GL1X · GenesisL1 explorer

MolNFT v1 · #70297 · protein

Crystal structure of rabbit muscle aldolase-SNX9 LC4 complex

3LGE · Fructose-bisphosphate aldolase a: “Crystal structure of rabbit muscle aldolase-SNX9 LC4 complex”. X-ray diffraction, 17 pockets (best druggability 0.89). MolNFT v1 #70297 on GenesisL1: 3D structure, binding sites and pockets in GL1X.

PDB
3LGE
Type
protein
Length
1,454 residues
Chains
8
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Fructose-bisphosphate aldolase a; Sorting nexin-9
EC
4.1.2.13
UniProt
P00883, Q9Y5X1
Pockets
17 · best druggability 0.89

Structure

x-ray diffraction · 4 distinct chains · 47% helix, 15% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, DFructose-bisphosphate aldolase a (EC 4.1.2.13)protein34946% helix, 15% strandP00883
B, CFructose-bisphosphate aldolase a (EC 4.1.2.13)protein35248% helix, 15% strandP00883
E, HSorting nexin-9protein70% helix, 0% strandQ9Y5X1
F, GSorting nexin-9protein1953% helix, 0% strandQ9Y5X1

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
110810.890.90115empty
25500.830.8879empty
37640.790.82106empty
4600.700.9724empty
52330.670.8446empty

Interfaces

10 interfaces between chains.

  • A–B · 1485 Ų buried · 20 hydrogen bonds · protein-protein
  • C–D · 1469 Ų buried · 19 hydrogen bonds · protein-protein
  • A–D · 1368 Ų buried · 24 hydrogen bonds · protein-protein
  • B–C · 1367 Ų buried · 24 hydrogen bonds · protein-protein
  • C–G · 986 Ų buried · 10 hydrogen bonds · protein-protein

Compared structures

  • 3LGE · Crystal structure of rabbit muscle aldolase-SNX9 LC4 complex · the same entry in another collection · chain H against H, TM-score 1.00
  • P00883 · AlphaFold monomer V2.0 prediction for fructose-bisphosphate aldolase a (P00883) · a predicted model of the same protein · chain A against A, TM-score 0.98

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