| Literature DB >> 15642336 |
W Nerinckx1, T Desmet, K Piens, M Claeyssens.
Abstract
An in silico survey of all known 3D-structures of glycoside hydrolases that contain a ligand in the -1 subsite is presented. A recurrent crucial positioning of active site residues indicates a common general strategy for electrostatic stabilisation directed to the carbohydrate's ring-oxygen at the transition state. This is substantially different depending on whether the enzyme's proton donor is syn or anti positioned versus the substrate. A comprehensive list of enzymes belonging to 42 different families is given and selected examples are described. An implication for an early evolution scenario of glycoside hydrolases is discussed.Entities:
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Year: 2005 PMID: 15642336 DOI: 10.1016/j.febslet.2004.12.021
Source DB: PubMed Journal: FEBS Lett ISSN: 0014-5793 Impact factor: 4.124