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Crystal structure of the Holliday junction DNA in complex with a single RuvA tetramerCrystal structure of the RuvA-RuvB complex: a structural basis for the Holliday junction migrating motor machineryNbs1 Flexibly Tethers Ctp1 and Mre11-Rad50 to Coordinate DNA Double-Strand Break Processing and RepairAtomic structure of the RuvC resolvase: a holliday junction-specific endonuclease from E. coliA yeast gene, MGS1, encoding a DNA-dependent AAA(+) ATPase is required to maintain genome stability.Reconstitution of DNA strand exchange mediated by Rhp51 recombinase and two mediatorsRAD6-RAD18-RAD5-pathway-dependent tolerance to chronic low-dose ultraviolet light.The fission yeast meiosis-specific Dmc1 recombinase mediates formation and branch migration of Holliday junctions by preferentially promoting strand exchange in a direction opposite to that of Rad51.Role of the Schizosaccharomyces pombe F-Box DNA helicase in processing recombination intermediatesEvidence that phenylalanine 69 in Escherichia coli RuvC resolvase forms a stacking interaction during binding and destabilization of a Holliday junction DNA substrate.Two different Swi5-containing protein complexes are involved in mating-type switching and recombination repair in fission yeast.The Swi5-Sfr1 complex stimulates Rhp51/Rad51- and Dmc1-mediated DNA strand exchange in vitro.A DNA polymerase alpha accessory protein, Mcl1, is required for propagation of centromere structures in fission yeastRecA protein-dependent cleavage of UmuD protein and SOS mutagenesis.Identification of four acidic amino acids that constitute the catalytic center of the RuvC Holliday junction resolvase.The Schizosaccharomyces pombe rad60 gene is essential for repairing double-strand DNA breaks spontaneously occurring during replication and induced by DNA-damaging agents.Analysis of substrate specificity of the RuvC holliday junction resolvase with synthetic Holliday junctions.Formation and branch migration of Holliday junctions mediated by eukaryotic recombinases.Dual regulation of Dmc1-driven DNA strand exchange by Swi5-Sfr1 activation and Rad22 inhibitionCompetition between the Rad50 complex and the Ku heterodimer reveals a role for Exo1 in processing double-strand breaks but not telomeresMultiple regulation of Rad51-mediated homologous recombination by fission yeast Fbh1.Fission yeast Swi5/Sfr1 and Rhp55/Rhp57 differentially regulate Rhp51-dependent recombination outcomes.Molecular characterization of the Schizosaccharomyces pombe nbs1+ gene involved in DNA repair and telomere maintenanceStructure and regulation of the Escherichia coli ruv operon involved in DNA repair and recombination.Direct evidence that a conserved arginine in RuvB AAA+ ATPase acts as an allosteric effector for the ATPase activity of the adjacent subunit in a hexamer.Molecular characterization of the role of the Schizosaccharomyces pombe nip1+/ctp1+ gene in DNA double-strand break repair in association with the Mre11-Rad50-Nbs1 complex.SOS-inducible DNA polymerase II of E coli is homologous to replicative DNA polymerase of eukaryotes.Role of the Escherichia coli RecQ DNA helicase in SOS signaling and genome stabilization at stalled replication forks.Rad62 protein functionally and physically associates with the smc5/smc6 protein complex and is required for chromosome integrity and recombination repair in fission yeast.Swi5-Sfr1 protein stimulates Rad51-mediated DNA strand exchange reaction through organization of DNA bases in the presynaptic filament.Cell polarity in Saccharomyces cerevisiae depends on proper localization of the Bud9 landmark protein by the EKC/KEOPS complex.The differentiated and conserved roles of Swi5-Sfr1 in homologous recombination.Molecular mechanisms of Holliday junction processing in Escherichia coli.Expression, purification and crystallization of Swi5 and the Swi5-Sfr1 complex from fission yeastSrs2 plays a critical role in reversible G2 arrest upon chronic and low doses of UV irradiation via two distinct homologous recombination-dependent mechanisms in postreplication repair-deficient cells.Overproduction of human immunodeficiency virus type I reverse transcriptase in Escherichia coli and purification of the enzyme.Proteolytic processing of MucA protein in SOS mutagenesis: both processed and unprocessed MucA may be active in the mutagenesis.Genetic and physical interactions between Schizosaccharomyces pombe Mcl1 and Rad2, Dna2 and DNA polymerase alpha: evidence for a multifunctional role of Mcl1 in DNA replication and repair.Recruitment and delivery of the fission yeast Rst2 transcription factor via a local genome structure counteracts repression by Tup1-family corepressors.In vitro site-specific recombination mediated by the tyrosine recombinase XerA of Thermoplasma acidophilum.
P50
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P50
description
researcher ORCID ID = 0000-0002-0153-6873
@en
name
Hiroshi Iwasaki
@ast
Hiroshi Iwasaki
@en
Hiroshi Iwasaki
@es
Hiroshi Iwasaki
@nl
type
label
Hiroshi Iwasaki
@ast
Hiroshi Iwasaki
@en
Hiroshi Iwasaki
@es
Hiroshi Iwasaki
@nl
prefLabel
Hiroshi Iwasaki
@ast
Hiroshi Iwasaki
@en
Hiroshi Iwasaki
@es
Hiroshi Iwasaki
@nl
P1153
57080285800
P31
P496
0000-0002-0153-6873