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Expression, purification and molecular modeling of the NIa protease of Cardamom mosaic virus.
- Source :
-
Journal of biomolecular structure & dynamics [J Biomol Struct Dyn] 2013; Vol. 31 (6), pp. 602-11. Date of Electronic Publication: 2012 Aug 13. - Publication Year :
- 2013
-
Abstract
- The NIa protease of Potyviridae is the major viral protease that processes potyviral polyproteins. The NIa protease coding region of Cardamom mosaic virus (CdMV) is amplified from the viral cDNA, cloned and expressed in Escherichia coli. NIa protease forms inclusion bodies in E.coli. The inclusion bodies are solubilized with 8 M urea, refolded and purified by Nickel-Nitrilotriacetic acid affinity chromatography. Three-dimensional modeling of the CdMV NIa protease is achieved by threading approach using the homologous X-ray crystallographic structure of Tobacco etch mosaic virus NIa protease. The model gave an insight in to the substrate specificities of the NIa proteases and predicted the complementation of nearby residues in the catalytic triad (H42, D74 and C141) mutants in the cis protease activity of CdMV NIa protease.
- Subjects :
- Amino Acid Sequence
DNA, Complementary chemistry
DNA, Complementary metabolism
DNA, Viral chemistry
DNA, Viral metabolism
Elettaria virology
Endopeptidases metabolism
Escherichia coli genetics
Escherichia coli metabolism
Models, Molecular
Molecular Sequence Data
Mosaic Viruses metabolism
Substrate Specificity
Viral Proteins metabolism
Endopeptidases chemistry
Endopeptidases isolation & purification
Mosaic Viruses enzymology
Viral Proteins chemistry
Viral Proteins isolation & purification
Subjects
Details
- Language :
- English
- ISSN :
- 1538-0254
- Volume :
- 31
- Issue :
- 6
- Database :
- MEDLINE
- Journal :
- Journal of biomolecular structure & dynamics
- Publication Type :
- Academic Journal
- Accession number :
- 22888800
- Full Text :
- https://doi.org/10.1080/07391102.2012.706078