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I-TASSER results for job id S814235

(Click on S814235_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

>protein
LNKEFAECALISLASSPEPTIDEMTKQNYSKPSIEKIAGFKESTRGLWTGKFRDVFGGRA
LFQVVIYY

  Predicted Secondary Structure

Sequence                  20                  40                  60
                   |                   |                   |        
LNKEFAECALISLASSPEPTIDEMTKQNYSKPSIEKIAGFKESTRGLWTGKFRDVFGGRALFQVVIYY
PredictionCCCHHHHHHSSSSCCCCCCCHHHHHHHCCCCCHHHHHHCCCCCCCCSSCCCHHHHCCCSSSSSSSSSC
Conf.Score93065443023112689975778856154560188872544356530016212101880689999869
H:Helix; S:Strand; C:Coil

  Predicted Solvent Accessibility

Sequence                  20                  40                  60
                   |                   |                   |        
LNKEFAECALISLASSPEPTIDEMTKQNYSKPSIEKIAGFKESTRGLWTGKFRDVFGGRALFQVVIYY
Prediction86552341112313544443244336452343316413414642432133423522423111303154
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
Hit		Iden1Iden2CovNorm.
Z-score		Download
Align.		                   20                  40                  60
                   |                   |                   |        
Sec.Str
Seq		CCCHHHHHHSSSSCCCCCCCHHHHHHHCCCCCHHHHHHCCCCCCCCSSCCCHHHHCCCSSSSSSSSSC
LNKEFAECALISLASSPEPTIDEMTKQNYSKPSIEKIAGFKESTRGLWTGKFRDVFGGRALFQVVIYY
13ltlA 0.23 0.23 0.69 0.43Download QQKEIIEQGIDLFNKKPKRGIQYLQEQGMLGTTPEDIAQFLHQEERL---------------------
27ml0R 0.18 0.19 0.74 0.88Download PKKEILDYLFKLFDEYDYWSLKERTRQAHLKECLDKVATLVKKYAFKYTL------------------
34w78B 0.16 0.28 0.93 0.73Download HDRDKAVA-----QGSKDIFVNILTDTGLVQRYVTDWAGLGVPWYYTFSGEVTAVNDGLITVKVVGRN
43ungA 0.38 0.29 0.62 0.92Download LGKRFIYHVLREVDTWPKVGIDEMLK-------FEVIRHIKEETKELRE-------------------
57lvsF 0.25 0.22 0.81 0.52Download IDEEVLMSLVIEMGLDRIKELPELTSY-----DCEVNAPI-QGSRNLLQG--EELL--RALDQVN---
62mlgA 0.19 0.19 0.94 0.91Download ---SLTQLILIRLSNRGCQTLEELEEFTQAKREVLLVTLTRLHQRGVIYRKWRHFS-GRKYREYCLKH
72vqpA 0.23 0.21 0.51 0.78Download MPSKFTICANVSLD--------D--KLAYDVTTPCEIKACSLTCL-----------------------
85l85A 0.40 0.15 0.29 0.20Download LFVEFADCCLGIVESQNEES------------------------------------------------
96ezn 0.13 0.38 0.99 0.44Download SEEQHLLWETNRLPLSAYDTKKASFTL-IGSSSFEEYHPGKANGNSFEFGPWEDIPRFSSTLAIVYSH
107fivA 0.16 0.23 1.00 0.44Download PTQKELRDTMSKKIKHPDPAVVAGRKSVLQDNFMEHIKYFKGQDEGCWSGVLGQRFTEEKIGGIDNPL
(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: SP3   4: HHSEARCH   5: wdPPAS   6: Neff-PPAS   7: HHSEARCH2   8: pGenTHREADER   9: HHSEARCH I   10: PROSPECT2   

   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=-2.04 (Read more about C-score)
  • Estimated TM-score = 0.47±0.15
  • Estimated RMSD = 7.4±4.3Å

  • Download Model 2
  • C-score = -4.48

  • Download Model 3
  • C-score = -4.73

  • Download Model 4
  • C-score = -5

  • Download Model 5
  • C-score = -4.44


  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

Click
to view		RankPDB HitTM-scoreRMSDaIDENaCovAlignment
17yw2A10.649 2.790.0630.941Download
25u8jA20.632 2.620.0770.941Download
33l4gC0.630 2.510.0910.971Download
43zplA0.630 2.700.1820.956Download
52v1uA0.629 2.470.1090.941Download
64nb5A0.629 2.480.1110.912Download
72lnbA0.626 2.330.0670.882Download
87kuaA0.626 2.620.2150.941Download
92fxaB0.624 2.610.0940.926Download
107l1iA0.624 2.680.0920.941Download

(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


Click
to view		RankC-scoreCluster
size		 PDB
Hit		 Lig
Name		 Download
Complex		 Ligand Binding Site Residues
10.10 5 4chuB Nuc.Acid Rep, Mult 20,21,35,42,50,53,54,55,63,64
20.10 5 1llrE k-mer N/A 50,51,53
30.06 3 3d5bF MG N/A 59,61,64
40.06 3 5bmzB Nuc.Acid Rep, Mult 4,29,30,32,33,36,37,56,60
50.04 2 4llnD Nuc.Acid Rep, Mult 4,6,29,30,32,33,40


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


Click
to view		RankCscoreECPDB
Hit		TM-scoreRMSDaIDENaCovEC NumberActive Site Residues
10.1693l4gC0.630 2.510.0910.971 6.1.1.20  NA
20.1613ilwA0.581 2.760.1320.897 5.99.1.3  NA
30.1561zaoA0.586 2.400.0490.882 2.7.11.1  NA
40.1552ewnA0.581 2.750.1000.882 6.3.4.15  NA
50.1511bibA0.574 2.720.1000.868 6.3.4.15  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 0.240.6056 2.49 0.12 0.883gfiA GO:0005622 GO:0003677 GO:0006355 GO:0006351 GO:0003700
2 0.170.6225 2.55 0.11 0.942cweA GO:0006355 GO:0006351 GO:0003700 GO:0005622 GO:0003677
3 0.170.6101 2.53 0.17 0.941z9cC GO:0003677 GO:0006351 GO:0006355 GO:0005737 GO:0003700 GO:0005622
4 0.170.6303 2.51 0.09 0.973l4gC GO:0005515 GO:0005829 GO:0006412 GO:0004812 GO:0000049 GO:0000166 GO:0043039 GO:0006432 GO:0005524 GO:0010467 GO:0004826 GO:0005625 GO:0006418 GO:0005737 GO:0016874
5 0.170.6212 2.63 0.14 0.913f3xA GO:0006351 GO:0003677 GO:0003700 GO:0006355 GO:0005622
6 0.170.6295 2.47 0.11 0.942v1uA GO:0006260 GO:0005524 GO:0000166 GO:0017111
7 0.170.6110 2.53 0.09 0.931ub9A GO:0006351 GO:0003700 GO:0006355 GO:0005622 GO:0003677
8 0.160.6069 2.53 0.12 0.911s3jA GO:0006351 GO:0005622 GO:0003677 GO:0003700 GO:0006355
9 0.160.6086 2.73 0.11 0.933g3zA GO:0006351 GO:0006355 GO:0003677 GO:0003700 GO:0005622
10 0.160.6114 2.80 0.16 0.932a61A GO:0003677 GO:0006351 GO:0006355 GO:0003700 GO:0005622


Consensus prediction of GO terms		 
Molecular Function GO:0003677 GO:0003700 GO:0016875 GO:0032559 GO:0035639
GO-Score 0.56 0.56 0.34 0.34 0.34
Biological Process GO:0006355 GO:0006399 GO:0043038 GO:0019538
GO-Score 0.56 0.34 0.34 0.30
Cellular Component GO:0000267 GO:0044444
GO-Score 0.34 0.34

(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 S814235_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.