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Crystal structure of the fv fragment of a monoclonal antibody specific for poly-glutamine

Analyse Crystal structure of the fv fragment of a monoclonal antibody specific for… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
2GSG
Type
protein
Length
464 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Monoclonal antibody light chain; Monoclonal antibody heavy chain
Ligands
SO4
Pockets
8 · best druggability 0.76

Structure

x-ray diffraction · 2 distinct chains · 5% helix, 53% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, CMonoclonal antibody light chainprotein1145% helix, 53% strand—
B, DMonoclonal antibody heavy chainprotein1185% helix, 53% strand—

Ligands and binding sites

  • SO4 · Sulfate ion · ion · 3 copies · chains B, D

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
19860.760.7888empty
21660.480.7730empty
31150.410.7619empty
4720.310.7417empty
5590.300.7513empty

Interfaces

5 interfaces between chains.

  • C–D · 926 Ų buried · 6 hydrogen bonds · protein-protein
  • A–B · 902 Ų buried · 8 hydrogen bonds · protein-protein
  • A–C · 285 Ų buried · 4 hydrogen bonds · protein-protein
  • B–D · 250 Ų buried · 6 hydrogen bonds · protein-protein
  • B–C · 98 Ų buried · 2 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 4 disulfide (disulfide).

Compared structures

  • 2GSG · Crystal structure of the Fv fragment of a monoclonal antibody specific for poly-glutamine · the same entry in another collection · chain A against A, TM-score 1.00

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