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MolNFT v1 · #82614 · protein

Crystal structure of native 1,6-apd (with iron), 2-animophenol-1,6- dioxygenase

3VSH · 2-amino-5-chlorophenol 1,6-dioxygenase alpha subunit: “Crystal structure of native 1,6-apd (with iron), 2-animophenol-1,6- dioxygenase”. X-ray diffraction, 1 ligand (FE2), 5 pockets (best druggability 0.85). MolNFT v1 #82614 on…

PDB
3VSH
Type
protein
Length
1,146 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
2-amino-5-chlorophenol 1,6-dioxygenase alpha subunit; 2-amino-5-chlorophenol…
EC
1.13.11.8
UniProt
Q38M40, Q38M41
Ligands
FE2
Pockets
5 · best druggability 0.85

Structure

x-ray diffraction · 3 distinct chains · 40% helix, 25% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, C2-amino-5-chlorophenol 1,6-dioxygenase alpha subunit (EC 1.13.11.8)protein27041% helix, 26% strandQ38M40
B2-amino-5-chlorophenol 1,6-dioxygenase beta subunit (EC 1.13.11.8)protein30239% helix, 24% strandQ38M41
D2-amino-5-chlorophenol 1,6-dioxygenase beta subunit (EC 1.13.11.8)protein30439% helix, 26% strandQ38M41

Ligands and binding sites

  • FE2 · Fe (II) ion · metal · 2 copies · chains B, D

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
12110.850.9824empty
210340.830.8478FE2
311280.820.8387FE2
41340.610.8527empty
5780.340.7517empty

Interfaces

3 interfaces between chains.

  • C–D · 1653 Ų buried · 22 hydrogen bonds · protein-protein
  • A–B · 1630 Ų buried · 19 hydrogen bonds · protein-protein
  • B–D · 1152 Ų buried · 13 hydrogen bonds · protein-protein

Compared structures

  • 3VSH · Crystal structure of native 1,6-APD (with Iron), 2-Animophenol-1,6-Dioxygenase · the same entry in another collection · chain A against A, TM-score 1.00

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