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Crystal structure of PDE2 catalytic domain in space group P1

Analyse Crystal structure of PDE2 catalytic domain in space group P1 in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4HTZ
Type
protein
Length
1,326 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Cgmp-dependent 3',5'-cyclic phosphodiesterase
EC
3.1.4.17
UniProt
O00408
Ligands
ZN, MG
Pockets
9 · best druggability 0.75

Structure

x-ray diffraction · 4 distinct chains · 69% helix, 0% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ACgmp-dependent 3',5'-cyclic phosphodiesterase (EC 3.1.4.17)protein33870% helix, 0% strandO00408
BCgmp-dependent 3',5'-cyclic phosphodiesterase (EC 3.1.4.17)protein33768% helix, 0% strandO00408
CCgmp-dependent 3',5'-cyclic phosphodiesterase (EC 3.1.4.17)protein32568% helix, 0% strandO00408
DCgmp-dependent 3',5'-cyclic phosphodiesterase (EC 3.1.4.17)protein32669% helix, 0% strandO00408

Ligands and binding sites

  • ZN · Zinc ion · metal · 4 copies · chains A, B, C, D
  • MG · Magnesium ion · metal · 4 copies · chains A, B, C, D

Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.

Pockets

9 pockets found on a 1 Å grid, 5 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
14270.750.8540MG
24260.750.8442MG
34180.730.8341MG
43740.720.8338MG
54260.580.7443empty

Interfaces

3 interfaces between chains.

  • B–D · 1248 Ų buried · 10 hydrogen bonds · protein-protein
  • A–C · 1180 Ų buried · 7 hydrogen bonds · protein-protein
  • A–B · 758 Ų buried · 5 hydrogen bonds · protein-protein

Compared structures

  • 4HTZ · Crystal structure of PDE2 catalytic domain in space group P1 · the same entry in another collection · chain A against A, TM-score 1.00

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