. Authors: Zuanning Yuan / Roxana Georgescu / Nina Y Yao / Olga Yurieva / Michael E O'Donnell / Huilin Li / ![]() Abstract: The proliferating cell nuclear antigen (PCNA) clamp encircles DNA to hold DNA polymerases (Pols) to DNA for processivity. The Ctf18-RFC PCNA loader, a replication factor C (RFC) variant, is specific ...The proliferating cell nuclear antigen (PCNA) clamp encircles DNA to hold DNA polymerases (Pols) to DNA for processivity. The Ctf18-RFC PCNA loader, a replication factor C (RFC) variant, is specific to the leading-strand Pol (Polε). We reveal here the underlying mechanism of Ctf18-RFC specificity to Polε using cryo-electron microscopy and biochemical studies. We found that both Ctf18-RFC and Polε contain specific structural features that direct PCNA loading onto DNA. Unlike other clamp loaders, Ctf18-RFC has a disordered ATPase associated with a diverse cellular activities (AAA+) motor that requires Polε to bind and stabilize it for efficient PCNA loading. In addition, Ctf18-RFC can pry prebound Polε off of DNA, then load PCNA onto DNA and transfer the PCNA-DNA back to Polε. These elements in both Ctf18-RFC and Polε provide specificity in loading PCNA onto DNA for Polε. | ||||||||||||
| History |
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Structure visualization
| Structure viewer | Molecule: Molmil Jmol/JSmol |
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Downloads & links
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Download
| PDBx/mmCIF format | 8twa.cif.gz | 772.9 KB | Display | PDBx/mmCIF format |
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| PDB format | pdb8twa.ent.gz | Display | PDB format | |
| PDBx/mmJSON format | 8twa.json.gz | Tree view | PDBx/mmJSON format | |
| Others | Other downloads |
-Validation report
| Summary document | 8twa_validation.pdf.gz | 1.6 MB | Display | wwPDB validaton report |
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| Full document | 8twa_full_validation.pdf.gz | 1.6 MB | Display | |
| Data in XML | 8twa_validation.xml.gz | 113.1 KB | Display | |
| Data in CIF | 8twa_validation.cif.gz | 172.3 KB | Display | |
| Arichive directory | https://data.pdbj.org/pub/pdb/validation_reports/tw/8twa ftp://data.pdbj.org/pub/pdb/validation_reports/tw/8twa | HTTPS FTP |
-Related structure data
| Related structure data | ![]() 41664MC ![]() 9b8rC M: map data used to model this data C: citing same article ( |
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| Similar structure data | Similarity search - Function & homology F&H Search |
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Links
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Assembly
| Deposited unit | ![]()
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Components
-Chromosome transmission fidelity protein ... , 3 types, 3 molecules CD1
| #1: Protein/peptide | Mass: 3171.607 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Source: (gene. exp.) ![]() Gene: CTF18 / Production host: ![]() |
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| #5: Protein | Mass: 15058.493 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Source: (gene. exp.) ![]() Gene: CTF8 / Production host: ![]() |
| #11: Protein | Mass: 84487.195 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Source: (gene. exp.) ![]() Gene: CTF18, CHL12, YMR078C, YM9582.03C / Production host: ![]() |
-DNA chain , 2 types, 2 molecules PT
| #2: DNA chain | Mass: 2737.795 Da / Num. of mol.: 1 / Source method: obtained synthetically / Source: (synth.) synthetic construct (others) |
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| #3: DNA chain | Mass: 4567.998 Da / Num. of mol.: 1 / Source method: obtained synthetically / Source: (synth.) synthetic construct (others) |
-Protein , 3 types, 5 molecules EBXYZ
| #4: Protein | Mass: 255992.484 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Source: (gene. exp.) ![]() Gene: POL2, DUN2, YNL262W, N0825 / Production host: ![]() References: UniProt: P21951, DNA-directed DNA polymerase, Hydrolases; Acting on ester bonds; Exodeoxyribonucleases producing 5'-phosphomonoesters |
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| #6: Protein | Mass: 44133.785 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Source: (gene. exp.) ![]() Gene: DCC1, YCL016C, YCL16C / Production host: ![]() |
| #12: Protein | Mass: 28944.051 Da / Num. of mol.: 3 Source method: isolated from a genetically manipulated source Source: (gene. exp.) ![]() Gene: POL30, YBR088C, YBR0811 / Production host: ![]() |
-Replication factor C subunit ... , 4 types, 4 molecules 4325
| #7: Protein | Mass: 35782.516 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Source: (gene. exp.) ![]() Gene: RFC4 / Production host: ![]() |
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| #8: Protein | Mass: 36818.879 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Source: (gene. exp.) ![]() Gene: RFC3 / Production host: ![]() |
| #9: Protein | Mass: 38256.617 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Source: (gene. exp.) ![]() Gene: RFC2 / Production host: ![]() |
| #10: Protein | Mass: 39993.582 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Source: (gene. exp.) ![]() Gene: RFC5 / Production host: ![]() |
-Non-polymers , 4 types, 8 molecules 






| #13: Chemical | ChemComp-SF4 / | ||||
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| #14: Chemical | | #15: Chemical | #16: Chemical | ChemComp-ADP / | |
-Details
| Has ligand of interest | N |
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| Has protein modification | N |
-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
| Component | Name: Ctf18-RFC-PCNA-PolE-DNA complex / Type: COMPLEX / Entity ID: #1-#12 / Source: MULTIPLE SOURCES |
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| Molecular weight | Experimental value: NO |
| Source (natural) | Organism: ![]() |
| Source (recombinant) | Organism: ![]() |
| Buffer solution | pH: 7.4 |
| 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: FLOOD BEAM |
| Electron lens | Mode: BRIGHT FIELD / Nominal defocus max: 2500 nm / Nominal defocus min: 1500 nm |
| Image recording | Electron dose: 60 e/Å2 / Film or detector model: GATAN K3 BIOQUANTUM (6k x 4k) |
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Processing
| CTF correction | Type: PHASE FLIPPING AND AMPLITUDE CORRECTION |
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| 3D reconstruction | Resolution: 4.1 Å / Resolution method: FSC 0.143 CUT-OFF / Num. of particles: 87643 / Symmetry type: POINT |
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FIELD EMISSION GUN