D-I-TASSER Q02218-D2

D-I-TASSER results for Q02218-D2

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

Input Sequence in FASTA format

>Q02218 (106 residues)
LSRGSLAAVAHAQSLVEAQPNVDKLVEDHLAVQSLIRAYQIRGHHVAQLDPLGILDADLD
SSVPADIISSTDKLGFYGLDESDLDKVFHLPTTTFIGGQESALPLR

Predicted Secondary Structure

Sequence	20 40 60 80 100 \| \| \| \| \| LSRGSLAAVAHAQSLVEAQPNVDKLVEDHLAVQSLIRAYQIRGHHVAQLDPLGILDADLDSSVPADIISSTDKLGFYGLDESDLDKVFHLPTTTFIGGQESALPLR
Prediction	CCCCCCCCCCCCCCCCCCCCCHHHHHHHHHHHHHHHHHHHHHCHHHHHCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCHHHCCCSSSCCCCCSCCCCCCCCCCC
Confidence	9986556556677766677642788999999999999999973355407988787665556788456861146321689978859457569863327986646789
	H:Helix; S:Strand; C:Coil

Predicted Solvent Accessibility

Sequence	20 40 60 80 100 \| \| \| \| \| LSRGSLAAVAHAQSLVEAQPNVDKLVEDHLAVQSLIRAYQIRGHHVAQLDPLGILDADLDSSVPADIISSTDKLGFYGLDESDLDKVFHLPTTTFIGGQESALPLR
Prediction	8557635544755444545453464144122023004203430122042220313456454544563437625352341345216441613543133475651648
	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

                   |                   |                   |                   |                   |

SS
Seq

CCCCCCCCCCCCCCCCCCCCCHHHHHHHHHHHHHHHHHHHHHCHHHHHCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCHHHCCCSSSCCCCCSCCCCCCCCCCC
LSRGSLAAVAHAQSLVEAQPNVDKLVEDHLAVQSLIRAYQIRGHHVAQLDPLGILDADLDSSVPADIISSTDKLGFYGLDESDLDKVFHLPTTTFIGGQESALPLR

3edvA

0.09

0.08

2.86

1.00

DEthreader

VLEAWKSLLDACESRRVRLVDTGDKFRFFSMVRDLMLWMEDVIRQIEA------QEKPLNHQGIAEID---ARNDSFTTCIELGKLLHA----------EEIEKLT

2xt6A2

0.31

0.23

6.84

2.44

SPARKS-K

------------------TDNPDSIEDKNARVIELIAAYRNRGHLMADIDPLRLDNTRFRS--HPDL-----DVNSHGLTLWDLDREFKVDG----FAGVQRKKLR

4zxjA

0.10

0.09

3.47

0.71

MapAlign

--------LVAEQAAKTPDAPASYREMREQVVALANLLREGVKDSVAVIVEAGAAWLPLARPSLLITTDSLCYNAPLPLQLSQPHHTAIIFTSGTGRPKGVMVGQT

2xt6A2

0.30

0.22

6.58

0.79

CEthreader

------------------TDNPDSIEDKNARVIELIAAYRNRGHLMADIDPLRLDNTRFRSHPD-------LDVNSHGLTLWDLDREFKVDGF----AGVQRKKLR

2xt6A

0.25

0.23

7.01

1.32

MUSTER

LLDDDFELGIPYEPVRWRTDNPDSIEDKNARVIELIAAYRNRGHLMADIDPLRLDNTRFRS-------HPDLDVNSHGLTLWDLDREFKVDGF----AGVQRKKLR

2xt6A2

0.32

0.24

7.09

2.85

HHsearch

------------------TDNPDSIEDKNARVIELIAAYRNRGHLMADIDPLRLDNTRF--RSHPDLDV-----NSHGLTLWDLDREFKVDG--FAG--VQRKKLR

2xt6A2

0.30

0.22

6.58

1.24

FFAS-3D

------------------TDNPDSIEDKNARVIELIAAYRNRGHLMADIDPLRLDNTRFRS-------HPDLDVNSHGLTLWDLDREFKVDGFA----GVQRKKLR

2rjsB2

0.08

3.00

0.67

EigenThreader

VEHADLRRELQKIFHGANFHGQPIAFAMDLTQLGVLAERQINRVLNRHLSYGLPEFLVSHSGFAGAQYPATALVAENRTIG----PASTQSPSNGDNQDVVSMGLI

2xt6A

0.30

0.20

6.01

1.08

CNFpred

-------------------------EDKNARVIELIAAYRNRGHLMADIDPLRLDNTRFR--SHPDLD-----VNSHGLTLWDLDREFKVDGFAG----VQRKKLR

6m3pA

0.08

0.07

2.59

1.00

DEthreader

VDKLYAGLKDLAEERRGKLDERHRLFQLNREVDDLEQWIAEREVVAGS------HELVLRFRFADTGNIGQERVD--TVNNMADIAATI------------AEWKN

(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	0.6415

(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	5qj2B	0.59	3.99	0.059	0.943	model1_5qj2B.pdb.gz
2	3faqA	0.58	4.23	0.058	0.962	model1_3faqA.pdb.gz
3	6ercA	0.58	3.78	0.038	0.887	model1_6ercA.pdb.gz
4	4hhrA	0.57	3.87	0.066	0.877	model1_4hhrA.pdb.gz
5	1cqeB2	0.56	3.88	0.040	0.868	model1_1cqeB2.pdb.gz
6	4kvjA2	0.56	3.96	0.075	0.877	model1_4kvjA2.pdb.gz
7	1cvuA2	0.56	3.67	0.049	0.840	model1_1cvuA2.pdb.gz
8	2bneB	0.42	4.62	0.100	0.783	model1_2bneB.pdb.gz
9	3e6sA	0.42	4.06	0.022	0.698	model1_3e6sA.pdb.gz
10	3gkaB	0.41	4.69	0.045	0.774	model1_3gkaB.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:0004591	1.00	oxoglutarate dehydrogenase (succinyl-transferring) 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:0008152	0.98	metabolic process
GO:0044699	0.97	single-organism process
GO:0044237	0.97	cellular metabolic process
GO:0044281	0.95	small molecule metabolic process
GO:0071704	0.94	organic substance metabolic process
GO:0044763	0.94	single-organism cellular process
GO:0044238	0.93	primary metabolic process
GO:0006082	0.92	organic acid metabolic process
GO:0006099	0.90	tricarboxylic acid cycle

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:0044444	0.99	cytoplasmic part
GO:0043226	0.93	organelle
GO:0043229	0.92	intracellular organelle
GO:0043227	0.92	membrane-bounded organelle
GO:0043234	0.91	protein complex
GO:0043231	0.91	intracellular membrane-bounded organelle
GO:0005829	0.90	cytosol
GO:0005739	0.90	mitochondrion
GO:0045252	0.89	oxoglutarate dehydrogenase complex
GO:0044422	0.52	organelle part
GO:0044446	0.51	intracellular 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	0.060	2e9eA	0.546	4.18	0.060	0.896	1.11.1.7	NA
2	0.060	2iz1B	0.529	4.37	0.093	0.896	1.1.1.44	NA
3	0.060	1y791	0.534	4.14	0.088	0.849	3.4.15.5	NA
4	0.060	1eulA	0.531	3.87	0.040	0.840	3.6.3.8	NA
5	0.060	2p4qA	0.534	4.43	0.093	0.896	1.1.1.44	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	0.15	1mypD	0.589	4.24	0.068	0.962	0.15	HEM	complex1.pdb.gz	36,39,40,44,95
2	0.02	2o86A	0.549	4.00	0.112	0.877	0.10	HEM	complex2.pdb.gz	40,43,44
3	0.01	1ht5B	0.569	3.51	0.031	0.840	0.19	HEM	complex3.pdb.gz	40,41,44,45
4	0.01	2gj1A	0.518	4.42	0.067	0.953	0.16	UUU	complex4.pdb.gz	35,38,40,43,44,47,64,67
5	0.01	2qqtA	0.521	4.48	0.086	0.962	0.11	AIN	complex5.pdb.gz	43,50,51,52
6	0.01	2oyeP	0.565	3.57	0.031	0.840	0.11	IM8	complex6.pdb.gz	43,46,47
7	0.01	3zs0C	0.593	4.16	0.067	0.962	0.12	UUU	complex7.pdb.gz	35,39,40,43,44,47

	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.