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Crystal structure of a dyp-type peroxidase from pseudomonas putida

Analyse Crystal structure of a dyp-type peroxidase from pseudomonas putida in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
7QYQ
Type
protein
Length
1,133 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Dyp-type peroxidase family protein
UniProt
Q88HV5
Ligands
HEM
Pockets
14 · best druggability 0.82

Structure

x-ray diffraction · 2 distinct chains · 27% helix, 27% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, C, DDyp-type peroxidase family proteinprotein28327% helix, 27% strandQ88HV5
BDyp-type peroxidase family proteinprotein28427% helix, 27% strandQ88HV5

Ligands and binding sites

  • HEM · Protoporphyrin IX containing Fe · ligand · 4 copies · chains A, B, C, D

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

Pockets

14 pockets found on a 1 Å grid, 6 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
13000.820.9234HEM
22930.820.9234HEM
33040.810.9134HEM
44280.800.8856HEM
56840.740.8079empty

Interfaces

4 interfaces between chains.

  • A–C · 1211 Ų buried · 20 hydrogen bonds · protein-protein
  • B–D · 1210 Ų buried · 14 hydrogen bonds · protein-protein
  • B–C · 907 Ų buried · 16 hydrogen bonds · protein-protein
  • A–D · 899 Ų buried · 13 hydrogen bonds · protein-protein

Compared structures

  • 7QYQ · Crystal structure of a DyP-type peroxidase from Pseudomonas putida · the same entry in another collection · chain A against A, TM-score 1.00

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