In silico structural analysis, physicochemical characterization and homology modeling of Arabidopsis thaliana Na+/H+ exchanger 1 protein

This thesis report is submitted in partial fulfillment of the requirement for the degree of Bachelor of Science in Biotechnology, 2015.

Detalhes bibliográficos
Autor principal: Feisal, Mohammad Rafid
Outros Autores: Islam, Dr. Aparna
Formato: Tese
Idioma:English
Publicado em: BRAC University 2015
Assuntos:
Acesso em linha:http://hdl.handle.net/10361/4550
id 10361-4550
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spelling 10361-45502019-09-30T04:12:23Z In silico structural analysis, physicochemical characterization and homology modeling of Arabidopsis thaliana Na+/H+ exchanger 1 protein Feisal, Mohammad Rafid Islam, Dr. Aparna Department of Mathematical and Natural Science, BRAC University Biotechnology Mathematics and Natural Sciences This thesis report is submitted in partial fulfillment of the requirement for the degree of Bachelor of Science in Biotechnology, 2015. Cataloged from PDF version of thesis. Includes bibliographical references (page 79-89). Climate changes have detrimental effects on the plants such as an increased susceptibility towards pathogens or ill health leading to food insecurity. This is eminently observed in developing countries such as Bangladesh. Hence, it is of crucial importance to comprehend the mechanisms the plants use to adapt to environmental stresses, such as, salinity. NHX-type antiporter facilitates the exchange of Na+ for H+ across the membranes. It sequesters Na+ form the cytoplasm to vacuoles via the electrochemical H+ gradient generated by two H+- pumps. In Arabidopsis thaliana, NHX1 encodes the vacuolar sodium or proton antiporter and it is identified as a significant salt tolerance determinant that is able to catalyze Na+ accumulation in vacuoles. As such, it is necessary to determine the structure of the protein encoded by the NHX1 gene in Arabidopsis thaliana. This would allow us to establish the regions (e.g. active sites and secondary structural motifs) in the protein that affect the function and protein-protein interaction network in regard to the mechanisms involved in salinity tolerance. The objective of this study is to predict the three-dimensional structure of Arabidopsis thaliana sodium/hydrogen exchanger 1 protein via homology modeling and examine its physicochemical properties using in silico approaches. Biocomputational analyses of the target protein were performed using an array of online bioinformatics tools and databases and the homology model was developed using 3 different softwares (I-TASSER, Phyre2 and Easymodeller) and the best model was selected upon evaluation. In addition, the secondary structural motifs were identified within the model. The results suggested that the EasyModeller model, EM_Model 01, was the best amongst the three. It had the highest stereochemical quality scores and was considered to be the least unusual. The model consisted of α/β/γ topology where a single β-sheet constituted the β-hairpin as observed in the secondary structure schematic and topology diagrams. It was predicted that the presence of the β-hairpin allowed the protein to act as a membrane channel protein to facilitate the exchange of Na+ and H+. Mohammad Rafid Feisal B. Biotechnology 2015-10-31T07:05:30Z 2015-10-31T07:05:30Z 2015 2015-09 Thesis ID 11236003 http://hdl.handle.net/10361/4550 en BRAC University thesis are protected by copyright. They may be viewed from this source for any purpose, but reproduction or distribution in any format is prohibited without written permission. 89 pages application/pdf BRAC University
institution Brac University
collection Institutional Repository
language English
topic Biotechnology
Mathematics and Natural Sciences
spellingShingle Biotechnology
Mathematics and Natural Sciences
Feisal, Mohammad Rafid
In silico structural analysis, physicochemical characterization and homology modeling of Arabidopsis thaliana Na+/H+ exchanger 1 protein
description This thesis report is submitted in partial fulfillment of the requirement for the degree of Bachelor of Science in Biotechnology, 2015.
author2 Islam, Dr. Aparna
author_facet Islam, Dr. Aparna
Feisal, Mohammad Rafid
format Thesis
author Feisal, Mohammad Rafid
author_sort Feisal, Mohammad Rafid
title In silico structural analysis, physicochemical characterization and homology modeling of Arabidopsis thaliana Na+/H+ exchanger 1 protein
title_short In silico structural analysis, physicochemical characterization and homology modeling of Arabidopsis thaliana Na+/H+ exchanger 1 protein
title_full In silico structural analysis, physicochemical characterization and homology modeling of Arabidopsis thaliana Na+/H+ exchanger 1 protein
title_fullStr In silico structural analysis, physicochemical characterization and homology modeling of Arabidopsis thaliana Na+/H+ exchanger 1 protein
title_full_unstemmed In silico structural analysis, physicochemical characterization and homology modeling of Arabidopsis thaliana Na+/H+ exchanger 1 protein
title_sort in silico structural analysis, physicochemical characterization and homology modeling of arabidopsis thaliana na+/h+ exchanger 1 protein
publisher BRAC University
publishDate 2015
url http://hdl.handle.net/10361/4550
work_keys_str_mv AT feisalmohammadrafid insilicostructuralanalysisphysicochemicalcharacterizationandhomologymodelingofarabidopsisthaliananahexchanger1protein
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