IN SILICO ANALYSIS OF INHIBITOR AND SUBSTRATE BINDING SITE OF SERRAPEPTIDASE FROM SERRATIA MARCESCENS MTCC 8708

Abstract

Objective: Serrapeptidase is a therapeutic enzyme broadly used as an anti-inflammatory drug to treat inflammatory diseases like arthritis, bronchitis, fibrocystic breast disease and sinusitis. The objective of present study is in silco analyzes of the substrate and inhibitor binding sites of serratiopeptidase, expressed from a cloned gene.Methods: The gene encoding Serrapeptidase was amplified from genomic DNA of Serratia marcescens MTCC 8707, an isolated from the flowers of summer squash plants. The gene was sequenced, the nucleotide sequence of 1464 nucleotides was submitted to Gen Bank nucleotide database and accession number GI: KP869847 obtained. The develop amino acid sequence was used to predict 3D structure using different bioinformatics tools and software’s Further, CABS-dock and Swiss Dock, the docking servers were used for enzyme-substrate/inhibitor binding site analysis. The inflammatory mediators, bradykinin, and substance-P were used as substrates, whereas, EDTA and Lisinopril were used as an inhibitor for serrapeptidase. UCSF Chimera program was used for interactive visualization and analysis of docked results.Results: The docking studies show substrates bradykinin and substance-P bind near zinc binding site with minimum RMSD value and the inhibitors EDTA and lisinopril showed favorable interaction at zinc binding site of serrapeptidase with minimum free energy.Conclusion: The result of docking studies confirm that the substrate or inhibitor binds near zinc binding domain (HEXXH.) and the peptide bond of the substrate can be effectively cleaved by serrapeptidase.Keywords: Serrapeptidase, Anti-inflammation, Arthritis, Molecular docking, Drug discovery, Protein-peptide interaction, Bradykinin, Substance-P

Authors and Affiliations

N. S. Kaviyarasi, C. N. Prashantha, V. V. s. Suryanarayana

Keywords

Related Articles

SYNTHESIS, CHARACTERISATION AND DNA PHOTOCLEAVAGE ACTIVITY OF NEW 2-(THIOXO/OXO) QUINOLINE-4,6-DIMETHYL PYRIMIDINYL HYDRAZONES

Objective: The main objective of present work is to synthesize, characterize and evaluate DNA photocleavage activity of hydrazones containing quinoline and pyrimidine rings.Methods: The syntheses of new 2-(Thioxo/Oxo)qui...

ANTI-INFLAMMATORY, ANTIBACTERIAL, AND ANTIOXIDANT ACTIVITIES OF THAI MEDICINAL PLANTS

Objective: Acacia farnesiana (L.) Willd, Senna alata (L.) Roxb., Sesbania grandiflora (L.) Pers., Syzygium cumini (L.) Skeels and Tabernaemontana divaricate (L.) R. Br. ex Roem. & Schult. are used in Thai traditional...

IDENTIFICATION AND SCREENING OF EXTRACELLULAR VIRULENCE FACTORS OF AEROMONAS SPP. IN ENVIRONMENTAL WATER SAMPLES FROM TAMILNADU, SOUTH INDIA

Objective: Aeromonas species (spp.) are emerging pathogen that is present in drinking water supplies which are a major reason for public health concern. Factors contributing to virulence include toxins, haemolysins, adhe...

BACTERIOCIN: A NOVEL APPROACH FOR PRESERVATION OF FOOD

Bacteriocins are antimicrobial peptides which are ribosomally synthesized and produced by Lactic acid bacteria. They play a major role in prevention of human disease such as cancer, inflammatory disease, respiratory in...

DEVELOPMENT OF COLON-SPECIFIC MULTI PARTICULATE DRUG DELIVERY SYSTEM OF FENOVERINE

Objective: The main objective of this study was to formulate and evaluate colon-specific multi- particulate drug delivery system of fenoverine, using Eudragit S 100 as enteric coating polymer.Methods: Microparticles were...

Download PDF file
  • EP ID EP577702
  • DOI -
  • Views 60
  • Downloads 0

How To Cite

N. S. Kaviyarasi, C. N. Prashantha, V. V. s. Suryanarayana (2016). IN SILICO ANALYSIS OF INHIBITOR AND SUBSTRATE BINDING SITE OF SERRAPEPTIDASE FROM SERRATIA MARCESCENS MTCC 8708. International Journal of Pharmacy and Pharmaceutical Sciences, 8(4), 123-128. https://europub.co.uk./articles/-A-577702