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Crystal structure of trehalose synthase tret from P. horikoshii (seleno derivative)

Analyse Crystal structure of trehalose synthase tret from P. horikoshii (seleno… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
2XA1
Type
protein
Length
810 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Trehalose-synthase tret
UniProt
O58762
Pockets
4 · best druggability 0.73

Structure

x-ray diffraction · 2 distinct chains · 46% helix, 15% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ATrehalose-synthase tretprotein40446% helix, 15% strandO58762
BTrehalose-synthase tretprotein40646% helix, 15% strandO58762

Pockets

4 pockets found on a 1 Å grid, 3 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
110560.730.7673empty
29460.730.7769empty
311310.720.7577empty
4630.290.7316empty

Interfaces

1 interface between chains.

  • A–B · 317 Ų buried · 6 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 16 modified (engineered).

Compared structures

  • 2XA1 · Crystal structure of trehalose synthase TreT from P.horikoshii (Seleno derivative) · the same entry in another collection · chain A against A, TM-score 1.00
  • O58762 · AlphaFold monomer V2.0 prediction for trehalose synthase (O58762) · a predicted model of the same protein · chain B against A, TM-score 1.00

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