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PDBsum entry 5cvl

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protein ligands metals links
Protein binding PDB id
5cvl

 

 

 

 

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Contents
Protein chain
526 a.a.
Ligands
PO4 ×2
Metals
_AU ×7
Waters ×137
PDB id:
5cvl
Name: Protein binding
Title: Wdr48 (uaf-1), residues 2-580
Structure: Wd repeat-containing protein 48. Chain: a. Fragment: unp residues 2-580. Synonym: usp1-associated factor 1,wd repeat endosomal protein,p80. Engineered: yes
Source: Homo sapiens. Human. Organism_taxid: 9606. Gene: wdr48, kiaa1449, uaf1. Expressed in: trichoplusia ni. Expression_system_taxid: 7111.
Resolution:
3.00Å     R-factor:   0.190     R-free:   0.233
Authors: S.F.Harris,J.Yin
Key ref: J.Yin et al. (2015). Structural Insights into WD-Repeat 48 Activation of Ubiquitin-Specific Protease 46. Structure, 23, 2043-2054. PubMed id: 26388029 DOI: 10.1016/j.str.2015.08.010
Date:
27-Jul-15     Release date:   07-Oct-15    
PROCHECK
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 Headers
 References

Protein chain
Pfam   ArchSchema ?
Q8TAF3  (WDR48_HUMAN) -  WD repeat-containing protein 48 from Homo sapiens
Seq:
Struc:
 
Seq:
Struc:
677 a.a.
526 a.a.
Key:    PfamA domain  Secondary structure

 

 
DOI no: 10.1016/j.str.2015.08.010 Structure 23:2043-2054 (2015)
PubMed id: 26388029  
 
 
Structural Insights into WD-Repeat 48 Activation of Ubiquitin-Specific Protease 46.
J.Yin, A.J.Schoeffler, K.Wickliffe, K.Newton, M.A.Starovasnik, E.C.Dueber, S.F.Harris.
 
  ABSTRACT  
 
Protein ubiquitination patterns are an important component of cellular signaling. The WD-repeat protein WDR48 (USP1-associated factor UAF-1) stimulates activity of ubiquitin-specific proteases USP1, USP12, and USP46. To understand how WDR48 exerts its effect on the USP scaffold, we determined structures of the ternary WDR48:USP46:ubiquitin complex. WDR48 interacts with the USP46 fingers subdomain via a relatively small, highly polar surface on the top center of the WDR48 β propeller. In addition, WDR48 has a novel ancillary domain and a C-terminal SUMO-like domain encircling the USP46-bound ubiquitin. Mutation of residues involved in the WDR48:USP46 interaction abrogated both binding and deubiquitinase activity of the complex. An analogous mutation in USP1 similarly blocked WDR48-dependent activation. Our data suggest a possible mechanism of deubiquitinase stimulation via stabilization and prolonged residence time of substrate. The unprecedented mode of interaction between the USP fingers domain and the WD-repeat β propeller serves as a prototypical example for this family of deubiquitinases.
 

 

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