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Fxr bound to a quinolinecarboxylic acid

Analyse Fxr bound to a quinolinecarboxylic acid in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
3P89
Type
protein
Length
234 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Farnesoid X receptor; Nuclear receptor coactivator 1
EC
2.3.1.48
UniProt
B6ZGS9, A8K1V4
Ligands
89P, SO4
Pockets
2 · best druggability 0.85

Structure

x-ray diffraction · 2 distinct chains · 74% helix, 0% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AFarnesoid X receptorprotein22374% helix, 0% strandB6ZGS9
BNuclear receptor coactivator 1 (EC 2.3.1.48)protein1173% helix, 0% strandA8K1V4

Ligands and binding sites

  • 89P · 6-(4-{[3-(2,6-dichlorophenyl)-5-(1-methylethyl)isoxazol-4-yl]methoxy}phenyl)quinoline-2-carboxylic acid · ligand · chains A
  • SO4 · Sulfate ion · ion · chains A

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
13920.850.924589P
21130.380.7421empty

Interfaces

1 interface between chains.

  • A–B · 558 Ų buried · 10 hydrogen bonds · protein-protein

Compared structures

  • 3P89 · FXR bound to a quinolinecarboxylic acid · the same entry in another collection · chain A against A, TM-score 1.00

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