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MolNFT v1 · #119936 · protein

Native structure of fructose 1,6-bisphosphate aldolase from escherichia COLI at 2.0 ångström resolution

5GK4 · Fructose-bisphosphate aldolase class 2: “Native structure of fructose 1,6-bisphosphate aldolase from escherichia COLI at 2.0 ångström resolution”. X-ray diffraction, 1 ligand (ZN), 6 pockets (best druggability 0.73). MolNFT v1…

PDB
5GK4
Type
protein
Length
659 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
ZN
Pockets
6 · best druggability 0.73

Structure

x-ray diffraction · 2 distinct chains · 53% helix, 14% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AFructose-bisphosphate aldolase class 2 (EC 4.1.2.13)protein32953% helix, 15% strandP0AB71
BFructose-bisphosphate aldolase class 2 (EC 4.1.2.13)protein33054% helix, 14% strandP0AB71

Ligands and binding sites

  • ZN · Zinc ion · metal · 4 copies · chains A, B
  • GOL · Glycerol · additive · 2 copies · chains A
  • PEG · Di(hydroxyethyl)ether · additive · chains A, B

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
1810.730.9628empty
21010.690.9228empty
31790.420.7320empty
4770.370.7715empty
5710.360.7714GOL

Interfaces

1 interface between chains.

  • A–B · 2429 Ų buried · 24 hydrogen bonds · protein-protein

Compared structures

  • 5GK4 · Native structure of fructose 1,6-bisphosphate aldolase from Escherichia coli at 2.0… · 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 1.00

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