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PDBsum entry 5e80

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protein ligands Protein-protein interface(s) links
Lipid binding protein PDB id
5e80

 

 

 

 

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Contents
Protein chains
149 a.a.
Ligands
5KP ×2
Waters ×15
PDB id:
5e80
Name: Lipid binding protein
Title: The crystal structure of pded in complex with inhibitor-2a
Structure: Retinal rod rhodopsin-sensitive cgmp 3',5'-cyclic phosphodiesterase subunit delta. Chain: b, a. Synonym: gmp-pde delta,protein p17. Engineered: yes
Source: Homo sapiens. Human. Organism_taxid: 9606. Gene: pde6d, pded. Expressed in: escherichia coli. Expression_system_taxid: 562
Resolution:
2.60Å     R-factor:   0.188     R-free:   0.247
Authors: S.Ismail,E.K.Fansa,S.Murarka,A.Wittinghofer
Key ref: B.Papke et al. (2016). Identification of pyrazolopyridazinones as PDEδ inhibitors. Nat Commun, 7, 11360. PubMed id: 27094677 DOI: 10.1038/ncomms11360
Date:
13-Oct-15     Release date:   04-May-16    
PROCHECK
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 Headers
 References

Protein chains
Pfam   ArchSchema ?
O43924  (PDE6D_HUMAN) -  Retinal rod rhodopsin-sensitive cGMP 3',5'-cyclic phosphodiesterase subunit delta from Homo sapiens
Seq:
Struc:
150 a.a.
149 a.a.*
Key:    PfamA domain  Secondary structure  CATH domain
* PDB and UniProt seqs differ at 1 residue position (black cross)

 

 
DOI no: 10.1038/ncomms11360 Nat Commun 7:11360 (2016)
PubMed id: 27094677  
 
 
Identification of pyrazolopyridazinones as PDEδ inhibitors.
B.Papke, S.Murarka, H.A.Vogel, P.Martín-Gago, M.Kovacevic, D.C.Truxius, E.K.Fansa, S.Ismail, G.Zimmermann, K.Heinelt, C.Schultz-Fademrecht, A.Al Saabi, M.Baumann, P.Nussbaumer, A.Wittinghofer, H.Waldmann, P.I.Bastiaens.
 
  ABSTRACT  
 
The prenyl-binding protein PDEδ is crucial for the plasma membrane localization of prenylated Ras. Recently, we have reported that the small-molecule Deltarasin binds to the prenyl-binding pocket of PDEδ, and impairs Ras enrichment at the plasma membrane, thereby affecting the proliferation of KRas-dependent human pancreatic ductal adenocarcinoma cell lines. Here, using structure-based compound design, we have now identified pyrazolopyridazinones as a novel, unrelated chemotype that binds to the prenyl-binding pocket of PDEδ with high affinity, thereby displacing prenylated Ras proteins in cells. Our results show that the new PDEδ inhibitor, named Deltazinone 1, is highly selective, exhibits less unspecific cytotoxicity than the previously reported Deltarasin and demonstrates a high correlation with the phenotypic effect of PDEδ knockdown in a set of human pancreatic cancer cell lines.
 

 

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