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PDBsum entry 4wyu

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protein ligands metals Protein-protein interface(s) links
Structural protein/peptide PDB id
4wyu

 

 

 

 

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Contents
Protein chains
201 a.a.
Ligands
SER-TRP-PHE-GLN-
THR-ASP-LEU
×2
Metals
IOD ×7
Waters ×108
PDB id:
4wyu
Name: Structural protein/peptide
Title: Crystal structure of scribble pdz34 tandem in complex with its target peptide
Structure: Protein scribble homolog. Chain: a, b. Fragment: pdz3/pdz4 tandem (unp residues 992-1203). Synonym: hscrib,protein lap4. Engineered: yes. Peptide ser-trp-phe-gln-thr-asp-leu. Chain: d, c. Synonym: synthetic pdz binding motif. Engineered: yes
Source: Homo sapiens. Human. Organism_taxid: 9606. Gene: scrib, crib1, kiaa0147, lap4, scrb1, vartul. Expressed in: escherichia coli. Expression_system_taxid: 469008. Synthetic: yes. Synthetic construct. Organism_taxid: 32630.
Resolution:
2.50Å     R-factor:   0.191     R-free:   0.227
Authors: J.Q.Ren,H.H.Pei,W.Feng
Key ref: J.Ren et al. (2015). Interdomain interface-mediated target recognition by the Scribble PDZ34 supramodule. Biochem J, 468, 133-144. PubMed id: 25734361 DOI: 10.1042/BJ20141473
Date:
18-Nov-14     Release date:   21-Oct-15    
PROCHECK
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 Headers
 References

Protein chains
Pfam   ArchSchema ?
Q14160  (SCRIB_HUMAN) -  Protein scribble homolog from Homo sapiens
Seq:
Struc:
 
Seq:
Struc:
 
Seq:
Struc:
 
Seq:
Struc:
1655 a.a.
201 a.a.
Key:    PfamA domain  Secondary structure  CATH domain

 

 
DOI no: 10.1042/BJ20141473 Biochem J 468:133-144 (2015)
PubMed id: 25734361  
 
 
Interdomain interface-mediated target recognition by the Scribble PDZ34 supramodule.
J.Ren, L.Feng, Y.Bai, H.Pei, Z.Yuan, W.Feng.
 
  ABSTRACT  
 
Tandem-arranged PDZ [PSD-95 (postsynaptic density-95), Dlg (discs large homologue) and ZO-1 (zonula occludens-1)] domains often form structural and functional supramodules with distinct target-binding properties. In the present study, we found that the two PDZ domains within the PDZ34 tandem of Scribble, a cell polarity regulator, tightly pack in a 'front-to-back' mode to form a compact supramodule. Although PDZ4 contains a distorted αB/βB pocket, the attachment of PDZ4 to PDZ3 generates an unexpected interdomain pocket that is adjacent to and integrates with the canonical αB/βB pocket of PDZ3 to form an expanded target-binding groove. The structure of the PDZ34-target peptide complex further demonstrated that the peptide binds to this expanded target-binding groove with its upstream residues anchoring into the interdomain pocket directly. Mutations of the interdomain pocket and disruptions of the PDZ34 supramodule both interfere with its target-binding capacity. Therefore, the interdomain interface between the PDZ34 supramodule is intrinsically required for its target recognition and determines its target-binding specificity. This interdomain interface-mediated specific recognition may represent a novel mode of target recognition and would broaden the target-binding versatility for PDZ supramodules. The supramodular nature and target recognition mode of the PDZ34 tandem found in the present study would also help to identify the new binding partners of Scribble and thus may direct further research on the PDZ domain-mediated assembly of Scribble polarity complexes.
 

 

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