Homology Modeling of ARS A
Contents
Proteins used as templates
From the previous alignment TASK (see Alignment TASK), we took four proteins which might serve as suitable templates for the modeling. The proteins are depicted in the below table. The information about active and binding sites were obtained from Uniprot and will serve as additional information for the manual modification of the alignments in order to try to improve the accuracy of the models. Interestingly, our potential templates - identified by the database searches - contain all homologs with known structure, regarding to HSSP.
| SeqIdentifier | Seq Identity (from TASK 2) | source | Protein function | True homolog (HSSP) | Seq Identity (pairw. ali.) | Active site | Substrate binding site | Metal binding site |
|---|---|---|---|---|---|---|---|---|
| 1P49 | 39.0% | Homo Sapiens | Steryl-Sulfatase | yes | 31.9% | 136 | 333, 459 | 35, 36, 75, 342, 343, |
| 1FSU | 28.0% | Homo Sapiens | Arylsulfatase B | yes | 26.5% | 147 | 145, 242, 318 | 53, 54, 91, 300, 301 |
| 2VQR | 20.0% | Rhizobium leguminosarum | Monoester Hydrolase | no | 20.3% | not avail. | not avail. | 12, 57, 324, 325 |
| 3ED4 | 32.0% | Escherichia coli | Arylsulfatase | yes | 27.7% | not avail. | not avail. | not avail. |
| ARSA (1AUK) | - | Homo Sapiens | - | - | - | 125 | 123, 150, 229, 302 | 29, 30, 69, 281, 282 |
Furthermore, we used the HHsearch webserver to see if we could extend this list towards even more remotely related sequences. But the results did not yield significant hits that were more distantly related than 2VQR, so we decided to stick with the above proteins for modelling with Modeller.
Modeller
Modeller is a program for comparative modeling of the 3D structure of a protein with unknown structure. It provides different methods for the calculation of the initial target-template alignment. Given the alignments, Modeller generates the backbone and optimizes a probablility function reflecting spatial restraints. The input alignments can be either pairwise sequence alignment - for single template modeling - or multiple sequence alignments - for multiple template modeling. <ref>AA. Sali, T.L. Blundell. Comparative protein modelling by satisfaction of spatial restraints. J. Mol. Biol. 234, 779-815, 1993</ref>
In this section, we use Modeller to model the 3D structure of ARSA and compare the results to the known structure from PDB. We wrote a tutorial ( Using Modeller for TASK 4 ) comprising all necessary steps in the following analysis. It provides generic scripts and example code and executes all methods using default parameters.
Single template modelling
In order to predict the structure using a single template structure, modeller needs pairwise sequence alignments in PIR format. Modeller provides two different methods to calculate pairwise sequence alignments. alignment.malign() uses classical dynamic programming to align two sequences. alignment.alig2dn() also uses a dynamic programming approach, but includes structural information to optimize the alignment (e.g. tries to place gaps outside of secondary structure elements). We applied both alignment methods and created eight pairwise sequence alignments of the above templates with the target. Then we modelled the structure with default parameters using the automodel() class. The scripts used for this purpose can be seen in our protocol: Using Modeller for TASK 4 .
Next, we calculated RMSD and TM scores of the models to get a first impression on how much the models deviate from the original structure. In order to calculate the TM-scores, we downloaded the TMscore FORTRAN source code from http://zhanglab.ccmb.med.umich.edu/TM-score/ and compiled it using
gfortran -static -O3 -ffast-math -lm -o TMscore TMscore.f
The TM-scores were calculated as follows:
./TMscore MODEL.pdb REAL_STRUCTURE.pdb
In order to calculate the RMSD scores, we used DaliLite
The results are depicted below:
| PDB Identifier | TM-score | RMSD | |
|---|---|---|---|
| Dynamic Programing with structural information | |||
| 1P49 | 0.7960 | 2.0 | |
| 2VQR | 0.4825 | 3.5 | |
| 1FSU | 0.7146 | 1.5 - 2.3 | |
| 3ED4 | 0.3881 | 1.9 - 2.8 | |
| Dynamic Programing without structural information | |||
| 1P49 | 0.7731 | 2.2 | |
| 2VQR | 0.3183 | 3.5 | |
| 1FSU | 0.7223 | 2.7 | |
| 3ED4 | 0.3122 | 4.1 | |
The RMSD score measures the root mean square deviation of the two structures. This is a straightforward measure to assess the similarity of our models. The TM-score also measures the deviation of the two structures from each other, but includes weight, i.e. the distances between close residues get a higher weight than the distances between distant residues. <ref>Y. Zhang, J. Skolnick, Scoring function for automated assessment of protein structure template quality, Proteins, 2004 57: 702-710 </ref>
The TM-score is more sensitive in detecting the same fold. Assume two proteins for which 80 % of the residues lie in a very similar fold, but the remaining 20 % of the residues fold completely different. One would consider these two proteins still as similar, but the RMSD might become very large regarding to the high distances in these 20 %.
Further on, we visualised the models using pymol. We loaded all pairs of model and real structure into the program and performed a structural alignment to superimpose and compare them visually. The pymol commands and the images are shown below:
align 1AUK, MODEL
hide all
show cartoon
# select color of modelled structure via graphical interface
ray
cmd.png("MODEL.png")
| Alignment method | 1P49 | 2VQR | 1FSU | 3ED4 |
| Classical Dynamic Programming |
||||
| Dynamic Programming with structural information from the template |
3ED4
Despite its evolutionary relationship, 3ED4 is a very poor template structure for modeling. Thus, we considered the structure of 3ED4 in more detail to figure out the reason for this behaviour.
First of all, we looked at the PDB entry of the protein and found out that 3ED4 consists of 4 different chains. Next, we plotted 3ED4 coloring each of the four chains (Figure is depicted below).
This visual inspection let us speculate that each of the individual chains structurally resemble our target protein ARSA. Thus we decided to use each individual chain for modeling. We again computed TM- and RMSD scores and used pymol to visualise the model together with the real structure of ARSA.
| chain | TM-score | RMSD |
| 3ED4A | 0.7268 | 2.9 |
| 3ED4B | 0.7251 | 2.8 |
| 3ED4C | 0.6518 | 2.8 |
| 3ED4D | 0.7303 | 2.8 |
| Alignment method | 3ED4A | 3ED4B | 3ED4C | 3ED4D |
| Dynamic Programming with structural information from the template |
Modification of Alignments
Using 1P49 as template structure for the modeling process yielded the best results thus we decided to manually modify this alignment to see if we can improve the model. We created two different modified alignments. For the first alignment we only made sure that active site, substrate binding sites and metal binding sites were aligned. For the second modified alignment we additionally removed gaps in secondary structure elements. For modification of the initial alignments, we used JalView. Images of the initial and the two modified alignments are depicted on the right border. Altogether, we performed the following changes:
- The gap between residue 74 and 75 in 1P49 was removed to align metal-binding site 75 with metal-binding site 69. This also induced the alignment of both active sites, which were not aligned in the initial alignment. The region around the active site is well conserved between both enzymes. However, this conservation seems to be shifted, thus the amino acids at the active sites differ and an alignment of both sites decreases the alignment of conserved residues within this region. An image of the structural model together with the real structure is depcited below.
After this change we caluclated one model. The TM-score of this model drops to 0.6940. This might be due to the fact that the amino acids are conserved in the region around the active sites, but the alignment of the active sites thmeselves decreases the alignment quality because the conservation is somehow shifted by one amino acid (i.e. the active site in 1AUK/ARSA is identical to the amino acid before the active site in 1P49).
Normally, one does not have information about the secondary structure of the target sequence, but in our case, this information was available and thus we modified the alignments such that gaps within the secondary structure were avoided. There were no gaps in secondary structure elements of 1P49. This is due to the fact that we modified the output of align2d() , which already uses secondary structure information to place gaps outside of these regions.
- The gap between residue 154 and 155 was moved out of the beta strand between residues 152 and 153.
- The gap between residues 190-191 was moved out of beta strand between residues 191-192.
- All gaps within the helix from residue 197-214 were moved out of the helix (at the right border).
- The gap between 290-291 was moved to the right end of the helix.
Surprisingly, the TM-score was decreased even more to 0.5561. An image of the structural model together with the real structure is depcited below.
Multiple Template Modeling
For the multiple template model, we first needed to create a multiple sequence alignment of the templates and the target. We used the salign() function, which uses (like align2d() ) structural information from the template to place gaps in coil regions. Then we calculated the model using this MSA. The detaild workflow is agian described in ( Using Modeller for TASK 4 ). We calculated three models:
- Model 1 was calculated from a multiple sequence alignment (MSA) of ARS A and the four proteins/chains, which yielded the best TM-score/RMSD in the single template modeling: 1FSU, 1P49, 2VQR, 3ED4D.
- Model 2 was calculated from a MSA of ARS A and the three proteins/chains, which yielded the best TM-score/RMSD in the single template modeling: 1FSU, 1P49, 3ED4D.
- Model 3 was calculated from a MSA of ARS A and the two proteins/chains, which yielded the best TM-score/RMSD in the single template modeling: 1P49, 3ED4D.
Below are depicted the TM- and RMSD scores, as well as images of the structural model and the real structure of ARS A.
| Model 1 | Model 2 | Model 3 |
| PDB Identifier | TM-score | RMSD |
|---|---|---|
| model1 | 0.5409 | 2.4 |
| model2 | 0.6701 | 2.4 - 3.1 |
| model3 | 0.6819 | 3.2 |
Modification of the MSA
Analogously to the previous section, we modified the alignment of Model 2 such that all active and binding sites were aligned. Images of the alignments and the structural model vs. the real structure are depicted on the right, below respectively.
The TM-score of the new model drops to 0.5685.
Discussion
Modeller yields good results. The initial alignments are very important for the quality of the resulting model. When using the 2d-alignment method for single template modeling, we could improve the prediction accuracy, regarding to both measures (RMSD, TMscore).
Surprisingly, the multiple template models all perform worse than the three best single template models. Also the manual modification of the alignments results in a decreased modelling accuracy.
This could be due to the fact that the automatic alignments are optimized over the whole alignment while the manual modified alignments are optimized in one region which seems to lead to a decrease of quality in other areas of the alignment.
iTasser
iTasser is a server to model 3D-structure by homology. Also function-predctions are provided. As Zhang-Server iTasser participated in CASP7, CASP8 and CASP9 and was the ranked best in CASP7 and CASP8 and ranked second in CASP9. iTasser uses a threading-approach to build the models. Unaligned regions (mainly loops) are modelled ab initio. <ref>Ambrish Roy, Alper Kucukural, Yang Zhang. I-TASSER: a unified platform for automated protein structure and function prediction. Nature Protocols, vol 5, 725-738 (2010)</ref><ref>Yang Zhang. Template-based modeling and free modeling by I-TASSER in CASP7. Proteins, vol 69 (Suppl 8), 108-117 (2007)</ref>
The confidence of a model is measured with the C-score which is based on the significance of the template alignments and the convergence parameters of the structure assembly simulations. The typical range for the C-score is [-5,2], where a higher C-score means higher confidence in the model. <ref>http://zhanglab.ccmb.med.umich.edu/I-TASSER/output/S72828/cscore.txt</ref>
Modelling without template
As one can see, model 1 is the model with the highest confidence. Model 1 has a TM-score of 0.84 ± 0.08 and a RMSD of 5.3 ± 3.4Å.
To compare the models, TM-score and RMSD to 1AUK were calculated:
| prediction by iTasser without template | |||
|---|---|---|---|
| model | TM-score | RMSD | |
| model1 | 0.9971 | 0.5 | |
| model2 | 0.9972 | 0.5 | |
| model3 | 0.9891 | 0.8 | |
| model4 | 0.9220 | 1.8 | |
| model5 | 0.9972 | 0.5 | |
Modelling with single template
To specify a single template, one can specify a pdb-id or upload a pdb-file. Due to the long runtime of iTasser we only built a model based on 1P49.
As one can see, model 1 is the model with the highest confidence. Model 1 has a TM-score of 0.93 ± 0.06 and a RMSD of 4.0 ± 2.7Å.
To compare the models, TM-score and RMSD to 1AUK were calculated:
| prediction by iTasser with 1P49 as template | |||
|---|---|---|---|
| model | TM-score | RMSD | |
| model1 | 0.2059 | 2.1 | |
| model2 | 0.2057 | 2.1 | |
| model3 | 0.2063 | 2.0 | |
| model4 | 0.2065 | 1.9 | |
| model5 | 0.2052 | 2.2 | |
Discussion
SWISS-MODEL
SWISS-MODEL is a online tool to model 3D-structure <ref>Arnold K., Bordoli L., Kopp J., and Schwede T. (2006). The SWISS-MODEL Workspace: A web-based environment for protein structure homology modelling. Bioinformatics, 22,195-201.</ref><ref>Kiefer F, Arnold K, Künzli M, Bordoli L, Schwede T (2009). The SWISS-MODEL Repository and associated resources. Nucleic Acids Research. 37, D387-D392. </ref><ref>Peitsch, M. C. (1995) Protein modeling by E-mail Bio/Technology 13: 658-660.</ref>. There are three different modes available: automated mode, alignment mode and project mode. We only used the automated and the alignment mode.
Modelling without template
In automated mode without template, suitable templates are selected by a BLAST-run via an e-value treshold. It is used by pasting a protein sequence or a UniProt AC code into a text-field.
Template
SWISS-MODEL identified 1N2LA as best template. The name of the PDB-Entry of 1N2LA is "Crystal structure of a covalent intermediate of endogenous human arylsulfatase A". So the result should be very good, as we are using a human Arylsulfatase A as a template. As expected, the Alignment quality was very high:
TARGET 19 RPPNIVLI FADDLGYGDL GCYGHPSSTT PNLDQLAAGG LRFTDFYVPV
1n2lA 19 rppnivli faddlgygdl gcyghpsstt pnldqlaagg lrftdfyvpv
TARGET sssss ss hhhhhhhh ssss sss
1n2lA sssss ss hhhhhhhh ssssssss
TARGET 67 SLCTPSRAAL LTGRLPVRMG MYPGVLVPSS RGGLPLEEVT VAEVLAARGY
1n2lA 67 sl-tpsraal ltgrlpvrmg mypgvlvpss rgglpleevt vaevlaargy
TARGET hhhhh hh hhh ss s hhhhhhhh
1n2lA hhhhhh hh hh ss s hhhhhhhh
TARGET 117 LTGMAGKWHL GVGPEGAFLP PHQGFHRFLG IPYSHDQGPC QNLTCFPPAT
1n2lA 117 ltgmagkwhl gvgpegaflp phqgfhrflg ipyshdqgpc qnltcfppat
TARGET ssssssss sss sss hhh ssss s sss s
1n2lA ssssssss sss sss hhh ssss s sss s
TARGET 167 PCDGGCDQGL VPIPLLANLS VEAQPPWLPG LEARYMAFAH DLMADAQRQD
1n2lA 167 pcdggcdqgl vpipllanls veaqppwlpg learymafah dlmadaqrqd
TARGET ss ssss s ss hhhhhhhhh hhhhhhhh
1n2lA ss ssss s ss hhhhhhhhh hhhhhhhh
TARGET 217 RPFFLYYASH HTHYPQFSGQ SFAERSGRGP FGDSLMELDA AVGTLMTAIG
1n2lA 217 rpfflyyash hthypqfsgq sfaersgrgp fgdslmelda avgtlmtaig
TARGET ssssssss h hhhhhhhhhh hhhhhhhhhh
1n2lA ssssssss h hhhhhhhhhh hhhhhhhhhh
TARGET 267 DLGLLEETLV IFTADNGPET MRMSRGGCSG LLRCGKGTTY EGGVREPALA
1n2lA 267 dlglleetlv iftadngpet mrmsrggcsg llrcgkgtty eggvrepala
TARGET hh ssss sss sss sss
1n2lA h ssss sss hhhsss sss
TARGET 317 FWPGHIAPGV THELASSLDL LPTLAALAGA PLPNVTLDGF DLSPLLLGTG
1n2lA 317 fwpghiapgv thelassldl lptlaalaga plpnvtldgf dlsplllgtg
TARGET s ss s hhh hhhhhhhh hhhhh
1n2lA s ss s ssshhh hhhhhhhh hhhhh
TARGET 367 KSPRQSLFFY PSYPDEVRGV FAVRTGKYKA HFFTQGSAHS DTTADPACHA
1n2lA 367 ksprqslffy psypdevrgv favrtgkyka hfftqgsahs dttadpacha
TARGET sssss ssssssssss ssss
1n2lA sssss ssssssssss ssss
TARGET 417 SSSLTAHEPP LLYDLSKDPG ENYNLLGGVA GATPEVLQAL KQLQLLKAQL
1n2lA 417 sssltahepp llydlskdpg enynllg--- gatpevlqal kqlqllkaql
TARGET sss sssss hhhhhhh hhhhhhhhhh
1n2lA sss sssss hhhhhhh hhhhhhhhhh
TARGET 467 DAAVTFGPSQ VARGEDPALQ ICCHPGCTPR PACCHCPD
1n2lA 467 daavtfgpsq vargedpalq icchpgctpr pacchcpd-
TARGET hhh hh sss
1n2lA hhh hh sss
Results
As one can see in the images above, the model quality is quite good, with uncertainties especially in the loop-regions. The result is not really surprising, as 1N2L is the structure of a human Arylsulfatase A.
Modelling with single template without alignment
It is possible to specify a template in automated mode by specifing a PDB-ID or by uploading a pdb-file.
1P49
1P49 has 39% sequence identity with human arylsulfatase which is the highest identity in all our templates. With this low sequence identity the alignment quality was rather poor:
TARGET 1 RPPNIV LIFADDLGYG DLGCYGHPSS TTPNLDQLAA GGLRFTDFYV
userX 23 aa--srpnii lvmaddlgig dpgcygnkti rtpnidrlas ggvkltqhla
TARGET sss ssss hhhh ssssssss
userX sss ssss hhhh sss ssss
TARGET 47 PVSLGTPSRA ALLTGRLPVR MGMYPGVLVP SS-----RGG LPLEEVTVAE
userX 71 a-spltpsra afmtgrypvr sgmaswsrtg vflftassgg lptdeitfak
TARGET hhh hhh hh h hhh
userX hhhh hhhh hh h hhh
TARGET 92 VLAARGYLTG MAGKWHLGVG PEG----AFL PPHQGFHRFL GIPYSHDQGP
userX 121 llkdqgysta ligkwhlgms chsktdfchh plhhgfnyfy gisltnlrdc
TARGET hhhh sss sssss sss ss
userX hhhh sss sssss sss ss
TARGET 138 CQNLT-CFPP ATPCDG---- ---------- ---------- ---------G
userX 171 kpgegsvftt gfkrlvflpl qivgvtlltl aalnclgllh vplgvffsll
TARGET hh hhhhh
userX hhh hhhh hhh hhhhhhhhhh hhhhhh hhhhhhh
TARGET 154 CD--QGLVPI PLLANLSVEA QP-------- ----PWLPGL EARYMAFAHD
userX 221 flaaliltlf lgflhyfrpl ncfmmrnyei iqqpmsydnl tqrltveaaq
TARGET hhhh hhhhhhh hhhhhhhhh
userX hhhhhhhhhh hhhhhhhhhh ssss ss sss h hhhhhhhhhh
TARGET 190 LMADAQRQDR PFFLYYASHH THYPQFSGQS FAERSGRGPF GDSLMELDAA
userX 271 fiq--rntet pfllvlsylh vhtalfsskd fagksqhgvy gdaveemdws
TARGET hh ssssssss hh hhhhhhhhhh
userX hhh ssssssss hh hhhhhhhhhh
TARGET 240 VGTLMTAIGD LGLLEETLVI FTADNGPETM RM-----SRG GCSGLLRCGK
userX 319 vgqilnllde lrlandtliy ftsdqgahve evsskgeihg gsngiykggk
TARGET hhhhhhhhhh h sssss ssss
userX hhhhhhhhhh h sssss ssss sss sss
TARGET 285 GTTYEGGVRE PALAFWPGHI -APGVTHELA SSLDLLPTLA ALAGAPLPN-
userX 369 annweggirv pgilrwprvi qagqkidept snmdifptva klagaplped
TARGET hhsss ssss sss s sshhhhhhhh hhh
userX sss ssss s sshhhhhhhh hhh
TARGET 333 VTLDGFDLSP LLLGTGKSPR QSLFFYPS-- YPDEVRGVFA VRTGKYKAHF
userX 419 riidgrdlmp llegksqrsd heflfhycna ylnavrwhpq nstsiwkaff
TARGET hh hhh hhhhhh h ssssss
userX hh hhh sssssss ssssssss ssssss
TARGET 381 FTQGSAHSDT TADPACHASS SLTAHEPPLL YDLSKDPGEN YNLLGGVAGA
userX 469 ftpnfnpvcf athvcfcfgs yvthhdppll fdiskdprer nplt----pa
TARGET ss sss ss sss sss sss
userX ss sss ss sss
TARGET 431 TPEVLQAL-K QLQLLKAQLD AAVTFGPSQV A---RGEDPA LQICCHPGCT
userX 519 seprfyeilk vmqeaadrht qtlpevpdqf swnnflwkpw lqlccp---s
TARGET hh hh hhhhhhhhh
userX hhh hhhhhhhhhh
TARGET 477 PRPACC ---
userX 566 tglscqcdre
TARGET
userX sss
Results
As one can see in the images above, the model quality is not really good, due to the fact that the template seems to be too far related
2VQR
2VQR has 20% sequence identity with human arylsulfatase which is the lowest identity in all our templates. With this even lower sequence identity the alignment quality was really poor:
TARGET 2 PPNIVLIFAD DLGYGDLG-- --CYGHPS-S TTPNLDQLAA GGLRFTDFYV
userX 3 kknvllivvd qwradfvphv lradgkidfl ktpnldrlcr egvtfrnhvt
TARGET sssssss hhhhhhhh h ssssssss
userX sssssss hhh hhhh hhhhhhhh h ssssssss
TARGET 47 PVSLGTPSRA ALLTGRLPVR MGMYPGVLVP SSRGGLPLEE VTVAEVLAAR
userX 53 tcvpxgpara slltglylmn hravqntv-- ----pldqrh lnlgkalrgv
TARGET hhhhhh hhh hhh h hhhhhhhh
userX hhhh hhh hhh h hhhhhh
TARGET 97 GYLTGMAGKW HLGVGPEGAF LPPHQGFHRF LGIPYSHDQG PCQ-----NL
userX 97 gydpaligyt ttvpdprtt- spndprfrvl gdlmdgfhpv gafepnmegy
TARGET ssss hh sss h
userX ssss hh sss hhh
TARGET 142 TCFPPATPCD GGCD-----Q GLVPIPLLAN LSVEAQPPWL PGLEARYMAF
userX 146 fgwvaqngfd lpehrpdiwl pegedavaga tdrpsripke fsdstffter
TARGET hhhhhh hhhhhhhh
userX hhhhhh hhhhhhhh
TARGET 187 AHDLMADAQR QDRPFFLYYA SHHTHYPQFS GQSFAERSGR ----------
userX 196 altylkg--r dgkpfflhlg yyrphppfva sapyhamyrp edmpapiraa
TARGET hhhhhh ssssss s
userX hhhhhhh h ssssss s
TARGET 227 ---------- ---------- ---------- ---------- ----GPFGDS
userX 244 npdieaaqhp lmkfyvdsir rgsffqgaeg sgatldeael rqmratycgl
TARGET hhhh
userX hhhhhh hhhhhhhhss s s ss hhhh hhhhhhhhhh
TARGET 233 LMELDAAVGT LMTAIGDLGL LEETLVIFTA DNGPETMRMS RGGCSGLLRC
userX 294 itevddclgr vfsyldetgq wddtliifts dhgeqlgdhh ll--------
TARGET hhhhhhhhhh hhhhhh h ssssss s
userX hhhhhhhhhh hhhhhh h ssssss s
TARGET 283 GKGTTYEGGV REPALAFWPG HI--APGVTH ELASSLDLLP TLAALAGAPL
userX 336 gkigyndpsf riplvikdag enaragaies gftesidvmp tildwlggki
TARGET hhs ss ssss sss ssshhhhh hhhhhh
userX hhs ss ssss sss ssshhhhh hhhhhh
TARGET 331 PNVTLDGFDL SPLLLGTGKS PRQ-SLFFYP SYP------- -------DEV
userX 386 ph-acdglsl lpflsegrpq dwrtelhyey dfrdvyysep qsflglgmnd
TARGET hhh sssss
userX hhh sssss ss hhhh
TARGET 366 RGVFAVRTGK YKAHFFTQGS AHSDTTADPA CHASSSLTAH EPPLLYDLSK
userX 435 cslcviqder ykyvhfaa-- ---------- ---------- lpplffdlrh
TARGET sssssss s sssssss s ss ss s sssss
userX ssssssss s sssssss sssss
TARGET 416 DPGENYNLLG GVAGATPEVL QAL-KQLQLL KAQLDAA -- ----------
userX 463 dpneftnlad d--payaalv rdyaqkalsw rlkhadrtlt hyrsgpegls
TARGET hhhh hh hhhh hhh
userX hhh hhhhhhhhhh hhh sssss sss
TARGET ----
userX 511 ersh
TARGET
userX ss
Results
Due to the low alignment quality, the model quality was so low, that the only result was a plot of the local quality.
Modelling with single template with alignment
1P49
SWISS-MODEL was not able to build a model based on our alignment.
2VQR
TARGET 4 PRSLLLA LAAGLAVARP PNIVLIFADD LGYGDLGCYG HPSSTTPNLD
2vqrA 3 kknvlli vvdqwradfv phvlr--adg -kidfl---- ----ktpnld
TARGET sssss ss sss hhhh sss sss hhhh
2vqrA sssss ss hhhhh hh hhhh
TARGET 51 QLAAGGLRFT DFYVPVSLCT PSRAALLTGR LPVRMGMYPG VLVPSSRGGL
2vqrA 39 rlcregvtfr nhvttcvpcg paraslltgl ylmnhravqn t-vpldqrhl
TARGET hhhhh ssss ssss hh hhhhhhh hhhh
2vqrA hhhhh ssss ssss hh hhhhhhh hhhh
TARGET 101 PLEEV--TVA EVLAARGYLT GM-------- -------AGK WHLGVGPEGA
2vqrA 88 nlgkalrgvg ydpaligytt tvpdprttsp ndprfrvlgd lmdgfhpvga
TARGET ssss sss
2vqrA hhhhhh ssss hh sss
TARGET 134 FLPPHQGFHR FL------GI PYSHDQGPC- ---------- ---QNLTCFP
2vqrA 138 fepnmegyfg wvaqngfdlp ehrpdiwlpe gedavagatd rpsripkefs
TARGET hhhhh hh hhh
2vqrA hhhhh hhhh
TARGET 164 PATPCDGGCD ---QGLVPIP LLANLSV-EA QPPWLPGLEA R-------YM
2vqrA 188 dstffteral tylkgrdgkp fflhlgyyrp hppfvasapy hamyrpedmp
TARGET hhhhhhhhh ssssss
2vqrA hhhhhhhhhh hhhhhh sssssss
TARGET 203 AFAHDLMADA QRQDRPFFLY YASHHTHY-- ---PQFSGQS FAE---RSGR
2vqrA 238 apiraanpdi eaaqhplmkf yvdsirrgsf fqgaegsgat ldeaelrqmr
TARGET hhh hhh hhhh hhhh hh
2vqrA hhh hhh hhhh hhhhsss sss hhhhhhhh
TARGET 245 GPFGDSLMEL DAAVGTLMTA IGDLGLLEET LVIFTADNGP ETMRMSRGGC
2vqrA 288 atycglitev ddclgrvfsy ldetgqwddt liiftsdhg- eql-----gd
TARGET hhhhhhhhhh hhhhhhhhhh hh h ssssssssss
2vqrA hhhhhhhhhh hhhhhhhhhh hh h sssssss
TARGET 295 SGLLRCGKGT TYEGGVREPA LAFWPGHI-A PGVTH-ELAS SLDLLPTLAA
2vqrA 332 hhll--gkig yndpsfripl vikdagenar agaiesgfte sidvmptild
TARGET hhsss s sss sss ss shhhhhhhhh
2vqrA hhsss s sss sss ss shhhhhhhhh
TARGET 343 LAGAPLPNVT LDGFDLSPLL LGTGKSPRQS LFFYPSYPDE VRGVFAVRTG
2vqrA 380 wlggkiph-a cdglsllpfl s-egr-p-qd wrtelhyeyd frdvy---ys
TARGET hh hhhh ssssss s
2vqrA hh hhh ssssss s
TARGET 393 KYKAHFFTQG S-AHSDTTAD PACHASSSLT AHEPPLLYDL SKDPGENYNL
2vqrA 423 epqs-flglg mndcslcviq derykyvhfa al-pplffdl rhdpneftnl
TARGET sssssss s ssssssss sssss
2vqrA hh hh sssssss s ssssssss sssss
TARGET 442 LGGVAGATPE VLQALKQLQL LKAQLDAAVT FGPSQVARGE DPALQICCHP
2vqrA 471 addpayaalv rdyaqkalsw rlkhadrtlt ----hyrsg- -pe-------
TARGET hhhh hhhhhhhhhh hhh sssss sss ssss
2vqrA hhh hhhhhhhhhh hhh sssss
TARGET 492 GCTPRPACCH CPDPH
2vqrA 508 glser----- ---sh-
TARGET ssss
2vqrA sssss
Results
As one can see in the images above, the model was even worse than the one built with 2VQR without alignment.
Discussion
To compare the models, TM-score and RMSD were calculated. For the calculation of the TM-score, TM-Score was used, for the calculation of the RMSD, DaliLite was used.
| prediction by SWISS-MODEL | |||
|---|---|---|---|
| template | TM-score | RMSD | |
| none | 0.9977 | 0.4 | |
| 1P49 | 0.2037 | 2.2 | |
| 2VQR | no common residue | no calculation possible | |
| 1P49 ali | no model | no model | |
| 2VQR ali | 0.4732 | 3.4 | |
3D-Jigsaw
Without knowing the real TM-score and RMSD, we decided to build a combined structure out of the following predictions:
- modeller prediction without structure information based on 1P49
- modeller prediction with structure information based on 1P49
- iTasser prediction with single template based on 1P49
- SWISS-MODEL prediction with single template based on 1P49
In the following the models are evaluated using RMSD and TM score and visually superimposed with the real structure using pymol:
| Model 1 | Model 2 | Model 3 | Model 4 | Model 5 |
To compare the models, TM-score and RMSD were calculated. For the calculation of the TM-score, TM-Score was used, for the calculation of the RMSD, DaliLite was used.
| prediction by 3D-jigsaw | ||
|---|---|---|
| model | TM-score | RMSD |
| Model 1 | 0.9120 | 2.3 |
| Model 2 | 0.9106 | 2.3 |
| Model 3 | 0.9121 | 2.3 |
| Model 4 | 0.9121 | 2.1 |
| Model 5 | 0.9121 | 1.1 – 1.3 |
Comparison of the methods
The RMSDs of all methods range from 2 to 3.5 Angstrom. This suggests, that all methods produced accteptable models, but none of them were outstanding (except of the two models for iTasser and SWISS-MODEL, which are better due to the self-hit during the template recognition).
The TM-scores for all models vary more than the RMSDs. An RMSD of < 0.5 suggests that the model is not good and a TM score of >= 0.5 suggests that the model exhibits a very similar fold as the original structure. The TM scores for Modeller range from 0.4 - 0.8. Using multiple templates or manual modifications of the alignments decreased the accuracy. Surprisingly all iTasser (excluding self-hit) models yield a very low TM-score (around 0.4), despite the RMSDs are very similar to the predictions of modeller. Also the SWISS-MODEL TM-scores are low compared to that of iTasser (all below 0.5).
Regarding to the RMSD scores, no method performs substantially better than another one. Regarding to the TM scores Modeller performs best and regarding to both measures also modeller outperforms iTasser and SWISS-MODEL. For all methods, 1P49 was the best template, thus we included the models generated when using 1P49 to 3D-Jigsaw. 3D-Jigsaw generated 5 models; all with very high TM scores (around 0.9) and low RMSDs (1-2 Angstrom). Thus 3D-Jigsaw was able to substantially improve the models generated by our previously applied methods. The best model is model 5 with an RMSD of 1.1-1.3 and a TM score of 0.91.
References
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