Protein Structural Bioinformatics
3-Day Course in 3D Macromolecular Visualization & Analysis with Protein Explorer

Washington University, Saint Louis

Lead Instructor Eric Martz (author of Protein Explorer; Prof. Emeritus, Univ. Mass. Amherst; emartz@microbio.umass.edu)
with co-instructors Wil Cruz and Raul Alcantara.

Organized by Sarah Elgin and April Bednarski
Registration: http://becker.wustl.edu/news/bioinfo-workshop-form.htm
Supported in part by the Washington University Biology Dept. and Becker Medical Library and by a grant to Washington University, St Louis, in support of Sarah C.R. Elgin from the Howard Hughes Medical Institute through its Professors Program.

This document is on-line: At proteinexplorer.org click on Workshops, or
http://www.umass.edu/molvis/workshop/washu04.htm
or at Washington University
www.nslc.wustl.edu/martz/PEsyllabus.htm

Rationale & Goals: In this day of exploding bioinformatics information from genomics and proteomics, it is ever more important to be conversant with macromolecular three-dimensional structure, and how it relates to protein and nucleic acid function and drug design. This workshop will enable participants to find published macromolecular structure data, and visualize and interpret 3D macromolecular structure. Participants will be enabled to incorporate computer visualization and qualitative analysis of 3D structure of protein, DNA, RNA, and protein-ligand interactions into their teaching and research.

Software: The central tool for this workshop is Protein Explorer (www.proteinexplorer.org). Protein Explorer is free, operates on Windows or Macintosh (also linux in a Windows subsystem), and is much easier to use, yet much more powerful than RasMol. Protein Explorer won the 2003 MERLOT Classic Award in Biology for exemplary online learning resources: "The Protein Explorer has revolutionized the teaching of biology at a molecular level". Protein Explorer integrates several key bioinformatics servers, and has been adopted by numerous bioinformatics resources.

Level & Pace: This workshop is designed for researchers familiar with basic biochemistry, but with no previous molecular visualization software experience. It progresses rapidly to powerful tools that will be of interest to specialists in protein structure and bioinformatics. Experienced participants are encouraged to work at their own speed, ahead of the group -- there is plenty of power to discover within Protein Explorer and its links to other resources!

Day 1, Tuesday August 24. Basics. How to use Protein Explorer to visualize structural features of proteins and protein-ligand interactions.

    Netscape 4.8 is best, but Internet Explorer is OK.
    Go to www.proteinexplorer.org

    Skip the PE Demo Movies -- use them for review (if you haven't used PE for a few months) or to start friends who didn't attend this course.

    FirstView

  1. Click Quick-Start ... to display Gal4:DNA.
  2. Organization of PE into 3 frames: control panel, molecular image, and messages.
  3. Use the mouse to rotate the molecule; click to identify atoms.
  4. Identify and become familiar with the computer representations for chains, backbones, disulfide bonds, solvent, and ligands.

    Features of the Molecule

  5. Understanding and using information provided in the PDB file header by the authors of the structure.
  6. The Help/Index/Glossary (green for "go"), a major component of PE's knowledge base.

    QuickViews

  7. Selecting, emphasizing, and hiding portions of the molecule.
  8. Selecting arbitrary atoms/chains/residues by clicking on them.
  9. Saving/recalling selected sets.
  10. Zooming, centering.
  11. Backbone, trace, cartoon, stick, ball and stick, spacefill to van der Waals radii.
  12. Coloring by element (Corey, Pauling, Koltun color scheme).
  13. Coloring cartoons by secondary structure.
  14. Identifying the amino and carboxy termini (5', 3' ends): N->C Rainbow (Group) color scheme.
  15. Interpreting the distribution of hydrophobic, polar, and charged residues (Polarity color schemes).
    1. Potassium channel: 1bl8. Trp prefers lipid-water interface.
    2. Gramicidin in a lipid bilayer: bilagram.pdb
  16. Coloring to distinguish A, T, G, C, U. How to distinguish DNA from RNA. (Cf. 104d)
  17. Coloring by disorder: temperature factor coloring.

  18. PE Site Map

    Global Protein Structure Issues

  19. How are 3D macromolecular structures obtained? Crystallography, NMR, and homology modeling.
  20. What fraction of the human proteome has known structure? A few percent.
  21. Is Structural Genomics the answer? Not in the next few years.
  22. Intrinsicially unstructured proteins:

  23. Finding published molecules of interest:
      Browsing
    1. Atlas of MacroMolecules: molvis.sdsc.edu/atlas/atlas.htm
    2. PDB at a Glance: cmm.info.nih.gov/modeling/pdb_at_a_glance.html

      Searching

    3. PDB Lite: www.pdblite.org
    4. SearchFields at the Protein Data Bank www.pdb.org
    5. Prilusky's OCA http://bioportal.weizmann.ac.il/oca-bin/ocamain

    Sequences
    Residue ranges for the CDR's in the Fab of 1FDL are:
      Heavy chain (H)
    • CDR1: 31-35
    • CDR2: 50-66
    • CDR3: 98-105

      Light chain (L)

    • CDR1: 24-34
    • CDR2: 50-56
    • CDR3: 90-97
    For shortcuts and tricks in using PE to visualize epitope-paratope contacts, see step #35 in this Antibody Structure Tutorial.

  24. OPTIONAL: Protein Explorer's Sequence display - finding gaps
    1. Insertions and non-physical gaps: 1igt.
    2. Physical gaps: 2ace, 1fod.
    3. Microheterogeneity: 1cbn.
  25. Protein Explorer's clickable Seq3D
    1. Sequence to 3D structure mapping.
    2. Finding all instances of one amino acid (e.g. cysteine).
    3. Selecting and coloring an arbitrary range of residues (see example in box at right).

  26. Noncovalent Bonds: Contact surfaces. Example: Gal4 contacting DNA (1d66), showing:
    1. Sequence specific recognition DNA bases by zinc finger domain of protein
    2. Hydrophobic protein-protein interaction
    3. Nonspecific charge interactions at DNA backbone phosphates

Day 2, Wednesday August 25. Supplementary Bioinformatics Servers and PE at Full Power

  1. External Resources (via PE Site Map)
      Model of SV40
      Capsid

      showing
      icosahedron.
    1. Probable Quaternary Structures: specific oligomers: 1k28, 1k93, virus capsids.
      vs. Crystal Contacts (4mdh).
    2. ConSurf: regions conserved or hypermutable in evolution
    3. MolProbity: all-atom contact analysis -- add hydrogens, then
      • See and correct Asn, Gln, His side-chain flips
      • See atomic clashes and evaluate overall clash score (1cbx)

  2. Visualizing Cation-Pi interactions and Salt Bridges (QuickViews, DISPLAY; 1b07, 1axi)

  3. QuickViews Boolean (scroll down in the QuickViews control panel).
    1. Example: In 1FDL, display Fab atoms contacting lysozyme, then overlay (DISPLAY) a cartoon display of all protein. Color the cartoon by Chain, then by N->C Rainbow, then by Structure.

  4. Multiple-Model NMR Results (1JSA, 1CFC)
    1. Most representative model (via PE Site Map -> External Resources).
    2. NMR Control Panel.
    3. Animation simulates thermal motion (Click "Animations" at the FrontDoor).

  5. Animations: Morphing conformational changes (Click "Animations" at the FrontDoor).

  6. Protein Comparator (via Quick-Start Comparator at the FrontDoor; (snapshot)
  7. Preferences in Protein Explorer (beneath the message box).
  8. Aliases for RasMol/Chime commands (beneath the message box).

Day 3 - Thursday August 26: Resources for Educators and Special Projects

The Day 3 agenda will be flexible. Individual help will be available for those with special projects.


    MolVis Resources for Educators

  1. Lesson Plans (at PE's FrontDoor)

  2. About Protein Structure (at PE's FrontDoor)

  3. World Index of Molecular Visualization Resources molvisindex.org
    1. Hundreds of Chime-based tutorials indexed by macromolecule
    2. Chime-based resources en Español
    3. Sources of atomic coordinate (PDB) files (metabolites, inorganic crystals, lipid micelles, etc.)
    4. Galleries, Molecular Sculpture and Physical Models, Software

  4. Martz Chime Resources www.umass.edu/microbio/chime
    1. Amino Acid Quizzer
    2. DNA, Hemoglobin, Antibody, MHC
    3. Lipid Bilayers and Gramicidin Channel
    4. IR Spectra with animated vibrations
    5. Toobers in Science Education
    6. History of Visualization of Biological Macromolecules
        Where did Chime come from? What about Fred's Folly and Byron's Bender? See early computer images, physical models including the latest by computer-driven laser-powered rapid-prototype engineering, and the latest molecular sculpture.
    7. Knots in Proteins

  5. Building a web page with hyperlinks to Protein Explorer that prespecify molecules for your teaching or research. Examples.   Methods.   Detailed methods.

  6. Presenting molecular structures in Chime websites:
    1. A well tested and debugged template for Chime presentations exists but is nearly obsolete.
    2. A Chime-based Script recorder within PE is nearly completed. With it, views achieved in PE can be saved (as Chime command scripts) and played back. Although not yet released, a pre-release working version is available.
    3. Support for Presentations in Protein Explorer (PiPE) remains under development and has not been released. A partial implementation of a new design has a viewable example and is downloadable. Although it is in rough shape at this time, a couple of people have already developed educational resources with it. An earlier design is now deemed obsolete and will not be supported.


    Additional topics by request, time permitting (or to explore on your own):

  7. Aligning two or more chains or molecules, and how to view the alignment.
    1. The CE site cl.sdsc.edu/ce.html will align any two protein chains quickly and easily (but hetero atoms are discarded).
    2. DeepView www.expasy.ch/spdbv/mainpage.html can align anything (one or more than one chains), selecting any subset of atoms for the alignment (other atoms following), and retaining hetero atoms. The results can be saved as a PDB file, but will need manual editing to separate models with MODEL [N] and ENDMDL records so that Protein Explorer can distinguish the models. Gale Rhodes provides a DeepView tutorial: click on the section Comparing Proteins.

  8. Mutating your model:
    1. Changing residue sidechains and rotamer minimization with DeepView
    2. DeepView beginners should start with the superb Molecular Modeling for Beginners by Gale Rhodes, Univ. Southern Maine.
    3. DeepView resources are indexed at molvisindex.org.

  9. Searching by structure without reference to sequence: (Try the bacterial cell division protein 1FSZ§.)
    Structure is more conserved than sequence! (Chothia et al., 2003; Precis)
    1. Shindyalov & Bourne's Combinatorial Extension cl.sdsc.edu/ce.html
    2. NCBI's Vector Alignment Search Tool (VAST) www.ncbi.nlm.nih.gov/Structure/VAST/vast.shtml

  10. External Resources (via PE Site Map)
    1. Crystal Contacts
    2. Fewer or Single Chains
    3. Model Quality (& examples of errors in published PDB files)
    4. RCSB's Structure Explorer
    5. NCBI's Entrez Structure

    Advanced Explorer

  11. The Noncovalent Bond Finder
  12. Rolling probe surfaces and molecular electrostatic potential coloring
  13. Including ligands in displays of cation-pi interactions and salt bridges

  14. Morphing conformational changes to view as animations in PE: see Protein Morpher.

  15. Homology (comparative) modeling: Introduction.


Keep in touch!


§ Example 1FSZ thanks to Gabe McCool. See also his presentation on 1FSZ in PE.