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dnasis max 3.0 software  (Hitachi Ltd)


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    Hitachi Ltd dnasis max 3.0 software
    Dnasis Max 3.0 Software, supplied by Hitachi Ltd, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/dnasis max 3.0 software/product/Hitachi Ltd
    Average 90 stars, based on 1 article reviews
    dnasis max 3.0 software - by Bioz Stars, 2026-04
    90/100 stars

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    dnasis max bioinformatics software  (Hitachi Ltd)
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    (a) The predicted amino acid sequence of the splice variant protein is aligned with the amino acid sequence of native Nox2 (Acc: BAE31076). Hyphens indicate region of spliced sequence. Asterisks indicate histidine residues reported to be important in heme binding. Underlined amino acids specify putative NADPH binding sites and hatched boxes signify predicted p47phox binding regions. Spotted boxes indicate the putative FAD binding motifs and the hash indicate predicted glycosylation sites. Alignment was achieved using <t>DNASIS</t> <t>MAX</t> software. (b) Hydrophobicity plot generated by “ The Molecular Toolkit: Colorado State University”. Red boxes indicate two regions of significant hydrophobicity.
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    (a) The predicted amino acid sequence of the splice variant protein is aligned with the amino acid sequence of native Nox2 (Acc: BAE31076). Hyphens indicate region of spliced sequence. Asterisks indicate histidine residues reported to be important in heme binding. Underlined amino acids specify putative NADPH binding sites and hatched boxes signify predicted p47phox binding regions. Spotted boxes indicate the putative FAD binding motifs and the hash indicate predicted glycosylation sites. Alignment was achieved using DNASIS MAX software. (b) Hydrophobicity plot generated by “ The Molecular Toolkit: Colorado State University”. Red boxes indicate two regions of significant hydrophobicity.

    Journal: PLoS ONE

    Article Title: NOX2β: A Novel Splice Variant of NOX2 That Regulates NADPH Oxidase Activity in Macrophages

    doi: 10.1371/journal.pone.0048326

    Figure Lengend Snippet: (a) The predicted amino acid sequence of the splice variant protein is aligned with the amino acid sequence of native Nox2 (Acc: BAE31076). Hyphens indicate region of spliced sequence. Asterisks indicate histidine residues reported to be important in heme binding. Underlined amino acids specify putative NADPH binding sites and hatched boxes signify predicted p47phox binding regions. Spotted boxes indicate the putative FAD binding motifs and the hash indicate predicted glycosylation sites. Alignment was achieved using DNASIS MAX software. (b) Hydrophobicity plot generated by “ The Molecular Toolkit: Colorado State University”. Red boxes indicate two regions of significant hydrophobicity.

    Article Snippet: Sequence alignment and analysis was performed using DNASIS MAX bioinformatics software from Hitachi Solutions America Ltd. LUSTAL.

    Techniques: Sequencing, Variant Assay, Binding Assay, Software, Generated