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X-ray structure of O-succinylbenzoate synthase complexed with O-succinylbenzoic acid

Analyse X-ray structure of O-succinylbenzoate synthase complexed with O-succinylbenzoic… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
1SJB
Type
protein
Length
1,470 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
N-acylamino acid racemase
UniProt
Q44244
Ligands
OSB, MG
Pockets
10 · best druggability 0.88

Structure

x-ray diffraction · 2 distinct chains · 38% helix, 23% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, CN-acylamino acid racemaseprotein36737% helix, 23% strandQ44244
B, DN-acylamino acid racemaseprotein36838% helix, 23% strandQ44244

Ligands and binding sites

  • OSB · 2-succinylbenzoate · ligand · 4 copies · chains A, B, C, D
  • MG · Magnesium ion · metal · 4 copies · chains A, B, C, D

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

Pockets

10 pockets found on a 1 Å grid, 7 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
110140.880.89124empty
29200.870.89121empty
3730.720.9724OSB
41620.690.8938OSB
51690.690.8837OSB

Interfaces

5 interfaces between chains.

  • A–B · 1261 Ų buried · 18 hydrogen bonds · protein-protein
  • C–D · 1234 Ų buried · 17 hydrogen bonds · protein-protein
  • B–C · 1042 Ų buried · 11 hydrogen bonds · protein-protein
  • A–C · 143 Ų buried · 0 hydrogen bonds · protein-protein
  • B–D · 126 Ų buried · 0 hydrogen bonds · protein-protein

Compared structures

  • 1SJB · X-ray structure of o-succinylbenzoate synthase complexed with o-succinylbenzoic acid · the same entry in another collection · chain A against A, TM-score 1.00

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