MolNFT v1 · #70406 · protein
Glucose-6-phosphate isomerase from francisella tularensis.
3LJK: “Glucose-6-phosphate isomerase from francisella tularensis.”. X-ray diffraction, 1 ligand (CA), 4 pockets (best druggability 0.65). MolNFT v1 #70406 on GenesisL1: 3D structure, binding sites and pockets in GL1X.
- PDB
- 3LJK
- Type
- protein
- Length
- 543 residues
- Chains
- 1
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Glucose-6-phosphate isomerase
- EC
- 5.3.1.9
- UniProt
- Q5NFC4
- Ligands
- CA
- Pockets
- 4 · best druggability 0.65
Structure
x-ray diffraction · 1 distinct chain · 55% helix, 12% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | Glucose-6-phosphate isomerase (EC 5.3.1.9) | protein | 543 | 55% helix, 12% strand | Q5NFC4 |
Ligands and binding sites
- CA · Calcium ion · metal · chains A
- MES · 2-(N-morpholino)-ethanesulfonic acid · additive · chains A
- GOL · Glycerol · additive · chains A
- IPA · Isopropyl alcohol · additive · chains A
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
4 pockets found on a 1 Å grid, 1 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 369 | 0.65 | 0.79 | 40 | empty |
| 2 | 58 | 0.50 | 0.86 | 17 | empty |
| 3 | 54 | 0.47 | 0.85 | 15 | empty |
| 4 | 66 | 0.31 | 0.75 | 15 | empty |
Modifications
Observed in the structure: 10 modified, 1 disulfide (engineered, disulfide).
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 Q5NFC4
- Elsewhere: RCSB PDB 3LJK · PDBe 3LJK · UniProt Q5NFC4
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