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Crystal structure of the 580 germline antibody bound to circumsporozoite protein nanp 5-mer

Analyse Crystal structure of the 580 germline antibody bound to circumsporozoite… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
6AZM
Type
protein
Length
904 residues
Chains
6
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
580 germline antibody, light chain; 580 germline antibody, heavy chain; Circumsporozoite…
Pockets
8 · best druggability 0.66

Structure

x-ray diffraction · 3 distinct chains · 7% helix, 49% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, C580 germline antibody, light chainprotein2195% helix, 52% strand—
B, D580 germline antibody, heavy chainprotein2258% helix, 48% strand—
F, ECircumsporozoite protein nanp 5-merprotein80% helix, 0% strand—

Ligands and binding sites

  • GOL · Glycerol · additive · chains A, B

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

Pockets

8 pockets found on a 1 Å grid, 3 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
17350.660.7576empty
24710.590.7457empty
33350.540.7442empty
41060.370.7421empty
5790.330.7525empty

Interfaces

7 interfaces between chains.

  • C–D · 1883 Ų buried · 16 hydrogen bonds · protein-protein
  • A–B · 1869 Ų buried · 16 hydrogen bonds · protein-protein
  • A–C · 991 Ų buried · 8 hydrogen bonds · protein-protein
  • A–E · 269 Ų buried · 1 hydrogen bond · protein-protein
  • C–F · 259 Ų buried · 1 hydrogen bond · protein-protein

Modifications

Observed in the structure: 8 disulfide (disulfide).

Compared structures

  • 6AZM · Crystal structure of the 580 germline antibody bound to circumsporozoite protein NANP… · the same entry in another collection · chain A against A, TM-score 1.00

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