1exa

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spinqualitylabelsall models 1exa, resolution 1.59Å Show:Asymmetric Unit Biological Assembly Drag the structure with the mouse to rotate   Export Animated Image

ENANTIOMER DISCRIMINATION ILLUSTRATED BY CRYSTAL STRUCTURES OF THE HUMAN RETINOIC ACID RECEPTOR HRARGAMMA LIGAND BINDING DOMAIN: THE COMPLEX WITH THE ACTIVE R-ENANTIOMER BMS270394.

Overview

The human retinoic acid receptor (hRAR) is a member of the nuclear, receptor superfamily that regulates the transcription of target genes in a, ligand-dependent manner. The three hRAR isotypes are targets for retinoids, that are used in the treatment of various diseases, including breast, cancer and skin diseases. Drug efficiency and safety depend on the, pharmacological activity of enantiomers, which can differ because of the, chiral environment generated by the target. We report the crystal, structures of the hRARgamma ligand-binding domain bound to two, enantiomers, the active BMS270394 and the inactive BMS270395, solved at, 1.6 A and 1.7 A resolution, respectively. The crystal structures reveal, that in both enantiomers, the hydroxyl moiety attached to the chiral, center forms a hydrogen bond to the Met-272 sulfur atom, thus imposing a, conformation of BMS270395 that differs significantly from that observed, for BMS270394 and other known retinoids. BMS270395 adopts an energetically, unfavorable conformation, accounting for its inactivity; in contrast, the, conformation of BMS270394 is close to an energy minimum. Our, high-resolution data allow rationalization of enantiomer discrimination by, the receptor and provide a model system for the pharmacological properties, of enantiomeric pairs.

About this Structure

1EXA is a Single protein structure of sequence from Homo sapiens with 394 and LMU as ligands. Full crystallographic information is available from OCA.

Reference

Enantiomer discrimination illustrated by high-resolution crystal structures of the human nuclear receptor hRARgamma., Klaholz BP, Mitschler A, Belema M, Zusi C, Moras D, Proc Natl Acad Sci U S A. 2000 Jun 6;97(12):6322-7. PMID:10841540

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