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Crystal structure of PDE4D catalytic domain complexed with compound 4E

Analyse Crystal structure of PDE4D catalytic domain complexed with compound 4E in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
6KK0
Type
protein
Length
649 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Camp-specific 3',5'-cyclic phosphodiesterase 4D
EC
3.1.4.53
UniProt
Q08499
Ligands
M36, ZN, MG
Pockets
5 · best druggability 0.73

Structure

x-ray diffraction · 2 distinct chains · 67% helix, 1% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ACamp-specific 3',5'-cyclic phosphodiesterase 4D (EC 3.1.4.53)protein32367% helix, 1% strandQ08499
BCamp-specific 3',5'-cyclic phosphodiesterase 4D (EC 3.1.4.53)protein32667% helix, 1% strandQ08499

Ligands and binding sites

  • M36 · 7-[8-methoxy-2,2-dimethyl-7-(3-methylbut-2-enyl)-5-oxidanyl-6-oxidanylidene-pyrano[3,2-b]xanthen-9-yl]oxyheptanoic acid · ligand · 2 copies · chains A, B
  • ZN · Zinc ion · metal · 2 copies · chains A, B
  • MG · Magnesium ion · metal · 2 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
14500.730.8344M36, MG
25090.720.8149M36, MG
32280.570.7924empty
41490.520.8019empty
51280.420.7618empty

Interfaces

1 interface between chains.

  • A–B · 794 Ų buried · 16 hydrogen bonds · protein-protein

Compared structures

  • 6KK0 · Crystal structure of PDE4D catalytic domain complexed with compound 4e · the same entry in another collection · chain A against A, TM-score 1.00

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