(Q27649882)

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Pathogenicity of the BRCA1 missense variant M1775K is determined by the disruption of the BRCT phosphopeptide-binding pocket: a multi-modal approach

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Pathogenicity of the BRCA1 missense variant M1775K is determined by the disruption of the BRCT phosphopeptide-binding pocket: a multi-modal approach (English)

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Marcelo A Carvalho

object named as

Marcelo A Carvalho

3

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Gabriel Birrane

object named as

Gabriel Birrane

4

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Alvaro Monteiro

object named as

Alvaro N Monteiro

16

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William David Foulkes

object named as

William D Foulkes

18

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14

object named as

David E Goldgar

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Sean V Tavtigian

15

object named as

Sean V Tavtigian

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2

object named as

Nancy Hamel

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11

object named as

Scott A Grist

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Marc Tischkowitz

1

object named as

Marc Tischkowitz

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author name string

Aditi Soni

5

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Erik H van Beers

6

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Simon A Joosse

7

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Nora Wong

8

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David Novak

9

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Louise A Quenneville

10

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Petra M Nederlof

13

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John A A Ladias

17

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publication date

July 2008

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European Journal of Human Genetics

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16

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7

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820-32

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DNA damage-induced cell cycle checkpoint control requires CtIP, a phosphorylation-dependent binding partner of BRCA1 C-terminal domains

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Structural consequences of a cancer-causing BRCA1-BRCT missense mutation

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BACH1, a novel helicase-like protein, interacts directly with BRCA1 and contributes to its DNA repair function

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BRCT Repeats As Phosphopeptide-Binding Modules Involved in Protein Targeting

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Functional impact of missense variants in BRCA1 predicted by supervised learning

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Structure and mechanism of BRCA1 BRCT domain recognition of phosphorylated BACH1 with implications for cancer

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Structure of the BRCT repeats of BRCA1 bound to a BACH1 phosphopeptide: implications for signaling

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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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20 March 2017

Structure of the BRCT Repeats of BRCA1 Bound to a BACH1 Phosphopeptide

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Determination of cancer risk associated with germ line BRCA1 missense variants by functional analysis

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Genetic analysis of BRCA1 ubiquitin ligase activity and its relationship to breast cancer susceptibility

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Comprehensive statistical study of 452 BRCA1 missense substitutions with classification of eight recurrent substitutions as neutral

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Structural basis of phosphopeptide recognition by the BRCT domain of BRCA1.

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Cancer risk assessment at the atomic level

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Processing of X-ray diffraction data collected in oscillation mode

1 reference

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1 reference

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10.1038/EJHG.2008.13

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