Research workbench
Crystal structure, recombinant expression and mutagenesis studies of the bifunctional catalase-phenol oxidase from scytalidium thermophilum
Analyse Crystal structure, recombinant expression and mutagenesis studies of the… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 4AUE
- Type
- protein
- Length
- 2,679 residues
- Chains
- 4
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Catalase-phenol oxidase
- EC
- 1.11.1.6
- Ligands
- HDD, NAG, CA
- Pockets
- 20 · best druggability 0.86
Structure
x-ray diffraction · 4 distinct chains · 33% helix, 18% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | Catalase-phenol oxidase (EC 1.11.1.6) | protein | 669 | 33% helix, 18% strand | — |
| B | Catalase-phenol oxidase (EC 1.11.1.6) | protein | 671 | 33% helix, 18% strand | — |
| C | Catalase-phenol oxidase (EC 1.11.1.6) | protein | 670 | 33% helix, 19% strand | — |
| D | Catalase-phenol oxidase (EC 1.11.1.6) | protein | 669 | 33% helix, 18% strand | — |
Ligands and binding sites
- HDD · Cis-heme D hydroxychlorin gamma-spirolactone · ligand · 4 copies · chains A, C, B, D
- NAG · 2-acetamido-2-deoxy-beta-D-glucopyranose · sugar · 21 copies · chains A, B, C, D
- CA · Calcium ion · metal · chains A, 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.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 1074 | 0.86 | 0.87 | 115 | empty |
| 2 | 1078 | 0.85 | 0.87 | 116 | empty |
| 3 | 360 | 0.85 | 0.94 | 64 | empty |
| 4 | 259 | 0.85 | 0.96 | 42 | HDD |
| 5 | 257 | 0.85 | 0.96 | 45 | HDD |
Interfaces
6 interfaces between chains.
- B–D · 5770 Ų buried · 78 hydrogen bonds · protein-protein
- A–C · 5758 Ų buried · 84 hydrogen bonds · protein-protein
- B–C · 5014 Ų buried · 63 hydrogen bonds · protein-protein
- A–D · 4997 Ų buried · 63 hydrogen bonds · protein-protein
- C–D · 2040 Ų buried · 32 hydrogen bonds · protein-protein
Modifications
Observed in the structure: 11 glycan (N-glycosylation).
Compared structures
- 4AUE · Crystal structure, recombinant expression and mutagenesis studies of the bifunctional… · 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
- Elsewhere: RCSB PDB 4AUE · PDBe 4AUE
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