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Structure of GH84 with ligand

Analyse Structure of GH84 with ligand in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
5ABF
Type
protein
Length
1,314 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
O-glcnacase BT_4395
EC
3.2.1.169
UniProt
Q89ZI2
Ligands
XRJ, CA
Pockets
20 · best druggability 0.67

Structure

x-ray diffraction · 2 distinct chains · 40% helix, 19% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AO-glcnacase BT_4395 (EC 3.2.1.169)protein66340% helix, 19% strandQ89ZI2
BO-glcnacase BT_4395 (EC 3.2.1.169)protein65141% helix, 19% strandQ89ZI2

Ligands and binding sites

  • XRJ · 2-[(2S,3R,4R,5R)-5-(hydroxymethyl)-3,4-bis(oxidanyl)-1-pentyl-pyrrolidin-2-yl]-N-methyl-ethanamide · ligand · 2 copies · chains A, B
  • CA · Calcium ion · metal · chains B
  • EDO · 1,2-ethanediol · additive · 2 copies · chains A, B

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

Pockets

20 pockets found on a 1 Å grid, 6 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
15060.670.7853empty
24150.640.7856empty
32610.600.7923empty
41040.580.8520XRJ
5990.550.8419XRJ

Interfaces

1 interface between chains.

  • A–B · 1110 Ų buried · 22 hydrogen bonds · protein-protein

Compared structures

  • 5ABF · Structure of GH84 with ligand · the same entry in another collection · chain A against A, TM-score 1.00
  • Q89ZI2 · AlphaFold monomer V2.0 prediction for O-glcnacase BT_4395 (Q89ZI2) · a predicted model of the same protein · chain A against A, TM-score 1.00

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