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Crystal structure of the enterobactin esterase fes from shigella flexneri in the presence of 2,3-di-hydroxy-N- benzoyl-serine

Analyse Crystal structure of the enterobactin esterase fes from shigella flexneri in… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
3C8H
Type
protein
Length
1,532 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Enterochelin esterase
UniProt
Q83SB9
Pockets
15 · best druggability 0.82

Structure

x-ray diffraction · 2 distinct chains · 31% helix, 25% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, CEnterochelin esteraseprotein38331% helix, 25% strandQ83SB9
B, DEnterochelin esteraseprotein38331% helix, 26% strandQ83SB9

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
15160.820.8853empty
25040.810.8855empty
38960.810.8365empty
49240.790.8163empty
57160.720.7860empty

Interfaces

3 interfaces between chains.

  • A–B · 1681 Ų buried · 9 hydrogen bonds · protein-protein
  • C–D · 1677 Ų buried · 10 hydrogen bonds · protein-protein
  • A–C · 349 Ų buried · 1 hydrogen bond · protein-protein

Modifications

Observed in the structure: 28 modified (engineered).

Compared structures

  • 3C8H · Crystal structure of the enterobactin esterase FES from Shigella flexneri in the presence… · the same entry in another collection · chain A against A, TM-score 1.00

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