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QM/MM studies of monozinc ?-lactamase CphA suggest that the crystal structure of an enzyme-intermediate complex represents a minor pathway.


ABSTRACT: QM/MM studies of the hydrolysis of a ?-lactam antibiotic molecule (biapenem) catalyzed by a monozinc ?-lactamase (CphA) have revealed the complete reaction mechanism and shown that an experimentally determined enzyme-intermediate complex is a stable intermediate or product in a minor pathway.

SUBMITTER: Wu S 

PROVIDER: S-EPMC3009838 | biostudies-literature | 2010 Dec

REPOSITORIES: biostudies-literature

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QM/MM studies of monozinc β-lactamase CphA suggest that the crystal structure of an enzyme-intermediate complex represents a minor pathway.

Wu Shanshan S   Xu Dingguo D   Guo Hua H  

Journal of the American Chemical Society 20101207 51


QM/MM studies of the hydrolysis of a β-lactam antibiotic molecule (biapenem) catalyzed by a monozinc β-lactamase (CphA) have revealed the complete reaction mechanism and shown that an experimentally determined enzyme-intermediate complex is a stable intermediate or product in a minor pathway. ...[more]

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