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Preparation, characterization and crystallization of an antibody Fab fragment that recognizes RNA. crystal structures of native Fab and three Fab-mononucleotide complexes

Analyse Preparation, characterization and crystallization of an antibody Fab fragment… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
1MRE
Type
protein
Length
426 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
IGG2B-kappa JEL103 Fab (light chain); IGG2B-kappa JEL103 Fab (heavy chain)
Ligands
GDP, ZN
Pockets
6 · best druggability 0.56

Structure

x-ray diffraction · 2 distinct chains · 6% helix, 53% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
LIGG2B-kappa JEL103 Fab (light chain)protein2184% helix, 51% strand—
HIGG2B-kappa JEL103 Fab (heavy chain)protein2089% helix, 54% strand—

Ligands and binding sites

  • GDP · Guanosine-5'-diphosphate · ligand · chains L, H
  • ZN · Zinc ion · metal · chains L
  • IMD · Imidazole · additive · chains L

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
13390.560.7541empty
21360.470.7822empty
3760.300.7320empty
4580.280.7415empty
5560.260.7315empty

Interfaces

1 interface between chains.

  • L–H · 1736 Ų buried · 15 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 4 disulfide (disulfide).

Compared structures

  • 1MRE · Preparation, characterization and crystallization of an antibody Fab fragment that… · the same entry in another collection · chain L against L, TM-score 1.00

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