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PDBsum entry 3tcp
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Transferase/transferase inhibitor
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PDB id
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3tcp
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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 the catalytic domain of the proto-oncogene tyrosine-protein kinase mer in complex with inhibitor unc569
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Structure:
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Tyrosine-protein kinase mer. Chain: a, b. Fragment: catalytic domain, unp residues 570-864. Synonym: proto-oncogenE C-mer, receptor tyrosine kinase mertk. Engineered: yes
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Source:
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Homo sapiens. Human. Organism_taxid: 9606. Gene: mertk, mer. Expressed in: escherichia coli. Expression_system_taxid: 469008.
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Resolution:
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2.69Å
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R-factor:
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0.228
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R-free:
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0.298
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Authors:
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J.Liu,C.Yang,C.Simpson,D.Deryckere,A.Van Deusen,M.Miley,D.B.Kireev, J.Norris-Drouin,S.Sather,D.Hunter,H.S.Patel,W.P.Janzen,M.Machius, G.Johnson,H.S.Earp,D.K.Graham,S.Frye,X.Wang
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Key ref:
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J.Liu
et al.
(2012).
Discovery of Novel Small Molecule Mer Kinase Inhibitors for the Treatment of Pediatric Acute Lymphoblastic Leukemia.
Acs Med Chem Lett,
3,
129-134.
PubMed id:
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Date:
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09-Aug-11
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Release date:
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20-Jun-12
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PROCHECK
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Headers
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References
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Q12866
(MERTK_HUMAN) -
Tyrosine-protein kinase Mer from Homo sapiens
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Seq: Struc:
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999 a.a.
256 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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Enzyme class:
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E.C.2.7.10.1
- receptor 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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Acs Med Chem Lett
3:129-134
(2012)
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PubMed id:
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Discovery of Novel Small Molecule Mer Kinase Inhibitors for the Treatment of Pediatric Acute Lymphoblastic Leukemia.
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J.Liu,
C.Yang,
C.Simpson,
D.Deryckere,
A.Van Deusen,
M.J.Miley,
D.Kireev,
J.Norris-Drouin,
S.Sather,
D.Hunter,
V.K.Korboukh,
H.S.Patel,
W.P.Janzen,
M.Machius,
G.L.Johnson,
H.S.Earp,
D.K.Graham,
S.V.Frye,
X.Wang.
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ABSTRACT
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');
}
}
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