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  • Structure view
  • Controls
    Leftclick + Mousemove: Rotate
    Scroll: Zoom
    Rightclick + Mousemove: Move
    Shift+Scroll: Adjust clipping-plane
    Ctrl+Leftclick on residue: Select residue
    Ctrl+Leftclick on empty space: Deselect residue

    Structure coloring
    The structure is colored according to the probability that the split sites are active (blue) and inactive (red).



    Residue selection
    Residues can be selected via Ctrl+Leftclick (a green sphere will show the selection) which treat the selected residue as the site where the protein is split. The split occurs after the selected residue. Additionally the two split fragments are shown with two colors (red and blue). Selected residues can be deselected via Ctrl-Leftclicking anywhere but on a residue. A tooltip will appear when hovering the mouse over the residue. The residues' chain information is displayed after a colon.

    Additional features
    The current camera view can be saved via this button.

    The size of the structure window can be resized via this button.


  • Split Sites
  • Groups of split sites
    Different groups of split sites can be selected outputting a list of split sites ordered from the highest activity probability to lowest. The high active probability group encompasses sites with a activity probability of at least 0.6. The high inactive probability encompasses sites with a activity probability of less than 0.4. The active and inactive groups have all sites that the model would predict to be active (at least 0.5) and inactive (less than 0.5) respectively.



    Additional features
    The list can be copied to the clipboard with this button.

  • Selection
  • Additional information
    When a residue is selected, additional information concerning the conservation, binding affinity, surface accessibility and secondary structure properties are shown here which are used to calculate the activity probability in the model. It is important to note that conservation and surface accessibility are given as means of the surrounding residues of the split site, as this was shown to work best for predicting the activity, so the values do not show single residue values (which can be accessed in the raw files) (*). The split site is considered to be in a secondary structure if both flanking residues of the split site are in a secondary structure region.



    Deselection
    Deselecting residues can be done in the structure view or with this button located at the top of the Data tab.

    Multiple files
    If multiple files were uploaded via batch upload, the single files can be selected via a dropdown menu.

  • Data
  • Data graphs
    Residues on the graph can be clicked on which will also show the selection in the structure view. Zooming can be done via clicking and holding the mouse at the start of the desired region and moving the mouse towards the end of the desired region. If the graph is zoomed in, it can be moved by holding Shift and dragging with the left mouse button. All graphs are color coded according to the activity probability (red = low probability, blue = high probability of being active).
    Deselecting residues can be done in the structure view or with this button located at the top of the Data tab.

    Zooming out can be done via a double-click on the graph or via this button that appears at the top-left of the graph (if it is zoomed in).




    Predictions
    This tab shows the models prediction for each possible split site. There are 4 categories given with 4 colors. Generally speaking the model predicts split sites with a probability of at least 0.5 to be active and below 0.5 to be inactive. Sites with a probability of at least 0.75 have been shown to contain the highest ratio of true positives to false positives at the dispense of loosing some true positive split sites. Sites with a probability of less than 0.25 have been shown to contain the highest ratio of true negatives to false negatives.



    Logit
    This tab shows the logit function, which what the model's prediction is based on. The points are sorted by the lowest prediction to the highest (Meaning the splits are not in order like with the other tabs).



    Binding affinity, conservation, surface accessibility and secondary structure
    Those four properties are used to calculate the activity probability. The binding affinity gives the affinity between the two fragments towards each other. The conservation and surface accessibility is given by the surrounding residues of the split site.

    Sequence
    The sequence tab shows the sequence with the activity probability color codes, residue id's and whether the residue belongs to a secondary structure region (marked with Sec).



    Download
    The raw data can be downloaded in this tab as a zip file. The zip contains the output from DSSP, hmmer, muscle and rate4site as well as the pdb file that was generated through pdb2pqr at a pH of 7.