MolNFT v2 · #8278 · protein
Crystal Structure of Laccase from Melanocarpus albomyces in Four Copper Form
1GW0 · Laccase-1: “Crystal Structure of Laccase from Melanocarpus albomyces in Four Copper Form”. X-ray diffraction at 2.4, 7 ligands (NAG, MAN, BMA), 12 pockets (best druggability 0.85). MolNFT v2 #8278 on GenesisL1: 3D structure, binding…
- PDB
- 1GW0
- Type
- protein
- Length
- 1,118 residues
- Chains
- 2
- Method
- x-ray diffraction
- Collection
- MolNFT v2 / PDB Bank
- Contract
- 0xd58B01f6C18086e5202cdC5D7Ad3E41790360102
- Owner
- 0xF4e1AA6f26B7DA48EeAD9B24a97927303eeA07b8
- Resolution
- 2.4
- Source
- MELANOCARPUS ALBOMYCES
- Molecule
- Laccase-1
- EC
- 1.10.3.2
- UniProt
- Q70KY3
- Ligands
- NAG, MAN, BMA, CU, SO4, OXY, CL
- Pockets
- 12 · best druggability 0.85
Structure
x-ray diffraction · resolution 2.4 · 1 distinct chain · 11% helix, 38% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A, B | Laccase-1 (EC 1.10.3.2) | protein | 559 | 11% helix, 38% strand | Q70KY3 |
Ligands and binding sites
- NAG · 2-acetamido-2-deoxy-beta-D-glucopyranose · sugar · 23 copies · chains A, B
- MAN · alpha-D-mannopyranose · sugar · 10 copies · chains A, B
- BMA · beta-D-mannopyranose · sugar · 6 copies · chains A, B
- CU · Copper (II) ion · metal · 8 copies · chains A, B
- SO4 · Sulfate ion · ion · 3 copies · chains A, B
- OXY · Oxygen molecule · ion · 2 copies · chains A, B
- CL · Chloride ion · ion · 2 copies · chains A, B
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
12 pockets found on a 1 Å grid, 8 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 584 | 0.85 | 0.90 | 80 | empty |
| 2 | 104 | 0.77 | 0.97 | 28 | empty |
| 3 | 102 | 0.77 | 0.97 | 30 | empty |
| 4 | 844 | 0.70 | 0.76 | 94 | NAG |
| 5 | 106 | 0.64 | 0.89 | 32 | empty |
Interfaces
1 interface between chains.
- A–B · 786 Ų buried · 7 hydrogen bonds · protein-protein
Modifications
Observed in the structure: 15 glycan, 6 disulfide (N-glycosylation, disulfide).
Compared structures
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 Q70KY3
- Elsewhere: RCSB PDB 1GW0 · PDBe 1GW0 · UniProt Q70KY3
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