MolNFT v1 · #72195 · protein
Crystal stricture of E145G/Y227F chitinase in complex with nag from bacillus cereus NCTU2
3N18 · Chitinase a: “Crystal stricture of E145G/Y227F chitinase in complex with nag from bacillus cereus NCTU2”. X-ray diffraction, 1 ligand (NAG), 2 pockets (best druggability 0.52). MolNFT v1 #72195 on GenesisL1: 3D structure, binding…
- PDB
- 3N18
- Type
- protein
- Length
- 327 residues
- Chains
- 1
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Chitinase a
- EC
- 3.2.1.14
- UniProt
- D0VV09
- Ligands
- NAG
- Pockets
- 2 · best druggability 0.52
Structure
x-ray diffraction · 1 distinct chain · 34% helix, 22% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | Chitinase a (EC 3.2.1.14) | protein | 327 | 34% helix, 22% strand | D0VV09 |
Ligands and binding sites
- NAG · 2-acetamido-2-deoxy-beta-D-glucopyranose · sugar · 4 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 | 162 | 0.52 | 0.79 | 24 | NAG |
| 2 | 52 | 0.27 | 0.74 | 17 | empty |
Compared structures
- 3N18 · Crystal stricture of E145G/Y227F chitinase in complex with NAG from Bacillus cereus NCTU2 · 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 D0VV09
- Elsewhere: RCSB PDB 3N18 · PDBe 3N18 · UniProt D0VV09
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