lasergene software  (DNASTAR)

 
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    Name:
    Lasergene
    Description:
    The Lasergene software package includes all of the applications from the genomics molecular biology and structural biology suites If your work focuses on next gen sequencing assembly and analysis clinical research or traditional sequence analysis the DNASTAR Lasergene package will cover your research needs The software is available for desktop download and via cloud
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    219018325
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    Structured Review

    DNASTAR lasergene software
    Lasergene
    The Lasergene software package includes all of the applications from the genomics molecular biology and structural biology suites If your work focuses on next gen sequencing assembly and analysis clinical research or traditional sequence analysis the DNASTAR Lasergene package will cover your research needs The software is available for desktop download and via cloud
    https://www.bioz.com/result/lasergene software/product/DNASTAR
    Average 99 stars, based on 16 article reviews
    Price from $9.99 to $1999.99
    lasergene software - by Bioz Stars, 2020-08
    99/100 stars

    Images

    1) Product Images from "Multi-Locus Typing of Histomonas meleagridis Isolates Demonstrates the Existence of Two Different Genotypes"

    Article Title: Multi-Locus Typing of Histomonas meleagridis Isolates Demonstrates the Existence of Two Different Genotypes

    Journal: PLoS ONE

    doi: 10.1371/journal.pone.0092438

    Analysis of ITS1-5.8S rRNA sequences from different H. meleagridis clonal cultures demonstrates the presence of multiple sequence variants within a single clone. (A) Phylogenetic tree based on the complete ITS1-5.8S rRNA-ITS2 region. Phylogenetic analysis of ITS1-5.8S rRNA-ITS2 region was performed using MegAlign application of Lasergene software (DNASTAR Inc.) by applying distance methods with default settings. Different clones are labelled with c and number, e.g. c1. (B) Sequence alignment of 5.8S rDNA region. Only sequence differences are shown, conserved nucleotides are designated as dots. Sequences originating from the same clonal culture are separated with lines.
    Figure Legend Snippet: Analysis of ITS1-5.8S rRNA sequences from different H. meleagridis clonal cultures demonstrates the presence of multiple sequence variants within a single clone. (A) Phylogenetic tree based on the complete ITS1-5.8S rRNA-ITS2 region. Phylogenetic analysis of ITS1-5.8S rRNA-ITS2 region was performed using MegAlign application of Lasergene software (DNASTAR Inc.) by applying distance methods with default settings. Different clones are labelled with c and number, e.g. c1. (B) Sequence alignment of 5.8S rDNA region. Only sequence differences are shown, conserved nucleotides are designated as dots. Sequences originating from the same clonal culture are separated with lines.

    Techniques Used: Sequencing, Software, Clone Assay

    2) Product Images from "Genetic Diversity of the 28-Kilodalton Outer Membrane Protein Gene in Human Isolates of Ehrlichia chaffeensis"

    Article Title: Genetic Diversity of the 28-Kilodalton Outer Membrane Protein Gene in Human Isolates of Ehrlichia chaffeensis

    Journal: Journal of Clinical Microbiology

    doi:

    Phylogenetic tree constructed on the basis of the predicted amino acid sequences from the p28 genes of the E. chaffeensis strains. The predicted amino acid sequences of E. chaffeensis ) and C. ruminantium ) were included in the analysis to build the root of the tree. The Megalign program of Lasergene software was used to construct the tree. The length of each pair of branches represents the distance between sequence pairs. The scale beneath the tree measures the distance between the sequences.
    Figure Legend Snippet: Phylogenetic tree constructed on the basis of the predicted amino acid sequences from the p28 genes of the E. chaffeensis strains. The predicted amino acid sequences of E. chaffeensis ) and C. ruminantium ) were included in the analysis to build the root of the tree. The Megalign program of Lasergene software was used to construct the tree. The length of each pair of branches represents the distance between sequence pairs. The scale beneath the tree measures the distance between the sequences.

    Techniques Used: Construct, Software, Sequencing

    3) Product Images from "A Novel Streptococcus Organism Identified in a Case of Fulminant Endocarditis Using 16S rDNA Sequencing"

    Article Title: A Novel Streptococcus Organism Identified in a Case of Fulminant Endocarditis Using 16S rDNA Sequencing

    Journal: The Journal of molecular diagnostics : JMD

    doi:

    Phylogenetic tree of 12 closely related Streptococcus species generated by LaserGene software.
    Figure Legend Snippet: Phylogenetic tree of 12 closely related Streptococcus species generated by LaserGene software.

    Techniques Used: Generated, Software

    4) Product Images from "Sequence and structural determinants of human APOBEC3H deaminase and anti-HIV-1 activities"

    Article Title: Sequence and structural determinants of human APOBEC3H deaminase and anti-HIV-1 activities

    Journal: Retrovirology

    doi: 10.1186/s12977-014-0130-8

    Sequence alignment of A3H HapII (residues 1 to 183) and four A3 deaminase-active proteins whose structures have been solved: A3A (1 to 199) [ 41 ], A3C (1 to 190) [ 49 ], A3F-CTD (185–373) [ 54 , 55 ], and A3G-CTD (191–384) [ 53 ] (also see refs. [ 43 , 50 - 52 ]). The A3H residues mutated in this study are highlighted with green asterisks and the active site residues are highlighted in blue. The region inside the square brackets represents the Z domain sequences for all of the proteins. The amino acids that comprise A3H loop 7 are also shown. The sequence alignment was generated using Lasergene software (DNASTAR, Inc., Madison, WI, USA).
    Figure Legend Snippet: Sequence alignment of A3H HapII (residues 1 to 183) and four A3 deaminase-active proteins whose structures have been solved: A3A (1 to 199) [ 41 ], A3C (1 to 190) [ 49 ], A3F-CTD (185–373) [ 54 , 55 ], and A3G-CTD (191–384) [ 53 ] (also see refs. [ 43 , 50 - 52 ]). The A3H residues mutated in this study are highlighted with green asterisks and the active site residues are highlighted in blue. The region inside the square brackets represents the Z domain sequences for all of the proteins. The amino acids that comprise A3H loop 7 are also shown. The sequence alignment was generated using Lasergene software (DNASTAR, Inc., Madison, WI, USA).

    Techniques Used: Sequencing, Generated, Software

    5) Product Images from "Identification of a New Broadly Cross-reactive Epitope within Domain III of the Duck Tembusu Virus E Protein"

    Article Title: Identification of a New Broadly Cross-reactive Epitope within Domain III of the Duck Tembusu Virus E Protein

    Journal: Scientific Reports

    doi: 10.1038/srep36288

    Sequence alignment of a minimal epitope in the E protein of flavivirus strains. The EXE/DPPFG epitope of various strains of DTMUV and other mosquito-borne flaviviruses were aligned using Lasergene software. Amino acid positions for each sequence are numbered on both sides. Dashes indicate identical amino acids. The identified epitope region is indicated by grey shading.
    Figure Legend Snippet: Sequence alignment of a minimal epitope in the E protein of flavivirus strains. The EXE/DPPFG epitope of various strains of DTMUV and other mosquito-borne flaviviruses were aligned using Lasergene software. Amino acid positions for each sequence are numbered on both sides. Dashes indicate identical amino acids. The identified epitope region is indicated by grey shading.

    Techniques Used: Sequencing, Software

    6) Product Images from "Reinfection of adult cattle with rotavirus B during repeated outbreaks of epidemic diarrhea"

    Article Title: Reinfection of adult cattle with rotavirus B during repeated outbreaks of epidemic diarrhea

    Journal: Canadian Journal of Veterinary Research

    doi:

    Phylogenetic trees for the VP7 gene (a) and the 5′-terminal region of VP4 gene (b) of bovine and human rotavirus B (RVB). The trees were generated using the MegAlign program of the Lasergene software (DNASTAR) on the basis of 772–816 bp
    Figure Legend Snippet: Phylogenetic trees for the VP7 gene (a) and the 5′-terminal region of VP4 gene (b) of bovine and human rotavirus B (RVB). The trees were generated using the MegAlign program of the Lasergene software (DNASTAR) on the basis of 772–816 bp

    Techniques Used: Generated, Software

    7) Product Images from "Genetically divergent methicillin-resistant Staphylococcus aureus and sec-dependent mastitis of dairy goats in Taiwan"

    Article Title: Genetically divergent methicillin-resistant Staphylococcus aureus and sec-dependent mastitis of dairy goats in Taiwan

    Journal: BMC Veterinary Research

    doi: 10.1186/1746-6148-8-39

    Phylogenetic tree of sec genes from eight Staphylococcus aureus isolates from goats with mastitis . The tree was constructed using the Megalign program of the Lasergene software. Scale bar represents number of nucleotide substitutions per? bases.
    Figure Legend Snippet: Phylogenetic tree of sec genes from eight Staphylococcus aureus isolates from goats with mastitis . The tree was constructed using the Megalign program of the Lasergene software. Scale bar represents number of nucleotide substitutions per? bases.

    Techniques Used: Size-exclusion Chromatography, Construct, Software

    8) Product Images from "Molecular epidemiology of Japanese encephalitis virus circulating in South Korea, 1983-2005"

    Article Title: Molecular epidemiology of Japanese encephalitis virus circulating in South Korea, 1983-2005

    Journal: Virology Journal

    doi: 10.1186/1743-422X-7-127

    Nucleotide and amino acid sequence similarities among Korean JEV strains . The percentage similarities between the aligned nucleotide and deduced amino acid sequences were calculated (uncorrected p-distances) with the MegAlign program implemented in the Lasergene software. The nucleotide similarities (%) are shown above the diagonal and the deduced amino acid identities (%) are shown below the diagonal.
    Figure Legend Snippet: Nucleotide and amino acid sequence similarities among Korean JEV strains . The percentage similarities between the aligned nucleotide and deduced amino acid sequences were calculated (uncorrected p-distances) with the MegAlign program implemented in the Lasergene software. The nucleotide similarities (%) are shown above the diagonal and the deduced amino acid identities (%) are shown below the diagonal.

    Techniques Used: Sequencing, Software

    Related Articles

    Sequencing:

    Article Title: De Novo Assembly and Functional Annotation of the Olive (Olea europaea) Transcriptome
    Article Snippet: .. Based on preliminary data using different computational assembly pipelines, including the 454 GS Assembler software, we chose to assemble the 454 sequence data using SeqMan Pro 8.1.1 (DNASTAR Lasergene v8.0 Suite, DNASTAR, USA). .. During pre-assembly, sequencing ends were trimmed using a medium-stringency criteria, with the following SeqMan parameters: average quality score Q/n threshold of 12, a non-trace window size of 50, and a maximum of 2 Ns.

    Article Title: Identification of a Single-Nucleotide Insertion in the Promoter Region Affecting the sodC Promoter Activity in Brucella neotomae
    Article Snippet: .. The nucleotide sequences were analyzed using LaserGene sequence analysis software (DNASTAR, Inc.). ..

    Article Title: Necessity of Quality-Controlled 16S rRNA Gene Sequence Databases: Identifying Nontuberculous Mycobacterium Species
    Article Snippet: .. The Lasergene program (version 4.01; DNASTAR, Inc., Madison, Wis.) was used for sequence assembly, sequence alignment, and phylogenetic analysis. .. Multiple sequence alignments were determined using the CLUSTAL method algorithm.

    Article Title: Decreased Serologic Response in Vaccinated Military Recruits during 2011 Correspond to Genetic Drift in Concurrent Circulating Pandemic A/H1N1 Viruses
    Article Snippet: .. Sequencing and Phylogenetic Analysis of Isolated Viruses To examine whether decreased serologic response from the A/CA/7/2009 H1N1 vaccine strain to circulating pH1N1 viruses isolated from recruits training in the southeastern United States in early 2011 correlated with antigenic drift, the HA1 genes from previous circulating and contemporaneous representative viruses were sequenced and a phylogenetic tree constructed using the neighbor-joining method (CLUSTAL W) of the MegAlign program (Lasergene software suite; DNASTAR Inc., Madison, WI) ( ). ..

    Article Title: A Polyclonal Antibody Against Recombinant Bovine Haptoglobin Expressed in Escherichia coli
    Article Snippet: .. The signal sequence of the BoHp protein was predicted and analyzed using SignalP-4 software (available at ). The B-cell antigenic regions of the BoHp protein were predicted using the Protean program included in the Lasergene DNASTAR™ software package, v. 5.06 ( ) on the basis of antigenic index (Jameson–Wolf ), surface probability plot (Emini), hydrophilicity plot (Kyte–Doolittle), flexible regions (Karlus-Schulz), and alpha regions (Chou–Fasman) ( ). .. The nucleotide sequence of the predicted immunodominant region of BoHp (pirBoHp) containing the Bam HI and Xho I restriction sites at the 5’ and 3’ terminals, respectively, was synthesized based on the codon usage bias of E. coli .

    Isolation:

    Article Title: Decreased Serologic Response in Vaccinated Military Recruits during 2011 Correspond to Genetic Drift in Concurrent Circulating Pandemic A/H1N1 Viruses
    Article Snippet: .. Sequencing and Phylogenetic Analysis of Isolated Viruses To examine whether decreased serologic response from the A/CA/7/2009 H1N1 vaccine strain to circulating pH1N1 viruses isolated from recruits training in the southeastern United States in early 2011 correlated with antigenic drift, the HA1 genes from previous circulating and contemporaneous representative viruses were sequenced and a phylogenetic tree constructed using the neighbor-joining method (CLUSTAL W) of the MegAlign program (Lasergene software suite; DNASTAR Inc., Madison, WI) ( ). ..

    Construct:

    Article Title: Decreased Serologic Response in Vaccinated Military Recruits during 2011 Correspond to Genetic Drift in Concurrent Circulating Pandemic A/H1N1 Viruses
    Article Snippet: .. Sequencing and Phylogenetic Analysis of Isolated Viruses To examine whether decreased serologic response from the A/CA/7/2009 H1N1 vaccine strain to circulating pH1N1 viruses isolated from recruits training in the southeastern United States in early 2011 correlated with antigenic drift, the HA1 genes from previous circulating and contemporaneous representative viruses were sequenced and a phylogenetic tree constructed using the neighbor-joining method (CLUSTAL W) of the MegAlign program (Lasergene software suite; DNASTAR Inc., Madison, WI) ( ). ..

    Marker:

    Article Title: Sequence Characterization of Mitochondrial 12S rRNA Gene in Mouse Deer (Moschiola indica) for PCR-RFLP Based Species Identification
    Article Snippet: .. Sequence analysis and restriction mapping in Lasergene (DNAstar Inc., Madison, WI, USA) confirmed the usefulness of 12S rRNA gene as molecular marker for differentiation of mouse deer from other species. .. Thus, it can be concluded that PCR-RFLP based analysis of mitochondrial 12S rRNA gene can be used as a tool for identification of mouse deer.

    Polymerase Chain Reaction:

    Article Title: Identification of cis-Regulatory Elements in the dmyc Gene of Drosophila Melanogaster
    Article Snippet: .. Polymerase chain reaction primers were designed for the lacZ reporter gene and Drosophila actin gene using PrimerSelect from the Lasergene software suite (DNASTAR, Madison, WI). ..

    Software:

    Article Title: De Novo Assembly and Functional Annotation of the Olive (Olea europaea) Transcriptome
    Article Snippet: .. Based on preliminary data using different computational assembly pipelines, including the 454 GS Assembler software, we chose to assemble the 454 sequence data using SeqMan Pro 8.1.1 (DNASTAR Lasergene v8.0 Suite, DNASTAR, USA). .. During pre-assembly, sequencing ends were trimmed using a medium-stringency criteria, with the following SeqMan parameters: average quality score Q/n threshold of 12, a non-trace window size of 50, and a maximum of 2 Ns.

    Article Title: Identification of a Single-Nucleotide Insertion in the Promoter Region Affecting the sodC Promoter Activity in Brucella neotomae
    Article Snippet: .. The nucleotide sequences were analyzed using LaserGene sequence analysis software (DNASTAR, Inc.). ..

    Article Title: Decreased Serologic Response in Vaccinated Military Recruits during 2011 Correspond to Genetic Drift in Concurrent Circulating Pandemic A/H1N1 Viruses
    Article Snippet: .. Sequencing and Phylogenetic Analysis of Isolated Viruses To examine whether decreased serologic response from the A/CA/7/2009 H1N1 vaccine strain to circulating pH1N1 viruses isolated from recruits training in the southeastern United States in early 2011 correlated with antigenic drift, the HA1 genes from previous circulating and contemporaneous representative viruses were sequenced and a phylogenetic tree constructed using the neighbor-joining method (CLUSTAL W) of the MegAlign program (Lasergene software suite; DNASTAR Inc., Madison, WI) ( ). ..

    Article Title: Identification of cis-Regulatory Elements in the dmyc Gene of Drosophila Melanogaster
    Article Snippet: .. Polymerase chain reaction primers were designed for the lacZ reporter gene and Drosophila actin gene using PrimerSelect from the Lasergene software suite (DNASTAR, Madison, WI). ..

    Article Title: A Polyclonal Antibody Against Recombinant Bovine Haptoglobin Expressed in Escherichia coli
    Article Snippet: .. The signal sequence of the BoHp protein was predicted and analyzed using SignalP-4 software (available at ). The B-cell antigenic regions of the BoHp protein were predicted using the Protean program included in the Lasergene DNASTAR™ software package, v. 5.06 ( ) on the basis of antigenic index (Jameson–Wolf ), surface probability plot (Emini), hydrophilicity plot (Kyte–Doolittle), flexible regions (Karlus-Schulz), and alpha regions (Chou–Fasman) ( ). .. The nucleotide sequence of the predicted immunodominant region of BoHp (pirBoHp) containing the Bam HI and Xho I restriction sites at the 5’ and 3’ terminals, respectively, was synthesized based on the codon usage bias of E. coli .

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  • 99
    DNASTAR megalign program
    Phylogenetic analysis of the hemagglutinin (HA) gene of influenza pH1N1 isolates. The phylogenetic tree was constructed using the neighbor-joining method (CLUSTAL W method) of the <t>MegAlign</t> program (Lasergene software suite, DNASTAR Inc., Madison, WI). The tree represents amino acids 111 through 360 of the mature HA protein. Reference strains for the six circulating subclades (2–7) are shown in bold text, with their defining mutations shown to the right. The vaccine strain, A/CA/7/2009, is shown in bold and italicized. Isolates collected by NHRC from recruits who had been vaccinated greater than 14 days are italicized. Strains from the same geographical location and time of collection from the GISAID database are included in the tree as well as two samples collected from the same recruit training sites in 2009. The scale indicates the distance created by a one amino-acid difference between sequences. The number of amino acid changes between subclades is denoted by a delta symbol (Δ).
    Megalign Program, supplied by DNASTAR, used in various techniques. Bioz Stars score: 99/100, based on 184 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/megalign program/product/DNASTAR
    Average 99 stars, based on 184 article reviews
    Price from $9.99 to $1999.99
    megalign program - by Bioz Stars, 2020-08
    99/100 stars
      Buy from Supplier

    Image Search Results


    Phylogenetic analysis of the hemagglutinin (HA) gene of influenza pH1N1 isolates. The phylogenetic tree was constructed using the neighbor-joining method (CLUSTAL W method) of the MegAlign program (Lasergene software suite, DNASTAR Inc., Madison, WI). The tree represents amino acids 111 through 360 of the mature HA protein. Reference strains for the six circulating subclades (2–7) are shown in bold text, with their defining mutations shown to the right. The vaccine strain, A/CA/7/2009, is shown in bold and italicized. Isolates collected by NHRC from recruits who had been vaccinated greater than 14 days are italicized. Strains from the same geographical location and time of collection from the GISAID database are included in the tree as well as two samples collected from the same recruit training sites in 2009. The scale indicates the distance created by a one amino-acid difference between sequences. The number of amino acid changes between subclades is denoted by a delta symbol (Δ).

    Journal: PLoS ONE

    Article Title: Decreased Serologic Response in Vaccinated Military Recruits during 2011 Correspond to Genetic Drift in Concurrent Circulating Pandemic A/H1N1 Viruses

    doi: 10.1371/journal.pone.0034581

    Figure Lengend Snippet: Phylogenetic analysis of the hemagglutinin (HA) gene of influenza pH1N1 isolates. The phylogenetic tree was constructed using the neighbor-joining method (CLUSTAL W method) of the MegAlign program (Lasergene software suite, DNASTAR Inc., Madison, WI). The tree represents amino acids 111 through 360 of the mature HA protein. Reference strains for the six circulating subclades (2–7) are shown in bold text, with their defining mutations shown to the right. The vaccine strain, A/CA/7/2009, is shown in bold and italicized. Isolates collected by NHRC from recruits who had been vaccinated greater than 14 days are italicized. Strains from the same geographical location and time of collection from the GISAID database are included in the tree as well as two samples collected from the same recruit training sites in 2009. The scale indicates the distance created by a one amino-acid difference between sequences. The number of amino acid changes between subclades is denoted by a delta symbol (Δ).

    Article Snippet: Sequencing and Phylogenetic Analysis of Isolated Viruses To examine whether decreased serologic response from the A/CA/7/2009 H1N1 vaccine strain to circulating pH1N1 viruses isolated from recruits training in the southeastern United States in early 2011 correlated with antigenic drift, the HA1 genes from previous circulating and contemporaneous representative viruses were sequenced and a phylogenetic tree constructed using the neighbor-joining method (CLUSTAL W) of the MegAlign program (Lasergene software suite; DNASTAR Inc., Madison, WI) ( ).

    Techniques: Construct, Software

    Prediction and synthesis of immunodominant region of bovine haptogobin (pirBoHp). ( A ) Prediction of B-cell antigenic regions of bovine haptogobin by Lasergene DNASTAR software. ( B ) Synthesis of the nucleotide sequence of pirBoHp. Note : underlined small

    Journal: Monoclonal Antibodies in Immunodiagnosis and Immunotherapy

    Article Title: A Polyclonal Antibody Against Recombinant Bovine Haptoglobin Expressed in Escherichia coli

    doi: 10.1089/mab.2013.0061

    Figure Lengend Snippet: Prediction and synthesis of immunodominant region of bovine haptogobin (pirBoHp). ( A ) Prediction of B-cell antigenic regions of bovine haptogobin by Lasergene DNASTAR software. ( B ) Synthesis of the nucleotide sequence of pirBoHp. Note : underlined small

    Article Snippet: The signal sequence of the BoHp protein was predicted and analyzed using SignalP-4 software (available at ). The B-cell antigenic regions of the BoHp protein were predicted using the Protean program included in the Lasergene DNASTAR™ software package, v. 5.06 ( ) on the basis of antigenic index (Jameson–Wolf ), surface probability plot (Emini), hydrophilicity plot (Kyte–Doolittle), flexible regions (Karlus-Schulz), and alpha regions (Chou–Fasman) ( ).

    Techniques: Software, Sequencing

    Multiple alignment of nucleotide sequences of the 5′ flanking region of sodC start codon from B. abortus , B. suis biovars 4 (strain 40) or 1 (strain 1330) and 2 (strain Thomsen), and B. neotomae . Alignment was performed with the Clustal method of the MegAlign program of LaserGene software. Gaps are indicated by dashes. The nucleotides differing between B. suis and B. abortus or B. neotomae are in bold and underlined. Note: B. melitensis nucleotide sequences are identical to those of B. abortus shown above.

    Journal: PLoS ONE

    Article Title: Identification of a Single-Nucleotide Insertion in the Promoter Region Affecting the sodC Promoter Activity in Brucella neotomae

    doi: 10.1371/journal.pone.0014112

    Figure Lengend Snippet: Multiple alignment of nucleotide sequences of the 5′ flanking region of sodC start codon from B. abortus , B. suis biovars 4 (strain 40) or 1 (strain 1330) and 2 (strain Thomsen), and B. neotomae . Alignment was performed with the Clustal method of the MegAlign program of LaserGene software. Gaps are indicated by dashes. The nucleotides differing between B. suis and B. abortus or B. neotomae are in bold and underlined. Note: B. melitensis nucleotide sequences are identical to those of B. abortus shown above.

    Article Snippet: The nucleotide sequences were analyzed using LaserGene sequence analysis software (DNASTAR, Inc.).

    Techniques: Software

    Comparison of partial sequences of DOX and CYP domains. A: Partial alignment of the DOX domains of COX-1 and -2, 7,8- and 5,8-LDS, ATEG_02036, and FOXB_01332 by ClustalW. The catalytically important Tyr residue and the proximal His ligand are in red,

    Journal: Journal of Lipid Research

    Article Title: Discovery of a linoleate 9S-dioxygenase and an allene oxide synthase in a fusion protein of Fusarium oxysporum [S]

    doi: 10.1194/jlr.M044347

    Figure Lengend Snippet: Comparison of partial sequences of DOX and CYP domains. A: Partial alignment of the DOX domains of COX-1 and -2, 7,8- and 5,8-LDS, ATEG_02036, and FOXB_01332 by ClustalW. The catalytically important Tyr residue and the proximal His ligand are in red,

    Article Snippet: Proteins were aligned with the ClustalW algorithm (Lasergene, DNASTAR, Inc.).

    Techniques: