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Structural and biochemical insights into FKBP51 as a Hsp90 co-chaperone.
Baischew, Asat; Engel, Sarah; Geiger, Thomas M; Taubert, Martha C; Hausch, Felix.
Afiliación
  • Baischew A; Department of Chemistry, Institute for Organic Chemistry and Biochemistry, Technical University Darmstadt, Darmstadt, Germany.
  • Engel S; Department of Chemistry, Institute for Organic Chemistry and Biochemistry, Technical University Darmstadt, Darmstadt, Germany.
  • Geiger TM; Department of Chemistry, Institute for Organic Chemistry and Biochemistry, Technical University Darmstadt, Darmstadt, Germany.
  • Taubert MC; Department of Chemistry, Institute for Organic Chemistry and Biochemistry, Technical University Darmstadt, Darmstadt, Germany.
  • Hausch F; Department of Chemistry, Institute for Organic Chemistry and Biochemistry, Technical University Darmstadt, Darmstadt, Germany.
J Cell Biochem ; 2023 Feb 15.
Article en En | MEDLINE | ID: mdl-36791213
The FK506-binding protein 51 (FKBP51) is a high-molecular-weight immunophilin that emerged as an important drug target for stress-related disorders, chronic pain, and obesity. It has been implicated in a plethora of molecular pathways but remains best characterized as a co-chaperone of Hsp90 in the steroid hormone receptor (SHR) maturation cycle. However, the mechanistic and structural basis for the regulation of SHRs by FKBP51 and the usually antagonistic function compared with its closest homolog FKBP52 remains enigmatic. Here we review recent structural and biochemical studies of FKBPs as regulators in the Hsp90 machinery. These advances provide important insights into the roles of FKBP51 and FKBP52 in SHR regulation.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: J Cell Biochem Año: 2023 Tipo del documento: Article País de afiliación: Alemania

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: J Cell Biochem Año: 2023 Tipo del documento: Article País de afiliación: Alemania