D-I-TASSER Q9H7Z6-D1

D-I-TASSER results for Q9H7Z6-D1

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

Input Sequence in FASTA format

>Q9H7Z6 (233 residues)
MAAQGAAAAVAAGTSGVAGEGEPGPGENAAAEGTAPSPGRVSPPTPARGEPEVTVEIGET
YLCRRPDSTWHSAEVIQSRVNDQEGREEFYVHYVGFNRRLDEWVDKNRLALTKTVKDAVQ
KNSEKYLSELAEQPERKITRNQKRKHDEINHVQKTYAEMDPTTAALEKEHEAITKVKYVD
KIHIGNYEIDAWYFSPFPEDYGKQPKLWLCEYCLKYMKYEKSYRFHLGQCQWR

Predicted Secondary Structure

Sequence	20 40 60 80 100 120 140 160 180 200 220 \| \| \| \| \| \| \| \| \| \| \| MAAQGAAAAVAAGTSGVAGEGEPGPGENAAAEGTAPSPGRVSPPTPARGEPEVTVEIGETYLCRRPDSTWHSAEVIQSRVNDQEGREEFYVHYVGFNRRLDEWVDKNRLALTKTVKDAVQKNSEKYLSELAEQPERKITRNQKRKHDEINHVQKTYAEMDPTTAALEKEHEAITKVKYVDKIHIGNYEIDAWYFSPFPEDYGKQPKLWLCEYCLKYMKYEKSYRFHLGQCQWR
Prediction	CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCSCCCCSSSSSSCCCCSSSSSSSSSSSCCCCCCSSSSSSCCCCCCCCCCCCCHHHCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCHHHCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCSSSSCCSSSSCCCCCCCCHHHCCCCSSSSSCCCHHHHCCHHHHHHHHHHCCCC
Confidence	99777876666777888877888988777667788777666788877776543311681999991799675579999763378896589998167665422023502111112333332233321121234543321112322211000001122111122212101222222334543147627777500316876355436983899535332328999999999977899
	H:Helix; S:Strand; C:Coil

Predicted Solvent Accessibility

Sequence	20 40 60 80 100 120 140 160 180 200 220 \| \| \| \| \| \| \| \| \| \| \| MAAQGAAAAVAAGTSGVAGEGEPGPGENAAAEGTAPSPGRVSPPTPARGEPEVTVEIGETYLCRRPDSTWHSAEVIQSRVNDQEGREEFYVHYVGFNRRLDEWVDKNRLALTKTVKDAVQKNSEKYLSELAEQPERKITRNQKRKHDEINHVQKTYAEMDPTTAALEKEHEAITKVKYVDKIHIGNYEIDAWYFSPFPEDYGKQPKLWLCEYCLKYMKYEKSYRFHLGQCQWR
Prediction	74566455546645554556454555655555555565565555465554452304212301032676541403013223556844320000034224321311447344334344434444455344443545435435434454444444444443444434434344443434434421302413040002000344146231000010003004345004203640738
	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                 200                 220

                   |                   |                   |                   |                   |                   |                   |                   |                   |                   |                   |

SS
Seq

CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCSCCCCSSSSSSCCCCSSSSSSSSSSSCCCCCCSSSSSSCCCCCCCCCCCCCHHHCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCHHHCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCSSSSCCSSSSCCCCCCCCHHHCCCCSSSSSCCCHHHHCCHHHHHHHHHHCCCC
MAAQGAAAAVAAGTSGVAGEGEPGPGENAAAEGTAPSPGRVSPPTPARGEPEVTVEIGETYLCRRPDSTWHSAEVIQSRVNDQEGREEFYVHYVGFNRRLDEWVDKNRLALTKTVKDAVQKNSEKYLSELAEQPERKITRNQKRKHDEINHVQKTYAEMDPTTAALEKEHEAITKVKYVDKIHIGNYEIDAWYFSPFPEDYGKQPKLWLCEYCLKYMKYEKSYRFHLGQCQWR

1wgsA

0.92

0.52

14.58

1.17

FFAS-3D

-------------------------------------------SSGSSGEPEVTVEIGETYLCRRPDSTWHSAEVIQSRVNDQEGREEFYVHYVGFNRRLDEWVDKNRLALTKTVKDAVQKNSEKYLSELAEQPERKITRNQKRKHDEINHVQKTYAEMDPTTAALEKESGPSS-----------------------------------------------------------

2ou2A

0.40

0.10

2.91

1.72

SPARKS-K

--------------------------------------------------------------------------------------------------------------------------------------------------------------------------------KNIECIELGRHRLKPWYFSPYPQELTTLPVLYLCEFCLKYGRSLKCLQRHLTKCDLR

1wgsA

0.91

0.52

14.59

2.86

CNFpred

------------------------------------------GSSGSSGEPEVTVEIGETYLCRRPDSTWHSAEVIQSRVNDQEGREEFYVHYVGFNRRLDEWVDKNRLALTKTVKDAVQKNSEKYLSELAEQPERKITRNQKRKHDEINHVQKTYAEMDPTTAALEKESGPSSG----------------------------------------------------------

1wgsA

0.91

0.52

14.59

1.44

MUSTER

------------------------------------------GSSGSSGEPEVTVEIGETYLCRRPDSTWHSAEVIQSRVNDQEGREEFYVHYVGFNRRLDEWVDKNRLALTKTVKDAVQKNSEKYLSELAEQPERKITRNQKRKHDEINHVQKTYAEMDPTTAALEKESGPSSG----------------------------------------------------------

1wgsA

0.91

0.52

14.59

3.30

HHsearch

------------------------------------------GSSGSSGEPEVTVEIGETYLCRRPDSTWHSAEVIQSRVNDQEGREEFYVHYVGFNRRLDEWVDKNRLALTKTVKDAVQKNSEKYLSELAEQPERKITRNQKRKHDEINHVQKTYAEMDPTTAALEKESGPSSG----------------------------------------------------------

2pq8A

1.00

0.24

6.85

1.72

SPARKS-K

--------------------------------------------------------------------------------------------------------------------------------------------------------------------------------KYVDKIHIGNYEIDAWYFSPFPEDYGKQPKLWLCEYCLKYMKYEKSYRFHLGQCQWR

2y0mA

1.00

0.24

6.85

1.95

CNFpred

--------------------------------------------------------------------------------------------------------------------------------------------------------------------------------KYVDKIHIGNYEIDAWYFSPFPEDYGKQPKLWLCEYCLKYMKYEKSYRFHLGQCQWR

1fy7A

0.30

0.08

2.34

3.03

HHsearch

-----------------------------------------------------------------------------------------------------------------------------------------------------------------------------ARVRNLNRIIMGKYEIEPWYFSPYPIELTDEDFIYIDDFTLQYFGSKKQYERYRKKCTLR

1wgsA

0.91

0.52

14.59

1.68

SPARKS-K

------------------------------------------GSSGSSGEPEVTVEIGETYLCRRPDSTWHSAEVIQSRVNDQEGREEFYVHYVGFNRRLDEWVDKNRLALTKTVKDAVQKNSEKYLSELAEQPERKITRNQKRKHDEINHVQKTYAEMDPTTAALEKESGPSSG----------------------------------------------------------

2pq8A

1.00

0.24

6.85

1.92

CNFpred

--------------------------------------------------------------------------------------------------------------------------------------------------------------------------------KYVDKIHIGNYEIDAWYFSPFPEDYGKQPKLWLCEYCLKYMKYEKSYRFHLGQCQWR

(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	0.5584

(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	5xjcA	0.47	5.34	0.050	0.768	model1_5xjcA.pdb.gz
2	3jb9A1	0.47	5.51	0.049	0.777	model1_3jb9A1.pdb.gz
3	7aavA	0.43	5.57	0.041	0.730	model1_7aavA.pdb.gz
4	6kldA	0.43	5.54	0.029	0.700	model1_6kldA.pdb.gz
5	5ifeA	0.42	5.81	0.049	0.725	model1_5ifeA.pdb.gz
6	6y6kA	0.42	5.70	0.031	0.682	model1_6y6kA.pdb.gz
7	5x7oA	0.42	6.18	0.041	0.760	model1_5x7oA.pdb.gz
8	5t8vA	0.41	5.59	0.043	0.682	model1_5t8vA.pdb.gz
9	4a2lA	0.41	5.97	0.056	0.712	model1_4a2lA.pdb.gz
10	6rc9A1	0.41	5.99	0.036	0.712	model1_6rc9A1.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:0004402	0.95	histone acetyltransferase activity
GO:0010485	0.60	H4 histone acetyltransferase 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	1.00	cellular process
GO:0044260	0.96	cellular macromolecule metabolic process
GO:0044238	0.96	primary metabolic process
GO:0065007	0.89	biological regulation
GO:0050789	0.89	regulation of biological process
GO:0016043	0.87	cellular component organization
GO:0006325	0.86	chromatin organization
GO:0016570	0.85	histone modification
GO:0018193	0.84	peptidyl-amino acid modification
GO:0050794	0.83	regulation of cellular process
GO:0016573	0.83	histone acetylation
GO:0019222	0.82	regulation of metabolic process
GO:0060255	0.81	regulation of macromolecule metabolic process
GO:0031326	0.79	regulation of cellular biosynthetic process
GO:0019219	0.79	regulation of nucleobase-containing compound metabolic process
GO:0010556	0.79	regulation of macromolecule biosynthetic process
GO:2000112	0.78	regulation of cellular macromolecule biosynthetic process
GO:0010468	0.78	regulation of gene expression
GO:0006355	0.76	regulation of transcription, DNA-templated
GO:0048518	0.74	positive regulation of biological process
GO:0048522	0.67	positive regulation of cellular process
GO:0045935	0.64	positive regulation of nucleobase-containing compound metabolic process
GO:0010604	0.64	positive regulation of macromolecule metabolic process
GO:0045893	0.63	positive regulation of transcription, DNA-templated
GO:0044699	0.61	single-organism process
GO:0048519	0.60	negative regulation of biological process
GO:0048523	0.59	negative regulation of cellular process
GO:0043967	0.58	histone H4 acetylation
GO:0044763	0.56	single-organism cellular process
GO:0006807	0.53	nitrogen compound metabolic process
GO:0090304	0.52	nucleic acid metabolic process
GO:2000113	0.50	negative regulation of cellular macromolecule biosynthetic process
GO:0051172	0.50	negative regulation of nitrogen compound 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:0044446	0.88	intracellular organelle part
GO:0044428	0.87	nuclear part
GO:0043229	0.86	intracellular organelle
GO:0043227	0.82	membrane-bounded organelle
GO:0043231	0.81	intracellular membrane-bounded organelle
GO:0032991	0.80	macromolecular complex
GO:0005634	0.80	nucleus
GO:0043234	0.76	protein complex
GO:0044451	0.74	nucleoplasm part
GO:1990234	0.73	transferase complex
GO:0000123	0.71	histone acetyltransferase complex

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	2vz9B	0.364	6.21	0.076	0.669	2.3.1.85	NA
2	0.060	2vz8A	0.356	6.04	0.057	0.631	2.3.1.85	NA
3	0.060	1uyvA	0.254	6.49	0.030	0.481	6.3.4.14 6.4.1.2	NA
4	0.060	2eabA	0.360	5.66	0.024	0.597	3.2.1.63	NA
5	0.060	1t3tA	0.376	6.73	0.027	0.734	6.3.5.3	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	1ce8G	0.384	6.37	0.027	0.712	0.15	IMP	complex1.pdb.gz	76,93,94
2	0.01	1ce8E	0.385	6.09	0.037	0.678	0.24	ADP	complex2.pdb.gz	63,73,74
3	0.01	1bxrA	0.382	6.45	0.039	0.717	0.10	ANP	complex3.pdb.gz	58,59,63,73,74
4	0.01	3cf4A	0.383	5.59	0.066	0.618	0.30	SF4	complex4.pdb.gz	213,223,224,225,227,228
5	0.01	1a9xG	0.375	6.67	0.059	0.734	0.24	ADP	complex5.pdb.gz	58,59,73,74,94,95,96
6	0.01	3cf4A	0.383	5.59	0.066	0.618	0.39	SF4	complex6.pdb.gz	58,60,74,75,91,93
7	0.01	1ahpA	0.329	6.50	0.047	0.627	0.13	PLP	complex7.pdb.gz	75,95,96
8	0.01	2ecpA	0.383	6.45	0.036	0.704	0.14	PLP	complex8.pdb.gz	184,203,218
9	0.01	1a9x2	0.383	6.47	0.050	0.721	0.32	III	complex9.pdb.gz	59,62,95
10	0.01	1jdbB	0.374	6.40	0.050	0.712	0.23	GLN	complex10.pdb.gz	59,60,61,91

	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.