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I33M (I3.2 mutant from CH103 lineage)

Analyse I33M (I3.2 mutant from CH103 lineage) in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
6VPY
Type
protein
Length
851 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
I33M light chain; I33M heavy chain
UniProt
Q8N355, Q6GMX6
Ligands
CL
Pockets
6 · best druggability 0.75

Structure

x-ray diffraction · 4 distinct chains · 8% helix, 53% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
BI33M light chainprotein2088% helix, 50% strandQ8N355
AI33M heavy chainprotein2167% helix, 55% strandQ6GMX6
HI33M heavy chainprotein2187% helix, 55% strandQ6GMX6
LI33M light chainprotein2098% helix, 51% strandQ8N355

Ligands and binding sites

  • CL · Chloride ion · ion · chains B
  • GOL · Glycerol · additive · 2 copies · chains A, L

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

Pockets

6 pockets found on a 1 Å grid, 4 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
111210.750.78113empty
24690.650.7748empty
32560.610.8039GOL
42220.550.7829empty
51020.340.7325empty

Interfaces

5 interfaces between chains.

  • H–L · 1793 Ų buried · 14 hydrogen bonds · protein-protein
  • B–A · 1769 Ų buried · 11 hydrogen bonds · protein-protein
  • A–L · 305 Ų buried · 4 hydrogen bonds · protein-protein
  • B–L · 188 Ų buried · 1 hydrogen bond · protein-protein
  • B–H · 178 Ų buried · 0 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 8 disulfide (disulfide).

Compared structures

  • 6VPY · I33M (I3.2 mutant from CH103 Lineage) · the same entry in another collection · chain B against B, TM-score 1.00

Analyse

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