Evaluation of Synthetic FK506 Analogues as Ligands for the FK506-Binding Proteins 51 and 52
Author:
Affiliation:
1. Max Planck Institute of Psychiatry, Kraepelinstrasse 2, 80804 Munich, Germany
2. Max Planck Institute of Biochemistry, Am Klopferspitz 18, 82152 Martinsried, Germany
Publisher
American Chemical Society (ACS)
Subject
Drug Discovery,Molecular Medicine
Link
https://pubs.acs.org/doi/pdf/10.1021/jm201746x
Reference49 articles.
1. The Chemical Biology of Immunophilin Ligands
2. Crystal Structure of the Cytoplasmic Domain of the Type I TGF β Receptor in Complex with FKBP12
3. The Hsp90-binding peptidylprolyl isomerase FKBP52 potentiates glucocorticoid signaling in vivo
4. FK506-binding Proteins 51 and 52 Differentially Regulate Dynein Interaction and Nuclear Translocation of the Glucocorticoid Receptor in Mammalian Cells
5. Differential Control of Glucocorticoid Receptor Hormone-Binding Function by Tetratricopeptide Repeat (TPR) Proteins and the Immunosuppressive Ligand FK506
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