Homology modelling TSD
There will be no curiosity, no enjoyment of the process of life. All competing pleasures will be destroyed. But always — do not forget this, Winston — always there will be the intoxication of power, constantly increasing and constantly growing subtler. Always, at every moment, there will be the thrill of victory, the sensation of trampling on an enemy who is helpless. If you want a picture of the future, imagine a boot stamping on a human face — forever.
1984
Templates
Since similar sets were already collected for Task 2, the information was reused. In addition searches with HHpred on pdb70 and with COMA on pdb40 were performed. If two structures were mapped to the same Uniprot entry, only one, the 'most native' one, was used. The set of chosen templates is displayed in <xr id="tab:templates" />.
None of the searches revealed any structure with >80% sequence identity, other than the two already known structures 2gjx and 2gk1 which share 100% sequence identity. To still perform the task, 2gjx, which is the native structure <ref name="2gjxref">Lemieux,M. et al. (2006) Crystallographic Structure of Human beta-Hexosaminidase A: Interpretation of Tay-Sachs Mutations and Loss of GM2 Ganglioside Hydrolysis. Journal of molecular biology, 359, 913-29.</ref>, was chosen as reference and 2gk1, which has the inhibitor NGT bound, will be used as template. In the range between 40/80% sequence identity only one entry could be added from COMA. Most of the hits found by either COMA or HHpred turned out to have a sequence identity of lower than 25%.
<figtable id="tab:templates">
| PDB id | Sequence identity | Method | |
|---|---|---|---|
| > 80% identity | 2gk1 chain A | 100% | Task2/HHpred/COMA |
| 40% - 80% identity | 1o7a chain D | 56.6% | Task 2 |
| 3lmy chain A | 54% | COMA | |
| < 30% identity | 3nsm chain A | 27.5% | Task 2 |
| 3gh5 chain A | 20.7% | Task 2 |
Table TODO: </figtable>
Important residues
TODO, jonas?
Modeller
Automatic alignments
2gk1
The alignments produced by the simple and 2D alignments methods within modeller are very similar. One differing position is located at the and of the first alpha helix: Since the preceding loop region is not part of the structure a large gap is needed and found by both alignment methods. However the first residue after the helix, therefore belonging to the loop region is positioned before the gap in the normal alignment and after it in the structure based one. Clearly this is a borderline case and the choice should not make a difference. Placing the threonine after the gap however aligns it with another threonine and is therefore the slightly more convincing choice.
1o7a
The two alignments (simple, 2D) of this structure with intermediate sequence identity exhibit the same difference with the placement of threonine before or after the gap. Two gaps in the middle of the sequence, both of length three, do not differ between the two alignments. A second difference is found at the end of the alignment where the 2D-Aligner inserts a five residue gap before the last two residues, while the normal alignment simply ends in the gap. Since this is the loop region at the end of the structure, there is nothing to support the shift of the last two residues and the simple alignment is the more convincing one. It also aligns asparagine with glutamine instead of the more distant glutamic acid. Whatever the choice, one would not expect a difference in the produced models.
3gh5
Since the sequence similarity is very low in this case which is reflected in the differing alignments. It is easily observable that the simple alignment methods tries to group gaps together instead of creating short breaks. The structure based alignment introduces several short gaps in looped regions for no apparent reason. More importantly the 2D-Aligner introduces a gap in the middle of the first helix, while it is preserved in the simple alignment. This is very unexpected since the whole point of the 2D-Aligner is that such cases are smoothed out instead of created in the first place. Another helix is broken by both methods, however the 2D-Aligner performs worse again, since it introduces two gaps in the helix, instead of only one. The last residue of 3gh5 is separated by a gap in both alignment methods for no apparent reason, however the structural alignment method again introduces two gaps instead of one, with no clear explanation.
Evaluation of alignment methods
While the templates with higher sequence similarity result in almost equal alignments with both methods, the low similarity template shows that the 2D-Aligner exhibits exactly the opposite of the expected behaviour and actually makes the alignment worse by introducing more gaps that do not conserve but destroy secondary structure elements. Therefore the simple alignment methods is much more convincing.
Manually edited alignments
All the alignments created in the previous step were analysed in respect to the correct alignment of important residues. For the 2gk1 and 1o7a alignments there is nothing to improve upon. The only editing operations that come to mind would turn the simple method based alignment into the 2D based one and vice versa. Since this has already been discussed above no further analysis is performed for these two templates.
The alignment of 3gh5 allowed for some editing operations. Taking the alignment produced by the simple method as a basis all important residues but N423 are already correctly aligned. Before that residue however there is the alpha helix, that is broken by both alignments methods. In the edited alignment this helix has been completely aligned and a gap placed before and after it, thereby only affecting loop regions. N423 is left as is, since there is no asparagine nearby that would result in a better alignment and since it is aligned to an aspartic acid which is a likely substitution that should not affect the formation of the hydrogen bond. Finally, the last residue is not placed separately and the alignment instead ends with gaps. The resulting alignment is shown in <xr id="fig:modeller3gh5edited"/>.
<figure id="fig:modeller3gh5edited">
>P1;3GH5 structureX:../../input/3GH5.pdb: -16 :A:+507 :A:MOL_ID 1; MOLECULE BETA-HEXOSAMINIDASE; CHAIN A; [...] HHHHSSGLVPRGSHMASMSQPSILPKPVSYTVGSGQFVLTKNASIFVAGNNVGETDELFNIGQALAKKLNAS TG-------YTISVVKSNQPTAGSIYLTTVGGN---AALGNEGYDLITTSNQVTLTANKPEGVFRGNQTLLQ LLPAGIEKNTVVSGVQWVIPHSNISDKPEYEYRGLMLDVARHFFTVDEVKRQIDLASQYKINKFHMHLSDDQ GWRIEIKSWPDLIEIGSKGQVGGGPGGYYTQEQFKDIVSYAAERYIEVIPEIDMPGHTNAALASYGELNPDG KRKAMRTDTAVGYSTLMPRAEITYQFVEDVISELAAISPSPYIHLGGDESNAT----------------SAA DYDYFFGRVTAIANSY----GKKVVGWDPS-DTSSGATSDSVLQNWTCSASTGTAAKAKGMKVIVSPANAYL DMKYYSDS-PIGLQWRGF-VNTNRAYNWDPTDCIKGANIYGVESTLWTETFVTQDHLDYMLYPKLLSNAEVG WTARGDRNWDDFKERLIEHTPRLQNKGIKFFADPIV---------* >P1;P06865 sequence:: : : : :::-1.00:-1.00 MTSSRLWFSLLLAAAFAGRATALWPWPQNFQTSDQRYVLYPNNFQFQYDVSSAAQPGCSVLDEAFQRYRDLL FGSGSWPRPYLTGKRHTLEKNVLVVSVVTPGCNQLPTLESVENYTLTINDDQCLLLSETVWGALRGLETFSQ LVWKSAEGT-------FFINKTEIEDFPRFPHRGLLLDTSRHYLPLSSILDTLDVMAYNKLNVFHWHLVDDP SFPYESFTFPELMRKGSYNPVTH----IYTAQDVKEVIEYARLRGIRVLAEFDTPGHTLSWGPGIPGLLTPC YSGSEPSGT---FGPVNPSLNNTYEFMSTFFLEVSSVFPDFYLHLGGDEVDFTCWKSNPEIQDFMRKKGFGE DFKQLESFYIQTLLDIVSSYGKGYVVWQEVFDNKVKIQPDTIIQVWREDIPVNYMKELE--LVTKAGFRALL SAPWYLNRISYGPDWKDFYIVEPLAFEGTPE---QKALVIGGEACMWGE-YVDNTNLVPRLWPRAGAVAERL WSNKLTSDLTFAYERLSHFRCELLRRGVQAQPLNVGFCEQEFEQT*
Edited Alignment of 3gh5_A with P06865 based on the simple (non-structural) alignment produced by Modeller. The helix region and single residue at the end that were changed are highlighted in red. Bold, blue residues are those deemed important (c.f. TODO) </figure>
3gh5
SWISS-MODEL
General
The SWISS-MODEL server provides as output a model in pdb format and the corresponding target template alignment. Besides it also offers diverse scores and functions for the model evaluation.
ANOLEA is the atomic empirical mean force potential. Therefore a program performs energy calculations on a protein chain. Negative energy values (in green) represent favourable energy environment whereas positive values (in red) unfavourable energy environment.
There is also a local model reliability score, the residue error computed along the sequence
QMEAN is a composite scoring function for both the estimation of the global quality of the entire model as well as for the local per-residue analysis of different regions within a model.
QMEAN4 is a scoring function to describe the model quality. It is a linear combination of the 4 statistical potential terms C_beta interaction energy, all-atom pairwise energy, solvation energy and torsion angle energy.
Hereby the QMEAN raw score ranges from 0 to 1 and indicates the reliability of the model.
The QMEAN Z-score represents the absolute quality of the model by describing the likelihood that a given model is of comparable quality to experimental structures. Is calculated by comparison to reference structures and has a range of -4 to 4; the smaller the value the worse the model quality.
For a more detailed explanation, see [1].
Default Modelling
2gjx chain E gets automatically assigned as template. this is not surprising as the 2gjx_a is the reference and all the chains are virtually identical. The resulting alignment between target and template consists of identical matches. Only in the first region a loop in the template is missing and therefore a gap is inserted (see <xr id="fig:2gjxali"/>).
<figure id="fig:2gjxali">
TARGET 1 LWPWPQNF QTSDQRYVLY PNNFQFQYDV SSAAQPGCSV LDEAFQRYRD 2gjxE 23 lwpwpqnf qtsdqryvly pnnfqfqydv ssaaqpgcsv ldeafqryrd TARGET ss sss sssss hh hhhhhhhhhh 2gjxE ss sss sssss hh hhhhhhhhhh TARGET 49 LLFGSGSWPR PYLTGKRHTL EKNVLVVSVV TPGCNQLPTL ESVENYTLTI 2gjxE 71 llfg------ --------tl eknvlvvsvv tpgcnqlptl esvenytlti TARGET hh sssss ssssss 2gjxE hh sssss ssssss
Alignment of 2gjx_E with P06865 </figure>
For the whole alignment see Swissmodel 2gjx alignment.
<figure id="fig:2gjxanolea">
</figure> As the 2gjx chain is our chosen reference sequence it is expected to provide a perfect model. ANOLEA displays only one weakness of the model which is found at the beginning between position 70 and 90, see <xr id="fig:2gjxanolea"/>. This is also supported by the QMEAN, which signalises a potential error at this site.
<figtable id="tab:swissevalsap">
| Scoring function term | Raw score | Z-score |
|---|---|---|
| C_beta interaction energy | -106 | -0.99 |
| All-atom pairwise energy | -13340 | -0.33 |
| Solvation energy | -37 | -0.62 |
| Torsion angle energy | -93 | -1.62 |
| QMEAN4 score | 0.68 | -1.63 |
Table TODO: Scores for default modelling of P06865 by SWISS-MODEL. </figtable>
<figure id="fig:2gjxswissmodel">
</figure> In <xr id="fig:2gjxswissmodel"/> the computed model is display (blue-red, depending on error) together with the reference (green). It is clear that the model fits the reference perfectly which was the expectancy as the the template is the reference just with another chain (template 2gjx_E, reference 2gjx_A). The only region where the target and reference do not is the loop region colored in red, which was correctly detected by the SWISS-MODEL error scores. The active site and the important residues are matched perfectly by the model.
High sequence identity
The model with 2gk1 as template is very much alike the previous model, which is not surprising as the templates have 100% sequence identity. The alignment of the Hex A subunit and the template expresses the same gap as shown above (for the whole alignment see Swismsmodel 2gk1 alignment) This alignment also correspond to the structural alignment from Modeller. <figure id="fig:2gk1anolea">
</figure> The ANOLEA and QMEAN are very good for the alignment, again except for the first region, where there are some signs of lower model quality, see <xr id="fig:2gk1anolea"/>.
<figtable id="tab:swissscores2gk1">
| Scoring function term | Raw score | Z-score |
|---|---|---|
| C_beta interaction energy | -122 | -0.81 |
| All-atom pairwise energy | -13468 | -0.34 |
| Solvation energy | -44 | -0.12 |
| Torsion angle energy | -109 | -1.06 |
| QMEAN4 score | 0.69 | -0.96 |
Table TODO: Scores for the model of P06865 with 2gk1 as template by SWISS-MODEL. </figtable>
<figure id="fig:2gjxswissmodel">
</figure>
Medium Sequence identity
<figure id="fig:2gjxali">
TARGET 1 TALWPWPQ NFQTSDQRYV LYPNNFQFQY DVSSAAQPGC SVLDEAFQRY 1o7aD 54 palwplpl svkmtpnllh lapenfyish spnstagpsc tlleeafr-- TARGET sssss ssss s ssss s hhhhhh 1o7aD sssss ssss s ssss s hhhhhhhh TARGET 49 RDLLFGSGSW PRPYLTGKRH TLEKNVLVVS VVTPGCNQLP TLESVENYTL 1o7aD 100 -----ryhgy ifgtqvq--- q---llvsi- tlqsecdafp nissdesytl TARGET sss hhhh sss ssssss sss 1o7aD hhhhh h s sssss s sss
Alignment of 2gjx_E with P06865 </figure>
<figure id="fig:1o7aanolea">
</figure>
<figtable id="tab:swissscore1o7a">
| Scoring function term | Raw score | Z-score |
|---|---|---|
| C_beta interaction energy | -97 | -1.15 |
| All-atom pairwise energy | -11181 | -0.99 |
| Solvation energy | -29 | -1.24 |
| Torsion angle energy | -72 | -2.33 |
| QMEAN4 score | 0.594 | -2.73 |
Table TODO: Scores for default modelling of P06865 by SWISS-MODEL. </figtable>
Low sequence identity
With the 3gh5 as template the automated SWISS-MODEL was not able to calculate a model structure for the Hex A subunit. Two alignments were produced, one with Blast and one with HHsearch. While the Blast alignment quality between target and template was too low to start with, the HHsearch alignment reached the next level and was sent to modelling but the building of a model was not successful.
The same occured for 3nsm which has a sequence identity about 7% higher than 3gh5. A sequence identity lower than 30% seems to be too low for modelling.
Evaluation
<figtable id="tab:swissOwneval">
| QMEAN raw score | QMEAN Z-score | |
|---|---|---|
| 2gjx | 0.658 | -1.63 |
| 2gk1 | 0.698 | -0.96 |
| 1o7a | 0.594 | -2.73 |
Table TODO: Scores provided by SWISS-MODEL. </figtable>
<figtable id="tab:swisseval">
| Residues in common | Common residue RMSD | TM | GDT-TS | GDT-HA | |
|---|---|---|---|---|---|
| 2gjx | 492 | 0.573 | 0.995 | 0.983 | 0.924 |
| 2gk1 | 492 | 0.213 | 0.999 | 1.000 | 0.999 |
| 1o7a | 486 | 2.411 | 0.952 | 0.913 | 0.802 |
Table TODO: Calculated TM scores. </figtable>
<figtable id="tab:swissevalsap">
| Residues in common | Weighted RMSD | Unweighted RMSD | RMSD 6A around active site | |
|---|---|---|---|---|
| 2gjx | 492 | 0.414 | 0.573 | |
| 2gk1 | 491 | 0.189 | 0.212 | |
| 1o7a | 471 | 0.486 | 1.455 |
Table TODO: Calculated RMSD scores with SAP and Pymol.
</figtable>
iTasser
3D-Jigsaw
References
<references/>
