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MolNFT v1 · #3038 · protein

Structure of the mutant VAL169CYS of catalase hpii from escherichia COLI

1CF9 · Protein (catalase hpii): “Structure of the mutant VAL169CYS of catalase hpii from escherichia COLI”. X-ray diffraction, 1 ligand (HEM), 20 pockets (best druggability 0.89). MolNFT v1 #3038 on GenesisL1: 3D structure, binding sites…

PDB
1CF9
Type
protein
Length
2,908 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Protein (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, DProtein (catalase 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
15130.890.9662empty
25060.890.9659empty
33220.860.9651HEM
43200.860.9651HEM
54770.860.9355empty

Interfaces

6 interfaces between chains.

  • A–D · 6171 Ų buried · 119 hydrogen bonds · protein-protein
  • B–C · 6128 Ų buried · 116 hydrogen bonds · protein-protein
  • B–D · 5949 Ų buried · 78 hydrogen bonds · protein-protein
  • A–C · 5865 Ų buried · 84 hydrogen bonds · protein-protein
  • C–D · 2259 Ų buried · 43 hydrogen bonds · protein-protein

Compared structures

  • 1CF9 · Structure of the mutant VAL169CYS of catalase HPII from Escherichia coli · the same entry in another collection · chain A against A, TM-score 1.00
  • P21179 · AlphaFold monomer V2.0 prediction for catalase hpii (P21179) · a predicted model of the same protein · chain A against A, TM-score 1.00

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