Research workbench
Structure of mineralized bfrb (double soak) from pseudomonas aeruginosa to 2.8A resolution
Analyse Structure of mineralized bfrb (double soak) from pseudomonas aeruginosa to 2.8A… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 3ISE
- Type
- protein
- Length
- 3,700 residues
- Chains
- 24
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Bacterioferritin
- UniProt
- Q9HY79
- Ligands
- HEM, FE, K
- Pockets
- 20 · best druggability 0.73
Structure
x-ray diffraction · 3 distinct chains · 79% helix, 0% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A, B, C, D, E, F, G, I, J, K, L, M, N, O, P, Q, S, T, U, V, X | Bacterioferritin | protein | 154 | 80% helix, 0% strand | Q9HY79 |
| H, R | Bacterioferritin | protein | 155 | 79% helix, 0% strand | Q9HY79 |
| W | Bacterioferritin | protein | 156 | 79% helix, 0% strand | Q9HY79 |
Ligands and binding sites
- HEM · Protoporphyrin IX containing Fe · ligand · 12 copies · chains A, B, C, D, E, F, G, H, I, J, K, L, M, N, O, P, Q, R, S, T, U, V, W, X
- FE · Fe (III) ion · metal · 24 copies · chains A, X, L, B, H, D, C, U, F, E, J, G, I, W, O, K, S, M, N, T, P, R, Q, V
- K · Potassium ion · metal · 6 copies · chains A, L, M, X, B, D, F, H, C, K, S, U, G, I, O, W, N, P, R, T, E, J, Q, V
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 | 214 | 0.73 | 0.88 | 34 | HEM |
| 2 | 219 | 0.73 | 0.88 | 31 | HEM |
| 3 | 213 | 0.73 | 0.88 | 31 | HEM |
| 4 | 218 | 0.72 | 0.87 | 30 | HEM |
| 5 | 214 | 0.72 | 0.88 | 32 | HEM |
Interfaces
72 interfaces between chains.
- Q–R · 914 Ų buried · 13 hydrogen bonds · protein-protein
- M–N · 912 Ų buried · 13 hydrogen bonds · protein-protein
- W–X · 909 Ų buried · 12 hydrogen bonds · protein-protein
- O–P · 909 Ų buried · 13 hydrogen bonds · protein-protein
- G–H · 908 Ų buried · 13 hydrogen bonds · protein-protein
Compared structures
- 3ISE · Structure of mineralized Bfrb (double soak) from Pseudomonas aeruginosa to 2.8A Resolution · 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 Q9HY79
- Elsewhere: RCSB PDB 3ISE · PDBe 3ISE · UniProt Q9HY79
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