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PDBsum entry 4ff8

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protein ligands links
Transferase/transferase inhibitor PDB id
4ff8

 

 

 

 

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JSmol PyMol  
Contents
Protein chain
169 a.a.
Ligands
14S
Waters ×3
PDB id:
4ff8
Name: Transferase/transferase inhibitor
Title: Inhibitor bound structure of the kinase domain of the murine receptor tyrosine kinase tyro3 (sky)
Structure: Tyrosine-protein kinase receptor tyro3. Chain: a. Synonym: etk2/tyro3, tk19-2, tyrosine-protein kinase dtk, tyrosine- protein kinase rse. Engineered: yes. Mutation: yes
Source: Mus musculus. Mouse. Organism_taxid: 10090. Gene: tyro3, dtk, rse. Expressed in: spodoptera frugiperda. Expression_system_taxid: 7108
Resolution:
2.40Å     R-factor:   0.279     R-free:   0.324
Authors: J.F.Ohren,N.A.Powell,J.Kohrt,L.A.Perrin
Key ref: N.A.Powell et al. (2013). Highly selective 2,4-diaminopyrimidine-5-carboxamide inhibitors of Sky kinase. Bioorg Med Chem Lett, 23, 1046-1050. PubMed id: 23312472
Date:
31-May-12     Release date:   13-Mar-13    
PROCHECK
Go to PROCHECK summary
 Headers
 References

Protein chain
Pfam   ArchSchema ?
P55144  (TYRO3_MOUSE) -  Tyrosine-protein kinase receptor TYRO3 from Mus musculus
Seq:
Struc:
 
Seq:
Struc:
880 a.a.
169 a.a.
Key:    PfamA domain  Secondary structure  CATH domain

 Enzyme reactions 
   Enzyme class: E.C.2.7.10.1  - receptor protein-tyrosine kinase.
[IntEnz]   [ExPASy]   [KEGG]   [BRENDA]
      Reaction: L-tyrosyl-[protein] + ATP = O-phospho-L-tyrosyl-[protein] + ADP + H+
L-tyrosyl-[protein]
+ ATP
= O-phospho-L-tyrosyl-[protein]
+ ADP
+ H(+)
Molecule diagrams generated from .mol files obtained from the KEGG ftp site

 

 
    Added reference    
 
 
Bioorg Med Chem Lett 23:1046-1050 (2013)
PubMed id: 23312472  
 
 
Highly selective 2,4-diaminopyrimidine-5-carboxamide inhibitors of Sky kinase.
N.A.Powell, J.K.Hoffman, F.L.Ciske, M.D.Kaufman, J.T.Kohrt, J.Quin, D.J.Sheehan, A.Delaney, S.M.Baxi, C.Catana, P.McConnell, J.Ohren, L.A.Perrin, J.J.Edmunds.
 
  ABSTRACT  
 
We report the SAR around a series of 2,4-diaminopyrimidine-5-carboxamide inhibitors of Sky kinase. 2-Aminophenethyl analogs demonstrate excellent potency but moderate kinase selectivity, while 2-aminobenzyl analogs that fill the Ala571 subpocket exhibit good inhibition activity and excellent kinase selectivity.
 

 

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