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Bence jones kwr protein- immunoglobulin light chain dimer, P3(1)21 crystal form

Analyse Bence jones kwr protein- immunoglobulin light chain dimer, P3(1)21 crystal form in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
2OMB
Type
protein
Length
868 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Bence jones kwr protein - immunoglobulin light chain
Ligands
IPH, SO4
Pockets
14 · best druggability 0.73

Structure

x-ray diffraction · 1 distinct chain · 6% helix, 47% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, B, C, DBence jones kwr protein - immunoglobulin light chainprotein2176% helix, 47% strand—

Ligands and binding sites

  • IPH · Phenol · ligand · 2 copies · chains A, B, C, D
  • SO4 · Sulfate ion · ion · 9 copies · chains A, B, C, D

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

Pockets

14 pockets found on a 1 Å grid, 9 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
1690.730.9710IPH
2670.710.9512IPH
39860.700.75105empty
45080.650.7753empty
52720.620.8043empty

Interfaces

3 interfaces between chains.

  • C–D · 1851 Ų buried · 21 hydrogen bonds · protein-protein
  • A–B · 1746 Ų buried · 5 hydrogen bonds · protein-protein
  • B–D · 739 Ų buried · 13 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 10 disulfide, 4 modified (disulfide, cyclization).

Compared structures

  • 2OMB · Bence Jones KWR Protein- Immunoglobulin Light Chain Dimer, P3(1)21 Crystal Form · the same entry in another collection · chain A against A, TM-score 1.00

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