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PDBsum entry 7wcw

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protein ligands links
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
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
Go to PROCHECK summary
 Headers
 References

Protein chain
Pfam   ArchSchema ?
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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