GL1X · GenesisL1 explorer

Research workbench

De novo designed protein 4E1H_95 in complex with 101F antibody

Analyse De novo designed protein 4E1H_95 in complex with 101F antibody in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
6YWC
Type
protein
Length
994 residues
Chains
6
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Antibody 101F, heavy chain; Antibody 101F, light chain; De novo design 4E1H_95
Pockets
10 · best druggability 0.74

Structure

x-ray diffraction · 4 distinct chains · 9% helix, 52% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, DAntibody 101F, heavy chainprotein22111% helix, 52% strand—
BAntibody 101F, light chainprotein2186% helix, 54% strand—
C, FDe novo design 4E1H_95protein5824% helix, 45% strand—
EAntibody 101F, light chainprotein2186% helix, 52% strand—

Pockets

10 pockets found on a 1 Å grid, 2 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
110620.740.77111empty
26210.640.7547empty
31970.490.7626empty
4720.450.8115empty
51390.410.7420empty

Interfaces

7 interfaces between chains.

  • D–E · 2128 Ų buried · 12 hydrogen bonds · protein-protein
  • A–B · 2031 Ų buried · 11 hydrogen bonds · protein-protein
  • A–D · 672 Ų buried · 11 hydrogen bonds · protein-protein
  • A–C · 587 Ų buried · 7 hydrogen bonds · protein-protein
  • D–F · 572 Ų buried · 10 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 10 disulfide (disulfide).

Compared structures

  • 6YWC · De novo designed protein 4E1H_95 in complex with 101F antibody · 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.