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3型M蛋白基因(emm3)的克隆及核苷酸序列,该基因由N端可变部分和C端保守C重复区域组成:与化脓性链球菌其他基因的关系。链球菌疾病研究组

Cloning and nucleotide sequence of type 3 M protein gene (emm3) consisting of an N-terminal variable portion and C-terminal conserved C repeat regions: relation to other genes of Streptococcus pyogenes. Streptococcal Diseases Study Group.

作者信息

Katsukawa C

机构信息

Laboratory of Microbiology, Osaka Prefectural Institute of Public Health.

出版信息

Kansenshogaku Zasshi. 1994 May;68(5):698-705. doi: 10.11150/kansenshogakuzasshi1970.68.698.

Abstract

The structural gene for type 3 M protein of Streptococcus pyogenes, which consists of an N-terminal variable portion and C-terminal conserved repeat regions, has been cloned by the polymerase chain reaction (PCR) with two primers (K-1 and K-2). They were selected from the best conserved region of the leader sequences and of the C-terminal portion near the Hexapeptide (LPSTGE) sequence found in different M proteins. From the nucleotide sequence of the product, 1645 base pairs were determined, including 32 amino acids of the leader sequences, the complete N-terminal variable region and the conserved C repeat region. Analysis of the deduced amino acids of the sequence revealed the existence of two major repeat regions, the B and C repeat regions. Comparison of the C-repeat regions among M3 and other M proteins showed them to be more than 90% identical. The two B repeat blocks in M3 protein are also similar to those in M12 protein. Predictive secondary structure analysis of M3 protein reveals a strong alpha-helical potential. The algorithm also shows that the beta-sheet and turn potential for region 23-42 in M3 protein are similar to those for region 28-50 in M12 protein. The results indicate that M3 protein is closely related to M12 protein.

摘要

化脓性链球菌3型M蛋白的结构基因由N端可变部分和C端保守重复区域组成,已通过聚合酶链反应(PCR)用两种引物(K-1和K-2)进行克隆。这两种引物是从不同M蛋白中发现的前导序列最佳保守区域以及靠近六肽(LPSTGE)序列的C端部分中挑选出来的。从产物的核苷酸序列中确定了1645个碱基对,包括前导序列的32个氨基酸、完整的N端可变区域和保守的C重复区域。对推导的氨基酸序列进行分析,发现存在两个主要的重复区域,即B和C重复区域。比较M3和其他M蛋白中的C重复区域,发现它们的同源性超过90%。M3蛋白中的两个B重复块也与M12蛋白中的相似。对M3蛋白的预测二级结构分析显示出很强的α螺旋潜力。该算法还表明,M3蛋白中23-42区域的β折叠和转角潜力与M12蛋白中28-50区域的相似。结果表明M3蛋白与M12蛋白密切相关。

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