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JAK2 JH1 in complex with SY5-103

Analyse JAK2 JH1 in complex with SY5-103 in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
6VNM
Type
protein
Length
587 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Tyrosine-protein kinase JAK2
EC
2.7.10.2
UniProt
O60674
Ligands
R5Y
Pockets
4 · best druggability 0.75

Structure

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

ChainMoleculeTypeResiduesSecondary structureUniProt
BTyrosine-protein kinase JAK2 (EC 2.7.10.2)protein28944% helix, 20% strandO60674
ATyrosine-protein kinase JAK2 (EC 2.7.10.2)protein29843% helix, 20% strandO60674

Ligands and binding sites

  • R5Y · 4-[1-(but-3-en-1-yl)-1H-pyrazol-4-yl]-N-[4-(piperidin-4-yl)phenyl]-7H-pyrrolo[2,3-d]pyrimidin-2-amine · ligand · 2 copies · chains B, A

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
16620.750.8169empty
25100.700.8061R5Y
33070.640.8146R5Y
4680.390.7922empty

Interfaces

1 interface between chains.

  • B–A · 471 Ų buried · 7 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 2 modified (phosphorylation).

Compared structures

  • 6VNM · JAK2 JH1 in complex with SY5-103 · the same entry in another collection · chain B against B, TM-score 1.00

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