Signaling pathways regulated by UBR box-containing E3 ligases

Cited 32 time in scopus
Metadata Downloads

Full metadata record

DC FieldValueLanguage
dc.contributor.authorJung Gi Kim-
dc.contributor.authorHo Chul Shin-
dc.contributor.authorTaewook Seo-
dc.contributor.authorL Nawale-
dc.contributor.authorGoeun Han-
dc.contributor.authorBo Yeon Kim-
dc.contributor.authorSeung Jun Kim-
dc.contributor.authorHyunjoo Cha-Molstad-
dc.date.accessioned2021-08-09T15:30:20Z-
dc.date.available2021-08-09T15:30:20Z-
dc.date.issued2021-
dc.identifier.issn1661-6596-
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/24619-
dc.description.abstractUBR box E3 ligases, also called N-recognins, are integral components of the N-degron pathway. Representative N-recognins include UBR1, UBR2, UBR4, and UBR5, and they bind destabilizing N-terminal residues, termed N-degrons. Understanding the molecular bases of their substrate recognition and the biological impact of the clearance of their substrates on cellular signaling pathways can provide valuable insights into the regulation of these pathways. This review provides an overview of the current knowledge of the binding mechanism of UBR box N-recognin/N-degron interactions and their roles in signaling pathways linked to G-protein-coupled receptors, apoptosis, mitochondrial quality control, inflammation, and DNA damage. The targeting of these UBR box N-recognins can provide potential therapies to treat diseases such as cancer and neurodegenerative diseases.-
dc.publisherMDPI-
dc.titleSignaling pathways regulated by UBR box-containing E3 ligases-
dc.title.alternativeSignaling pathways regulated by UBR box-containing E3 ligases-
dc.typeArticle-
dc.citation.titleInternational Journal of Molecular Sciences-
dc.citation.number15-
dc.citation.endPage8323-
dc.citation.startPage8323-
dc.citation.volume22-
dc.contributor.affiliatedAuthorJung Gi Kim-
dc.contributor.affiliatedAuthorHo Chul Shin-
dc.contributor.affiliatedAuthorTaewook Seo-
dc.contributor.affiliatedAuthorGoeun Han-
dc.contributor.affiliatedAuthorBo Yeon Kim-
dc.contributor.affiliatedAuthorSeung Jun Kim-
dc.contributor.affiliatedAuthorHyunjoo Cha-Molstad-
dc.contributor.alternativeName김정기-
dc.contributor.alternativeName신호철-
dc.contributor.alternativeName서태욱-
dc.contributor.alternativeNameNawale-
dc.contributor.alternativeName한고은-
dc.contributor.alternativeName김보연-
dc.contributor.alternativeName김승준-
dc.contributor.alternativeName차현주-
dc.identifier.bibliographicCitationInternational Journal of Molecular Sciences, vol. 22, no. 15, pp. 8323-8323-
dc.identifier.doi10.3390/ijms22158323-
dc.subject.keywordUBR Box E3 ligases-
dc.subject.keywordN-recognin-
dc.subject.keywordArg/N-degron pathway-
dc.subject.keywordN-degron-
dc.subject.keywordG-protein signaling-
dc.subject.keywordApoptosis-
dc.subject.keywordMitochondrial quality control-
dc.subject.keywordInflammatory response-
dc.subject.keywordDNA damage-
dc.subject.localUBR Box E3 ligases-
dc.subject.localN-recognin-
dc.subject.localArg/N-degron pathway-
dc.subject.localN-degron-
dc.subject.localG-protein signaling-
dc.subject.localapoptosis-
dc.subject.localApoptosis-
dc.subject.localMitochondrial quality control-
dc.subject.localInflammatory Response-
dc.subject.localinflammatory response-
dc.subject.localInflammatory response-
dc.subject.localDNA damage-
dc.description.journalClassY-
Appears in Collections:
Critical Diseases Diagnostics Convergence Research Center > 1. Journal Articles
Ochang Branch Institute > Chemical Biology Research Center > 1. Journal Articles
Ochang Branch Institute > Nucleic Acid Therapeutics Research Center > 1. Journal Articles
Files in This Item:
  • There are no files associated with this item.


Items in OpenAccess@KRIBB are protected by copyright, with all rights reserved, unless otherwise indicated.