Schluckebier G, O'Gara M, Saenger W, Cheng X
Institut für Kristallographie Freie Universität, Berlin, Germany.
J Mol Biol. 1995 Mar 17;247(1):16-20. doi: 10.1006/jmbi.1994.0117.
The DNA methyltransferases, M.HhaI and M.TaqI, and catechol O-methyl-transferase (COMT) catalyze the transfer of a methyl group from the cofactor S-adenosyl-L-methionine (AdoMet) to carbon-5 of cytosine, to nitrogen-6 of adenine, and to a hydroxyl group of catechol, respectively. The catalytic domains of the bilobal proteins, M.HhaI and M.TaqI, and the entire single domain of COMT have similar folding with an alpha/beta structure containing a mixed central beta-sheet. The functional residues are located in equivalent regions at the carboxyl ends of the parallel beta-strands. The cofactor binding sites are almost identical and the essential catalytic amino acids coincide. The comparable protein folding and the existence of equivalent amino acids in similar secondary and tertiary positions indicate that many (if not all) AdoMet-dependent methyltransferases have a common catalytic domain structure. This permits tertiary structure prediction of other DNA, RNA, protein, and small-molecule AdoMet-dependent methyltransferases from their amino acid sequences.
DNA甲基转移酶M.HhaI和M.TaqI以及儿茶酚O-甲基转移酶(COMT)分别催化辅因子S-腺苷-L-甲硫氨酸(AdoMet)的甲基转移至胞嘧啶的C-5位、腺嘌呤的N-6位以及儿茶酚的羟基上。双叶蛋白M.HhaI和M.TaqI的催化结构域以及COMT的整个单结构域具有相似的折叠方式,其α/β结构包含一个混合的中央β折叠片层。功能残基位于平行β链羧基端的等效区域。辅因子结合位点几乎相同,关键催化氨基酸也一致。相似的蛋白质折叠以及在相似二级和三级位置存在等效氨基酸表明,许多(如果不是全部)依赖AdoMet的甲基转移酶具有共同的催化结构域结构。这使得能够根据其他DNA、RNA、蛋白质和小分子依赖AdoMet的甲基转移酶的氨基酸序列预测其三级结构。