Retroviral integrase superfamily: the structural perspective

被引:144
作者
Nowotny, Marcin [1 ]
机构
[1] Int Inst Mol & Cell Biol, Lab Prot Struct, PL-02109 Warsaw, Poland
基金
英国惠康基金;
关键词
Argonaute; integrase; protein structure; RNase H; transposase; JUNCTION-SPECIFIC ENDONUCLEASE; RNASE-H; CRYSTAL-STRUCTURE; ACTIVE-SITE; 3-DIMENSIONAL STRUCTURE; SUBSTRATE-SPECIFICITY; MUTATIONAL ANALYSIS; RIBONUCLEASE-H; RUVC RESOLVASE; RNA/DNA HYBRID;
D O I
10.1038/embor.2008.256
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The retroviral integrase superfamily (RISF) comprises numerous important nucleic acid-processing enzymes, including transposases, integrases and various nucleases. These enzymes are involved in a wide range of processes such as transposition, replication and repair of DNA, homologous recombination, and RNA-mediated gene silencing. Two out of the four enzymes that are encoded by the human immunodeficiency virus-RNase H1 and integrase-are members of this superfamily. RISF enzymes act on various substrates, and yet show remarkable mechanistic and structural similarities. All share a common fold of the catalytic core and the active site, which is composed primarily of carboxylate residues. Here, I present RISF proteins from a structural perspective, describing the individual members and the common and divergent elements of their structures, as well as the mechanistic insights gained from the structures of RNase H1 enzyme complexes with RNA/DNA hybrids.
引用
收藏
页码:144 / 151
页数:8
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