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Crystal structure analysis of the anti-arsonate germline antibody 36- 65 in complex with a phage display derived dodecapeptide rlliadppspre

Analyse Crystal structure analysis of the anti-arsonate germline antibody 36- 65 in… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
2A6D
Type
protein
Length
877 residues
Chains
5
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Germline antibody 36-65 Fab light chain; Germline antibody 36-65 Fab heavy chain…
Pockets
9 · best druggability 0.52

Structure

x-ray diffraction · 4 distinct chains · 6% helix, 49% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
L, AGermline antibody 36-65 Fab light chainprotein2147% helix, 48% strand—
HGermline antibody 36-65 Fab heavy chainprotein2186% helix, 50% strand—
BGermline antibody 36-65 Fab heavy chainprotein2195% helix, 51% strand—
PDodecapeptide, rlliadppspreprotein120% helix, 0% strand—

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
13010.520.7442empty
22590.500.7445empty
31280.410.7525empty
41100.370.7424empty
5700.360.7715empty

Interfaces

4 interfaces between chains.

  • L–H · 1899 Ų buried · 16 hydrogen bonds · protein-protein
  • A–B · 1840 Ų buried · 17 hydrogen bonds · protein-protein
  • A–P · 268 Ų buried · 8 hydrogen bonds · protein-protein
  • B–P · 146 Ų buried · 1 hydrogen bond · protein-protein

Modifications

Observed in the structure: 8 disulfide (disulfide).

Compared structures

  • 2A6D · Crystal structure analysis of the anti-arsonate germline antibody 36-65 in complex with a… · the same entry in another collection · chain L against L, TM-score 1.00

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