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Structure of catalytic elimination antibody 13G5 from a crystal in space group P2(1)

Analyse Structure of catalytic elimination antibody 13G5 from a crystal in space group… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
2GJZ
Type
protein
Length
876 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Catalytic elimination antibody 13G5 light chain; Catalytic elimination antibody 13G5…
Ligands
ZN
Pockets
9 · best druggability 0.59

Structure

x-ray diffraction · 2 distinct chains · 5% helix, 51% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
L, ACatalytic elimination antibody 13G5 light chainprotein2176% helix, 52% strand—
H, BCatalytic elimination antibody 13G5 heavy chainprotein2214% helix, 51% strand—

Ligands and binding sites

  • ZN · Zinc ion · metal · 11 copies · chains L, H, A, B

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
12990.590.7845empty
23860.570.7553empty
31130.570.8422ZN
43770.560.7447empty
5510.550.9019ZN

Interfaces

3 interfaces between chains.

  • L–H · 1841 Ų buried · 17 hydrogen bonds · protein-protein
  • A–B · 1774 Ų buried · 14 hydrogen bonds · protein-protein
  • H–A · 62 Ų buried · 2 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 8 disulfide (disulfide).

Compared structures

  • 2GJZ · Structure of Catalytic Elimination Antibody 13G5 from a crystal in space group P2(1) · the same entry in another collection · chain L against L, TM-score 1.00

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