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Predicted structural elements of Bcr-Abl oncoprotein isoforms in | 25048
Journal of Proteomics & Bioinformatics

Journal of Proteomics & Bioinformatics
Open Access

ISSN: 0974-276X

+44 1223 790975

Predicted structural elements of Bcr-Abl oncoprotein isoforms in Chronic Myelogenous leukemia


4th International Conference on Proteomics & Bioinformatics

August 04-06, 2014 Hilton-Chicago/Northbrook, Chicago, USA

Nadeem A Kizilbash

Scientific Tracks Abstracts: J Proteomics Bioinform

Abstract :

The structural elements of Bcr-Abl oncoprotein (p210BCR-ABL) isoforms, b2a2 and b3a2, expressed in Chronic Myelogenous Leukemia (CML), were predicted by Psipred and ExPASy servers. These proteins are tyrosine kinases with masses of 210-kDa. Structural differences were found in five a-helices (a25, a?, a26, a27 and a29) and nine β-strands (β12, β13, β15, β?, β17, β30, β?, β34 and β35). These differences are present in the SH3, SH2, SH1 and DNA-binding domains. The structural differences might be able to explain the different roles played by the two isoforms in mediating signal transduction during the development of CML.

Biography :

Nadeem A Kizilbash received his Bachelor?s degree in Chemistry from Longwood College in USA. His Master?s degree was also in Chemistry from Washington University in St. Louis, USA. His doctoral degree was awarded in Biophysics from Boston University in USA. He is presently working as an Assistant Professor of Biochemistry at Northern Border University in Arar, Saudi Arabia. He has published fifteen papers in various journals on topics as diverse as Proteomics, Protein Structure, Drug Delivery and Gene Polymorphism. He is currently a member of editorial board of three international research journals.

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