Structural basis of divergent cyclin‐dependent kinase activation by Spy1/ RINGO proteins-Reference-Cited by-同舟云学术

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Structural basis of divergent cyclin‐dependent kinase activation by Spy1/ RINGO proteins

Published:2017-06-30 Issue:15 Volume:36 Page:2251-2262
ISSN:0261-4189
Container-title:The EMBO Journal
language:en
Short-container-title:EMBO J

Author:

McGrath Denise A¹,Fifield Bre‐Anne²,Marceau Aimee H¹,Tripathi Sarvind¹^ORCID,Porter Lisa A²,Rubin Seth M¹^ORCID

Affiliation:

1. Department of Chemistry and Biochemistry University of California Santa Cruz CA USA

2. Department of Biological Sciences University of Windsor Windsor ON Canada

Funder

Canadian Breast Cancer Foundation

Canadian Institutes of Health Research

American Cancer Society

National Cancer Institute

Publisher

EMBO

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,Molecular Biology,General Neuroscience

Link

https://onlinelibrary.wiley.com/doi/pdf/10.15252/embj.201796905

Reference55 articles.

1. Retinoblastoma Protein Contains a C-terminal Motif That Targets It for Phosphorylation by Cyclin-cdk Complexes

2. PHENIX: a comprehensive Python-based system for macromolecular structure solution

3. The Cyclin-dependent Kinase Activator, Spy1A, Is Targeted for Degradation by the Ubiquitin Ligase NEDD4

4. The cyclin-like protein Spy1/RINGO promotes mammary transformation and is elevated in human breast cancer

5. Direct interactions with both p27 and Cdk2 regulate Spy1-mediated proliferation in vivo and in vitro

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