MolNFT v1 · #177491 · protein
Prawn ferritin to coordinate with heavy metal ions
7EK4: “Prawn ferritin to coordinate with heavy metal ions”. X-ray diffraction, 2 ligands (HG, FE), 11 pockets (best druggability 0.79). MolNFT v1 #177491 on GenesisL1: 3D structure, binding sites and pockets in GL1X.
- PDB
- 7EK4
- Type
- protein
- Length
- 1,008 residues
- Chains
- 6
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Ferritin
- EC
- 1.16.3.1
- UniProt
- T2B7E1
- Ligands
- HG, FE
- Pockets
- 11 · best druggability 0.79
Structure
x-ray diffraction · 1 distinct chain · 73% helix, 1% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A, B, C, D, E, F | Ferritin (EC 1.16.3.1) | protein | 168 | 73% helix, 1% strand | T2B7E1 |
Ligands and binding sites
- HG · Mercury (II) ion · metal · 6 copies · chains A, B, C, D, E, F
- FE · Fe (III) ion · metal · 6 copies · chains A, B, C, D, E, F
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
11 pockets found on a 1 Å grid, 6 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 718 | 0.79 | 0.83 | 74 | empty |
| 2 | 95 | 0.77 | 0.97 | 16 | empty |
| 3 | 90 | 0.76 | 0.97 | 18 | empty |
| 4 | 95 | 0.76 | 0.97 | 17 | empty |
| 5 | 73 | 0.61 | 0.90 | 25 | empty |
Interfaces
9 interfaces between chains.
- E–F · 1429 Ų buried · 24 hydrogen bonds · protein-protein
- A–B · 1406 Ų buried · 25 hydrogen bonds · protein-protein
- C–D · 1375 Ų buried · 22 hydrogen bonds · protein-protein
- B–C · 772 Ų buried · 8 hydrogen bonds · protein-protein
- B–D · 551 Ų buried · 7 hydrogen bonds · protein-protein
Compared structures
- 7EK4 · prawn ferritin to coordinate with heavy metal ions · 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 T2B7E1
- Elsewhere: RCSB PDB 7EK4 · PDBe 7EK4 · UniProt T2B7E1
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