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PDBsum entry 3sxr

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protein ligands Protein-protein interface(s) links
Transferase/transferase inhibitor PDB id
3sxr

 

 

 

 

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Contents
Protein chains
260 a.a.
Ligands
1N1 ×2
SO4 ×3
Waters ×212
PDB id:
3sxr
Name: Transferase/transferase inhibitor
Title: Crystal structure of bmx non-receptor tyrosine kinase complex with dasatinib
Structure: Cytoplasmic tyrosine-protein kinase bmx. Chain: a, b. Fragment: unp residues 411-675. Synonym: bone marrow tyrosine kinase gene in chromosome x protein, epithelial and endothelial tyrosine kinase, etk, ntk38. Engineered: yes. Mutation: yes
Source: Homo sapiens. Human. Organism_taxid: 9606. Gene: agmx1, atk, bmx, bpk, btk. Expressed in: spodoptera frugiperda. Expression_system_taxid: 7108. Expression_system_cell_line: sf9.
Resolution:
2.40Å     R-factor:   0.189     R-free:   0.231
Authors: J.Sack,J.Muckelbauer
Key ref: J.Muckelbauer et al. (2011). X-ray crystal structure of bone marrow kinase in the x chromosome: a Tec family kinase. Chem Biol Drug Des, 78, 739-748. PubMed id: 21883956
Date:
15-Jul-11     Release date:   21-Sep-11    
PROCHECK
Go to PROCHECK summary
 Headers
 References

Protein chains
Pfam   ArchSchema ?
P51813  (BMX_HUMAN) -  Cytoplasmic tyrosine-protein kinase BMX from Homo sapiens
Seq:
Struc:
 
Seq:
Struc:
675 a.a.
260 a.a.*
Key:    PfamA domain  Secondary structure  CATH domain
* PDB and UniProt seqs differ at 6 residue positions (black crosses)

 Enzyme reactions 
   Enzyme class: E.C.2.7.10.2  - non-specific 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    
 
 
Chem Biol Drug Des 78:739-748 (2011)
PubMed id: 21883956  
 
 
X-ray crystal structure of bone marrow kinase in the x chromosome: a Tec family kinase.
J.Muckelbauer, J.S.Sack, N.Ahmed, J.Burke, C.Y.Chang, M.Gao, J.Tino, D.Xie, A.J.Tebben.
 
  ABSTRACT  
 
No abstract given.

 

 

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