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PDBsum entry 2xb7

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Transferase PDB id
2xb7

 

 

 

 

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Contents
Protein chain
286 a.a. *
Ligands
GUI
Waters ×66
* Residue conservation analysis
PDB id:
2xb7
Name: Transferase
Title: Structure of human anaplastic lymphoma kinase in complex with nvp- tae684
Structure: Alk tyrosine kinase receptor. Chain: a. Fragment: kinase domain, residues 1094-1407. Synonym: anaplastic lymphoma kinase, cd246. Engineered: yes
Source: Homo sapiens. Human. Organism_taxid: 9606. Expressed in: spodoptera frugiperda. Expression_system_taxid: 7108.
Resolution:
2.50Å     R-factor:   0.195     R-free:   0.243
Authors: R.T.Bossi,M.B.Saccardo,E.Ardini,M.Menichincheri,L.Rusconi,P.Magnaghi, P.Orsini,G.Fogliatto,J.A.Bertrand
Key ref: R.T.Bossi et al. (2010). Crystal structures of anaplastic lymphoma kinase in complex with ATP competitive inhibitors. Biochemistry, 49, 6813-6825. PubMed id: 20695522
Date:
08-Apr-10     Release date:   28-Jul-10    
PROCHECK
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 Headers
 References

Protein chain
Pfam   ArchSchema ?
Q9UM73  (ALK_HUMAN) -  ALK tyrosine kinase receptor from Homo sapiens
Seq:
Struc:
 
Seq:
Struc:
 
Seq:
Struc:
 
Seq:
Struc:
1620 a.a.
286 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    
 
 
Biochemistry 49:6813-6825 (2010)
PubMed id: 20695522  
 
 
Crystal structures of anaplastic lymphoma kinase in complex with ATP competitive inhibitors.
R.T.Bossi, M.B.Saccardo, E.Ardini, M.Menichincheri, L.Rusconi, P.Magnaghi, P.Orsini, N.Avanzi, A.L.Borgia, M.Nesi, T.Bandiera, G.Fogliatto, J.A.Bertrand.
 
  ABSTRACT  
 
No abstract given.

 

Literature references that cite this PDB file's key reference

  PubMed id Reference
22585002 E.L.Carpenter, and Y.P.Mossé (2012).
Targeting ALK in neuroblastoma--preclinical and clinical advancements.
  Nat Rev Clin Oncol, 9, 391-399.  
21561771 K.Kinoshita, Y.Ono, T.Emura, K.Asoh, N.Furuichi, T.Ito, H.Kawada, S.Tanaka, K.Morikami, T.Tsukaguchi, H.Sakamoto, T.Tsukuda, and N.Oikawa (2011).
Discovery of novel tetracyclic compounds as anaplastic lymphoma kinase inhibitors.
  Bioorg Med Chem Lett, 21, 3788-3793.  
21515061 M.Okamoto, H.Kojima, N.Saito, T.Okabe, Y.Masuda, T.Furuya, and T.Nagano (2011).
Virtual screening and further development of novel ALK inhibitors.
  Bioorg Med Chem, 19, 3086-3095.  
21030459 T.Sasaki, K.Okuda, W.Zheng, J.Butrynski, M.Capelletti, L.Wang, N.S.Gray, K.Wilner, J.G.Christensen, G.Demetri, G.I.Shapiro, S.J.Rodig, M.J.Eck, and P.A.Jänne (2010).
The neuroblastoma-associated F1174L ALK mutation causes resistance to an ALK kinase inhibitor in ALK-translocated cancers.
  Cancer Res, 70, 10038-10043.  
The most recent references are shown first. Citation data come partly from CiteXplore and partly from an automated harvesting procedure. Note that this is likely to be only a partial list as not all journals are covered by either method. However, we are continually building up the citation data so more and more references will be included with time.

 

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