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PDBsum entry 5da3
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Transferase/transferase inhibitor
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PDB id
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5da3
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PDB id:
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| Name: |
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Transferase/transferase inhibitor
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Title:
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Crystal structure of ptk6 kinase domain with inhibitor
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Structure:
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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
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Source:
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Homo sapiens. Human. Organism_taxid: 9606. Gene: ptk6. Expressed in: spodoptera frugiperda. Expression_system_taxid: 7108. Expression_system_cell_line: sf9.
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Resolution:
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1.70Å
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R-factor:
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0.199
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R-free:
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0.230
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Authors:
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M.K.Thakur,S.Birudukota,S.Swaminathan,S.K.Battula,S.Vadivelu,R.Tyagi, R.Gosu
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Key ref:
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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:
DOI:
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Date:
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19-Aug-15
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Release date:
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24-Aug-16
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PROCHECK
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Headers
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References
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Q13882
(PTK6_HUMAN) -
Protein-tyrosine kinase 6 from Homo sapiens
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Seq: Struc:
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451 a.a.
264 a.a.*
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Key: |
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PfamA domain |
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Secondary structure |
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CATH domain |
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*
PDB and UniProt seqs differ
at 4 residue positions (black
crosses)
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Enzyme class:
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E.C.2.7.10.2
- non-specific protein-tyrosine kinase.
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Reaction:
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L-tyrosyl-[protein] + ATP = O-phospho-L-tyrosyl-[protein] + ADP + H+
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L-tyrosyl-[protein]
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+
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ATP
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=
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O-phospho-L-tyrosyl-[protein]
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+
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ADP
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+
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H(+)
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Molecule diagrams generated from .mol files obtained from the
KEGG ftp site
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DOI no:
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Biochem Biophys Res Commun
482:1289-1295
(2017)
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PubMed id:
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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.
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M.K.Thakur,
S.Birudukota,
S.Swaminathan,
S.K.Battula,
S.Vadivelu,
R.Tyagi,
R.Gosu.
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ABSTRACT
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');
}
}
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