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Specificity of coenzyme binding in thiamin diphosphate dependent enzymes: crystal structures of yeast transketolase in complex with analogs of thiamin diphosphate

Analyse Specificity of coenzyme binding in thiamin diphosphate dependent enzymes… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
1TKA
Type
protein
Length
1,356 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Transketolase
EC
2.2.1.1
UniProt
P23254
Ligands
N3T, CA
Pockets
13 · best druggability 0.80

Structure

x-ray diffraction · 1 distinct chain · 44% helix, 13% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, BTransketolase (EC 2.2.1.1)protein67844% helix, 13% strandP23254

Ligands and binding sites

  • N3T · 3'-deazo-thiamin diphosphate · ligand · 2 copies · chains A, B
  • CA · Calcium ion · metal · 2 copies · chains A, B

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
19290.800.8285empty
23760.760.8650CA, N3T
33980.750.8549CA, N3T
43440.630.7946empty
52800.540.7634empty

Interfaces

1 interface between chains.

  • A–B · 4583 Ų buried · 81 hydrogen bonds · protein-protein

Compared structures

  • 1TKA · Specificity of coenzyme binding in thiamin diphosphate dependent enzymes: crystal… · the same entry in another collection · chain A against A, TM-score 1.00
  • P23254 · AlphaFold monomer V2.0 prediction for transketolase 1 (P23254) · a predicted model of the same protein · chain A against A, TM-score 1.00

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