GL1X · GenesisL1 explorer

MolNFT v1 · #7766 · protein

Crystal structure of catalase hpii from escherichia COLI, ASN201HIS variant.

1GGK: “Crystal structure of catalase hpii from escherichia COLI, ASN201HIS variant.”. X-ray diffraction, 1 ligand (HEM), 20 pockets (best druggability 0.89). MolNFT v1 #7766 on GenesisL1: 3D structure, binding sites and pockets in GL1X.

PDB
1GGK
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, 20 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
15800.890.9562empty
25660.890.9560empty
33370.860.9654HEM
43340.860.9550HEM
53310.860.9552HEM

Interfaces

6 interfaces between chains.

  • B–C · 6258 Ų buried · 118 hydrogen bonds · protein-protein
  • A–D · 6237 Ų buried · 109 hydrogen bonds · protein-protein
  • B–D · 5929 Ų buried · 82 hydrogen bonds · protein-protein
  • A–C · 5905 Ų buried · 77 hydrogen bonds · protein-protein
  • A–B · 2263 Ų buried · 34 hydrogen bonds · protein-protein

Compared structures

  • 1GGK · Crystal structure of catalase hpii from escherichia COLI, ASN201HIS variant. · 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

Analyse

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