The covalent binding of genistein to the non-prosthetic-heme-moiety of bovine lactoperoxidase leads to enzymatic inactivation

Biomedical and Environmental Sciences

Volumn 24, Issue 3, 2011, Pages 284-290

  Chang, Hebron C ^a   Doerge, Daniel R ^b   Hsieh, Chenghong ^a   Lin, Yingju ^c   Tsai, Fuujen ^c  

^a ASIA UNIVERSITY   (Taiwan)

^b NATIONAL CENTER FOR TOXICOLOGICAL RESEARCH   (United States)

^c CHINA MEDICAL UNIVERSITY   (Taiwan)

Author keywords

Covalent binding; Genistein; Lactoperoxidase; Modification of heme; Peptide fragments

Indexed keywords

GENISTEIN; HYDROGEN PEROXIDE; ISOFLAVONE DERIVATIVE; LACTOPEROXIDASE; PLACENTA LACTOGEN;

ANIMAL; ARTICLE; CATTLE; DRUG EFFECT; ENZYME ACTIVATION; METABOLISM; PROTEIN BINDING;

ANIMALS; CATTLE; ENZYME ACTIVATION; GENISTEIN; HYDROGEN PEROXIDE; ISOFLAVONES; LACTOPEROXIDASE; PLACENTAL LACTOGEN; PROTEIN BINDING;

BOVINAE;

EID: 79960759885     PISSN: 08953988     EISSN: None     Source Type: Journal    
DOI: 10.3967/0895-3988.2011.03.012     Document Type: Article

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