Task 5: Homology Modeling

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lab journal task 5

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 multiple templates.


Single template

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<figtable id="Modeller single">

Template Seq. identity std Alignment 2d alignment curated Alignment
RMSD TM score RMSD TM score RMSD TM score
1QVO_A 39% 3.647 0.6241 4.994 0.5653
1S7X_A 29% 15.806 0.3355 18.099 0.2509
1CD1_A 21% 18.066 0.3640 5.640 0.4697
Table 1:Template structures and their sequence identity to the target, as computed by Blast. The RMSD and TM score are given as a quality measure for the different models based on a pairwise sequence alignment with dynamic programming (std Alignment), pairwise sequence alignment with additional secondary structure information (2d Alignment) and manually curated alignments (curated Alignment).

</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 alignment.alig2dn() method to improve the alignment by including secondary structure information and improved the alignments manually. The RMSD and TM score are given for all models. The TM score ranges in the interval of (0, 1]. A value below 0.17 indicates a random similarity and a TM score above 0.5 corresponds to two structures with the same fold in CATH or SCOP (see TM score). Including the secondary structure information did only improve the model of the most distant homolog 1CD1_A.

<figtable id="pymol str. al.">

a) classical pairwise sequence alignment
b) inclusion of secondary structure information in the alignment
Figure 1:Superposition of the target 1A6Z_A (green), the template 1QVO_A (red) and the model (purple). Two different alignment methods were used to create the input alignment. for Modeller.

</figtable>


<figtable id="pymol str. al.">

a) classical pairwise sequence alignment
b) inclusion of secondary structure information in the alignment
Figure 2:Superposition of the target 1A6Z_A (green), the template 1S7X_A (red) and the model (purple). Two different alignment methods were used to create the input alignment. for Modeller.

</figtable>


<figtable id="pymol str. al.">

a) classical pairwise sequence alignment
b) inclusion of secondary structure information in the alignment
Figure 3:Superposition of the target 1A6Z_A (green), the template 1CD1_A (red) and the model (purple). Two different alignment methods were used to create the input alignment. for Modeller.

</figtable>

Multiple templates

We also user more than one template in a modeling step. Therefore, we created three sets of structures, one with close homologes, one with distant homologes and one combined 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%
Table 2: The three different sets used as templates for Modeller: two sets of close and distant homologs and a mixed set.

</figtable>

<xr id="multiple sets"/> specifies the three sets.

<figtable id="multiple sets">

close homology distant homology mixed homology
1QVO_A, 1ZAG_A 1QVO_A, 1ZAG_A, 1RJZ_D 3HUJ_C, 1CD1_A 3HUJ_C, 1CD1_A, 1VZY_A 1QVO_A, 1CD1_A
RMSD 3.432 2.431 4.130 7.741 3.974
TM score 0.6553 0.7638 0.5607 0.3814 0.5846
Table 2: Results of the modeling with multiple templates. We computed models using 2 structures as templates and also using three structures.

</figtable>

Swiss-Modell

I-TASSER