Results 11 to 20 of about 684,735 (325)
Adapalene inhibits the activity of cyclin-dependent kinase 2 in colorectal carcinoma. [PDF]
Cyclin-dependent kinase 2 (CDK2) has been reported to be overexpressed in human colorectal cancer; it is responsible for the G1‑to‑S‑phase transition in the cell cycle and its deregulation is a hallmark of cancer. The present study was the first to use idock, a free and open‑source protein‑ligand docking software developed by our group, to identify ...
Shi XN+7 more
europepmc +5 more sources
Phosphorylation of cyclin-dependent kinase 2 peptides enhances metal binding [PDF]
The cyclin-dependent kinase CDK2 is inactivated by phosphorylation on either of the two neighbouring residues Thr14 or Tyr15. The effect of phosphorylation on metal ion binding has been investigated with peptides incorporating residues 6-20 of CDK2. The stoichiometry of Ca(2+) binding increased from 1 in the un- and singly-phosphorylated peptides to 2 ...
Graham S. Baldwin
openalex +4 more sources
COMPUTATIONAL STUDY OF THE INTERACTION BETWEEN INDENE PYRAZOLE AND CYCLIN DEPENDENT KINASE 2
Proteins have been traditionally out of reach of electronic structure methods. But with technological advances in the development of powerful computers and the need to extend the methods of computational chemistry to problems of biological interest, such
Juan Enrique Torres+4 more
doaj +4 more sources
Coupling function of cyclin-dependent kinase 2 and Septin2 in the promotion of hepatocellular carcinoma. [PDF]
Hepatocellular carcinoma (HCC) is a common and aggressive malignant tumor with a poorly defined molecular mechanism. Cyclin‐dependent kinase 2 (CDK2) and Septin2 (SEPT2) are 2 known oncogenic molecules but the mechanism of functional interactions remains unclear.
Xu C+10 more
europepmc +5 more sources
A Simple and Efficient Docking Method to the Cyclin-Dependent Kinase 2 [PDF]
The subtle but significant differences and thereby the lack of consensus in active site structures among the crystal structures of cyclin-dependent kinase 2 (CDK2) has hampered structure-based drug design. In this study, we devised a simple but effective ‘mutation, pharmacophore-guided docking, followed by mutation' strategy to generate an “average ...
Kwang‐Su Park+3 more
openalex +4 more sources
Binding Study of Naringenin Derivatives and Cyclin Dependent Kinase 2 [PDF]
Among several classes ofphenolic compounds, a group with the core structure of C6-C3-C6 is named flavonoids (benzo-γ-pyran derivatives),consisting of phenolic and pyran rings. According to theoxidation state of pyran ring, flavonoids can be furthersubdivided into five major subclasses as follows: flavonols,flavanols, flavones, isoflavones, and ...
Ho Jung Kim+8 more
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Structure-based discovery of the first allosteric inhibitors of cyclin-dependent kinase 2. [PDF]
Allosteric targeting of protein kinases via displacement of the structural αC helix with type III allosteric inhibitors is currently gaining a foothold in drug discovery. Recently, the first crystal structure of CDK2 with an open allosteric pocket adjacent to the αC helix has been described, prospecting new opportunities to design more selective ...
Rastelli G+4 more
europepmc +5 more sources
Understanding selectivity-dependent molecular mechanism of inhibitors towards CDK2 over CDK6 is prominent for improving drug design towards the CDK family.
Lifei Wang+5 more
doaj +1 more source
CDK2 (cyclin dependent kinase 2) [PDF]
Review on CDK2, with data on DNA, on the protein encoded, and where the gene is implicated.
Wingren, Anette Gjörloff+1 more
openaire +3 more sources
ASSOCIATION OF RS2069502 CYCLIN-DEPENDENT KINASE 4 GENE WITH BREAST CANCER [PDF]
The goal of this project was to evaluate the association of candidate genetic variant rs2069502 of the CDK4 gene with breast cancer and the effect of variant genotypes on the serum concentration of CDK4 enzyme and consequently, on the occurrence of ...
Dalya Shakir Al-owaidi
doaj +1 more source