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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: , /Temperature acclimation protein B OS= Pseudomonas fluorescens (strain ATCC BAA-477 / NRRL B-23,932 / Pf-5) OX=220,664 GN=tapB , Q4K7Q5_PSEF5 , 7.736 , 40 , 34.43 , SwissP_ P. protegens.

Techniques: 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, 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: , /Temperature acclimation protein B OS= Pseudomonas fluorescens (strain ATCC BAA-477 / NRRL B-23,932 / Pf-5) OX=220,664 GN=tapB , Q4K7Q5_PSEF5 , 7.736 , 40 , 34.43 , SwissP_ P. protegens.

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: , /Temperature acclimation protein B OS= Pseudomonas fluorescens (strain ATCC BAA-477 / NRRL B-23,932 / Pf-5) OX=220,664 GN=tapB , Q4K7Q5_PSEF5 , 7.736 , 40 , 34.43 , SwissP_ P. protegens.

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: , /Temperature acclimation protein B OS= Pseudomonas fluorescens (strain ATCC BAA-477 / NRRL B-23,932 / Pf-5) OX=220,664 GN=tapB , Q4K7Q5_PSEF5 , 7.736 , 40 , 34.43 , SwissP_ P. protegens.

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: , /Temperature acclimation protein B OS= Pseudomonas fluorescens (strain ATCC BAA-477 / NRRL B-23,932 / Pf-5) OX=220,664 GN=tapB , Q4K7Q5_PSEF5 , 7.736 , 40 , 34.43 , SwissP_ P. protegens.

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: , /Temperature acclimation protein B OS= Pseudomonas fluorescens (strain ATCC BAA-477 / NRRL B-23,932 / Pf-5) OX=220,664 GN=tapB , Q4K7Q5_PSEF5 , 7.736 , 40 , 34.43 , SwissP_ P. protegens.

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: , /Temperature acclimation protein B OS= Pseudomonas fluorescens (strain ATCC BAA-477 / NRRL B-23,932 / Pf-5) OX=220,664 GN=tapB , Q4K7Q5_PSEF5 , 7.736 , 40 , 34.43 , SwissP_ P. protegens.

Techniques: Molecular Weight, Sequencing, Bacteria