MOLECULAR MODELLING AND DOCKING STUDIES OF HUMAN ACROSIN BINDING PROTEIN (ACRBP/OY-TES-1)

Authors

  • Sabitha Kesavan Department of Molecular Oncology, Cancer Institute (WIA) 38, Sardar Patel Road, Guindy, Chennai 600036, Tamil Nadu, India
  • Priya Ramanathan Department of Molecular Oncology, Cancer Institute (WIA) 38, Sardar Patel Road, Guindy, Chennai 600036, Tamil Nadu, India
  • Rajkumar Thangarajan Department of Molecular Oncology, Cancer Institute (WIA) 38, Sardar Patel Road, Guindy, Chennai 600036, Tamil Nadu, India

Keywords:

ACRBPOY-TES-1, Docking, Glide, Immunotherapy, Modeling

Abstract

Objective: We have made an attempt to identify inhibitors that are bound with Acrosin binding protein (ACRBP/OY-TES-1) through In silico molecular docking studies.

Methods: Modeling of ACRBP/OY-TES-1 was performed using Iterative Threading Assembly Refinement (I-TASSER) software. Docking calculations were carried out using Glide. Glide Score (GS core) was used to rank the ligands on the basis of their relative binding affinities.

Results: Food and Drug Administration (FDA)-approved drugs were docked with ACRBP/OY-TES-1 to identify potent inhibitors. Leuprolide a decapeptide interacts with the protein at residues Tyr116, Gly421, Leu433, Asp480 and Gln483 with Glide score-14.188. Other compounds that showed high affinity to the protein are triptorelin, nafatarelin, goserelin and sincalide.

Conclusion: The investigation concluded that these drugs could be used as potential inhibitors against ACRBP/OY-TES-1 in cancer treatment.


 

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Published

01-09-2015

How to Cite

Kesavan, S., P. Ramanathan, and R. Thangarajan. “MOLECULAR MODELLING AND DOCKING STUDIES OF HUMAN ACROSIN BINDING PROTEIN (ACRBP/OY-TES-1)”. International Journal of Pharmacy and Pharmaceutical Sciences, vol. 7, no. 9, Sept. 2015, pp. 491-5, https://mail.innovareacademics.in/journals/index.php/ijpps/article/view/6673.

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