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Crystal structure at 2.2 ångström of hsl-homolog ESTE7 from a metagenome library

Analyse Crystal structure at 2.2 ångström of hsl-homolog ESTE7 from a metagenome library in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
3K6K
Type
protein
Length
1,177 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
ESTERASE/LIPASE
EC
3.1.1.-
UniProt
Q0GMU1
Ligands
SO4
Pockets
11 · best druggability 0.75

Structure

x-ray diffraction · 3 distinct chains · 43% helix, 17% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, BESTERASE/LIPASE (EC 3.1.1.-)protein29744% helix, 16% strandQ0GMU1
CESTERASE/LIPASE (EC 3.1.1.-)protein29043% helix, 17% strandQ0GMU1
DESTERASE/LIPASE (EC 3.1.1.-)protein29342% helix, 18% strandQ0GMU1

Ligands and binding sites

  • SO4 · Sulfate ion · ion · 9 copies · chains A, B, C, D
  • BME · Beta-mercaptoethanol · additive · chains 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, 6 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
15810.750.8248empty
26270.750.8153empty
35730.740.8146BME
44290.700.8140empty
52390.580.7922empty

Interfaces

3 interfaces between chains.

  • A–B · 954 Ų buried · 15 hydrogen bonds · protein-protein
  • C–D · 944 Ų buried · 16 hydrogen bonds · protein-protein
  • B–C · 313 Ų buried · 9 hydrogen bonds · protein-protein

Compared structures

  • 3K6K · Crystal structure at 2.2 angstrom of HSL-homolog EstE7 from a metagenome library · the same entry in another collection · chain A against A, TM-score 1.00

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