Task 5: Homology Modeling
1A6Z chain A was used as modeling target for all three methods.
Modeller
We used Modeller to create models based on a single template and also multiple templates.
Single template
<css> table.colBasic2 { margin-left: auto; margin-right: auto; border: 2px solid black; border-collapse:collapse; width: 60%; } .colBasic2 th,td { padding: 3px; border: 2px solid black; } .colBasic2 td { text-align:left; } .colBasic2 tr th { background-color:#efefef; color: black;} .colBasic2 tr:first-child th { background-color:#adceff; color:black;} </css>
<figtable id="Modeller single">
| Template | Seq. identity | std Alignment | 2d alignment | ||||
|---|---|---|---|---|---|---|---|
| DOPE score | RMSD | GDT score | DOPE score | RMSD | GDT score | ||
| 1QVO_A | 39% | -27772 | 3.647 | 0.6241 | -20467 | 18.789 | 0.3410 |
| 1S7X_A | 29% | -19941 | 15.806 | 0.3355 | -22681 | 18.101 | 0.3649 |
| 1CD1_A | 21% | -19034 | 18.066 | 0.3640 | -18938 | 21.670 | 0.2822 |
</figtable>
<xr id="Modeller single"/> lists the selected templates and the Modeller results for the different template structures and alignment methods. In addition to the standard pairwise sequence alignment based on dynamic programming, we also used Modeller's alig2dn() method to improve the alignment by including secondary structure information of the template. The method tries to place gaps outside secondary structure segments. This is especially useful for alignments between more distant related sequences, because those alignments usually contain more gaps than alignments between more close related sequences.
As Modeller quality score, we chose the DOPE score, which is a statistical potential that was optimized for the assessment of model quality. The DOPE score has an arbitrary scale, but scores for structures of the same protein are comparable and can be used to select the best model from a collection of structures. The lower the score, the better the model. In addition to the DOPE score, we also computed the RMSD and GDT scores. The RMSD is a a good measure of the average distance between all pairs of corresponding atoms in two structures. Therefore, the lower the RMSD the better. For the GDT score, the average coverage of the target sequence under four defined distance cutoffs is computed. Normally, 1, 2, 4 and 8 Å are used as distance thresholds. The GDT score ranges between 0 and 1, with random superpositions of unrelated structures having a score of 0.1 to 0.2.
<figure id="pymol modeller 1QVO">
</figure>
<xr id="pymol modeller 1QVO"/> shows a visualisation of the two models (purple) created from the template 1QVO_A (red) with the closest homology to the target (green). The first model a) is obviously very good ant much better than the second model b), because its secondary structure features match the target quite good and the position of the alpha helices of the second model differs a lot from the target.
<figure id="pymol modeller 1S7X">
</figure>
The models created from the template 1S7X_A are worse than those from the more closely related 1QVO_A. The 3D representation in <xr id="pymol modeller 1S7X"/> shows several regions in both models, where the secondary structure elements could not be superimposed correctly to the reference. The beta sheets in the second model b) match those of the immunoglobulin domain (lower part of the protein) in the target, but there are no beta sheets in that region in the first model a). Although the RMSD is better for model a) , we would agree with the DOPE score that the model b) is better.
<figure id="pymol modeller 1CD1">
</figure>
<xr id="pymol modeller 1CD1"/> shows 3D representations for the models created form the most distant related homolog 1CD1. Both model a) and b) are very different from the target and also the template. The 21% sequence identity between the two proteins is obvious too low to create good alignments. Nevertheless, the secondary structure guided alignment method from Modeller was especially designed for this task: the alignment of sequences with low identity. But including the secondary structure information in the alignments did only slightly improve the alignment for the template 1S7X.
<figure id="1CD1 alignments">
| std alignment | 2D alignment |
|---|---|
</figure>
The alignments of 1QVO_A and the target in <xr id="1CD1 alignments"/> show, that the standard alignment is already quite good, it only contains a few gaps. Including the 2D information could not improve the alignment and lead to a fragmented alignment with an increased number of gaps. Thus, the resulting model is of decreased quality.
The DOPE score has a positive correlation with the the GDT score, as well as with the RMSD. The scores differ a bit in some cases, but all in all, they agree that the model created from 1QVO_A and the standard alignment is the best. This is not surprising, since the 3D visualisations show that 1QVO_A is already very similar to the target, whereas the other two templates differ much more.
Multiple templates
We also created templates using more than one template in a single modeling step. Therefore, we created three sets of structures, one with close homologs, one with distant homologs and one mixed set.
<figtable id="multiple sets">
| close homology | distant homology | mixed | |||
|---|---|---|---|---|---|
| Template | Seq. identity | Template | Seq. identity | Template | Seq. identity |
| 1QVO_A | 39% | 3HUJ_C | 23% | 1QVO_A | 39% |
| 1ZAG_A | 36% | 1CD1_A | 21% | 1CD1_A | 21% |
| 1RJZ_D | 34% | 1VZY_A | 14% | ||
</figtable>
<figtable id="multiple sets">
| close homology | ||
|---|---|---|
| Template | 1QVO_A, 1ZAG_A | 1QVO_A, 1ZAG_A, 1RJZ_D |
| DOPE score | -28073 | -27460 |
| RMSD | 3.432 | 2.431 |
| GDT score | 0.6553 | 0.7638 |
| Pymol visualisation | ||
| distant homology | ||
| Template | 3HUJ_C, 1CD1_A | 3HUJ_C, 1CD1_A, 1VZY_A |
| DOPE score | -25967 | -20588 |
| RMSD | 4.130 | 7.741 |
| GDT score | 0.5607 | 0.3814 |
| Pymol visualisation | ||
| mixed homology | ||
| Template | 1QVO_A, 1CD1_A | |
| DOPE score | -25894 | |
| RMSD | 3.974 | |
| GDT score | 0.5846 | |
| Pymol visualisation | ||
</figtable>
Including more templates improves the quality of the models. However, we got the best results with two template sequences, because three templates led to a bit worse model than two templates. However, the three template models are still better than those created from a single template. Surprisingly, the two templates with low sequence identity to the target led to a good model with an RMSD of 4.12 which is nearly as good as the model created with the mixed set.
Swiss-Model
We used Swiss-Model to create models using 1QVO_A, 1S7X_A and 1CD1_A as template.
Swiss-Model outputs a raw score and also a Z-score that represents an absolute measure of the model quality. It relates the model's raw score to the scores that high-resolution X-ray structures get and thus gives an estimate of how likely the model has a quality comparable to an experimental structure. A low quality model is indicated by a strong negative Z-score, which means that the raw score is several standard deviations lower as the scores of experimental structures with similar size (see Swiss-Model help).
Swiss-Model also provides plots that help to analyse the local energy of the model. For this, the atomic empirical mean force potential (Anolea) and the Gromos simulation package are used. Both are used calculate the energy of each amino acid in the sequence. The two plots show the protein sequence on the x-axis and the calculated energy of each residue on the y-axis. A low energy corresponds to a favorable energy environment for an amino acid and a positive energy represents an unfavorable energy environment.
<figtable id="swiss-model">
| 1QVO_A | 1S7X_A | 1CD1_A | |
|---|---|---|---|
| Seq. identity | 39% | 29% | 21% |
| Z-score | -1.977 | -2.005 | -2.707 |
| RMSD | 2.847 | 2.757 | 3.604 |
| GDT score | 0.6774 | 0.7086 | 0.6121 |
| Pymol visualisation | |||
| Anolea and Gromos energy |
</figtable>
<xr id="swiss-model"/> contains the Swiss-Model results. The models from 1QVO_A and 1S7X_A are both very good having a RMSD of 2.847 and 2.757. The GDT score agrees with the RMSD that the model from 1S7X_A is slightly better than the one from 1QVO_A. However, the Z-score decreases with the sequence identity. Looking at the two models in 3D does not clearly reveal the best model. Some secondary structure segments are more correct in one model and some are better modeled in the other one. We therefore would rank both models as equally good. The Anolea and Gromos plots for each model are also given in the table. For the first model, they show that the residues at the N and C termini are in a favorable energy environments, but there are some less favorable segments in the middle of the model. Since the first two models are better than the third, we expected to see this also trend represented in the energy landscape. But the energy plot of the third model is not very different from the other two.
I-TASSER
I-Tasser was used to create models from two different templates. Due to I-Tasser's very long runtime of over 60h for one protein and because we were only allowed to run one job at a time, we only created 2 models.
I-Tasser uses threading in the first step to search for several template structures with high secondary structure similarity to the target in addition to the user specified template(s). Fragments of those structures are then reassembled to create several models for the target. The models are clustered and the lowest energy models are reported. We only selected the first and best model, because we wanted to make it comparable to the results from Modeller and Swiss-Model, both methods only report a single model.
The results contain a confidence score (C-score) as quality measure for the created models. It ranges between -5 and 2, with a high score indicating a high confidence (see cscore.txt).
<figtable id="i-tasser">
| 1QVO_A | 1CD1_A | |
|---|---|---|
| Seq. identity | 39% | 21% |
| C-score | 1.73 | 1.38 |
| RMSD | 3.062 | 3.478 |
| GDT score | 0.6719 | 0.6103 |
| Pymol visualisation |
</figtable>
The two models and different quality measures are listed in <xr id="i-tasser"/>. Both models are quite good, and especially the second model from 1CD1 is remarkable, since the sequence identity of the template is only 21%. The model has a RMSD of 3.478, which is very close to the RMSD of the first model (3.062). The GDT and C-score both also rank the first model as the better one. In the Pymol visualisation is clearly visible that the second model is worse especially in the immunoglobulin domain, where it does not contain all beta sheet, but an alpha helix instead.
Summary
The GDT score is negatively correlated with the RMSD in nearly all cases. If the RMSD is lgets lower, then the GDT score gets higher and vice versa.There are only a few exceptions among the models created by Modeller.
The DOPE score from Modeller is also suited to get a first impression of how good the models are. However, there are some models where it indicates a medium quality, but the RMSD and GDT score are actually bad. Swiss-Models's Z-score and I-Tassers C-score are both stronger correlated with the RMSD and GDT score than the DOPE score.
All methods were able to create good models, although Modeller created the best one from three close homology sequences with an RMSD of 2.431. Nevertheless, the Modeller models have the highest RMSDs and lowest GDT scores and are thus the worst, only the models created with multiple templates are all good. Swiss-Model created the second best model with an RMSD of 2.757. Itasser is also very good and especially in creating models from low sequence identity templates.
