Research workbench
SAXIPHILIN:STX complex, co-crystal
Analyse SAXIPHILIN:STX complex, co-crystal in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 6O0F
- Type
- protein
- Length
- 1,628 residues
- Chains
- 2
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Saxiphilin
- UniProt
- P31226
- Ligands
- 9SL
- Pockets
- 20 · best druggability 0.78
Structure
x-ray diffraction · 2 distinct chains · 29% helix, 17% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | Saxiphilin | protein | 812 | 29% helix, 17% strand | P31226 |
| B | Saxiphilin | protein | 816 | 28% helix, 18% strand | P31226 |
Ligands and binding sites
- 9SL · [(3aS,4R,10aS)-2,6-diamino-10,10-dihydroxy-3a,4,9,10-tetrahydro-3H,8H-pyrrolo[1,2-c]purin-4-yl]methyl carbamate · ligand · 2 copies · chains A, B
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
20 pockets found on a 1 Å grid, 11 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 1020 | 0.78 | 0.80 | 107 | empty |
| 2 | 797 | 0.76 | 0.80 | 79 | empty |
| 3 | 181 | 0.71 | 0.89 | 38 | empty |
| 4 | 434 | 0.70 | 0.81 | 58 | empty |
| 5 | 582 | 0.65 | 0.76 | 52 | empty |
Interfaces
1 interface between chains.
- A–B · 303 Ų buried · 8 hydrogen bonds · protein-protein
Modifications
Observed in the structure: 42 disulfide, 1 covalent (disulfide, covalent ligand).
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 P31226
- Elsewhere: RCSB PDB 6O0F · PDBe 6O0F · UniProt P31226
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