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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
1MRC
Type
protein
Length
420 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
ZN, SO4
Pockets
5 · best druggability 0.58

Structure

x-ray diffraction · 2 distinct chains · 5% helix, 52% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
LIGG2B-kappa JEL103 Fab (light chain)protein2166% helix, 52% strand—
HIGG2B-kappa JEL103 Fab (heavy chain)protein2044% helix, 52% strand—

Ligands and binding sites

  • ZN · Zinc ion · metal · chains L
  • SO4 · Sulfate ion · ion · chains L, H
  • IMD · Imidazole · additive · chains L

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
14030.580.7544empty
21090.400.7621empty
3920.330.7324empty
4690.320.7517empty
5650.280.7314empty

Interfaces

1 interface between chains.

  • L–H · 1621 Ų buried · 11 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 4 disulfide (disulfide).

Compared structures

  • 1MRC · 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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