Structure of the A20 OTU domain and mechanistic insights into deubiquitination.

The NF-kappaB (nuclear factor kappaB) regulator A20 antagonises IKK [IkappaB (inhibitor of kappaB) kinase] activation by modulating Lys63-linked polyubiquitination of cytokine-receptor-associated factors including TRAF2/6 (tumour-necrosis-factor-receptor-associated factor 2/6) and RIP1 (receptor-interacting protein 1). In the present paper we describe the crystal structure of the N-terminal OTU (ovarian tumour) deubiquitinase domain of ...
A20, which differs from other deubiquitinases but shares the minimal catalytic core with otubain-2. Analysis of conserved surface regions allows prediction of ubiquitin-binding sites for the proximal and distal ubiquitin molecules. Structural and biochemical analysis suggests a novel architecture of the catalytic triad, which might be present in a subset of OTU domains including Cezanne and TRABID (TRAF-binding domain). Biochemical analysis shows a preference of the isolated A20 OTU domain for Lys48-linked tetraubiquitin in vitro suggesting that additional specificity factors might be required for the physiological function of A20 in cells.
Mesh Terms:
Amino Acid Sequence, Biochemistry, Catalysis, Catalytic Domain, Cloning, Molecular, Humans, I-kappa B Kinase, Intracellular Signaling Peptides and Proteins, Lysine, Molecular Sequence Data, Nuclear Pore Complex Proteins, Nuclear Proteins, Phosphorylation, Protein Structure, Tertiary, RNA-Binding Proteins, Thiolester Hydrolases, Ubiquitin
Biochem. J.
Date: Jan. 01, 2008
Download Curated Data For This Publication
86549
Switch View:
  • Interactions 1