The Bloom's syndrome gene product interacts with topoisomerase III - Test2 - elhamkhani - TriplyDB

The Bloom's syndrome gene product interacts with topoisomerase III

The Bloom's syndrome gene product interacts with topoisomerase III

http://www.wikidata.org/entity/Q28139703

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Replication protein A physically interacts with the Bloom's syndrome protein and stimulates its helicase activity Colocalization, physical, and functional interaction between Werner and Bloom syndrome proteins RECQL5 cooperates with Topoisomerase II alpha in DNA decatenation and cell cycle progression Physical and functional mapping of the replication protein a interaction domain of the werner and bloom syndrome helicases Human topoisomerase IIIalpha is a single-stranded DNA decatenase that is stimulated by BLM and RMI1 Functional interaction between the Bloom's syndrome helicase and the RAD51 paralog, RAD51L3 (RAD51D)Interaction between the helicases genetically linked to Fanconi anemia group J and Bloom's syndrome POT1 and TRF2 cooperate to maintain telomeric integrity Dual localization of human DNA topoisomerase IIIalpha to mitochondria and nucleus The Bloom's syndrome helicase stimulates the activity of human topoisomerase IIIalpha BLAP75/RMI1 promotes the BLM-dependent dissolution of homologous recombination intermediates MPS1-dependent mitotic BLM phosphorylation is important for chromosome stability Direct association of Bloom's syndrome gene product with the human mismatch repair protein MLH1 Cleavage of the Bloom's syndrome gene product during apoptosis by caspase-3 results in an impaired interaction with topoisomerase IIIalpha The RecQ DNA helicases in DNA repair Physical and functional interaction between the Bloom's syndrome gene product and the largest subunit of chromatin assembly factor 1 Analysis of the unwinding activity of the dimeric RECQ1 helicase in the presence of human replication protein A Genome-wide comprehensive analysis of human helicases More complexity to the Bloom's syndrome complex RMI, a new OB-fold complex essential for Bloom syndrome protein to maintain genome stability The Bloom's syndrome helicase (BLM) interacts physically and functionally with p12, the smallest subunit of human DNA polymerase delta A multiprotein nuclear complex connects Fanconi anemia and Bloom syndrome Human premature aging, DNA repair and RecQ helicases Mus81 functions in the quality control of replication forks at the rDNA and is involved in the maintenance of rDNA repeat number in Saccharomyces cerevisiae The role of the Zn(II) binding domain in the mechanism of E. coli DNA topoisomerase I The C-terminal domain of the Bloom syndrome DNA helicase is essential for genomic stability Structural and functional characterizations reveal the importance of a zinc binding domain in Bloom's syndrome helicase The Bloom's syndrome helicase promotes the annealing of complementary single-stranded DNA Structure and function of the regulatory HRDC domain from human Bloom syndrome protein Structure and Cellular Roles of the RMI Core Complex from the Bloom Syndrome Dissolvasome Crystal structures of RMI1 and RMI2, two OB-fold regulatory subunits of the BLM complex RecQ helicases in DNA double strand break repair and telomere maintenance.Mutations in homologous recombination genes rescue top3 slow growth in Saccharomyces cerevisiae.Slx1-Slx4 is a second structure-specific endonuclease functionally redundant with Sgs1-Top3.An essential DNA strand-exchange activity is conserved in the divergent N-termini of BLM orthologs.Functional overlap between Sgs1-Top3 and the Mms4-Mus81 endonuclease Role of SGS1 and SLX4 in maintaining rDNA structure in Saccharomyces cerevisiae.Decatenation of DNA by the S. cerevisiae Sgs1-Top3-Rmi1 and RPA complex: a mechanism for disentangling chromosomes.Esc2 and Sgs1 act in functionally distinct branches of the homologous recombination repair pathway in Saccharomyces cerevisiae.Yeast Rmi1/Nce4 controls genome stability as a subunit of the Sgs1-Top3 complex.

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The Bloom's syndrome gene product interacts with topoisomerase III

http://www.wikidata.org/entity/Q28139703

description

2000 nî lūn-bûn

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2000 թուականի Մարտին հրատարակուած գիտական յօդուած

@hyw

2000 թվականի մարտին հրատարակված գիտական հոդված

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2000年の論文

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2000年論文

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2000年論文

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2000年論文

@zh-hk

2000年論文

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2000年論文

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2000年论文

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name

The Bloom's syndrome gene product interacts with topoisomerase III

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The Bloom's syndrome gene product interacts with topoisomerase III

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The Bloom's syndrome gene product interacts with topoisomerase III

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type

label

The Bloom's syndrome gene product interacts with topoisomerase III

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The Bloom's syndrome gene product interacts with topoisomerase III

@en

The Bloom's syndrome gene product interacts with topoisomerase III

@nl

prefLabel

The Bloom's syndrome gene product interacts with topoisomerase III

@ast

The Bloom's syndrome gene product interacts with topoisomerase III

@en

The Bloom's syndrome gene product interacts with topoisomerase III

@nl

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JBC.275.13.9636

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Journal of Biological Chemistry

P1476

The Bloom's syndrome gene product interacts with topoisomerase III

@en

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H Goulaouic

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H Turley

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I D Hickson

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K C Gatter

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L Wu

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P S North

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S L Davies

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P2860

Cloning of cDNA encoding a novel mouse DNA topoisomerase III (Topo IIIbeta) possessing negatively supercoiled DNA relaxing activity, whose message is highly expressed in the testis

Mutations in RECQL4 cause a subset of cases of Rothmund-Thomson syndrome

Oligomeric ring structure of the Bloom's syndrome helicase

Human TOP3: a single-copy gene encoding DNA topoisomerase III

The Werner syndrome protein is a DNA helicase

The Bloom's syndrome gene product is a 3'-5' DNA helicase

The Bloom's syndrome gene product is homologous to RecQ helicases

Bloom's and Werner's syndrome genes suppress hyperrecombination in yeast sgs1 mutant: implication for genomic instability in human diseases

Nucleolar localization of the Werner syndrome protein in human cells

Structure and function of type II DNA topoisomerases

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674496

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10.1074/JBC.275.13.9636

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13

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275

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Jean-François Riou

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2000-03-01T00:00:00Z

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12582328

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10734115

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