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PDBsum entry 4uwc
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PDB id:
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Transferase
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Title:
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Fibroblast growth factor receptor 1 kinase in complex with jk-p3
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Structure:
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Fibroblast growth factor receptor 1. Chain: a, b. Fragment: kinase domain, residues 458-765. Synonym: fgfr-1, basic fibroblast growth factor receptor 1, bfgfr, b fgf-r-1, fms-like tyrosine kinase 2, flt-2, n-sam, proto-oncogenE C- fgr, fibroblast growth factor receptor 1 kinase. 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: star.
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Resolution:
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1.96Å
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R-factor:
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0.179
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R-free:
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0.206
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Authors:
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H.Beeston,J.Tucker,J.Kankanala
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Key ref:
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h.beeston
(2021).
Validation of IMS-MS as a screening tool to identify type II kinase inhibitors of FGFR1 kinase.
Rapid Commun Mass Spectrom,
0,
e9130.
PubMed id:
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Date:
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11-Aug-14
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Release date:
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02-Sep-15
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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.
301 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 2 residue positions (black
crosses)
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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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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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Rapid Commun Mass Spectrom
0:e9130
(2021)
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PubMed id:
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Validation of IMS-MS as a screening tool to identify type II kinase inhibitors of FGFR1 kinase.
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h.beeston.
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ABSTRACT
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');
}
}
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