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The crystal structure of a protease from helicobacter pylori

Analyse The crystal structure of a protease from helicobacter pylori in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
5EUF
Type
protein
Length
829 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Protease
EC
3.4.-.-
UniProt
I9VHL9
Ligands
ZN
Pockets
12 · best druggability 0.65

Structure

x-ray diffraction · 2 distinct chains · 46% helix, 19% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AProtease (EC 3.4.-.-)protein41347% helix, 19% strandI9VHL9
BProtease (EC 3.4.-.-)protein41645% helix, 19% strandI9VHL9

Ligands and binding sites

  • ZN · Zinc ion · metal · 4 copies · chains A, B
  • GOL · Glycerol · additive · 2 copies · 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, 4 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
14890.650.7751ZN
24180.610.7638ZN
34490.610.7537empty
41200.510.8119empty
51220.480.7921empty

Interfaces

1 interface between chains.

  • A–B · 1247 Ų buried · 22 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 14 modified (engineered).

Compared structures

  • 5EUF · The crystal structure of a protease from Helicobacter pylori · the same entry in another collection · chain A against A, TM-score 1.00

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