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Crystal structure of bacillus licheniformis gamma glutamyl transpeptidase with azaserine

Analyse Crystal structure of bacillus licheniformis gamma glutamyl transpeptidase with… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
5Y8X
Type
protein
Length
543 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Gamma glutamyl transpeptidase
EC
2.3.2.2
Ligands
AZS, CA
Pockets
1 · best druggability 0.74

Structure

x-ray diffraction · 2 distinct chains · 38% helix, 18% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AGamma glutamyl transpeptidase (EC 2.3.2.2)protein36147% helix, 12% strand—
BGamma glutamyl transpeptidase (EC 2.3.2.2)protein18220% helix, 30% strand—

Ligands and binding sites

  • AZS · O-diazoacetyl-L-serine · ligand · chains A, B
  • CA · Calcium ion · metal · 3 copies · chains A, B
  • GOL · Glycerol · additive · 2 copies · chains A, B
  • EDO · 1,2-ethanediol · additive · chains B

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

Pockets

1 pocket found on a 1 Å grid, 1 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
17010.740.8064AZS

Interfaces

1 interface between chains.

  • A–B · 6761 Ų buried · 128 hydrogen bonds · protein-protein

Compared structures

  • 5Y8X · Crystal structure of Bacillus licheniformis Gamma glutamyl transpeptidase with Azaserine · the same entry in another collection · chain A against A, TM-score 1.00

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