Literature DB >> 12121073

Asymmetric sulfoxidation and amine binding by H64D/V68A and H64D/V68S Mb: mechanistic insight into the chiral discrimination step.

Shigeru Kato1, Hui-Jun Yang, Takafumi Ueno, Shin-ichi Ozaki, George N Phillips, Shunichi Fukuzumi, Yoshihito Watanabe.   

Abstract

The H64D/V68A and H64D/V68S mutants of Myoglobin are found to oxidize thioanisole with high enantioselectivity and reactivity. These mutants are also capable of enantioselective binding of alpha-methylbenzylamine, which mimics an expected sulfoxidation intermediate. The kinetic study of the amine binding shows that the Fe-O bond cleavage in the intermediate may be the chiral discrimination step of the sulfoxidation.

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Year:  2002        PMID: 12121073     DOI: 10.1021/ja0256414

Source DB:  PubMed          Journal:  J Am Chem Soc        ISSN: 0002-7863            Impact factor:   15.419


  1 in total

1.  Efficient conversion of primary azides to aldehydes catalyzed by active site variants of myoglobin.

Authors:  Simone Giovani; Ritesh Singh; Rudi Fasan
Journal:  Chem Sci       Date:  2015-09-28       Impact factor: 9.825

  1 in total

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