D-I-TASSER Q8N668-D1

D-I-TASSER results for Q8N668-D1

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

Input Sequence in FASTA format

>Q8N668 (116 residues)
MAAGELEGGKPLSGLLNALAQDTFHGYPGITEELLRSQLYPEVPPEEFRPFLAKMRGILK
SIASADMDFNQLEAFLTAQTKKQGGITSDQAAVISKFWKSHKTKIRESLMNQSRWN

Predicted Secondary Structure

Sequence	20 40 60 80 100 \| \| \| \| \| MAAGELEGGKPLSGLLNALAQDTFHGYPGITEELLRSQLYPEVPPEEFRPFLAKMRGILKSIASADMDFNQLEAFLTAQTKKQGGITSDQAAVISKFWKSHKTKIRESLMNQSRWN
Prediction	CCCCCCCCCCHHHHHHHHHHHHHHCCCCCCCHHHHHHHHCCCCCHHHHHHHHHHHHHHHHHHHHCCCCHHHHHHHHHHHHHHHCCCCHHHHHHHHHHHHHCHHHHHHHHHHHHCCC
Confidence	98542234534999999999999808865419999998658999999999999999999999981699789999999988871799999999999999970699999999970359
	H:Helix; S:Strand; C:Coil

Predicted Solvent Accessibility

Sequence	20 40 60 80 100 \| \| \| \| \| MAAGELEGGKPLSGLLNALAQDTFHGYPGITEELLRSQLYPEVPPEEFRPFLAKMRGILKSIASADMDFNQLEAFLTAQTKKQGGITSDQAAVISKFWKSHKTKIRESLMNQSRWN
Prediction	76454274343021003210444136476144620354125614474045026404410431244514364044204543677551466215302411543444035303643538
	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 DeepPotential. 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

                   |                   |                   |                   |                   |

SS
Seq

CCCCCCCCCCHHHHHHHHHHHHHHCCCCCCCHHHHHHHHCCCCCHHHHHHHHHHHHHHHHHHHHCCCCHHHHHHHHHHHHHHHCCCCHHHHHHHHHHHHHCHHHHHHHHHHHHCCC
MAAGELEGGKPLSGLLNALAQDTFHGYPGITEELLRSQLYPEVPPEEFRPFLAKMRGILKSIASADMDFNQLEAFLTAQTKKQGGITSDQAAVISKFWKSHKTKIRESLMNQSRWN

2h2mA

1.00

0.93

26.07

1.35

SPARKS-K

MAAGELEGGKPLSGLLNALAQDTFHGYPGITEELLRSQLYPEVPPEEFRPFLAKMRGILKSIASADMDFNQLEAFLTAQTKKQGGITSDQAAVISKFWKSHKTKIRES--------

2h2mA

1.00

0.93

26.07

1.73

MUSTER

MAAGELEGGKPLSGLLNALAQDTFHGYPGITEELLRSQLYPEVPPEEFRPFLAKMRGILKSIASADMDFNQLEAFLTAQTKKQGGITSDQAAVISKFWKSHKTKIRES--------

2h2mA

1.00

0.93

26.07

4.33

HHsearch

MAAGELEGGKPLSGLLNALAQDTFHGYPGITEELLRSQLYPEVPPEEFRPFLAKMRGILKSIASADMDFNQLEAFLTAQTKKQGGITSDQAAVISKFWKSHKTKIRES--------

2h2mA

1.00

0.92

25.83

1.69

FFAS-3D

MAAGELEGGKPLSGLLNALAQDTFHGYPGITEELLRSQLYPEVPPEEFRPFLAKMRGILKSIASADMDFNQLEAFLTAQTKKQGGITSDQAAVISKFWKSHKTKIRE---------

3dsiA

0.06

0.05

2.30

1.00

DEthreader

----RNRIFPEFQTYSELFSLELKADFGGSSDGTAF-NFLAFLTCFNWGGMKILFPNMVKRIGRAGVRLELTKSVVYELRVLWSKVV-LVARLFVIEIFRRYD-SFD-IEFSS---

6w2rA1

0.08

0.07

2.77

0.64

SPARKS-K

--GTTEDERRELEKVARKAIEAAREGNTDEVREQLQRALESG-TKTAVKLALDVALRVAQEAAKRGNKIDEAAEVVVRIAEESNN------SDALEQALRVLEEIAKAVLKSEK--

1t5jA

0.04

0.03

1.91

0.66

MapAlign

KITHNNKTAIAGALAIAFFVSSALKDRKSL-LDECYNYIK-DIDEEFAKKLLEIKNFLDYIYDYFGTGVVPSAIATYLLTDNFKEG-MLKCINATDSLASMYGAMAGAYYGFKNIP

2h2mA

1.00

0.93

26.07

0.51

CEthreader

MAAGELEGGKPLSGLLNALAQDTFHGYPGITEELLRSQLYPEVPPEEFRPFLAKMRGILKSIASADMDFNQLEAFLTAQTKKQGGITSDQAAVISKFWKSHKTKIRES--------

1rjvA

0.09

0.08

3.00

0.53

MUSTER

MSMTDLLNAEDIKKAVGAF------ATDSFDKKFFQMVGLKKKSADDVKKVFHMLDK-----KSGFIEEDELGFILKGFSPDARDLSAKETKMLMAAGKDGDGKIVDEFSTLVAES

6bq1A

0.14

0.13

4.43

0.35

HHsearch

LGATPACVKKDYSNFMASLNLRNRYAGFDL-NKMMVQDLHSRSHPQHYTQAMFKLTAMLISS--KD-CDPQLLHHLCW---GPLMFNEHGMETALACWEWGKDGFMREMAGAWHMT

(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	0.7725

(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 DeepPotential, 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	2h2mA	0.62	2.86	0.718	0.828	model1_2h2mA.pdb.gz
2	2wj8S1	0.58	3.80	0.072	0.922	model1_2wj8S1.pdb.gz
3	5fvcA2	0.57	3.87	0.073	0.914	model1_5fvcA2.pdb.gz
4	6rwtA	0.57	3.84	0.102	0.845	model1_6rwtA.pdb.gz
5	3o1aA	0.56	4.23	0.054	0.905	model1_3o1aA.pdb.gz
6	4z5pA	0.56	4.20	0.084	0.897	model1_4z5pA.pdb.gz
7	3nc3A	0.56	4.20	0.053	0.948	model1_3nc3A.pdb.gz
8	3pm0A	0.56	4.37	0.079	0.957	model1_3pm0A.pdb.gz
9	6m7lA	0.56	4.21	0.036	0.897	model1_6m7lA.pdb.gz
10	3wecA	0.56	4.25	0.056	0.888	model1_3wecA.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:0005507	1.00	copper ion binding
GO:0042802	0.53	identical protein binding
GO:0008289	0.53	lipid binding
GO:0080025	0.52	phosphatidylinositol-3,5-bisphosphate binding
GO:0070300	0.52	phosphatidic acid binding
GO:0043325	0.52	phosphatidylinositol-3,4-bisphosphate binding
GO:0042803	0.52	protein homodimerization activity
GO:0005547	0.52	phosphatidylinositol-3,4,5-trisphosphate binding
GO:0005546	0.52	phosphatidylinositol-4,5-bisphosphate binding

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:2000009	1.00	negative regulation of protein localization to cell surface
GO:1902306	1.00	negative regulation of sodium ion transmembrane transport
GO:0055070	1.00	copper ion homeostasis
GO:0032434	1.00	regulation of proteasomal ubiquitin-dependent protein catabolic process
GO:0031398	1.00	positive regulation of protein ubiquitination

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:0005768	1.00	endosome

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	0.060	3hf2A	0.534	4.48	0.096	0.940	1.14.14.1 1.6.2.4	NA
2	0.060	2uvnA	0.505	4.60	0.043	0.905	1.14.-.-	NA
3	0.060	1oxaA	0.510	4.72	0.061	0.905	3.4.23.23	NA
4	0.060	2f7fA	0.504	4.16	0.074	0.810	2.4.2.11	NA
5	0.060	2vn0A	0.540	4.44	0.035	0.940	1.14.14.1	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	3eqmA	0.541	4.27	0.091	0.922	0.13	HEM	complex1.pdb.gz	12,16,20,100,101
2	0.01	3p3lA	0.540	4.34	0.036	0.897	0.18	HEM	complex2.pdb.gz	8,9,12,13,16,52,87,89,92,93,96
3	0.01	2wj8A	0.581	3.80	0.072	0.922	0.15	QNA	complex3.pdb.gz	15,23,27
4	0.01	2z3uA	0.432	4.75	0.063	0.759	0.10	HEM	complex4.pdb.gz	5,12,13,62,76,80
5	0.01	2x9pA	0.542	4.48	0.070	0.966	0.14	HEM	complex5.pdb.gz	52,56,59,63

	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, Qiqige Wuyun, Yang Li, Quancheng Liu, Xiaogen Zhou, Yiheng Zhu, P. Lydia Freddolino, Yang Zhang. Integrating deep learning potentials with I-TASSER for single- and multi-domain protein structure prediction. Submitted. 2023.