| Literature DB >> 28261912 |
Christopher Selleck1, Daniel Clayton1, Lawrence R Gahan1, Nataša Mitić2, Ross P McGeary1, Marcelo Monteiro Pedroso1, Luke W Guddat1, Gerhard Schenk1.
Abstract
Metallohydrolases are a vast family of enzymes that play crucial roles in numerous metabolic pathways. Several members have emerged as targets for chemotherapeutics. Knowledge about their reaction mechanisms and associated transition states greatly aids the design of potent and highly specific drug leads. By using a high-resolution crystal structure, we have probed the trajectory of the reaction catalyzed by purple acid phosphatase, an enzyme essential for the integrity of bone structure. In particular, the transition state is visualized, thus providing detailed structural information that may be exploited in the design of specific inhibitors for the development of new anti-osteoporotic chemotherapeutics.Entities:
Keywords: enzymes; hydrolases; metallohydrolases; transition states
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Year: 2017 PMID: 28261912 DOI: 10.1002/chem.201700866
Source DB: PubMed Journal: Chemistry ISSN: 0947-6539 Impact factor: 5.236