GL1X · GenesisL1 explorer

Research workbench

Crystal structure of lacto-N-biosidase from bifidobacterium bifidum complexed with lnb-thiazoline

Analyse Crystal structure of lacto-N-biosidase from bifidobacterium bifidum complexed… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4JAW
Type
protein
Length
1,265 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Lacto-N-biosidase
EC
3.2.1.140
UniProt
B3TLD6
Ligands
NGT, GAL, SO4
Pockets
12 · best druggability 0.67

Structure

x-ray diffraction · 2 distinct chains · 31% helix, 24% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ALacto-N-biosidase (EC 3.2.1.140)protein63331% helix, 24% strandB3TLD6
BLacto-N-biosidase (EC 3.2.1.140)protein63231% helix, 25% strandB3TLD6

Ligands and binding sites

  • NGT · 3ar,5r,6s,7r,7ar-5-hydroxymethyl-2-methyl-5,6,7,7A-tetrahydro-3AH-pyrano[3,2-d]thiazole-6,7-diol · ligand · 2 copies · chains A, B
  • GAL · beta-D-galactopyranose · sugar · 2 copies · chains A, B
  • SO4 · Sulfate ion · ion · 7 copies · chains A, B

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
15900.670.7769empty
25680.660.7759empty
31960.650.8432GAL, NGT, SO4
41770.640.8528GAL, NGT
52110.540.7835empty

Interfaces

1 interface between chains.

  • A–B · 1847 Ų buried · 33 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 4 disulfide (disulfide).

Compared structures

  • 4JAW · Crystal Structure of Lacto-N-Biosidase from Bifidobacterium bifidum complexed with… · the same entry in another collection · chain A against A, TM-score 1.00

Analyse

GL1X is a live explorer of the GenesisL1 blockchain. Turn on JavaScript for search, charts and interactive views.