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Hemoglobin protease (hbp) passenger missing domain-2

Analyse Hemoglobin protease (hbp) passenger missing domain-2 in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
3AK5
Type
protein
Length
3,840 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Hemoglobin-binding protease hbp
EC
3.4.21.-
UniProt
O88093
Ligands
CA
Pockets
20 · best druggability 0.71

Structure

x-ray diffraction · 3 distinct chains · 7% helix, 46% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, BHemoglobin-binding protease hbp (EC 3.4.21.-)protein9707% helix, 46% strandO88093
CHemoglobin-binding protease hbp (EC 3.4.21.-)protein9527% helix, 46% strandO88093
DHemoglobin-binding protease hbp (EC 3.4.21.-)protein9487% helix, 46% strandO88093

Ligands and binding sites

  • CA · Calcium ion · metal · 4 copies · chains A, B, C, D

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

Pockets

20 pockets found on a 1 Å grid, 7 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
14530.710.8247empty
24330.710.8244empty
34570.710.8146empty
46890.700.7873empty
54040.700.8247empty

Interfaces

2 interfaces between chains.

  • C–D · 1239 Ų buried · 14 hydrogen bonds · protein-protein
  • A–B · 413 Ų buried · 4 hydrogen bonds · protein-protein

Compared structures

  • 3AK5 · Hemoglobin protease (Hbp) passenger missing domain-2 · the same entry in another collection · chain A against A, TM-score 1.00
  • O88093 · AlphaFold monomer V2.0 prediction for hemoglobin-binding protease hbp autotransporter… · a predicted model of the same protein · chain A against A, TM-score 0.98

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