Journal:JBSD:8
From Proteopedia
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<b>Molecular Tour</b><br> | <b>Molecular Tour</b><br> | ||
''Fusarium solani'' causes stem and fruit rot disease in ''Capsicum sp.'' causing severe losses. Use of peptides as antimicrobials has been reported earlier. The peptide designing for a specific fungus using its own protein (enzyme) may be a useful strategy for the control of disease. Polyamine biosynthesis is responsible for growth of ''Fusarium solani''. The rate-limiting step of this process is decarboxylation of ornithine. [http://en.wikipedia.org/wiki/Ornithine_decarboxylase Ornithine decarboxylase] (ODC) [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=4.1.1.17 (EC 4.1.1.17)] is an enzyme that catalyzes the decarboxylation of ornithine to putrescine. <scene name='Journal:JBSD:8/Cv/9'>Ornithine</scene> is an amino acid, whereas <scene name='Journal:JBSD:8/Cv/5'>putrescine</scene> is a polyamine. Inhibitors of <scene name='Journal:JBSD:8/Cv/10'>ODC</scene> having higher binding capacity than ornithine can be used for treating the plant from fungal disease. | ''Fusarium solani'' causes stem and fruit rot disease in ''Capsicum sp.'' causing severe losses. Use of peptides as antimicrobials has been reported earlier. The peptide designing for a specific fungus using its own protein (enzyme) may be a useful strategy for the control of disease. Polyamine biosynthesis is responsible for growth of ''Fusarium solani''. The rate-limiting step of this process is decarboxylation of ornithine. [http://en.wikipedia.org/wiki/Ornithine_decarboxylase Ornithine decarboxylase] (ODC) [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=4.1.1.17 (EC 4.1.1.17)] is an enzyme that catalyzes the decarboxylation of ornithine to putrescine. <scene name='Journal:JBSD:8/Cv/9'>Ornithine</scene> is an amino acid, whereas <scene name='Journal:JBSD:8/Cv/5'>putrescine</scene> is a polyamine. Inhibitors of <scene name='Journal:JBSD:8/Cv/10'>ODC</scene> having higher binding capacity than ornithine can be used for treating the plant from fungal disease. | ||
- | In this study, we designed 15 peptide inhibitors by the random alteration of active site residues at which ornithine binds. These inhibitors were peptides of the length of nine residues. The peptide, <scene name='Journal:JBSD:8/Cv/13'>GLIWGNGPF showed highest docking with active site of ODC</scene> (<span style="color:orange;background-color:black;font-weight:bold;">peptide GLIWGNGPF is colored in orange</span> and <font color='darkmagenta'><b>residues of ODC active site are colored in darkmagenta</b></font>, which is four times greater than ornithine. Thus, peptides can be used as a potential inhibitor to block the pathway responsible for the growth of the pathogen. | + | In this study, we designed 15 peptide inhibitors by the random alteration of active site residues at which ornithine binds. These inhibitors were peptides of the length of nine residues. The peptide, <scene name='Journal:JBSD:8/Cv/13'>GLIWGNGPF showed highest docking with active site of ODC</scene> (<span style="color:orange;background-color:black;font-weight:bold;">peptide GLIWGNGPF is colored in orange</span>) and <font color='darkmagenta'><b>residues of ODC active site are colored in darkmagenta</b></font>, which is four times greater than ornithine. Thus, peptides can be used as a potential inhibitor to block the pathway responsible for the growth of the pathogen. |
</StructureSection> | </StructureSection> |
Revision as of 11:13, 22 August 2012
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- ↑ REF
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