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PDBsum entry 5lwm
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PDB id:
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Transferase
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Title:
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Crystal structure of jak3 in complex with compound 4 (fm381)
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Structure:
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Tyrosine-protein kinase jak3. Chain: a. Synonym: janus kinase 3,jak-3,leukocyte janus kinase,l-jak. Engineered: yes
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Source:
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Homo sapiens. Human. Organism_taxid: 9606. Gene: jak3. Expressed in: spodoptera frugiperda. Expression_system_taxid: 7108
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Resolution:
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1.55Å
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R-factor:
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0.166
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R-free:
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0.204
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Authors:
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A.Chaikuad,M.Forster,S.Mukhopadhyay,K.Kupinska,K.Ellis,P.Mahajan, N.Burgess-Brown,A.M.Edwards,C.H.Arrowsmith,C.Bountra,S.A.Laufer, S.Knapp,Structural Genomics Consortium (Sgc)
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Key ref:
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M.Forster
et al.
(2016).
Selective JAK3 Inhibitors with a Covalent Reversible Binding Mode Targeting a New Induced Fit Binding Pocket.
Cell Chem Biol,
23,
1335-1340.
PubMed id:
DOI:
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Date:
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18-Sep-16
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Release date:
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26-Oct-16
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PROCHECK
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Headers
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References
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P52333
(JAK3_HUMAN) -
Tyrosine-protein kinase JAK3 from Homo sapiens
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Seq: Struc:
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1124 a.a.
290 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 3 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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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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Cell Chem Biol
23:1335-1340
(2016)
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PubMed id:
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Selective JAK3 Inhibitors with a Covalent Reversible Binding Mode Targeting a New Induced Fit Binding Pocket.
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M.Forster,
A.Chaikuad,
S.M.Bauer,
J.Holstein,
M.B.Robers,
C.R.Corona,
M.Gehringer,
E.Pfaffenrot,
K.Ghoreschi,
S.Knapp,
S.A.Laufer.
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ABSTRACT
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');
}
}
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