MolNFT v1 · #98217 · protein
Human leukotriene A4 hydrolase complexed with ligand 4-(4- BENZYLPHENYL)THIAZOL-2-amine
4L2L · Leukotriene a-4 hydrolase: “Human leukotriene A4 hydrolase complexed with ligand 4-(4- BENZYLPHENYL)THIAZOL-2-amine”. X-ray diffraction, 3 ligands (1V6, YB, ZN), 5 pockets (best druggability 0.86). MolNFT v1 #98217 on GenesisL1: 3D…
- PDB
- 4L2L
- Type
- protein
- Length
- 607 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
- 1V6, YB, ZN
- Pockets
- 5 · best druggability 0.86
Structure
x-ray diffraction · 1 distinct chain · 44% helix, 24% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | Leukotriene a-4 hydrolase (EC 3.3.2.6) | protein | 607 | 44% helix, 24% strand | P09960 |
Ligands and binding sites
- 1V6 · 4-(4-benzylphenyl)-1,3-thiazol-2-amine · ligand · chains A
- YB · Ytterbium (III) ion · metal · 4 copies · chains A
- ZN · Zinc ion · metal · chains A
- ACT · Acetate ion · additive · 3 copies · 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 | 984 | 0.86 | 0.87 | 85 | 1V6, ACT |
| 2 | 115 | 0.56 | 0.84 | 18 | empty |
| 3 | 209 | 0.51 | 0.76 | 26 | empty |
| 4 | 123 | 0.44 | 0.77 | 25 | empty |
| 5 | 76 | 0.34 | 0.75 | 20 | empty |
Compared structures
- 4L2L · Human Leukotriene A4 Hydrolase complexed with ligand 4-(4-benzylphenyl)thiazol-2-amine · 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 P09960
- Elsewhere: RCSB PDB 4L2L · PDBe 4L2L · UniProt P09960
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