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PDBsum entry 4dei

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protein ligands links
Transferase/transferase inhibitor PDB id
4dei

 

 

 

 

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JSmol PyMol  
Contents
Protein chain
287 a.a.
Ligands
0JL
Waters ×167
PDB id:
4dei
Name: Transferase/transferase inhibitor
Title: Crystal structure of c-met in complex with triazolopyridinone inhibitor 24
Structure: Hepatocyte growth factor receptor. Chain: a. Synonym: hgf receptor, hgf/sf receptor, proto-oncogenE C-met, scatter factor receptor, sf receptor, tyrosine-protein kinase met. Engineered: yes
Source: Homo sapiens. Human. Organism_taxid: 9606. Gene: met. Expressed in: trichoplusia ni. Expression_system_taxid: 7111.
Resolution:
2.05Å     R-factor:   0.224     R-free:   0.289
Authors: D.A.Whittington,A.M.Long
Key ref: C.M.Bode et al. (2012). Discovery and optimization of a potent and selective triazolopyridinone series of c-Met inhibitors. Bioorg Med Chem Lett, 22, 4089-4093. PubMed id: 22595176
Date:
20-Jan-12     Release date:   30-May-12    
PROCHECK
Go to PROCHECK summary
 Headers
 References

Protein chain
Pfam   ArchSchema ?
P08581  (MET_HUMAN) -  Hepatocyte growth factor receptor from Homo sapiens
Seq:
Struc:
 
Seq:
Struc:
 
Seq:
Struc:
1390 a.a.
287 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 22:4089-4093 (2012)
PubMed id: 22595176  
 
 
Discovery and optimization of a potent and selective triazolopyridinone series of c-Met inhibitors.
C.M.Bode, A.A.Boezio, B.K.Albrecht, S.F.Bellon, L.Berry, M.A.Broome, D.Choquette, I.Dussault, R.T.Lewis, M.H.Lin, K.Rex, D.A.Whittington, Y.Yang, J.C.Harmange.
 
  ABSTRACT  
 
No abstract given.

 

 

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