Research workbench
Crystal structure of ara H 8.0201
Analyse Crystal structure of ara H 8.0201 in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 6V8H
- Type
- protein
- Length
- 1,214 residues
- Chains
- 8
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Ara H 8 allergen isoform
- UniProt
- B0YIU5
- Ligands
- SO4
- Pockets
- 13 · best druggability 0.89
Structure
x-ray diffraction · 2 distinct chains · 30% helix, 47% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A, C, J, L, M, N, O | Ara H 8 allergen isoform | protein | 152 | 30% helix, 47% strand | B0YIU5 |
| G | Ara H 8 allergen isoform | protein | 150 | 30% helix, 47% strand | B0YIU5 |
Ligands and binding sites
- SO4 · Sulfate ion · ion · 2 copies · chains C, J
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
13 pockets found on a 1 Å grid, 7 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 1114 | 0.89 | 0.90 | 136 | empty |
| 2 | 1165 | 0.88 | 0.89 | 132 | empty |
| 3 | 661 | 0.84 | 0.89 | 83 | empty |
| 4 | 530 | 0.84 | 0.90 | 76 | empty |
| 5 | 450 | 0.84 | 0.91 | 58 | empty |
Interfaces
17 interfaces between chains.
- C–G · 898 Ų buried · 7 hydrogen bonds · protein-protein
- J–L · 865 Ų buried · 10 hydrogen bonds · protein-protein
- M–O · 823 Ų buried · 2 hydrogen bonds · protein-protein
- A–N · 787 Ų buried · 4 hydrogen bonds · protein-protein
- A–L · 308 Ų buried · 5 hydrogen bonds · protein-protein
Compared structures
- 6V8H · Crystal structure of Ara h 8.0201 · 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 B0YIU5
- Elsewhere: RCSB PDB 6V8H · PDBe 6V8H · UniProt B0YIU5
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