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Structural and kinetic analysis of the beef liver catalase complexed with nitric oxide

Analyse Structural and kinetic analysis of the beef liver catalase complexed with… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
3RGP
Type
protein
Length
1,996 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Catalase
EC
1.11.1.6
UniProt
P00432
Ligands
HEM, NO
Pockets
20 · best druggability 0.88

Structure

x-ray diffraction · 1 distinct chain · 33% helix, 19% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, B, C, DCatalase (EC 1.11.1.6)protein49933% helix, 19% strandP00432

Ligands and binding sites

  • HEM · Protoporphyrin IX containing Fe · ligand · 4 copies · chains A, D, B, C
  • NO · Nitric oxide · ion · 4 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, 19 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
16580.880.9251empty
23830.870.9646empty
33990.870.9650empty
42720.850.9648HEM, NO
52600.850.9644HEM, NO

Interfaces

6 interfaces between chains.

  • A–D · 4947 Ų buried · 77 hydrogen bonds · protein-protein
  • B–C · 4941 Ų buried · 70 hydrogen bonds · protein-protein
  • A–C · 4790 Ų buried · 57 hydrogen bonds · protein-protein
  • B–D · 4736 Ų buried · 59 hydrogen bonds · protein-protein
  • C–D · 2159 Ų buried · 29 hydrogen bonds · protein-protein

Compared structures

  • 3RGP · Structural and Kinetic Analysis of the Beef liver Catalase complexed with Nitric Oxide · the same entry in another collection · chain D against D, TM-score 1.00
  • P00432 · AlphaFold monomer V2.0 prediction for catalase (P00432) · a predicted model of the same protein · chain C against A, TM-score 1.00

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