Research workbench
Cholera toxin el tor B-pentamer in complex with lewis-Y
Analyse Cholera toxin el tor B-pentamer in complex with lewis-Y in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 5ELC
- Type
- protein
- Length
- 1,030 residues
- Chains
- 10
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Cholera enterotoxin subunit B
- UniProt
- P01556
- Ligands
- BCN, FUC, GAL, NDG, NAG, CA
- Pockets
- 10 · best druggability 0.82
Structure
x-ray diffraction · 1 distinct chain · 24% helix, 38% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A, B, C, D, E, F, G, H, I, J | Cholera enterotoxin subunit B | protein | 103 | 24% helix, 38% strand | P01556 |
Ligands and binding sites
- BCN · Bicine · ligand · 10 copies · chains A, E, F, J, B, I, C, H, D, G
- FUC · alpha-L-fucopyranose · sugar · 19 copies · chains A, E, B, C, D, F, G, H, I, J
- GAL · beta-D-galactopyranose · sugar · 9 copies · chains A, B, C, D, E, G, H, I, J
- NDG · 2-acetamido-2-deoxy-alpha-D-glucopyranose · sugar · 7 copies · chains A, B, C, E, G, H, I, J
- NAG · 2-acetamido-2-deoxy-beta-D-glucopyranose · sugar · 2 copies · chains G
- CA · Calcium ion · metal · 10 copies · chains A, F, J, B, I, C, H, D, E, G
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
10 pockets found on a 1 Å grid, 5 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 696 | 0.82 | 0.86 | 93 | CA, BCN |
| 2 | 828 | 0.75 | 0.79 | 43 | empty |
| 3 | 719 | 0.73 | 0.79 | 37 | empty |
| 4 | 254 | 0.70 | 0.86 | 39 | CA, BCN |
| 5 | 90 | 0.57 | 0.86 | 20 | CA, BCN |
Interfaces
22 interfaces between chains.
- F–G · 1363 Ų buried · 30 hydrogen bonds · protein-protein
- F–J · 1352 Ų buried · 25 hydrogen bonds · protein-protein
- D–E · 1329 Ų buried · 27 hydrogen bonds · protein-protein
- A–B · 1327 Ų buried · 23 hydrogen bonds · protein-protein
- I–J · 1321 Ų buried · 24 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 P01556
- Elsewhere: RCSB PDB 5ELC · PDBe 5ELC · UniProt P01556
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