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Structure of native catalytic antibody HA5-19A4

Analyse Structure of native catalytic antibody HA5-19A4 in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
1HQ4
Type
protein
Length
862 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Antibody HA5-19A4 Fab light chain; Antibody HA5-19A4 Fab heavy chain
UniProt
Q91W12, P01867
Ligands
CD
Pockets
13 · best druggability 0.74

Structure

x-ray diffraction · 2 distinct chains · 5% helix, 50% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, CAntibody HA5-19A4 Fab light chainprotein2157% helix, 50% strandQ91W12
B, DAntibody HA5-19A4 Fab heavy chainprotein2163% helix, 50% strandP01867

Ligands and binding sites

  • CD · Cadmium ion · metal · 2 copies · chains A, C

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
19000.740.78102empty
21490.690.8821empty
31460.680.8819empty
43180.550.7549empty
52820.520.7535empty

Interfaces

4 interfaces between chains.

  • C–D · 1851 Ų buried · 14 hydrogen bonds · protein-protein
  • A–B · 1839 Ų buried · 14 hydrogen bonds · protein-protein
  • B–C · 579 Ų buried · 8 hydrogen bonds · protein-protein
  • B–D · 63 Ų buried · 0 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 8 disulfide (disulfide).

Compared structures

  • 1HQ4 · Structure of native catalytic antibody HA5-19A4 · the same entry in another collection · chain A against A, TM-score 1.00
  • P01867 · AlphaFold monomer V2.0 prediction for ig gamma-2B chain C region (P01867) · a predicted model of the same protein · chain B against A, TM-score 0.50

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