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JAK1 kinase (JH1 domain) in complex with compound 72

Analyse JAK1 kinase (JH1 domain) in complex with compound 72 in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4FK6
Type
protein
Length
573 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Tyrosine-protein kinase JAK1
EC
2.7.10.2
UniProt
P23458
Ligands
0UJ
Pockets
4 · best druggability 0.74

Structure

x-ray diffraction · 2 distinct chains · 42% helix, 20% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ATyrosine-protein kinase JAK1 (EC 2.7.10.2)protein28742% helix, 20% strandP23458
BTyrosine-protein kinase JAK1 (EC 2.7.10.2)protein28642% helix, 20% strandP23458

Ligands and binding sites

  • 0UJ · N-({1-[(1R,2R,4S)-bicyclo[2.2.1]hept-2-yl]-1,6-dihydroimidazo[4,5-d]pyrrolo[2,3-b]pyridin-2-yl}methyl)methanesulfonamide · ligand · 2 copies · chains A, 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
15410.740.82610UJ
24730.710.81540UJ
3560.510.8713empty
4650.300.7417empty

Interfaces

1 interface between chains.

  • A–B · 929 Ų buried · 20 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 4 modified (phosphorylation).

Compared structures

  • 4FK6 · JAK1 kinase (JH1 domain) in complex with compound 72 · the same entry in another collection · chain A against A, TM-score 1.00
  • P23458 · AlphaFold monomer V2.0 prediction for tyrosine-protein kinase JAK1 (P23458) · a predicted model of the same protein · chain B against A, TM-score 0.98

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