MolNFT v1 · #138818 · protein
Crystal structure of a mutant insect group III chitinase complex with (GLCNAC)6 (CAD1-E217L-(GLCNAC)6 ) from ostrinia furnacalis
5WVB: “Crystal structure of a mutant insect group III chitinase complex with (GLCNAC)6 (CAD1-E217L-(GLCNAC)6 ) from…”. X-ray diffraction, 1 ligand (NAG), 2 pockets (best druggability 0.66). MolNFT v1 #138818 on GenesisL1: 3D structure…
- PDB
- 5WVB
- Type
- protein
- Length
- 391 residues
- Chains
- 1
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Chitinase
- EC
- 3.2.1.14
- UniProt
- U5LUV7
- Ligands
- NAG
- Pockets
- 2 · best druggability 0.66
Structure
x-ray diffraction · 1 distinct chain · 36% helix, 21% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | Chitinase (EC 3.2.1.14) | protein | 391 | 36% helix, 21% strand | U5LUV7 |
Ligands and binding sites
- NAG · 2-acetamido-2-deoxy-beta-D-glucopyranose · sugar · 6 copies · chains A
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
2 pockets found on a 1 Å grid, 1 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 409 | 0.66 | 0.79 | 45 | NAG |
| 2 | 50 | 0.30 | 0.77 | 15 | empty |
Modifications
Observed in the structure: 2 disulfide (disulfide).
Compared structures
- 5WVB · Crystal structure of a mutant insect group III chitinase complex with (GlcNAc)6… · 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 U5LUV7
- Elsewhere: RCSB PDB 5WVB · PDBe 5WVB · UniProt U5LUV7
GL1X is a live explorer of the GenesisL1 blockchain. Turn on JavaScript for search, charts and interactive views.