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Crystal structure of the E190A mutant of O-succinylbenzoate synthase from escherichia COLI

Analyse Crystal structure of the E190A mutant of O-succinylbenzoate synthase from… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
2OFJ
Type
protein
Length
1,194 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
O-succinylbenzoate synthase
EC
4.2.1.-
UniProt
P29208
Pockets
13 · best druggability 0.81

Structure

x-ray diffraction · 3 distinct chains · 35% helix, 24% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, BO-succinylbenzoate synthase (EC 4.2.1.-)protein30035% helix, 24% strandP29208
CO-succinylbenzoate synthase (EC 4.2.1.-)protein29634% helix, 24% strandP29208
DO-succinylbenzoate synthase (EC 4.2.1.-)protein29837% helix, 22% strandP29208

Pockets

13 pockets found on a 1 Å grid, 5 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
18080.810.8389empty
22560.690.8434empty
31970.600.8139empty
42320.530.7730empty
52730.500.7430empty

Interfaces

5 interfaces between chains.

  • A–B · 1140 Ų buried · 17 hydrogen bonds · protein-protein
  • A–D · 678 Ų buried · 4 hydrogen bonds · protein-protein
  • B–C · 563 Ų buried · 8 hydrogen bonds · protein-protein
  • B–D · 130 Ų buried · 1 hydrogen bond · protein-protein
  • A–C · 118 Ų buried · 3 hydrogen bonds · protein-protein

Compared structures

  • 2OFJ · Crystal structure of the E190A mutant of o-succinylbenzoate synthase from Escherichia coli · the same entry in another collection · chain A against A, TM-score 1.00
  • P29208 · AlphaFold monomer V2.0 prediction for O-succinylbenzoate synthase (P29208) · a predicted model of the same protein · chain A against A, TM-score 0.99

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