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MolNFT v1 · #22634 · protein

Catalytic domain of human phosphodiesterase 4D in complex with AMP

1TB7 · Camp-specific 3',5'-cyclic phosphodiesterase 4D: “Catalytic domain of human phosphodiesterase 4D in complex with AMP”. X-ray diffraction, 3 ligands (AMP, ZN, MG), 4 pockets (best druggability 0.71). MolNFT v1 #22634 on GenesisL1: 3D…

PDB
1TB7
Type
protein
Length
647 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Camp-specific 3',5'-cyclic phosphodiesterase 4D
EC
3.1.4.17
UniProt
Q08499
Ligands
AMP, ZN, MG
Pockets
4 · best druggability 0.71

Structure

x-ray diffraction · 2 distinct chains · 67% helix, 0% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ACamp-specific 3',5'-cyclic phosphodiesterase 4D (EC 3.1.4.17)protein32168% helix, 0% strandQ08499
BCamp-specific 3',5'-cyclic phosphodiesterase 4D (EC 3.1.4.17)protein32667% helix, 1% strandQ08499

Ligands and binding sites

  • AMP · Adenosine monophosphate · 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 · 27 copies · chains A, B
  • B3P · 2-[3-(2-hydroxy-1,1-dihydroxymethyl-ethylamino)-propylamino]-2-hydroxymethyl-propane-1,3-diol · additive · 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, 4 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
14010.710.8236MG, AMP, EDO
24040.690.8142MG, AMP, EDO
33310.610.7843EDO
42070.570.8024EDO

Interfaces

1 interface between chains.

  • A–B · 775 Ų buried · 15 hydrogen bonds · protein-protein

Compared structures

  • 1TB7 · Catalytic Domain Of Human Phosphodiesterase 4D In Complex With AMP · the same entry in another collection · chain A against A, TM-score 1.00

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