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PDBsum entry 7wcw
Go to PDB code:
Transferase/transferase inhibitor
PDB id
7wcw
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Contents
Protein chain
300 a.a.
Ligands
90F
SO4
×3
Waters
×123
PDB id:
7wcw
Links
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Name:
Transferase/transferase inhibitor
Title:
Crystal structure of fgfr4(v550l) kinase domain with 7v
Structure:
Fibroblast growth factor receptor 4. Chain: a. Synonym: fgfr-4. Engineered: yes. Mutation: yes
Source:
Homo sapiens. Human. Organism_taxid: 9606. Gene: fgfr4, jtk2, tkf. Expressed in: escherichia coli. Expression_system_taxid: 562
Resolution:
2.32Å
R-factor:
0.179
R-free:
0.221
Authors:
X.J.Chen,Q.M.Lin,S.Y.Dai,Y.H.Chen
Key ref:
M.Shao et al. Design, Synthesis, And biological evaluation of aminoindazole derivatives as highly selective covalen inhibitors of wild-Type and gatekeeper mutant fgfr4..
J med chem
, .
PubMed id:
35271262
Date:
20-Dec-21
Release date:
30-Mar-22
PROCHECK
Headers
References
Protein chain
?
P22455
(FGFR4_HUMAN) - Fibroblast growth factor receptor 4 from Homo sapiens
Seq:
Struc:
 
Seq:
Struc:
802 a.a.
300 a.a.
*
Key:
PfamA domain
Secondary structure
*
PDB and UniProt seqs differ at 3 residue positions (black crosses)
Enzyme reactions
Enzyme class:
E.C.2.7.10.1
- receptor protein-tyrosine kinase.
[IntEnz]
[ExPASy]
[KEGG]
[BRENDA]
Reaction:
L-tyrosyl-[protein] + ATP = O-phospho-L-tyrosyl-[protein] + ADP + H
+
L-tyrosyl-[protein]
+
ATP
=
O-phospho-L-tyrosyl-[protein]
+
ADP
+
H(+)
Molecule diagrams generated from .mol files obtained from the
KEGG ftp site
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