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Thermobaculum terrenum O-GlcNAc transferase mutant - K341M

Analyse Thermobaculum terrenum O-GlcNAc transferase mutant - K341M in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
5DJS
Type
protein
Length
2,080 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v2 / PDB Bank
Contract
0xd58B01f6C18086e5202cdC5D7Ad3E41790360102
Owner
0xF4e1AA6f26B7DA48EeAD9B24a97927303eeA07b8
Resolution
2.8
Source
Thermobaculum terrenum
Molecule
Tetratricopeptide TPR_2 repeat protein
UniProt
D1CIY5
Ligands
UDP
Pockets
20 · best druggability 0.82

Structure

x-ray diffraction · resolution 2.8 · 1 distinct chain · 54% helix, 11% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, B, C, DTetratricopeptide TPR_2 repeat proteinprotein52054% helix, 11% strandD1CIY5

Ligands and binding sites

  • UDP · Uridine-5'-diphosphate · ligand · 4 copies · chains A, B, C, D

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

Pockets

20 pockets found on a 1 Å grid, 11 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
110020.820.8380UDP
211930.800.8186UDP
311420.800.8185UDP
410600.800.8177UDP
54610.670.7953empty

Interfaces

5 interfaces between chains.

  • B–D · 946 Ų buried · 10 hydrogen bonds · protein-protein
  • A–C · 945 Ų buried · 10 hydrogen bonds · protein-protein
  • A–B · 931 Ų buried · 10 hydrogen bonds · protein-protein
  • C–D · 232 Ų buried · 2 hydrogen bonds · protein-protein
  • B–C · 14 Ų buried · 0 hydrogen bonds · protein-protein

Compared structures

  • 5DJS · Thermobaculum terrenum O-glcnac transferase mutant - K341M · the same entry in another collection · chain A against A, TM-score 1.00

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