GL1X · GenesisL1 explorer

Research workbench

Crystal structure of FAB399 in complex with NPNA3 peptide from circumsporozoite protein

Analyse Crystal structure of FAB399 in complex with NPNA3 peptide from circumsporozoite… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
6WFZ
Type
protein
Length
890 residues
Chains
6
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
FAB399 heavy chain; FAB399 light chain; NPNA3 peptide
Pockets
12 · best druggability 0.65

Structure

x-ray diffraction · 5 distinct chains · 8% helix, 51% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AFAB399 heavy chainprotein21610% helix, 52% strand—
BFAB399 light chainprotein2195% helix, 50% strand—
C, PNPNA3 peptideprotein1127% helix, 0% strand—
HFAB399 heavy chainprotein21510% helix, 52% strand—
LFAB399 light chainprotein2185% helix, 50% strand—

Pockets

12 pockets found on a 1 Å grid, 4 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
1530.650.9516empty
24540.580.7457empty
34580.570.7452empty
42750.570.7846empty
5610.460.8423empty

Interfaces

14 interfaces between chains.

  • A–B · 1760 Ų buried · 15 hydrogen bonds · protein-protein
  • H–L · 1736 Ų buried · 15 hydrogen bonds · protein-protein
  • A–H · 544 Ų buried · 8 hydrogen bonds · protein-protein
  • A–C · 382 Ų buried · 6 hydrogen bonds · protein-protein
  • H–P · 382 Ų buried · 6 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 8 disulfide (disulfide).

Compared structures

  • 6WFZ · Crystal structure of Fab399 in complex with NPNA3 peptide from circumsporozoite protein · the same entry in another collection · chain A against A, TM-score 1.00

Analyse

GL1X is a live explorer of the GenesisL1 blockchain. Turn on JavaScript for search, charts and interactive views.