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Crystal structure of the bifunctional chorismate synthase from saccharomyces cerevisiae

Analyse Crystal structure of the bifunctional chorismate synthase from saccharomyces… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
1R52
Type
protein
Length
1,130 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Chorismate synthase
EC
4.2.3.5
UniProt
P28777
Pockets
16 · best druggability 0.88

Structure

x-ray diffraction · 3 distinct chains · 36% helix, 23% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AChorismate synthase (EC 4.2.3.5)protein28336% helix, 23% strandP28777
B, DChorismate synthase (EC 4.2.3.5)protein28235% helix, 23% strandP28777
CChorismate synthase (EC 4.2.3.5)protein28336% helix, 23% strandP28777

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
110300.880.8985empty
25210.650.7768empty
33890.630.7854empty
43320.610.7849empty
52840.560.7742empty

Interfaces

6 interfaces between chains.

  • C–D · 2390 Ų buried · 32 hydrogen bonds · protein-protein
  • A–B · 2357 Ų buried · 30 hydrogen bonds · protein-protein
  • B–C · 1126 Ų buried · 15 hydrogen bonds · protein-protein
  • A–D · 1119 Ų buried · 19 hydrogen bonds · protein-protein
  • B–D · 775 Ų buried · 9 hydrogen bonds · protein-protein

Compared structures

  • 1R52 · Crystal structure of the bifunctional chorismate synthase from Saccharomyces cerevisiae · the same entry in another collection · chain D against D, TM-score 1.00
  • P28777 · AlphaFold monomer V2.0 prediction for chorismate synthase (P28777) · a predicted model of the same protein · chain D against A, TM-score 0.97

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