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Crystal structure of H. pylori htra with PDZ2 deletion

Analyse Crystal structure of H. pylori htra with PDZ2 deletion in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
5Y28
Type
protein
Length
752 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Periplasmic serine endoprotease degp-like; Unk-unk-unk-unk
EC
3.4.21.107
UniProt
G2J5T2
Pockets
6 · best druggability 0.62

Structure

x-ray diffraction · 4 distinct chains · 13% helix, 33% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
APeriplasmic serine endoprotease degp-like (EC 3.4.21.107)protein26812% helix, 31% strandG2J5T2
BPeriplasmic serine endoprotease degp-like (EC 3.4.21.107)protein20214% helix, 37% strandG2J5T2
CPeriplasmic serine endoprotease degp-like (EC 3.4.21.107)protein27814% helix, 34% strandG2J5T2
GUnk-unk-unk-unkprotein40% helix, 0% strand—

Ligands and binding sites

  • EDO · 1,2-ethanediol · additive · chains A

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

Pockets

6 pockets found on a 1 Å grid, 2 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
13330.620.7944empty
21800.520.7929empty
3710.310.7421empty
4510.300.7610EDO
5620.280.7422empty

Interfaces

4 interfaces between chains.

  • A–B · 1824 Ų buried · 31 hydrogen bonds · protein-protein
  • A–C · 1780 Ų buried · 20 hydrogen bonds · protein-protein
  • B–C · 1619 Ų buried · 30 hydrogen bonds · protein-protein
  • A–G · 243 Ų buried · 1 hydrogen bond · protein-protein

Compared structures

  • 5Y28 · Crystal structure of H. pylori HtrA with PDZ2 deletion · the same entry in another collection · chain A against A, TM-score 1.00

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