Mühlebach S M, Gross M, Wirz T, Wallimann T, Perriard J C, Wyss M
Institute for Cell Biology, ETH Hönggerberg, Zürich, Switzerland.
Mol Cell Biochem. 1994 Apr-May;133-134:245-62. doi: 10.1007/BF01267958.
Comparisons of the protein sequences and gene structures of the known creatine kinase isoenzymes and other guanidino kinases revealed high homology and were used to determine the evolutionary relationships of the various guanidino kinases. A 'CK framework' is defined, consisting of the most conserved sequence blocks, and 'diagnostic boxes' are identified which are characteristic for anyone creatine kinase isoenzyme (e.g. for vertebrate B-CK) and which may serve to distinguish this isoenzyme from all others (e.g. from M-CKs and Mi-CKs). Comparison of the guanidino kinases by near-UV and far-UV circular dichroism further indicates pronounced conservation of secondary structure as well as of aromatic amino acids that are involved in catalysis.
对已知肌酸激酶同工酶和其他胍基激酶的蛋白质序列及基因结构进行比较,发现它们具有高度同源性,并被用于确定各种胍基激酶的进化关系。定义了一个由最保守序列块组成的“CK框架”,并识别出“诊断框”,这些“诊断框”是任何一种肌酸激酶同工酶(如脊椎动物B-CK)所特有的,可用于将该同工酶与所有其他同工酶(如M-CK和Mi-CK)区分开来。通过近紫外和远紫外圆二色性对胍基激酶进行比较,进一步表明二级结构以及参与催化的芳香族氨基酸具有明显的保守性。