Sequence homology and structure predictions of the creatine kinase isoenzymes |
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Authors: | Mühlebach S. M. Gross M. Wirz T. Wallimann T. Perriard J. -C. Wyss M. |
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Affiliation: | (1) Institute for Cell Biology, ETH Hönggerberg, CH-8093 Zürich, Switzerland;(2) Department of Transplant Surgery, Research Division, University Hospital, Anichstr. 35, A-6020 Innsbruck, Austria |
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Abstract: | 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 guamidino 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.Abbreviations GuaK guanidino kinase - CK creatine kinase - B-and M-CK brain and muscle cytosolic CK isoenzyme - Mi-CK mitochondrial CK isoenzyme - ArgK arginine kinase - Cr creatine - PCr phosphorylcreatine - PArg phosphorylarginine |
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Keywords: | creatine kinase arginine kinase protein sequence comparison evolution CK framework /content/m1h185160j6688n2/xxlarge8216.gif" alt=" lsquo" align=" BASELINE" BORDER=" 0" >diagnostic boxes /content/m1h185160j6688n2/xxlarge8217.gif" alt=" rsquo" align=" BASELINE" BORDER=" 0" > secondary structure prediction |
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