Workshop I

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 Session I Exercises

   Working with bound substrates and cofactors: Arginine kinase

Launch guide window Launch NCBI Home Page

Goals

  • Find structure records using the Taxonomy Browser
  • Locate and identify heterogens in a structure
  • Locate and annotate binding site residues

Steps

  1. Find a species using the Taxonomy Browser
    • On the NCBI home page, click TaxBrowser on the black bar at the top.
    • In the left blue side bar, click Taxonomy browser.
    • Type "horseshoe crab" in the box and set the menu to "token set".
    • Click Go.

  2. Find structure records for a single species
    • In the results list, click on the common name "Atlantic horseshoe crab".
    • In the table, click on the number of structure records.

  3. Refine the set of structure records
    • Add the following to the current query in the search box:
      AND 1.0:1.5[resolution]
      and click Go.
    • Find the record in the list labeled as a transition state and click on the accession number to open the structure summary page.

  4. Find ligands linked to the structure record
    • Scroll down to the bottom of the page and make a note of the heterogens present.

  5. Locate relevant literature about a structure
    • Click on the "All References" link at the top of the page, and then open the 1998 abstract by Zhou et al.
    • Make a note of the comments about the positioning of the bound ligands.

  6. Locate and identify heterogens in a structure
    • Return to the structure summary page by going back twice in your browser, and click the structure image.
    • Choose Style / Coloring Shortcuts / Molecule
    • Locate the three heterogens next to the magnesium (Mg) ion. They will each be colored differently. Note their relative locations.

  7. Locate a bound co-factor
    • Zoom in and locate the nitrate ion bound to the Mg ion. (Nitrate has four atoms, and is directly bound to Mg).
    • Double click on the nitrate ion (it should turn yellow).

  8. Locate binding site residues
    • Choose Show/Hide / Select by Distance / Residues Only and set the distance to 4.5 Angstroms.
    • Find the five arginines among the highlighted residues. Holding down the Control key, click on the highlighted residues that are NOT arginine to deselect them.

  9. Create a custom annotation
    • Choose Style / Annotate, click "New", and give the annotation the name "Arg".
    • Click Edit Style, check the protein side chain box, and render them as "Tubes" with a color of your choice.

  10. Label residues in the annotation
    • Click the Labels tab and set the protein backbone spacing to 1 and the type to One Letter.
    • Click Done, OK, and then Done. Now deselect the residues to see the annotated color.

  11. Add a second annotation
    • The catalytic residue is thought to be either E225 or E314. Using Style / Annotate, create a new annotation where the sidechains of these residues are rendered as ball-and-stick models colored by charge. Label these with one letter labels as before.

  12. Save your work
    • Experiment with turning the annotations on and off in the Annotation panel. You can now save the annotated file for future use.

Revised December 3, 2007