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The crystal structure of ferritin from vibrio cholerae O1 biovar el tor str. N16961
Analyse The crystal structure of ferritin from vibrio cholerae O1 biovar el tor str.… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 3QZ3
- Type
- protein
- Length
- 492 residues
- Chains
- 3
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Ferritin
- UniProt
- Q9KVR1
- Pockets
- 3 · best druggability 0.58
Structure
x-ray diffraction · 3 distinct chains · 80% helix, 0% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | Ferritin | protein | 165 | 80% helix, 1% strand | Q9KVR1 |
| B | Ferritin | protein | 163 | 81% helix, 0% strand | Q9KVR1 |
| C | Ferritin | protein | 164 | 80% helix, 1% strand | Q9KVR1 |
Ligands and binding sites
- EDO · 1,2-ethanediol · additive · 4 copies · chains A, B, C
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
3 pockets found on a 1 Å grid, 2 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 231 | 0.58 | 0.79 | 39 | empty |
| 2 | 143 | 0.52 | 0.79 | 22 | empty |
| 3 | 58 | 0.32 | 0.76 | 15 | empty |
Interfaces
3 interfaces between chains.
- A–C · 1064 Ų buried · 7 hydrogen bonds · protein-protein
- A–B · 559 Ų buried · 4 hydrogen bonds · protein-protein
- B–C · 421 Ų buried · 5 hydrogen bonds · protein-protein
Modifications
Observed in the structure: 15 modified (engineered).
Compared structures
- 3QZ3 · The crystal structure of ferritin from Vibrio cholerae O1 biovar El Tor str. N16961 · 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 Q9KVR1
- Elsewhere: RCSB PDB 3QZ3 · PDBe 3QZ3 · UniProt Q9KVR1
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