Sequences and Structures Tutorial

This tutorial is an introduction to working with sequence alignments and associated structures using Multalign Viewer. Data are taken from the enolase superfamily:

The enolase superfamily: a general strategy for enzyme-catalyzed abstraction of the alpha-protons of carboxylic acids. Babbitt PC, Hasson MS, Wedekind JE, Palmer DR, Barrett WC, Reed GH, Rayment I, Ringe D, Kenyon GL, Gerlt JA. Biochemistry. 1996 Dec 24;35(51):16489-501.

On Windows/Mac, click the chimera icon; on UNIX, start Chimera from the system prompt:

unix: chimera

Multalign Viewer sequence window

Multalign Viewer has its own set of preferences, including several that control display. From the alignment window menu, choose Preferences... Appearance and adjust display options as desired for Multiple alignments, then Close the preferences dialog.

Size and place the sequence window and main Chimera window so that both are visible. If the sequence window becomes obscured at any point, it can be raised from the Chimera Tools menu (Tools... MAV - super8.msf... Raise).

Sequence names are shown on the left, and a Consensus sequence and Conservation histogram are shown above the sequences. Red capital letters in the consensus sequence indicate a few positions in which all of the sequences have the same type of residue.

The first sequence in the alignment, named mr, corresponds to the barrel domain of mandelate racemase from Pseudomonas putida. The next-to-the last sequence in the alignment, named enolyeast, corresponds to the barrel domain of enolase from Saccharomyces cerevisiae. There are multiple structures in the Protein Data Bank for each of these sequences; 2mnr (mandelate racemase) and 4enl (enolase) are used in this tutorial.

If you have internet connectivity, structures can be obtained directly from the Protein Data Bank. Choose File... Fetch by ID from the Chimera menu. In the resulting dialog, check the PDB option (if it is not already checked) and the option to Keep dialog up after Fetch. Fetch 2mnr, then 4enl, and then Close the dialog. If you do not have internet connectivity, instead download the files 2mnr.pdb and 4enl.pdb included with this tutorial and open them in that order with File... Open.

The view is initially centered on a protein colored white, the mandelate racemase structure. Off to the side and possibly out of view is the enolase structure, which is colored magenta. Use the menu to bring everything within view:

Actions... Focus

Presets... Interactive 1 (ribbons)

sequence window after structure association

Notice that in the sequence window, the sequence names mr and enolyeast are now shown in bold within boxes colored white and magenta, respectively. Each structure was automatically associated with its best-matching sequence, and the colors indicate the pairing.

Association enables several types of crosstalk, which will be explored in more detail below:

• selecting in the sequence window selects residues in the structure(s) and vice versa
• information from the sequences can be shown on the structures and vice versa
• the structures can be superimposed using the sequence alignment

First, we will use the sequence alignment to guide a structural match. From the Multalign Viewer menu, choose Structure... Match and click Apply without checking any boxes. This superimposes the structures using the alpha-carbons of all pairs of residues aligned in the sequence alignment. Readjust the view to focus on the structures:

Actions... Focus

active sites

The structures have N-terminal and barrel domains, but only the barrel domains are included in the sequence alignment. With the mouse, drag a box to highlight the entire sequence alignment. That will select the corresponding parts of the proteins. Invert the selection to the parts of the proteins not included in the sequence alignment, then hide the ribbon for those parts:

Select... Invert (all models)
Actions... Ribbon... hide
Select... Clear Selection

Communication also goes in the opposite direction: a selection in the structures is shown on the sequence alignment as a region. For example, select all aromatic residues in the structures:

Select... Residue... amino acid category... aromatic

Placing the cursor over any structure-associated residue in the sequence alignment shows the corresponding structure residue number near the bottom of the sequence window. For example, clicking into the sequence window and then placing the cursor over the first residue in the mr sequence shows that it is associated with Val 134 in chain A of model #0 (2mnr, mandelate racemase).

Next, see where some of the conserved residues are within the structures. In the sequence window, find the first completely conserved residue in the alignment. It is an aspartic acid, D, at alignment position 99. Drag with the mouse to create a region containing just that column of the alignment. The corresponding structure residues will be selected.

These aspartic acid residues are already displayed because the ribbons preset (used above) shows not just ribbons, but also bound molecules, ions, and nearby sidechains. Several of the highly conserved residues ligate a catalytically important metal ion. Clicking into the graphics window and then hovering the cursor over the ions shows that they are manganese and zinc, respectively.

At alignment position 150, there is a completely conserved proline (P). Create another region for this column (this time, press Ctrl along with the mouse button to start a new region instead of replacing the first). Only ribbons are shown for these residues; display the sidechain atoms too:

Actions... Atoms/Bonds... show

The region names are listed in the Region Browser (Tools... Region Browser in the Multalign Viewer menu). Clicking the Active checkbox for a region will select the corresponding residues in any associated structures. Only one region can be active at a time, but the Region Browser allows recoloring or deleting one or more regions simultaneously. Close the Region Browser.

conservation shown with color

Choose Tools... General Controls... Command Line from the main Chimera menu and use a command to close the enolase structure:

Command: close 1

A structure can be colored according to the conservation in an associated sequence alignment. Choose Structure... Render by Conservation from the Multalign Viewer menu. The resulting Render by Attribute tool shows a histogram of the residue attribute named mavConservation. The "mav" part of the name is shorthand for Multalign Viewer, and "Conservation" indicates the values correspond to what is shown in the Conservation line of the sequence window. By default, the value for a column is the fraction of sequences with the most common residue type at that position, for example: 1.0 where all 8 sequences have the same type of residue, and 2/8 = 0.25 where only 2 (but any 2) share a type.

The Render by Attribute histogram contains vertical bars (or thresholds) for mapping the attribute values to colors or other visual cues. Use the Colors section. You can define your own color mapping by moving thresholds along the histogram and/or changing their colors. The Value and Color are shown for the most recently clicked or moved threshold. The Value changes when the threshold is moved, or the position can be changed by entering a value and pressing return. The Color can be changed by clicking the square color well and using the Color Editor. Thresholds can be added or deleted by Ctrl-clicking on the histogram. Adjust the color mapping as desired before clicking Apply. Coloring the structure shows the high conservation of the metal-binding residues and the low conservation of most residues around the outside of the barrel.

Attributes can also be used in the command line. For example, show only the residues with mavConservation values greater than 0.7:

Command: show :/mavConservation>.7

Multalign Viewer includes many features, only a few of which are sampled here. Users are encouraged to explore the menus and documentation for more information.

End the Chimera session:

Command: stop now