Literature DB >> 15333774

Expression of the C-terminus of HIV-1 reverse transcriptase p66 and p51 subunits as a single polypeptide with RNase H activity.

Roberto Zúñiga1, Sonali Sengupta, Christine Snyder, Oscar Leon, Monica J Roth.   

Abstract

The C-terminus of the HIV-1 reverse transcriptase heterodimer was reconstructed into a single polypeptide. The construct encodes the p51 thumb (T) and connection (C) subdomains joined through a linker region to the p66 connection (C) and RNase H (R) domain. The TCCR protein was purified from insoluble fractions of Escherichia coli lysates. The TCCR construct maintains Mn(2+)-dependent RNase H activity and specifically cleaves the substrate mimicking the tRNA removal required for second-strand transfer reactions.

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Year:  2004        PMID: 15333774     DOI: 10.1093/protein/gzh071

Source DB:  PubMed          Journal:  Protein Eng Des Sel        ISSN: 1741-0126            Impact factor:   1.650


  4 in total

1.  Expression of an Mg2+-dependent HIV-1 RNase H construct for drug screening.

Authors:  Richard V Farias; Deborah A Vargas; Andres E Castillo; Beatriz Valenzuela; Marie L Coté; Monica J Roth; Oscar Leon
Journal:  Antimicrob Agents Chemother       Date:  2011-07-18       Impact factor: 5.191

2.  Structural and inhibition studies of the RNase H function of xenotropic murine leukemia virus-related virus reverse transcriptase.

Authors:  Karen A Kirby; Bruno Marchand; Yee Tsuey Ong; Tanyaradzwa P Ndongwe; Atsuko Hachiya; Eleftherios Michailidis; Maxwell D Leslie; Daniel V Sietsema; Tracy L Fetterly; Christopher A Dorst; Kamalendra Singh; Zhengqiang Wang; Michael A Parniak; Stefan G Sarafianos
Journal:  Antimicrob Agents Chemother       Date:  2012-01-17       Impact factor: 5.191

3.  Enzymatic Activities of RNase H Domains of HIV-1 Reverse Transcriptase with Substrate Binding Domains of Bacterial RNases H1 and H2.

Authors:  Etin-Diah Permanasari; Kiyoshi Yasukawa; Shigenori Kanaya
Journal:  Mol Biotechnol       Date:  2015-06       Impact factor: 2.695

4.  Eukaryotic RNases H1 act processively by interactions through the duplex RNA-binding domain.

Authors:  Sergei A Gaidamakov; Inna I Gorshkova; Peter Schuck; Peter J Steinbach; Hirofumi Yamada; Robert J Crouch; Susana M Cerritelli
Journal:  Nucleic Acids Res       Date:  2005-04-14       Impact factor: 16.971

  4 in total

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