Morris Sidney M
Department of Molecular Genetics and Biochemistry, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania 15261, USA.
Ann N Y Acad Sci. 2003 Dec;1009:30-3. doi: 10.1196/annals.1304.003.
Whereas agmatine in vertebrates may be derived from multiple sources such as the diet, endogenous synthesis via arginine decarboxylase, and possibly also from enteric bacteria, agmatinase is the only enzyme specific for agmatine catabolism. As it hydrolyzes a guanidino group within agmatine and also contains signature amino acid residues that act as ligand binding sites for the Mn(++) cofactor, agmatinase is classified as a member of the arginase superfamily. Very little information is available regarding how much agmatine in vertebrate species is catabolized by agmatinase versus other enzymes such as diamine and amine oxidases. Moreover, comparisons of primary sequences of several vertebrate agmatinases demonstrate that several residues essential for catalytic activity are not conserved in the mouse. This leads to the prediction that the agmatinase protein in mouse has little or no catalytic activity, not only raising questions about the physiologic routes of agmatine disposal in this organism, but also suggesting the existence of species-specific differences in mechanisms for regulating agmatine levels.
在脊椎动物中,胍丁胺可能来源于多种途径,如饮食、通过精氨酸脱羧酶进行的内源性合成,也可能来自肠道细菌,而胍丁胺酶是唯一一种特异性参与胍丁胺分解代谢的酶。由于它能水解胍丁胺中的胍基,并且还含有作为锰离子(Mn(++))辅因子配体结合位点的特征性氨基酸残基,因此胍丁胺酶被归类为精氨酸酶超家族的一员。关于脊椎动物物种中胍丁胺被胍丁胺酶与其他酶(如二胺和胺氧化酶)分解代谢的比例,目前所知甚少。此外,对几种脊椎动物胍丁胺酶一级序列的比较表明,一些对催化活性至关重要的残基在小鼠中并不保守。这导致人们预测,小鼠中的胍丁胺酶蛋白几乎没有或没有催化活性,这不仅引发了关于该生物体中胍丁胺处置生理途径的问题,也暗示了在调节胍丁胺水平的机制上存在物种特异性差异。