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Structural analysis of the human fibroblast growth factor receptor 4 kinase

Analyse Structural analysis of the human fibroblast growth factor receptor 4 kinase in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4TYE
Type
protein
Length
292 residues
Chains
1
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Fibroblast growth factor receptor 4
EC
2.7.10.1
UniProt
P22455
Ligands
PO4
Pockets
3 · best druggability 0.68

Structure

x-ray diffraction · 1 distinct chain · 35% helix, 17% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AFibroblast growth factor receptor 4 (EC 2.7.10.1)protein29235% helix, 17% strandP22455

Ligands and binding sites

  • PO4 · Phosphate ion · ion · 2 copies · chains A

Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.

Pockets

3 pockets found on a 1 Å grid, 1 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
12390.680.8445empty
21480.400.7325empty
3550.270.7315empty

Compared structures

  • 4TYE · Structural analysis of the human Fibroblast Growth Factor Receptor 4 Kinase · the same entry in another collection · chain A against A, TM-score 1.00
  • P22455 · AlphaFold monomer V2.0 prediction for fibroblast growth factor receptor 4 (P22455) · a predicted model of the same protein · chain A against A, TM-score 0.88

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