Bioinformatics study of the 3-hydroxy-3-methylglotaryl-coenzyme A reductase (HMGR) gene in Gramineae
Isoprenoids or terpenoids are synthesized by two important units’ including dimethylallyl diphosphate and isopentenyl diphosphate (IPP). Plants use two different methods for formation of IPP, which is a cytosolic and a plastidial method. The 3-hydroxy-3-methylglutaryl-CoA reductase (HMGR, EC 1.1.1.3...
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Veröffentlicht in: | Molecular biology reports 2012-09, Vol.39 (9), p.8925-8935 |
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description | Isoprenoids or terpenoids are synthesized by two important units’ including dimethylallyl diphosphate and isopentenyl diphosphate (IPP). Plants use two different methods for formation of IPP, which is a cytosolic and a plastidial method. The 3-hydroxy-3-methylglutaryl-CoA reductase (HMGR, EC 1.1.1.34) catalyzes the conversion of HMG-CoA to mevalonate, which is the first stage in the cytosolic pathway for biosynthesis of isoprenoid in plants. In this study, a total of fifty HMGR protein sequences from Gramineae and three animal samples including human, mouse and fruit fly were aligned and analyzed by computational tools to predict the protein properties, such as molecular mass, pI, signal peptide, transmembrane and conserved domains, secondary and spatial structures. Sequence comparison analysis revealed that there is high identity between plants and animals. Three catalytic regions including L domain, N domain and S domain were detected by structural modeling of HMGR. The tertiary structure model of
Oryza sativa
HMGR (Accession Number: NP_001063541) was further checked by PROCHECK algorithm, and showed that 90.3 % of the amino acid residues were located in the most favored regions in Ramachandran plot, indicating that the simulated three-dimensional structure was reliable. Phylogenetic analysis indicated that there is a relationship among species of Gramineae and other organisms. According to these results, HMGRs should be derived from a common ancestor. |
doi_str_mv | 10.1007/s11033-012-1761-2 |
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Oryza sativa
HMGR (Accession Number: NP_001063541) was further checked by PROCHECK algorithm, and showed that 90.3 % of the amino acid residues were located in the most favored regions in Ramachandran plot, indicating that the simulated three-dimensional structure was reliable. Phylogenetic analysis indicated that there is a relationship among species of Gramineae and other organisms. According to these results, HMGRs should be derived from a common ancestor.</description><identifier>ISSN: 0301-4851</identifier><identifier>EISSN: 1573-4978</identifier><identifier>DOI: 10.1007/s11033-012-1761-2</identifier><identifier>PMID: 22722993</identifier><language>eng</language><publisher>Dordrecht: Springer Netherlands</publisher><subject>Algorithms ; Amino Acid Motifs ; Amino Acid Sequence ; Animal Anatomy ; Animal Biochemistry ; Bioinformatics ; Biomedical and Life Sciences ; Catalytic reforming ; Computational Biology ; Consensus Sequence ; Drosophila ; Enzymes ; Genes ; Histology ; Hydroxymethylglutaryl CoA Reductases - chemistry ; Hydroxymethylglutaryl CoA Reductases - genetics ; Hydroxymethylglutaryl CoA Reductases - metabolism ; Life Sciences ; Mevalonic Acid - metabolism ; Models, Molecular ; Molecular Sequence Data ; Morphology ; Phylogeny ; Poaceae - genetics ; Poaceae - metabolism ; Protein Structure, Tertiary ; Sequence Alignment ; Sequence Homology, Amino Acid</subject><ispartof>Molecular biology reports, 2012-09, Vol.39 (9), p.8925-8935</ispartof><rights>Springer Science+Business Media B.V. 2012</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c405t-94209d50b835e71eba4d9c673b53c6e663ccb0027b37207fcbd176726fade6d33</citedby><cites>FETCH-LOGICAL-c405t-94209d50b835e71eba4d9c673b53c6e663ccb0027b37207fcbd176726fade6d33</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s11033-012-1761-2$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s11033-012-1761-2$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,27903,27904,41467,42536,51297</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22722993$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Darabi, Maryam</creatorcontrib><creatorcontrib>Masoudi-Nejad, Ali</creatorcontrib><creatorcontrib>Nemat-Zadeh, Ghorbanali</creatorcontrib><title>Bioinformatics study of the 3-hydroxy-3-methylglotaryl-coenzyme A reductase (HMGR) gene in Gramineae</title><title>Molecular biology reports</title><addtitle>Mol Biol Rep</addtitle><addtitle>Mol Biol Rep</addtitle><description>Isoprenoids or terpenoids are synthesized by two important units’ including dimethylallyl diphosphate and isopentenyl diphosphate (IPP). Plants use two different methods for formation of IPP, which is a cytosolic and a plastidial method. The 3-hydroxy-3-methylglutaryl-CoA reductase (HMGR, EC 1.1.1.34) catalyzes the conversion of HMG-CoA to mevalonate, which is the first stage in the cytosolic pathway for biosynthesis of isoprenoid in plants. In this study, a total of fifty HMGR protein sequences from Gramineae and three animal samples including human, mouse and fruit fly were aligned and analyzed by computational tools to predict the protein properties, such as molecular mass, pI, signal peptide, transmembrane and conserved domains, secondary and spatial structures. Sequence comparison analysis revealed that there is high identity between plants and animals. Three catalytic regions including L domain, N domain and S domain were detected by structural modeling of HMGR. The tertiary structure model of
Oryza sativa
HMGR (Accession Number: NP_001063541) was further checked by PROCHECK algorithm, and showed that 90.3 % of the amino acid residues were located in the most favored regions in Ramachandran plot, indicating that the simulated three-dimensional structure was reliable. Phylogenetic analysis indicated that there is a relationship among species of Gramineae and other organisms. According to these results, HMGRs should be derived from a common ancestor.</description><subject>Algorithms</subject><subject>Amino Acid Motifs</subject><subject>Amino Acid Sequence</subject><subject>Animal Anatomy</subject><subject>Animal Biochemistry</subject><subject>Bioinformatics</subject><subject>Biomedical and Life Sciences</subject><subject>Catalytic reforming</subject><subject>Computational Biology</subject><subject>Consensus Sequence</subject><subject>Drosophila</subject><subject>Enzymes</subject><subject>Genes</subject><subject>Histology</subject><subject>Hydroxymethylglutaryl CoA Reductases - chemistry</subject><subject>Hydroxymethylglutaryl CoA Reductases - genetics</subject><subject>Hydroxymethylglutaryl CoA Reductases - metabolism</subject><subject>Life Sciences</subject><subject>Mevalonic Acid - metabolism</subject><subject>Models, Molecular</subject><subject>Molecular Sequence Data</subject><subject>Morphology</subject><subject>Phylogeny</subject><subject>Poaceae - genetics</subject><subject>Poaceae - 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chemistry</topic><topic>Hydroxymethylglutaryl CoA Reductases - genetics</topic><topic>Hydroxymethylglutaryl CoA Reductases - metabolism</topic><topic>Life Sciences</topic><topic>Mevalonic Acid - metabolism</topic><topic>Models, Molecular</topic><topic>Molecular Sequence Data</topic><topic>Morphology</topic><topic>Phylogeny</topic><topic>Poaceae - genetics</topic><topic>Poaceae - metabolism</topic><topic>Protein Structure, Tertiary</topic><topic>Sequence Alignment</topic><topic>Sequence Homology, Amino Acid</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Darabi, Maryam</creatorcontrib><creatorcontrib>Masoudi-Nejad, Ali</creatorcontrib><creatorcontrib>Nemat-Zadeh, Ghorbanali</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection (ProQuest)</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Science Database</collection><collection>Biological Science Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>Biotechnology Research Abstracts</collection><jtitle>Molecular biology reports</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Darabi, Maryam</au><au>Masoudi-Nejad, Ali</au><au>Nemat-Zadeh, Ghorbanali</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Bioinformatics study of the 3-hydroxy-3-methylglotaryl-coenzyme A reductase (HMGR) gene in Gramineae</atitle><jtitle>Molecular biology reports</jtitle><stitle>Mol Biol Rep</stitle><addtitle>Mol Biol Rep</addtitle><date>2012-09-01</date><risdate>2012</risdate><volume>39</volume><issue>9</issue><spage>8925</spage><epage>8935</epage><pages>8925-8935</pages><issn>0301-4851</issn><eissn>1573-4978</eissn><abstract>Isoprenoids or terpenoids are synthesized by two important units’ including dimethylallyl diphosphate and isopentenyl diphosphate (IPP). Plants use two different methods for formation of IPP, which is a cytosolic and a plastidial method. The 3-hydroxy-3-methylglutaryl-CoA reductase (HMGR, EC 1.1.1.34) catalyzes the conversion of HMG-CoA to mevalonate, which is the first stage in the cytosolic pathway for biosynthesis of isoprenoid in plants. In this study, a total of fifty HMGR protein sequences from Gramineae and three animal samples including human, mouse and fruit fly were aligned and analyzed by computational tools to predict the protein properties, such as molecular mass, pI, signal peptide, transmembrane and conserved domains, secondary and spatial structures. Sequence comparison analysis revealed that there is high identity between plants and animals. Three catalytic regions including L domain, N domain and S domain were detected by structural modeling of HMGR. The tertiary structure model of
Oryza sativa
HMGR (Accession Number: NP_001063541) was further checked by PROCHECK algorithm, and showed that 90.3 % of the amino acid residues were located in the most favored regions in Ramachandran plot, indicating that the simulated three-dimensional structure was reliable. Phylogenetic analysis indicated that there is a relationship among species of Gramineae and other organisms. According to these results, HMGRs should be derived from a common ancestor.</abstract><cop>Dordrecht</cop><pub>Springer Netherlands</pub><pmid>22722993</pmid><doi>10.1007/s11033-012-1761-2</doi><tpages>11</tpages></addata></record> |
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subjects | Algorithms Amino Acid Motifs Amino Acid Sequence Animal Anatomy Animal Biochemistry Bioinformatics Biomedical and Life Sciences Catalytic reforming Computational Biology Consensus Sequence Drosophila Enzymes Genes Histology Hydroxymethylglutaryl CoA Reductases - chemistry Hydroxymethylglutaryl CoA Reductases - genetics Hydroxymethylglutaryl CoA Reductases - metabolism Life Sciences Mevalonic Acid - metabolism Models, Molecular Molecular Sequence Data Morphology Phylogeny Poaceae - genetics Poaceae - metabolism Protein Structure, Tertiary Sequence Alignment Sequence Homology, Amino Acid |
title | Bioinformatics study of the 3-hydroxy-3-methylglotaryl-coenzyme A reductase (HMGR) gene in Gramineae |
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