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Structure of D25 Fab in complex with scaffold S0_2.126

Analyse Structure of D25 Fab in complex with scaffold S0_2.126 in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
6S3D
Type
protein
Length
1,921 residues
Chains
12
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Heavy chain; Light chain; S0_2.126
Pockets
20 · best druggability 0.80

Structure

x-ray diffraction · 9 distinct chains · 9% helix, 47% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, HHeavy chainprotein2124% helix, 50% strand—
BLight chainprotein2103% helix, 50% strand—
CHeavy chainprotein2154% helix, 53% strand—
DLight chainprotein2065% helix, 49% strand—
EHeavy chainprotein2154% helix, 53% strand—
FLight chainprotein2063% helix, 49% strand—
LLight chainprotein2115% helix, 51% strand—
M, OS0_2.126protein5963% helix, 3% strand—
N, PS0_2.126protein5866% helix, 7% strand—

Pockets

20 pockets found on a 1 Å grid, 13 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
19760.800.82107empty
27560.790.8376empty
37230.770.8271empty
47330.770.8270empty
56830.720.7977empty

Interfaces

28 interfaces between chains.

  • H–L · 1608 Ų buried · 9 hydrogen bonds · protein-protein
  • A–B · 1590 Ų buried · 9 hydrogen bonds · protein-protein
  • C–D · 1577 Ų buried · 11 hydrogen bonds · protein-protein
  • E–F · 1563 Ų buried · 12 hydrogen bonds · protein-protein
  • E–O · 758 Ų buried · 18 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 24 disulfide (disulfide).

Compared structures

  • 6S3D · Structure of D25 Fab in complex with scaffold S0_2.126 · the same entry in another collection · chain A against A, TM-score 1.00

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