Archaeoglobus fulgidus/enzymology* ; Enzyme Stability ; Esterases/chemistry* ; Esterases/metabolism* ; Hot Temperature* ; Hydrophobic and Hydrophilic Interactions ; Models, Molecular ; Molecular Sequence Data ; Protein Denaturation ; Protein Structure, Secondary ; Sequence Alignment ; Structure-Activity Relationship
Abstract
The three-dimensional (3D) structure of the hyperthermophilic esterase EstE1 was constructed by homology modeling using Archaeoglobus fulgidus esterase as a reference, and the thermostability-structure relationship was analyzed. Our results verified the predicted 3D structure of EstE1 and identified the ion pair networks and hydrophobic interactions that are critical determinants for the thermostability of EstE1.