Research workbench
Crystal structure of myeloperoxidase subform C (mpo) complex with compound-37 A.K.A 7-(1-phenyl-3-(((1S,3S)-3-phenyl-2,3-dihydro-1H- inden-1-YL)AMINO)PROPYL)-1H-[1,2,3]TRIAZOLO[4,5-B]PYRIDIN-5-amine
Analyse Crystal structure of myeloperoxidase subform C (mpo) complex with compound-37… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 6WY5
- Type
- protein
- Length
- 1,137 residues
- Chains
- 4
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Myeloperoxidase light chain; Myeloperoxidase heavy chain
- EC
- 1.11.2.2
- UniProt
- P05164
- Ligands
- HEC, UF7, NAG, MAN, BMA, FUC, CA, CL
- Pockets
- 11 · best druggability 0.83
Structure
x-ray diffraction · 3 distinct chains · 39% helix, 9% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A, D | Myeloperoxidase light chain (EC 1.11.2.2) | protein | 104 | 25% helix, 11% strand | P05164 |
| B | Myeloperoxidase heavy chain (EC 1.11.2.2) | protein | 464 | 40% helix, 9% strand | P05164 |
| E | Myeloperoxidase heavy chain (EC 1.11.2.2) | protein | 465 | 40% helix, 9% strand | P05164 |
Ligands and binding sites
- HEC · Heme C · ligand · 2 copies · chains A, B, D, E
- UF7 · 7-[(1R)-1-phenyl-3-{[(1S,3S)-3-phenyl-2,3-dihydro-1H-inden-1-yl]amino}propyl]-3H-[1,2,3]triazolo[4,5-b]pyridin-5-amine · ligand · 2 copies · chains A, B, D, E
- NAG · 2-acetamido-2-deoxy-beta-D-glucopyranose · sugar · 9 copies · chains B, E, D, A
- MAN · alpha-D-mannopyranose · sugar · 4 copies · chains E, D, B, A
- BMA · beta-D-mannopyranose · sugar · 2 copies · chains E, B
- FUC · alpha-L-fucopyranose · sugar · 2 copies · chains B, E
- CA · Calcium ion · metal · 2 copies · chains A, B, D, E
- CL · Chloride ion · ion · 3 copies · chains A, B, D, E
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
11 pockets found on a 1 Å grid, 4 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 465 | 0.83 | 0.89 | 72 | empty |
| 2 | 792 | 0.80 | 0.83 | 88 | MAN |
| 3 | 746 | 0.79 | 0.83 | 61 | HEC, UF7 |
| 4 | 761 | 0.78 | 0.82 | 59 | HEC, UF7 |
| 5 | 54 | 0.44 | 0.84 | 17 | empty |
Interfaces
6 interfaces between chains.
- D–E · 5659 Ų buried · 109 hydrogen bonds · protein-protein
- A–B · 5483 Ų buried · 113 hydrogen bonds · protein-protein
- A–D · 620 Ų buried · 4 hydrogen bonds · protein-protein
- B–E · 391 Ų buried · 2 hydrogen bonds · protein-protein
- A–E · 275 Ų buried · 2 hydrogen bonds · protein-protein
Modifications
Observed in the structure: 6 cofactor, 5 glycan, 2 modified (heme c attachment, N-glycosylation, oxidation).
Compared structures
- 6WY5 · CRYSTAL STRUCTURE OF MYELOPEROXIDASE SUBFORM C (MPO) COMPLEX WITH Compound-37 A.K.A… · the same entry in another collection · chain A against A, TM-score 1.00
- P05164 · AlphaFold monomer V2.0 prediction for myeloperoxidase (P05164) · 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 P05164
- Elsewhere: RCSB PDB 6WY5 · PDBe 6WY5 · UniProt P05164
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