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Transketolase from E. COLI in complex with substrate D-xylulose-5- phosphate

Analyse Transketolase from E. COLI in complex with substrate D-xylulose-5- phosphate in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
2R8O
Type
protein
Length
1,329 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Transketolase 1
EC
2.2.1.1
UniProt
P27302
Ligands
T5X, CA
Pockets
13 · best druggability 0.75

Structure

x-ray diffraction · 2 distinct chains · 47% helix, 14% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ATransketolase 1 (EC 2.2.1.1)protein66247% helix, 14% strandP27302
BTransketolase 1 (EC 2.2.1.1)protein66748% helix, 14% strandP27302

Ligands and binding sites

  • T5X · 2-C-{3-[(4-amino-2-methylpyrimidin-5-yl)methyl]-5-(2-{[(R)-hydroxy(phosphonooxy)phosphoryl]oxy}ethyl)-4-methyl-1,3-thiazol-3-ium-2-yl}-5-O-phosphono-D-xylitol · ligand · 2 copies · chains A, B
  • CA · Calcium ion · metal · 2 copies · chains A, B
  • EDO · 1,2-ethanediol · additive · 11 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, 6 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
13380.750.8651CA, T5X
23380.750.8650CA, T5X
33470.570.7650empty
43590.570.7549empty
53410.570.7649EDO

Interfaces

1 interface between chains.

  • A–B · 4287 Ų buried · 79 hydrogen bonds · protein-protein

Compared structures

  • 2R8O · Transketolase from E. coli in complex with substrate D-xylulose-5-phosphate · the same entry in another collection · chain A against A, TM-score 1.00
  • P27302 · AlphaFold monomer V2.0 prediction for transketolase 1 (P27302) · a predicted model of the same protein · chain A against A, TM-score 1.00

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