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Class II fructose-1,6-bisphosphate aldolase from helicobacter pylori in complex with N-(3-hydroxypropyl)-glycolohydroxamic acid bisphosphate, a competitive inhibitor

Analyse Class II fructose-1,6-bisphosphate aldolase from helicobacter pylori in complex… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
3C56
Type
protein
Length
591 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Fructose-bisphosphate aldolase
EC
4.1.2.13
UniProt
P56109
Ligands
PH4, ZN
Pockets
2 · best druggability 0.44

Structure

x-ray diffraction · 2 distinct chains · 52% helix, 15% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AFructose-bisphosphate aldolase (EC 4.1.2.13)protein29751% helix, 15% strandP56109
BFructose-bisphosphate aldolase (EC 4.1.2.13)protein29452% helix, 15% strandP56109

Ligands and binding sites

  • PH4 · 3-{hydroxy[(phosphonooxy)acetyl]amino}propyl dihydrogen phosphate · ligand · 2 copies · chains A, B
  • ZN · Zinc ion · metal · 2 copies · chains A, B

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

Pockets

2 pockets found on a 1 Å grid, 0 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
1780.440.8122ZN, PH4
2920.410.7822ZN, PH4

Interfaces

1 interface between chains.

  • A–B · 1933 Ų buried · 29 hydrogen bonds · protein-protein

Compared structures

  • 3C56 · Class II fructose-1,6-bisphosphate aldolase from helicobacter pylori in complex with… · the same entry in another collection · chain A against A, TM-score 1.00
  • P56109 · AlphaFold monomer V2.0 prediction for fructose-bisphosphate aldolase (P56109) · a predicted model of the same protein · chain B against A, TM-score 0.99

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