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PDBsum entry 5am7
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PDB id:
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Transferase
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Title:
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Fgfr1 mutant with an inhibitor
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Structure:
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Fibroblast growth factor receptor 1. Chain: a, b. Fragment: kinase domain, unp residues 458-765. Synonym: fgfr-1, basic fibroblast growth factor receptor 1, bfgfr, bfgf-r-1, fms-like tyrosine kinase 2, flt-2, n-sam, proto-oncogenE C- fgr, fibroblast growth factor 1. Engineered: yes. Mutation: yes
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Source:
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Homo sapiens. Human. Organism_taxid: 9606. Expressed in: escherichia coli. Expression_system_taxid: 469008. Expression_system_variant: c41 lambda 37.
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Resolution:
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1.96Å
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R-factor:
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0.201
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R-free:
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0.254
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Authors:
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T.D.Bunney,S.Wan,N.Thiyagarajan,L.Sutto,S.V.Williams,P.Ashford, H.Koss,M.A.Knowles,F.L.Gervasio,P.V.Coveney,M.Katan
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Key ref:
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T.D.Bunney
et al.
(2015).
The Effect of Mutations on Drug Sensitivity and Kinase Activity of Fibroblast Growth Factor Receptors: A Combined Experimental and Theoretical Study.
Ebiomedicine,
2,
194-204.
PubMed id:
DOI:
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Date:
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10-Mar-15
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Release date:
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18-Mar-15
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Supersedes:
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PROCHECK
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Headers
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References
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P11362
(FGFR1_HUMAN) -
Fibroblast growth factor receptor 1 from Homo sapiens
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Seq: Struc:
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822 a.a.
294 a.a.*
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Key: |
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Secondary structure |
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CATH domain |
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*
PDB and UniProt seqs differ
at 1 residue position (black
cross)
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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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DOI no:
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Ebiomedicine
2:194-204
(2015)
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PubMed id:
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The Effect of Mutations on Drug Sensitivity and Kinase Activity of Fibroblast Growth Factor Receptors: A Combined Experimental and Theoretical Study.
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T.D.Bunney,
S.Wan,
N.Thiyagarajan,
L.Sutto,
S.V.Williams,
P.Ashford,
H.Koss,
M.A.Knowles,
F.L.Gervasio,
P.V.Coveney,
M.Katan.
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ABSTRACT
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');
}
}
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