Rap80

RAP80 binding to polyubiquitin a Schematic of human RAP80 showing the

RAP80 suppresses the vulnerability of Rloops during DNA doublestrand

RAP80 regulates HR a RAP80 binds to and protects polyubiquitin chains

RAP80 suppresses the vulnerability of Rloops during DNA doublestrand

Rap80 uses a molecular ruler mechanism to respond to K63linked

RAP80 Protein Is Important for Genomic Stability and Is Required for

RAP80 binding models RAP80 binds to ubiquitinSUMO hybrid chains

RAP80 and BRCA1 PARsylation protect chromosome integrity by preventing

DOT1Lmediated RAP80 methylation promotes BRCA1 recruitment to elicit

RAP80 Protein Is Important for Genomic Stability and Is Required for

RAP80 and BRCA1 PARsylation protect chromosome integrity by preventing

The UIMcontaining protein RAP80 interacts with BRCA1 and functions in

Rap80 Protein Recruitment to DNA Doublestrand Breaks Requires Binding

DOT1Lmediated RAP80 methylation promotes BRCA1 recruitment to elicit

Rap80 Protein Recruitment to DNA Doublestrand Breaks Requires Binding

DOT1Lmediated RAP80 methylation promotes BRCA1 recruitment to elicit

The UIMcontaining protein RAP80 interacts with BRCA1 and functions in

RAP80 and BRCA1 PARsylation protect chromosome integrity by preventing

The UIMcontaining protein RAP80 interacts with BRCA1 and functions in

RAP80 and BRCA1 PARsylation protect chromosome integrity by preventing

RAP80 suppresses the vulnerability of Rloops during DNA doublestrand

The UIMcontaining protein RAP80 interacts with BRCA1 and functions in

RAP80 Protein Is Important for Genomic Stability and Is Required for

RAP80 and BRCA1 PARsylation protect chromosome integrity by preventing

RAP80 suppresses the vulnerability of Rloops during DNA doublestrand

Abraxas and Rap80 form a novel BRCA1 protein complex required for the

DOT1Lmediated RAP80 methylation promotes BRCA1 recruitment to elicit

RAP80 suppresses the vulnerability of Rloops during DNA doublestrand

DOT1Lmediated RAP80 methylation promotes BRCA1 recruitment to elicit

RAP80 Protein Is Important for Genomic Stability and Is Required for

Rap80 Protein Recruitment to DNA Doublestrand Breaks Requires Binding

RAP80 localizes to the nucleus pEGFPRAP80 A pEGFPRAP80NLS1 B

Abraxas and Rap80 form a novel BRCA1 protein complex required for the

The amino terminus of RAP80 contains a repressor function CHO or CV1

Rap80 Protein Recruitment to DNA Doublestrand Breaks Requires Binding

A Expression of exogenous RAP80 in TOV21G cells B Cells loss of

RAP80 suppresses the vulnerability of Rloops during DNA doublestrand

RAP80 expression increases the level of ER protein A HeLa cells

RNF8 and RNF168 promote the accumulation of 53BP1 and RAP80 at DSB

RAP80 associates with p53 A HeLa cells were cotransfected with

RAP80 binding to polyubiquitin a Schematic of human RAP80 showing the

RAP80 interacts with ubiquitinated H2A and H2B A Endogenous RAP80

Figure 2 from The ubiquitininteracting motif containing protein RAP80

RAP80 Targets BRCA1 to Specific Ubiquitin Structures at DNA Damage

Mutation screening of RAP80 reveals RAP80 delE81 a RAP80 protein

RAP80 suppresses the vulnerability of Rloops during DNA doublestrand

Biochemical reconstitution of the Rap80 complex in vitro A

RAP80 and RNF8 key players in the recruitment of repair proteins to

RAP80 binding models RAP80 binds to ubiquitinSUMO hybrid chains

RNF169 negatively regulates 53BP1 and RAP80 recruitment to DSBs to

RAP80 LLPS regulates HR genomic stability and radiosensitivity A

Both UIMs of RAP80 are required for interaction with monoubiquitinated

PDF The UbiquitinInteracting Motif Containing Protein RAP80

RAP80 suppresses the vulnerability of Rloops during DNA doublestrand

RAP80 interacts with ubiquitinated H2A and H2B A Endogenous RAP80

Binding interaction of RAP80 UIMs and D E81 with DiUb K63 linked

Knockdown of JMJD1C impairs accumulation of RAP80 and BRCA1 on

RAP80 positively regulates ATM activity to promote cell survival by

UIMs of RAP80 are required for its translocation to DNA damage foci

RAP80 binding to polyubiquitin a Schematic of human RAP80 showing the

Ubc13Rnf8 ubiquitin ligases control foci formation of the Rap80

RAP80 delE81 shows reduced ubiquitin binding and localization to damage

DOT1Lmediated RAP80 methylation promotes BRCA1 recruitment to elicit

RAP80 associates with p53 A HeLa cells were cotransfected with

Rap80 Protein Recruitment to DNA Doublestrand Breaks Requires Binding

RNF8 and RNF168 promote the accumulation of 53BP1 and RAP80 at DSB

RAP80 suppresses spontaneous and IRinduced genomic instability A and

Cells expressing RAP80 delE81 show an increase in chromosomal

RAP80 Controls BRE Conformation and Prevents Dimerization A A fusion

RAP80 modulates p53 transactivation activity A effect of RAP80 on p53

Abraxas and Rap80 form a novel BRCA1 protein complex required for the

Ubc13Rnf8 ubiquitin ligases control foci formation of the Rap80

BRCC36 requires interactions within the RAP80 complex for DUB activity

TOV21G is a RAP80null cell line A The expression of RAP80 in 293T

RAP80 forms liquidlike condensates in the nucleus A B HeLa

Anticipated mechanism of consequence due to RAP80 D E81 The model

RAP80 suppresses the vulnerability of Rloops during DNA doublestrand

Epithelialmesenchymal transition is induced by RAP80 knockdown a

RAP80 Targets BRCA1 to Specific Ubiquitin Structures at DNA Damage

A Integration of RAP80 into the BRCA1A complex RAP80 and BRCC36 are

Binding interaction of RAP80 UIMs and E81 with DiUb K63

PDF RAP80 and BRCA1 PARsylation protect chromosome integrity by

RAP80 is an in vivo target of BRCC36 Lys 63 specific DUB activity A

Rap80 Protein Recruitment to DNA Doublestrand Breaks Requires Binding

RAP80 suppresses spontaneous and IRinduced genomic instability A and

Structural Basis of BRCC36 Function in DNA Repair and Immune Regulation

The BRCA1RAP80 Complex Regulates DNA Repair Mechanism Utilization by

K63linked polyubiquitin chains bind to DNA to facilitate DNA damage

The BRCA1RAP80 Complex Regulates DNA Repair Mechanism Utilization by

Molecular Basis for Phosphorylationdependent SUMO Recognition by the

The Rap80BRCC36 deubiquitinating enzyme complex antagonizes RNF8

Cdk1 Proteinmediated Phosphorylation of Receptorassociated Protein 80

PARP1driven PolyADPribosylation Regulates BRCA1 Function in

The Rap80BRCC36 deubiquitinating enzyme complex antagonizes RNF8

A Regulatory Loop Composed of RAP80HDM2p53 Provides RAP80enhanced

Structural Basis of BRCC36 Function in DNA Repair and Immune Regulation

Early recruitment of RAP80BRCA1 to DNA damage sites requires PARP1

Increased chromosomal instability after DNA damage in RAP80depleted

Molecular Basis for Impaired DNA Damage Response Function Associated

Lab Spotlight Biochemistry

The Rap80BRCC36 deubiquitinating enzyme complex antagonizes RNF8

PARP1driven PolyADPribosylation Regulates BRCA1 Function in

RAP80 a Novel Nuclear Protein That Interacts with the Retinoidrelated

Tandem Protein Interaction Modules Organize the UbiquitinDependent

Opposing roles of RNF8RNF168 and deubiquitinating enzymes in

Model showing the removal of the inhibitory barriers posed to resection

Playing the End Game DNA DoubleStrand Break Repair Pathway Choice

USP13 regulates the RAP80BRCA1 complex dependent DNA damage response

RAP80 a Novel Nuclear Protein That Interacts with the Retinoidrelated

A nucleotide and amino acid sequence of human RAP80 The deduced amino

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