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Engineered streptavidin variant (enagy) in complex with the twin- strep-tag peptide

Analyse Engineered streptavidin variant (enagy) in complex with the twin- strep-tag… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
6SOS
Type
protein
Length
518 residues
Chains
6
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Streptavidin; Twin-strep-tag peptide
UniProt
P22629
Ligands
NH2
Pockets
6 · best druggability 0.62

Structure

x-ray diffraction · 5 distinct chains · 9% helix, 51% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AStreptavidinprotein1227% helix, 56% strandP22629
BStreptavidinprotein1227% helix, 55% strandP22629
C, DStreptavidinprotein1217% helix, 55% strandP22629
PTwin-strep-tag peptideprotein1817% helix, 0% strand—
RTwin-strep-tag peptideprotein1443% helix, 0% strand—

Ligands and binding sites

  • NH2 · Amino group · ion · 2 copies · chains C, P, D, R

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
12380.620.8236empty
22870.620.8035empty
32730.620.8034empty
42190.610.8232empty
51650.460.7633empty

Interfaces

10 interfaces between chains.

  • A–B · 1652 Ų buried · 26 hydrogen bonds · protein-protein
  • C–D · 1613 Ų buried · 28 hydrogen bonds · protein-protein
  • B–P · 741 Ų buried · 8 hydrogen bonds · protein-protein
  • A–R · 617 Ų buried · 8 hydrogen bonds · protein-protein
  • D–R · 608 Ų buried · 6 hydrogen bonds · protein-protein

Compared structures

  • 6SOS · Engineered streptavidin variant (ENAGY) in complex with the Twin-Strep-tag peptide · the same entry in another collection · chain A against A, TM-score 1.00

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