Ontology highlight
ABSTRACT:
SUBMITTER: Smith H
PROVIDER: S-EPMC2651833 | biostudies-literature | 2009 Mar
REPOSITORIES: biostudies-literature
Smith Hilary H Peggie Mark M Campbell David G DG Vandermoere Franck F Carrick Emma E Cohen Philip P
Proceedings of the National Academy of Sciences of the United States of America 20090305 12
The E3 ubiquitin ligase Pellino can be activated by phosphorylation in vitro, catalyzed by IL-1 receptor-associated kinase 1 (IRAK1) or IRAK4. Here, we show that phosphorylation enhances the E3 ligase activity of Pellino 1 similarly with any of several E2-conjugating enzymes (Ubc13-Uev1a, UbcH4, or UbcH5a/5b) and identify 7 amino acid residues in Pellino 1 whose phosphorylation is critical for activation. Five of these sites are clustered between residues 76 and 86 (Ser-76, Ser-78, Thr-80, Ser-8 ...[more]