(1)H, (13)C and (15)N resonance assignments for the tandem CUE domains from chromatin remodeler SMARCAD1

SMARCAD1 is a non-canonical chromatin remodelling ATPase, unique in its domain organization in that is encodes tandem ubiquitin binding CUE domains along with a classical SNF2 helicase ATP-dependent motor. SMARCAD1 is conserved from yeast to humans and has reported roles in the maintenance of hetero...

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Autores principales: Biasutto, Antonio J., West, Philip M., Mancini, Erika J., Redfield, Christina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Netherlands 2019
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6713675/
https://www.ncbi.nlm.nih.gov/pubmed/30919308
http://dx.doi.org/10.1007/s12104-019-09888-9
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author Biasutto, Antonio J.
West, Philip M.
Mancini, Erika J.
Redfield, Christina
author_facet Biasutto, Antonio J.
West, Philip M.
Mancini, Erika J.
Redfield, Christina
author_sort Biasutto, Antonio J.
collection PubMed
description SMARCAD1 is a non-canonical chromatin remodelling ATPase, unique in its domain organization in that is encodes tandem ubiquitin binding CUE domains along with a classical SNF2 helicase ATP-dependent motor. SMARCAD1 is conserved from yeast to humans and has reported roles in the maintenance of heterochromatin following replication and in double-strand break repair. Here we present the (1)H, (13)C and (15)N assignments for the tandem CUE domains and for the disordered regions that flank them. These assignments provide the starting point for detailed investigations of the structure and interactions of this region of SMARCAD1.
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spelling pubmed-67136752019-09-13 (1)H, (13)C and (15)N resonance assignments for the tandem CUE domains from chromatin remodeler SMARCAD1 Biasutto, Antonio J. West, Philip M. Mancini, Erika J. Redfield, Christina Biomol NMR Assign Article SMARCAD1 is a non-canonical chromatin remodelling ATPase, unique in its domain organization in that is encodes tandem ubiquitin binding CUE domains along with a classical SNF2 helicase ATP-dependent motor. SMARCAD1 is conserved from yeast to humans and has reported roles in the maintenance of heterochromatin following replication and in double-strand break repair. Here we present the (1)H, (13)C and (15)N assignments for the tandem CUE domains and for the disordered regions that flank them. These assignments provide the starting point for detailed investigations of the structure and interactions of this region of SMARCAD1. Springer Netherlands 2019-03-27 2019 /pmc/articles/PMC6713675/ /pubmed/30919308 http://dx.doi.org/10.1007/s12104-019-09888-9 Text en © The Author(s) 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Article
Biasutto, Antonio J.
West, Philip M.
Mancini, Erika J.
Redfield, Christina
(1)H, (13)C and (15)N resonance assignments for the tandem CUE domains from chromatin remodeler SMARCAD1
title (1)H, (13)C and (15)N resonance assignments for the tandem CUE domains from chromatin remodeler SMARCAD1
title_full (1)H, (13)C and (15)N resonance assignments for the tandem CUE domains from chromatin remodeler SMARCAD1
title_fullStr (1)H, (13)C and (15)N resonance assignments for the tandem CUE domains from chromatin remodeler SMARCAD1
title_full_unstemmed (1)H, (13)C and (15)N resonance assignments for the tandem CUE domains from chromatin remodeler SMARCAD1
title_short (1)H, (13)C and (15)N resonance assignments for the tandem CUE domains from chromatin remodeler SMARCAD1
title_sort (1)h, (13)c and (15)n resonance assignments for the tandem cue domains from chromatin remodeler smarcad1
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6713675/
https://www.ncbi.nlm.nih.gov/pubmed/30919308
http://dx.doi.org/10.1007/s12104-019-09888-9
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