Structural and functional consequences of the STAT5BN642H driver mutation
Hyper-activated STAT5B and its disease-causing variants are of interest as cancer drug targets. Here the authors combine cell based studies, X-ray crystallography, biophysical experiments and MD simulations to structurally and functionally characterize the STAT5BN642H mutant found in aggressive T-ce...
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2019
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oai:doaj.org-article:f8b672c48f8f4b91911646f53ce84f0b2021-12-02T16:57:08ZStructural and functional consequences of the STAT5BN642H driver mutation10.1038/s41467-019-10422-72041-1723https://doaj.org/article/f8b672c48f8f4b91911646f53ce84f0b2019-06-01T00:00:00Zhttps://doi.org/10.1038/s41467-019-10422-7https://doaj.org/toc/2041-1723Hyper-activated STAT5B and its disease-causing variants are of interest as cancer drug targets. Here the authors combine cell based studies, X-ray crystallography, biophysical experiments and MD simulations to structurally and functionally characterize the STAT5BN642H mutant found in aggressive T-cell leukemia and lymphomas and find that it has an increased affinity for self-dimerization.Elvin D. de AraujoFettah ErdoganHeidi A. NeubauerDeniz Meneksedag-ErolPimyupa ManaswiyoungkulMohammad S. EramHyuk-Soo SeoAbdul K. QadreeJohan IsraelianAnna OrlovaTobias SuskeHa T. T. PhamAuke BoersmaSimone TangermannLukas KennerThomas RülickeAiping DongManimekalai RavichandranPeter J. BrownGerald F. AudetteSarah RauscherSirano Dhe-PaganonRichard MorigglPatrick T. GunningNature PortfolioarticleScienceQENNature Communications, Vol 10, Iss 1, Pp 1-15 (2019) |
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Science Q Elvin D. de Araujo Fettah Erdogan Heidi A. Neubauer Deniz Meneksedag-Erol Pimyupa Manaswiyoungkul Mohammad S. Eram Hyuk-Soo Seo Abdul K. Qadree Johan Israelian Anna Orlova Tobias Suske Ha T. T. Pham Auke Boersma Simone Tangermann Lukas Kenner Thomas Rülicke Aiping Dong Manimekalai Ravichandran Peter J. Brown Gerald F. Audette Sarah Rauscher Sirano Dhe-Paganon Richard Moriggl Patrick T. Gunning Structural and functional consequences of the STAT5BN642H driver mutation |
description |
Hyper-activated STAT5B and its disease-causing variants are of interest as cancer drug targets. Here the authors combine cell based studies, X-ray crystallography, biophysical experiments and MD simulations to structurally and functionally characterize the STAT5BN642H mutant found in aggressive T-cell leukemia and lymphomas and find that it has an increased affinity for self-dimerization. |
format |
article |
author |
Elvin D. de Araujo Fettah Erdogan Heidi A. Neubauer Deniz Meneksedag-Erol Pimyupa Manaswiyoungkul Mohammad S. Eram Hyuk-Soo Seo Abdul K. Qadree Johan Israelian Anna Orlova Tobias Suske Ha T. T. Pham Auke Boersma Simone Tangermann Lukas Kenner Thomas Rülicke Aiping Dong Manimekalai Ravichandran Peter J. Brown Gerald F. Audette Sarah Rauscher Sirano Dhe-Paganon Richard Moriggl Patrick T. Gunning |
author_facet |
Elvin D. de Araujo Fettah Erdogan Heidi A. Neubauer Deniz Meneksedag-Erol Pimyupa Manaswiyoungkul Mohammad S. Eram Hyuk-Soo Seo Abdul K. Qadree Johan Israelian Anna Orlova Tobias Suske Ha T. T. Pham Auke Boersma Simone Tangermann Lukas Kenner Thomas Rülicke Aiping Dong Manimekalai Ravichandran Peter J. Brown Gerald F. Audette Sarah Rauscher Sirano Dhe-Paganon Richard Moriggl Patrick T. Gunning |
author_sort |
Elvin D. de Araujo |
title |
Structural and functional consequences of the STAT5BN642H driver mutation |
title_short |
Structural and functional consequences of the STAT5BN642H driver mutation |
title_full |
Structural and functional consequences of the STAT5BN642H driver mutation |
title_fullStr |
Structural and functional consequences of the STAT5BN642H driver mutation |
title_full_unstemmed |
Structural and functional consequences of the STAT5BN642H driver mutation |
title_sort |
structural and functional consequences of the stat5bn642h driver mutation |
publisher |
Nature Portfolio |
publishDate |
2019 |
url |
https://doaj.org/article/f8b672c48f8f4b91911646f53ce84f0b |
work_keys_str_mv |
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