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Crystal structure of protein STHE_2403 from sphaerobacter thermophilus

Analyse Crystal structure of protein STHE_2403 from sphaerobacter thermophilus in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
5TGN
Type
protein
Length
433 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Uncharacterized protein
UniProt
D1C7H4
Ligands
CL
Pockets
5 · best druggability 0.80

Structure

x-ray diffraction · 3 distinct chains · 25% helix, 47% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, DUncharacterized proteinprotein10925% helix, 47% strandD1C7H4
BUncharacterized proteinprotein10825% helix, 48% strandD1C7H4
CUncharacterized proteinprotein10726% helix, 47% strandD1C7H4

Ligands and binding sites

  • CL · Chloride ion · ion · 4 copies · chains A, D, B, C
  • GOL · Glycerol · additive · 5 copies · chains A, D, B, C

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
11880.800.9531GOL, CL
27600.780.8286GOL, CL
31340.470.7827GOL
41060.410.7627empty
51100.360.7417empty

Interfaces

5 interfaces between chains.

  • B–C · 799 Ų buried · 9 hydrogen bonds · protein-protein
  • A–D · 776 Ų buried · 8 hydrogen bonds · protein-protein
  • B–D · 627 Ų buried · 7 hydrogen bonds · protein-protein
  • A–C · 626 Ų buried · 7 hydrogen bonds · protein-protein
  • A–B · 587 Ų buried · 5 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 8 modified (engineered).

Compared structures

  • 5TGN · Crystal structure of protein Sthe_2403 from Sphaerobacter thermophilus · the same entry in another collection · chain A against A, TM-score 1.00

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