MolNFT v1 · #180761 · protein
Crystal structure of myeloperoxidase subform C (mpo) complex with compound-4
7LAE: “Crystal structure of myeloperoxidase subform C (mpo) complex with compound-4”. X-ray diffraction, 8 ligands (HEM, XRV, NAG). MolNFT v1 #180761 on GenesisL1: 3D structure, binding sites and pockets in GL1X.
- PDB
- 7LAE
- Type
- protein
- Length
- 1,135 residues
- Chains
- 4
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- UniProt
- P05164
- Ligands
- HEM, XRV, NAG, MAN, FUC, BMA, CA, CL
Structure
x-ray diffraction · 3 distinct chains.
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A, D | — | protein | 103 | — | P05164 |
| B | — | protein | 464 | — | P05164 |
| E | — | protein | 465 | — | P05164 |
Ligands and binding sites
- HEM · Protoporphyrin IX containing Fe · ligand · 2 copies · chains A, B, D, E
- XRV · 7-{[1-(4-fluorophenyl)-1H-pyrazol-4-yl]methyl}-1H-[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 · 10 copies · chains B, E, D, A
- MAN · alpha-D-mannopyranose · sugar · 4 copies · chains B, A, E, D
- FUC · alpha-L-fucopyranose · sugar · 2 copies · chains B, E
- BMA · beta-D-mannopyranose · sugar · 2 copies · chains B, E
- CA · Calcium ion · metal · 2 copies · chains A, B, D, E
- CL · Chloride ion · ion · 2 copies · chains A, B
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Compared structures
- 7LAE · CRYSTAL STRUCTURE OF MYELOPEROXIDASE SUBFORM C (MPO) COMPLEX WITH Compound-4 · 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 P05164
- Elsewhere: RCSB PDB 7LAE · PDBe 7LAE · UniProt P05164
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