The Gene Ontology terms assigned to this protein are listed if expanding the Gene ontology column. Parent protein classes are in bold font and subclasses are listed under the parent class. The protein classes assigned to this protein are shown if expanding the data in the protein class column. The data in the UniProt column can be expanded to show links to all matching UniProt identifiers for this protein. The ENSP identifier links to the Ensembl website protein summary, while the ENST identifier links to the Ensembl website transcript summary for the selected splice variant. The protein information section displays alternative protein-coding transcripts (splice variants) encoded by this gene according to the Ensembl database. curves according to the protein condition value assigned for the well. Common (purple) and unique (grey) regions between different splice variants of the gene are also displayed ( read more), and at the bottom of the protein view is the protein scale. Regarding the analysis of the docking results, the selection of hit compounds considered the docking score and the top 10 of docking compounds, therefore, 100 hit compounds of each package were considered for further study. Low complexity regions are shown in yellow and InterPro regions in green. ROC curves generated from the results of 197 compounds docked with 3V5W. If a signal peptide is predicted by a majority of the signal peptide predictors SPOCTOPUS, SignalP 4.0, and Phobius (turquoise) and/or transmembrane regions (orange) are predicted by MDM, these are displayed. the tendency for different regions of the protein to generate an immune response, with peak regions being predicted to be more antigenic.The curve shows average values based on a sliding window approach using an in-house propensity scale. The curve in blue displays the predicted antigenicity i.e. The region with the lowest possible identity is always selected for antigen design, with a maximum identity of 60% allowed for designing a single-target antigen ( read more). A yellow triangle on the bar indicates a <100% sequence identity to the protein target.īelow the antigens, the maximum percent sequence identity of the protein to all other proteins from other human genes is displayed, using a sliding window of 10 aa residues (HsID 10) or 50 aa residues (HsID 50). The tabs at the top of the protein view section can be used to switch between the different splice variants to which an antigen has been mapped.Īt the top of the view, the position of the antigen (identified by the corresponding HPA identifier) is shown as a green bar. In both ranges, the normalized SCOOP scores achieve. Figure 1a shows the curves for a large number of false matches, whereas Figure 1b focuses on the region of the curves with few false matches. The protein browser displays the antigen location on the target protein(s) and the features of the target protein. Figure 1 shows an ROC curve demonstrating the performance of SCOOP compared to other methods using the conservative definition of false positives.
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