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血管紧张素原和激肽原:cDNA的克隆与序列分析

Angiotensinogen and kininogen: cloning and sequence analysis of the cDNAs.

作者信息

Nakanishi S, Ohkubo H, Nawa H, Kitamura N, Kageyama R, Ujihara M

出版信息

Clin Exp Hypertens A. 1983;5(7-8):997-1003. doi: 10.3109/10641968309048837.

Abstract

The primary structures of the angiotensinogen precursor and the low molecular weight (LMW) kininogen precursors have been deduced by determining the nucleotide sequences of cloned DNAs complementary to their mRNAs. The angiotensinogen precursor consists of a mature angiotensinogen of 453 amino acid residues and a putative signal peptide of 24 amino acid residues. An angiotensin moiety is located at the amino-terminal part of angiotensinogen, preceded directly by the signal peptide and followed by a large carboxyl-terminal sequence that contains two internally homologous sequences and three potential glycosylation sites. The LMW kininogen precursors are encoded by two very similar but distinct mRNAs and composed of 436 and 434 amino acid residues. Both kininogens contain two internally homologous sequences in which all amino acid differences between the two kininogens are located. This suggests that these homologous regions may be biologically significant in relation to the existence of two LMW kininogens.

摘要

通过测定与血管紧张素原前体和低分子量(LMW)激肽原前体的mRNA互补的克隆DNA的核苷酸序列,已推断出它们的一级结构。血管紧张素原前体由一个含453个氨基酸残基的成熟血管紧张素原和一个含24个氨基酸残基的假定信号肽组成。血管紧张素部分位于血管紧张素原的氨基末端,其直接前面是信号肽,后面是一个大的羧基末端序列,该序列包含两个内部同源序列和三个潜在的糖基化位点。LMW激肽原前体由两个非常相似但不同的mRNA编码,由436和434个氨基酸残基组成。两种激肽原都含有两个内部同源序列,两种激肽原之间所有的氨基酸差异都位于这些序列中。这表明这些同源区域可能与两种LMW激肽原的存在具有生物学意义。

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