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Journal of Biochemistry 2005 137(4):455-461; doi:10.1093/jb/mvi062
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© 2005 The Japanese Biochemical Society

Rapid Communication

Structural Reorganization of the Copper Binding Site Involving Thr15 of Mavicyanin from Cucurbita pepo medullosa (Zucchini) upon Reduction

Yong Xie1, Tsuyoshi Inoue1,2, Yoichi Miyamoto1, Hiroyoshi Matsumura1, Kunishige Kataoka3,*, Kazuya Yamaguchi3, Masaki Nojini3, Shinnichiro Suzuki3 and Yasushi Kai1,{dagger}

1 Department of Materials Chemistry, Graduate School of Engineering, Osaka University, 2-1 Yamada-oka, Suita, Osaka 565-0871; 2 Structure and Function of Biomolecules Group, PRESTO, Japan Science and Technology Agency, 4-1-8 Honcho, Kawaguchi, Saitama 332-0012; and 3 Department of Chemistry, Graduate School of Science, Osaka University, 1-14 Machikaneyama, Toyonaka, Osaka 560-0043

{dagger} To whom correspondence should be addressed. Tel: +81-6-6879-7408, Fax: +81-6-6879-7409, E-mail: kai{at}chem.eng.osaka-u.ac.jp

Mavicyanin, a glycosylated protein isolated from Cucurbita pepo medullosa (zucchini), is a member of the phytocyanin subfamily containing one polypeptide chain of 109 amino residues and an unusual type-I Cu site in which the copper ligands are His45, Cys86, His91, and Gln96. The crystal structures of oxidized and reduced mavicyanin were determined at 1.6 and 1.9 Å resolution, respectively. Mavicyanin has a core structure of seven polypeptide ß-strands arranged as a ß-sandwich organized into two ß-sheets, and the structure considerably resembles that of stellacyanin from cucumber (CST) or cucumber basic protein (CBP). A flexible region was not observed on superimpositioning of the oxidized and reduced mavicyanin structures. However, the CuII-{varepsilon}-O-Gln96 bond length was extended by 0.47 Å, and the Thr15 residue was rotated by 60.0 degrees and O-{gamma}1-Thr15 moved from a distance of 4.78 to 2.58 Å from the ligand Gln96 forming a new hydrogen bond between O-{gamma}1-Thr15 and {varepsilon}-O-Gln96 upon reduction. The reorganization of copper coordination geometry of mavicyanin upon reduction arouses reduction potential decreased above pH 8 [Battistuzzi et al. (2001) J. Inorg. Biochem. 83, 223–227]. The rotation of Thr15 and the hydrogen bonding with the ligand Gln96 may constitute structural evidence of the decrease in the reduction potential at high pH.

* Present address: Department of Chemistry, Faculty of Science, Kanazawa University, Kakuma-machi, Kanazawa 920-1192.


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