Loading
PDBj
MenuPDBj@FacebookPDBj@X(formerly Twitter)PDBj@BlueSkyPDBj@YouTubewwPDB FoundationwwPDBDonate
RCSB PDBPDBeBMRBAdv. SearchSearch help

5OHP

Crystal structure of USP30 (C77A) in complex with Lys6-linked diubiquitin

Summary for 5OHP
Entry DOI10.2210/pdb5ohp/pdb
Related5OHK
DescriptorUbiquitin carboxyl-terminal hydrolase 30, Polyubiquitin-B, ZINC ION, ... (4 entities in total)
Functional Keywordsdub, ubiquitin, usp, k6, hydrolase
Biological sourceHomo sapiens (Human)
More
Total number of polymer chains3
Total formula weight55656.43
Authors
Gersch, M.,Komander, D. (deposition date: 2017-07-17, release date: 2017-09-20, Last modification date: 2024-01-17)
Primary citationGersch, 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: 28945249
DOI: 10.1038/nsmb.3475
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.8 Å)
Structure validation

246031

数据于2025-12-10公开中

PDB statisticsPDBj update infoContact PDBjnumon