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chaperone protein dnak  (ATCC)


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    ATCC chaperone protein dnak
    Chaperone Protein Dnak, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 1527 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/chaperone+protein+dnak/pmc12475490__41467_2025_63426_MOESM3_ESM-593-196-201?v=ATCC
    Average 99 stars, based on 1527 article reviews
    chaperone protein dnak - by Bioz Stars, 2026-07
    99/100 stars

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    Image Search Results


    TCS data for Fl4BN1, Fl4BN2 and Fl5BN2. ** above cut-off (> 0.999), * in range (> 0.989), below cut-off (< 0.989).

    Journal: Data in Brief

    Article Title: Dataset on phenotypic characterization, on protein and genome analysis of three fluorescent Pseudomonas strains from mid-mountain water

    doi: 10.1016/j.dib.2020.105466

    Figure Lengend Snippet: TCS data for Fl4BN1, Fl4BN2 and Fl5BN2. ** above cut-off (> 0.999), * in range (> 0.989), below cut-off (< 0.989).

    Article Snippet: , , Chaperone protein DnaK OS= Pseudomonas fluorescens (strain ATCC BAA-477 / NRRL B-23,932 / Pf-5) GN=dnaK , DNAK_PSEF5 , 68.476 , 12 , 171.05 , SwissP_ Bacteria _R.

    Techniques: Bacteria

    Identification of the proteins released by Fl4BN1, Fl4BN2 and Fl5BN2. They migrated in a gel with an isoelectric point gradient from 3 to 10 and were identified by the technique of peptide mapping by mass through the “Mascot” search algorithm. ( http://www.matrixscience.com/cgi/search_form.pl?FORMVER=2&SEARCH=PMF ). In the algorithm Mascot with the SwissProt and NCBI

    Journal: Data in Brief

    Article Title: Dataset on phenotypic characterization, on protein and genome analysis of three fluorescent Pseudomonas strains from mid-mountain water

    doi: 10.1016/j.dib.2020.105466

    Figure Lengend Snippet: Identification of the proteins released by Fl4BN1, Fl4BN2 and Fl5BN2. They migrated in a gel with an isoelectric point gradient from 3 to 10 and were identified by the technique of peptide mapping by mass through the “Mascot” search algorithm. ( http://www.matrixscience.com/cgi/search_form.pl?FORMVER=2&SEARCH=PMF ). In the algorithm Mascot with the SwissProt and NCBI "National Center for Biotechnology Information" databases, protein identification was “significant” if the probability MOWSE score was greater than the signification threshold where P was the probability that the observed match was a random event. (Spot no.) spot number. (MW) molecular weight. (Nb) number of experimental peptides recognized. Maximum ≠ between theoretical/experimental masses = maximum difference between theoretical peptide masses and experimental ones, expressed in ppm (parts per million).

    Article Snippet: , , Chaperone protein DnaK OS= Pseudomonas fluorescens (strain ATCC BAA-477 / NRRL B-23,932 / Pf-5) GN=dnaK , DNAK_PSEF5 , 68.476 , 12 , 171.05 , SwissP_ Bacteria _R.

    Techniques: Molecular Weight, Sequencing

    Identification of the proteins released by Fl4BN1. They migrated in a gel with an isoelectric point gradient from 3 to 10 and were identified by the technique of peptide mapping by mass through the “PEAKS studio” search algorithm, NCBI database. In the algorithm of PEAKS studio with the SwissProt and NCBI “National Center for Biotechnology Information” databases, protein identification was “significant” if the (−10lgP) score was greater than the peptide hit threshold (30.0). P was the probability that the observed match was a random event. (Spot no.) spot number. (MW) molecular weight. (R) reviewed. (NR) not reviewed. ( P. protegens ) Pseudomonas protegens .

    Journal: Data in Brief

    Article Title: Dataset on phenotypic characterization, on protein and genome analysis of three fluorescent Pseudomonas strains from mid-mountain water

    doi: 10.1016/j.dib.2020.105466

    Figure Lengend Snippet: Identification of the proteins released by Fl4BN1. They migrated in a gel with an isoelectric point gradient from 3 to 10 and were identified by the technique of peptide mapping by mass through the “PEAKS studio” search algorithm, NCBI database. In the algorithm of PEAKS studio with the SwissProt and NCBI “National Center for Biotechnology Information” databases, protein identification was “significant” if the (−10lgP) score was greater than the peptide hit threshold (30.0). P was the probability that the observed match was a random event. (Spot no.) spot number. (MW) molecular weight. (R) reviewed. (NR) not reviewed. ( P. protegens ) Pseudomonas protegens .

    Article Snippet: , , Chaperone protein DnaK OS= Pseudomonas fluorescens (strain ATCC BAA-477 / NRRL B-23,932 / Pf-5) GN=dnaK , DNAK_PSEF5 , 68.476 , 12 , 171.05 , SwissP_ Bacteria _R.

    Techniques: Molecular Weight, Sequencing, Bacteria

    Identification of the proteins released by Fl4BN1. They migrated in a gel with an isoelectric point gradient from 3 to 10 and were identified by the technique of peptide mapping by mass through the “PEAKS studio” search algorithm, SwissProt database. In the algorithm of PEAKS studio with the SwissProt and NCBI

    Journal: Data in Brief

    Article Title: Dataset on phenotypic characterization, on protein and genome analysis of three fluorescent Pseudomonas strains from mid-mountain water

    doi: 10.1016/j.dib.2020.105466

    Figure Lengend Snippet: Identification of the proteins released by Fl4BN1. They migrated in a gel with an isoelectric point gradient from 3 to 10 and were identified by the technique of peptide mapping by mass through the “PEAKS studio” search algorithm, SwissProt database. In the algorithm of PEAKS studio with the SwissProt and NCBI "National Center for Biotechnology Information" databases, protein identification was "significant" if the (−10lgP) score was greater than the peptide hit threshold (30.0). P was the probability that the observed match was a random event. (Spot no.) spot number. (MW) molecular weight. (R) reviewed. (NR) not reviewed. ( P. protegens ) Pseudomonas protegens .

    Article Snippet: , , Chaperone protein DnaK OS= Pseudomonas fluorescens (strain ATCC BAA-477 / NRRL B-23,932 / Pf-5) GN=dnaK , DNAK_PSEF5 , 68.476 , 12 , 171.05 , SwissP_ Bacteria _R.

    Techniques: Molecular Weight, Sequencing, Bacteria

    Identification of the proteins released by Fl4BN2 culture. They migrated in a gel with an isoelectric point gradient from 3 to 10 and were identified by the technique of peptide mapping by mass through the “PEAKS studio” search algorithm, NCBI database. In the algorithm of PEAKS studio with the SwissProt and NCBI

    Journal: Data in Brief

    Article Title: Dataset on phenotypic characterization, on protein and genome analysis of three fluorescent Pseudomonas strains from mid-mountain water

    doi: 10.1016/j.dib.2020.105466

    Figure Lengend Snippet: Identification of the proteins released by Fl4BN2 culture. They migrated in a gel with an isoelectric point gradient from 3 to 10 and were identified by the technique of peptide mapping by mass through the “PEAKS studio” search algorithm, NCBI database. In the algorithm of PEAKS studio with the SwissProt and NCBI "National Center for Biotechnology Information" databases, protein identification was "significant" if the (−10lgP) score was greater than the peptide hit threshold (30.0). P was the probability that the observed match was a random event. (Spot no.) spot number. (MW) molecular weight. (R) reviewed. (NR) not reviewed. ( P. protegens ) Pseudomonas protegens .

    Article Snippet: , , Chaperone protein DnaK OS= Pseudomonas fluorescens (strain ATCC BAA-477 / NRRL B-23,932 / Pf-5) GN=dnaK , DNAK_PSEF5 , 68.476 , 12 , 171.05 , SwissP_ Bacteria _R.

    Techniques: Molecular Weight, Sequencing, Bacteria

    Identification of the proteins released by Fl4BN2. They migrated in a gel with an isoelectric point gradient from 3 to 10 and were identified by the technique of peptide mapping by mass through the “PEAKS studio” search algorithm, SwissProt database. In the algorithm of PEAKS studio with the SwissProt and NCBI “National Center for Biotechnology Information” databases, protein identification was “significant” if the (−10lgP) score was greater than the peptide hit threshold (30.0). P was the probability that the observed match was a random event. (Spot no.) spot number. (MW) molecular weight. (R) reviewed. (NR) not reviewed. ( P. protegens ) Pseudomonas protegens .

    Journal: Data in Brief

    Article Title: Dataset on phenotypic characterization, on protein and genome analysis of three fluorescent Pseudomonas strains from mid-mountain water

    doi: 10.1016/j.dib.2020.105466

    Figure Lengend Snippet: Identification of the proteins released by Fl4BN2. They migrated in a gel with an isoelectric point gradient from 3 to 10 and were identified by the technique of peptide mapping by mass through the “PEAKS studio” search algorithm, SwissProt database. In the algorithm of PEAKS studio with the SwissProt and NCBI “National Center for Biotechnology Information” databases, protein identification was “significant” if the (−10lgP) score was greater than the peptide hit threshold (30.0). P was the probability that the observed match was a random event. (Spot no.) spot number. (MW) molecular weight. (R) reviewed. (NR) not reviewed. ( P. protegens ) Pseudomonas protegens .

    Article Snippet: , , Chaperone protein DnaK OS= Pseudomonas fluorescens (strain ATCC BAA-477 / NRRL B-23,932 / Pf-5) GN=dnaK , DNAK_PSEF5 , 68.476 , 12 , 171.05 , SwissP_ Bacteria _R.

    Techniques: Molecular Weight, Sequencing, Bacteria

    Identification of the proteins released by Fl5BN2. They migrated in a gel with an isoelectric point gradient from 3 to 10 and were identified by the technique of peptide mapping by mass through the “PEAKS studio” search algorithm, NCBI database. In the algorithm of PEAKS studio with the SwissProt and NCBI

    Journal: Data in Brief

    Article Title: Dataset on phenotypic characterization, on protein and genome analysis of three fluorescent Pseudomonas strains from mid-mountain water

    doi: 10.1016/j.dib.2020.105466

    Figure Lengend Snippet: Identification of the proteins released by Fl5BN2. They migrated in a gel with an isoelectric point gradient from 3 to 10 and were identified by the technique of peptide mapping by mass through the “PEAKS studio” search algorithm, NCBI database. In the algorithm of PEAKS studio with the SwissProt and NCBI "National Center for Biotechnology Information" databases, protein identification was "significant" if the (−10lgP) score was greater than the peptide hit threshold (30.0). P was the probability that the observed match was a random event. (Spot no.) spot number. (MW) molecular weight. (R) reviewed. (NR) not reviewed. ( P. protegens ) Pseudomonas protegens .

    Article Snippet: , , Chaperone protein DnaK OS= Pseudomonas fluorescens (strain ATCC BAA-477 / NRRL B-23,932 / Pf-5) GN=dnaK , DNAK_PSEF5 , 68.476 , 12 , 171.05 , SwissP_ Bacteria _R.

    Techniques: Molecular Weight, Sequencing, Bacteria

    Identification of the proteins released by Fl5BN2. They migrated in a gel with an isoelectric point gradient from 3 to 10 and were identified by the technique of peptide mapping by mass through the “PEAKS studio” search algorithm, SwissProt database. In the algorithm of PEAKS studio with the SwissProt and NCBI

    Journal: Data in Brief

    Article Title: Dataset on phenotypic characterization, on protein and genome analysis of three fluorescent Pseudomonas strains from mid-mountain water

    doi: 10.1016/j.dib.2020.105466

    Figure Lengend Snippet: Identification of the proteins released by Fl5BN2. They migrated in a gel with an isoelectric point gradient from 3 to 10 and were identified by the technique of peptide mapping by mass through the “PEAKS studio” search algorithm, SwissProt database. In the algorithm of PEAKS studio with the SwissProt and NCBI "National Center for Biotechnology Information" databases, protein identification was "significant" if the (−10lgP) score was greater than the peptide hit threshold (30.0). P was the probability that the observed match was a random event. (Spot no.) spot number. (MW) molecular weight. (R) reviewed. (NR) not reviewed. ( P. protegens ) Pseudomonas protegens .

    Article Snippet: , , Chaperone protein DnaK OS= Pseudomonas fluorescens (strain ATCC BAA-477 / NRRL B-23,932 / Pf-5) GN=dnaK , DNAK_PSEF5 , 68.476 , 12 , 171.05 , SwissP_ Bacteria _R.

    Techniques: Molecular Weight, Sequencing, Bacteria