MolNFT v1 · #17108 · protein
Gafd (F17C-type) fimbrial adhesin from escherichia COLI
1OIO · Fimbrial lectin: “Gafd (F17C-type) fimbrial adhesin from escherichia COLI”. X-ray diffraction, 1 ligand (NAG), 1 pocket (best druggability 0.56). MolNFT v1 #17108 on GenesisL1: 3D structure, binding sites and pockets in GL1X.
- PDB
- 1OIO
- Type
- protein
- Length
- 356 residues
- Chains
- 2
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Fimbrial lectin
- UniProt
- Q47341
- Ligands
- NAG
- Pockets
- 1 · best druggability 0.56
Structure
x-ray diffraction · 1 distinct chain · 2% helix, 60% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A, B | Fimbrial lectin | protein | 178 | 2% helix, 60% strand | Q47341 |
Ligands and binding sites
- NAG · 2-acetamido-2-deoxy-beta-D-glucopyranose · sugar · 4 copies · chains A, B
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 | 226 | 0.56 | 0.78 | 24 | empty |
Interfaces
1 interface between chains.
- A–B · 333 Ų buried · 8 hydrogen bonds · protein-protein
Modifications
Observed in the structure: 2 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 Q47341
- Elsewhere: RCSB PDB 1OIO · PDBe 1OIO · UniProt Q47341
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