DESIGNING OF ANTI-CANCEROUS HISTONE DEACETYLASE INHIBITORS THROUGH MIMICKING OF PROTEIN-PROTEIN INTERFACES

Authors

  • K. Rajaganapathy Department of Pharmacy, Annamalai University, Annamalai Nagar 608002
  • R. Sathiyasundar Department of Pharmacy, Annamalai University, Annamalai Nagar 608002
  • G. Ramesh Kumar Department of Bioinformatics, AU-KBC Research Center, MIT, Anna University, Chromepet, Chennai 600044
  • V. K. Kalaichelvan Department of Pharmacy, Annamalai University, Annamalai Nagar 608002

Keywords:

HDAC, SIN3-NcoR, Docking and protein-protein interfaces

Abstract

Objective: The objective of the study was to come up with of the small molecular modulators that inhibit protein – protein interfaces or interaction site in HDAC complexes. The main focus is on the mimicking or forming of tiny molecule wherever by inhibiting the protein-protein interactions in specifically HDAC protein complexes. 

Methods: By mimicking of the interface of the protein interaction site like SIN3A-SMRT complex as well as SIN3A-NcoR complexes.

Results: Totally 10 molecular structures were designed through molecular docking with HDAC2 PDB Id 3MAX and were downloaded from protein data bank.

Conclusion: The results clearly indicate that before synthesis and biochemical testing of new lead and its analogs; one can use molecular modeling based methods for qualitative assessment.

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References

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Published

01-11-2014

How to Cite

Rajaganapathy, K., R. Sathiyasundar, G. R. Kumar, and V. K. Kalaichelvan. “DESIGNING OF ANTI-CANCEROUS HISTONE DEACETYLASE INHIBITORS THROUGH MIMICKING OF PROTEIN-PROTEIN INTERFACES”. International Journal of Pharmacy and Pharmaceutical Sciences, vol. 6, no. 11, Nov. 2014, pp. 208-12, https://mail.innovareacademics.in/journals/index.php/ijpps/article/view/2695.

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Original Article(s)