Research workbench
Formation of a protein intermediate and its trapping by the simultaneous crystallization process: crystal structure of an iron-saturated intermediate in the FE3+ binding pathway of camel lactoferrin at 2.7 resolution
Analyse Formation of a protein intermediate and its trapping by the simultaneous… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 1I6Q
- Type
- protein
- Length
- 689 residues
- Chains
- 1
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Lactoferrin
- UniProt
- Q9TUM0
- Ligands
- FE, CO3
- Pockets
- 8 · best druggability 0.72
Structure
x-ray diffraction · 1 distinct chain · 29% helix, 19% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | Lactoferrin | protein | 689 | 29% helix, 19% strand | Q9TUM0 |
Ligands and binding sites
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
8 pockets found on a 1 Å grid, 3 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 350 | 0.72 | 0.84 | 38 | empty |
| 2 | 215 | 0.57 | 0.80 | 24 | empty |
| 3 | 329 | 0.55 | 0.75 | 44 | FE, CO3 |
| 4 | 192 | 0.46 | 0.74 | 37 | empty |
| 5 | 91 | 0.38 | 0.76 | 16 | empty |
Modifications
Observed in the structure: 15 disulfide (disulfide).
Compared structures
- 1I6Q · Formation of a protein intermediate and its trapping by the simultaneous crystallization… · the same entry in another collection · chain A against A, TM-score 1.00
- Q9TUM0 · AlphaFold monomer V2.0 prediction for lactotransferrin (Q9TUM0) · a predicted model of the same protein · chain A against A, TM-score 0.68
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 Q9TUM0
- Elsewhere: RCSB PDB 1I6Q · PDBe 1I6Q · UniProt Q9TUM0
GL1X is a live explorer of the GenesisL1 blockchain. Turn on JavaScript for search, charts and interactive views.