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I-TASSER results for job id S692938

[Click on S692938_results.tar.bz2 to download the tarball file including all modeling results listed on this page]


  Submitted Sequence in FASTA format

>protein
MGRSPCCDKVGLKKGPWTPEEDQKLLAYIEEHGHGSWRALPAKAGLQRCGKSCRLRWTNY
LRPDIKRGKFTLQEEQTIIQLHALLGNRWSAIATHLPKRTDNEIKNYWNTHLKKRLVKMG
IDPVTHKPKNDALLSNDGQSKNAANLSHMAQWESARLEAEARLARQSKLRSNSFQNSLAS
QEFTAPSPSSPLSKPVMGPARCLNVLKAWNGVWTKPINEGSIASASAGISVTGALARDLE
SPTSTLGYFENAQHISSSGIGASSNTVLYEFVGNSSGSSEGGIMNNEESEEDWKEFGNSS
TGHLPQYNKDVINENSISFTSGLQDLTLPMDTTWTAESLRSNTEQISPANFVETFTDLLL
SNSGDGDLSEGGGTESDNGGEGSGSGNASENCEDNKNYWNSIFNLVNNPSPSDSAMF

  Predicted Secondary Structure

Sequence                  20                  40                  60                  80                 100                 120                 140                 160                 180                 200                 220                 240                 260                 280                 300                 320                 340                 360                 380                 400
                   |                   |                   |                   |                   |                   |                   |                   |                   |                   |                   |                   |                   |                   |                   |                   |                   |                   |                   |                   |                 
MGRSPCCDKVGLKKGPWTPEEDQKLLAYIEEHGHGSWRALPAKAGLQRCGKSCRLRWTNYLRPDIKRGKFTLQEEQTIIQLHALLGNRWSAIATHLPKRTDNEIKNYWNTHLKKRLVKMGIDPVTHKPKNDALLSNDGQSKNAANLSHMAQWESARLEAEARLARQSKLRSNSFQNSLASQEFTAPSPSSPLSKPVMGPARCLNVLKAWNGVWTKPINEGSIASASAGISVTGALARDLESPTSTLGYFENAQHISSSGIGASSNTVLYEFVGNSSGSSEGGIMNNEESEEDWKEFGNSSTGHLPQYNKDVINENSISFTSGLQDLTLPMDTTWTAESLRSNTEQISPANFVETFTDLLLSNSGDGDLSEGGGTESDNGGEGSGSGNASENCEDNKNYWNSIFNLVNNPSPSDSAMF
PredictionCCCCCCCCCCCCCCCCCCHHHHHHHHHHHHHHCCCCHHHHHHHHCCCCCCCHHHHHHHHCCCCCCCCCCCCHHHHHHHHHHHHHHCCHHHHHHHHCCCCCHHHHHHHHHHHHHHHHHHCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCHHHHCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCHHHHHCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCHHHHHHHHHCCCCCCCCCCCC
Conf.Score998876677878779999899999999999978984999999866775651063431203685665798998999999999987386999999878898512325532567999987607886666766554435677776766667654202244676652012203566766666555557788876555677778766500555424676677766665667666666543345668985223677775666776667788752012467776566665334555544334555433444543455555346676666555566775443566543567655677633246643221477777767777755556766545676556455540357878760167898899999
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
                   |                   |                   |                   |                   |                   |                   |                   |                   |                   |                   |                   |                   |                   |                   |                   |                   |                   |                   |                   |                 
MGRSPCCDKVGLKKGPWTPEEDQKLLAYIEEHGHGSWRALPAKAGLQRCGKSCRLRWTNYLRPDIKRGKFTLQEEQTIIQLHALLGNRWSAIATHLPKRTDNEIKNYWNTHLKKRLVKMGIDPVTHKPKNDALLSNDGQSKNAANLSHMAQWESARLEAEARLARQSKLRSNSFQNSLASQEFTAPSPSSPLSKPVMGPARCLNVLKAWNGVWTKPINEGSIASASAGISVTGALARDLESPTSTLGYFENAQHISSSGIGASSNTVLYEFVGNSSGSSEGGIMNNEESEEDWKEFGNSSTGHLPQYNKDVINENSISFTSGLQDLTLPMDTTWTAESLRSNTEQISPANFVETFTDLLLSNSGDGDLSEGGGTESDNGGEGSGSGNASENCEDNKNYWNSIFNLVNNPSPSDSAMF
Prediction772411142652632301451152014004610311023004402042013001010201010103415025501410040033112200300540361112202220102013103736131422313354344445444434434343333334143524234434344343444343433443444443443434343133204123322433344433333333333333334315233131333433433434444434333244223343313333223333334314323343333234334433434324233332334233333333432323143133231211000000232424433444444443344433333333323333200210010013432661335
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                 400
                   |                   |                   |                   |                   |                   |                   |                   |                   |                   |                   |                   |                   |                   |                   |                   |                   |                   |                   |                   |                 
Sec.Str
Seq
CCCCCCCCCCCCCCCCCCHHHHHHHHHHHHHHCCCCHHHHHHHHCCCCCCCHHHHHHHHCCCCCCCCCCCCHHHHHHHHHHHHHHCCHHHHHHHHCCCCCHHHHHHHHHHHHHHHHHHCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCHHHHCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCHHHHHCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCHHHHHHHHHCCCCCCCCCCCC
MGRSPCCDKVGLKKGPWTPEEDQKLLAYIEEHGHGSWRALPAKAGLQRCGKSCRLRWTNYLRPDIKRGKFTLQEEQTIIQLHALLGNRWSAIATHLPKRTDNEIKNYWNTHLKKRLVKMGIDPVTHKPKNDALLSNDGQSKNAANLSHMAQWESARLEAEARLARQSKLRSNSFQNSLASQEFTAPSPSSPLSKPVMGPARCLNVLKAWNGVWTKPINEGSIASASAGISVTGALARDLESPTSTLGYFENAQHISSSGIGASSNTVLYEFVGNSSGSSEGGIMNNEESEEDWKEFGNSSTGHLPQYNKDVINENSISFTSGLQDLTLPMDTTWTAESLRSNTEQISPANFVETFTDLLLSNSGDGDLSEGGGTESDNGGEGSGSGNASENCEDNKNYWNSIFNLVNNPSPSDSAMF
16kksA 0.62 0.16 0.25 2.08Download ---------NEYKKGLWTVEEDKILMDYVKAHGKGHWNRIAKKTGLKRCGKSCRLRWMNYLSPNVKRGNFTEQEEDLIIRLHKLLGNRWSLIAKRVPGRTDNQVKNYWNTHLSKK--------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------
27e2cI 0.08 0.26 0.92 1.05Download ------------QVPFESSSKSDESLGSIIIEGTLDKFQLHKYFFIRRLRLL------------KLEDQTLTAFVGAFQLIKNFIELEFKHYFITYFEFENCEIKAELLMLKRDNWVQGVMATSGYRL--MDKNYPNSKETFVDETVFQENFLTLTKEILSLFNKCEGKRQRIVDILSIEIGLLYYQGKKYEEAVSLFLSCGLKILQVFSAVLTNAFLNILKLCKDNDSKEIKFMDLQMKVHLRANVSAIEVNLKSYGFPEDISTKTMRLSLKNMDVIVFGASDFLLKKGENKLILECRDIMYEFSLLSFEIIVEGITFVKEFPENQDEFIVVPEIYCKESTKVLVKQAHNLNEYALELKSVQSDALESLQVEVEVQKNIGNMKNLPVSFSMDEIQ---------ARKRYNTPFENV
36qdv 0.15 0.19 0.68 1.37Download HRKSAKKLDPSIKKTEWSREEEEKLLHLAKLMP-TQWRTIAPIIG--RTAAQCLEHYEFLLDKAAQPIDMDEDELEMLSEARARLANTQGKKAKRKAREKQLEEARRLAALQKRRLRAAGIEIQKKRKRKRGVDYNAEIPKKPAGFYDTS-EENYQ----------------ALDADF-------RKLRQQ---DLDGELRSEDKLKRKKES-------D--------------------LPS-A------ILQTSA-D-V----DARKQAI-----------RDAE-RVKEMKR--------------------------M----HLQK----------------SEELIKKEMITMLHYDLLHHKLKKQDVLVQEMEVV-KQGM----SHGSLEKRLEINRGHMTT-EAKRARTF
45gmkC 0.14 0.17 0.76 3.13Download ------------KGGVWTNVEDQILKAAVQKYGTHQWSKVASLLQ-KKTARQSELRWNEYLNPKLNFTEFSKEEDAQLLDLARELPNQWRTIADMM-ARPAQVCVERYNRLLESEDSEDEEKEMLAEARARLL---NTQGKKATRKIRERMLEESKRIAELQKRRELKQAGINVAIKKKYGTDIDYNEDIVYEQAPMPGIYDTSTEDRQIKKKFEQFERKVNRKGLESRMQHITQGRTSMKIQFKTAMPPTEVLLESIQSKVESIEQLQRKLQHVQPLEQQNNEMCSTLCHHSLPALIEGQRKYYADYYAYRQEIRSLEGRRKRLQAMLNSS-------------------------------------------------------------------------------------
56qdv 0.20 0.19 0.28 1.96Download --------DPSIKKTEWSREEEEKLLHLAKLMP-TQWRTIAP--IIGRTAAQCLEHYEFLLDKAAQPIDMDEDELEMLSEARARLANTQGKKAKRKAREKQLEEARRLAALQKRRLRAAGIEIQKKRKR------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------
66exnO 0.15 0.16 0.73 1.42Download ----PV--PIYVKGGVWTNVEDQILKAAVQKYGTHQWSKVASLLQ-KKTARQSELRWNEYLNPKLNFTEFSKEEDAQLLDLARELPNQWRTIADMM-ARPAQVCVERYNRLLELKVGDINPNAETQMARPDNGDLEDEEKEMLAEARLNTQGKKATRKIRERMLEESKAGINVAIKKPKKKYGTDIDYNEDIVYEQAPMPGIYDTSTEDRQIKKKFEQFERKVNRKGTEVLLESIQSKVESIEQLQRKLQHVQPLEQQN-NEMCSTLCHHSLPALIEGQRKYYADYYAYRQEIRSLEGRRK----RLQAMLNSSSSI----------------------------------------------------------------------------------------------------
77e2cI 0.10 0.26 1.00 1.31Download QVIEGTLDKFQLHDQTLTAFVGQLIKNFIESISIEYFKHYFITSMLSYFEFEKRDNWVQGVYPNSKETFVDETVKEILSLFNKCEGKRFIDSLSHCPKGESLCKDNDSKEIWWKKFMDLQMKVHLARANVSAIEVNLKSYGFPEDISTKTMRLSLKNMGGDVIVFGASDFLLKKGENKLILECRDIMYGEFSLLSFEIIVEGITFVKEFPENQDEFIVVPEIYCKESTKVLVKQAHNLNLGEYALELKSVQSDALESLQVEVEVQKNIGNMKNLPVSFSMDEIQARKRYNTPFENVRLEYYLLDQITAFDLIIKTSFTKKNDQGTAPDTRNDYNIRGDYIATTPALITFDGNESFINCYEITANNNFDSKDIKLKYDYDAFKENRIIRLLKTSIDLNKTKSKIRNLNTDMDEYVRNL
83zqcA 0.36 0.11 0.28 5.30Download ------------MKGPFTEAEDDLIREYVKENGPQNWPRITSFLP-NRSPKQCRERWFNHLDPAVVKHAWTPEEDETIFRNYLKLGSKWSVIAKLIPGRTDNAIKNRWNSSISKRISTNSNHKEILLPDRS----------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------
96exn 0.15 0.16 0.69 1.70Download PVP------IYVKGGVWTNVEDQILKAAVQKYGTHQWSKV-ASLLQKKTARQSELRWNEYLNPKLNFTEFSKEEDAQLLDLARELPNQWRTIADMM-ARPAQVCVERYNRLLELKVGNGDLEDEEKEMLAEARARLLNTQGKKATRKISKRIAELQKRRELK---QAGINVAIKKPKKKYGTDIDYNEDIVYE--QAPMPGIYDTSTEDRQI-KKK------FEQFERKVNR--KGT-------------------EV-L---L-----ES------------I-QSKVEEQLQRKLQHVQPLEQQNNE---MCSTHHSLPALIEGQ----RKYYADYYAYRQEIRSLQAMLNSSSSI-----------------------------------------------------------
106kksA 0.63 0.16 0.25 3.92Download ----------EYKKGLWTVEEDKILMDYVKAHGKGHWNRIAKKTGLKRCGKSCRLRWMNYLSPNVKRGNFTEQEEDLIIRLHKLLGNRWSLIAKRVPGRTDNQVKNYWNTHLSKK--------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------
(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: HHSEARCH I   4: Neff-PPAS   5: HHSEARCH   6: wdPPAS   7: PROSPECT2   8: SP3   9: HHSEARCH2   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=-1.79 (Read more about C-score)
  • Estimated TM-score = 0.50±0.15
  • Estimated RMSD = 11.1±4.6Å

  • Download Model 2
  • C-score = -3.84

  • Download Model 3
  • C-score = -3.71

  • Download Model 4
  • C-score = -4.08

  • Download Model 5
  • C-score = -3.67


  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
17e2cI0.861 2.030.0810.902Download
27q2xD0.486 6.560.0850.770Download
34uvkA0.481 6.550.0470.758Download
46yufD0.477 6.790.0660.772Download
57dxjA0.475 6.120.0540.727Download
65vkqA0.469 6.600.0540.741Download
76bq1A0.469 6.740.0440.758Download
87jq9A0.464 6.260.0590.703Download
97lheA0.464 6.500.0560.729Download
106qj3A0.459 6.520.0440.715Download

(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 7 1mseC Nuc.Acid N/A 14,15,16,17,48,51,52,55,56,59,60,67,68,69,70,106,107,110,111,114
20.05 4 1mseC Nuc.Acid N/A 35,36,37,38,51,54,55,87,88,89,90,94,101,105,109,113
30.05 4 2imaA ZN Rep, Mult 111,115,153
40.04 3 2kdzA Nuc.Acid N/A 15,35,51,52,54,55,87,89,90,101,102,105
50.04 3 3osfA Nuc.Acid N/A 13,14,15,16,17,51,52,56,60,102,106,109,110


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
10.1363btaA0.371 7.160.0440.628 3.4.24.69  NA
20.1342np0A0.327 6.860.0230.542 3.4.24.69  NA
30.1111dceA0.365 5.520.0660.523 2.5.1.60  NA
40.1092vkzG0.370 7.140.0380.619 2.3.1.38 3.1.2.14  NA
50.1092uv8G0.374 7.240.0430.633 2.3.1.86  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 0.140.3889 6.66 0.04 0.623gb8A GO:0005737 GO:0015031 GO:0000776 GO:0000278 GO:0005654 GO:0003723 GO:0016070 GO:0006810 GO:0044419 GO:0005829 GO:0006886 GO:0030529 GO:0046796 GO:0000087 GO:0051028 GO:0005730 GO:0016032 GO:0005635 GO:0016071 GO:0005488 GO:0005634 GO:0005642 GO:0015030 GO:0000236 GO:0005515 GO:0008565 GO:0019058
2 0.120.3979 6.29 0.06 0.613a6pA GO:0005515 GO:0015031 GO:0005730 GO:0005829 GO:0003723 GO:0000049 GO:0031047 GO:0005634 GO:0006810 GO:0006886 GO:0005654 GO:0008565 GO:0005488 GO:0005737 GO:0006611
3 0.120.4067 6.32 0.04 0.632x1gF GO:0005622 GO:0007270 GO:0008565 GO:0006886 GO:0042331 GO:0050804 GO:0005488
4 0.120.4137 6.52 0.05 0.653icqT GO:0003723 GO:0006810 GO:0006605 GO:0005525 GO:0005737 GO:0005643 GO:0000049 GO:0005829 GO:0005635 GO:0008033 GO:0005634 GO:0005488
5 0.120.4188 5.99 0.04 0.611b3uA 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
6 0.120.3986 6.79 0.04 0.631wa5C GO:0008565 GO:0051301 GO:0005634 GO:0005635 GO:0006810 GO:0006886 GO:0005737 GO:0007049 GO:0005488 GO:0008262 GO:0006611 GO:0008283 GO:0007067 GO:0015031
7 0.120.4084 6.66 0.06 0.653m1iC 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
8 0.120.4012 6.92 0.04 0.663fhnA GO:0015031 GO:0006810 GO:0016020 GO:0005515 GO:0005783 GO:0070939 GO:0016192 GO:0042802 GO:0005789 GO:0003674 GO:0006890
9 0.120.4070 6.45 0.07 0.631u6gC GO:0043086 GO:0030154 GO:0006351 GO:0000151 GO:0005488 GO:0005515 GO:0016567 GO:0005634 GO:0006355
10 0.120.3839 5.79 0.04 0.561n11A GO:0005515


Consensus prediction of GO terms
 
Molecular Function GO:0003723 GO:0008565 GO:0005515
GO-Score 0.33 0.33 0.33
Biological Process GO:0006886
GO-Score 0.33
Cellular Component GO:0031981 GO:0043232 GO:0031967 GO:0012505 GO:0005829
GO-Score 0.48 0.48 0.48 0.48 0.41

(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 S692938_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.