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Expression, purification, crystallization and X-ray data collection for RAS and its mutants
This article expands on crystal structure data for human H-RAS with mutations at position Y137, briefly described in a paper on the effects of phosphorylation of Y137 by ABL kinases (Tyrosine phosphorylation of RAS by ABL allosterically enhances effector binding, published in the FASEB Journal [1])....
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4710794/ https://www.ncbi.nlm.nih.gov/pubmed/26866052 http://dx.doi.org/10.1016/j.dib.2015.12.007 |
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author | Johnson, Christian W. Buhrman, Greg Ting, Pamela Y. Colicelli, John Mattos, Carla |
author_facet | Johnson, Christian W. Buhrman, Greg Ting, Pamela Y. Colicelli, John Mattos, Carla |
author_sort | Johnson, Christian W. |
collection | PubMed |
description | This article expands on crystal structure data for human H-RAS with mutations at position Y137, briefly described in a paper on the effects of phosphorylation of Y137 by ABL kinases (Tyrosine phosphorylation of RAS by ABL allosterically enhances effector binding, published in the FASEB Journal [1]). The crystal structures of the Y137E mutant (phosphorylation mimic) and of the Y137F mutant (without the hydroxyl group where phosphorylation occurs) were deposited in the Protein Data Bank with PDB codes 4XVQ (H-RAS(Y137E)) and 4XVR (H-RAS(Y137F)). This article includes details for expression and purification of RAS and its mutants with no affinity tags, in vitro exchange of guanine nucleotides, protein crystallization, X-ray data collection and structure refinement. |
format | Online Article Text |
id | pubmed-4710794 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-47107942016-02-10 Expression, purification, crystallization and X-ray data collection for RAS and its mutants Johnson, Christian W. Buhrman, Greg Ting, Pamela Y. Colicelli, John Mattos, Carla Data Brief Data Article This article expands on crystal structure data for human H-RAS with mutations at position Y137, briefly described in a paper on the effects of phosphorylation of Y137 by ABL kinases (Tyrosine phosphorylation of RAS by ABL allosterically enhances effector binding, published in the FASEB Journal [1]). The crystal structures of the Y137E mutant (phosphorylation mimic) and of the Y137F mutant (without the hydroxyl group where phosphorylation occurs) were deposited in the Protein Data Bank with PDB codes 4XVQ (H-RAS(Y137E)) and 4XVR (H-RAS(Y137F)). This article includes details for expression and purification of RAS and its mutants with no affinity tags, in vitro exchange of guanine nucleotides, protein crystallization, X-ray data collection and structure refinement. Elsevier 2015-12-17 /pmc/articles/PMC4710794/ /pubmed/26866052 http://dx.doi.org/10.1016/j.dib.2015.12.007 Text en © 2015 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Data Article Johnson, Christian W. Buhrman, Greg Ting, Pamela Y. Colicelli, John Mattos, Carla Expression, purification, crystallization and X-ray data collection for RAS and its mutants |
title | Expression, purification, crystallization and X-ray data collection for RAS and its mutants |
title_full | Expression, purification, crystallization and X-ray data collection for RAS and its mutants |
title_fullStr | Expression, purification, crystallization and X-ray data collection for RAS and its mutants |
title_full_unstemmed | Expression, purification, crystallization and X-ray data collection for RAS and its mutants |
title_short | Expression, purification, crystallization and X-ray data collection for RAS and its mutants |
title_sort | expression, purification, crystallization and x-ray data collection for ras and its mutants |
topic | Data Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4710794/ https://www.ncbi.nlm.nih.gov/pubmed/26866052 http://dx.doi.org/10.1016/j.dib.2015.12.007 |
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