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Anthrax toxin prepore in complex with the neutralizing Fab CAB29

Analyse Anthrax toxin prepore in complex with the neutralizing Fab CAB29 in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
7O85
Type
protein
Length
3,843 residues
Chains
21
Method
electron microscopy
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Protective antigen pa-63; Fab
UniProt
P13423
Ligands
CA
Pockets
20 · best druggability 0.80

Structure

electron microscopy · 3 distinct chains · 13% helix, 28% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, D, G, J, M, P, SProtective antigen pa-63protein33220% helix, 22% strandP13423
B, E, H, K, N, Q, TFabprotein1040% helix, 43% strand—
C, F, I, L, O, R, UFabprotein1135% helix, 31% strand—

Ligands and binding sites

  • CA · Calcium ion · metal · 14 copies · chains A, D, G, J, M, P, S

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

Pockets

20 pockets found on a 1 Å grid, 20 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
11210.800.9826empty
21180.800.9825empty
31140.790.9826empty
41130.790.9825empty
51090.780.9826empty

Interfaces

28 interfaces between chains.

  • G–J · 1453 Ų buried · 13 hydrogen bonds · protein-protein
  • J–M · 1451 Ų buried · 13 hydrogen bonds · protein-protein
  • M–P · 1450 Ų buried · 13 hydrogen bonds · protein-protein
  • D–G · 1450 Ų buried · 13 hydrogen bonds · protein-protein
  • P–S · 1448 Ų buried · 13 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 7 disulfide (disulfide).

Compared structures

  • 7O85 · Anthrax toxin prepore in complex with the neutralizing Fab cAb29 · the same entry in another collection · chain U against U, TM-score 1.00

Analyse

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