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PDBsum entry 3o23

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protein ligands links
Transferase/transferase inhibitor PDB id
3o23

 

 

 

 

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JSmol PyMol  
Contents
Protein chain
293 a.a.
Ligands
MQY
Waters ×85
PDB id:
3o23
Name: Transferase/transferase inhibitor
Title: Human unphosphorylated igf1-r kinase domain in complex with an hydantoin inhibitor
Structure: Insulin-like growth factor 1 receptor. Chain: a. Fragment: kinase domain. Synonym: insulin-like growth factor i receptor, igf-i receptor, insulin-like growth factor 1 receptor alpha chain, insulin-like growth factor 1 receptor beta chain. Engineered: yes. Mutation: yes
Source: Homo sapiens. Human. Organism_taxid: 9606. Gene: igf1r. Expressed in: escherichia coli. Expression_system_taxid: 562
Resolution:
2.10Å     R-factor:   0.238     R-free:   0.278
Authors: S.Maignan,J.P.Guilloteau,A.Dupuy
Key ref: D.Lesuisse et al. (2011). Discovery of the first non-ATP competitive IGF-1R kinase inhibitors: advantages in comparison with competitive inhibitors. Bioorg Med Chem Lett, 21, 2224-2228. PubMed id: 21441024
Date:
22-Jul-10     Release date:   04-May-11    
PROCHECK
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 Headers
 References

Protein chain
Pfam   ArchSchema ?
P08069  (IGF1R_HUMAN) -  Insulin-like growth factor 1 receptor from Homo sapiens
Seq:
Struc:
 
Seq:
Struc:
 
Seq:
Struc:
1367 a.a.
293 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 21:2224-2228 (2011)
PubMed id: 21441024  
 
 
Discovery of the first non-ATP competitive IGF-1R kinase inhibitors: advantages in comparison with competitive inhibitors.
D.Lesuisse, J.Mauger, C.Nemecek, S.Maignan, J.Boiziau, G.Harlow, A.Hittinger, S.Ruf, H.Strobel, A.Nair, K.Ritter, J.L.Malleron, A.Dagallier, Y.El-Ahmad, J.P.Guilloteau, H.Guizani, H.Bouchard, C.Venot.
 
  ABSTRACT  
 
No abstract given.

 

 

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