3BW7
Maize cytokinin oxidase/dehydrogenase complexed with the allenic cytokinin analog HA-1
3BW7 の概要
エントリーDOI | 10.2210/pdb3bw7/pdb |
関連するPDBエントリー | 2QKN 2QPM |
分子名称 | Cytokinin dehydrogenase 1, 2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose, 2-acetamido-2-deoxy-beta-D-glucopyranose, ... (7 entities in total) |
機能のキーワード | cytokinin oxidase/dehydrogenase, fad, ha-1 inhibitor, oxidoreductase |
由来する生物種 | Zea mays (maize) |
タンパク質・核酸の鎖数 | 1 |
化学式量合計 | 58151.68 |
構造登録者 | |
主引用文献 | Kopecny, D.,Sebela, M.,Briozzo, P.,Spichal, L.,Houba-Herin, N.,Masek, V.,Joly, N.,Madzak, C.,Anzenbacher, P.,Laloue, M. Mechanism-based inhibitors of cytokinin oxidase/dehydrogenase attack FAD cofactor J.Mol.Biol., 380:886-899, 2008 Cited by PubMed Abstract: Cytokinin oxidases/dehydrogenases (CKOs) mediate catabolic regulation of cytokinin levels in plants. Several substrate analogs containing an unsaturated side chain were studied for their possible inhibitory effect on maize CKO (ZmCKO1) by use of various bioanalytical methods. Two allenic derivatives, N(6)-(buta-2,3-dienyl)adenine (HA-8) and N(6)-(penta-2,3-dienyl)adenine (HA-1), were identified as strong mechanism-based inhibitors of the enzyme. Despite exhaustive dialysis, the enzyme remained inhibited. Conversely, substrate analogs with a triple bond in the side chain were much weaker inactivators. The crystal structures of recombinant ZmCKO1 complexed with HA-1 or HA-8 were solved to 1.95 A resolution. Together with Raman spectra of the inactivated enzyme, it was revealed that reactive imine intermediates generated by oxidation of the allenic inhibitors covalently bind to the flavin adenine dinucleotide (FAD) cofactor. The binding occurs at the C4a atom of the isoalloxazine ring of FAD, the planarity of which is consequently disrupted. All the compounds under study were also analyzed for binding to the Arabidopsis cytokinin receptors AHK3 and AHK4 in a bacterial receptor assay and for cytokinin activity in the Amaranthus bioassay. HA-1 and HA-8 were found to be good receptor ligands with a significant cytokinin activity. Nevertheless, due to their ability to inactivate CKO in the desired time intervals or developmental stages, they both represent attractive compounds for physiological studies, as the inhibition mechanism of HA-1 and HA-8 is mainly FAD dependent. PubMed: 18571199DOI: 10.1016/j.jmb.2008.05.044 主引用文献が同じPDBエントリー |
実験手法 | X-RAY DIFFRACTION (1.95 Å) |
構造検証レポート
検証レポート(詳細版)
をダウンロード
