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Structure of bacillus pumilus catalase with catechol bound.
Analyse Structure of bacillus pumilus catalase with catechol bound. in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 4QON
- Type
- protein
- Length
- 1,920 residues
- Chains
- 4
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Catalase
- EC
- 1.11.1.6
- UniProt
- W8QL66
- Ligands
- CAQ, HEM, NA, CL
- Pockets
- 20 · best druggability 0.87
Structure
x-ray diffraction · 1 distinct chain · 32% helix, 18% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A, B, C, D | Catalase (EC 1.11.1.6) | protein | 480 | 32% helix, 18% strand | W8QL66 |
Ligands and binding sites
- CAQ · Catechol · ligand · 11 copies · chains A, B, C, D
- HEM · Protoporphyrin IX containing Fe · ligand · 8 copies · chains A, D, B, C
- NA · Sodium ion · metal · 2 copies · chains A, B
- CL · Chloride ion · ion · 6 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.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 345 | 0.87 | 0.97 | 55 | empty |
| 2 | 350 | 0.86 | 0.96 | 59 | empty |
| 3 | 499 | 0.86 | 0.92 | 41 | CL |
| 4 | 638 | 0.83 | 0.87 | 67 | HEM, CAQ |
| 5 | 639 | 0.83 | 0.87 | 68 | HEM, CAQ |
Interfaces
6 interfaces between chains.
- B–D · 4684 Ų buried · 50 hydrogen bonds · protein-protein
- A–D · 4670 Ų buried · 71 hydrogen bonds · protein-protein
- A–C · 4661 Ų buried · 48 hydrogen bonds · protein-protein
- B–C · 4650 Ų buried · 73 hydrogen bonds · protein-protein
- C–D · 2500 Ų buried · 54 hydrogen bonds · protein-protein
Compared structures
- 4QON · Structure of Bacillus pumilus catalase with catechol bound. · the same entry in another collection · chain A against A, TM-score 1.00
Analyse
- Open in the research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides and crosslinks on the 3D structure
- Every structure of UniProt W8QL66
- Elsewhere: RCSB PDB 4QON · PDBe 4QON · UniProt W8QL66
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