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Crystal structure of a lipase carboxylesterase from Sulfolobus islandicus

Analyse Crystal structure of a lipase carboxylesterase from Sulfolobus islandicus in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
5LK6
Type
protein
Length
1,208 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v2 / PDB Bank
Contract
0xd58B01f6C18086e5202cdC5D7Ad3E41790360102
Owner
0xF4e1AA6f26B7DA48EeAD9B24a97927303eeA07b8
Resolution
2.6
Source
Sulfolobus islandicus (strain REY15A)
Molecule
Alpha/beta hydrolase fold-3 domain protein
UniProt
F0NDQ1
Ligands
SO4
Pockets
11 · best druggability 0.79

Structure

x-ray diffraction · resolution 2.6 · 1 distinct chain · 40% helix, 18% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, B, C, DAlpha/beta hydrolase fold-3 domain proteinprotein30240% helix, 18% strandF0NDQ1

Ligands and binding sites

  • SO4 · Sulfate ion · ion · 8 copies · chains A, B, C, D

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

Pockets

11 pockets found on a 1 Å grid, 11 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
17910.790.8390empty
2940.750.9619empty
38350.750.7979empty
4970.740.9520empty
5860.740.9620empty

Interfaces

6 interfaces between chains.

  • C–D · 1362 Ų buried · 29 hydrogen bonds · protein-protein
  • A–B · 1317 Ų buried · 31 hydrogen bonds · protein-protein
  • A–D · 867 Ų buried · 2 hydrogen bonds · protein-protein
  • B–C · 837 Ų buried · 2 hydrogen bonds · protein-protein
  • A–C · 266 Ų buried · 8 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 4 disulfide (disulfide).

Compared structures

  • 5LK6 · Crystal structure of a lipase carboxylesterase from sulfolobus islandicus · the same entry in another collection · chain A against A, TM-score 1.00

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