GL1X · GenesisL1 explorer

MolNFT v1 · #177451 · protein

Human histidine decarboxylase mutant Y334F

7EIX: “Human histidine decarboxylase mutant Y334F”. X-ray diffraction, 2 ligands (PLP, SO4), 12 pockets (best druggability 0.65). MolNFT v1 #177451 on GenesisL1: 3D structure, binding sites and pockets in GL1X.

PDB
7EIX
Type
protein
Length
931 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Histidine decarboxylase
EC
4.1.1.22
UniProt
P19113
Ligands
PLP, SO4
Pockets
12 · best druggability 0.65

Structure

x-ray diffraction · 2 distinct chains · 51% helix, 14% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AHistidine decarboxylase (EC 4.1.1.22)protein46750% helix, 13% strandP19113
BHistidine decarboxylase (EC 4.1.1.22)protein46451% helix, 14% strandP19113

Ligands and binding sites

  • PLP · Pyridoxal-5'-phosphate · ligand · 2 copies · chains A, B
  • SO4 · Sulfate ion · ion · chains A, B

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

Pockets

12 pockets found on a 1 Å grid, 3 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
13120.650.8152PLP
22810.630.8047PLP
31470.520.8024empty
41010.470.8023empty
51280.420.7524empty

Interfaces

1 interface between chains.

  • A–B · 6036 Ų buried · 81 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 2 cofactor, 2 modified (pyridoxal phosphate Schiff base, oxidation).

Compared structures

  • 7EIX · Human histidine decarboxylase mutant Y334F · the same entry in another collection · chain A against A, TM-score 1.00
  • P19113 · AlphaFold monomer V2.0 prediction for histidine decarboxylase (P19113) · a predicted model of the same protein · chain B against A, TM-score 1.00

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