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Crystal structure of chimeric H.2140 / K.1210 Fab in complex with circumsporozoite protein NANP3

Analyse Crystal structure of chimeric H.2140 / K.1210 Fab in complex with… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
6D0X
Type
protein
Length
446 residues
Chains
3
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
2140 antibody, heavy chain; 1210 antibody, light chain; NANP3
Pockets
5 · best druggability 0.53

Structure

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

ChainMoleculeTypeResiduesSecondary structureUniProt
A2140 antibody, heavy chainprotein2248% helix, 50% strand—
B1210 antibody, light chainprotein2115% helix, 51% strand—
CNANP3protein110% helix, 0% strand—

Ligands and binding sites

  • GOL · Glycerol · additive · 3 copies · chains A, B
  • PEG · Di(hydroxyethyl)ether · additive · chains B

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

Pockets

5 pockets found on a 1 Å grid, 2 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
1590.530.8825empty
22640.530.7633GOL
31490.410.7418empty
4920.370.7523empty
5570.270.7316empty

Interfaces

3 interfaces between chains.

  • A–B · 1803 Ų buried · 17 hydrogen bonds · protein-protein
  • A–C · 482 Ų buried · 6 hydrogen bonds · protein-protein
  • B–C · 153 Ų buried · 5 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 4 disulfide (disulfide).

Compared structures

  • 6D0X · Crystal structure of chimeric H.2140 / K.1210 Fab in complex with circumsporozoite… · the same entry in another collection · chain A against A, TM-score 1.00

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