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CRYSTAL STRUCTURE OF HUMAN INDOLEAMINE 2,3-DIOXYGENASE 1 (IDO1) in complex with ferric heme and an Epacadostat analog
Analyse CRYSTAL STRUCTURE OF HUMAN INDOLEAMINE 2,3-DIOXYGENASE 1 (IDO1) in complex with… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 6E41
- Type
- protein
- Length
- 1,507 residues
- Chains
- 4
- Method
- x-ray diffraction
- Collection
- MolNFT v2 / PDB Bank
- Contract
- 0xd58B01f6C18086e5202cdC5D7Ad3E41790360102
- Owner
- 0xF4e1AA6f26B7DA48EeAD9B24a97927303eeA07b8
- Resolution
- 2.291
- Source
- Homo sapiens
- Molecule
- Indoleamine 2,3-dioxygenase 1
- EC
- 1.13.11.52
- UniProt
- P14902
- Ligands
- HQS, HEM
- Pockets
- 19 · best druggability 0.82
Structure
x-ray diffraction · resolution 2.291 · 3 distinct chains · 61% helix, 3% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | Indoleamine 2,3-dioxygenase 1 (EC 1.13.11.52) | protein | 377 | 61% helix, 4% strand | P14902 |
| B, C | Indoleamine 2,3-dioxygenase 1 (EC 1.13.11.52) | protein | 376 | 60% helix, 3% strand | P14902 |
| D | Indoleamine 2,3-dioxygenase 1 (EC 1.13.11.52) | protein | 378 | 61% helix, 3% strand | P14902 |
Ligands and binding sites
- HQS · N-(3-bromo-4-fluorophenyl)-N'-hydroxy-4-{[2-(sulfamoylamino)ethyl]sulfanyl}-1,2,5-oxadiazole-3-carboximidamide · ligand · 6 copies · chains A, B, C, D
- HEM · Protoporphyrin IX containing Fe · ligand · 4 copies · chains A, B, C, D
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
19 pockets found on a 1 Å grid, 9 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 982 | 0.82 | 0.83 | 73 | HEM, HQS |
| 2 | 954 | 0.81 | 0.82 | 72 | HEM, HQS |
| 3 | 1072 | 0.81 | 0.82 | 90 | HEM, HQS |
| 4 | 842 | 0.80 | 0.83 | 58 | HEM, HQS |
| 5 | 945 | 0.76 | 0.79 | 75 | empty |
Interfaces
3 interfaces between chains.
- A–B · 594 Ų buried · 6 hydrogen bonds · protein-protein
- C–D · 514 Ų buried · 5 hydrogen bonds · protein-protein
- A–D · 27 Ų buried · 0 hydrogen bonds · protein-protein
Compared structures
- 6E41 · Crystal structure of human indoleamine 2,3-dioxygenase 1 (IDO1) in complex with ferric… · the same entry in another collection · chain A against A, TM-score 1.00
- P14902 · AlphaFold monomer V2.0 prediction for indoleamine 2,3-dioxygenase 1 (P14902) · a predicted model of the same protein · chain B against A, TM-score 0.98
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 P14902
- Elsewhere: RCSB PDB 6E41 · PDBe 6E41 · UniProt P14902
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