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Crystal structure of HBR3 bound to CB3S-Fab

Analyse Crystal structure of HBR3 bound to CB3S-Fab in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
2HFG
Type
protein
Length
460 residues
Chains
3
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
CB3S Fab light chain (kappa); CB3S Fab heavy chain; Tumor necrosis factor receptor…
UniProt
Q6PIH7, Q6N093, Q96RJ3
Pockets
5 · best druggability 0.57

Structure

x-ray diffraction · 3 distinct chains · 6% helix, 53% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
LCB3S Fab light chain (kappa)protein2137% helix, 51% strandQ6PIH7
HCB3S Fab heavy chainprotein2207% helix, 57% strandQ6N093
RTumor necrosis factor receptor superfamily member 13Cprotein270% helix, 37% strandQ96RJ3

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
13930.570.7447empty
2620.520.8720empty
31550.410.7430empty
41030.360.7422empty
5600.270.7319empty

Interfaces

3 interfaces between chains.

  • L–H · 1860 Ų buried · 18 hydrogen bonds · protein-protein
  • H–R · 665 Ų buried · 7 hydrogen bonds · protein-protein
  • L–R · 243 Ų buried · 1 hydrogen bond · protein-protein

Modifications

Observed in the structure: 7 disulfide (disulfide).

Compared structures

  • 2HFG · Crystal structure of hBR3 bound to CB3s-Fab · the same entry in another collection · chain L against L, TM-score 1.00
  • Q96RJ3 · AlphaFold monomer V2.0 prediction for tumor necrosis factor receptor superfamily member… · a predicted model of the same protein · chain R against A, TM-score 0.71

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