نتایج جستجو برای: cdk2

تعداد نتایج: 2662  

Journal: :Journal of cell science 2009
Alberto Viera Julio S Rufas Inés Martínez José L Barbero Sagrario Ortega José A Suja

Cyclin-dependent kinase 2 (CDK2) was assumed to be essential in the mammalian cell cycle both at the G1-S transition and throughout the S phase. Interestingly, ablation of Cdk2 in mice does not have substantial consequences for embryonic or postnatal development, but both males and females are infertile. In the present study, we have analysed the meiotic alterations leading to infertility in Cd...

پایان نامه :وزارت علوم، تحقیقات و فناوری - دانشگاه شیراز - دانشکده علوم پایه 1391

از ویژگی‎های پروتئین‏ کینازهای یوکاریوتیک، وجود دو ناحیه ساختاری با هم تکامل‏یافته قطعه فعال‎کننده و زیردمین ghi می‏باشد. قطعه فعال‎کننده بین و شامل دو موتیف حفاظت‏شده آسپارتات-فنیل‏آلانین-گلیسین (dfg) و آلانین-پرولین-گلوتامات (ape) می‏باشد و زیردمین ghi نیز از مارپیچ‏های g، h و i تشکیل شده است. این دو قطعه توسط پل‏نمکی حفاظت‏شده‏‏ایی که بین گلوتامیک‎اسید موتیف ape و آرژنینی که در زیردمین ghi ق...

2013
Dariush Etemadmoghadam George Au-Yeung Meaghan Wall Chris Mitchell Maya Kansara Elizabeth Loehrer Crisoula Batzios Joshy George Sarah Ftouni Barbara A. Weir Scott Carter Irma Gresshoff Linda Mileshkin Danny Rischin William C. Hahn Paul M. Waring Gad Getz Carleen Cullinane Lynda J. Campbell David D. Bowtell

Purpose: Amplification of cyclin E1 (CCNE1) is associated with poor outcome in breast, lung, and other solid cancers, and is themost prominent structural variant associatedwith primary treatment failure in highgrade serous ovarian cancer (HGSC). We have previously shown that CCNE1-amplified tumors show amplicon-dependent sensitivity to CCNE1 suppression. Here, we explore targeting CDK2 as a nov...

2007
Fang Yu Judit Megyesi Robert L. Safirstein Peter M. Price

E2F1 is a key regulator that links cell cycle progression and cell death. E2F1 activity is controlled by Cdk2-cyclin complexes via several mechanisms, such as phosphorylation of retinoblastoma protein (pRb) to release E2F1, direct phosphorylation, and stable physical interaction. We have demonstrated that cisplatin cytotoxicity depends on Cdk2 activity, and Cdk2 inhibition protects kidney cells...

Journal: :The EMBO journal 1998
K Alevizopoulos B Catarin J Vlach B Amati

We show here that the adenovirus E1A oncoprotein prevents growth arrest by the CDK2 inhibitor p27(Kip1) (p27) in rodent fibroblasts. However, E1A neither binds p27 nor prevents inhibition of CDK2 complexes in vivo. In contrast, the amount of free p27 available to inhibit cyclin E/CDK2 is increased in E1A-expressing cells, owing to reduced expression of cyclins D1 and D3. Moreover, E1A allows ce...

Journal: :Journal of virology 2003
Wanxia He Doug Staples Clark Smith Chris Fisher

Addition of human papillomavirus (HPV) E7 CDK2/cyclin A or CDK2/cyclin E, purified from either insect cells or bacteria, dramatically upregulates histone H1 kinase activity. Activation is substrate specific, with a smaller effect noted for retinoblastoma protein (Rb). The CDK2 stimulatory activity is equivalent in high-risk (HPV type 16 [HPV16] and HPV31) and low-risk (HPV6b) E7. Mutational ana...

2015
Elizabeth Anscombe Elisa Meschini Regina Mora-Vidal Mathew P. Martin David Staunton Matthis Geitmann U. Helena Danielson Will A. Stanley Lan Z. Wang Tristan Reuillon Bernard T. Golding Celine Cano David R. Newell Martin E.M. Noble Stephen R. Wedge Jane A. Endicott Roger J. Griffin

Irreversible inhibitors that modify cysteine or lysine residues within a protein kinase ATP binding site offer, through their distinctive mode of action, an alternative to ATP-competitive agents. 4-((6-(Cyclohexylmethoxy)-9H-purin-2-yl)amino)benzenesulfonamide (NU6102) is a potent and selective ATP-competitive inhibitor of CDK2 in which the sulfonamide moiety is positioned close to a pair of ly...

Journal: :Cell 2007
Isabel Chu Jun Sun Angel Arnaout Harriette Kahn Wedad Hanna Steven Narod Ping Sun Cheng-Keat Tan Ludger Hengst Joyce Slingerland

The kinase inhibitor p27Kip1 regulates the G1 cell cycle phase. Here, we present data indicating that the oncogenic kinase Src regulates p27 stability through phosphorylation of p27 at tyrosine 74 and tyrosine 88. Src inhibitors increase cellular p27 stability, and Src overexpression accelerates p27 proteolysis. Src-phosphorylated p27 is shown to inhibit cyclin E-Cdk2 poorly in vitro, and Src t...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2013
Bridget T Hughes Julia Sidorova Jherek Swanger Raymond J Monnat Bruce E Clurman

Cyclin-dependent kinases (Cdks) coordinate cell division, and their activities are tightly controlled. Phosphorylation of threonine 14 (T14) and tyrosine 15 (Y15) inhibits Cdks and regulates their activities in numerous physiologic contexts. Although the roles of Cdk1 inhibitory phosphorylation during mitosis are well described, studies of Cdk2 inhibitory phosphorylation during S phrase have la...

Journal: :American journal of physiology. Cell physiology 1998
Qing-Ming Ding Tien C Ko B Mark Evers

The cellular mechanisms regulating intestinal proliferation and differentiation remain largely undefined. Previously, we showed an early induction of the cyclin-dependent kinase (CDK) inhibitor p21Waf1/Cip1 in Caco-2 cells, a human colon cancer line that spontaneously differentiates into a small bowel phenotype. The purpose of our present study was to assess the timing of cell cycle arrest in r...

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