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MolNFT v1 · #38024 · protein

Structure of catalytic elimination antibody 13G5 from a twinned crystal in space group C2

2GK0 · Catalytic elimination antibody 13G5 light chain: “Structure of catalytic elimination antibody 13G5 from a twinned crystal in space group C2”. X-ray diffraction, 14 pockets (best druggability 0.77). MolNFT v1 #38024 on GenesisL1: 3D…

PDB
2GK0
Type
protein
Length
871 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…
UniProt
Q65ZC0, Q91Z05
Pockets
14 · best druggability 0.77

Structure

x-ray diffraction · 3 distinct chains · 4% helix, 43% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
L, ACatalytic elimination antibody 13G5 light chainprotein2174% helix, 47% strandQ65ZC0
HCatalytic elimination antibody 13G5 heavy chainprotein2214% helix, 44% strandQ91Z05
BCatalytic elimination antibody 13G5 heavy chainprotein2164% helix, 38% strandQ91Z05

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
19000.770.8091empty
25770.610.7451empty
33430.600.7741empty
4750.590.8923empty
51390.580.8426empty

Interfaces

4 interfaces between chains.

  • L–H · 1793 Ų buried · 17 hydrogen bonds · protein-protein
  • A–B · 1622 Ų buried · 14 hydrogen bonds · protein-protein
  • L–A · 331 Ų buried · 6 hydrogen bonds · protein-protein
  • L–B · 275 Ų buried · 2 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 8 disulfide (disulfide).

Compared structures

  • 2GK0 · Structure of Catalytic Elimination Antibody 13G5 from a twinned crystal in space group C2 · the same entry in another collection · chain L against L, TM-score 1.00

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