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Crystal structure of a lytic polysaccharide MONOOXYGENASE,BTLPMO10A, from bacillus thuringiensis
Analyse Crystal structure of a lytic polysaccharide MONOOXYGENASE,BTLPMO10A, from… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 5WSZ
- Type
- protein
- Length
- 673 residues
- Chains
- 4
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- LPMO10A
- UniProt
- A0A0C5K362
- Ligands
- CU
- Pockets
- 3 · best druggability 0.74
Structure
x-ray diffraction · 2 distinct chains · 12% helix, 40% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | LPMO10A | protein | 169 | 12% helix, 39% strand | A0A0C5K362 |
| B, C, D | LPMO10A | protein | 168 | 12% helix, 41% strand | A0A0C5K362 |
Ligands and binding sites
- CU · Copper (II) ion · metal · 4 copies · chains A, D, B, C
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
3 pockets found on a 1 Å grid, 2 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 675 | 0.74 | 0.80 | 71 | empty |
| 2 | 121 | 0.51 | 0.82 | 26 | empty |
| 3 | 59 | 0.35 | 0.78 | 18 | empty |
Interfaces
5 interfaces between chains.
- B–C · 472 Ų buried · 5 hydrogen bonds · protein-protein
- A–B · 394 Ų buried · 4 hydrogen bonds · protein-protein
- B–D · 237 Ų buried · 2 hydrogen bonds · protein-protein
- A–D · 165 Ų buried · 1 hydrogen bond · protein-protein
- A–C · 40 Ų buried · 0 hydrogen bonds · protein-protein
Modifications
Observed in the structure: 4 disulfide (disulfide).
Compared structures
- 5WSZ · Crystal structure of a lytic polysaccharide monooxygenase,BtLPMO10A, from Bacillus… · 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 A0A0C5K362
- Elsewhere: RCSB PDB 5WSZ · PDBe 5WSZ · UniProt A0A0C5K362
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