D-I-TASSER Q70EL4-D3

D-I-TASSER results for Q70EL4-D3

[Click result.zip to download all results on this page]

Input Sequence in FASTA format

>Q70EL4 (181 residues)
GLKNHGNTCFMNAVVQCLSNTDLLAEFLALGRYRAAPGRAEVTEQLAALVRALWTREYTP
QLSAEFKNAVSKYGSQFQGNSQHDALEFLLWLLDRVHEDLEGSSRGPVSEKLPPEATKTS
ENCLSPSAQLPLGQSFVQSHFQAQYRSSLTCPHCLKQSNTFDPFLCVSLPIPNSEDGGRA
I

Predicted Secondary Structure

Sequence	20 40 60 80 100 120 140 160 180 \| \| \| \| \| \| \| \| \| GLKNHGNTCFMNAVVQCLSNTDLLAEFLALGRYRAAPGRAEVTEQLAALVRALWTREYTPQLSAEFKNAVSKYGSQFQGNSQHDALEFLLWLLDRVHEDLEGSSRGPVSEKLPPEATKTSENCLSPSAQLPLGQSFVQSHFQAQYRSSLTCPHCLKQSNTFDPFLCVSLPIPNSEDGGRAI
Prediction	CCCCCCCCHHHHHHHHHHHCCHHHHHHHHCCCCCCCCCCHHHHHHHHHHHHHHHCCCCCCCCHHHHHHHHHHHHHHCCCCCCCCHHHHHHHHHHHHHHHHHHHCCCCCCCCCCCCCCCHHHHHHHHHHHCCCCCCCCSSSCCSSSSSSSSSCCCCCSSSSSCCCSSSSSSCCCCCCCCCCC
Confidence	9867786378999999986497888776327654456420999999999999980999953839999999886150499987588999999999999999861168866678755676178887666420358990201312088789998899988643568545786479998620049
	H:Helix; S:Strand; C:Coil

Predicted Solvent Accessibility

Sequence	20 40 60 80 100 120 140 160 180 \| \| \| \| \| \| \| \| \| GLKNHGNTCFMNAVVQCLSNTDLLAEFLALGRYRAAPGRAEVTEQLAALVRALWTREYTPQLSAEFKNAVSKYGSQFQGNSQHDALEFLLWLLDRVHEDLEGSSRGPVSEKLPPEATKTSENCLSPSAQLPLGQSFVQSHFQAQYRSSLTCPHCLKQSNTFDPFLCVSLPIPNSEDGGRAI
Prediction	7352333200000000002304302402445414544342200300140044033574322103302420341254046331400300031004203520443444433343444344454334434533543412033103132313030461654133313123020402557425516
	Values range from 0 (buried residue) to 8 (highly exposed residue)

Predicted Contact, Hydrogen and Distance Map Used in D-I-TASSER simulation

Contact Map

Distance Map

Hydrogen bond networks

D-I-TASSER simulation is guided by the consensus contact map (left figure), distance map (middle figure) and Hydrogen bond network (right figure) derived based on confidence scores of AttentionPotential. In the contact, distance map and hydrogen bond networks, the axes mark the residue index along the sequence. For the contact map, each dot represents a residue pair with predicted contact, while for the distance map and hydrogen bond network, a color scale represents a distance of 1-20+ angstroms or a angle of 0-180 degree.

Top 10 threading templates used by D-I-TASSER

Rank

PDB
hit

ID1

ID2

Cov

Norm.
Zscore

Download
alignment

                  20                  40                  60                  80                 100                 120                 140                 160                 180

                   |                   |                   |                   |                   |                   |                   |                   |                   |

SS
Seq

CCCCCCCCHHHHHHHHHHHCCHHHHHHHHCCCCCCCCCCHHHHHHHHHHHHHHHCCCCCCCCHHHHHHHHHHHHHHCCCCCCCCHHHHHHHHHHHHHHHHHHHCCCCCCCCCCCCCCCHHHHHHHHHHHCCCCCCCCSSSCCSSSSSSSSSCCCCCSSSSSCCCSSSSSSCCCCCCCCCCC
GLKNHGNTCFMNAVVQCLSNTDLLAEFLALGRYRAAPGRAEVTEQLAALVRALWTREYTPQLSAEFKNAVSKYGSQFQGNSQHDALEFLLWLLDRVHEDLEGSSRGPVSEKLPPEATKTSENCLSPSAQLPLGQSFVQSHFQAQYRSSLTCPHCLKQSNTFDPFLCVSLPIPNSEDGGRAI

2ibiA

0.35

0.33

9.73

1.33

DEthreader

GLRNLGNTCFMNSILQCLSNTRELRDYCLQRLYMLHHNHTALVEEFAKLIQTIWTSSNDVVSPSEFKTQIQRYAPRFVGYNQQDAQEFLRFLLDGLHNEVN-RVTL-P----LPDD------EKGRQMWKYLEDSRIGDLFVGQLKSSLTCTDCGYCSTVFDPFWDLSLPIAKVLTTSSDA

2ibiA

0.33

9.80

1.95

SPARKS-K

GLRNLGNTCFMNSILQCLSNTRELRDYCLQRLYMRDNAHTALVEEFAKLIQTIWTSSPDVVSPSEFKTQIQRYAPRFVGYNQQDAQEFLRFLLDGLHNEVNRVTLRPKNPENLDHLPDDEKGRQMWRKYLEREDSRIGDLFVGQLKSSLTCTDCGYCSTVFDPFWDLSLPIAKRGPEVTLM

2y6eA

0.31

9.35

1.18

MapAlign

GLGNLGNT-FMNSALQCLSNTAPLTDYFLKDEYINLGMKGEIAEAYAELIKQMWSGRDAHVAPRMFKTQVGRFAPQFSGYQQQDSQELLAFLLDGLHEDLNRVKKKPYLELKDANGRPDAVVAKEAWENHLRNDSVIVDTFHGLFKSTLVCPECAKVSVTFDPFCYLTLDPWYCPNCKKHQ

2y6eA

0.33

9.80

1.03

CEthreader

GLGNLGNT-FMNSALQCLSNTAPLTDYFLKDEYNPLGMKGEIAEAYAELIKQMWSGRDAHVAPRMFKTQVGRFAPQFSGYQQQDSQELLAFLLDGLHEDLNRVKKKPYLELKDANGRPDAVVAKEAWENHLRNDSVIVDTFHGLFKSTLVCPECAKVSVTFDPFCYLTLPLPLTVALRDCI

2ibiA

0.33

9.80

1.86

MUSTER

GLRNLGNTCFMNSILQCLSNTRELRDYCLQRLYMRDLHHTALVEEFAKLIQTIWTSSPDVVSPSEFKTQIQRYAPRFVGYNQQDAQEFLRFLLDGLHNEVNRVTLRPKNPENLDHLPDDEKGRQMWRKYLEREDSRIGDLFVGQLKSSLTCTDCGYCSTVFDPFWDLSLPIAKRGPEVDCM

3ihpB

0.23

0.19

5.89

2.03

HHsearch

GIRNLGNSCYLNSVVQVLFSIPDFQRKYVDKLEAPTDPTQDFSTQVAKLGHGLLSG--EGIAPRMFKALIGKGHPEFSTNRQQDAQEFFLHLINMVERNCRS-------------------------------SENPNEVFRFLVEEKIKCLATEKVKYTQRVDYIMQLPVPMDAALNSCL

6dgfA

0.35

0.32

9.57

1.65

FFAS-3D

GLRNLGNTCFMNSILQCLSNTRELRDYCLQRLYMRDLHHGSVEEFAKLIQTIWTSSPNDVVSPSEFKTQIQRYAPRFVGYNQQDAQEFLRFLLDGLHNEVNRVDHLPDDEKGRQM----------WRKYLEREDSRIGDLFVGQLKSSLTCTDCGYCSTVFDPFWDLSLPIAKYPE-----

2ibiA

0.29

0.28

8.58

1.52

EigenThreader

LAGNLGNTCFMNSILQCLSNTRELRDYCLQRLHHGSNAHTALVEEFAKLIQTIWTSSPNDVVPSEFKTQIQRYAPRFVGYNQQDAQEFLRFLLDGLHNEVNRVTLRPKNPENLD--HLPDDEKGRQMWRKYLERERIGDLFVGQLKSSLTCTDCGYCSTVFDPFWDLLPIAKRG---PEVT

6crnA

0.33

9.95

1.50

CNFpred

GLSNLGNTCFMNSAIQCLSNTPPLTEYFLNDKYQEELNRGEIAKSYAELIKQMWSGKFSYVTPRAFKTQVGRFAPQFSGYQQQDCQELLAFLLDGLHEDLNRIRKKPYIQLKDADGRPDKVVAEAWENHLKRNDSIIVDIFHGLFKSTLVCPECAKISVTFDPFCYLTLPLPMPKKPFVKL

6dgfA

0.36

0.33

9.72

1.33

DEthreader

GLRNLGNTCFMNSILQCLSNTRELRDYCLQRLYMLHHAHTALVEEFAKLIQTIWTSSNDVVSPSEFKTQIQRYAPRFVGYNQQDAQEFLRFLLDGLHNEVN--RV-------LPDD------EKGRQMWKYLEDSRIGDLFVGQLKSSLTCTDCGYCSTVFDPFWDLSLPIAKPLTTSSDA

(a)	ID1 is the number of template residues identical to query divided by number of aligned residues.
(b)	ID2 is the number of template residues identical to query divided by query sequence length.
(c)	Cov is equal the number of aligned template residues divided by query sequence length.
(d)	Norm. Zscore is the normalized Z-score of the threading alignments. A Normalized Z-score >1 means a good alignment and is highlighted in bold.
(e)	Download alignment lists the threading program used to identify the template, and provide the 3D structure of aligned regions of threading templates (threading[1-10].pdb.gz).
(f)	Template residues identical to query sequence are highlighted in color.

Top 1 final models from D-I-TASSER

Click to view	Rank^a	Download	Estimated TM-score^b
	1	model1.pdb.gz	0.837

(a)

D-I-TASSER simulations generate a large ensemble of structural conformations, i.e. decoys. These decoys are clustered by SPICKER based on pairwise structure similarity to report up to five final models from the five largest clusters. Models are ranked in descending order of cluster size. If the simulations converge well, it is possible to have less than 5 models generated, which is usually an indication of good model quality.

(b)

The model confidence is quantitatified by estimated TM-score (eTM-score), calculated based on significance of threading template alignments, contact map satisfaction rate, mean absolute error between distance of model and distance of AttentionPotential, and convergence of D-I-TASSER simulations. eTM-score is typically in the range of [0, 1], with higher eTM-score signifies higher model confidence.

Proteins with similar structure

Top 10 structural analogs in PDB (as identified by TM-align)

Rank	PDB Hit	TM-score	RMSD^a	IDEN^a	Cov.	Download Alignment
1	2ibiA	0.92	1.82	0.326	1.000	model1_2ibiA.pdb.gz
2	2y6eA	0.91	1.95	0.322	0.995	model1_2y6eA.pdb.gz
3	3i3tC	0.86	1.89	0.359	0.923	model1_3i3tC.pdb.gz
4	2gfoA	0.84	2.24	0.345	0.928	model1_2gfoA.pdb.gz
5	5cvmA	0.75	2.53	0.242	0.845	model1_5cvmA.pdb.gz
6	5txkA	0.74	2.42	0.247	0.834	model1_5txkA.pdb.gz
7	6tbmQ	0.74	3.01	0.252	0.878	model1_6tbmQ.pdb.gz
8	2ayoA	0.73	2.56	0.224	0.834	model1_2ayoA.pdb.gz
9	5wchA	0.73	2.72	0.222	0.845	model1_5wchA.pdb.gz
10	4zuxe	0.72	2.96	0.253	0.873	model1_4zuxe.pdb.gz

(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 Gene Ontology (GO) Terms

Molecular Function (MF)

GO term	Cscore^GO	Name
GO:0003824	0.96	catalytic activity
GO:0070011	0.95	peptidase activity, acting on L-amino acid peptides
GO:0008234	0.94	cysteine-type peptidase activity
GO:0019783	0.91	ubiquitin-like protein-specific protease activity
GO:0004843	0.89	thiol-dependent ubiquitin-specific protease activity

Download full result of the above consensus prediction.

Click the graph to show a high resolution version.

(a)

Cscore^GO is the confidence score of predicted GO terms. Cscore^GO values range in between [0-1]; where a higher value indicates a better confidence in predicting the function using the template.

(b)

The graph shows the predicted terms within the Gene Ontology hierachy for Molecular Function. Confidently predicted terms are color coded by Cscore^GO:

[0.4,0.5)

[0.5,0.6)

[0.6,0.7)

[0.7,0.8)

[0.8,0.9)

[0.9,1.0]

Biological Process (BP)

GO term	Cscore^GO	Name
GO:0009987	0.98	cellular process
GO:0044260	0.95	cellular macromolecule metabolic process
GO:0044238	0.95	primary metabolic process
GO:0019538	0.93	protein metabolic process
GO:0006508	0.92	proteolysis
GO:0070647	0.85	protein modification by small protein conjugation or removal
GO:0016579	0.83	protein deubiquitination
GO:0065007	0.69	biological regulation
GO:0050789	0.68	regulation of biological process
GO:0050794	0.67	regulation of cellular process
GO:0080090	0.52	regulation of primary metabolic process
GO:0060255	0.52	regulation of macromolecule metabolic process
GO:0031323	0.52	regulation of cellular metabolic process

Download full result of the above consensus prediction.

Click the graph to show a high resolution version.

(a)

Cscore^GO is the confidence score of predicted GO terms. Cscore^GO values range in between [0-1]; where a higher value indicates a better confidence in predicting the function using the template.

(b)

The graph shows the predicted terms within the Gene Ontology hierachy for Biological Process. Confidently predicted terms are color coded by Cscore^GO:

[0.4,0.5)

[0.5,0.6)

[0.6,0.7)

[0.7,0.8)

[0.8,0.9)

[0.9,1.0]

Cellular Component (CC)

GO term	Cscore^GO	Name
GO:0044424	1.00	intracellular part
GO:0043226	0.84	organelle
GO:0043229	0.83	intracellular organelle
GO:0043227	0.82	membrane-bounded organelle
GO:0043231	0.81	intracellular membrane-bounded organelle
GO:0005634	0.70	nucleus
GO:0044422	0.50	organelle part

Download full result of the above consensus prediction.

Click the graph to show a high resolution version.

(a)

Cscore^GO is the confidence score of predicted GO terms. Cscore^GO values range in between [0-1]; where a higher value indicates a better confidence in predicting the function using the template.

(b)

The graph shows the predicted terms within the Gene Ontology hierachy for Cellular Component. Confidently predicted terms are color coded by Cscore^GO:

[0.4,0.5)

[0.5,0.6)

[0.6,0.7)

[0.7,0.8)

[0.8,0.9)

[0.9,1.0]

Predicted Enzyme Commission (EC) Numbers

Top 5 enzyme homologs in PDB

Rank	Cscore^EC	PDB Hit	TM-score	RMSD^a	IDEN^a	Cov.	EC Number	Predicted Active Site Residues
1	0.107	3i3tC	0.861	1.89	0.359	0.923	3.4.19.12	70
2	0.079	2hd5A	0.851	2.01	0.347	0.923	3.1.2.15	NA
3	0.060	3e9sA	0.489	4.74	0.099	0.751	3.4.22.69	19
4	0.060	1lmlA	0.466	5.34	0.030	0.773	3.4.24.36	NA
5	0.060	1nb8B	0.683	2.63	0.207	0.790	3.1.2.15	NA

	Click on the radio buttons to visualize predicted active site residues.
(a)	Cscore^EC is the confidence score for the Enzyme Commission (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.

Predicted Ligand Binding Sites

Template proteins with similar binding site:

Rank	Cscore^LB	PDB Hit	TM-score	RMSD^a	IDEN^a	Cov.	BS-score	Lig. Name	Download Complex	Predicted binding site residues
1	0.01	3e9sA	0.489	4.86	0.105	0.757	0.26	TTT	complex1.pdb.gz	3,4,9,15
2	0.01	1a9x1	0.445	5.12	0.051	0.729	0.39	III	complex2.pdb.gz	4,9,10,12,13
3	0.01	1a9xG	0.445	4.92	0.032	0.718	0.14	ADP	complex3.pdb.gz	48,49,50,52
4	0.01	1bxrE	0.435	5.07	0.037	0.713	0.10	ANP	complex4.pdb.gz	44,46,63,78
5	0.01	1ce8A	0.446	5.17	0.051	0.735	0.22	IMP	complex5.pdb.gz	2,3,4,11,12,14
6	0.01	1bxrA	0.446	5.11	0.038	0.729	0.11	ANP	complex6.pdb.gz	5,6,8,9,81
7	0.01	1ce8C	0.444	5.22	0.044	0.740	0.13	ADP	complex7.pdb.gz	5,9,10,11,77
8	0.01	1a9x2	0.444	5.13	0.038	0.729	0.34	III	complex8.pdb.gz	4,9,12,13,16
9	0.01	1ce8A	0.446	5.17	0.051	0.735	0.15	ADP	complex9.pdb.gz	4,5,6
10	0.01	1a9x3	0.444	5.13	0.038	0.729	0.18	III	complex10.pdb.gz	3,8,9,10,11,16,20

	Click on the radio buttons to visualize predicted binding site and residues.
(a)	Cscore^LB is the confidence score of predicted binding site. Cscore^LB values range in between [0-1]; where a higher score indicates a more reliable ligand-binding site prediction.
(b)	BS-score is a measure of local similarity (sequence & structure) between template binding site and predicted binding site in the query structure. Based on large scale benchmarking analysis, we have observed that a BS-score >1 reflects a significant local match between the predicted and template binding site.
(c)	TM-score is a measure of global structural similarity between query and template protein.
(d)	RMSD^a the RMSD between residues that are structurally aligned by TM-align.
(e)	IDEN^a is the percentage sequence identity in the structurally aligned region.
(f)	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.

[Click result.zip to download all results on this page]

References:
1.	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. In preparation, 2020.