GL1X · GenesisL1 explorer

MolNFT v1 · #161723 · protein

Structure of bovine anti-rsv hybrid Fab B13HC-B4LC

6QNA · B13 heavy chain: “Structure of bovine anti-rsv hybrid Fab B13HC-B4LC”. X-ray diffraction, 20 pockets (best druggability 0.74). MolNFT v1 #161723 on GenesisL1: 3D structure, binding sites and pockets in GL1X.

PDB
6QNA
Type
protein
Length
1,760 residues
Chains
8
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
B13 heavy chain; B4 light chain
Pockets
20 · best druggability 0.74

Structure

x-ray diffraction · 5 distinct chains · 5% helix, 52% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
HB13 heavy chainprotein2325% helix, 52% strand—
L, B, D, FB4 light chainprotein2116% helix, 51% strand—
AB13 heavy chainprotein2295% helix, 52% strand—
CB13 heavy chainprotein2275% helix, 53% strand—
EB13 heavy chainprotein2285% helix, 52% strand—

Ligands and binding sites

  • GOL · Glycerol · additive · chains A, B

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

Pockets

20 pockets found on a 1 Å grid, 12 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
18490.740.7885empty
28250.710.7789empty
35700.610.7467empty
41270.600.8526empty
53350.580.7743empty

Interfaces

11 interfaces between chains.

  • H–L · 2065 Ų buried · 19 hydrogen bonds · protein-protein
  • C–D · 2032 Ų buried · 14 hydrogen bonds · protein-protein
  • A–B · 2009 Ų buried · 17 hydrogen bonds · protein-protein
  • E–F · 2008 Ų buried · 13 hydrogen bonds · protein-protein
  • L–F · 490 Ų buried · 6 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 28 disulfide (disulfide).

Compared structures

  • 6QNA · Structure of bovine anti-RSV hybrid Fab B13HC-B4LC · the same entry in another collection · chain H against H, TM-score 1.00

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