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8B9B

S. cerevisiae replisome + Ctf4, bound by pol alpha. Complex engaged with a fork DNA substrate containing a 60 nucleotide lagging strand.

This is a non-PDB format compatible entry.
Summary for 8B9B
Entry DOI10.2210/pdb8b9b/pdb
EMDB information15309 15310
DescriptorDNA replication licensing factor MCM2, DNA replication complex GINS protein PSF2, DNA replication complex GINS protein PSF3, ... (24 entities in total)
Functional Keywordsreplication, helicase, polymerase, pol alpha, priming
Biological sourceSaccharomyces cerevisiae (baker's yeast)
More
Total number of polymer chains23
Total formula weight1843993.88
Authors
Jones, M.L.,Yeeles, J.T.P. (deposition date: 2022-10-05, release date: 2023-08-09, Last modification date: 2023-08-30)
Primary citationJones, M.L.,Aria, V.,Baris, Y.,Yeeles, J.T.P.
How Pol alpha-primase is targeted to replisomes to prime eukaryotic DNA replication.
Mol.Cell, 83:2911-, 2023
Cited by
PubMed Abstract: During eukaryotic DNA replication, Pol α-primase generates primers at replication origins to start leading-strand synthesis and every few hundred nucleotides during discontinuous lagging-strand replication. How Pol α-primase is targeted to replication forks to prime DNA synthesis is not fully understood. Here, by determining cryoelectron microscopy (cryo-EM) structures of budding yeast and human replisomes containing Pol α-primase, we reveal a conserved mechanism for the coordination of priming by the replisome. Pol α-primase binds directly to the leading edge of the CMG (CDC45-MCM-GINS) replicative helicase via a complex interaction network. The non-catalytic PRIM2/Pri2 subunit forms two interfaces with CMG that are critical for in vitro DNA replication and yeast cell growth. These interactions position the primase catalytic subunit PRIM1/Pri1 directly above the exit channel for lagging-strand template single-stranded DNA (ssDNA), revealing why priming occurs efficiently only on the lagging-strand template and elucidating a mechanism for Pol α-primase to overcome competition from RPA to initiate primer synthesis.
PubMed: 37506699
DOI: 10.1016/j.molcel.2023.06.035
PDB entries with the same primary citation
Experimental method
ELECTRON MICROSCOPY (3.5 Å)
Structure validation

237735

数据于2025-06-18公开中

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