GL1X · GenesisL1 explorer

Research workbench

Complex of CH28/11 Fab and ssea-4 (tetragonal form)

Analyse Complex of CH28/11 Fab and ssea-4 (tetragonal form) in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
6UG7
Type
protein
Length
424 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
CH28/11 Fab light chain; CH28/11 Fab heavy chain
Ligands
GAL, BGC, GLA, NGA, SIA, SO4
Pockets
2 · best druggability 0.63

Structure

x-ray diffraction · 2 distinct chains · 7% helix, 51% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
LCH28/11 Fab light chainprotein2116% helix, 51% strand—
HCH28/11 Fab heavy chainprotein2138% helix, 52% strand—

Ligands and binding sites

  • GAL · beta-D-galactopyranose · sugar · 2 copies · chains L, H
  • BGC · beta-D-glucopyranose · sugar · chains L
  • GLA · alpha-D-galactopyranose · sugar · chains L, H
  • NGA · 2-acetamido-2-deoxy-beta-D-galactopyranose · sugar · chains L, H
  • SIA · N-acetyl-alpha-neuraminic acid · sugar · chains H
  • SO4 · Sulfate ion · ion · 4 copies · chains L, H
  • EDO · 1,2-ethanediol · additive · 5 copies · chains L, H

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
16100.630.7574empty
2570.270.7316empty

Interfaces

1 interface between chains.

  • L–H · 1692 Ų buried · 16 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 4 disulfide (disulfide).

Compared structures

  • 6UG7 · Complex of ch28/11 Fab and SSEA-4 (tetragonal form) · the same entry in another collection · chain L against L, TM-score 1.00

Analyse

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