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Class II fructose-1,6-bisphosphate aldolase of escherichia COLI with dhap

Analyse Class II fructose-1,6-bisphosphate aldolase of escherichia COLI with dhap in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
5VJD
Type
protein
Length
686 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Fructose-bisphosphate aldolase class 2
EC
4.1.2.13
UniProt
P0AB71
Ligands
13P, NA, ZN
Pockets
8 · best druggability 0.73

Structure

x-ray diffraction · 2 distinct chains · 51% helix, 15% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AFructose-bisphosphate aldolase class 2 (EC 4.1.2.13)protein34351% helix, 15% strandP0AB71
BFructose-bisphosphate aldolase class 2 (EC 4.1.2.13)protein34351% helix, 15% strandP0AB71

Ligands and binding sites

  • 13P · 1,3-dihydroxyacetonephosphate · ligand · 2 copies · chains A, B
  • NA · Sodium ion · metal · 4 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

8 pockets found on a 1 Å grid, 3 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
1720.730.9825empty
2690.720.9726empty
32090.510.773813P
4950.410.782213P
5610.380.8019empty

Interfaces

1 interface between chains.

  • A–B · 2721 Ų buried · 26 hydrogen bonds · protein-protein

Compared structures

  • 5VJD · Class II fructose-1,6-bisphosphate aldolase of Escherichia coli with DHAP · the same entry in another collection · chain A against A, TM-score 1.00
  • P0AB71 · AlphaFold monomer V2.0 prediction for fructose-bisphosphate aldolase class 2 (P0AB71) · a predicted model of the same protein · chain A against A, TM-score 0.99

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