Academic Journal

RET Functions as a Dual-Specificity Kinase that Requires Allosteric Inputs from Juxtamembrane Elements

التفاصيل البيبلوغرافية
العنوان: RET Functions as a Dual-Specificity Kinase that Requires Allosteric Inputs from Juxtamembrane Elements
المؤلفون: Iván Plaza-Menacho, Karin Barnouin, Rachael Barry, Annabel Borg, Mariam Orme, Rakhee Chauhan, Stephane Mouilleron, Rubén J. Martínez-Torres, Pascal Meier, Neil Q. McDonald
المصدر: Cell Reports, Vol 17, Iss 12, Pp 3319-3332 (2016)
بيانات النشر: Elsevier, 2016.
سنة النشر: 2016
المجموعة: LCC:Biology (General)
مصطلحات موضوعية: receptor tyrosine kinase, RTK, structure-function, phosphorylation, dual-specificity, signaling, oncogene, Drosophila, Biology (General), QH301-705.5
الوصف: Receptor tyrosine kinases exhibit a variety of activation mechanisms despite highly homologous catalytic domains. Such diversity arises through coupling of extracellular ligand-binding portions with highly variable intracellular sequences flanking the tyrosine kinase domain and specific patterns of autophosphorylation sites. Here, we show that the juxtamembrane (JM) segment enhances RET catalytic domain activity through Y687. This phospho-site is also required by the JM region to rescue an otherwise catalytically deficient RET activation-loop mutant lacking tyrosines. Structure-function analyses identified interactions between the JM hinge, αC helix, and an unconventional activation-loop serine phosphorylation site that engages the HRD motif and promotes phospho-tyrosine conformational accessibility and regulatory spine assembly. We demonstrate that this phospho-S909 arises from an intrinsic RET dual-specificity kinase activity and show that an equivalent serine is required for RET signaling in Drosophila. Our findings reveal dual-specificity and allosteric components for the mechanism of RET activation and signaling with direct implications for drug discovery.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 2211-1247
Relation: http://www.sciencedirect.com/science/article/pii/S2211124716316345; https://doaj.org/toc/2211-1247
DOI: 10.1016/j.celrep.2016.11.061
URL الوصول: https://doaj.org/article/d79f670d6e0b48388c49a0287b96fbce
رقم الانضمام: edsdoj.79f670d6e0b48388c49a0287b96fbce
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:22111247
DOI:10.1016/j.celrep.2016.11.061