The consensus motif for phosphorylation by cyclin D1‐Cdk4 is different from that for phosphorylation by cyclin A/E‐Cdk2.

…, H Higashi, HK Jung, I SuzukiTakahashi… - The EMBO …, 1996 - embopress.org
Cyclin D‐Cdk4/6 and cyclin A/E‐Cdk2 are suggested to be involved in phosphorylation of
the retinoblastoma protein (pRB) during the G1/S transition of the cell cycle. However, it is …

Structure-Based Generation of a New Class of Potent Cdk4 Inhibitors:  New de Novo Design Strategy and Library Design

…, C Ikeura, M Ikuta, I Suzuki-Takahashi… - Journal of Medicinal …, 2001 - ACS Publications
As a first step in structure-based design of highly selective and potent Cdk4 inhibitors, we
performed structure-based generation of a novel series of Cdk4 inhibitors. A Cdk4 homology …

Butyrolactone I, a selective inhibitor of cdk2 and cdc2 kinase.

…, T Okabe, H Ogino, H Matsumoto, I Suzuki-Takahashi… - Oncogene, 1993 - europepmc.org
We screened cdc2 kinase inhibitors from cultured mediums of micro organisms using purified
mouse cyclin B-cdc2 kinase and a specific substrate peptide for cdc2 kinase. A selective …

A novel approach for the development of selective Cdk4 inhibitors: library design based on locations of Cdk4 specific amino acid residues

…, C Ikeura, M Ikuta, I Suzuki-Takahashi… - Journal of medicinal …, 2001 - ACS Publications
Identification of a selective inhibitor for a particular protein kinase without inhibition of other
kinases is critical for use as a biological tool or drug. However, this is very difficult because …

[HTML][HTML] Crystallographic approach to identification of cyclin-dependent kinase 4 (CDK4)-specific inhibitors by using CDK4 mimic CDK2 protein

…, T Machida, H Hirai, I Suzuki-Takahashi… - Journal of Biological …, 2001 - ASBMB
Genetic alteration of one or more components of the p16 INK4A -CDK4,6/cyclin D-retinoblastoma
pathway is found in more than half of all human cancers. Therefore, CDK4 is an …

Phosphorylation of E2F-1 by cyclin A-cdk2.

M Kitagawa, H Higashi, I Suzuki-Takahashi, K Segawa… - Oncogene, 1995 - europepmc.org
Transcription factor E2F-1 has a putative consensus sequence for phosphorylation by cyclin
dependent kinase (Ser-Pro-X-Lys/Arg). Therefore, we studied the phosphorylation of E2F-1 …

The K252a derivatives, inhibitors for the PAK/MLK kinase family, selectively block the growth of HAS transformants

…, L Florin, ML Schmitz, I Suzuki-Takahashi… - The Cancer …, 2002 - journals.lww.com
BACKGROUND Oncogenic RAS mutants such as v-Ha-RAS activate members of Rac/CDC42-dependent
kinases (PAKs) and appear to contribute to the development of more than 30…

Preferences for Phosphorylation Sites in the Retinoblastoma Protein of D-Type Cyclin–Dependent Kinases, Cdk4 and Cdk6, In Vitro

T Takaki, K Fukasawa, I Suzuki-Takahashi… - Journal of …, 2005 - academic.oup.com
D-type cyclin–dependent kinases (Cdk4 and Cdk6) regulate the G1 to S phase progression
of the mammalian cell cycle. It has been suggested that Cdk4 and Cdk6 may have distinct …

The interactions of E2F with pRB and with p107 are regulated via the phosphorylation of pRB and p107 by a cyclin-dependent kinase.

I Suzuki-Takahashi, M Kitagawa, M Saijo, H Higashi… - Oncogene, 1995 - europepmc.org
It has been postulated that the product (pRB) of the retinoblastoma gene dissociates from
the E2F-pRB complex upon phosphorylation by cyclin-dependent kinase (s)(cdk). However, …

Cdk-mediated phosphorylation of pRB regulates HDAC binding in vitro

T Takaki, K Fukasawa, I Suzuki-Takahashi… - … and biophysical research …, 2004 - Elsevier
Retinoblastoma protein (pRB) controls the G1/S transition in the cell cycle by binding and
inactivating E2F transcription factor. pRB changes the chromatin structure at the E2F-…