Research workbench
Lt-iib-B5 S74D mutant
Analyse Lt-iib-B5 S74D mutant in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 4FNF
- Type
- protein
- Length
- 980 residues
- Chains
- 10
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Heat-labile enterotoxin iib, B chain
- UniProt
- P43529
- Pockets
- 2 · best druggability 0.75
Structure
x-ray diffraction · 1 distinct chain · 30% helix, 40% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| D, E, F, G, H, A, B, C, I, J | Heat-labile enterotoxin iib, B chain | protein | 98 | 30% helix, 40% strand | P43529 |
Ligands and binding sites
- ACT · Acetate ion · additive · 10 copies · chains E, F, G, H, A, B, C, I, J
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
2 pockets found on a 1 Å grid, 2 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 1040 | 0.75 | 0.78 | 60 | empty |
| 2 | 1000 | 0.75 | 0.78 | 62 | empty |
Interfaces
10 interfaces between chains.
- E–F · 1218 Ų buried · 16 hydrogen bonds · protein-protein
- A–J · 1210 Ų buried · 15 hydrogen bonds · protein-protein
- C–I · 1210 Ų buried · 15 hydrogen bonds · protein-protein
- D–H · 1207 Ų buried · 16 hydrogen bonds · protein-protein
- G–H · 1204 Ų buried · 16 hydrogen bonds · protein-protein
Modifications
Observed in the structure: 10 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 P43529
- Elsewhere: RCSB PDB 4FNF · PDBe 4FNF · UniProt P43529
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