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The details of glycolipid glycan hydrolysis by the structural analysis of a family 123 glycoside hydrolase from clostridium perfringens

Analyse The details of glycolipid glycan hydrolysis by the structural analysis of a… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
5FQE
Type
protein
Length
1,159 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Beta-N-acetylgalactosaminidase
UniProt
A0A0H2YNR7
Ligands
BR
Pockets
14 · best druggability 0.83

Structure

x-ray diffraction · 2 distinct chains · 31% helix, 28% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ABeta-N-acetylgalactosaminidaseprotein58031% helix, 29% strandA0A0H2YNR7
BBeta-N-acetylgalactosaminidaseprotein57931% helix, 28% strandA0A0H2YNR7

Ligands and binding sites

  • BR · Bromide ion · ion · 133 copies · chains A, B
  • FMT · Formic acid · additive · 4 copies · chains A, B
  • MPD · (4S)-2-methyl-2,4-pentanediol · additive · chains B

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

Pockets

14 pockets found on a 1 Å grid, 7 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
110020.830.84115BR, MPD
24780.760.8551FMT, BR
33570.650.8036BR
43150.630.7936BR
51460.580.8320BR

Interfaces

1 interface between chains.

  • A–B · 631 Ų buried · 8 hydrogen bonds · protein-protein

Compared structures

  • 5FQE · The details of glycolipid glycan hydrolysis by the structural analysis of a family 123… · the same entry in another collection · chain A against A, TM-score 1.00

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