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Structure of single domain antibody SD83

Analyse Structure of single domain antibody SD83 in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
6FYS
Type
protein
Length
1,009 residues
Chains
8
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Single domain antibody SD83
Pockets
10 · best druggability 0.59

Structure

x-ray diffraction · 3 distinct chains · 9% helix, 46% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
C, B, D, F, G, HSingle domain antibody SD83protein12713% helix, 45% strand—
ASingle domain antibody SD83protein1267% helix, 44% strand—
ESingle domain antibody SD83protein1218% helix, 49% strand—

Ligands and binding sites

  • EDO · 1,2-ethanediol · additive · 5 copies · chains D, F, H

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
13380.590.7753empty
24780.580.7337empty
32950.560.7753empty
41190.550.8324empty
51960.490.7636empty

Interfaces

13 interfaces between chains.

  • A–H · 617 Ų buried · 7 hydrogen bonds · protein-protein
  • C–G · 599 Ų buried · 7 hydrogen bonds · protein-protein
  • A–D · 562 Ų buried · 13 hydrogen bonds · protein-protein
  • C–B · 547 Ų buried · 11 hydrogen bonds · protein-protein
  • C–A · 527 Ų buried · 7 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 16 disulfide (disulfide).

Compared structures

  • 6FYS · Structure of single domain antibody SD83 · the same entry in another collection · chain C against C, TM-score 1.00

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