| Literature DB >> 28869863 |
Piyusha P Pagare1, Saheem A Zaidi1, Xiaomei Zhang2, Xia Li3, Xiaofei Yu3, Xiang-Yang Wang3, Yan Zhang4.
Abstract
Scavenger receptor A (SRA), as an immune regulator, has been shown to play important roles in lipid metabolism, cardiovascular diseases, and pathogen recognition. Several natural product inhibitors of SRA have been studied for their potential application in modulating SRA functions. To understand the binding mode of these inhibitors on SRA, we conducted systematic molecular modeling studies in order to identify putative binding domain(s) that may be responsible for their recognition to the receptor as well as their inhibitory activity. Treatment of SRA with one of the natural product inhibitors, rhein, led to significant dissociation of SRA oligomers to its trimer and dimer forms, which further supported our hypothesis on their putative mechanism of action. Such information is believed to shed light on design of more potent inhibitors for the receptor in order to develop potential therapeutics through immune system modulation. Published by Elsevier Inc.Entities:
Keywords: Binding modes; Docking; Inhibitor; Molecular dynamics simulation; Natural products; SRA
Mesh:
Substances:
Year: 2017 PMID: 28869863 PMCID: PMC5696021 DOI: 10.1016/j.jmgm.2017.08.013
Source DB: PubMed Journal: J Mol Graph Model ISSN: 1093-3263 Impact factor: 2.518