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Crystal structure of protein RHA08564, thioesterase superfamily protein

Analyse Crystal structure of protein RHA08564, thioesterase superfamily protein in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
2OV9
Type
protein
Length
807 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Hypothetical protein
UniProt
Q0S4E1
Ligands
SO4
Pockets
13 · best druggability 0.71

Structure

x-ray diffraction · 4 distinct chains · 29% helix, 27% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AHypothetical proteinprotein20329% helix, 27% strandQ0S4E1
BHypothetical proteinprotein20529% helix, 27% strandQ0S4E1
CHypothetical proteinprotein20629% helix, 27% strandQ0S4E1
DHypothetical proteinprotein19331% helix, 27% strandQ0S4E1

Ligands and binding sites

  • SO4 · Sulfate ion · ion · chains C

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

Pockets

13 pockets found on a 1 Å grid, 7 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
16130.710.7968empty
21220.590.8523empty
32890.590.7843empty
4710.580.8918empty
5610.550.8817empty

Interfaces

3 interfaces between chains.

  • C–D · 3436 Ų buried · 35 hydrogen bonds · protein-protein
  • A–B · 3408 Ų buried · 36 hydrogen bonds · protein-protein
  • B–C · 627 Ų buried · 6 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 12 modified (engineered).

Compared structures

  • 2OV9 · Crystal structure of protein RHA08564, thioesterase superfamily protein · the same entry in another collection · chain A against A, TM-score 1.00

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