MolNFT v1 · #19835 · protein
Crystal structure of a family 51 alpha-L-arabinofuranosidase in complex with ara-ALPHA(1,3)-xyl
1QW8: “Crystal structure of a family 51 alpha-L-arabinofuranosidase in complex with ara-ALPHA(1,3)-xyl”. X-ray diffraction, 2 ligands (XYP, AHR), 6 pockets (best druggability 0.69). MolNFT v1 #19835 on GenesisL1: 3D structure, binding…
- PDB
- 1QW8
- Type
- protein
- Length
- 994 residues
- Chains
- 2
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Alpha-L-arabinofuranosidase
- EC
- 3.2.1.55
- UniProt
- Q9XBQ3
- Ligands
- XYP, AHR
- Pockets
- 6 · best druggability 0.69
Structure
x-ray diffraction · 1 distinct chain · 29% helix, 27% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A, B | Alpha-L-arabinofuranosidase (EC 3.2.1.55) | protein | 497 | 29% helix, 27% strand | Q9XBQ3 |
Ligands and binding sites
- XYP · beta-D-xylopyranose · sugar · 2 copies · chains A, B
- AHR · alpha-L-arabinofuranose · sugar · 2 copies · chains A, B
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
6 pockets found on a 1 Å grid, 3 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 898 | 0.69 | 0.75 | 83 | empty |
| 2 | 223 | 0.54 | 0.77 | 36 | XYP, AHR |
| 3 | 234 | 0.54 | 0.77 | 38 | XYP, AHR |
| 4 | 84 | 0.47 | 0.82 | 16 | empty |
| 5 | 60 | 0.30 | 0.74 | 16 | empty |
Interfaces
1 interface between chains.
- A–B · 1023 Ų buried · 5 hydrogen bonds · protein-protein
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 Q9XBQ3
- Elsewhere: RCSB PDB 1QW8 · PDBe 1QW8 · UniProt Q9XBQ3
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