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Cryo-EM structure of the S. typhimurium oxaloacetate decarboxylase beta-gamma sub-complex

Analyse Cryo-EM structure of the S. typhimurium oxaloacetate decarboxylase beta-gamma… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
6IWW
Type
protein
Length
1,386 residues
Chains
6
Method
electron microscopy
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Oxaloacetate decarboxylase beta chain; Probable oxaloacetate decarboxylase gamma chain
EC
7.2.4.2
UniProt
A0A0F7JAV8, A0A0F7JC72
Pockets
20 · best druggability 0.83

Structure

electron microscopy · 2 distinct chains · 72% helix, 0% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, C, EOxaloacetate decarboxylase beta chain (EC 7.2.4.2)protein42070% helix, 0% strandA0A0F7JAV8
B, D, FProbable oxaloacetate decarboxylase gamma chain (EC 7.2.4.2)protein4295% helix, 0% strandA0A0F7JC72

Ligands and binding sites

  • LMT · Dodecyl-beta-D-maltoside · additive · 3 copies · chains A, C, E

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

Pockets

20 pockets found on a 1 Å grid, 9 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
17310.830.8640LMT
24970.730.8261empty
36560.720.7962empty
42480.670.8330empty
52930.670.8234empty

Interfaces

6 interfaces between chains.

  • A–B · 1600 Ų buried · 1 hydrogen bond · protein-protein
  • C–D · 1580 Ų buried · 1 hydrogen bond · protein-protein
  • E–F · 1578 Ų buried · 1 hydrogen bond · protein-protein
  • A–C · 1539 Ų buried · 4 hydrogen bonds · protein-protein
  • C–E · 1538 Ų buried · 4 hydrogen bonds · protein-protein

Compared structures

  • 6IWW · Cryo-EM structure of the S. typhimurium oxaloacetate decarboxylase beta-gamma sub-complex · the same entry in another collection · chain A against A, TM-score 1.00

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