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The crystal structure E. COLI spy

Analyse The crystal structure E. COLI spy in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
3OEO
Type
protein
Length
364 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Spheroplast protein Y
UniProt
C5W4R8
Ligands
CD
Pockets
8 · best druggability 0.59

Structure

x-ray diffraction · 1 distinct chain · 66% helix, 0% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, B, C, DSpheroplast protein Yprotein9166% helix, 0% strandC5W4R8

Ligands and binding sites

  • CD · Cadmium ion · metal · 22 copies · chains A, C, B, D

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

Pockets

8 pockets found on a 1 Å grid, 2 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
13060.590.7743empty
23480.590.7650CD
3970.450.7915empty
4970.430.7813empty
5790.400.7810empty

Interfaces

6 interfaces between chains.

  • A–C · 1573 Ų buried · 12 hydrogen bonds · protein-protein
  • B–D · 1487 Ų buried · 13 hydrogen bonds · protein-protein
  • B–C · 297 Ų buried · 1 hydrogen bond · protein-protein
  • A–D · 233 Ų buried · 0 hydrogen bonds · protein-protein
  • A–B · 181 Ų buried · 5 hydrogen bonds · protein-protein

Compared structures

  • 3OEO · The crystal structure E. coli Spy · the same entry in another collection · chain A against A, TM-score 1.00

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