Ontology highlight
ABSTRACT:
SUBMITTER: Huang G
PROVIDER: S-EPMC4263876 | biostudies-literature | 2014 Dec
REPOSITORIES: biostudies-literature
Huang Guochang G Stock Cameron C Bommeljé Claire C CC Weeda Víola B VB Shah Kushyup K Bains Sarina S Buss Elizabeth E Shaha Manish M Rechler Willi W Ramanathan Suresh Y SY Singh Bhuvanesh B
The Journal of biological chemistry 20141027 50
The activity of cullin-RING type ubiquitination E3 ligases is regulated by neddylation, a process analogous to ubiquitination that culminates in covalent attachment of the ubiquitin-like protein Nedd8 to cullins. As a component of the E3 for neddylation, SCCRO/DCUN1D1 plays a key regulatory role in neddylation and, consequently, cullin-RING ligase activity. The essential contribution of SCCRO to neddylation is to promote nuclear translocation of the cullin-ROC1 complex. The presence of a myristo ...[more]