Back to search

Article

Impaired transitioning of the FXR ligand binding domain to an active state underlies an FXR-associated PFIC phenotype

2024-02-12

Abstract excerpt

Nuclear receptor farnesoid X receptor (FXR) acts as a key regulator of bile acid pool homeostasis and metabolism. Within the enterohepatic circulation, reabsorbed bile acids act as FXR agonists, which transcriptionally controls the synthesis and transport of bile acids. Binding occurs in the ligand binding domain (LBD), favoring a conformational change to the active state in which helix 12 interacts with the LBD t...

Topics

Open a Topic to create a Post that cites this publication.

Identifiers and source

Literature Corpus work
d93f6394-6d27-5812-97d8-a4ca6a1d085f
DOI
10.1101/2024.02.08.579530
Open publication

Related research

Semantic proximity does not establish scientific evidence.

Click a neighbor to travelStep 1 · 12 closest
Interactive article relationship graphSelect a related publication card to move it into the centre and load its closest explainable connections. Solid lines are source-backed structured connections. Dashed lines are semantic discovery signals and are not scientific evidence.
Impaired transitioning of the FXR ligand binding domain to an active state underlies an FXR-associated PFIC phenotypeDOI 10.1101/2024.02.08.579530
Select a neighboring publication to make it the new centre.