DC Field | Value | Language |
---|---|---|
dc.contributor.author | S M Sriram | - |
dc.contributor.author | Bo Yeon Kim | - |
dc.contributor.author | Y T Kwon | - |
dc.date.accessioned | 2017-04-19T09:25:57Z | - |
dc.date.available | 2017-04-19T09:25:57Z | - |
dc.date.issued | 2011 | - |
dc.identifier.issn | 1471-0072 | - |
dc.identifier.uri | 10.1038/nrm3217 | ko |
dc.identifier.uri | https://oak.kribb.re.kr/handle/201005/10412 | - |
dc.description.abstract | The N-end rule defines the protein-destabilizing activity of a given amino-terminal residue and its post-translational modification. Since its discovery 25 years ago, the pathway involved in the N-end rule has been thought to target only a limited set of specific substrates of the ubiquitin-proteasome system. Recent studies have provided insights into the components, substrates, functions and structural basis of substrate recognition. The N-end rule pathway is now emerging as a major cellular proteolytic system, in which the majority of proteins are born with or acquire specific N-terminal degradation determinants through protein-specific or global post-translational modifications. | - |
dc.publisher | Springer-Nature Pub Group | - |
dc.title | The N-end rule pathway: emerging functions and molecular principles of substrate recognition | - |
dc.title.alternative | The N-end rule pathway: emerging functions and molecular principles of substrate recognition | - |
dc.type | Article | - |
dc.citation.title | Nature Reviews Molecular Cell Biology | - |
dc.citation.number | 12 | - |
dc.citation.endPage | 747 | - |
dc.citation.startPage | 735 | - |
dc.citation.volume | 12 | - |
dc.contributor.affiliatedAuthor | Bo Yeon Kim | - |
dc.contributor.alternativeName | Sriram | - |
dc.contributor.alternativeName | 김보연 | - |
dc.contributor.alternativeName | 권용태 | - |
dc.identifier.bibliographicCitation | Nature Reviews Molecular Cell Biology, vol. 12, no. 12, pp. 735-747 | - |
dc.identifier.doi | 10.1038/nrm3217 | - |
dc.description.journalClass | Y | - |
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