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Structure of the D181N variant of catalase hpii from E. COLI

Analyse Structure of the D181N variant of catalase hpii from E. COLI in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
1QWS
Type
protein
Length
2,908 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Catalase hpii
EC
1.11.1.6
UniProt
P21179
Ligands
HEM
Pockets
20 · best druggability 0.89

Structure

x-ray diffraction · 1 distinct chain · 32% helix, 18% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, B, C, DCatalase hpii (EC 1.11.1.6)protein72732% helix, 18% strandP21179

Ligands and binding sites

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

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
14970.890.9658empty
25040.890.9657empty
34240.860.9443empty
42950.860.9651HEM
52550.850.9636HEM

Interfaces

6 interfaces between chains.

  • A–D · 6213 Ų buried · 118 hydrogen bonds · protein-protein
  • B–C · 6130 Ų buried · 120 hydrogen bonds · protein-protein
  • B–D · 5969 Ų buried · 86 hydrogen bonds · protein-protein
  • A–C · 5946 Ų buried · 82 hydrogen bonds · protein-protein
  • C–D · 2295 Ų buried · 43 hydrogen bonds · protein-protein

Compared structures

  • 1QWS · Structure of the D181N variant of catalase HPII from E. coli · the same entry in another collection · chain D against D, TM-score 1.00
  • P21179 · AlphaFold monomer V2.0 prediction for catalase hpii (P21179) · a predicted model of the same protein · chain B against A, TM-score 1.00

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