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Structural and Functional Analysis of the Engineered Type I DNA Methyltransferase EcoR124I(NT)
The Type I R–M system EcoR124I is encoded by three genes. HsdM is responsible for modification (DNA methylation), HsdS for DNA sequence specificity and HsdR for restriction endonuclease activity. The trimeric methyltransferase (M(2)S) recognises the asymmetric sequence (GAAN(6)RTCG). An engineered R...
Autores principales: | , , , |
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Formato: | Texto |
Lenguaje: | English |
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Elsevier
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2877798/ https://www.ncbi.nlm.nih.gov/pubmed/20302878 http://dx.doi.org/10.1016/j.jmb.2010.03.008 |
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author | Taylor, James E.N. Callow, Phil Swiderska, Anna Kneale, G. Geoff |
author_facet | Taylor, James E.N. Callow, Phil Swiderska, Anna Kneale, G. Geoff |
author_sort | Taylor, James E.N. |
collection | PubMed |
description | The Type I R–M system EcoR124I is encoded by three genes. HsdM is responsible for modification (DNA methylation), HsdS for DNA sequence specificity and HsdR for restriction endonuclease activity. The trimeric methyltransferase (M(2)S) recognises the asymmetric sequence (GAAN(6)RTCG). An engineered R–M system, denoted EcoR124I(NT), has two copies of the N-terminal domain of the HsdS subunit of EcoR124I, instead of a single S subunit with two domains, and recognises the symmetrical sequence GAAN(7)TTC. We investigate the methyltransferase activity of EcoR124I(NT), characterise the enzyme and its subunits by analytical ultracentrifugation and obtain low-resolution structural models from small-angle neutron scattering experiments using contrast variation and selective deuteration of subunits. |
format | Text |
id | pubmed-2877798 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-28777982010-06-21 Structural and Functional Analysis of the Engineered Type I DNA Methyltransferase EcoR124I(NT) Taylor, James E.N. Callow, Phil Swiderska, Anna Kneale, G. Geoff J Mol Biol Article The Type I R–M system EcoR124I is encoded by three genes. HsdM is responsible for modification (DNA methylation), HsdS for DNA sequence specificity and HsdR for restriction endonuclease activity. The trimeric methyltransferase (M(2)S) recognises the asymmetric sequence (GAAN(6)RTCG). An engineered R–M system, denoted EcoR124I(NT), has two copies of the N-terminal domain of the HsdS subunit of EcoR124I, instead of a single S subunit with two domains, and recognises the symmetrical sequence GAAN(7)TTC. We investigate the methyltransferase activity of EcoR124I(NT), characterise the enzyme and its subunits by analytical ultracentrifugation and obtain low-resolution structural models from small-angle neutron scattering experiments using contrast variation and selective deuteration of subunits. Elsevier 2010-05-07 /pmc/articles/PMC2877798/ /pubmed/20302878 http://dx.doi.org/10.1016/j.jmb.2010.03.008 Text en © 2010 Elsevier Ltd. . https://creativecommons.org/licenses/by/3.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/3.0/). |
spellingShingle | Article Taylor, James E.N. Callow, Phil Swiderska, Anna Kneale, G. Geoff Structural and Functional Analysis of the Engineered Type I DNA Methyltransferase EcoR124I(NT) |
title | Structural and Functional Analysis of the Engineered Type I DNA Methyltransferase EcoR124I(NT) |
title_full | Structural and Functional Analysis of the Engineered Type I DNA Methyltransferase EcoR124I(NT) |
title_fullStr | Structural and Functional Analysis of the Engineered Type I DNA Methyltransferase EcoR124I(NT) |
title_full_unstemmed | Structural and Functional Analysis of the Engineered Type I DNA Methyltransferase EcoR124I(NT) |
title_short | Structural and Functional Analysis of the Engineered Type I DNA Methyltransferase EcoR124I(NT) |
title_sort | structural and functional analysis of the engineered type i dna methyltransferase ecor124i(nt) |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2877798/ https://www.ncbi.nlm.nih.gov/pubmed/20302878 http://dx.doi.org/10.1016/j.jmb.2010.03.008 |
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