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Crystal structure of S25-39 in complex with KDO(2.4)KDO(2.4)KDO

Analyse Crystal structure of S25-39 in complex with KDO(2.4)KDO(2.4)KDO in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
3OKN
Type
protein
Length
434 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
S25-39 Fab (IGG1K) light chain; S25-39 Fab (IGG1K) heavy chain
Ligands
KDA, KDO, ZN
Pockets
4 · best druggability 0.62

Structure

x-ray diffraction · 2 distinct chains · 6% helix, 52% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AS25-39 Fab (IGG1K) light chainprotein2186% helix, 53% strand—
BS25-39 Fab (IGG1K) heavy chainprotein2166% helix, 50% strand—

Ligands and binding sites

  • KDA · prop-2-en-1-yl 3-deoxy-alpha-D-manno-oct-2-ulopyranosidonic acid · ligand · chains A
  • KDO · 3-deoxy-alpha-D-manno-oct-2-ulopyranosonic acid · sugar · 2 copies · chains B, A
  • ZN · Zinc ion · metal · chains A

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
15800.620.7466empty
2660.460.8323empty
3630.290.7418empty
4680.280.7321empty

Interfaces

1 interface between chains.

  • A–B · 1792 Ų buried · 22 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 4 disulfide (disulfide).

Compared structures

  • 3OKN · Crystal structure of S25-39 in complex with Kdo(2.4)Kdo(2.4)Kdo · the same entry in another collection · chain A against A, TM-score 1.00

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