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I-TASSER results for job id S805763

(Click on S805763_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
MSRAFIIDPTISAIDGLYDLLGIGIPNQGGILYSSLEYFEKALEELAAAFPGDGWLGSAA
DKYAGKNRNHVNFFQELADLDRQLISLIHDQANAVQTTRDILEGAKKGLEFVRPVAVDLT
YIPVVGHALSAAFQAPFCAGAMAVVGGALAYLVVKTLINATQLLKLLAKLAELVAAAIAD
IISDVADIIKGILGEVWEFITNALNGLKELWDKLTGWVTGLFSRGWSNLESFFAGVPGLT
GATSGLSQVTGLFGAAGLSASSGLAHADSLASSASLPALAGIGGGSGFGGLPSLAQVHAA
STRQALRPRADGPVGAAAEQVGGQSQLVSAQGSQGMGGPVGMGGMHPSSGASKGTTTKKY
SEGAAAGTEDAERAPVEADAGGGQKVLVRNVV

  Predicted Secondary Structure

Sequence                  20                  40                  60                  80                 100                 120                 140                 160                 180                 200                 220                 240                 260                 280                 300                 320                 340                 360                 380
                   |                   |                   |                   |                   |                   |                   |                   |                   |                   |                   |                   |                   |                   |                   |                   |                   |                   |                   |            
MSRAFIIDPTISAIDGLYDLLGIGIPNQGGILYSSLEYFEKALEELAAAFPGDGWLGSAADKYAGKNRNHVNFFQELADLDRQLISLIHDQANAVQTTRDILEGAKKGLEFVRPVAVDLTYIPVVGHALSAAFQAPFCAGAMAVVGGALAYLVVKTLINATQLLKLLAKLAELVAAAIADIISDVADIIKGILGEVWEFITNALNGLKELWDKLTGWVTGLFSRGWSNLESFFAGVPGLTGATSGLSQVTGLFGAAGLSASSGLAHADSLASSASLPALAGIGGGSGFGGLPSLAQVHAASTRQALRPRADGPVGAAAEQVGGQSQLVSAQGSQGMGGPVGMGGMHPSSGASKGTTTKKYSEGAAAGTEDAERAPVEADAGGGQKVLVRNVV
PredictionCCCCSSHHHHHHHHHHHHHHCCCCCCCCCCCCCCHHHHHHHHHHHHHHHCCCCCCCCHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHCCCCCHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC
Conf.Score98765358689999999996488889887430207999999999999727999974748999999999999999999999999999999999999999999999999988889999998726860188999989999999999999999999999998799999999998877740367865668777789877677888876688887777787777788888889988888999999988899999999998888888999999999998888999899988888899998667787656667777788887767776676677877777899888888778788877777887777866545799865668976667876556557779
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
                   |                   |                   |                   |                   |                   |                   |                   |                   |                   |                   |                   |                   |                   |                   |                   |                   |                   |                   |            
MSRAFIIDPTISAIDGLYDLLGIGIPNQGGILYSSLEYFEKALEELAAAFPGDGWLGSAADKYAGKNRNHVNFFQELADLDRQLISLIHDQANAVQTTRDILEGAKKGLEFVRPVAVDLTYIPVVGHALSAAFQAPFCAGAMAVVGGALAYLVVKTLINATQLLKLLAKLAELVAAAIADIISDVADIIKGILGEVWEFITNALNGLKELWDKLTGWVTGLFSRGWSNLESFFAGVPGLTGATSGLSQVTGLFGAAGLSASSGLAHADSLASSASLPALAGIGGGSGFGGLPSLAQVHAASTRQALRPRADGPVGAAAEQVGGQSQLVSAQGSQGMGGPVGMGGMHPSSGASKGTTTKKYSEGAAAGTEDAERAPVEADAGGGQKVLVRNVV
Prediction75201002001100100121023121542330340142045015303413247403120043024304403400430230043024203500530340142031013100200100200121222020002201010011000000200010022024314403400432241234334333362161242233332423244142146245334342343222424414212111131222443333212012124133242143323333234234034134362243111233143335434434345244343354344444334433454344443343344444446435466345333443664320113334455444454416
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                  80                 100                 120                 140                 160                 180                 200                 220                 240                 260                 280                 300                 320                 340                 360                 380
                   |                   |                   |                   |                   |                   |                   |                   |                   |                   |                   |                   |                   |                   |                   |                   |                   |                   |                   |            
Sec.Str
Seq		CCCCSSHHHHHHHHHHHHHHCCCCCCCCCCCCCCHHHHHHHHHHHHHHHCCCCCCCCHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHCCCCCHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC
MSRAFIIDPTISAIDGLYDLLGIGIPNQGGILYSSLEYFEKALEELAAAFPGDGWLGSAADKYAGKNRNHVNFFQELADLDRQLISLIHDQANAVQTTRDILEGAKKGLEFVRPVAVDLTYIPVVGHALSAAFQAPFCAGAMAVVGGALAYLVVKTLINATQLLKLLAKLAELVAAAIADIISDVADIIKGILGEVWEFITNALNGLKELWDKLTGWVTGLFSRGWSNLESFFAGVPGLTGATSGLSQVTGLFGAAGLSASSGLAHADSLASSASLPALAGIGGGSGFGGLPSLAQVHAASTRQALRPRADGPVGAAAEQVGGQSQLVSAQGSQGMGGPVGMGGMHPSSGASKGTTTKKYSEGAAAGTEDAERAPVEADAGGGQKVLVRNVV
11vt4I 0.14 0.12 0.91 1.19Download ---EYALHRSIVDHYNIPKTF-----DSDDLIPPYQYFYSHIGHHLKNIEHP-----ERMTLFRMVFLDFRFLEQKIRH-DSASGSILNTLQQLKFYKPYICDNDPKYERLVNAILDFLPKIELICSKYTDLLRIALMA---------------------EAIFEEAHKQVQR-GGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG-GGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG
27nd2A 0.07 0.16 0.61 0.67Download VQDLVTALLNFHTYTEQRIQIF---PVTSQYLHENASYVRPLEEGMLHLFEDTVTVLETTVKLKTFSEHLTSYICFLRKILPYQLKSLEEECERNLELSQDMKKMTAVFEKLQTYIALLALPSLRTNYSSVLTNVGAALHGFHDVMKDISKHYSQKAAIEHESVVALTNGAGKIASFFSNNLDYFIASLSYGPKAASGFISPLSAECMLQYKKKAAAYMKSLRKPLLESVPYEEALANRRILL-----------------------------------------------------------------------------------------------------------------------------------------------------
33zbh 0.12 0.03 0.21 1.46Download --------------------------LTPEELRGVARNVTELIARLDQMSHQGIWEGASSEAFIQQYQELRPSFEKMAVLLNEVGQQLHNSATILEDTDQQIASQIR---------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------
43hr2 0.16 0.19 0.59 1.72Download ----------------------------------------------------------------------------------------------------------------------------------------------------------QM---SYGYDE--KSAGVSVPGPMGPSGPRGLGPGAGPQGFQGPGEGEGGSGPMGPPGPAGKPGRGEPGPQGAKGDTGPAGPKGEGSGENGQMGPRGL-GERGGPGTAGARGNDGAVGAAGPTGAKGEAGPQGARGSEGPQGVRGAAGPAGNGDGQGAKGANGAAGAFGARGPSGPQGPSG-AGPKGTSGEGAGNKGADGVAGPKGPSGERGSAGPKGGEAGRGEAGLPGARGQAGVM
51vt4I 0.16 0.12 0.84 1.15Download ---------------------------------------------------------RSIVDHYNIPKTFDSDDLIPPYLDQYFYSHIGHHLKNIEHPERMTLFRMVFLDFRFLEQKIRHDSTAWNASGS----ILNTLQQLKFYKPYICDNDPKYERLVNAILDFLPKIEENLICSGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG-GGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG--GGGGGGGGGGGGGGGGGGGGGGGGGGGGGG
63zbh 0.13 0.03 0.18 1.44Download -----------------------------------SSNVTELIARLDQMSHQGIWEGASSEAFIQQYQELRPSFEKMAVLLNEVGQQLHNSATILEDTDQQIAS------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------
74dmuA 0.16 0.06 0.20 0.81Download ------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------PGPPGPPGPRGQPGVMGFPGPPGPPGPPGPPGPPGPRGQPGVMGFPGPPGPPGPPGPPGPPGPRGQPGVM----GFPGPPGPP---------------------------------
87aqxA 0.09 0.18 0.84 1.50Download AAEKGFKQAFWQPLCQVSEELDD------------------------------------QPKGALFTLQAAASKIQKMRDAALRASIYAEINHGTNRAKAAV--------------------------IVANHYAMKADSGLEALKQTLSSQEVTATATASYLKGRIDEYLNLLLQTKESGTSGCMMDTSGTNTVTKAGGTIGGVPCKLQLSPIQPKRPAATYLGKAGYVGLTRQADAANNFHSGHNTNGLGKSGQLSAAVTMAAGYVTVANSQTAVTVQALDALQEASGAAHQPWIDAWKAKKALTGAETAEFRNETAGIAGKTGVTKLVEEALLKKKDSEASGHENEQWTAIEKLISEQPVAQNLVGDNQPTKLGELEGNAKAGKFEVLT
95zi1A 0.08 0.18 0.96 1.16Download FAGHGTAGGIIGLFTEVLRLL---WPNKQN------DLWESFMNEVEALI-NQE---ITEAVVSKALSELEGLRNALEGYTSALEAWQNNDKLKQLLVYERFVSTENLFKFAMPSFRSVGFEGPLAQAANLHLFLLKNAELQYEIDLFYNEQKGYVEEYTDHCVKWYKEGLNKLKNASGVKGKPIYDARTYPMETVTELTRQIFTDPIGLTGINETKYPDWYGAASSEFVLIENRAIPKPGLFQWLTKINVRARV--VEPNDRFAIWTGHSVVTQYTKSTTENTFNGTSSGSTLSHTFDLLSKDIYQTYSIAAANKSATWYQAVPLLRLYGINSSNVLSEDAFSFSNNIPSSKCKSTYSSDQLPIELLDEPIYGDLEEYGEIFKETGSGTIP
102gd5A 0.14 0.09 0.30 0.39Download -------------------------------------------------------------------NEWSLKIRKERVVDRQIRDI---QREEEKVKRSVKDAAKKGKDVCIVLAKEISKLYASKAHNSVLGKNQLAVLRVAGSLQKSTEVKAQSLVKIPEIQATRELSKEKAGIIEAEEIDRILFEI-----------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------
(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: MUSTER   2: SPARKS-X   3: HHSEARCH2   4: HHSEARCH I   5: Neff-PPAS   6: HHSEARCH   7: pGenTHREADER   8: PROSPECT2   9: SP3   10: FFAS03   

   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=-1.94 (Read more about C-score)
  • Estimated TM-score = 0.48±0.15
  • Estimated RMSD = 11.3±4.5Å

  • Download Model 2
  • C-score = -3.66

  • Download Model 3
  • C-score = -4.11

  • Download Model 4
  • C-score = -4.28

  • Download Model 5
  • C-score = -4.07


  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
11vt4I0.868 2.150.1360.921Download
23iytA30.673 4.430.0540.857Download
33izaA0.673 4.470.0530.860Download
46jp6A0.582 4.880.0390.750Download
55julA0.570 5.380.0570.804Download
65wbiA0.552 4.880.0640.707Download
76bcuW0.548 5.080.0560.712Download
86zpnA0.544 5.010.0500.702Download
95teeA0.517 3.820.0670.620Download
102ymuA0.513 3.940.0640.612Download

(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
10.06 1 N/A N/A N/A 200,308,310,349
20.06 1 N/A N/A N/A 325,333,351,355,367
30.06 1 4a0bB k-mer Rep, Mult 191,210,211,275,290,320
40.06 1 N/A N/A N/A 199,226,245,248,260,261,262,263
50.06 1 N/A N/A N/A 249,259,269,283,284,285,286


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
10.1321hn0A0.468 5.910.0410.694 4.2.2.20  NA
20.1302ebsB0.480 5.710.0500.686 3.2.1.150  NA
30.1291k3iA0.463 5.870.0640.681 1.1.3.9  NA
40.1282q1fA0.473 5.490.0650.668 4.2.2.21  NA
50.1243elqB0.461 5.070.0550.617 2.8.2.22  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 0.220.8678 2.15 0.03 0.921vt4I GO:0005524 GO:0006915
2 0.170.6733 4.47 0.05 0.863izaA GO:0005794 GO:0005515 GO:0005829 GO:0006919 GO:0008656 GO:0006915 GO:0008635 GO:0005634 GO:0007399 GO:0008629 GO:0005737 GO:0000166 GO:0005524 GO:0005730 GO:0042981 GO:0005622 GO:0006952
3 0.130.4680 5.91 0.04 0.691hn0A GO:0005975 GO:0016829 GO:0016837 GO:0005576 GO:0030246 GO:0003824
4 0.130.4804 5.76 0.05 0.691sqjB GO:0005975 GO:0016787 GO:0030245 GO:0008152 GO:0016798 GO:0033945 GO:0000272
5 0.120.4605 5.07 0.06 0.623elqB GO:0047686 GO:0016740
6 0.120.4675 2.18 0.07 0.501vyhC GO:0021540 GO:0043005 GO:0071445 GO:0030154 GO:0000226 GO:0042598 GO:0048471 GO:0006810 GO:0030036 GO:0021819 GO:0019226 GO:0007017 GO:0033267 GO:0045505 GO:0005829 GO:0030426 GO:0007049 GO:0005737 GO:0016042 GO:0005625 GO:0005815 GO:0016020 GO:0008090 GO:0005813 GO:0042803 GO:0031513 GO:0007405 GO:0031512 GO:0015630 GO:0031252 GO:0007611 GO:0005938 GO:0032403 GO:0051660 GO:0051081 GO:0051219 GO:0045773 GO:0045931 GO:0007420 GO:0017145 GO:0007399 GO:0007067 GO:0007275 GO:0001675 GO:0005634 GO:0051301 GO:0050885 GO:0000132 GO:0031023 GO:0001764 GO:0007097 GO:0005875 GO:0007268 GO:0008017 GO:0005626 GO:0005635 GO:0045502 GO:0010977 GO:0043025 GO:0005874 GO:0048854 GO:0005819 GO:0021895 GO:0005871 GO:0005856 GO:0031965 GO:0032319 GO:0021766 GO:0005515 GO:0000235 GO:0000776 GO:0021987 GO:0008344 GO:0016477
7 0.120.4612 2.75 0.06 0.511erjC GO:0005515
8 0.120.4617 2.40 0.06 0.503fm0A GO:0071817 GO:0006357 GO:0005515 GO:0007059 GO:0016226 GO:0008284
9 0.120.4731 3.31 0.06 0.551nr0A GO:0003779 GO:0040017 GO:0030837 GO:0040010 GO:0051015 GO:0002119 GO:0005515 GO:0005737 GO:0016528 GO:0018991 GO:0040011 GO:0042643 GO:0005856 GO:0030836
10 0.110.4608 3.93 0.05 0.553fcuA GO:0009897 GO:0007155 GO:0005887 GO:0007229 GO:0042802 GO:0016020 GO:0030168 GO:0002576 GO:0007596 GO:0050840 GO:0007411 GO:0004872 GO:0005925 GO:0016021 GO:0031092 GO:0005886 GO:0007160 GO:0008305


Consensus prediction of GO terms		 
Molecular Function GO:0005524 GO:0043028 GO:0016505
GO-Score 0.36 0.35 0.35
Biological Process GO:0044238 GO:0006919 GO:0006917 GO:0048731 GO:0050896
GO-Score 0.49 0.35 0.35 0.35 0.35
Cellular Component GO:0043232 GO:0031981 GO:0044444
GO-Score 0.35 0.35 0.35

(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 S805763_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.