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Bacterial chalcone isomerase in closed conformation from eubacterium ramulus at 2.8 a resolution

Analyse Bacterial chalcone isomerase in closed conformation from eubacterium ramulus at… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
3ZPH
Type
protein
Length
1,574 residues
Chains
6
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Chalcone isomerase
EC
5.5.1.6
Ligands
CL
Pockets
15 · best druggability 0.87

Structure

x-ray diffraction · 3 distinct chains · 29% helix, 25% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AChalcone isomerase (EC 5.5.1.6)protein26028% helix, 25% strand—
BChalcone isomerase (EC 5.5.1.6)protein28230% helix, 24% strand—
C, D, E, FChalcone isomerase (EC 5.5.1.6)protein25830% helix, 25% strand—

Ligands and binding sites

  • CL · Chloride ion · ion · 4 copies · chains A, B, C, E
  • GOL · Glycerol · additive · 5 copies · chains A, C, D, E, F

Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.

Pockets

15 pockets found on a 1 Å grid, 14 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
14990.870.9474empty
25150.860.9372empty
33720.820.9152empty
43550.810.9047empty
53700.800.8941empty

Interfaces

12 interfaces between chains.

  • A–E · 2226 Ų buried · 36 hydrogen bonds · protein-protein
  • B–D · 2221 Ų buried · 34 hydrogen bonds · protein-protein
  • C–F · 2205 Ų buried · 33 hydrogen bonds · protein-protein
  • B–F · 1031 Ų buried · 11 hydrogen bonds · protein-protein
  • E–F · 982 Ų buried · 12 hydrogen bonds · protein-protein

Compared structures

  • 3ZPH · Bacterial chalcone isomerase in closed conformation from Eubacterium ramulus at 2.8 A… · the same entry in another collection · chain A against A, TM-score 1.00

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