MolNFT v1 · #6170 · protein
E. COLI (lacz) beta-galactosidase (orthorhombic)
1F4H: “E. COLI (lacz) beta-galactosidase (orthorhombic)”. X-ray diffraction, 1 ligand (MG), 20 pockets (best druggability 0.81). MolNFT v1 #6170 on GenesisL1: 3D structure, binding sites and pockets in GL1X.
- PDB
- 1F4H
- Type
- protein
- Length
- 4,084 residues
- Chains
- 4
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Beta-galactosidase
- EC
- 3.2.1.23
- UniProt
- P00722
- Ligands
- MG
- Pockets
- 20 · best druggability 0.81
Structure
x-ray diffraction · 1 distinct chain · 14% helix, 39% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A, B, C, D | Beta-galactosidase (EC 3.2.1.23) | protein | 1021 | 14% helix, 39% strand | P00722 |
Ligands and binding sites
- MG · Magnesium ion · metal · 8 copies · chains A, B, C, D
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
20 pockets found on a 1 Å grid, 20 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 932 | 0.81 | 0.83 | 89 | empty |
| 2 | 825 | 0.81 | 0.84 | 113 | empty |
| 3 | 713 | 0.80 | 0.84 | 88 | empty |
| 4 | 704 | 0.78 | 0.83 | 78 | empty |
| 5 | 79 | 0.76 | 0.99 | 22 | empty |
Interfaces
6 interfaces between chains.
- A–D · 2414 Ų buried · 27 hydrogen bonds · protein-protein
- B–C · 2366 Ų buried · 26 hydrogen bonds · protein-protein
- A–B · 2068 Ų buried · 28 hydrogen bonds · protein-protein
- C–D · 1972 Ų buried · 24 hydrogen bonds · protein-protein
- B–D · 101 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 P00722
- Elsewhere: RCSB PDB 1F4H · PDBe 1F4H · UniProt P00722
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