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蛋白质序列和结构的保守性与其功能的关系 被引量:12
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作者 黄京飞 tom l.blundell 《Zoological Research》 CAS CSCD 1999年第1期21-25,共5页
以蛋白质酪氨酸磷酸酶为模型,通过序列和结构的比较,对蛋白质序列、结构的保守性与其功能和进化的关系问题进行了研究。结果显示,虽然在酪氨酸磷酸酶超家族分子的序列中,仅有3个与其催化功能密切相关的残基是高度保守的,但它们功... 以蛋白质酪氨酸磷酸酶为模型,通过序列和结构的比较,对蛋白质序列、结构的保守性与其功能和进化的关系问题进行了研究。结果显示,虽然在酪氨酸磷酸酶超家族分子的序列中,仅有3个与其催化功能密切相关的残基是高度保守的,但它们功能结构域的核心拓扑结构却明显类似,其中存在着βαβ和βαβα2个保守的结构单元;此外,它们活性位点的拓扑结构也极其相似。因此,在保持蛋白质功能方面具有重要作用的残基是高度保守的,而具维持蛋白质结构作用的残基则是相对保守的。在进化过程中,蛋白质三维拓扑结构的保守性,似乎主要是体现在保持某些共同的特有二级结构单元和共同的折叠方式上。 展开更多
关键词 酪氨酸磷酸酶 保守性 功能 进化 蛋白质结构
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Crystal structure,biochemical and biophysical characterisation of NHR1 domain of E3 Ubiquitin ligase neutralized
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作者 Deepti Gupta Sylvie Beaufils +5 位作者 Veronique Vie Gilles Paboeuf Bill Broadhurst Francois Schweisguth tom l.blundell Victor M.Bolanos-Garcia 《Advances in Enzyme Research》 2013年第3期61-75,共15页
Notch signaling controls diverse developmental decisions of central importance to cell activity. One of the conserved positive regulators of Notch signaling is Neuralized, the E3 Ubiquitin ligase enzyme that regulates... Notch signaling controls diverse developmental decisions of central importance to cell activity. One of the conserved positive regulators of Notch signaling is Neuralized, the E3 Ubiquitin ligase enzyme that regulates signaling activity by endocytosis. Neuralized has two novel repeats, NHR1 and NHR2, with a RING finger motif at the C-terminus. Both endocytosis of the Notch ligand, Delta, and inhibition of Notch signaling by Tom, a bearded family member, require the NHR1 domain. Here we describe the first crystal structure of NHR1 domain from Drosophila melanogaster, solved to 2.1 A resolution by X-ray analysis. Using NMR and other biophysical techniques we define a minimal binding region of Tom, consisting of 12 residues, which interacts with NHR1 and show by interfacial analysis of protein monolayers that NHR1 binds PI4P. Taken together, the studies provide insight into molecular interactions that are important for Notch signaling. 展开更多
关键词 NOTCH Signaling Neuralized NHR1 Bearded TOM ENDOCYTOSIS NEUROGENESIS
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The crystal structure of fibroblast growth factor 18 (FGF18)
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作者 Alan Brown Lucy E.Adam tom l.blundell 《Protein & Cell》 SCIE CAS CSCD 2014年第5期343-347,共5页
Dear Editor, Fibroblast growth factors (FGFs) regulate a plethora of crit- ical processes in development (Beenken and Mohammadi, 2009). These processes are mediated by signaling through four FGF receptors (FGFR1-... Dear Editor, Fibroblast growth factors (FGFs) regulate a plethora of crit- ical processes in development (Beenken and Mohammadi, 2009). These processes are mediated by signaling through four FGF receptors (FGFR1-4), which are high-affinity cell surface receptor tyrosine kinases. Receptors 1-3 undergo alternative splicing to generate b- and c-isoforms with altered ligand specificities and affinities. Ligand to receptor binding is not unique and one receptor can be activated by several FGFs. Heparan sulfate (HS) proteoglycan, a variably poly- sulfated glycosaminoglycan related to heparin, is an essential requirement for FGF signaling with FGFs varying in their specificities for different HS sulfation patterns (Galla- gher et al., 1992). 展开更多
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