GL1X · GenesisL1 explorer

MolNFT v1 · #180438 · protein

Substrate-dependent divergence of leukotriene A4 hydrolase aminopeptidase activity

7KZE · Leukotriene a-4 hydrolase: “Substrate-dependent divergence of leukotriene A4 hydrolase aminopeptidase activity”. X-ray diffraction, 2 ligands (N0Y, ZN), 16 pockets (best druggability 0.87). MolNFT v1 #180438 on GenesisL1: 3D…

PDB
7KZE
Type
protein
Length
1,823 residues
Chains
3
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Leukotriene a-4 hydrolase
EC
3.3.2.6, 3.4.11.4
UniProt
P09960
Ligands
N0Y, ZN
Pockets
16 · best druggability 0.87

Structure

x-ray diffraction · 2 distinct chains · 42% helix, 23% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, BLeukotriene a-4 hydrolase (EC 3.3.2.6, 3.4.11.4)protein60843% helix, 24% strandP09960
CLeukotriene a-4 hydrolase (EC 3.3.2.6, 3.4.11.4)protein60742% helix, 23% strandP09960

Ligands and binding sites

  • N0Y · 1-benzyl-4-methoxybenzene · ligand · 2 copies · chains A, C
  • ZN · Zinc ion · metal · 3 copies · chains A, B, C
  • PGE · Triethylene glycol · additive · chains B

Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.

Pockets

16 pockets found on a 1 Å grid, 10 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
110740.870.88116PGE
210130.860.8794N0Y
310380.860.8695ZN, N0Y
43940.730.8466empty
53440.620.7841empty

Interfaces

3 interfaces between chains.

  • A–B · 651 Ų buried · 6 hydrogen bonds · protein-protein
  • B–C · 302 Ų buried · 4 hydrogen bonds · protein-protein
  • A–C · 30 Ų buried · 0 hydrogen bonds · protein-protein

Compared structures

  • 7KZE · Substrate-dependent divergence of leukotriene A4 hydrolase aminopeptidase activity · the same entry in another collection · chain A against A, TM-score 1.00

Analyse

GL1X is a live explorer of the GenesisL1 blockchain. Turn on JavaScript for search, charts and interactive views.