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The comparative amino acid sequences, substrate specificities and gene or cDNA nucleotide sequences of some prokaryote and eukaryote amidinotransferases: implications for evolution

机译:一些原核生物和真核生物转移酶的比较氨基酸序列,底物特异性和基因或cDNA核苷酸序列:对进化的影响

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The amino acid sequences of the amidinotransferases and the nucleotide sequences of their genes or cDNA from four Streptomyces species (seven genes) and from the kidneys of rat, pig, human and human pancreas were compared. The overall amino acid and nucleotide sequences of the prokaryotes and eukaryotes were very similar and further, three regions were identified that were highly identical. Evidence is presented that there is virtually zero chance that the overall and high identity regions of the amino acid sequence similarities and the overall nucleotide sequence similarities between Streptomyces and mammals represent random match. Both rat and lamprey amidinotransferases were able to use inosamine phosphate, the amidine group acceptor of Streptomyces. We have concluded that the structure and function of the amidinotransferases and their genes has been highly conserved through evolution from prokaryotes to eukaryotes. The evolution has occurred with: (1) a high degree of retention of nucleotide and amino acid sequences; (2) a high degree of retention of the primitive Streptomyces guanine + cytosine (G + C) third codon position composition in certain high identity regions of the eukaryote cDNA; (3) a decrease in the specificities for the amidine group accepters; and (4) most of the mutations silent in the regions suggested to code for active sites in the enzymes. (C) 1998 Elsevier Science Inc. All rights reserved. [References: 37]
机译:比较了酰胺转移酶的氨基酸序列和其基因或cDNA的核苷酸序列,从四种链霉菌物种(七种基因)和大鼠,猪,人和人类胰腺的肾脏中进行了比较。原核生物和真核生物的整体氨基酸和核苷酸序列非常相似,另外,鉴定了三个区域,其高度相同。提出了氨基酸序列相似性的总体和高分区域几乎有用的几乎是氨基酸序列的相似性和链霉菌和哺乳动物之间的整体核苷酸序列相似之处代表随机匹配。大鼠和羊斑酰胺转移酶均能够使用Inosamine磷酸盐,脒基受体的链霉菌。得出结论,酰胺转移酶及其基因的结构和功能通过从原核生物到真核生物的演变高度保守。进化发生了:(1)核苷酸和氨基酸序列的高度保持程度高; (2)原始链霉菌的高度保留鸟嘌呤+胞嘧啶(G + C)第三密码子位置组合物在真核生物cDNA的某些高同型区域中; (3)脒基团受体的特异性降低; (4)区域中沉默的大部分突变建议在酶中的活性位点代码。 (c)1998年elestvier科学公司保留所有权利。 [参考:37]

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