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7SGZ

Structure of the yeast Rad24-RFC loader bound to DNA and the closed 9-1-1 clamp

Summary for 7SGZ
Entry DOI10.2210/pdb7sgz/pdb
EMDB information25121 25122
DescriptorCheckpoint protein RAD24, Crick strand, PHOSPHOTHIOPHOSPHORIC ACID-ADENYLATE ESTER, ... (14 entities in total)
Functional Keywordsdna damage repair, rad24-rfc, 9-1-1 clamp, dna clamp, alternative clamp loader, dna damage signaling, dna binding protein-dna complex, dna binding protein/dna
Biological sourceSaccharomyces cerevisiae (Baker's yeast)
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Total number of polymer chains10
Total formula weight415760.75
Authors
Zheng, F.,Georgescu, R.,Yao, Y.N.,O'Donnell, M.E.,Li, H. (deposition date: 2021-10-07, release date: 2022-03-23, Last modification date: 2025-05-14)
Primary citationZheng, F.,Georgescu, R.E.,Yao, N.Y.,O'Donnell, M.E.,Li, H.
DNA is loaded through the 9-1-1 DNA checkpoint clamp in the opposite direction of the PCNA clamp.
Nat.Struct.Mol.Biol., 29:376-385, 2022
Cited by
PubMed Abstract: The 9-1-1 DNA checkpoint clamp is loaded onto 5'-recessed DNA to activate the DNA damage checkpoint that arrests the cell cycle. The 9-1-1 clamp is a heterotrimeric ring that is loaded in Saccharomyces cerevisiae by Rad24-RFC (hRAD17-RFC), an alternate clamp loader in which Rad24 replaces Rfc1 in the RFC1-5 clamp loader of proliferating cell nuclear antigen (PCNA). The 9-1-1 clamp loading mechanism has been a mystery, because, unlike RFC, which loads PCNA onto a 3'-recessed junction, Rad24-RFC loads the 9-1-1 ring onto a 5'-recessed DNA junction. Here we report two cryo-EM structures of Rad24-RFC-DNA with a closed or 27-Å open 9-1-1 clamp. The structures reveal a completely unexpected mechanism by which a clamp can be loaded onto DNA. Unlike RFC, which encircles DNA, Rad24 binds 5'-DNA on its surface, not inside the loader, and threads the 3' ssDNA overhang into the 9-1-1 clamp from above the ring.
PubMed: 35314830
DOI: 10.1038/s41594-022-00742-6
PDB entries with the same primary citation
Experimental method
ELECTRON MICROSCOPY (3.17 Å)
Structure validation

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