5OHP
Crystal structure of USP30 (C77A) in complex with Lys6-linked diubiquitin
Summary for 5OHP
| Entry DOI | 10.2210/pdb5ohp/pdb |
| Related | 5OHK |
| Descriptor | Ubiquitin carboxyl-terminal hydrolase 30, Polyubiquitin-B, ZINC ION, ... (4 entities in total) |
| Functional Keywords | dub, ubiquitin, usp, k6, hydrolase |
| Biological source | Homo sapiens (Human) More |
| Total number of polymer chains | 3 |
| Total formula weight | 55656.43 |
| Authors | Gersch, M.,Komander, D. (deposition date: 2017-07-17, release date: 2017-09-20, Last modification date: 2024-01-17) |
| Primary citation | Gersch, M.,Gladkova, C.,Schubert, A.F.,Michel, M.A.,Maslen, S.,Komander, D. Mechanism and regulation of the Lys6-selective deubiquitinase USP30. Nat. Struct. Mol. Biol., 24:920-930, 2017 Cited by PubMed Abstract: Damaged mitochondria undergo mitophagy, a specialized form of autophagy that is initiated by the protein kinase PINK1 and the ubiquitin E3 ligase Parkin. Ubiquitin-specific protease USP30 antagonizes Parkin-mediated ubiquitination events on mitochondria and is a key negative regulator of mitophagy. Parkin and USP30 both show a preference for assembly or disassembly, respectively, of Lys6-linked polyubiquitin, a chain type that has not been well studied. Here we report crystal structures of human USP30 bound to monoubiquitin and Lys6-linked diubiquitin, which explain how USP30 achieves Lys6-linkage preference through unique ubiquitin binding interfaces. We assess the interplay between USP30, PINK1 and Parkin and show that distally phosphorylated ubiquitin chains impair USP30 activity. Lys6-linkage-specific affimers identify numerous mitochondrial substrates for this modification, and we show that USP30 regulates Lys6-polyubiquitinated TOM20. Our work provides insights into the architecture, activity and regulation of USP30, which will aid drug design against this and related enzymes. PubMed: 28945249DOI: 10.1038/nsmb.3475 PDB entries with the same primary citation |
| Experimental method | X-RAY DIFFRACTION (2.8 Å) |
Structure validation
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