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9B8R

Cryo-EM structure of S. cerevisiae PolE-core-DNA

Summary for 9B8R
Entry DOI10.2210/pdb9b8r/pdb
EMDB information44356
DescriptorPrimer DNA, Template DNA, DNA polymerase epsilon catalytic subunit, ... (4 entities in total)
Functional Keywordspol2, dna, replication, dna binding protein-dna complex, dna binding protein/dna
Biological sourceSaccharomyces cerevisiae (brewer's yeast)
More
Total number of polymer chains3
Total formula weight140957.08
Authors
Yuan, Z.,Georgescu, R.,O'Donnell, M.,Li, H. (deposition date: 2024-03-31, release date: 2024-10-09, Last modification date: 2024-10-23)
Primary citationYuan, Z.,Georgescu, R.,Yao, N.Y.,Yurieva, O.,O'Donnell, M.E.,Li, H.
Mechanism of PCNA loading by Ctf18-RFC for leading-strand DNA synthesis.
Science, 385:eadk5901-eadk5901, 2024
Cited by
PubMed 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 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.
PubMed: 39088616
DOI: 10.1126/science.adk5901
PDB entries with the same primary citation
Experimental method
ELECTRON MICROSCOPY (3.5 Å)
Structure validation

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