GL1X · GenesisL1 explorer

Research workbench

Crystal structure of the human neutralizing antibody Fab fragment T025 bound to tbev ediii (far eastern subtype)

Analyse Crystal structure of the human neutralizing antibody Fab fragment T025 bound to… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
7LSE
Type
protein
Length
519 residues
Chains
3
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
T025 Fab heavy chain; T025 Fab light chain; Envelope protein E
UniProt
P07720
Pockets
5 · best druggability 0.58

Structure

x-ray diffraction · 3 distinct chains · 5% helix, 51% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
HT025 Fab heavy chainprotein2137% helix, 50% strand—
LT025 Fab light chainprotein2136% helix, 51% strand—
EEnvelope protein Eprotein930% helix, 56% strandP07720

Ligands and binding sites

  • GOL · Glycerol · additive · chains H, L

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
14180.580.7556empty
2560.500.8722GOL
31390.410.7429empty
4640.350.7818empty
5590.300.7515empty

Interfaces

3 interfaces between chains.

  • H–L · 1611 Ų buried · 14 hydrogen bonds · protein-protein
  • H–E · 383 Ų buried · 10 hydrogen bonds · protein-protein
  • L–E · 291 Ų buried · 8 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 5 disulfide (disulfide).

Compared structures

  • 7LSE · Crystal structure of the human neutralizing antibody Fab fragment T025 bound to TBEV… · the same entry in another collection · chain H against H, TM-score 1.00

Analyse

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