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Crystal structure of T. brucei pde-B1 catalytic domain with inhibitor npd-1361

Analyse Crystal structure of T. brucei pde-B1 catalytic domain with inhibitor npd-1361 in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
6QGU
Type
protein
Length
665 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Phosphodiesterase
EC
3.1.4.-
UniProt
Q8WQX9
Ligands
GAI, 863, ZN, MG
Pockets
4 · best druggability 0.74

Structure

x-ray diffraction · 2 distinct chains · 72% helix, 0% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
APhosphodiesterase (EC 3.1.4.-)protein33372% helix, 0% strandQ8WQX9
BPhosphodiesterase (EC 3.1.4.-)protein33272% helix, 0% strandQ8WQX9

Ligands and binding sites

  • GAI · Guanidine · ligand · 3 copies · chains A, B
  • 863 · 5-(3-(cyclopentyloxy)-4-methoxyphenyl)-2-isopropyl-4,4-dimethyl-2,4-dihydro-3H-pyrazol-3-one · ligand · chains B
  • ZN · Zinc ion · metal · 2 copies · chains A, B
  • MG · Magnesium ion · metal · 2 copies · chains A, B
  • GOL · Glycerol · additive · 4 copies · chains A, B
  • FMT · Formic acid · additive · 3 copies · chains 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
15780.740.8154MG
24830.730.8243MG, 863
32400.530.7634FMT
4590.260.7312empty

Interfaces

1 interface between chains.

  • A–B · 745 Ų buried · 4 hydrogen bonds · protein-protein

Compared structures

  • 6QGU · Crystal structure of T. brucei PDE-B1 catalytic domain with inhibitor NPD-1361 · the same entry in another collection · chain A against A, TM-score 1.00

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