کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
5907923 1160885 2013 10 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Putative drug and vaccine target protein identification using comparative genomic analysis of KEGG annotated metabolic pathways of Mycoplasma hyopneumoniae
موضوعات مرتبط
علوم زیستی و بیوفناوری بیوشیمی، ژنتیک و زیست شناسی مولکولی ژنتیک
پیش نمایش صفحه اول مقاله
Putative drug and vaccine target protein identification using comparative genomic analysis of KEGG annotated metabolic pathways of Mycoplasma hyopneumoniae
چکیده انگلیسی


- We used comparative genomics and metabolic pathways analysis with predefined workflow
- 41 annotated metabolic pathways 5 of which unique to M. hyopneumoniae were identified
- A total of 234 proteins were identified to be involved in these metabolic pathways
- 125 non homologous and predicted essential proteins were found potential targets from total
- Further prioritization identified 21 vaccine candidate and 42 drug target proteins

In the present study, a computational comparative and subtractive genomic/proteomic analysis aimed at the identification of putative therapeutic target and vaccine candidate proteins from Kyoto Encyclopedia of Genes and Genomes (KEGG) annotated metabolic pathways of Mycoplasma hyopneumoniae was performed for drug design and vaccine production pipelines against M.hyopneumoniae. The employed comparative genomic and metabolic pathway analysis with a predefined computational systemic workflow extracted a total of 41 annotated metabolic pathways from KEGG among which five were unique to M. hyopneumoniae. A total of 234 proteins were identified to be involved in these metabolic pathways. Although 125 non homologous and predicted essential proteins were found from the total that could serve as potential drug targets and vaccine candidates, additional prioritizing parameters characterize 21 proteins as vaccine candidate while druggability of each of the identified proteins evaluated by the DrugBank database prioritized 42 proteins suitable for drug targets.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Genomics - Volume 102, Issue 1, July 2013, Pages 47-56
نویسندگان
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