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Crystal structure of TTBK2 in complex with VNG2.73 (compound 42)

Analyse Crystal structure of TTBK2 in complex with VNG2.73 (compound 42) in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
7Q8Y
Type
protein
Length
587 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Tau-tubulin kinase 2
EC
2.7.11.1
UniProt
Q6IQ55
Ligands
9IV, PO4
Pockets
5 · best druggability 0.66

Structure

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

ChainMoleculeTypeResiduesSecondary structureUniProt
ATau-tubulin kinase 2 (EC 2.7.11.1)protein29435% helix, 18% strandQ6IQ55
BTau-tubulin kinase 2 (EC 2.7.11.1)protein29337% helix, 18% strandQ6IQ55

Ligands and binding sites

  • 9IV · ~{N}-[4-(2-chloranylphenoxy)phenyl]-7~{H}-pyrrolo[2,3-d]pyrimidin-4-amine · ligand · 2 copies · chains A, B
  • PO4 · Phosphate ion · ion · 4 copies · chains A, B

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

Pockets

5 pockets found on a 1 Å grid, 4 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
12650.660.83359IV
23820.660.80489IV
31460.640.8621empty
41950.570.8028PO4
5750.320.7421PO4

Interfaces

1 interface between chains.

  • A–B · 602 Ų buried · 4 hydrogen bonds · protein-protein

Compared structures

  • 7Q8Y · Crystal structure of TTBK2 in complex with VNG2.73 (compound 42) · the same entry in another collection · chain A against A, TM-score 1.00
  • Q6IQ55 · AlphaFold monomer V2.0 prediction for tau-tubulin kinase 2 (Q6IQ55) · a predicted model of the same protein · chain B against A, TM-score 0.99

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