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Helicobacter pylori catalase compound I

Analyse Helicobacter pylori catalase compound I in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
2A9E
Type
protein
Length
982 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Kata catalase
EC
1.11.1.6
UniProt
P77872
Ligands
HEM, O
Pockets
17 · best druggability 0.84

Structure

x-ray diffraction · 1 distinct chain · 34% helix, 17% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, BKata catalase (EC 1.11.1.6)protein49134% helix, 17% strandP77872

Ligands and binding sites

  • HEM · Protoporphyrin IX containing Fe · ligand · 2 copies · chains A, B
  • O · Oxygen atom · ion · 2 copies · chains A, B
  • ACT · Acetate ion · additive · chains A, B

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

Pockets

17 pockets found on a 1 Å grid, 7 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
111340.840.85128ACT, HEM, O
24050.640.7837empty
33810.640.7932empty
44230.610.7643empty
53660.600.7734empty

Interfaces

1 interface between chains.

  • A–B · 2434 Ų buried · 40 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 8 modified (oxidation).

Compared structures

  • 2A9E · Helicobacter pylori catalase compound I · the same entry in another collection · chain A against A, TM-score 1.00
  • P77872 · AlphaFold monomer V2.0 prediction for catalase (P77872) · a predicted model of the same protein · chain B against A, TM-score 1.00

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