MolNFT v1 · #103890 · protein
Extracellulr xylanase from geobacillus stearothermophilus: E159Q mutant, with xylopentaose in active site
4PUD · Endo-1,4-beta-xylanase: “Extracellulr xylanase from geobacillus stearothermophilus: E159Q mutant, with xylopentaose in active site”. X-ray diffraction, 3 ligands (XYP, ZN, CL), 1 pocket (best druggability 0.49). MolNFT v1 #103890 on…
- PDB
- 4PUD
- Type
- protein
- Length
- 371 residues
- Chains
- 1
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Endo-1,4-beta-xylanase
- EC
- 3.2.1.8
- UniProt
- P40943
- Ligands
- XYP, ZN, CL
- Pockets
- 1 · best druggability 0.49
Structure
x-ray diffraction · 1 distinct chain · 42% helix, 19% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | Endo-1,4-beta-xylanase (EC 3.2.1.8) | protein | 371 | 42% helix, 19% strand | P40943 |
Ligands and binding sites
- XYP · beta-D-xylopyranose · sugar · 5 copies · chains A
- ZN · Zinc ion · metal · 9 copies · chains A
- CL · Chloride ion · ion · 3 copies · chains A
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
1 pocket found on a 1 Å grid, 0 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 134 | 0.49 | 0.79 | 27 | XYP |
Compared structures
- 4PUD · Extracellulr Xylanase from Geobacillus stearothermophilus: E159Q mutant, with… · the same entry in another collection · chain A against A, TM-score 1.00
- P40943 · AlphaFold monomer V2.0 prediction for endo-1,4-beta-xylanase (P40943) · a predicted model of the same protein · 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 P40943
- Elsewhere: RCSB PDB 4PUD · PDBe 4PUD · UniProt P40943
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