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Structural and thermodynamic characterization of the TYK2 and JAK3 kinase domains in complex with cp-690550 and cmp-6

Analyse Structural and thermodynamic characterization of the TYK2 and JAK3 kinase… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
3LXL
Type
protein
Length
281 residues
Chains
1
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Tyrosine-protein kinase JAK3
EC
2.7.10.2
UniProt
P52333
Ligands
IZA
Pockets
3 · best druggability 0.67

Structure

x-ray diffraction · 1 distinct chain · 44% helix, 22% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ATyrosine-protein kinase JAK3 (EC 2.7.10.2)protein28144% helix, 22% strandP52333

Ligands and binding sites

  • IZA · 2-tert-butyl-9-fluoro-3,6-dihydro-7H-benz[h]-imidaz[4,5-f]isoquinoline-7-one · ligand · 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, 2 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
12690.670.8335IZA
21350.500.7930empty
3500.300.7617empty

Compared structures

  • 3LXL · Structural and Thermodynamic Characterization of the TYK2 and JAK3 Kinase Domains in… · the same entry in another collection · chain A against A, TM-score 1.00
  • P52333 · AlphaFold monomer V2.0 prediction for tyrosine-protein kinase JAK3 (P52333) · a predicted model of the same protein · chain A against A, TM-score 0.96

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