The NMR‐based characterization of the FTY720‐SET complex reveals an alternative mechanism for the attenuation of the inhibitory SET‐PP2A interaction

Author:

De Palma Ryan M.12,Parnham Stuart R.3,Li Yitong4,Oaks Joshua J.5,Peterson Yuri K.6,Szulc Zdzislaw M.12,Roth Braden M.12,Xing Yongna4,Ogretmen Besim12

Affiliation:

1. Department of Biochemistry and Molecular BiologyMedical University of South CarolinaCharlestonSouth CarolinaUSA

2. Hollings Cancer CenterMedical University of South CarolinaCharlestonSouth CarolinaUSA

3. Department of Biochemistry and BiophysicsUniversity of North Carolina–Chapel HillChapel HillNorth CarolinaUSA

4. McArdle Laboratory for Cancer ResearchUniversity of Wisconsin–MadisonMadisonWisconsinUSA

5. Phanes TherapeuticsSan DiegoCaliforniaUSA

6. Department of Drug Discovery and Biomedical SciencesMedical University of South CarolinaCharlestonSouth CarolinaUSA

Funder

National Institutes of Health

National Cancer Institute

National Institute of Dental and Craniofacial Research

National Center for Research Resources

Hollings Cancer Center, Medical University of South Carolina

Publisher

Wiley

Subject

Genetics,Molecular Biology,Biochemistry,Biotechnology

Cited by 33 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Emerging Roles of B56 Phosphorylation and Binding Motif in PP2A-B56 Holoenzyme Biological Function;International Journal of Molecular Sciences;2024-03-10

2. PP2A complex disruptor SET prompts widespread hypertranscription of growth-essential genes in the pancreatic cancer cells;Science Advances;2024-01-26

3. Pharmacological Effects of FTY720 and its Derivatives;Current Topics in Medicinal Chemistry;2024-01

4. The next decade of SET: from an oncoprotein to beyond;Journal of Molecular Cell Biology;2023-12-29

5. Putting a Novel Emphysema Treatment on the SMAP;American Journal of Respiratory Cell and Molecular Biology;2023-11

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