Motif’s of aromatic and aliphatic nitrilases
Journal of Proteomics & Bioinformatics

Journal of Proteomics & Bioinformatics
Open Access

ISSN: 0974-276X

Motif’s of aromatic and aliphatic nitrilases

3rd International Conference on Proteomics & Bioinformatics

July 15-17, 2013 Courtyard by Marriott Philadelphia Downtown, USA

Nikhil Sharma and Tek Chand Bhalla

AcceptedAbstracts: J Proteomics Bioinform

Abstract :

Nitrilase is one of the nitrile metabolizing enzymes that catalyzes the conversion of nitriles to corresponding acids. Based on substrate specificities, nitrilases are classified as aliphatic and aromatic nitrilases. Number of nitrilases from microbial/ plant sources have been purified, characterized and their genes have been cloned and sequenced. In order to identify as to which group the sequences of nitrilases belong to, two types of motifs i.e. aliphatic nitrilase motifs (MDMAl) and aromatic nitrilase motifs (MDMAr) each with four motifs based on conserved catalytic triad (Glu-48, Lys-131, Cys-165) were designed. Conserved regions were identified by performing multiple sequence alignment (MSA) using multiple EM for motif elicitation (MEME). The manually designed motifs (MDM?s) were validated by ScanProsite and their presence was also confirmed by PRATT, Gblocks and MEME. The ScanProsite search against the MDMAr exhibited some new sources of aromatic nitrilase from plant, animals and microbes whereas MDMAl only exhibited nitrilase from microbes. Besides identifying unique motifs in nitrilase sequences and to confirm their specificity towards nitriles, randomly selected sequences were validated or motifs were validated by analyzing some important physiochemical parameters of corresponding nitrilases.

Biography :

Nikhil Sharma is currently pursuing his Ph.D. in the Department of Biotechnology and his research entails the study of microbial enzyme both in vitro and in silico. He has contributed chapters in books and research articles in peer review journals.