MolNFT v1 · #60097 · protein
Crystal structure of leukotriene A4 hydrolase in complex with 2-amino- N-[4-(PHENYLMETHOXY)PHENYL]-acetamide
3CHO · Leukotriene a-4 hydrolase: “Crystal structure of leukotriene A4 hydrolase in complex with 2-amino- N-[4-(PHENYLMETHOXY)PHENYL]-acetamide”. X-ray diffraction, 3 ligands (4BG, ZN, YB), 5 pockets (best druggability 0.85). MolNFT v1…
- PDB
- 3CHO
- Type
- protein
- Length
- 610 residues
- Chains
- 1
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Leukotriene a-4 hydrolase
- EC
- 3.3.2.6
- UniProt
- P09960
- Ligands
- 4BG, ZN, YB
- Pockets
- 5 · best druggability 0.85
Structure
x-ray diffraction · 1 distinct chain · 43% helix, 23% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | Leukotriene a-4 hydrolase (EC 3.3.2.6) | protein | 610 | 43% helix, 23% strand | P09960 |
Ligands and binding sites
- 4BG · N-[4-(benzyloxy)phenyl]glycinamide · ligand · chains A
- ZN · Zinc ion · metal · chains A
- YB · Ytterbium (III) ion · metal · chains A
- ACT · Acetate ion · additive · chains A
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
5 pockets found on a 1 Å grid, 3 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 1088 | 0.85 | 0.86 | 97 | 4BG |
| 2 | 198 | 0.52 | 0.78 | 29 | empty |
| 3 | 88 | 0.50 | 0.83 | 18 | empty |
| 4 | 95 | 0.41 | 0.77 | 24 | empty |
| 5 | 123 | 0.40 | 0.75 | 27 | empty |
Compared structures
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 P09960
- Elsewhere: RCSB PDB 3CHO · PDBe 3CHO · UniProt P09960
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