Interaction of wild-type S100A4 with ezrin constructs<sup>*</sup>.

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癌症转移机制

数据链接：

https://figshare.com/articles/dataset/Interaction_of_wild-type_S100A4_with_ezrin_constructs_sup_sup_/5000231 数据链接链接失效反馈

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Interaction of wild-type S100A4 with ezrin constructs*.

创建时间：

2017-05-12

Activated FGFR3:p-FRS2:p-PPTN11 binds GRB2:GAB1:PI3KR1

蛋白质相互作用

生物信息学

This event has been computationally inferred from an event that has been demonstrated in another species. The inference is based on the homology mapping from PANTHER. Briefly, reactions for which al

reactome.org90

shRNAi profiling of human MDA-MB-231 cells expressing anti-p53 (shp53) short-hairpin RNAs treated with TFGbeta or control

癌症转移机制

转录组功能分析

TGFβ ligands act as tumor suppressors in early stage tumors but are paradoxically diverted into potent prometastatic factors in advanced cancers. The molecular nature of this switch remains enigmatic.

NIAID Data Ecosystem30

Proteins co-precipitated with the EIF4AI wild-type.

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亲和纯化质谱

Only proteins represented by a minimum of two peptides in at least two of the replicates from the bait and with an enrichment ratio in comparison with the control equal to or greater than 1.5 were con

NIAID Data Ecosystem00

Validation by comparing NBEL algorithm with naïve Bayes via two human datasets.

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算法验证

In table 3, indicates the total number of protein pairs in a database that are overlapped with our collected 79,441 human PPIs; indicates the number of protein pairs in that are predicted by NBEL;

NIAID Data Ecosystem80

Table 5_Successful prediction of LC8 binding to intrinsically disordered proteins sheds light on AlphaFold’s black box.xlsx

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结构生物信息学

IntroductionLC8 is a hub protein involved in many processes from tumor suppression and cell cycle regulation to neurotransmission and viral infection. Despite recent progress, prediction of binding si

NIAID Data Ecosystem00

Interaction of wild-type S100A4 with ezrin constructs<sup>*</sup>.

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