NFBD1, a novel nuclear protein with signature motifs of FHA and BRCT, and an internal 41-amino acid repeat sequence, is an early participant in DNA damage response (Q28217141)

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scientific article (publication date: 21 February 2003)

Language	Label	Description	Also known as
English	NFBD1, a novel nuclear protein with signature motifs of FHA and BRCT, and an internal 41-amino acid repeat sequence, is an early participant in DNA damage response	scientific article (publication date: 21 February 2003)

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scholarly article

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NFBD1, a novel nuclear protein with signature motifs of FHA and BRCT, and an internal 41-amino acid repeat sequence, is an early participant in DNA damage response (English)

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author name string

Yong Lei Shang

1

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Amanda J Bodero

2

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Phang-Lang Chen

3

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language of work or name

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publication date

21 February 2003

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Journal of Biological Chemistry

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278

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8

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6323-9

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Defects in a cell cycle checkpoint may be responsible for the genomic instability of cancer cells

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Checkpoint pathways come of age.

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A unified view of the DNA-damage checkpoint

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Aerial dispersal of pathogens on the global and continental scales and its impact on plant disease

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The recognition of DNA damage

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Rad53 FHA domain associated with phosphorylated Rad9 in the DNA damage checkpoint

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The budding yeast Rad9 checkpoint protein is subjected to Mec1/Tel1-dependent hyperphosphorylation and interacts with Rad53 after DNA damage

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Rad9 phosphorylation sites couple Rad53 to the Saccharomyces cerevisiae DNA damage checkpoint

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Activation of Rad53 kinase in response to DNA damage and its effect in modulating phosphorylation of the lagging strand DNA polymerase.

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The set1Delta mutation unveils a novel signaling pathway relayed by the Rad53-dependent hyperphosphorylation of replication protein A that leads to transcriptional activation of repair genes

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The ribonucleotide reductase inhibitor Sml1 is a new target of the Mec1/Rad53 kinase cascade during growth and in response to DNA damage

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The human checkpoint protein hRad17 interacts with the PCNA-like proteins hRad1, hHus1, and hRad9

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Structure-based predictions of Rad1, Rad9, Hus1 and Rad17 participation in sliding clamp and clamp-loading complexes

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Phosphorylation of serines 635 and 645 of human Rad17 is cell cycle regulated and is required for G(1)/S checkpoint activation in response to DNA damage

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ATR/ATM-mediated phosphorylation of human Rad17 is required for genotoxic stress responses

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Regulation of ATR substrate selection by Rad17-dependent loading of Rad9 complexes onto chromatin

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Conservation of the Chk1 checkpoint pathway in mammals: linkage of DNA damage to Cdk regulation through Cdc25

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A human Cds1-related kinase that functions downstream of ATM protein in the cellular response to DNA damage

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Linkage of ATM to cell cycle regulation by the Chk2 protein kinase

1 reference

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ATR-mediated checkpoint pathways regulate phosphorylation and activation of human Chk1

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Mammalian G1- and S-phase checkpoints in response to DNA damage

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M210749200

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Regulation of the G2/M transition by p53.

1 reference

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21 January 2018

The RAD9 gene controls the cell cycle response to DNA damage in Saccharomyces cerevisiae

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M210749200

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BRCA1 protein products ... Functional motifs...

1 reference

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Requirement of ATM-dependent phosphorylation of brca1 in the DNA damage response to double-strand breaks

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M210749200

21 January 2018

Functional interactions between BRCA1 and the checkpoint kinase ATR during genotoxic stress

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M210749200

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Involvement of Brca1 in S-phase and G(2)-phase checkpoints after ionizing irradiation

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M210749200

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Centrosome amplification and a defective G2-M cell cycle checkpoint induce genetic instability in BRCA1 exon 11 isoform-deficient cells

1 reference

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21 January 2018

hCds1-mediated phosphorylation of BRCA1 regulates the DNA damage response

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M210749200

21 January 2018

Brca1 controls homology-directed DNA repair

1 reference

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The RING heterodimer BRCA1-BARD1 is a ubiquitin ligase inactivated by a breast cancer-derived mutation

1 reference

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Lessons learned from BRCA1 and BRCA2.

1 reference

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p53 binding protein 1 (53BP1) is an early participant in the cellular response to DNA double-strand breaks

1 reference

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Tumor suppressor p53 binding protein 1 (53BP1) is involved in DNA damage-signaling pathways

1 reference

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Negative cell cycle regulation and DNA damage-inducible phosphorylation of the BRCT protein 53BP1.

1 reference

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Phosphorylation and rapid relocalization of 53BP1 to nuclear foci upon DNA damage

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Prediction of the coding sequences of unidentified human genes. V. The coding sequences of 40 new genes (KIAA0161-KIAA0200) deduced by analysis of cDNA clones from human cell line KG-1

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NFBD1/KIAA0170 is a novel nuclear transcriptional transactivator with BRCT domain

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https://api.crossref.org/works/10.1074%2FJBC.M210749200

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The FHA domain: a putative nuclear signalling domain found in protein kinases and transcription factors

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https://api.crossref.org/works/10.1074%2FJBC.M210749200

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Phosphorylation of the retinoblastoma gene product is modulated during the cell cycle and cellular differentiation

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The amino-terminal region of the retinoblastoma gene product binds a novel nuclear matrix protein that co-localizes to centers for RNA processing

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Association of BRCA1 with the hRad50-hMre11-p95 complex and the DNA damage response

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M210749200

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DNA double-stranded breaks induce histone H2AX phosphorylation on serine 139

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M210749200

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Threonine 68 of Chk2 is phosphorylated at sites of DNA strand breaks

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https://api.crossref.org/works/10.1074%2FJBC.M210749200

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A critical role for histone H2AX in recruitment of repair factors to nuclear foci after DNA damage

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Ataxia telangiectasia-mutated phosphorylates Chk2 in vivo and in vitro

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Budding yeast Rad9 is an ATP-dependent Rad53 activating machine.

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Threonine 68 is required for radiation-induced phosphorylation and activation of Cds1.

1 reference

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Structure of an XRCC1 BRCT domain: a new protein-protein interaction module

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Crystal structure of the BRCT repeat region from the breast cancer-associated protein BRCA1

1 reference

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Structure of the 53BP1 BRCT region bound to p53 and its comparison to the Brca1 BRCT structure

1 reference

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Crystal structure of human 53BP1 BRCT domains bound to p53 tumour suppressor

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Characterization of a carboxy-terminal BRCA1 interacting protein

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The C-terminal (BRCT) domains of BRCA1 interact in vivo with CtIP, a protein implicated in the CtBP pathway of transcriptional repression

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Binding of CtIP to the BRCT repeats of BRCA1 involved in the transcription regulation of p21 is disrupted upon DNA damage

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Functional link of BRCA1 and ataxia telangiectasia gene product in DNA damage response

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Two cellular proteins that bind to wild-type but not mutant p53

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M210749200

21 January 2018

Regulation of p53 in response to DNA damage

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M210749200

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ATM phosphorylates histone H2AX in response to DNA double-strand breaks

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M210749200

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Histone H2AX is phosphorylated in an ATR-dependent manner in response to replicational stress

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M210749200

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Genomic instability in mice lacking histone H2AX

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M210749200

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BRCA1 mutations in primary breast and ovarian carcinomas

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Low-penetrance susceptibility to breast cancer due to CHEK2(*)1100delC in noncarriers of BRCA1 or BRCA2 mutations

1 reference

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21 January 2018

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10.1074/JBC.M210749200

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