Literature DB >> 31797816

Crystal structure of the Wheat dwarf virus Rep domain.

Blake A Everett1, Lauren A Litzau1, Kassidy Tompkins1, Ke Shi1, Andrew Nelson1, Hideki Aihara1, Robert L Evans Iii1, Wendy R Gordon1.   

Abstract

The Rep domain of Wheat dwarf virus (WDV Rep) is an HUH endonuclease involved in rolling-circle replication. HUH endonucleases coordinate a metal ion to enable the nicking of a specific ssDNA sequence and the subsequent formation of an intermediate phosphotyrosine bond. This covalent protein-ssDNA adduct makes HUH endonucleases attractive fusion tags (HUH-tags) in a diverse number of biotechnological applications. Solving the structure of an HUH endonuclease in complex with ssDNA will provide critical information about ssDNA recognition and sequence specificity, thus enabling rationally engineered protein-DNA interactions that are programmable. The structure of the WDV Rep domain reported here was solved in the apo state from a crystal diffracting to 1.24 Å resolution and represents an initial step in the direction of solving the structure of a protein-ssDNA complex.

Entities:  

Keywords:  HUH motif; HUH-tag; Rep domain; Wheat dwarf virus; crystal structure; engineered protein–ssDNA complexes; ssDNA

Mesh:

Substances:

Year:  2019        PMID: 31797816      PMCID: PMC6891580          DOI: 10.1107/S2053230X19015796

Source DB:  PubMed          Journal:  Acta Crystallogr F Struct Biol Commun        ISSN: 2053-230X            Impact factor:   1.056


  22 in total

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  1 in total

1.  Molecular underpinnings of ssDNA specificity by Rep HUH-endonucleases and implications for HUH-tag multiplexing and engineering.

Authors:  Kassidy J Tompkins; Mo Houtti; Lauren A Litzau; Eric J Aird; Blake A Everett; Andrew T Nelson; Leland Pornschloegl; Lidia K Limón-Swanson; Robert L Evans; Karen Evans; Ke Shi; Hideki Aihara; Wendy R Gordon
Journal:  Nucleic Acids Res       Date:  2021-01-25       Impact factor: 16.971

  1 in total

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