p27Kip1 regulates cell cycle progression by modulating the expression of p21Cip1

ChEBI2016-06-09 更新2026-07-12 收录

细胞周期调控

蛋白质相互作用

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https://www.ebi.ac.uk/biostudies/ArrayExpress/studies/E-MTAB-2790 数据链接链接失效反馈

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p27Kip1 regulates cell cycle progression by modulating the expression of p21Cip1

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2016-06-09

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

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

蛋白质相互作用

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

Proteins co-precipitated with the EIF4AI wild-type.

蛋白质相互作用

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

DataSheet4_PRR11 promotes cell proliferation by regulating PTTG1 through interacting with E2F1 transcription factor in pan-cancer.zip

癌症分子机制

细胞周期调控

The upregulated proline rich 11 (PRR11) plays a critical role in cancer progression. The relevant biological functions of PRR11 in pan-cancer development are not well understood. In the current study,

NIAID Data Ecosystem30

Data Sheet 3_Using AlphaFold-Multimer to study novel protein-protein interactions of predation essential hypothetical proteins in Bdellovibrio.zip

蛋白质相互作用

细菌捕食机制

Bdellovibrio bacteriovorus is the most studied member of a group of small motile Gram-negative bacteria called Bdellovibrio and Like Organisms (BALOs). B. bacteriovorus can prey on Gram-negative bacte

NIAID Data Ecosystem00

p27Kip1 regulates cell cycle progression by modulating the expression of p21Cip1

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