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Crystal structure of GH5_18 from bifidobacterium longum subsp. longum atcc 55813 in complex with glcnac

Analyse Crystal structure of GH5_18 from bifidobacterium longum subsp. longum atcc… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
7LR2
Type
protein
Length
1,693 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Glycosyl hydrolase BLGH5_18
UniProt
C2GY91
Ligands
NAG, SO4
Pockets
12 · best druggability 0.78

Structure

x-ray diffraction · 2 distinct chains · 40% helix, 15% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, C, DGlycosyl hydrolase BLGH5_18protein42340% helix, 15% strandC2GY91
BGlycosyl hydrolase BLGH5_18protein42440% helix, 15% strandC2GY91

Ligands and binding sites

  • NAG · 2-acetamido-2-deoxy-beta-D-glucopyranose · sugar · 4 copies · chains A, B, C, D
  • SO4 · Sulfate ion · ion · 10 copies · chains A, B, C, D
  • EDO · 1,2-ethanediol · additive · 21 copies · chains A, B, C, D

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

Pockets

12 pockets found on a 1 Å grid, 10 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
12860.780.9034NAG, EDO
22830.760.8838NAG, EDO
32600.750.8835NAG, EDO
42730.740.8734EDO, NAG
55780.690.7851empty

Interfaces

2 interfaces between chains.

  • B–C · 537 Ų buried · 11 hydrogen bonds · protein-protein
  • A–B · 434 Ų buried · 6 hydrogen bonds · protein-protein

Compared structures

  • 7LR2 · Crystal structure of GH5_18 from Bifidobacterium longum subsp. longum ATCC 55813 in… · the same entry in another collection · chain A against A, TM-score 1.00

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