Research workbench
Crystal structure of yoeb under peg condition
Analyse Crystal structure of yoeb under peg condition in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 2A6R
- Type
- protein
- Length
- 503 residues
- Chains
- 6
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Toxin yoeb
- UniProt
- P69348
- Ligands
- MG
- Pockets
- 2 · best druggability 0.60
Structure
x-ray diffraction · 2 distinct chains · 35% helix, 26% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A, B, D, E, F | Toxin yoeb | protein | 84 | 36% helix, 26% strand | P69348 |
| C | Toxin yoeb | protein | 83 | 35% helix, 27% strand | P69348 |
Ligands and binding sites
- MG · Magnesium ion · metal · 2 copies · chains A, D
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
2 pockets found on a 1 Å grid, 1 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 475 | 0.60 | 0.75 | 58 | empty |
| 2 | 130 | 0.43 | 0.76 | 29 | empty |
Interfaces
6 interfaces between chains.
- A–B · 689 Ų buried · 12 hydrogen bonds · protein-protein
- E–F · 684 Ų buried · 13 hydrogen bonds · protein-protein
- C–D · 674 Ų buried · 10 hydrogen bonds · protein-protein
- B–F · 248 Ų buried · 6 hydrogen bonds · protein-protein
- B–C · 176 Ų buried · 4 hydrogen bonds · protein-protein
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 P69348
- Elsewhere: RCSB PDB 2A6R · PDBe 2A6R · UniProt P69348
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