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I-TASSER results for job id S692807

(Click on S692807_results.tar.bz2 to download the tarball file including all modeling results listed on this page. Click on Annotation of I-TASSER Output to read the instructions for how to interpret the results on this page. Model results are kept on the server for 60 days, there is no way to retrieve the modeling data older than 2 months)

  Submitted Sequence in FASTA format


  Predicted Secondary Structure

Sequence                  20                  40                  60                  80                 100                 120                 140                 160                 180                 200                 220                 240                 260                 280                 300                 320                 340                 360                 380                 400                 420
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H:Helix; S:Strand; C:Coil

  Predicted Solvent Accessibility

Sequence                  20                  40                  60                  80                 100                 120                 140                 160                 180                 200                 220                 240                 260                 280                 300                 320                 340                 360                 380                 400                 420
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Values range from 0 (buried residue) to 9 (highly exposed residue)

   Predicted normalized B-factor

(B-factor is a value to indicate the extent of the inherent thermal mobility of residues/atoms in proteins. In I-TASSER, this value is deduced from threading template proteins from the PDB in combination with the sequence profiles derived from sequence databases. The reported B-factor profile in the figure below corresponds to the normalized B-factor of the target protein, defined by B=(B'-u)/s, where B' is the raw B-factor value, u and s are respectively the mean and standard deviation of the raw B-factors along the sequence. Click here to read more about predicted normalized B-factor)

  Top 10 threading templates used by I-TASSER

(I-TASSER modeling starts from the structure templates identified by LOMETS from the PDB library. LOMETS is a meta-server threading approach containing multiple threading programs, where each threading program can generate tens of thousands of template alignments. I-TASSER only uses the templates of the highest significance in the threading alignments, the significance of which are measured by the Z-score, i.e. the difference between the raw and average scores in the unit of standard deviation. The templates in this section are the 10 best templates selected from the LOMETS threading programs. Usually, one template of the highest Z-score is selected from each threading program, where the threading programs are sorted by the average performance in the large-scale benchmark test experiments.)

Rank PDB
                   20                  40                  60                  80                 100                 120                 140                 160                 180                 200                 220                 240                 260                 280                 300                 320                 340                 360                 380                 400                 420
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15h7bA 0.81 0.46 0.47 1.62Download ----KEQQNAFYEILHLPNLNEEQRNAFIQSLKDDPSQSANLLAEAKKLN----------------EQQAAFYEILSLPNLNEEQRNAFIQSLKDDPSQSANLLAEAKKLNEQQAPNLNEEQRNEQQAAFYEILHLPNLNEEQRNAFIQSLKDDPSQSANLLAEAKKLN-------------EQQAAFYEILHLPNLNEEQRNAFIQSLKDDPSQSANLLAEAKKLNDAQA-----------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------
95h7aA 0.84 0.39 0.45 3.07Download -KFNKEQQNAFYEILHLPNLNEEQRNAFIQSLKDDPSQSANLLAEAKKLN----------------EQQAAFYEILSLPNLNEEQRNAFIQSLKDDPSQSANLLAEAKKLN-------------EQQAAFYEILHLPNLNEEQRNAFIQSLKDDPSQSANLLAEAKKLN-------------EQQAAFYEILHLPNLNEEQRNAFIQSLKDDPSQSANLLAEAKKLNDAQA-----------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------
(a)All the residues are colored in black; however, those residues in template which are identical to the residue in the query sequence are highlighted in color. Coloring scheme is based on the property of amino acids, where polar are brightly coloured while non-polar residues are colored in dark shade. (more about the colors used)
(b)Rank of templates represents the top ten threading templates used by I-TASSER.
(c)Ident1 is the percentage sequence identity of the templates in the threading aligned region with the query sequence.
(d)Ident2 is the percentage sequence identity of the whole template chains with query sequence.
(e)Cov represents the coverage of the threading alignment and is equal to the number of aligned residues divided by the length of query protein.
(f)Norm. Z-score is the normalized Z-score of the threading alignments. Alignment with a Normalized Z-score >1 mean a good alignment and vice versa.
(g)Download Align. provides the 3D structure of the aligned regions of the threading templates.
(h)The top 10 alignments reported above (in order of their ranking) are from the following threading programs:
       1: FFAS-3D   2: SPARKS-X   3: Neff-PPAS   4: wdPPAS   5: PROSPECT2   6: SPARKS-X   7: Neff-PPAS   8: PROSPECT2   9: pGenTHREADER   10: HHSEARCH2   

   Top 5 final models predicted by I-TASSER

(For each target, I-TASSER simulations generate a large ensemble of structural conformations, called decoys. To select the final models, I-TASSER uses the SPICKER program to cluster all the decoys based on the pair-wise structure similarity, and reports up to five models which corresponds to the five largest structure clusters. The confidence of each model is quantitatively measured by C-score that is calculated based on the significance of threading template alignments and the convergence parameters of the structure assembly simulations. C-score is typically in the range of [-5, 2], where a C-score of a higher value signifies a model with a higher confidence and vice-versa. TM-score and RMSD are estimated based on C-score and protein length following the correlation observed between these qualities. Since the top 5 models are ranked by the cluster size, it is possible that the lower-rank models have a higher C-score in rare cases. Although the first model has a better quality in most cases, it is also possible that the lower-rank models have a better quality than the higher-rank models as seen in our benchmark tests. If the I-TASSER simulations converge, it is possible to have less than 5 clusters generated; this is usually an indication that the models have a good quality because of the converged simulations.)
    (By right-click on the images, you can export image file or change the configurations, e.g. modifying the background color or stopping the spin of your models)
  • Download Model 1
  • C-score=-1.49 (Read more about C-score)
  • Estimated TM-score = 0.53±0.15
  • Estimated RMSD = 10.4±4.6Å

  • Download Model 2
  • C-score = -1.04

  • Download Model 3
  • C-score = -2.53

  • Download Model 4
  • C-score = -4.23

  • Download Model 5
  • C-score = -2.78

  Proteins structurally close to the target in the PDB (as identified by TM-align)

(After the structure assembly simulation, I-TASSER uses the TM-align structural alignment program to match the first I-TASSER model to all structures in the PDB library. This section reports the top 10 proteins from the PDB that have the closest structural similarity, i.e. the highest TM-score, to the predicted I-TASSER model. Due to the structural similarity, these proteins often have similar function to the target. However, users are encouraged to use the data in the next section 'Predicted function using COACH' to infer the function of the target protein, since COACH has been extensively trained to derive biological functions from multi-source of sequence and structure features which has on average a higher accuracy than the function annotations derived only from the global structure comparison.)

Top 10 Identified stuctural analogs in PDB

to view
RankPDB HitTM-scoreRMSDaIDENaCovAlignment
15h7cA0.867 1.630.2780.903Download
25hb4B0.603 6.410.0640.926Download
36mu1A0.594 5.980.0390.867Download
47jq9A0.567 5.970.0460.820Download
57wkkA0.549 6.340.0690.844Download
67wo9A0.542 6.480.0450.853Download
76sytA0.539 6.550.0510.846Download
87w7gB0.537 5.910.0290.803Download
97wooF0.533 6.570.0430.832Download

(a)Query structure is shown in cartoon, while the structural analog is displayed using backbone trace.
(b)Ranking of proteins is based on TM-score of the structural alignment between the query structure and known structures in the PDB library.
(c)RMSDa is the RMSD between residues that are structurally aligned by TM-align.
(d)IDENa is the percentage sequence identity in the structurally aligned region.
(e)Cov represents the coverage of the alignment by TM-align and is equal to the number of structurally aligned residues divided by length of the query protein.

  Predicted function using COFACTOR and COACH

(This section reports biological annotations of the target protein by COFACTOR and COACH based on the I-TASSER structure prediction. While COFACTOR deduces protein functions (ligand-binding sites, EC and GO) using structure comparison and protein-protein networks, COACH is a meta-server approach that combines multiple function annotation results (on ligand-binding sites) from the COFACTOR, TM-SITE and S-SITE programs.)

  Ligand binding sites

to view
Ligand Binding Site Residues
10.06 4 4ev9A URE Rep, Mult 320,321,353,354,357
20.05 3 3r6yC CA Rep, Mult 308,312,335
30.05 3 4ev9A URE Rep, Mult 319,320,321,328,358,361
40.05 3 4evaA URE Rep, Mult 336,341,373,374
50.05 3 3eteC H3P Rep, Mult 281,282

Download the residue-specific ligand binding probability, which is estimated by SVM.
Download the all possible binding ligands and detailed prediction summary.
Download the templates clustering results.
(a)C-score is the confidence score of the prediction. C-score ranges [0-1], where a higher score indicates a more reliable prediction.
(b)Cluster size is the total number of templates in a cluster.
(c)Lig Name is name of possible binding ligand. Click the name to view its information in the BioLiP database.
(d)Rep is a single complex structure with the most representative ligand in the cluster, i.e., the one listed in the Lig Name column.
Mult is the complex structures with all potential binding ligands in the cluster.

  Enzyme Commission (EC) numbers and active sites

to view
TM-scoreRMSDaIDENaCovEC NumberActive Site Residues
10.1333ecqB0.393 7.190.0280.666  269
20.1252pziA0.398 6.570.0280.604  358,361
30.1212zxqA0.426 7.210.0650.718  NA
40.1211hn0A0.363 6.860.0310.581  NA
50.1183draA0.364 5.450.0640.512  NA

 Click on the radio buttons to visualize predicted active site residues.
(a)CscoreEC is the confidence score for the EC number prediction. CscoreEC values range in between [0-1];
where a higher score indicates a more reliable EC number prediction.
(b)TM-score is a measure of global structural similarity between query and template protein.
(c)RMSDa is the RMSD between residues that are structurally aligned by TM-align.
(d)IDENa is the percentage sequence identity in the structurally aligned region.
(e)Cov represents the coverage of global structural alignment and is equal to the number of structurally aligned residues divided
by length of the query protein.

  Gene Ontology (GO) terms
Top 10 homologous GO templates in PDB 
RankCscoreGOTM-scoreRMSDaIDENaCovPDB HitAssociated GO Terms
1 0.170.5294 5.99 0.04 0.802z6gA GO:0005488 GO:0005515 GO:2000008 GO:0016020 GO:0046332 GO:0048471 GO:0005886 GO:0034747 GO:0043065 GO:0071363 GO:0005915 GO:0070412 GO:0008022 GO:0045893 GO:0005938 GO:0005912 GO:0045768 GO:0005813 GO:0032993 GO:0061154 GO:0071681 GO:0005924 GO:0005102 GO:0035257 GO:0090279 GO:0014704 GO:0008285 GO:0010909 GO:0048660 GO:0060070 GO:0016342 GO:0005902 GO:0034333 GO:0044325 GO:0044336 GO:0044334 GO:0045294 GO:0070369 GO:0030057 GO:0045296 GO:0016337 GO:0042493 GO:0048262 GO:0000578 GO:0005634 GO:0005913 GO:0030054 GO:0070602 GO:0019900 GO:0005667 GO:0019899 GO:0007155 GO:0019903 GO:0034394 GO:0008134 GO:0030331 GO:0003713 GO:0030997 GO:0016055 GO:0005911 GO:0034742 GO:0070411 GO:0005737 GO:0016328 GO:0032355
2 0.160.5236 6.12 0.06 0.793opbA GO:0005515 GO:0017022 GO:0008298 GO:0030036 GO:0005737 GO:0007533 GO:0005488
3 0.160.4143 6.49 0.03 0.631xi4A GO:0030659 GO:0016020 GO:0005739 GO:0042470 GO:0031410 GO:0030117 GO:0005515 GO:0005905 GO:0005198 GO:0005488 GO:0006886 GO:0016192 GO:0030130 GO:0030132
4 0.160.5280 5.87 0.07 0.783ifqA GO:0005488 GO:0005515
5 0.160.4937 6.57 0.06 0.783c2hB GO:0005488
6 0.150.4792 5.96 0.05 0.721b3uA GO:0000775 GO:0015630 GO:0005515 GO:0005739 GO:0006917 GO:0008380 GO:0042518 GO:0006461 GO:0005737 GO:0005829 GO:0030155 GO:0019932 GO:0030308 GO:0046982 GO:0006470 GO:0006672 GO:0006275 GO:0000278 GO:0005634 GO:0030111 GO:0000188 GO:0003823 GO:0005694 GO:0000086 GO:0000159 GO:0005625 GO:0040008 GO:0010033 GO:0007059 GO:0045595 GO:0008601 GO:0016020 GO:0006355 GO:0005488 GO:0042981 GO:0070262 GO:0004722
7 0.150.4760 6.07 0.06 0.712vglB GO:0005488 GO:0006886 GO:0008565 GO:0015031 GO:0016192 GO:0030117
8 0.140.4658 5.99 0.09 0.691wa5B GO:0005737 GO:0006810 GO:0005634 GO:0008565 GO:0006606 GO:0048471 GO:0005515 GO:0006612 GO:0015031 GO:0000176 GO:0005488 GO:0005643 GO:0006886
9 0.140.4487 6.70 0.06 0.703m1iC GO:0006810 GO:0005634 GO:0005816 GO:0000776 GO:0048471 GO:0005515 GO:0015031 GO:0000055 GO:0005737 GO:0008565 GO:0006406 GO:0006611 GO:0034501 GO:0005488 GO:0006886
10 0.140.4827 6.12 0.06 0.713icqT GO:0003723 GO:0006810 GO:0006605 GO:0005525 GO:0005737 GO:0005643 GO:0000049 GO:0005829 GO:0005635 GO:0008033 GO:0005634 GO:0005488

Consensus prediction of GO terms
Molecular Function GO:0019902 GO:0035258 GO:0003712 GO:0050839 GO:0046332 GO:0008092
GO-Score 0.33 0.33 0.33 0.33 0.33 0.32
Biological Process GO:0032880 GO:0043627 GO:0010718 GO:0070507 GO:0042127 GO:0034765 GO:0010628 GO:0009953 GO:0060341 GO:0007063
GO-Score 0.33 0.33 0.33 0.33 0.33 0.33 0.33 0.33 0.33 0.33
Cellular Component GO:0044451 GO:0005815 GO:0019897 GO:0071664 GO:0044291 GO:0042995 GO:0043296 GO:0005913 GO:0030055 GO:0005905
GO-Score 0.33 0.33 0.33 0.33 0.33 0.33 0.33 0.33 0.33 0.32

(a)CscoreGO is a combined measure for evaluating global and local similarity between query and template protein. It's range is [0-1] and higher values indicate more confident predictions.
(b)TM-score is a measure of global structural similarity between query and template protein.
(c)RMSDa is the RMSD between residues that are structurally aligned by TM-align.
(d)IDENa is the percentage sequence identity in the structurally aligned region.
(e)Cov represents the coverage of global structural alignment and is equal to the number of structurally aligned residues divided by length of the query protein.
(f)The second table shows a consensus GO terms amongst the top scoring templates. The GO-Score associated with each prediction is defined as the average weight of the GO term, where the weights are assigned based on CscoreGO of the template.

[Click on S692807_results.tar.bz2 to download the tarball file including all modeling results listed on this page]

Please cite the following articles when you use the I-TASSER server:
  • Wei Zheng, Chengxin Zhang, Yang Li, Robin Pearce, Eric W. Bell, Yang Zhang. Folding non-homology proteins by coupling deep-learning contact maps with I-TASSER assembly simulations. Cell Reports Methods, 1: 100014 (2021).
  • Chengxin Zhang, Peter L. Freddolino, and Yang Zhang. COFACTOR: improved protein function prediction by combining structure, sequence and protein-protein interaction information. Nucleic Acids Research, 45: W291-299 (2017).
  • Jianyi Yang, Yang Zhang. I-TASSER server: new development for protein structure and function predictions, Nucleic Acids Research, 43: W174-W181, 2015.