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Conformational dynamics of human FXR-LBD ligand interactions studied by hydrogen/deuterium exchange mass spectrometry: Insights into the antagonism of the hypolipidemic agent Z-guggulsterone
Authors:Liping Yang  David Broderick  Yuan Jiang  Victor Hsu  Claudia S. Maier
Affiliation:1. Department of Chemistry, Oregon State University, Corvallis, OR 97331, USA;2. Department of Statistics, Oregon State University, Corvallis, OR 97331, USA;3. Biochemistry and Biophysics, Oregon State University, Corvallis, OR 97331, USA
Abstract:
Keywords:HDX, hydrogen/deuterium exchange   LC&ndash  ESI-MS, liquid chromatography electrospray ionization mass spectrometry   FXR-LBD, farnesoid X receptor ligand binding domain   LBC, ligand binding cavity   CDCA, chenodeoxycholic acid   GG, Z-guggulsterone   6ECDCA, 6-ethylchenodeoxycholic acid   UDCA, ursodeoxycholic acid   DMSO, dimethylsulfoxide   TCEP, Tris (2-carboxyethyl) phosphine hydrochloride   TOF, time of flight   PPARγ, peroxisome proliferator-activated receptor   RXR, retinoid X receptor   THR, thyroid hormone receptor   ER, estrogen receptor   VDR, vitamin D receptor   GR, glucocorticoid receptor
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