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7C9A

Human RAD51 post-synaptic complexes mutant (V273P, D274G)

Summary for 7C9A
Entry DOI10.2210/pdb7c9a/pdb
EMDB information30310
DescriptorDNA repair protein RAD51 homolog 1, DNA (5'-D(P*TP*TP*TP*TP*TP*TP*TP*TP*T)-3'), DNA (5'-D(P*AP*AP*AP*AP*AP*AP*AP*AP*A)-3'), ... (5 entities in total)
Functional Keywordsmeitotic homologous recombination, dna repair, atpase, recombination
Biological sourceHomo sapiens (Human)
More
Total number of polymer chains5
Total formula weight117952.73
Authors
Chi, H.Y.,Ho, M.C.,Tsai, M.D.,Luo, S.C.,Yeh, H.Y. (deposition date: 2020-06-05, release date: 2020-11-18, Last modification date: 2024-03-27)
Primary citationLuo, S.C.,Yeh, H.Y.,Lan, W.H.,Wu, Y.M.,Yang, C.H.,Chang, H.Y.,Su, G.C.,Lee, C.Y.,Wu, W.J.,Li, H.W.,Ho, M.C.,Chi, P.,Tsai, M.D.
Identification of fidelity-governing factors in human recombinases DMC1 and RAD51 from cryo-EM structures.
Nat Commun, 12:115-115, 2021
Cited by
PubMed Abstract: Both high-fidelity and mismatch-tolerant recombination, catalyzed by RAD51 and DMC1 recombinases, respectively, are indispensable for genomic integrity. Here, we use cryo-EM, MD simulation and functional analysis to elucidate the structural basis for the mismatch tolerance of DMC1. Structural analysis of DMC1 presynaptic and postsynaptic complexes suggested that the lineage-specific Loop 1 Gln244 (Met243 in RAD51) may help stabilize DNA backbone, whereas Loop 2 Pro274 and Gly275 (Val273/Asp274 in RAD51) may provide an open "triplet gate" for mismatch tolerance. In support, DMC1-Q244M displayed marked increase in DNA dynamics, leading to unobservable DNA map. MD simulation showed highly dispersive mismatched DNA ensemble in RAD51 but well-converged DNA in DMC1 and RAD51-V273P/D274G. Replacing Loop 1 or Loop 2 residues in DMC1 with RAD51 counterparts enhanced DMC1 fidelity, while reciprocal mutations in RAD51 attenuated its fidelity. Our results show that three Loop 1/Loop 2 residues jointly enact contrasting fidelities of DNA recombinases.
PubMed: 33446654
DOI: 10.1038/s41467-020-20258-1
PDB entries with the same primary citation
Experimental method
ELECTRON MICROSCOPY (3.43 Å)
Structure validation

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數據於2025-06-25公開中

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