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JAK2 JH1 in complex with PN4-014

Analyse JAK2 JH1 in complex with PN4-014 in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
6VNJ
Type
protein
Length
589 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v2 / PDB Bank
Contract
0xd58B01f6C18086e5202cdC5D7Ad3E41790360102
Owner
0xF4e1AA6f26B7DA48EeAD9B24a97927303eeA07b8
Resolution
1.9
Source
Homo sapiens
Molecule
Tyrosine-protein kinase JAK2
EC
2.7.10.2
UniProt
O60674
Ligands
R5S
Pockets
7 · best druggability 0.75

Structure

x-ray diffraction · resolution 1.9 · 2 distinct chains · 43% helix, 20% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
BTyrosine-protein kinase JAK2 (EC 2.7.10.2)protein29044% helix, 20% strandO60674
ATyrosine-protein kinase JAK2 (EC 2.7.10.2)protein29942% helix, 20% strandO60674

Ligands and binding sites

  • R5S · 3-[4-(2-{[4-(piperidin-4-yl)phenyl]amino}-6,7-dihydro-5H-pyrrolo[2,3-d]pyrimidin-4-yl)-1H-pyrazol-1-yl]propanenitrile · ligand · 2 copies · chains B, A

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

Pockets

7 pockets found on a 1 Å grid, 5 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
16150.750.8163R5S
24060.700.8244empty
32380.630.8229R5S
42630.610.8028empty
51570.560.8221empty

Interfaces

1 interface between chains.

  • B–A · 502 Ų buried · 8 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 2 modified (phosphorylation).

Compared structures

  • 6VNJ · JAK2 JH1 in complex with PN4-014 · the same entry in another collection · chain A against A, TM-score 1.00

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