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Crystal structure of DYRK2 in complex with eht 5372 (compound 1)

Analyse Crystal structure of DYRK2 in complex with eht 5372 (compound 1) in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
5LXC
Type
protein
Length
770 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Dual specificity tyrosine-phosphorylation-regulated kinase 2
EC
2.7.12.1
UniProt
Q92630
Ligands
7AA
Pockets
9 · best druggability 0.71

Structure

x-ray diffraction · 2 distinct chains · 36% helix, 18% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ADual specificity tyrosine-phosphorylation-regulated kinase 2 (EC 2.7.12.1)protein38436% helix, 18% strandQ92630
BDual specificity tyrosine-phosphorylation-regulated kinase 2 (EC 2.7.12.1)protein38637% helix, 18% strandQ92630

Ligands and binding sites

  • 7AA · methyl 9-[(2,4-dichlorophenyl)amino]-[1,3]thiazolo[5,4-f]quinazoline-2-carboximidate · ligand · 2 copies · chains A, B
  • EDO · 1,2-ethanediol · additive · 11 copies · chains A, B

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
14460.710.81507AA, EDO
22240.630.82277AA
33500.600.7749EDO
42020.580.8132empty
52970.540.7537EDO

Interfaces

1 interface between chains.

  • A–B · 828 Ų buried · 20 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 2 modified (phosphorylation).

Compared structures

  • 5LXC · Crystal structure of DYRK2 in complex with EHT 5372 (Compound 1) · the same entry in another collection · chain A against A, TM-score 1.00
  • Q92630 · AlphaFold monomer V2.0 prediction for dual specificity tyrosine… · a predicted model of the same protein · chain B against A, TM-score 0.99

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