Research workbench
Structure of the lectin bambl from burkholderia ambifaria in complex with blood group H type 1 tetrasaccharide
Analyse Structure of the lectin bambl from burkholderia ambifaria in complex with blood… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 3ZW2
- Type
- protein
- Length
- 261 residues
- Chains
- 3
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Bambl lectin
- UniProt
- Q0B4G1
- Ligands
- GAL, FUC, NAG, GLA
- Pockets
- 1 · best druggability 0.73
Structure
x-ray diffraction · 1 distinct chain · 0% helix, 68% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A, B, C | Bambl lectin | protein | 87 | 0% helix, 68% strand | Q0B4G1 |
Ligands and binding sites
- GAL · beta-D-galactopyranose · sugar · 6 copies · chains A, B, C
- FUC · alpha-L-fucopyranose · sugar · 6 copies · chains A, B, C
- NAG · 2-acetamido-2-deoxy-beta-D-glucopyranose · sugar · 5 copies · chains A, B, C
- GLA · alpha-D-galactopyranose · sugar · chains C
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
1 pocket found on a 1 Å grid, 1 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 551 | 0.73 | 0.82 | 55 | empty |
Interfaces
3 interfaces between chains.
- A–C · 729 Ų buried · 8 hydrogen bonds · protein-protein
- B–C · 713 Ų buried · 9 hydrogen bonds · protein-protein
- A–B · 706 Ų buried · 9 hydrogen bonds · protein-protein
Compared structures
- 3ZW2 · Structure of the lectin Bambl from Burkholderia ambifaria in complex with blood group H… · 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 Q0B4G1
- Elsewhere: RCSB PDB 3ZW2 · PDBe 3ZW2 · UniProt Q0B4G1
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