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Crystal structure of MAD2-6 IgA Fab in complex with pfcsp N-terminal peptide.

Analyse Crystal structure of MAD2-6 IgA Fab in complex with pfcsp N-terminal peptide. in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
7K75
Type
protein
Length
1,762 residues
Chains
10
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Heavy chain of MAD2-6 IgA Fab; Light chain of MAD2-6 IgA Fab; Pfcsp N-terminal peptide P17
Pockets
20 · best druggability 0.75

Structure

x-ray diffraction · 5 distinct chains · 4% helix, 49% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, CHeavy chain of MAD2-6 IgA Fabprotein2254% helix, 50% strand—
B, D, J, NLight chain of MAD2-6 IgA Fabprotein2136% helix, 50% strand—
IHeavy chain of MAD2-6 IgA Fabprotein2223% helix, 48% strand—
MHeavy chain of MAD2-6 IgA Fabprotein2223% helix, 50% strand—
E, FPfcsp N-terminal peptide P17protein80% helix, 25% strand—

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
1920.750.9628empty
2690.740.9820empty
32700.630.8152empty
43410.620.7939empty
53460.550.7554empty

Interfaces

20 interfaces between chains.

  • I–J · 1848 Ų buried · 23 hydrogen bonds · protein-protein
  • M–N · 1847 Ų buried · 20 hydrogen bonds · protein-protein
  • A–B · 1845 Ų buried · 28 hydrogen bonds · protein-protein
  • D–C · 1843 Ų buried · 25 hydrogen bonds · protein-protein
  • B–C · 533 Ų buried · 5 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 23 disulfide (disulfide).

Compared structures

  • 7K75 · Crystal structure of MAD2-6 IgA Fab in complex with PfCSP N-terminal peptide. · the same entry in another collection · chain A against A, TM-score 1.00

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