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Crystal structure of PDE4D catalytic domain in complex with compound 36

Analyse Crystal structure of PDE4D catalytic domain in complex with compound 36 in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
7CBJ
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
FTX, ZN, MG
Pockets
5 · best druggability 0.70

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)protein32667% helix, 1% strandQ08499
BCamp-specific 3',5'-cyclic phosphodiesterase 4D (EC 3.1.4.53)protein32366% helix, 1% strandQ08499

Ligands and binding sites

  • FTX · (1S)-1-[(7-chloranyl-1H-indol-3-yl)methyl]-6,7-dimethoxy-3,4-dihydro-1H-isoquinoline-2-carbaldehyde · ligand · 2 copies · chains A, B
  • ZN · Zinc ion · metal · 2 copies · chains A, B
  • MG · Magnesium ion · metal · 2 copies · chains A, B
  • EDO · 1,2-ethanediol · additive · 12 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
14270.700.8143MG, FTX, EDO
24110.690.8141MG, FTX, EDO
31870.570.8019EDO
42060.560.7925EDO
51030.370.7519EDO

Interfaces

1 interface between chains.

  • A–B · 808 Ų buried · 10 hydrogen bonds · protein-protein

Compared structures

  • 7CBJ · Crystal structure of PDE4D catalytic domain in complex with compound 36 · the same entry in another collection · chain A against A, TM-score 1.00

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