Research workbench
AVR2
Analyse AVR2 in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 1WBI
- Type
- protein
- Length
- 970 residues
- Chains
- 8
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Avidin-related protein 2
- UniProt
- P56732
- Ligands
- BTN, SO4
- Pockets
- 17 · best druggability 0.68
Structure
x-ray diffraction · 4 distinct chains · 7% helix, 49% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A, F | Avidin-related protein 2 | protein | 123 | 7% helix, 49% strand | P56732 |
| B, G | Avidin-related protein 2 | protein | 120 | 8% helix, 50% strand | P56732 |
| C, D, E | Avidin-related protein 2 | protein | 121 | 7% helix, 50% strand | P56732 |
| H | Avidin-related protein 2 | protein | 121 | 7% helix, 50% strand | P56732 |
Ligands and binding sites
- BTN · Biotin · ligand · 8 copies · chains A, D, B, C, E, F, G, H
- SO4 · Sulfate ion · ion · 14 copies · chains A, C, B, D, E, H, F, G
- GOL · Glycerol · additive · 6 copies · chains A, B, C, F, E, G
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
17 pockets found on a 1 Å grid, 9 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 85 | 0.68 | 0.92 | 23 | BTN |
| 2 | 94 | 0.67 | 0.91 | 25 | BTN |
| 3 | 94 | 0.66 | 0.91 | 25 | BTN |
| 4 | 87 | 0.66 | 0.91 | 25 | BTN |
| 5 | 96 | 0.66 | 0.90 | 24 | BTN |
Interfaces
13 interfaces between chains.
- B–D · 1779 Ų buried · 22 hydrogen bonds · protein-protein
- A–C · 1759 Ų buried · 22 hydrogen bonds · protein-protein
- F–G · 1756 Ų buried · 23 hydrogen bonds · protein-protein
- E–H · 1744 Ų buried · 24 hydrogen bonds · protein-protein
- B–C · 589 Ų buried · 3 hydrogen bonds · protein-protein
Modifications
Observed in the structure: 8 disulfide (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 P56732
- Elsewhere: RCSB PDB 1WBI · PDBe 1WBI · UniProt P56732
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