D-I-TASSER Q9BXF3-D8

D-I-TASSER results for Q9BXF3-D8

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

Input Sequence in FASTA format

>Q9BXF3 (80 residues)
YLYGTPPPLSSGMGFGSSAFPPHSVMLQTGPPYTPQRPASHFQPRAYSSPVAALPPHHPG
ATQPNGLSQEGPIYRCQEEG

Predicted Secondary Structure

Sequence	20 40 60 80 \| \| \| \| YLYGTPPPLSSGMGFGSSAFPPHSVMLQTGPPYTPQRPASHFQPRAYSSPVAALPPHHPGATQPNGLSQEGPIYRCQEEG
Prediction	CCCCCCCCCCCCCCCCCCCCCCCCSSCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCSSSCCCCC
Confidence	98789998878877788888986235147999998887555788677888777899998888988878888625404589
	H:Helix; S:Strand; C:Coil

Predicted Solvent Accessibility

Sequence	20 40 60 80 \| \| \| \| YLYGTPPPLSSGMGFGSSAFPPHSVMLQTGPPYTPQRPASHFQPRAYSSPVAALPPHHPGATQPNGLSQEGPIYRCQEEG
Prediction	74444444345434234642443223143445344744464154442544345334744445546424771322415788
	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

                   |                   |                   |                   |

SS
Seq

CCCCCCCCCCCCCCCCCCCCCCCCSSCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCSSSCCCCC
YLYGTPPPLSSGMGFGSSAFPPHSVMLQTGPPYTPQRPASHFQPRAYSSPVAALPPHHPGATQPNGLSQEGPIYRCQEEG

4m4dA1

0.07

3.02

0.54

CEthreader

ELRGSSLKLLPGQGLSLAISDSSIGVGKWKVRKSFLKLHGSFDLDVKGVTISVDLLRPTVSASGCSSRICDLDVHISGNV

6lkgA1

0.06

2.69

0.55

EigenThreader

NVLTVYSPYQSNLIRPILNEFEKIEIKSTQVLLSNLHNESERGDGVLSETIYQDQQLEDYRSNNKYVTSFVDGIALVKNA

2ftcN

0.14

4.67

0.45

FFAS-3D

---GDTVEILEGKDAGKQVIRQRNWVVVGGLNTHYRYKTMDYRGTMIPSEAPLLHRQDPMDRKPTEIEEAGERVRSTRSG

3bogA

0.11

0.10

3.64

1.37

SPARKS-K

GAHGVGCPGTAGAAGSVGGPGCDGGHGGNGGNGNPGCAGGVGGAGGASGGTGVGGRGGKGGSGTPKGADGAPGAP-----

5imtA

0.05

0.01

0.57

0.42

CNFpred

-------------------------------------------------------------SSREAFHRPGEYVVIEKKK

3w0fA

0.03

1.54

0.83

DEthreader

EGPTLGEFSSQQRV-RV-MEEDCSPFSFAEVLCDVLQRV--LPGVGIKNEALFSGL-QLS-D----QACHLMTFSFYCC-

6w09E1

0.03

1.52

0.87

MapAlign

VSLQIGIKTDDSHDWTKLRYMDNHMPA---------DAERARLFVRTSAPCTITGTMGHFILARCPKGETLTVGFTD---

5w3nA

0.16

0.12

4.14

0.88

MUSTER

-SYSGYSQSTDTSGYGQSSYSSYGQSQNTGYG-TQSTPQGYGSTGGYGSSQSSQSSYGQQSSY-----------------

2aklA

0.17

0.06

2.05

0.46

HHsearch

--------------------------------------------------MVSTLPPCPQCNSEYTYE-DGALLVCPECA

3kfuF1

0.05

2.35

0.48

CEthreader

LVFHRKNYFYPDLPKNYQISQYDLPLGRGGSLPLGERRVRIKRLHLEEDAGKSLHLEGRTLLDLNRAGSPLIELVTEPDL

(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	0.5882

(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	2artA	0.46	4.38	0.027	0.887	model1_2artA.pdb.gz
2	1oheA	0.46	3.77	0.043	0.875	model1_1oheA.pdb.gz
3	6ck0A	0.44	4.30	0.014	0.887	model1_6ck0A.pdb.gz
4	6s87D	0.44	3.65	0.027	0.775	model1_6s87D.pdb.gz
5	7juyB	0.44	3.90	0.014	0.787	model1_7juyB.pdb.gz
6	1lufA	0.44	4.18	0.028	0.838	model1_1lufA.pdb.gz
7	2c6xA	0.44	3.82	0.026	0.800	model1_2c6xA.pdb.gz
8	3igoA	0.44	3.97	0.028	0.825	model1_3igoA.pdb.gz
9	3ky2A2	0.43	3.99	0.043	0.800	model1_3ky2A2.pdb.gz
10	2ifcC1	0.43	3.62	0.026	0.787	model1_2ifcC1.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:1901363	0.49	heterocyclic compound binding
GO:0097159	0.49	organic cyclic compound binding
GO:0003676	0.37	nucleic acid binding
GO:0003677	0.30	DNA 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:0097194	1.00	execution phase of apoptosis
GO:0043044	1.00	ATP-dependent chromatin remodeling
GO:0032502	0.79	developmental process
GO:0048856	0.78	anatomical structure development
GO:0044767	0.78	single-organism developmental process
GO:0090102	0.77	cochlea development
GO:0060122	0.77	inner ear receptor stereocilium organization
GO:0021915	0.77	neural tube development
GO:0007338	0.77	single fertilization
GO:0001843	0.77	neural tube closure
GO:0001842	0.77	neural fold formation
GO:0008152	0.62	metabolic process
GO:0071704	0.61	organic substance metabolic process
GO:0044238	0.60	primary metabolic process
GO:0044237	0.60	cellular metabolic process
GO:0044260	0.59	cellular macromolecule metabolic process
GO:0006139	0.55	nucleobase-containing compound metabolic process
GO:0090304	0.54	nucleic acid 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:0090537	1.00	CERF complex
GO:0005634	1.00	nucleus
GO:0000785	0.78	chromatin
GO:0005719	0.77	nuclear euchromatin

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	2weiA	0.418	4.23	0.025	0.825	2.7.1.17	NA
2	0.060	2wzjD	0.401	4.36	0.056	0.838	2.7.11.1	NA
3	0.060	3db8A	0.310	4.45	0.050	0.650	2.7.11.21	9,19,25
4	0.060	1a25A	0.301	4.43	0.000	0.600	2.7.11.13	NA
5	0.060	2x4fA	0.424	3.96	0.029	0.825	2.7.11.1	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	2r26C	0.347	4.08	0.050	0.637	0.26	CMC	complex1.pdb.gz	13,15,16,17,18,72,73
2	0.01	2dxu0	0.418	4.26	0.058	0.850	0.26	III	complex2.pdb.gz	4,27,28,29,33,70
3	0.01	1wpyA	0.432	4.00	0.088	0.775	0.22	BTN	complex3.pdb.gz	4,5,27,45
4	0.01	2e41A	0.429	4.12	0.074	0.787	0.23	BTX	complex4.pdb.gz	3,4,5,25,29,30,32,33,73,74
5	0.01	2wqbA	0.325	4.38	0.013	0.675	0.19	QQ1	complex5.pdb.gz	29,46,64,65
6	0.01	2oscA	0.433	4.31	0.069	0.838	0.14	MUH	complex6.pdb.gz	3,10,33,34
7	0.01	2artA	0.459	4.38	0.027	0.887	0.13	UUU	complex7.pdb.gz	32,37,69
8	0.01	2c6xA	0.438	3.82	0.026	0.800	0.17	COZ	complex8.pdb.gz	17,28,29,30
9	0.01	1x01A	0.416	4.53	0.085	0.863	0.24	ATP	complex9.pdb.gz	5,28,29,33,66,77
10	0.01	3igoA	0.438	3.97	0.028	0.825	0.27	ANP	complex10.pdb.gz	5,7,14,25,27,42,43

	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.