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PDBsum entry 5da3

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protein ligands links
Transferase/transferase inhibitor PDB id
5da3

 

 

 

 

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Contents
Protein chain
264 a.a.
Ligands
GOL ×2
58V
Waters ×192
PDB id:
5da3
Name: Transferase/transferase inhibitor
Title: Crystal structure of ptk6 kinase domain with inhibitor
Structure: Protein-tyrosine kinase 6. Chain: a. Fragment: kinase domain, unp residues 185-446. Synonym: breast tumor kinase,tyrosine-protein kinase brk. Engineered: yes. Mutation: yes
Source: Homo sapiens. Human. Organism_taxid: 9606. Gene: ptk6. Expressed in: spodoptera frugiperda. Expression_system_taxid: 7108. Expression_system_cell_line: sf9.
Resolution:
1.70Å     R-factor:   0.199     R-free:   0.230
Authors: M.K.Thakur,S.Birudukota,S.Swaminathan,S.K.Battula,S.Vadivelu,R.Tyagi, R.Gosu
Key ref: M.K.Thakur et al. (2017). Co-crystal structures of PTK6: With Dasatinib at 2.24 Å, with novel imidazo[1,2-a]pyrazin-8-amine derivative inhibitor at 1.70 Å resolution. Biochem Biophys Res Commun, 482, 1289-1295. PubMed id: 27993680 DOI: 10.1016/j.bbrc.2016.12.030
Date:
19-Aug-15     Release date:   24-Aug-16    
PROCHECK
Go to PROCHECK summary
 Headers
 References

Protein chain
Pfam   ArchSchema ?
Q13882  (PTK6_HUMAN) -  Protein-tyrosine kinase 6 from Homo sapiens
Seq:
Struc:
451 a.a.
264 a.a.*
Key:    PfamA domain  Secondary structure  CATH domain
* PDB and UniProt seqs differ at 4 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    
 
 
DOI no: 10.1016/j.bbrc.2016.12.030 Biochem Biophys Res Commun 482:1289-1295 (2017)
PubMed id: 27993680  
 
 
Co-crystal structures of PTK6: With Dasatinib at 2.24 Å, with novel imidazo[1,2-a]pyrazin-8-amine derivative inhibitor at 1.70 Å resolution.
M.K.Thakur, S.Birudukota, S.Swaminathan, S.K.Battula, S.Vadivelu, R.Tyagi, R.Gosu.
 
  ABSTRACT  
 
No abstract given.

 

 

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