Literature DB >> 10872460

Nuclear-receptor ligands and ligand-binding domains.

R V Weatherman1, R J Fletterick, T S Scanlan.   

Abstract

The determination of several structures of nuclear receptor ligand binding domains (LBD) has led to new insights into the mechanism of action of this very important class of receptors. This review describes and compares the different LBD structures and their relationship to the function of the nuclear receptors. The role of the ligand in the LBD structures and the implications of ligand structure on receptor activity are also discussed. Structural information regarding interactions between the LBD and coactivator proteins and the potential role of these interactions in ligand agonism and antagonism is reviewed. Different pathways for nuclear receptor signaling and the use of new ligands to investigate these pathways are also described.

Mesh:

Substances:

Year:  1999        PMID: 10872460     DOI: 10.1146/annurev.biochem.68.1.559

Source DB:  PubMed          Journal:  Annu Rev Biochem        ISSN: 0066-4154            Impact factor:   23.643


  62 in total

1.  Identification of XPR-1, a progesterone receptor required for Xenopus oocyte activation.

Authors:  J Tian; S Kim; E Heilig; J V Ruderman
Journal:  Proc Natl Acad Sci U S A       Date:  2000-12-19       Impact factor: 11.205

Review 2.  Structure function studies: identification of vitamin D analogs for the ligand-binding domains of important proteins in the vitamin D-endocrine system.

Authors:  A W Norman; F R Silva
Journal:  Rev Endocr Metab Disord       Date:  2001-04       Impact factor: 6.514

3.  The stress response mediator ATF3 represses androgen signaling by binding the androgen receptor.

Authors:  Hongbo Wang; Ming Jiang; Hongmei Cui; Mengqian Chen; Ralph Buttyan; Simon W Hayward; Tsonwin Hai; Zhengxin Wang; Chunhong Yan
Journal:  Mol Cell Biol       Date:  2012-06-04       Impact factor: 4.272

4.  Improved docking, screening and selectivity prediction for small molecule nuclear receptor modulators using conformational ensembles.

Authors:  So-Jung Park; Irina Kufareva; Ruben Abagyan
Journal:  J Comput Aided Mol Des       Date:  2010-05-09       Impact factor: 3.686

5.  Molecular origins for the dominant negative function of human glucocorticoid receptor beta.

Authors:  Matthew R Yudt; Christine M Jewell; Rachelle J Bienstock; John A Cidlowski
Journal:  Mol Cell Biol       Date:  2003-06       Impact factor: 4.272

6.  Functional analysis of the Mad1-mSin3A repressor-corepressor interaction reveals determinants of specificity, affinity, and transcriptional response.

Authors:  Shaun M Cowley; Richard S Kang; John V Frangioni; Jason J Yada; Alec M DeGrand; Ishwar Radhakrishnan; Robert N Eisenman
Journal:  Mol Cell Biol       Date:  2004-04       Impact factor: 4.272

7.  Peroxisome proliferator-activated receptors target family landscape: a chemometrical approach to ligand selectivity based on protein binding site analysis.

Authors:  Bernard Pirard
Journal:  J Comput Aided Mol Des       Date:  2003-11       Impact factor: 3.686

8.  Tautomers and topomers: challenging the uncertainties of direct physicochemical modeling.

Authors:  Richard D Cramer
Journal:  J Comput Aided Mol Des       Date:  2010-03-21       Impact factor: 3.686

Review 9.  Diet, fatty acids, and regulation of genes important for heart disease.

Authors:  John P Vanden Heuvel
Journal:  Curr Atheroscler Rep       Date:  2004-11       Impact factor: 5.113

10.  Interactions of androgens, green tea catechins and the antiandrogen flutamide with the external glucose-binding site of the human erythrocyte glucose transporter GLUT1.

Authors:  Richard J Naftalin; Iram Afzal; Philip Cunningham; Mansur Halai; Clare Ross; Naguib Salleh; Stuart R Milligan
Journal:  Br J Pharmacol       Date:  2003-08-26       Impact factor: 8.739

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.