GL1X · GenesisL1 explorer

Research workbench

5'-nucleotidase (E. COLI) with an engineered disulfide bridge (P90C, L424C)

Analyse 5'-nucleotidase (E. COLI) with an engineered disulfide bridge (P90C, L424C) in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
1OI8
Type
protein
Length
1,050 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Protein usha
EC
3.1.3.5, 3.6.1.45
UniProt
P07024
Ligands
MN, SO4, CO3
Pockets
8 · best druggability 0.72

Structure

x-ray diffraction · 1 distinct chain · 30% helix, 30% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, BProtein usha (EC 3.1.3.5, 3.6.1.45)protein52530% helix, 30% strandP07024

Ligands and binding sites

  • MN · Manganese (II) ion · metal · 4 copies · chains A, B
  • SO4 · Sulfate ion · ion · 2 copies · chains A, B
  • CO3 · Carbonate ion · ion · 2 copies · chains A, B

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
16880.720.7971SO4, CO3
28270.720.7787SO4, CO3
33810.690.8145empty
42500.600.8035empty
52450.580.7925empty

Interfaces

1 interface between chains.

  • A–B · 222 Ų buried · 3 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 4 disulfide (disulfide).

Compared structures

  • 1OI8 · 5'-Nucleotidase (E. coli) with an Engineered Disulfide Bridge (P90C, L424C) · the same entry in another collection · chain A against A, TM-score 1.00
  • P07024 · AlphaFold monomer V2.0 prediction for protein usha (P07024) · a predicted model of the same protein · chain A against A, TM-score 0.85

Analyse

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