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Crystal structure of human tankyrase 2 in complex with ta-41

Analyse Crystal structure of human tankyrase 2 in complex with ta-41 in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4UI5
Type
protein
Length
417 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Tankyrase-2
EC
2.4.2.30
UniProt
Q9H2K2
Ligands
BJ4, ZN, SO4
Pockets
4 · best druggability 0.80

Structure

x-ray diffraction · 3 distinct chains · 26% helix, 28% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ATankyrase-2 (EC 2.4.2.30)protein16129% helix, 25% strandQ9H2K2
BTankyrase-2 (EC 2.4.2.30)protein16229% helix, 25% strandQ9H2K2
C, DTankyrase-2 (EC 2.4.2.30)protein476% helix, 45% strandQ9H2K2

Ligands and binding sites

  • BJ4 · 8-methoxy-2-(4-methylphenyl)-3,4-dihydroquinazolin-4-one · ligand · 2 copies · chains A, C, B, D
  • ZN · Zinc ion · metal · 2 copies · chains A, B
  • SO4 · Sulfate ion · ion · 4 copies · chains A, C, B, D
  • GOL · Glycerol · additive · 3 copies · chains A, C

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
14250.800.8961SO4, BJ4
22290.630.8236SO4, BJ4
31400.520.8019empty
4860.340.7416empty

Interfaces

5 interfaces between chains.

  • B–D · 3094 Ų buried · 64 hydrogen bonds · protein-protein
  • A–C · 3056 Ų buried · 62 hydrogen bonds · protein-protein
  • A–B · 574 Ų buried · 3 hydrogen bonds · protein-protein
  • A–D · 87 Ų buried · 0 hydrogen bonds · protein-protein
  • B–C · 53 Ų buried · 0 hydrogen bonds · protein-protein

Compared structures

  • 4UI5 · Crystal structure of human tankyrase 2 in complex with TA-41 · the same entry in another collection · chain A against A, TM-score 1.00

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