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Structure of teni from bacillus subtilis

Analyse Structure of teni from bacillus subtilis in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
1YAD
Type
protein
Length
763 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Regulatory protein teni
UniProt
P25053
Ligands
SO4
Pockets
3 · best druggability 0.70

Structure

x-ray diffraction · 2 distinct chains · 46% helix, 19% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, C, DRegulatory protein teniprotein19047% helix, 19% strandP25053
BRegulatory protein teniprotein19346% helix, 19% strandP25053

Ligands and binding sites

  • SO4 · Sulfate ion · ion · 8 copies · chains A, B, C, D
  • 144 · Tris-hydroxymethyl-methyl-ammonium · additive · 3 copies · chains A, B, D

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
15030.700.8074SO4, 144
24900.690.8073SO4, 144
31150.450.7820empty

Interfaces

4 interfaces between chains.

  • A–B · 799 Ų buried · 7 hydrogen bonds · protein-protein
  • C–D · 794 Ų buried · 10 hydrogen bonds · protein-protein
  • A–D · 407 Ų buried · 6 hydrogen bonds · protein-protein
  • B–D · 215 Ų buried · 3 hydrogen bonds · protein-protein

Compared structures

  • 1YAD · Structure of TenI from Bacillus subtilis · the same entry in another collection · chain A against A, TM-score 1.00
  • P25053 · AlphaFold monomer V2.0 prediction for thiazole tautomerase (P25053) · a predicted model of the same protein · chain A against A, TM-score 0.99

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