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9PER

Structure of the S. cerevisiae clamp loader Replication Factor C (RFC) with mixed nucleotide occupancy

Summary for 9PER
Entry DOI10.2210/pdb9per/pdb
EMDB information71574
DescriptorReplication factor C subunit 1, Replication factor C subunit 4, Replication factor C subunit 3, ... (8 entities in total)
Functional Keywordsaaa+ atpase, rossmann fold, complex, dna replication, replication
Biological sourceSaccharomyces cerevisiae (brewer's yeast)
More
Total number of polymer chains5
Total formula weight250280.32
Authors
Pajak, J.,Kelch, B.A. (deposition date: 2025-07-02, release date: 2025-11-12, Last modification date: 2025-11-26)
Primary citationPajak, J.,Landeck, J.T.,Liu, X.,Anand, K.,Litvak, S.,Kelch, B.A.
PCNA is a nucleotide exchange factor for the clamp loader ATPase complex.
Proc.Natl.Acad.Sci.USA, 122:e2518834122-e2518834122, 2025
Cited by
PubMed Abstract: All life requires loading ring-shaped sliding clamp protein complexes onto DNA. The sliding clamp loader is a conserved AAA+ ATPase that binds the sliding clamp, opens the ring, and places it onto DNA. While recent structural work on both the canonical and "alternative" clamp loaders has shed light into how these machines perform their task once, it remains unclear how clamp loaders are recycled to load multiple sliding clamps. Here, we present structures of the clamp loader Replication Factor C (RFC) in absence of sliding clamp or supplemented nucleotide. Our structures indicate that RFC holds onto ADP tightly in at least two of its four ATPase active sites, suggesting that nucleotide exchange is regulated. Our molecular dynamics simulations and biochemical data indicate that binding of the sliding clamp Proliferating Cell Nuclear Antigen (PCNA) causes rapid exchange of tightly bound ADP. Our data suggest that PCNA acts as a nucleotide exchange factor (NEF) by prying apart adjacent subunits, providing a pathway for ADP release. We propose that, by using its own substrate as a NEF, RFC excludes off-pathway states that would arise from binding DNA prior to PCNA.
PubMed: 41231947
DOI: 10.1073/pnas.2518834122
PDB entries with the same primary citation
Experimental method
ELECTRON MICROSCOPY (2.57 Å)
Structure validation

245663

数据于2025-12-03公开中

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