DDB1 is a cellular substrate of NS3/4A protease and required for hepatitis C virus replication (Q24302998)

viral release from host cell

GOA release 2020-03-11

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GOA release 2020-03-11

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1 reference

Xi Kang

1

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Xi Chen

2

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Ying He

3

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Deyin Guo

4

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Lin Guo

5

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Jin Zhong

6

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Hong-Bing Shu

The p127 subunit (DDB1) of the UV-DNA damage repair binding protein is essential for the targeted degradation of STAT1 by the V protein of the paramyxovirus simian virus 5

7

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language of work or name

English

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publication date

20 January 2013

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published in

Virology

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volume

435

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issue

2

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page(s)

385-94

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cites work

1 reference

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Degradation of STAT1 and STAT2 by the V proteins of simian virus 5 and human parainfluenza virus type 2, respectively: consequences for virus replication in the presence of alpha/beta and gamma interferons

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UV-damaged DNA-binding proteins are targets of CUL-4A-mediated ubiquitination and degradation

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Radiation-mediated proteolysis of CDT1 by CUL4–ROC1 and CSN complexes constitutes a new checkpoint

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CUL4-DDB1 ubiquitin ligase interacts with multiple WD40-repeat proteins and regulates histone methylation

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Hepatitis C virus glycoproteins mediate pH-dependent cell entry of pseudotyped retroviral particles

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Hepatitis C virus infection

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Hepatitis B virus X protein stimulates viral genome replication via a DDB1-dependent pathway distinct from that leading to cell death

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A promiscuous alpha-helical motif anchors viral hijackers and substrate receptors to the CUL4-DDB1 ubiquitin ligase machinery

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Hepatitis C virus protease NS3/4A cleaves mitochondrial antiviral signaling protein off the mitochondria to evade innate immunity

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Primate lentiviral Vpx commandeers DDB1 to counteract a macrophage restriction

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UV-induced ubiquitylation of XPC protein mediated by UV-DDB-ubiquitin ligase complex.

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Histone H3 and H4 ubiquitylation by the CUL4-DDB-ROC1 ubiquitin ligase facilitates cellular response to DNA damage

7 January 2021

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Human De-etiolated-1 regulates c-Jun by assembling a CUL4A ubiquitin ligase

7 January 2021

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VISA is an adapter protein required for virus-triggered IFN-beta signaling

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Hepatocyte-specific deletion of DDB1 induces liver regeneration and tumorigenesis

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Robust hepatitis C virus infection in vitro

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Nonstructural protein 3 of the hepatitis C virus encodes a serine-type proteinase required for cleavage at the NS3/4 and NS4/5 junctions

7 January 2021

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inferred from DOI database lookup

7 January 2021

based on heuristic

The V protein of simian virus 5 inhibits interferon signalling by targeting STAT1 for proteasome-mediated degradation

1 reference

https://api.crossref.org/works/10.1016%2FJ.VIROL.2012.10.025