GL1X · GenesisL1 explorer

MolNFT v2 · #211311 · protein

Crystal structure of anti-FIXa IgG fab with FAST-Ig mutations

8GUZ · Anti-factor IXa IgG fab heavy chain: “Crystal structure of anti-FIXa IgG fab with FAST-Ig mutations”. X-ray diffraction at 1.79, 10 pockets (best druggability 0.64). MolNFT v2 #211311 on GenesisL1: 3D structure, binding sites and…

PDB
8GUZ
Type
protein
Length
867 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v2 / PDB Bank
Contract
0xd58B01f6C18086e5202cdC5D7Ad3E41790360102
Owner
0xF4e1AA6f26B7DA48EeAD9B24a97927303eeA07b8
Resolution
1.79
Source
Homo sapiens
Molecule
Anti-factor IXa IgG fab heavy chain; Anti-factor IXa IgG fab light chain
Pockets
10 · best druggability 0.64

Structure

x-ray diffraction · resolution 1.79 · 3 distinct chains · 8% helix, 50% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AAnti-factor IXa IgG fab heavy chainprotein2198% helix, 50% strand—
B, DAnti-factor IXa IgG fab light chainprotein2147% helix, 50% strand—
CAnti-factor IXa IgG fab heavy chainprotein2209% helix, 51% strand—

Ligands and binding sites

  • EDO · 1,2-ethanediol · additive · 28 copies · chains A, B, C, D

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
16120.640.7564EDO
25960.630.7564empty
33630.620.7848EDO
41330.580.8424empty
5960.450.7917empty

Interfaces

4 interfaces between chains.

  • C–D · 1816 Ų buried · 14 hydrogen bonds · protein-protein
  • A–B · 1744 Ų buried · 15 hydrogen bonds · protein-protein
  • A–C · 214 Ų buried · 1 hydrogen bond · protein-protein
  • A–D · 70 Ų buried · 0 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 10 disulfide (disulfide).

Analyse

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