TY - JOUR
T1 - Analysis of crystal structures of LXR beta in relation to plasticity of the ligand-binding domain upon ligand binding
AU - Mallini, Nagullapailli
AU - Rajesh, Hariharan
AU - Berwal, Pooja
AU - Phukan, Samiron
AU - Balaji, Vittukudi Narayanaiyengar
PY - 2008
Y1 - 2008
N2 - Liver X receptors (LXRs) are a member of the nuclear hormone receptor superfamilly of ligand activated transcription factors. LXRs have gained importance as therapeutic targets because of their involvement in many diseases. Analysis of the protein-ligand complexes of X-ray crystallography-derived structures revealed that residues His435 and Trp457 act as a switch that mediates ligand activation. These residues show conservation for main chain (phi, psi) in His435 and moderate movement for Trp457. Hiis435 in Hellix11 (H11) is conserved in relation to Trp457 in Helix12 (H12). This shows that some induced fit effect can be incorporated while designing ligands for activation of LXR with relation to Trp457 rather than that of His435. Similarly, main chain movement in Phe329 and Leu330 showed significant conformational mobility leading to flexibility in the ligand-binding domain (LBD) along with Arg319 which has a moderate movement in (phi and psi) angles. It is interesting to know that for some sequence-ligand complex crystallizations using different conditions show considerable main chain and side chain mobility indicating plasticity in LBD of LXR beta. This study supports our understanding the relative movement of residues in the Ill of LXRs upon ligand binding which can provide insight for designing of LXRs modulators.
AB - Liver X receptors (LXRs) are a member of the nuclear hormone receptor superfamilly of ligand activated transcription factors. LXRs have gained importance as therapeutic targets because of their involvement in many diseases. Analysis of the protein-ligand complexes of X-ray crystallography-derived structures revealed that residues His435 and Trp457 act as a switch that mediates ligand activation. These residues show conservation for main chain (phi, psi) in His435 and moderate movement for Trp457. Hiis435 in Hellix11 (H11) is conserved in relation to Trp457 in Helix12 (H12). This shows that some induced fit effect can be incorporated while designing ligands for activation of LXR with relation to Trp457 rather than that of His435. Similarly, main chain movement in Phe329 and Leu330 showed significant conformational mobility leading to flexibility in the ligand-binding domain (LBD) along with Arg319 which has a moderate movement in (phi and psi) angles. It is interesting to know that for some sequence-ligand complex crystallizations using different conditions show considerable main chain and side chain mobility indicating plasticity in LBD of LXR beta. This study supports our understanding the relative movement of residues in the Ill of LXRs upon ligand binding which can provide insight for designing of LXRs modulators.
M3 - Article
SN - 1747-0277
VL - 71
SP - 140
EP - 154
JO - Chemical Biology and Drug Design
JF - Chemical Biology and Drug Design
IS - 2
ER -