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    InterPro Inc cluster of orthologous groups of proteins database
    Cluster Of Orthologous Groups Of Proteins Database, supplied by InterPro Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Article Snippet: Subsequently, these unigenes were annotated using seven public databases, including non-redundant protein database (NR), non-redundant nucleotide database (NT), gene ontology database (GO), cluster of orthologous groups of proteins database (COG), kyoto encyclopaedia of genes and genomes database (KEGG), Swiss-Prot protein database (Swiss-Prot) and Interpro.



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    Biotechnology Information cluster of orthologous groups of proteins (cogs) database
    The statistical results of subcellular localization and <t>COGs</t> functional categories <t>of</t> <t>DEPs.</t> ( A ) Subcellular localization of DEPs in the ‘Freezing-6 h vs. CK’ comparison. The percentage represents the ratio of DEPs located in a specific subcellular structure. ( B ) Subcellular localization of DEPs in the ‘Freezing-30 h vs. CK’ comparison. ( C ) The COGs functional categories of DEPs in the ‘Freezing-6 h vs. CK’ comparison. ( D ) The COGs functional categories of DEPs in the ‘Freezing-30 h vs. CK’ comparison.
    Cluster Of Orthologous Groups Of Proteins (Cogs) Database, supplied by Biotechnology Information, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    The statistical results of subcellular localization and <t>COGs</t> functional categories <t>of</t> <t>DEPs.</t> ( A ) Subcellular localization of DEPs in the ‘Freezing-6 h vs. CK’ comparison. The percentage represents the ratio of DEPs located in a specific subcellular structure. ( B ) Subcellular localization of DEPs in the ‘Freezing-30 h vs. CK’ comparison. ( C ) The COGs functional categories of DEPs in the ‘Freezing-6 h vs. CK’ comparison. ( D ) The COGs functional categories of DEPs in the ‘Freezing-30 h vs. CK’ comparison.
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    The statistical results of subcellular localization and <t>COGs</t> functional categories <t>of</t> <t>DEPs.</t> ( A ) Subcellular localization of DEPs in the ‘Freezing-6 h vs. CK’ comparison. The percentage represents the ratio of DEPs located in a specific subcellular structure. ( B ) Subcellular localization of DEPs in the ‘Freezing-30 h vs. CK’ comparison. ( C ) The COGs functional categories of DEPs in the ‘Freezing-6 h vs. CK’ comparison. ( D ) The COGs functional categories of DEPs in the ‘Freezing-30 h vs. CK’ comparison.
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    Structure of T6SS gene cluster analysis of the pathogenic strain Psa M228. (A) Molecular phylogenetic analysis by Maximum Likelihood method. The evolutionary history was inferred using the Maximum Likelihood method based on the Le_Gascuel_2008 model . The bootstrap consensus tree inferred from 1000 replicates was used to represent the evolutionary history of the taxa analyzed . Branches corresponding to partitions reproduced in less than 60% bootstrap replicates were collapsed. The percentage of replicate trees in which the associated taxa clustered together in the bootstrap test (1000 replicates) is shown next to the branches . The initial tree(s) for the heuristic search were obtained automatically by applying Neighbor-Join and BioNJ algorithms to a matrix of pairwise distances estimated using a JTT model, and the topology with a superior log likelihood value was selected. A discrete Gamma distribution was used to model evolutionary rate differences among sites [five categories (+G, parameter = 2.4316)]. The analysis involved 34 amino acid sequences. All positions containing gaps and missing data were eliminated. A total of 443 positions in the final dataset was obtained. Evolutionary analyses were conducted in MEGA6 . According to the results of the phylogenetic tree, one complete T6SS was found in Psa M228 and belonged to the same branch as that of the P. aeruginosa PAO1 H3-T6SS (HIS-III) gene cluster. “ ” indicates the functional T6SS that has been reported. (B) . Schematic diagram of theT6SS gene cluster of the pathogenic strain Psa M228. The name of the core genes of T6SS in Psa M228 are indicated by arrows. The direction of the arrows represents the direction of transcription of the genes in the genome. “//” indicates the presence of other genes not belonging to T6SS. “*” indicates the presence of frameshift mutation. The gene products are shown below the arrows. The database of Clusters <t>of</t> <t>Orthologous</t> Groups of proteins <t>(COGs)</t> was obtained from the National Center of Biotechnology Information (see text footnote 1).
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    Biotechnology Information national center for biotechnology information clusters of orthologous groups of proteins database
    Structure of T6SS gene cluster analysis of the pathogenic strain Psa M228. (A) Molecular phylogenetic analysis by Maximum Likelihood method. The evolutionary history was inferred using the Maximum Likelihood method based on the Le_Gascuel_2008 model . The bootstrap consensus tree inferred from 1000 replicates was used to represent the evolutionary history of the taxa analyzed . Branches corresponding to partitions reproduced in less than 60% bootstrap replicates were collapsed. The percentage of replicate trees in which the associated taxa clustered together in the bootstrap test (1000 replicates) is shown next to the branches . The initial tree(s) for the heuristic search were obtained automatically by applying Neighbor-Join and BioNJ algorithms to a matrix of pairwise distances estimated using a JTT model, and the topology with a superior log likelihood value was selected. A discrete Gamma distribution was used to model evolutionary rate differences among sites [five categories (+G, parameter = 2.4316)]. The analysis involved 34 amino acid sequences. All positions containing gaps and missing data were eliminated. A total of 443 positions in the final dataset was obtained. Evolutionary analyses were conducted in MEGA6 . According to the results of the phylogenetic tree, one complete T6SS was found in Psa M228 and belonged to the same branch as that of the P. aeruginosa PAO1 H3-T6SS (HIS-III) gene cluster. “ ” indicates the functional T6SS that has been reported. (B) . Schematic diagram of theT6SS gene cluster of the pathogenic strain Psa M228. The name of the core genes of T6SS in Psa M228 are indicated by arrows. The direction of the arrows represents the direction of transcription of the genes in the genome. “//” indicates the presence of other genes not belonging to T6SS. “*” indicates the presence of frameshift mutation. The gene products are shown below the arrows. The database of Clusters <t>of</t> <t>Orthologous</t> Groups of proteins <t>(COGs)</t> was obtained from the National Center of Biotechnology Information (see text footnote 1).
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    Biotechnology Information clusters of orthologous groups (cog) protein database
    Structure of T6SS gene cluster analysis of the pathogenic strain Psa M228. (A) Molecular phylogenetic analysis by Maximum Likelihood method. The evolutionary history was inferred using the Maximum Likelihood method based on the Le_Gascuel_2008 model . The bootstrap consensus tree inferred from 1000 replicates was used to represent the evolutionary history of the taxa analyzed . Branches corresponding to partitions reproduced in less than 60% bootstrap replicates were collapsed. The percentage of replicate trees in which the associated taxa clustered together in the bootstrap test (1000 replicates) is shown next to the branches . The initial tree(s) for the heuristic search were obtained automatically by applying Neighbor-Join and BioNJ algorithms to a matrix of pairwise distances estimated using a JTT model, and the topology with a superior log likelihood value was selected. A discrete Gamma distribution was used to model evolutionary rate differences among sites [five categories (+G, parameter = 2.4316)]. The analysis involved 34 amino acid sequences. All positions containing gaps and missing data were eliminated. A total of 443 positions in the final dataset was obtained. Evolutionary analyses were conducted in MEGA6 . According to the results of the phylogenetic tree, one complete T6SS was found in Psa M228 and belonged to the same branch as that of the P. aeruginosa PAO1 H3-T6SS (HIS-III) gene cluster. “ ” indicates the functional T6SS that has been reported. (B) . Schematic diagram of theT6SS gene cluster of the pathogenic strain Psa M228. The name of the core genes of T6SS in Psa M228 are indicated by arrows. The direction of the arrows represents the direction of transcription of the genes in the genome. “//” indicates the presence of other genes not belonging to T6SS. “*” indicates the presence of frameshift mutation. The gene products are shown below the arrows. The database of Clusters <t>of</t> <t>Orthologous</t> Groups of proteins <t>(COGs)</t> was obtained from the National Center of Biotechnology Information (see text footnote 1).
    Clusters Of Orthologous Groups (Cog) Protein Database, supplied by Biotechnology Information, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Biotechnology Information database of clusters of orthologous groups of proteins (cogs)
    Structure of T6SS gene cluster analysis of the pathogenic strain Psa M228. (A) Molecular phylogenetic analysis by Maximum Likelihood method. The evolutionary history was inferred using the Maximum Likelihood method based on the Le_Gascuel_2008 model . The bootstrap consensus tree inferred from 1000 replicates was used to represent the evolutionary history of the taxa analyzed . Branches corresponding to partitions reproduced in less than 60% bootstrap replicates were collapsed. The percentage of replicate trees in which the associated taxa clustered together in the bootstrap test (1000 replicates) is shown next to the branches . The initial tree(s) for the heuristic search were obtained automatically by applying Neighbor-Join and BioNJ algorithms to a matrix of pairwise distances estimated using a JTT model, and the topology with a superior log likelihood value was selected. A discrete Gamma distribution was used to model evolutionary rate differences among sites [five categories (+G, parameter = 2.4316)]. The analysis involved 34 amino acid sequences. All positions containing gaps and missing data were eliminated. A total of 443 positions in the final dataset was obtained. Evolutionary analyses were conducted in MEGA6 . According to the results of the phylogenetic tree, one complete T6SS was found in Psa M228 and belonged to the same branch as that of the P. aeruginosa PAO1 H3-T6SS (HIS-III) gene cluster. “ ” indicates the functional T6SS that has been reported. (B) . Schematic diagram of theT6SS gene cluster of the pathogenic strain Psa M228. The name of the core genes of T6SS in Psa M228 are indicated by arrows. The direction of the arrows represents the direction of transcription of the genes in the genome. “//” indicates the presence of other genes not belonging to T6SS. “*” indicates the presence of frameshift mutation. The gene products are shown below the arrows. The database of Clusters <t>of</t> <t>Orthologous</t> Groups of proteins <t>(COGs)</t> was obtained from the National Center of Biotechnology Information (see text footnote 1).
    Database Of Clusters Of Orthologous Groups Of Proteins (Cogs), supplied by Biotechnology Information, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    InterPro Inc cluster of orthologous groups of proteins database
    Structure of T6SS gene cluster analysis of the pathogenic strain Psa M228. (A) Molecular phylogenetic analysis by Maximum Likelihood method. The evolutionary history was inferred using the Maximum Likelihood method based on the Le_Gascuel_2008 model . The bootstrap consensus tree inferred from 1000 replicates was used to represent the evolutionary history of the taxa analyzed . Branches corresponding to partitions reproduced in less than 60% bootstrap replicates were collapsed. The percentage of replicate trees in which the associated taxa clustered together in the bootstrap test (1000 replicates) is shown next to the branches . The initial tree(s) for the heuristic search were obtained automatically by applying Neighbor-Join and BioNJ algorithms to a matrix of pairwise distances estimated using a JTT model, and the topology with a superior log likelihood value was selected. A discrete Gamma distribution was used to model evolutionary rate differences among sites [five categories (+G, parameter = 2.4316)]. The analysis involved 34 amino acid sequences. All positions containing gaps and missing data were eliminated. A total of 443 positions in the final dataset was obtained. Evolutionary analyses were conducted in MEGA6 . According to the results of the phylogenetic tree, one complete T6SS was found in Psa M228 and belonged to the same branch as that of the P. aeruginosa PAO1 H3-T6SS (HIS-III) gene cluster. “ ” indicates the functional T6SS that has been reported. (B) . Schematic diagram of theT6SS gene cluster of the pathogenic strain Psa M228. The name of the core genes of T6SS in Psa M228 are indicated by arrows. The direction of the arrows represents the direction of transcription of the genes in the genome. “//” indicates the presence of other genes not belonging to T6SS. “*” indicates the presence of frameshift mutation. The gene products are shown below the arrows. The database of Clusters <t>of</t> <t>Orthologous</t> Groups of proteins <t>(COGs)</t> was obtained from the National Center of Biotechnology Information (see text footnote 1).
    Cluster Of Orthologous Groups Of Proteins Database, supplied by InterPro Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Biotechnology Information database of the clusters of orthologous groups of proteins
    Structure of T6SS gene cluster analysis of the pathogenic strain Psa M228. (A) Molecular phylogenetic analysis by Maximum Likelihood method. The evolutionary history was inferred using the Maximum Likelihood method based on the Le_Gascuel_2008 model . The bootstrap consensus tree inferred from 1000 replicates was used to represent the evolutionary history of the taxa analyzed . Branches corresponding to partitions reproduced in less than 60% bootstrap replicates were collapsed. The percentage of replicate trees in which the associated taxa clustered together in the bootstrap test (1000 replicates) is shown next to the branches . The initial tree(s) for the heuristic search were obtained automatically by applying Neighbor-Join and BioNJ algorithms to a matrix of pairwise distances estimated using a JTT model, and the topology with a superior log likelihood value was selected. A discrete Gamma distribution was used to model evolutionary rate differences among sites [five categories (+G, parameter = 2.4316)]. The analysis involved 34 amino acid sequences. All positions containing gaps and missing data were eliminated. A total of 443 positions in the final dataset was obtained. Evolutionary analyses were conducted in MEGA6 . According to the results of the phylogenetic tree, one complete T6SS was found in Psa M228 and belonged to the same branch as that of the P. aeruginosa PAO1 H3-T6SS (HIS-III) gene cluster. “ ” indicates the functional T6SS that has been reported. (B) . Schematic diagram of theT6SS gene cluster of the pathogenic strain Psa M228. The name of the core genes of T6SS in Psa M228 are indicated by arrows. The direction of the arrows represents the direction of transcription of the genes in the genome. “//” indicates the presence of other genes not belonging to T6SS. “*” indicates the presence of frameshift mutation. The gene products are shown below the arrows. The database of Clusters <t>of</t> <t>Orthologous</t> Groups of proteins <t>(COGs)</t> was obtained from the National Center of Biotechnology Information (see text footnote 1).
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    Biotechnology Information clusters of orthologous groups of protein (cog) database
    Structure of T6SS gene cluster analysis of the pathogenic strain Psa M228. (A) Molecular phylogenetic analysis by Maximum Likelihood method. The evolutionary history was inferred using the Maximum Likelihood method based on the Le_Gascuel_2008 model . The bootstrap consensus tree inferred from 1000 replicates was used to represent the evolutionary history of the taxa analyzed . Branches corresponding to partitions reproduced in less than 60% bootstrap replicates were collapsed. The percentage of replicate trees in which the associated taxa clustered together in the bootstrap test (1000 replicates) is shown next to the branches . The initial tree(s) for the heuristic search were obtained automatically by applying Neighbor-Join and BioNJ algorithms to a matrix of pairwise distances estimated using a JTT model, and the topology with a superior log likelihood value was selected. A discrete Gamma distribution was used to model evolutionary rate differences among sites [five categories (+G, parameter = 2.4316)]. The analysis involved 34 amino acid sequences. All positions containing gaps and missing data were eliminated. A total of 443 positions in the final dataset was obtained. Evolutionary analyses were conducted in MEGA6 . According to the results of the phylogenetic tree, one complete T6SS was found in Psa M228 and belonged to the same branch as that of the P. aeruginosa PAO1 H3-T6SS (HIS-III) gene cluster. “ ” indicates the functional T6SS that has been reported. (B) . Schematic diagram of theT6SS gene cluster of the pathogenic strain Psa M228. The name of the core genes of T6SS in Psa M228 are indicated by arrows. The direction of the arrows represents the direction of transcription of the genes in the genome. “//” indicates the presence of other genes not belonging to T6SS. “*” indicates the presence of frameshift mutation. The gene products are shown below the arrows. The database of Clusters <t>of</t> <t>Orthologous</t> Groups of proteins <t>(COGs)</t> was obtained from the National Center of Biotechnology Information (see text footnote 1).
    Clusters Of Orthologous Groups Of Protein (Cog) Database, supplied by Biotechnology Information, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    The statistical results of subcellular localization and COGs functional categories of DEPs. ( A ) Subcellular localization of DEPs in the ‘Freezing-6 h vs. CK’ comparison. The percentage represents the ratio of DEPs located in a specific subcellular structure. ( B ) Subcellular localization of DEPs in the ‘Freezing-30 h vs. CK’ comparison. ( C ) The COGs functional categories of DEPs in the ‘Freezing-6 h vs. CK’ comparison. ( D ) The COGs functional categories of DEPs in the ‘Freezing-30 h vs. CK’ comparison.

    Journal: International Journal of Molecular Sciences

    Article Title: Proteomic Insights into the Regulatory Mechanisms of the Freezing Response in the Alpine Subnivale Plant Chorispora bungeana

    doi: 10.3390/ijms252413381

    Figure Lengend Snippet: The statistical results of subcellular localization and COGs functional categories of DEPs. ( A ) Subcellular localization of DEPs in the ‘Freezing-6 h vs. CK’ comparison. The percentage represents the ratio of DEPs located in a specific subcellular structure. ( B ) Subcellular localization of DEPs in the ‘Freezing-30 h vs. CK’ comparison. ( C ) The COGs functional categories of DEPs in the ‘Freezing-6 h vs. CK’ comparison. ( D ) The COGs functional categories of DEPs in the ‘Freezing-30 h vs. CK’ comparison.

    Article Snippet: For the functional classification of DEPs, the Cluster of Orthologous Groups of Proteins (COGs) database [ ] from the National Center for Biotechnology Information (NCBI) was used.

    Techniques: Functional Assay, Comparison

    Structure of T6SS gene cluster analysis of the pathogenic strain Psa M228. (A) Molecular phylogenetic analysis by Maximum Likelihood method. The evolutionary history was inferred using the Maximum Likelihood method based on the Le_Gascuel_2008 model . The bootstrap consensus tree inferred from 1000 replicates was used to represent the evolutionary history of the taxa analyzed . Branches corresponding to partitions reproduced in less than 60% bootstrap replicates were collapsed. The percentage of replicate trees in which the associated taxa clustered together in the bootstrap test (1000 replicates) is shown next to the branches . The initial tree(s) for the heuristic search were obtained automatically by applying Neighbor-Join and BioNJ algorithms to a matrix of pairwise distances estimated using a JTT model, and the topology with a superior log likelihood value was selected. A discrete Gamma distribution was used to model evolutionary rate differences among sites [five categories (+G, parameter = 2.4316)]. The analysis involved 34 amino acid sequences. All positions containing gaps and missing data were eliminated. A total of 443 positions in the final dataset was obtained. Evolutionary analyses were conducted in MEGA6 . According to the results of the phylogenetic tree, one complete T6SS was found in Psa M228 and belonged to the same branch as that of the P. aeruginosa PAO1 H3-T6SS (HIS-III) gene cluster. “ ” indicates the functional T6SS that has been reported. (B) . Schematic diagram of theT6SS gene cluster of the pathogenic strain Psa M228. The name of the core genes of T6SS in Psa M228 are indicated by arrows. The direction of the arrows represents the direction of transcription of the genes in the genome. “//” indicates the presence of other genes not belonging to T6SS. “*” indicates the presence of frameshift mutation. The gene products are shown below the arrows. The database of Clusters of Orthologous Groups of proteins (COGs) was obtained from the National Center of Biotechnology Information (see text footnote 1).

    Journal: Frontiers in Microbiology

    Article Title: Role of the Type VI Secretion System in the Pathogenicity of Pseudomonas syringae pv. actinidiae , the Causative Agent of Kiwifruit Bacterial Canker

    doi: 10.3389/fmicb.2021.627785

    Figure Lengend Snippet: Structure of T6SS gene cluster analysis of the pathogenic strain Psa M228. (A) Molecular phylogenetic analysis by Maximum Likelihood method. The evolutionary history was inferred using the Maximum Likelihood method based on the Le_Gascuel_2008 model . The bootstrap consensus tree inferred from 1000 replicates was used to represent the evolutionary history of the taxa analyzed . Branches corresponding to partitions reproduced in less than 60% bootstrap replicates were collapsed. The percentage of replicate trees in which the associated taxa clustered together in the bootstrap test (1000 replicates) is shown next to the branches . The initial tree(s) for the heuristic search were obtained automatically by applying Neighbor-Join and BioNJ algorithms to a matrix of pairwise distances estimated using a JTT model, and the topology with a superior log likelihood value was selected. A discrete Gamma distribution was used to model evolutionary rate differences among sites [five categories (+G, parameter = 2.4316)]. The analysis involved 34 amino acid sequences. All positions containing gaps and missing data were eliminated. A total of 443 positions in the final dataset was obtained. Evolutionary analyses were conducted in MEGA6 . According to the results of the phylogenetic tree, one complete T6SS was found in Psa M228 and belonged to the same branch as that of the P. aeruginosa PAO1 H3-T6SS (HIS-III) gene cluster. “ ” indicates the functional T6SS that has been reported. (B) . Schematic diagram of theT6SS gene cluster of the pathogenic strain Psa M228. The name of the core genes of T6SS in Psa M228 are indicated by arrows. The direction of the arrows represents the direction of transcription of the genes in the genome. “//” indicates the presence of other genes not belonging to T6SS. “*” indicates the presence of frameshift mutation. The gene products are shown below the arrows. The database of Clusters of Orthologous Groups of proteins (COGs) was obtained from the National Center of Biotechnology Information (see text footnote 1).

    Article Snippet: The database of Clusters of Orthologous Groups of proteins (COGs) was obtained from the National Center of Biotechnology Information .

    Techniques: Functional Assay, Mutagenesis