Literature DB >> 28261912

Visualization of the Reaction Trajectory and Transition State in a Hydrolytic Reaction Catalyzed by a Metalloenzyme.

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.
© 2017 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Keywords:  enzymes; hydrolases; metallohydrolases; transition states

Mesh:

Substances:

Year:  2017        PMID: 28261912     DOI: 10.1002/chem.201700866

Source DB:  PubMed          Journal:  Chemistry        ISSN: 0947-6539            Impact factor:   5.236


  2 in total

1.  Synthesis, Magnetic Properties, and Catalytic Properties of a Nickel(II)-Dependent Biomimetic of Metallohydrolases.

Authors:  Adolfo Horn; Daniel Englert; Asha E Roberts; Peter Comba; Gerhard Schenk; Elizabeth H Krenske; Lawrence R Gahan
Journal:  Front Chem       Date:  2018-09-25       Impact factor: 5.221

2.  Structure of a cereal purple acid phytase provides new insights to phytate degradation in plants.

Authors:  Raquel Faba-Rodriguez; Yinghong Gu; Melissa Salmon; Giuseppe Dionisio; Henrik Brinch-Pedersen; Charles A Brearley; Andrew M Hemmings
Journal:  Plant Commun       Date:  2022-02-19
  2 in total

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