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Positive Regulator Molecules02:39

Positive Regulator Molecules

7.0K
Mitotic cell division results in daughter cells that exactly resemble the parent cell. However, errors in the DNA replication or distribution of genetic material may lead to genetic mutations that may be passed down to every new cell formed from the resulting abnormal cell. Propagation of such mutant cells is restricted through checkpoint mechanisms present at different stages of the cell cycle. These checkpoints involve regulator molecules that either promote or demote cell cycle events.
7.0K
Positive Regulator Molecules01:45

Positive Regulator Molecules

136.8K
To consistently produce healthy cells, the cell cycle—the process that generates daughter cells—must be precisely regulated.
136.8K
Negative Regulator Molecules01:23

Negative Regulator Molecules

38.7K
Positive regulators allow a cell to advance through cell cycle checkpoints. Negative regulators have an equally important role as they terminate a cell’s progression through the cell cycle—or pause it—until the cell meets specific criteria.
38.7K
Anaphase Promoting Complex00:50

Anaphase Promoting Complex

3.5K
The stepwise destruction of specific proteins is necessary for the progression and completion of the cell cycle. Such proteins are ubiquitinated by ubiquitin ligases and then subsequently destroyed by the proteasome. The SCF (Skp1/Cullin/F-box) and the anaphase-promoting complex (APC) are two important ubiquitin ligases involved in cell cycle progression. While SCF is active throughout the cell cycle, APC gets activated during metaphase to anaphase transition. Cdc20 or Cdh1 binds to APC and...
3.5K
Inhibition of Cdk Activity02:34

Inhibition of Cdk Activity

6.1K
The orderly progression of the cell cycle depends on the activation of Cdk protein by binding to its cyclin partner. However, the cell cycle must be restricted when undergoing abnormal changes. Most cancers correlate to the deregulated cell cycle, and since Cdks are a central component of the cell cycle, Cdk inhibitors are extensively studied to develop anticancer agents. For instance, cyclin D associates with several Cdks, such as Cdk 4/6, to form an active complex. The cyclin D-Cdk4/6 complex...
6.1K
Separation of Sister Chromatids02:17

Separation of Sister Chromatids

4.6K
At the transition from prophase to metaphase, there is a reduction in cohesion along the chromosomal arms, resulting in the resolution of sister chromatids. However, residual cohesin connections remain to hold the sister chromatids together until the transition from metaphase to anaphase. The residual connection prevents any premature separation of sister chromatids, blocking the risks of aneuploidy within the daughter cells.
At the onset of anaphase, separase, a proteolytic enzyme, is...
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Related Experiment Video

Updated: Feb 28, 2026

Development of Inhibitors of Protein-protein Interactions through REPLACE: Application to the Design and Development Non-ATP Competitive CDK Inhibitors
10:33

Development of Inhibitors of Protein-protein Interactions through REPLACE: Application to the Design and Development Non-ATP Competitive CDK Inhibitors

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Pep5-Cpp, a Cyclin D2-Derived Antimicrobial.

Bianca Silva Souto1,2,3, Vitória Stephani Hasbahr1, Bárbara Ribeiro Lourenço da Silva1

  • 1Applied Toxinology Laboratory, Butantan Institute, Rua Rudolf Virchow 250, Butantã, São Paulo 05345-040, SP, Brazil.

Molecules (Basel, Switzerland)
|February 27, 2026
PubMed
Summary
This summary is machine-generated.

Antimicrobial peptides Pep5-Cpp and its derivatives show potential against bacteria and fungi, with selective activity and low toxicity. Further development is supported for pharmacological applications.

Keywords:
Pep5-Cppantimicrobial peptidescationic peptides

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Production, Crystallization and Structure Determination of C. difficile PPEP-1 via Microseeding and Zinc-SAD
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Production, Crystallization and Structure Determination of C. difficile PPEP-1 via Microseeding and Zinc-SAD

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Related Experiment Videos

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Development of Inhibitors of Protein-protein Interactions through REPLACE: Application to the Design and Development Non-ATP Competitive CDK Inhibitors
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Construction of Cyclic Cell-Penetrating Peptides for Enhanced Penetration of Biological Barriers
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Production, Crystallization and Structure Determination of C. difficile PPEP-1 via Microseeding and Zinc-SAD
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Production, Crystallization and Structure Determination of C. difficile PPEP-1 via Microseeding and Zinc-SAD

Published on: December 30, 2016

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Area of Science:

  • Microbiology
  • Peptide Science
  • Antimicrobial Research

Background:

  • Peptidomic studies identified antitumoral Pep5.
  • Coupling Pep5 to a carrier peptide (Cpp) yielded antimicrobial potential.

Purpose of the Study:

  • Evaluate antimicrobial activity of Pep5-Cpp and derivatives (ΔC3-Pep5-Cpp, ΔN-Pep5-Cpp).
  • Investigate their mechanisms of action.

Main Methods:

  • Minimum Inhibitory Concentration (MIC) assays against *Staphylococcus aureus*, *Candida albicans*, and *Aspergillus niger*.
  • DNA interaction studies, fluorescence assays, biofilm inhibition assays, microbicidal assays, and hemolytic assays.

Main Results:

  • Pep5-Cpp and derivatives exhibited varying MIC values against tested microbes.
  • Pep5-Cpp interacted with *S. aureus* DNA and increased its fluorescence.
  • ΔC3-Pep5-Cpp inhibited biofilm formation (>50%).
  • Peptides showed selective microbicidal activity and no significant hemolysis at MIC values.

Conclusions:

  • Pep5-Cpp and its derivatives possess significant antimicrobial potential and selectivity.
  • Findings support the future pharmacological development of these peptides.