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The complex structure of hssqs wtih LIGAND,BPH1344

Analyse The complex structure of hssqs wtih LIGAND,BPH1344 in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
3WCL
Type
protein
Length
2,004 residues
Chains
6
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Squalene synthase
EC
2.5.1.21
UniProt
P37268
Ligands
BH3
Pockets
16 · best druggability 0.85

Structure

x-ray diffraction · 1 distinct chain · 69% helix, 0% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, B, C, D, E, FSqualene synthase (EC 2.5.1.21)protein33469% helix, 0% strandP37268

Ligands and binding sites

  • BH3 · hydrogen [(1R)-2-(3-pentadecyl-1H-imidazol-3-ium-1-yl)-1-phosphonoethyl]phosphonate · ligand · chains A

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
110160.850.8597empty
211340.820.83103empty
310020.810.82103empty
46520.800.8560empty
59710.800.8174BH3

Interfaces

11 interfaces between chains.

  • A–C · 1001 Ų buried · 8 hydrogen bonds · protein-protein
  • D–F · 988 Ų buried · 11 hydrogen bonds · protein-protein
  • E–F · 975 Ų buried · 10 hydrogen bonds · protein-protein
  • D–E · 969 Ų buried · 12 hydrogen bonds · protein-protein
  • A–B · 956 Ų buried · 13 hydrogen bonds · protein-protein

Compared structures

  • 3WCL · The complex structure of HsSQS wtih ligand,BPH1344 · the same entry in another collection · chain F against F, TM-score 1.00
  • P37268 · AlphaFold monomer V2.0 prediction for squalene synthase (P37268) · a predicted model of the same protein · chain A against A, TM-score 0.97

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