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詹氏甲烷球菌中瓣状核酸内切酶-1的晶体结构。

The crystal structure of flap endonuclease-1 from Methanococcus jannaschii.

作者信息

Hwang K Y, Baek K, Kim H Y, Cho Y

机构信息

Structural Biology Center, Korea Institute of Science & Technology, Seoul, South Korea.

出版信息

Nat Struct Biol. 1998 Aug;5(8):707-13. doi: 10.1038/1406.

Abstract

Flap endonuclease-1 (FEN-1), a structure specific nuclease, is an essential enzyme for eukaryotic DNA replication and repair. The crystal structure of FEN-1 from Methanococcus jannaschii, determined at 2.0 A resolution, reveals an active site with two metal ions residing on top of a deep cleft where several conserved acidic residues are clustered. Near the active site, a long flexible loop comprised of many basic and aromatic residues forms a hole large enough to accommodate the DNA substrate. Deletion mutations in this loop significantly decreased the nuclease activity and specificity of FEN-1, suggesting that the loop is critical for recognition and cleavage of the junction between single and double-stranded regions of flap DNA.

摘要

瓣状核酸内切酶-1(FEN-1)是一种结构特异性核酸酶,是真核生物DNA复制和修复所必需的酶。嗜压甲烷球菌FEN-1的晶体结构在2.0埃分辨率下测定,揭示了一个活性位点,两个金属离子位于一个深裂隙顶部,几个保守的酸性残基聚集在此。在活性位点附近,一个由许多碱性和芳香族残基组成的长柔性环形成了一个足以容纳DNA底物的洞。该环中的缺失突变显著降低了FEN-1的核酸酶活性和特异性,表明该环对于识别和切割瓣状DNA单链和双链区域之间的连接处至关重要。

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