Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
15
pubmed:dateCreated
2001-8-2
pubmed:abstractText
NEDD8/Rub1 is a ubiquitin (Ub)-like post-translational modifier that is covalently linked to cullin (Cul)-family proteins in a manner analogous to ubiquitylation. NEDD8 is known to enhance the ubiquitylating activity of the SCF complex (composed of Skp1, Cul-1, ROC1 and F-box protein), but the mechanistic role is largely unknown. Using an in vitro reconstituted system, we report here that NEDD8 modification of Cul-1 enhances recruitment of Ub-conjugating enzyme Ubc4 (E2) to the SCF complex (E3). This recruitment requires thioester linkage of Ub to Ubc4. Our findings indicate that the NEDD8-modifying system accelerates the formation of the E2-E3 complex, which stimulates protein polyubiquitylation.
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/11483504-10072378, http://linkedlifedata.com/resource/pubmed/commentcorrection/11483504-10089879, http://linkedlifedata.com/resource/pubmed/commentcorrection/11483504-10207026, http://linkedlifedata.com/resource/pubmed/commentcorrection/11483504-10213691, http://linkedlifedata.com/resource/pubmed/commentcorrection/11483504-10230407, http://linkedlifedata.com/resource/pubmed/commentcorrection/11483504-10232975, http://linkedlifedata.com/resource/pubmed/commentcorrection/11483504-10385629, http://linkedlifedata.com/resource/pubmed/commentcorrection/11483504-10445024, http://linkedlifedata.com/resource/pubmed/commentcorrection/11483504-10579999, http://linkedlifedata.com/resource/pubmed/commentcorrection/11483504-10597293, http://linkedlifedata.com/resource/pubmed/commentcorrection/11483504-10611969, http://linkedlifedata.com/resource/pubmed/commentcorrection/11483504-10644755, http://linkedlifedata.com/resource/pubmed/commentcorrection/11483504-10694884, http://linkedlifedata.com/resource/pubmed/commentcorrection/11483504-10713156, http://linkedlifedata.com/resource/pubmed/commentcorrection/11483504-10722740, http://linkedlifedata.com/resource/pubmed/commentcorrection/11483504-10772955, http://linkedlifedata.com/resource/pubmed/commentcorrection/11483504-10781063, http://linkedlifedata.com/resource/pubmed/commentcorrection/11483504-10806345, http://linkedlifedata.com/resource/pubmed/commentcorrection/11483504-10872471, http://linkedlifedata.com/resource/pubmed/commentcorrection/11483504-10880460, http://linkedlifedata.com/resource/pubmed/commentcorrection/11483504-10884686, http://linkedlifedata.com/resource/pubmed/commentcorrection/11483504-10921923, http://linkedlifedata.com/resource/pubmed/commentcorrection/11483504-10934491, http://linkedlifedata.com/resource/pubmed/commentcorrection/11483504-11027288, http://linkedlifedata.com/resource/pubmed/commentcorrection/11483504-11178226, http://linkedlifedata.com/resource/pubmed/commentcorrection/11483504-11231585, http://linkedlifedata.com/resource/pubmed/commentcorrection/11483504-7724550, http://linkedlifedata.com/resource/pubmed/commentcorrection/11483504-8717528, http://linkedlifedata.com/resource/pubmed/commentcorrection/11483504-9008162, http://linkedlifedata.com/resource/pubmed/commentcorrection/11483504-9430629, http://linkedlifedata.com/resource/pubmed/commentcorrection/11483504-9531529, http://linkedlifedata.com/resource/pubmed/commentcorrection/11483504-9531531, http://linkedlifedata.com/resource/pubmed/commentcorrection/11483504-9545234, http://linkedlifedata.com/resource/pubmed/commentcorrection/11483504-9597130, http://linkedlifedata.com/resource/pubmed/commentcorrection/11483504-9624055, http://linkedlifedata.com/resource/pubmed/commentcorrection/11483504-9694792, http://linkedlifedata.com/resource/pubmed/commentcorrection/11483504-9759494, http://linkedlifedata.com/resource/pubmed/commentcorrection/11483504-9859996, http://linkedlifedata.com/resource/pubmed/commentcorrection/11483504-9990852
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/DNA-Binding Proteins, http://linkedlifedata.com/resource/pubmed/chemical/I-kappa B Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Ligases, http://linkedlifedata.com/resource/pubmed/chemical/NEDD8 protein, human, http://linkedlifedata.com/resource/pubmed/chemical/NF-kappaB inhibitor alpha, http://linkedlifedata.com/resource/pubmed/chemical/Peptide Synthases, http://linkedlifedata.com/resource/pubmed/chemical/SKP Cullin F-Box Protein Ligases, http://linkedlifedata.com/resource/pubmed/chemical/Ubiquitin-Conjugating Enzymes, http://linkedlifedata.com/resource/pubmed/chemical/Ubiquitin-Protein Ligase Complexes, http://linkedlifedata.com/resource/pubmed/chemical/Ubiquitin-Protein Ligases, http://linkedlifedata.com/resource/pubmed/chemical/Ubiquitins, http://linkedlifedata.com/resource/pubmed/chemical/anaphase-promoting complex, http://linkedlifedata.com/resource/pubmed/chemical/ubiquitin-conjugating enzyme UBC4
pubmed:status
MEDLINE
pubmed:month
Aug
pubmed:issn
0261-4189
pubmed:author
pubmed:issnType
Print
pubmed:day
1
pubmed:volume
20
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
4003-12
pubmed:dateRevised
2009-11-18
pubmed:meshHeading
pubmed:year
2001
pubmed:articleTitle
NEDD8 recruits E2-ubiquitin to SCF E3 ligase.
pubmed:affiliation
Department of Gastroenterology, Faculty of Medicine, University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo 113-8655, Japan.
pubmed:publicationType
Journal Article
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