Literature DB >> 1537459

Analysis of the catalytic specificity of cytochrome P450 enzymes through site-directed mutagenesis.

E F Johnson1, T Kronbach, M H Hsu.   

Abstract

The way in which structural diversity encodes the capacity of individual P450 enzymes to metabolize multiple, structurally distinct substrates remains largely unknown. The tools of molecular biology provide a means of identifying amino acid residues among closely related P450s that are determinants of their distinct catalytic properties. Work in our laboratory has identified two substrate specificity-determining segments of the amino acid sequences of subfamily 2C P450s. A pattern has emerged from this work, and that of others, which suggests a model for the structural basis of P450 catalytic diversity.

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Year:  1992        PMID: 1537459     DOI: 10.1096/fasebj.6.2.1537459

Source DB:  PubMed          Journal:  FASEB J        ISSN: 0892-6638            Impact factor:   5.191


  2 in total

1.  A host-inducible cytochrome P-450 from a host-specific caterpillar: molecular cloning and evolution.

Authors:  M B Cohen; M A Schuler; M R Berenbaum
Journal:  Proc Natl Acad Sci U S A       Date:  1992-11-15       Impact factor: 11.205

2.  Solution structure and topology of the N-terminal membrane anchor domain of a microsomal cytochrome P450: prostaglandin I2 synthase.

Authors:  Ke-He Ruan; Shui-Ping So; Weida Zheng; Jiaxin Wu; Dawei Li; Jennifer Kung
Journal:  Biochem J       Date:  2002-12-15       Impact factor: 3.857

  2 in total

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