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Probing the active center of catalase-phenol oxidase from scytalidium thermophilum

Analyse Probing the active center of catalase-phenol oxidase from scytalidium… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4B2Y
Type
protein
Length
2,693 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Catalase-phenol oxidase
EC
1.11.1.6
Ligands
HEM, CA
Pockets
20 · best druggability 0.86

Structure

x-ray diffraction · 3 distinct chains · 33% helix, 19% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ACatalase-phenol oxidase (EC 1.11.1.6)protein67533% helix, 20% strand—
BCatalase-phenol oxidase (EC 1.11.1.6)protein67434% helix, 19% strand—
C, DCatalase-phenol oxidase (EC 1.11.1.6)protein67233% helix, 19% strand—

Ligands and binding sites

  • HEM · Protoporphyrin IX containing Fe · ligand · 4 copies · chains A, C, B, D
  • CA · Calcium ion · metal · 6 copies · chains A, B, C, D

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

Pockets

20 pockets found on a 1 Å grid, 20 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
12950.860.9745HEM
22900.860.9646HEM
32980.860.9652HEM
411220.860.87114CA
511210.850.86112CA

Interfaces

6 interfaces between chains.

  • B–D · 5733 Ų buried · 86 hydrogen bonds · protein-protein
  • A–C · 5700 Ų buried · 85 hydrogen bonds · protein-protein
  • B–C · 5087 Ų buried · 66 hydrogen bonds · protein-protein
  • A–D · 5076 Ų buried · 66 hydrogen bonds · protein-protein
  • A–B · 2074 Ų buried · 27 hydrogen bonds · protein-protein

Compared structures

  • 4B2Y · Probing the active center of catalase-phenol oxidase from Scytalidium thermophilum · the same entry in another collection · chain A against A, TM-score 1.00

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