RAP80 interacts with the SUMO-conjugating enzyme UBC9 and is a novel target for sumoylation (Q24670038)

2

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Yong-Sik Kim

3

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Joung Hyuck Joo

4

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Anton M Jetten

Biochemical and Biophysical Research Communications

5

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language of work or name

English

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publication date

12 October 2007

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published in

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volume

362

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page(s)

132-8

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issue

1

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cites work

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Ubiquitin-binding protein RAP80 mediates BRCA1-dependent DNA damage response

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RAP80 targets BRCA1 to specific ubiquitin structures at DNA damage sites

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RAP80, a novel nuclear protein that interacts with the retinoid-related testis-associated receptor

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Transcription factor AP-2 interacts with the SUMO-conjugating enzyme UBC9 and is sumolated in vivo

7 April 2017

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SUMO-1 modification and its role in targeting the Ran GTPase-activating protein, RanGAP1, to the nuclear pore complex

7 April 2017

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Mammalian ubiquitin-conjugating enzyme Ubc9 interacts with Rad51 recombination protein and localizes in synaptonemal complexes

7 April 2017

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SUMO-1 modification of IkappaBalpha inhibits NF-kappaB activation

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SUMOylation of the corepressor N-CoR modulates its capacity to repress transcription.

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Protein modification by SUMO

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Ubiquitin-interaction motifs of RAP80 are critical in its regulation of estrogen receptor alpha.

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SARS-CoV nucleocapsid protein binds to hUbc9, a ubiquitin conjugating enzyme of the sumoylation system

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28 September 2017

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Role of SUMO/Ubc9 in DNA damage repair and tumorigenesis

28 September 2017

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Regulation of ubiquitin-binding proteins by monoubiquitination

28 September 2017

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Assembly of a polymeric chain of SUMO1 on human topoisomerase I in vitro

28 September 2017

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A field guide to ubiquitylation

28 September 2017

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SUMO: a regulator of gene expression and genome integrity.

28 September 2017

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Small ubiquitin-related modifier-1 modification mediates resolution of CREB-dependent responses to hypoxia

28 September 2017

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A SUMOry of DNA Replication: Synthesis, Damage, and Repair

28 September 2017

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SUMO-1/Ubc9 promotes nuclear accumulation and metabolic stability of tumor suppressor Smad4

28 November 2018

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https://pubmed.ncbi.nlm.nih.gov/17698038