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Phosphorylation-dependent activity of the deubiquitinase DUBA.

Nat. Struct. Mol. Biol.2012 Jan 15;19(2):171-5
Oscar W Huang 1 , Xiaolei Ma , JianPing Yin , Jeremy Flinders , Till Maurer , Nobuhiko Kayagaki , Qui Phung , Ivan Bosanac , David Arnott , Vishva M Dixit , Sarah G Hymowitz , Melissa A Starovasnik , Andrea G Cochran
Oscar W Huang 1 , Xiaolei Ma , JianPing Yin , Jeremy Flinders , Till Maurer , Nobuhiko Kayagaki , Qui Phung , Ivan Bosanac , David Arnott , Vishva M Dixit , Sarah G Hymowitz , Melissa A Starovasnik , Andrea G Cochran
+ et al

[No authors listed]

Author information
  • 1 Department of Early Discovery Biochemistry, Genentech, South San Francisco, California, USA.

摘要


Addition and removal of ubiquitin or ubiquitin chains to and from proteins is a tightly regulated process that contributes to cellular signaling and protein stability. Here we show that phosphorylation of the human deubiquitinase DUBA (OTUD5) at a single residue, Ser177, is both necessary and sufficient to activate the enzyme. The crystal structure of the ubiquitin aldehyde adduct of active DUBA reveals a marked cooperation between phosphorylation and substrate binding. An intricate web of interactions involving the phosphate and the C-terminal tail of ubiquitin cause DUBA to fold around its substrate, revealing why phosphorylation is essential for deubiquitinase activity. Phosphoactivation of DUBA represents an unprecedented mode of protease regulation and a clear link between two major cellular signal transduction systems: phosphorylation and ubiquitin modification.