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I-TASSER results for job id S777201

(Click on S777201_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
NGDLLLDHSGAYVAQYYITWDELSYNHQGKEVLTPKAWDRNGQDLTAHFTTSIPLKGNVR
NLSVKIREGTGLAFEWWRTVYEKTDLPLVRKRTISIWGTTLYPQVEDKVENEAAAKAKFV
AAWTLKAAAKKGYGVNANKKEKDYDAAVKKSEAAKKDYETAKKKAEDAQKKKKYDEDQKK
TEAKAKKSEAAKKDYETAKKKAEDAQKKYDEDQKKTEAKAEKERKAKKDITKNIAGDKID
LHGPGPGSENTPTVTSSGQDISGPGPGAAKKDYETAKKKAEDGPGPGKKDYETAKKKAED
AQGPGPGVNTTVDGYTVNENGEGGGSYYLEASGAMGGGSYYLNANGSMGGGSAKFVAAWT
LKAAA

Predicted Secondary Structure

Sequence	20 40 60 80 100 120 140 160 180 200 220 240 260 280 300 320 340 360 \| \| \| \| \| \| \| \| \| \| \| \| \| \| \| \| \| \| NGDLLLDHSGAYVAQYYITWDELSYNHQGKEVLTPKAWDRNGQDLTAHFTTSIPLKGNVRNLSVKIREGTGLAFEWWRTVYEKTDLPLVRKRTISIWGTTLYPQVEDKVENEAAAKAKFVAAWTLKAAAKKGYGVNANKKEKDYDAAVKKSEAAKKDYETAKKKAEDAQKKKKYDEDQKKTEAKAKKSEAAKKDYETAKKKAEDAQKKYDEDQKKTEAKAEKERKAKKDITKNIAGDKIDLHGPGPGSENTPTVTSSGQDISGPGPGAAKKDYETAKKKAEDGPGPGKKDYETAKKKAEDAQGPGPGVNTTVDGYTVNENGEGGGSYYLEASGAMGGGSYYLNANGSMGGGSAKFVAAWTLKAAA
Prediction	CCSSSSSSCCSSSSSSSSSSSSSSSCCCCCSSSSSCCCCCCCCCCCCCCSSSSSCCCCCCCSSSSSSSSSSSSHHHHHHCCCCCCCCCCCCSSSSSCCSSSSSSCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCHHHHHHHHHHHHHHHHHHHHHHCCCHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCSSCCCCCCCCCCCCSSSCCSSSSCCCCCCCCCSSSSCCCCCCCCCCSSSCCSSSSSCCC
Conf.Score	97268851450799998676550146889688541024678875667732887438873100676545422131132323566787866634899745486430235555422234543446666577111544210101231566554244555432343321000102221223332334434434454443444432223433201100023455310123555554444445543346788876677777775444567785445567775556666656755445544333567423798415316987000388561988998899967576468799877441753789999982379
	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 \| \| \| \| \| \| \| \| \| \| \| \| \| \| \| \| \| \| NGDLLLDHSGAYVAQYYITWDELSYNHQGKEVLTPKAWDRNGQDLTAHFTTSIPLKGNVRNLSVKIREGTGLAFEWWRTVYEKTDLPLVRKRTISIWGTTLYPQVEDKVENEAAAKAKFVAAWTLKAAAKKGYGVNANKKEKDYDAAVKKSEAAKKDYETAKKKAEDAQKKKKYDEDQKKTEAKAKKSEAAKKDYETAKKKAEDAQKKYDEDQKKTEAKAEKERKAKKDITKNIAGDKIDLHGPGPGSENTPTVTSSGQDISGPGPGAAKKDYETAKKKAEDGPGPGKKDYETAKKKAEDAQGPGPGVNTTVDGYTVNENGEGGGSYYLEASGAMGGGSYYLNANGSMGGGSAKFVAAWTLKAAA
Prediction	82403041310000103030430323761342142331454343322313340303330440303044110000220241245671322453413321541344245535654446452346464426546444463654466365345625544563653456365364444366445435634643652455356344635644452464345455654655644654654455344544545453653344465655465554434465353443443444333344244444444446473432223442313331344422010233131100001014401010003434330213358
	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

Iden1

Iden2

Cov

Norm.
Z-score

Download
Align.

                  20                  40                  60                  80                 100                 120                 140                 160                 180                 200                 220                 240                 260                 280                 300                 320                 340                 360
                   |                   |                   |                   |                   |                   |                   |                   |                   |                   |                   |                   |                   |                   |                   |                   |                   |                   |     

Sec.Str
Seq

CCSSSSSSCCSSSSSSSSSSSSSSSCCCCCSSSSSCCCCCCCCCCCCCCSSSSSCCCCCCCSSSSSSSSSSSSHHHHHHCCCCCCCCCCCCSSSSSCCSSSSSSCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCHHHHHHHHHHHHHHHHHHHHHHCCCHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCSSCCCCCCCCCCCCSSSCCSSSSCCCCCCCCCSSSSCCCCCCCCCCSSSCCSSSSSCCC
NGDLLLDHSGAYVAQYYITWDELSYNHQGKEVLTPKAWDRNGQDLTAHFTTSIPLKGNVRNLSVKIREGTGLAFEWWRTVYEKTDLPLVRKRTISIWGTTLYPQVEDKVENEAAAKAKFVAAWTLKAAAKKGYGVNANKKEKDYDAAVKKSEAAKKDYETAKKKAEDAQKKKKYDEDQKKTEAKAKKSEAAKKDYETAKKKAEDAQKKYDEDQKKTEAKAEKERKAKKDITKNIAGDKIDLHGPGPGSENTPTVTSSGQDISGPGPGAAKKDYETAKKKAEDGPGPGKKDYETAKKKAEDAQGPGPGVNTTVDGYTVNENGEGGGSYYLEASGAMGGGSYYLNANGSMGGGSAKFVAAWTLKAAA

4hscA

0.45

0.14

0.30

1.86

Download

SGKINLSHQGAYVAQYEILWDEINYDDKGKEVITKRRWDNNWYSKTSPFSTVIPLGANSRNIRIMARECTGLAWEWWRKVIDERDVKLSKEINVNISGSTLSPYGSITYK---------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------

8p0vK

0.07

0.17

0.78

1.24

Download

--------------------------------------LGTSQLHRRKVISLNKQIAQKTKHLEELRASHTSLQARYNEAKKTLTELKTYSEKLDKEQAALEKIESSILQNLRALVAMNENLKSQEQEFKAHCREEMTRLQQEIENLKAHDEDLDRRYNMEKEKLYKIRLLQARRNREIAILHRKIDEQKRFIELYRQISAVHKETKQFFTLYNTLDDKKVYLEKEISLLNSIHENFSQAMASPAARDQFLRQMEQIVEGIKQSRMKMEKKKQENKMRRDQLNDQYLELLEKQRLYFKTVKEFKEEGRKNEMLLSKVKAKAS-------------------------------------------

4cdb

0.54

0.21

0.30

3.10

Download

DGKINIDHSGGYVAQFNISWDEVNYDPEGNEIVQHKNWSENNKSKLAHFTSSIYLPGNARNINVYAKECTGLAWEWWRTVIDDRNLPLVKNRNISIWGTTLYPKYSNKVDN--------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------

8deoA

0.09

0.22

1.00

1.27

Download

IDITTVKGRDNYDFYGRVDIESNPTDLNATNLTRYNYGQPPGTTTDKDFDFNIREKGTPSAAGFRIDTGYYNNDPLDKIQKQAGQGYRGYGTFVKNDSQGNTSKVGSGTPSTDFLNYADNTTNDLDGKFHGQKLASNQTFTATYAGKTWTATLSELGLSPTDSYSGVMRADLDGATLTYTPKAVDGDPIISTKEIPFNKKREFDPNLAPGTEKVVQKGEPGIETTTTPTYVNPNTGEKVGEGEPTEKITKQPVDEIVHYGGEEIKPGHKDEFDPNAPKGSQTTQPGKPGVKNPDTGEVVTPPVDDVTKYGPVDGDPITSTEEIPFDKKREFNPDLKPGETKNPLTGGEPTEKITKQPVDEITEYG

4cdb

0.54

0.21

0.30

1.15

Download

DGKINIDHSGGYVAQFNISWDEVNYDPEGNEIVQHKNWSENNKSKLAHFTSSIYLPGNARNINVYAKECTGLAWEWWRTVIDDRNLPLVKNRNISIWGTTLYPKYSNKVDN--------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------

8p0vL

0.08

0.20

1.00

1.24

Download

PPDVQTLRAFTTELVVEAVVRCLRVINPAVGSGLSPLLPLAMSARFRLAMQACMDLGYPLELGYQNFLYPSELRDLLLFLAERLRRPEQVTAAQEQELESLREQLEGVNRSIEEVEADMKTLGVSFVQAESECRHSKLSTAEREQALRLKSRAVEGTANLAKLQLVVENSAQRVIHLAGQWEKHRVPLLAEYRHLRKLQDCRELESSRRLAEIQELHQSVRAAAEEARRKEEVYKLETLPRDVSRLAYTQRILEIVGNIRKQKEEITKILSDTKELQKEINSLSGKLDRTFAVTDELVFKDAKKDDAVRKAYKYLAALHENCSQLIQTIEDTGTIMREVRDLEEQIETELGKKTLSNLEKIREDY

4qqqA

0.96

0.29

0.30

2.00

Download

-GDLLLDHSGAYVAQYYITWNELSYDHQGKEVLTPKAWDRNGQDLTAHFTTSIPLKGNVRNLSVKIRECTGLAWEWWRTVYEKTDLPLVRKRTISIWGTTLYPQVEDKVEN--------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------

4cdb

0.54

0.21

0.30

2.38

Download

DGKINIDHSGGYVAQFNISWDEVNYDPEGNEIVQHKNWSENNKSKLAHFTSSIYLPGNARNINVYAKECTGLAWEWWRTVIDDRNLPLVKNRNISIWGTTLYPKYSNKVD---------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------

8t2iN

0.05

0.23

0.99

1.25

Download

MDD-----DNGLELSLGLSCGGSTGKAKGNNNNNAGSSSENYRAEGGDRSAKVIDPAEPSSGSQRSDSGQQPPQNFFNDLSKAPTTEAEASTKPLWVEDESRKEAGNKRKFGFPGMNDDKKKEKDSSHVDMHEKKTKASHVSTATDEGSTAENEDVAESEVGGGSSSNHAKEVVRPPTDTNIVDNLTGQRRSNHGGSGTEEFTMRNMSYTVPFTVHPQNVVTSMPYSLPTKESGQHAAATSLLQPNANAGNLPIMFGYSPVQLPDGSGGIVALSQSPFAGRVPSNSATAKGEGKQPVAEEGSSEDASERPTGDNSNLNTAFSFDFAADVKFGGSGARPNLPWVSTTGSGPHGRTISGVTYASAHT

5cr6D

0.97

0.30

0.31

1.88

Download

NGDLLLDHSGAYVAQYYITWDELSYNHQGKEVLTPKAWDRNGQDLTAHFTTSIPLKGNVRNLSVKIREATGLAWEWWRTVYEKTDLPLVRKRTISIWGTTLYPQVEDKVEND-------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------

(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: HHSEARCH2 4: PROSPECT2 5: HHSEARCH I 6: SPARKS-X 7: Neff-PPAS 8: HHSEARCH 9: PROSPECT2 10: pGenTHREADER

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=-1.64 (Read more about C-score) Estimated TM-score = 0.51±0.15 Estimated RMSD = 10.4±4.6Å	Download Model 2 C-score = -2.68	Download Model 3 C-score = -3.86	Download Model 4 C-score = -2.79	Download Model 5 C-score = -2.96

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

Rank	PDB Hit	TM-score	RMSD^a	IDEN^a	Cov	Alignment
1	8deoA	0.881	2.66	0.085	0.948	Download
2	4cciA	0.434	3.06	0.055	0.477	Download
3	2ycuA	0.422	7.04	0.063	0.737	Download
4	4cd9A	0.421	3.11	0.071	0.471	Download
5	7yl4A	0.414	6.03	0.029	0.649	Download
6	7sjkA	0.413	3.63	0.060	0.477	Download
7	7wooD	0.388	6.76	0.023	0.652	Download
8	6hydA	0.388	6.70	0.054	0.644	Download
9	1g8xA	0.382	6.93	0.036	0.657	Download
10	7zu0A	0.374	6.80	0.032	0.630	Download

(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)	RMSD^a is the RMSD between residues that are structurally aligned by TM-align.
(d)	IDEN^a 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

Rank	C-score	Cluster size	PDB Hit	Lig Name	Download Complex	Ligand Binding Site Residues
1	0.08	3	3qg6B	ZN	Rep, Mult	330,332
2	0.06	2	3dwoX	C8E	Rep, Mult	287,301,302
3	0.06	2	1w9lA	ALF	Rep, Mult	325,344,347,348
4	0.06	2	4fumA	ZN	Rep, Mult	204,258
5	0.06	2	5f2eA	GLY	Rep, Mult	328,357

	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

Rank	Cscore^EC	PDB Hit	TM-score	RMSD^a	IDEN^a	Cov	EC Number	Active Site Residues
1	0.106	2v5yA	0.321	6.50	0.038	0.518	3.1.3.48	NA
2	0.098	2q3zA	0.321	6.44	0.023	0.512	2.3.2.13	NA
3	0.092	2uv8G	0.368	6.26	0.043	0.575	2.3.1.86	NA
4	0.092	3kvnX	0.323	5.85	0.036	0.490	3.1.1.1	NA
5	0.090	2vkzG	0.367	6.72	0.026	0.606	2.3.1.38 3.1.2.14	NA

	Click on the radio buttons to visualize predicted active site residues.
(a)	Cscore^EC is the confidence score for the EC number prediction. Cscore^EC 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)	RMSD^a is the RMSD between residues that are structurally aligned by TM-align.
(d)	IDEN^a 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

Rank	Cscore^GO	TM-score	RMSD^a	IDEN^a	Cov	PDB Hit	Associated GO Terms
Top 10 homologous GO templates in PDB
1	0.12	0.3693	6.59	0.04	0.60	1sjjA	GO:0051017 GO:0003779 GO:0030018 GO:0005916 GO:0051015 GO:0005856 GO:0030017 GO:0005737 GO:0005509 GO:0005515
2	0.12	0.3643	6.75	0.08	0.62	3kg2A	GO:0043204 GO:0030672 GO:0043234 GO:0050806 GO:0030425 GO:0042734 GO:0004872 GO:0032839 GO:0030426 GO:0005783 GO:0016021 GO:0043198 GO:0014069 GO:0005886 GO:0043025 GO:0019901 GO:0016020 GO:0004971 GO:0008328 GO:0032279 GO:0045184 GO:0043197 GO:0030054 GO:0031623 GO:0005515 GO:0045211 GO:0043195 GO:0004970 GO:0045202 GO:0006811 GO:0001919 GO:0010226 GO:0051966 GO:0005216 GO:0030165 GO:0007268 GO:0032281 GO:0006810 GO:0005246 GO:0005789 GO:0060992 GO:0005234
3	0.11	0.3470	6.58	0.03	0.56	2pffB	GO:0004312 GO:0016296 GO:0055114 GO:0005739 GO:0005829 GO:0004319 GO:0004321 GO:0016297 GO:0019171 GO:0005737 GO:0006633 GO:0005835 GO:0005515 GO:0016295 GO:0016740 GO:0016829 GO:0004318 GO:0016409 GO:0008152 GO:0016491 GO:0004317 GO:0016787 GO:0004314 GO:0005811 GO:0004313 GO:0004320 GO:0003824 GO:0008610
4	0.11	0.3212	6.50	0.04	0.52	2v5yA	GO:0005515 GO:0016020
5	0.11	0.3679	6.26	0.04	0.58	2uv8G	GO:0016829 GO:0004318 GO:0016409 GO:0008152 GO:0016491 GO:0004317 GO:0005737 GO:0004314 GO:0005811 GO:0004313 GO:0004320 GO:0003824 GO:0008610 GO:0004312 GO:0016296 GO:0055114 GO:0005739 GO:0005829 GO:0004319 GO:0004321 GO:0016297 GO:0019171 GO:0006633 GO:0005835 GO:0005515 GO:0016295 GO:0016740 GO:0016787
6	0.11	0.3311	6.77	0.04	0.56	3k1qA	GO:0004482 GO:0004484 GO:0005524 GO:0019028 GO:0006370
7	0.10	0.3293	6.94	0.04	0.56	1e07A	GO:0016020 GO:0005887 GO:0005886 GO:0016323 GO:0031225 GO:0005515
8	0.10	0.3679	6.46	0.05	0.60	1hciA	GO:0005515
9	0.10	0.3283	6.18	0.04	0.52	3f83A	GO:0009289
10	0.10	0.3211	6.44	0.02	0.51	2q3zA	GO:0045785 GO:0005515 GO:0043277 GO:0060445 GO:0016740 GO:0046872 GO:0060662 GO:0003810 GO:0016746 GO:0018149

Consensus prediction of GO terms

Molecular Function GO:0005515 GO:0016408 GO:0016419 GO:0016418 GO:0016297 GO:0016628 GO:0016836

GO-Score 0.44 0.41 0.41 0.41 0.41 0.41 0.39

Biological Process GO:0046394 GO:0006631

GO-Score 0.41 0.31

Cellular Component GO:0044445 GO:0043231 GO:0032991

GO-Score 0.41 0.41 0.41

(a) Cscore^GO 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) RMSD^a is the RMSD between residues that are structurally aligned by TM-align.

(d) IDEN^a 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 Cscore^GO of the template.

[Click on S777201_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.