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Crystal structure of T. brucei pde-B1 catalytic domain with inhibitor npd-1335

Analyse Crystal structure of T. brucei pde-B1 catalytic domain with inhibitor npd-1335 in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
6GXQ
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, FFZ, MG, ZN
Pockets
5 · best druggability 0.72

Structure

x-ray diffraction · 2 distinct chains · 73% helix, 0% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
APhosphodiesterase (EC 3.1.4.-)protein33372% helix, 0% strandQ8WQX9
BPhosphodiesterase (EC 3.1.4.-)protein33273% helix, 0% strandQ8WQX9

Ligands and binding sites

  • GAI · Guanidine · ligand · 5 copies · chains A, B
  • FFZ · 3-[5-[(4ar,8as)-4-oxidanylidene-3-propan-2-yl-4A,5,8, 8A-tetrahydrophthalazin-1-yl]-2-methoxy-phenyl]-N-(phenylmethyl)prop-2-ynamide · ligand · chains A
  • MG · Magnesium ion · metal · 2 copies · chains A, B
  • ZN · Zinc ion · metal · 2 copies · chains A, B
  • GOL · Glycerol · additive · 3 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, 3 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
14840.720.8144MG, FFZ
24630.720.8146MG
32450.520.7633GOL
4630.280.7313empty
5570.260.7314empty

Interfaces

1 interface between chains.

  • A–B · 733 Ų buried · 7 hydrogen bonds · protein-protein

Compared structures

  • 6GXQ · Crystal structure of T. brucei PDE-B1 catalytic domain with inhibitor NPD-1335 · the same entry in another collection · chain B against B, TM-score 1.00

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