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Updated: Jun 21, 2026

Mutagenesis and Functional Analysis of Ion Channels Heterologously Expressed in Mammalian Cells
Published on: October 1, 2010
Mutagenesis studies of human cystathionine beta-synthase: residues important for heme binding and substrate
Shin-ichi Ozaki1, Chihori Sakaguchi, Akira Nakahara
1Department of Biological Sciences, Yamaguchi University, 1677-1 Yoshida, Yamaguchi, 753-8515, Japan. ozakis@yamaguchi-u.ac.jp
Abstract:
Human cystathionine beta-synthase (CBS) is a pyridoxal 5'-phosphate (PLP) dependent hemoprotein, which catalyzes the condensation of serine and homocysteine. Our mutagenesis studies suggest that Arg-266 is important to sense structural changes in heme-binding site, and that Gln-222 as well as Tyr-223 are involved in interactions with substrates.
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