GL1X · GenesisL1 explorer

MolNFT v1 · #128826 · protein

E. COLI fold apo

5O28 · Bifunctional protein fold: “E. COLI fold apo”. X-ray diffraction, 12 pockets (best druggability 0.74). MolNFT v1 #128826 on GenesisL1: 3D structure, binding sites and pockets in GL1X.

PDB
5O28
Type
protein
Length
1,139 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Bifunctional protein fold
EC
1.5.1.5, 3.5.4.9
UniProt
P24186
Pockets
12 · best druggability 0.74

Structure

x-ray diffraction · 3 distinct chains · 43% helix, 16% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ABifunctional protein fold (EC 1.5.1.5, 3.5.4.9)protein28544% helix, 16% strandP24186
B, DBifunctional protein fold (EC 1.5.1.5, 3.5.4.9)protein28542% helix, 16% strandP24186
CBifunctional protein fold (EC 1.5.1.5, 3.5.4.9)protein28441% helix, 16% strandP24186

Pockets

12 pockets found on a 1 Å grid, 6 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
17770.740.7976empty
24470.630.7659empty
33430.620.7830empty
43690.600.7650empty
52740.550.7636empty

Interfaces

5 interfaces between chains.

  • A–B · 1692 Ų buried · 32 hydrogen bonds · protein-protein
  • C–D · 1466 Ų buried · 24 hydrogen bonds · protein-protein
  • B–C · 242 Ų buried · 0 hydrogen bonds · protein-protein
  • B–D · 170 Ų buried · 3 hydrogen bonds · protein-protein
  • A–D · 19 Ų buried · 0 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 8 modified (methylation).

Compared structures

  • 5O28 · E. coli FolD apo · the same entry in another collection · chain D against D, TM-score 1.00
  • P24186 · AlphaFold monomer V2.0 prediction for bifunctional protein fold (P24186) · a predicted model of the same protein · chain B against A, TM-score 0.96

Analyse

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