MolNFT v1 · #40911 · protein
Beta-glucosidase from thermotoga maritima in complex with azafagomine
2J7H · Beta-glucosidase a: “Beta-glucosidase from thermotoga maritima in complex with azafagomine”. X-ray diffraction, 2 ligands (AZF, CA), 5 pockets (best druggability 0.73). MolNFT v1 #40911 on GenesisL1: 3D structure, binding sites and…
- PDB
- 2J7H
- Type
- protein
- Length
- 880 residues
- Chains
- 2
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Beta-glucosidase a
- EC
- 3.2.1.21
- UniProt
- Q08638
- Ligands
- AZF, CA
- Pockets
- 5 · best druggability 0.73
Structure
x-ray diffraction · 2 distinct chains · 45% helix, 19% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | Beta-glucosidase a (EC 3.2.1.21) | protein | 438 | 45% helix, 18% strand | Q08638 |
| B | Beta-glucosidase a (EC 3.2.1.21) | protein | 442 | 45% helix, 19% strand | Q08638 |
Ligands and binding sites
- AZF · Azafagomine · ligand · 2 copies · chains A, B
- CA · Calcium ion · metal · 3 copies · chains A, B
- ACT · Acetate ion · additive · 3 copies · chains A, B
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
5 pockets found on a 1 Å grid, 2 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 602 | 0.73 | 0.80 | 54 | AZF |
| 2 | 476 | 0.71 | 0.81 | 48 | AZF |
| 3 | 78 | 0.36 | 0.75 | 12 | empty |
| 4 | 96 | 0.34 | 0.73 | 17 | empty |
| 5 | 55 | 0.25 | 0.72 | 16 | empty |
Interfaces
1 interface between chains.
- A–B · 73 Ų buried · 0 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 Q08638
- Elsewhere: RCSB PDB 2J7H · PDBe 2J7H · UniProt Q08638
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