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Crystal structure of interleukin-2 inducible T-cell kinase itk catalytic domain with thienopyrazolylindole inhibitor 469

Analyse Crystal structure of interleukin-2 inducible T-cell kinase itk catalytic domain… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
3V8W
Type
protein
Length
485 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Tyrosine-protein kinase ITK/TSK
EC
2.7.10.2
UniProt
Q08881
Ligands
0G2, SO4
Pockets
4 · best druggability 0.77

Structure

x-ray diffraction · 2 distinct chains · 43% helix, 18% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ATyrosine-protein kinase ITK/TSK (EC 2.7.10.2)protein24343% helix, 18% strandQ08881
BTyrosine-protein kinase ITK/TSK (EC 2.7.10.2)protein24242% helix, 18% strandQ08881

Ligands and binding sites

  • 0G2 · 3-[2-(5-phenyl-2H-thieno[3,2-c]pyrazol-3-yl)-1H-indol-6-yl]pentan-3-ol · ligand · 2 copies · chains A, B
  • SO4 · Sulfate ion · ion · chains B

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
17430.770.8160empty
23280.630.79380G2
33000.590.77330G2
4500.490.8714empty

Interfaces

1 interface between chains.

  • A–B · 1339 Ų buried · 35 hydrogen bonds · protein-protein

Compared structures

  • 3V8W · Crystal Structure of Interleukin-2 Inducible T-cell Kinase Itk Catalytic Domain with… · the same entry in another collection · chain A against A, TM-score 1.00
  • Q08881 · AlphaFold monomer V2.0 prediction for tyrosine-protein kinase ITK/TSK (Q08881) · a predicted model of the same protein · chain B against A, TM-score 0.97

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