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Y97L/G100-/E101- mutant in organophosphorus hydrolase

Analyse Y97L/G100-/E101- mutant in organophosphorus hydrolase in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
3GU2
Type
protein
Length
330 residues
Chains
1
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Organophosphorus hydrolase
UniProt
Q9RVU2
Ligands
CO
Pockets
3 · best druggability 0.60

Structure

x-ray diffraction · 1 distinct chain · 44% helix, 15% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AOrganophosphorus hydrolaseprotein33044% helix, 15% strandQ9RVU2

Ligands and binding sites

  • CO · Cobalt (II) ion · metal · 2 copies · chains A

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
11740.600.8328CO
2500.440.8514empty
3560.250.7215empty

Modifications

Observed in the structure: 1 modified (carboxylation).

Compared structures

  • 3GU2 · Y97L/G100-/E101- mutant in organophosphorus hydrolase · the same entry in another collection · chain A against A, TM-score 1.00

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