Research workbench
Chitin deacetylase family member from encephalitozoon cuniculi
Analyse Chitin deacetylase family member from encephalitozoon cuniculi in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 2VYO
- Type
- protein
- Length
- 206 residues
- Chains
- 1
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Polysaccharide deacetylase domain-containing protein ECU11_0510
- EC
- 3.5.1.41
- UniProt
- Q8SU65
- Ligands
- CA, ZN, CL
- Pockets
- 1 · best druggability 0.36
Structure
x-ray diffraction · 1 distinct chain · 44% helix, 17% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | Polysaccharide deacetylase domain-containing protein ECU11_0510 (EC 3.5.1.41) | protein | 206 | 44% helix, 17% strand | Q8SU65 |
Ligands and binding sites
- CA · Calcium ion · metal · 4 copies · chains A
- ZN · Zinc ion · metal · 2 copies · chains A
- CL · Chloride ion · ion · chains A
- ACT · Acetate ion · additive · chains A
- IMD · Imidazole · additive · chains A
- EDO · 1,2-ethanediol · additive · 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 | 65 | 0.36 | 0.78 | 15 | empty |
Modifications
Observed in the structure: 1 disulfide (disulfide).
Compared structures
- 2VYO · Chitin deacetylase family member from Encephalitozoon cuniculi · the same entry in another collection · chain A against A, TM-score 1.00
- Q8SU65 · AlphaFold monomer V2.0 prediction for polysaccharide deacetylase domain-containing… · 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 Q8SU65
- Elsewhere: RCSB PDB 2VYO · PDBe 2VYO · UniProt Q8SU65
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