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multiple protein sequence alignments  (DNASTAR)


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    Structured Review

    DNASTAR multiple protein sequence alignments
    Multiple Protein Sequence Alignments, supplied by DNASTAR, used in various techniques. Bioz Stars score: 96/100, based on 283 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/protein+multiple+sequence+alignments/MegAlign+Pro/pm40447203-67-0-13
    Average 96 stars, based on 283 article reviews
    multiple protein sequence alignments - by Bioz Stars, 2026-11
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    other:

    Article Title: Sequence Analysis of the Hemagglutinin Gene of H9N2 Korean Avian Influenza Viruses and Assessment of the Pathogenic Potential of Isolate MS96
    Article Snippet: Sequence Analysis of the Hemagglutinin Gene of H9N2 Korean Avian Influenza Viruses and Assessment of the Pathogenic Potential of Isolate MS96 Author(s): Chang-Won Lee, Chang-Seon Song, Youn-Jeong Lee, In-Pil Mo, Maricarmen Garcia, David L. Suarez and Sun-Joong Kim Source: Avian Diseases, Vol.. 44, No. 3 (Jul.. - Sep., 2000), pp.

    Sequencing:

    Article Title: Identification of Phthiodiolone Ketoreductase, an Enzyme Required for Production of Mycobacterial Diacyl Phthiocerol Virulence Factors
    Article Snippet: .. Multiple protein sequence alignments were performed using Clustal W software bundled with the MegAlign sequence alignment software package (DNASTAR, Inc.). ..

    Article Title: Rab5b localization to early endosomes in the protozoan human pathogen Leishmania donovani.
    Article Snippet: Leishmania donovani is a primitive trypanosomatid pathogen of humans.. This protozoan is apically polarized such that the flagellar reservoir, the exclusive site of endocytosis and exocytosis, is situated at the anterior end.. Recent evidence for the existence of an endocytic pathway in Leishmania has prompted us to investigate candidate temporal markers for endocytosis.

    Article Title: La Crosse virus reassortants highlight genomic determinants of infection and pathogenesis
    Article Snippet: .. RNA conservation within WT strains was aligned using Smitt-Watermen RNA alignment and protein conservation within WT strains was generated using ClustalW Multiple Sequence alignment with MegAlign Pro (DNASTAR; Version 17.4.1.17). ..

    Article Title: Catalysis and structural properties of Leishmania infantum glyoxalase II: trypanothione specificity and phylogeny.
    Article Snippet: The glyoxalase pathway catalyzes the formation of D-lactate from methylglyoxal, a toxic byproduct of glycolysis.. In trypanosomatids, trypanothione replaces glutathione in this pathway, making it a potential drug target, since its selective inhibition might increase methylglyoxal concentration in the parasites.. Two glyoxalase II structures were solved.

    Article Title: Construction of an ~700-kb Transcript Map Around the Familial Mediterranean Fever Locus on Human Chromosome 16p13.3
    Article Snippet: Determination of open reading frames within clones was done using the MapDraw program (DNAStar, Madison, WI). .. DNA and protein sequence comparisons were done with Megalign multiple sequence alignment program (DNAStar) using a clustal algorithim with a gap penalty and gap-length penalty of 10. .. Identification of transmembrane domains in the putative olfactory receptor open reading frame was done using Protean software (DNAStar).

    Article Title: Origin of a novel protein-coding gene family with similar signal sequence in Schistosoma japonicum
    Article Snippet: .. All multiple sequence alignments of DNA and protein sequences were performed in parallel with ClustalW on MegAlign program in Lasergene 7 DNASTAR software, NCBI bl2seq, COBALT multiple alignment programs, and Multialin interface software [ ]. ..

    Article Title: Molecular cloning, expression, and functional analysis of cystatin B from silver pomfret (Pampus argenteus) under Vibrio parahaemolyticus challenge.
    Article Snippet: Cystatin B is an intracellular inhibitor that regulates the activity of cysteine proteases.. In this study, the coding sequence of silver pomfret cystatin B was successfully cloned and identified, which was 297 bp in length, predicted to encode 98 amino acids with a molecular weight of approximately 11.12 kDa.. Sequence analysis revealed that PaCystatin B (Pampus argenteus Cystatin B) exhibited a high degree of conservation with Cystatin B orthologs from other fish species, maintaining characteristic motifs essential for cysteine protease inhibition, such as the conserved QXVXG motif.

    Software:

    Article Title: Identification of Phthiodiolone Ketoreductase, an Enzyme Required for Production of Mycobacterial Diacyl Phthiocerol Virulence Factors
    Article Snippet: .. Multiple protein sequence alignments were performed using Clustal W software bundled with the MegAlign sequence alignment software package (DNASTAR, Inc.). ..

    Article Title: Origin of a novel protein-coding gene family with similar signal sequence in Schistosoma japonicum
    Article Snippet: .. All multiple sequence alignments of DNA and protein sequences were performed in parallel with ClustalW on MegAlign program in Lasergene 7 DNASTAR software, NCBI bl2seq, COBALT multiple alignment programs, and Multialin interface software [ ]. ..

    Article Title: Molecular cloning, expression, and functional analysis of cystatin B from silver pomfret (Pampus argenteus) under Vibrio parahaemolyticus challenge.
    Article Snippet: Cystatin B is an intracellular inhibitor that regulates the activity of cysteine proteases.. In this study, the coding sequence of silver pomfret cystatin B was successfully cloned and identified, which was 297 bp in length, predicted to encode 98 amino acids with a molecular weight of approximately 11.12 kDa.. Sequence analysis revealed that PaCystatin B (Pampus argenteus Cystatin B) exhibited a high degree of conservation with Cystatin B orthologs from other fish species, maintaining characteristic motifs essential for cysteine protease inhibition, such as the conserved QXVXG motif.

    Generated:

    Article Title: La Crosse virus reassortants highlight genomic determinants of infection and pathogenesis
    Article Snippet: .. RNA conservation within WT strains was aligned using Smitt-Watermen RNA alignment and protein conservation within WT strains was generated using ClustalW Multiple Sequence alignment with MegAlign Pro (DNASTAR; Version 17.4.1.17). ..



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    Image Search Results


    High and low frequency non-synonymous single nucleotide polymorphisms (SNPs) in human CEACAM1 N domain. ( A ) The amino acid sequences of the mature CEACAM1 N domain (leader sequences removed) from human (Hsa), bonobo (Ppa), and chimpanzee (Ptr) were aligned using the KALIGN multiple protein sequence alignment program. Amino acids deviating from the human sequence are underlined. The position of common SNPs found in certain African tribes are indicated by green boxes. A less common SNP at a position with variation in the other apes is marked in blue. A low frequency, functionally relevant SNP is boxed with red lines. The degree of conservation of the sequences is shown at the bottom of the graph [* = identical (red), : = conservative changes (green), . = less stringent conservative changes (blue)]. The location, sequence, and name of active human CEACAM1 peptides functionally tested in a granulocyte activation assay [ , , ] are highlighted and shown below the CEACAM1 N exon amino acid sequence alignment. ( B ) High and selected low frequency non-synonymous SNPs were derived from the 1000 Genomes Project Phase 3 and Gambian Genome Variation Project; their highest population frequency in the indicated population and corresponding identifiers are indicated below the human CEACAM1N domain sequence. Amino acid numbering (1) starts at the first amino acid of the leader sequence. SNPs commonly co-inherited (haplotype) are depicted as colored boxes connected by lines. #: A to V in human CEACAM1 increases the affinity to Helicobacter pylori HopQ AD-I adhesin 1.7-fold . The regions which contain critical amino acids important for pathogen adhesin binding are highlighted by blue lines . GWD, Gambian in Western Division—The Gambia, Mandinka; MSL, Mende, in Sierra Leone; YRI, Yoruba in Ibadan, Nigeria.

    Journal: Biology

    Article Title: Evolution of CEACAM1 N Domain Biologically Active Sites in Primates

    doi: 10.3390/biology14121744

    Figure Lengend Snippet: High and low frequency non-synonymous single nucleotide polymorphisms (SNPs) in human CEACAM1 N domain. ( A ) The amino acid sequences of the mature CEACAM1 N domain (leader sequences removed) from human (Hsa), bonobo (Ppa), and chimpanzee (Ptr) were aligned using the KALIGN multiple protein sequence alignment program. Amino acids deviating from the human sequence are underlined. The position of common SNPs found in certain African tribes are indicated by green boxes. A less common SNP at a position with variation in the other apes is marked in blue. A low frequency, functionally relevant SNP is boxed with red lines. The degree of conservation of the sequences is shown at the bottom of the graph [* = identical (red), : = conservative changes (green), . = less stringent conservative changes (blue)]. The location, sequence, and name of active human CEACAM1 peptides functionally tested in a granulocyte activation assay [ , , ] are highlighted and shown below the CEACAM1 N exon amino acid sequence alignment. ( B ) High and selected low frequency non-synonymous SNPs were derived from the 1000 Genomes Project Phase 3 and Gambian Genome Variation Project; their highest population frequency in the indicated population and corresponding identifiers are indicated below the human CEACAM1N domain sequence. Amino acid numbering (1) starts at the first amino acid of the leader sequence. SNPs commonly co-inherited (haplotype) are depicted as colored boxes connected by lines. #: A to V in human CEACAM1 increases the affinity to Helicobacter pylori HopQ AD-I adhesin 1.7-fold . The regions which contain critical amino acids important for pathogen adhesin binding are highlighted by blue lines . GWD, Gambian in Western Division—The Gambia, Mandinka; MSL, Mende, in Sierra Leone; YRI, Yoruba in Ibadan, Nigeria.

    Article Snippet: Amino acid sequence alignments were performed using the KALIGN multiple protein sequence alignment tool ( https://npsa.lyon.inserm.fr/cgi-bin/npsa_automat.pl?page=/NPSA/npsa_kalign.html , accessed 17 April 2025).

    Techniques: Sequencing, Activation Assay, Derivative Assay, Binding Assay, Western Blot