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Crystal structure of hoba (HP1230)FROM helicobacter pylori

Analyse Crystal structure of hoba (HP1230)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
2UVP
Type
protein
Length
723 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Hoba
UniProt
O25828
Ligands
CA
Pockets
11 · best druggability 0.72

Structure

x-ray diffraction · 4 distinct chains · 49% helix, 15% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AHobaprotein18049% helix, 15% strandO25828
BHobaprotein18148% helix, 15% strandO25828
CHobaprotein18647% helix, 14% strandO25828
DHobaprotein17650% helix, 15% strandO25828

Ligands and binding sites

  • CA · Calcium ion · metal · 5 copies · chains B, C, D
  • ACT · Acetate ion · additive · 3 copies · chains A, B, D, C
  • GOL · Glycerol · additive · 2 copies · chains B, C, D

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

Pockets

11 pockets found on a 1 Å grid, 4 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
110280.720.76106ACT
2690.720.9716ACT
3690.720.9717GOL
411440.720.76108ACT
5810.460.8116GOL, CA

Interfaces

4 interfaces between chains.

  • A–B · 2200 Ų buried · 15 hydrogen bonds · protein-protein
  • C–D · 2150 Ų buried · 14 hydrogen bonds · protein-protein
  • B–C · 991 Ų buried · 12 hydrogen bonds · protein-protein
  • A–D · 847 Ų buried · 11 hydrogen bonds · protein-protein

Compared structures

  • 2UVP · Crystal structure of HobA (HP1230)from Helicobacter pylori · the same entry in another collection · chain A against A, TM-score 1.00

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