D-I-TASSER A0A0G2JMH6-D1

D-I-TASSER results for A0A0G2JMH6-D1

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

Input Sequence in FASTA format

>A0A0G2JMH6 (108 residues)
MAISGVPVLGFFIIAVLMSAQESWAIKEEHVIIQAEFYLNPDQSGEFMFDFDGDEIFHVD
MAKKETVWRLEEFGRFASFEAQGALANIAVDKANLEIMTKRSNYTPIT

Predicted Secondary Structure

Sequence	20 40 60 80 100 \| \| \| \| \| MAISGVPVLGFFIIAVLMSAQESWAIKEEHVIIQAEFYLNPDQSGEFMFDFDGDEIFHVDMAKKETVWRLEEFGRFASFEAQGALANIAVDKANLEIMTKRSNYTPIT
Prediction	CCCCHCHHHHHHHHHHHHHCCCCCSSSCCSSSSSSSSSSSCCCCCCSSSCCCCCSSSSSSCCCCSSSSSCCCCCCCCCCCCHHHHHHHHHHHHHHHHHHHHHCCCCCC
Confidence	985421899999999998413543144352575368998449997332236896389985245738885886566677680133456899999999999862799999
	H:Helix; S:Strand; C:Coil

Predicted Solvent Accessibility

Sequence	20 40 60 80 100 \| \| \| \| \| MAISGVPVLGFFIIAVLMSAQESWAIKEEHVIIQAEFYLNPDQSGEFMFDFDGDEIFHVDMAKKETVWRLEEFGRFASFEAQGALANIAVDKANLEIMTKRSNYTPIT
Prediction	744441313123221101023435324443232213122344454423351554331222165553213134135346142231144133044104100432643658
	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

CCCCHCHHHHHHHHHHHHHCCCCCSSSCCSSSSSSSSSSSCCCCCCSSSCCCCCSSSSSSCCCCSSSSSCCCCCCCCCCCCHHHHHHHHHHHHHHHHHHHHHCCCCCC
MAISGVPVLGFFIIAVLMSAQESWAIKEEHVIIQAEFYLNPDQSGEFMFDFDGDEIFHVDMAKKETVWRLEEFGRFASFEAQGALANIAVDKANLEIMTKRSNYTPIT

3p73A

0.10

0.07

2.78

0.83

DEthreader

-----------------LPERYNKSKSHT-MQ-MMFGCDILDGSIRGYDQYAFDFLAFDMD--TMTFTAADPVEIKRWEYAERWKHELTVCVQNLRRYLEHGKLK---

1ymmA1

1.00

0.74

20.74

3.14

SPARKS-K

--------------------------KEEHVIIQAEFYLNPDQSGEFMFDFDGDEIFHVDMAKKETVWRLEEFGRFASFEAQGALANIAVDKANLEIMTKRSNYTP--

3d2uE1

0.07

0.06

2.67

0.55

MapAlign

GERAKGDLIFNQTEQNLLELEIALGY--RSQSVLTWTHECNTTAGYEGFGWDGETLMELKL--TLWTGPLKQQKTYIDGKITIQRNYLKNCTQWSVIYSGFQP-----

1kcgC

0.09

3.50

0.49

CEthreader

LYATDAWGKQLEMLREVGQRLRLELADTEPLTLQVRMSCECEIRGSWQFSFDGRKFLLFDSNNRKWTVVHAGARRMKEKDSGLTTFFKMVSMRDCKSWLRDFLMHRKK

1ymmA1

1.00

0.74

20.74

2.48

MUSTER

--------------------------KEEHVIIQAEFYLNPDQSGEFMFDFDGDEIFHVDMAKKETVWRLEEFGRFASFEAQGALANIAVDKANLEIMTKRSNYTP--

3lqzA1

0.57

0.43

12.25

3.67

HHsearch

-------------------------IKADHVSTYAAFVQTHRPTGEFMFEFDEDEMFYVDLDKKETVWHLEEFGQAFSFEAQGGLANIAILNNNLNTLIQRSNHTQ--

3lqzA1

0.57

0.43

12.25

1.87

FFAS-3D

-------------------------IKADHVSTYAAFVQTHRPTGEFMFEFDEDEMFYVDLDKKETVWHLEEFGQAFSFEAQGGLANIAILNNNLNTLIQRSNHTQ--

5gjxA1

0.06

2.50

0.75

EigenThreader

VDQQYWDRETETSRGNEQIFRVNLDTARRGSHTWQCMHGCGSIRGFQQCGYDGKDFIALDKDTLTYTAADAAAQITKRKWEQEGKNYLENCIEWLRKYVSYGKDVLER

3l6fA

1.00

0.75

21.00

1.01

CNFpred

---------------------------EEHVIIQAEFYLNPDQSGEFMFDFDGDEIFHVDMAKKETVWRLEEFGRFASFEAQGALANIAVDKANLEIMTKRSNYTPIT

2qriA3

0.10

0.08

3.07

0.83

DEthreader

-------------GGGGLLGYYNQSKGSHTIQ-VISGCEVG-RLLRGYQQYAYDYIALNED--LKTWTAADMAALITKWEAERLRAYLGTCVEWLRRYLKNGNALL--

(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	0.5854

(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	3p73A	0.63	3.65	0.093	0.991	model1_3p73A.pdb.gz
2	1je6A	0.62	3.74	0.084	0.982	model1_1je6A.pdb.gz
3	1mhcA1	0.61	3.52	0.099	0.935	model1_1mhcA1.pdb.gz
4	1kcgC	0.61	3.74	0.056	0.963	model1_1kcgC.pdb.gz
5	6xqpC	0.61	3.46	0.088	0.944	model1_6xqpC.pdb.gz
6	3bevA	0.61	3.28	0.108	0.935	model1_3bevA.pdb.gz
7	5gjxA	0.61	3.51	0.097	0.954	model1_5gjxA.pdb.gz
8	1d9kC	0.61	2.50	0.530	0.750	model1_1d9kC.pdb.gz
9	6v7yA	0.61	3.53	0.069	0.935	model1_6v7yA.pdb.gz
10	6a2bA	0.61	3.96	0.102	1.000	model1_6a2bA.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:0003823	0.91	antigen binding
GO:0042605	0.69	peptide antigen 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:0002682	1.00	regulation of immune system process
GO:0050794	0.96	regulation of cellular process
GO:0002376	0.96	immune system process
GO:0050863	0.95	regulation of T cell activation
GO:0002495	0.95	antigen processing and presentation of peptide antigen via MHC class II
GO:0019886	0.94	antigen processing and presentation of exogenous peptide antigen via MHC class II
GO:0002684	0.77	positive regulation of immune system process
GO:0050870	0.76	positive regulation of T cell activation
GO:0051239	0.69	regulation of multicellular organismal process
GO:0045619	0.63	regulation of lymphocyte differentiation
GO:0045580	0.62	regulation of T cell differentiation
GO:0051240	0.53	positive regulation of multicellular organismal process
GO:0009987	0.50	cellular 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:0044459	1.00	plasma membrane part
GO:0043234	0.96	protein complex
GO:0042613	0.95	MHC class II protein complex
GO:0044424	0.93	intracellular part
GO:0044444	0.90	cytoplasmic part
GO:0016020	0.89	membrane
GO:0005886	0.86	plasma membrane
GO:0043226	0.75	organelle
GO:0043227	0.74	membrane-bounded organelle
GO:0043229	0.72	intracellular organelle
GO:0043231	0.70	intracellular membrane-bounded organelle
GO:0005773	0.67	vacuole
GO:0005764	0.63	lysosome

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	2iamA	0.594	2.37	0.988	0.741	5.3.1.1	9,39,55
2	0.060	3n2oA	0.517	4.52	0.038	0.907	4.1.1.19	45,71
3	0.060	1bdgA	0.493	3.95	0.034	0.796	2.7.1.1	NA
4	0.060	3daxA	0.501	3.97	0.040	0.796	1.14.13.17	NA
5	0.060	1e27A	0.607	3.92	0.093	0.982	3.1.26.4	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	0.32	1d9kC	0.610	2.50	0.530	0.750	0.63	III	complex1.pdb.gz	49,76,77,78,79,87,90,91,93,94,97,101
2	0.08	1jl42	0.602	2.32	0.557	0.732	0.62	III	complex2.pdb.gz	30,31,32,33,36,37,38,51,52,53,54,55,56,69,70,73,77,87,95,98,99,101,102,104,105,106
3	0.01	1n361	0.206	4.45	0.020	0.370	0.51	III	complex3.pdb.gz	51,74,75,76,77,79

	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.