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Anti-streptococcus pneumoniae 23F Fab 023.102 with bound rhamnose- galactose

Analyse Anti-streptococcus pneumoniae 23F Fab 023.102 with bound rhamnose- galactose in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4HII
Type
protein
Length
823 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Fab 023.102 light chain; Fab 023.102 heavy chain
Ligands
GAL, RAM
Pockets
5 · best druggability 0.54

Structure

x-ray diffraction · 3 distinct chains · 6% helix, 52% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AFab 023.102 light chainprotein2126% helix, 51% strand—
B, DFab 023.102 heavy chainprotein2036% helix, 54% strand—
CFab 023.102 light chainprotein2057% helix, 51% strand—

Ligands and binding sites

  • GAL · beta-D-galactopyranose · sugar · 2 copies · chains A, B, C, D
  • RAM · alpha-L-rhamnopyranose · sugar · 2 copies · chains A, B, C, D

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
13480.540.7450empty
23140.520.7439empty
3870.370.7519empty
4660.350.7718RAM
5500.300.7616RAM

Interfaces

3 interfaces between chains.

  • A–B · 1897 Ų buried · 19 hydrogen bonds · protein-protein
  • C–D · 1873 Ų buried · 16 hydrogen bonds · protein-protein
  • B–D · 316 Ų buried · 8 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 8 disulfide (disulfide).

Compared structures

  • 4HII · Anti-Streptococcus pneumoniae 23F Fab 023.102 with bound rhamnose-galactose · the same entry in another collection · chain A against A, TM-score 1.00

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