Chitranshi Nitin, Gupta Vivek, Dheer Yogita, Gupta Veer, Vander Wall Roshana, Graham Stuart
Faculty of Medicine and Health Sciences, Macquarie University, F10A, 2 Technology Place, North Ryde, NSW 2109, Australia.
School of Medical Sciences, Edith Cowan University, Perth, Australia.
Data Brief. 2016 Jan 16;6:776-82. doi: 10.1016/j.dib.2016.01.016. eCollection 2016 Mar.
TrkB is a high affinity receptor for the brain derived neurotrophic factor (BDNF) and its phosphorylation stimulates activation of several intracellular signalling pathways linked to cellular growth, differentiation and maintenance. Identification of various activators and inhibitors of the TrkB receptor and greater understanding their binding mechanisms is critical to elucidate the biochemical and pharmacological pathways and analyse various protein crystallization studies. The data presented here is related to the research article entitled "Brain Derived neurotrophic factor is involved in the regulation of glycogen synthase kinase 3β (GSK3β) signalling" [1]. Cyclotraxin B (CTXB) is a disulphide bridge linked cyclic peptide molecule that interacts with TrkB receptor and inhibits the BDNF/TrkB downstream signalling. This article reports for the first time binding mechanism and interaction parameters of CTXB with the TrkB receptor. The molecular model of CTXB has been generated and it's docking with TrkB domain carried out to determine the critical residues involved in the protein peptide interaction.
TrkB是脑源性神经营养因子(BDNF)的高亲和力受体,其磷酸化会刺激与细胞生长、分化和维持相关的多种细胞内信号通路的激活。鉴定TrkB受体的各种激活剂和抑制剂,并更深入地了解它们的结合机制,对于阐明生化和药理途径以及分析各种蛋白质结晶研究至关重要。此处呈现的数据与题为“脑源性神经营养因子参与糖原合酶激酶3β(GSK3β)信号通路的调节”的研究文章相关[1]。环孢素B(CTXB)是一种二硫键连接的环肽分子,它与TrkB受体相互作用并抑制BDNF/TrkB下游信号传导。本文首次报道了CTXB与TrkB受体的结合机制和相互作用参数。已生成CTXB的分子模型,并将其与TrkB结构域进行对接,以确定参与蛋白质-肽相互作用的关键残基。