D-I-TASSER Q07817-D1

D-I-TASSER results for Q07817-D1

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

Input Sequence in FASTA format

>Q07817 (233 residues)
MSQSNRELVVDFLSYKLSQKGYSWSQFSDVEENRTEAPEGTESEMETPSAINGNPSWHLA
DSPAVNGATGHSSSLDAREVIPMAAVKQALREAGDEFELRYRRAFSDLTSQLHITPGTAY
QSFEQVVNELFRDGVNWGRIVAFFSFGGALCVESVDKEMQVLVSRIAAWMATYLNDHLEP
WIQENGGWDTFVELYGNNAAAESRKGQERFNRWFLTGMTVAGVVLLGSLFSRK

Predicted Secondary Structure

Sequence	20 40 60 80 100 120 140 160 180 200 220 \| \| \| \| \| \| \| \| \| \| \| MSQSNRELVVDFLSYKLSQKGYSWSQFSDVEENRTEAPEGTESEMETPSAINGNPSWHLADSPAVNGATGHSSSLDAREVIPMAAVKQALREAGDEFELRYRRAFSDLTSQLHITPGTAYQSFEQVVNELFRDGVNWGRIVAFFSFGGALCVESVDKEMQVLVSRIAAWMATYLNDHLEPWIQENGGWDTFVELYGNNAAAESRKGQERFNRWFLTGMTVAGVVLLGSLFSRK
Prediction	CCCCHHHHHHHHHHHHHHCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHCCCCCCHHHHHHHHHHHHHCCCCCHHHHHHHHHHHHHHHHHHHHHCCHHHHHHHHHHHHHHHHHHHHHHHHHCCCHHHHHHHHCCCCCCCCCCCCHHHHHHHHHHHHHHHHHHHHHHHSSC
Confidence	99617889999998874048987777766556778899864212255201036621101344333567765566666666656999999999999999996899999999837998728999999999993279978999999999999999999958868999999999999999899999981887899999555321122232136689999999999999999862119
	H:Helix; S:Strand; C:Coil

Predicted Solvent Accessibility

Sequence	20 40 60 80 100 120 140 160 180 200 220 \| \| \| \| \| \| \| \| \| \| \| MSQSNRELVVDFLSYKLSQKGYSWSQFSDVEENRTEAPEGTESEMETPSAINGNPSWHLADSPAVNGATGHSSSLDAREVIPMAAVKQALREAGDEFELRYRRAFSDLTSQLHITPGTAYQSFEQVVNELFRDGVNWGRIVAFFSFGGALCVESVDKEMQVLVSRIAAWMATYLNDHLEPWIQENGGWDTFVELYGNNAAAESRKGQERFNRWFLTGMTVAGVVLLGSLFSRK
Prediction	85552240023004320244614164354655446644554444453442345424443454544654455545464644432440150035005302531554144005404145730241022003200544021010000000002002201656246104300400040035403530474400320152135544454454443331121112133233322110034
	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                 120                 140                 160                 180                 200                 220

                   |                   |                   |                   |                   |                   |                   |                   |                   |                   |                   |

SS
Seq

CCCCHHHHHHHHHHHHHHCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHCCCCCCHHHHHHHHHHHHHCCCCCHHHHHHHHHHHHHHHHHHHHHCCHHHHHHHHHHHHHHHHHHHHHHHHHCCCHHHHHHHHCCCCCCCCCCCCHHHHHHHHHHHHHHHHHHHHHHHSSC
MSQSNRELVVDFLSYKLSQKGYSWSQFSDVEENRTEAPEGTESEMETPSAINGNPSWHLADSPAVNGATGHSSSLDAREVIPMAAVKQALREAGDEFELRYRRAFSDLTSQLHITPGTAYQSFEQVVNELFRDGVNWGRIVAFFSFGGALCVESVDKEMQVLVSRIAAWMATYLNDHLEPWIQENGGWDTFVELYGNNAAAESRKGQERFNRWFLTGMTVAGVVLLGSLFSRK

1lxlA

0.90

0.69

19.30

1.00

DEthreader

MSQSNRELVVDFLSYKLSQKGYSWSQFSDVEEN-RTEAP------------------------------------DAREVIPMAAVKQALREAGDEFELRYRRAFSDLTSQLHITPGTAYQSFEQVVNELFRDGVNWGRIVAFFSFGGALCVESVDKEMQVLVSRIAAWMATYLNDHLEPWIQENGGWDTFVELYGN-AA-ESR-KGQERLEHHH--HH--H-----------

1lxlA

0.96

0.90

25.15

2.12

SPARKS-K

MSQSNRELVVDFLSYKLSQKGYSWSQFSDVEENRTEAPEGTESEMETPSAINGNPSWHLADSPAVNGATGHSSSLDAREVIPMAAVKQALREAGDEFELRYRRAFSDLTSQLHITPGTAYQSFEQVVNELFRDGVNWGRIVAFFSFGGALCVESVDKEMQVLVSRIAAWMATYLNDHLEPWIQENGGWDTFVELYGNNAAAESRKGQERLEHHHHHH----------------

1lxlA

1.00

0.89

24.88

1.16

MapAlign

MSQSNRELVVDFLSYKLSQKGYSWSQFSDVEENRTEAPEGTESEMETPSAINGNPSWHLADSPAVNGATGHSSSLDAREVIPMAAVKQALREAGDEFELRYRRAFSDLTSQLHITPGTAYQSFEQVVNELFRDGVNWGRIVAFFSFGGALCVESVDKEMQVLVSRIAAWMATYLNDHLEPWIQENGGWDTFVELYGNNAAAESRKGQ--------------------------

1lxlA

0.96

0.90

25.15

0.90

CEthreader

MSQSNRELVVDFLSYKLSQKGYSWSQFSDVEENRTEAPEGTESEMETPSAINGNPSWHLADSPAVNGATGHSSSLDAREVIPMAAVKQALREAGDEFELRYRRAFSDLTSQLHITPGTAYQSFEQVVNELFRDGVNWGRIVAFFSFGGALCVESVDKEMQVLVSRIAAWMATYLNDHLEPWIQENGGWDTFVELYGNNAAAESRKGQERLEHHHHHH----------------

1lxlA

0.99

0.90

25.13

1.93

MUSTER

MSQSNRELVVDFLSYKLSQKGYSWSQFSDVEENRTEAPEGTESEMETPSAINGNPSWHLADSPAVNGATGHSSSLDAREVIPMAAVKQALREAGDEFELRYRRAFSDLTSQLHITPGTAYQSFEQVVNELFRDGVNWGRIVAFFSFGGALCVESVDKEMQVLVSRIAAWMATYLNDHLEPWIQENGGWDTFVELYGNNAAAESRKGQERLEH---------------------

1lxlA

0.96

0.90

25.15

3.22

HHsearch

MSQSNRELVVDFLSYKLSQKGYSWSQFSDVEENRTEAPEGTESEMETPSAINGNPSWHLADSPAVNGATGHSSSLDAREVIPMAAVKQALREAGDEFELRYRRAFSDLTSQLHITPGTAYQSFEQVVNELFRDGVNWGRIVAFFSFGGALCVESVDKEMQVLVSRIAAWMATYLNDHLEPWIQENGGWDTFVELYGNNAAAESRKGQERLEHHHHHH----------------

1lxlA

1.00

0.90

25.12

2.41

FFAS-3D

MSQSNRELVVDFLSYKLSQKGYSWSQFSDVEENRTEAPEGTESEMETPSAINGNPSWHLADSPAVNGATGHSSSLDAREVIPMAAVKQALREAGDEFELRYRRAFSDLTSQLHITPGTAYQSFEQVVNELFRDGVNWGRIVAFFSFGGALCVESVDKEMQVLVSRIAAWMATYLNDHLEPWIQENGGWDTFVELYGNNAAAESRKGQER------------------------

1lxlA

1.00

0.89

25.00

1.70

EigenThreader

MSQSNRELVVDFLSYKLSQKGYSWSQFSDVEENRTEAPEGTESEMETPSAINGNPSWHLADSPAVNGATGHSSSLDAREVIPMAAVKQALREAGDEFELRYRRAFSDLTSQLHITPGTAYQSFEQVVNELFRDGVNWGRIVAFFSFGGALCVESVDKEMQVLVSRIAAWMATYLNDHLEPWIQENGGWDTFVELYGNNAAAESRKGQEH------------------------

2lp8A

0.97

0.70

19.73

1.21

CNFpred

MSQSNRELVVDFLSYKLSQKGYSWSQFSDVEENRTEAP----------------------------------------EGTESEAVKQALREAGDEFELRYRRAFSDLTSQLHITPGTAYQSFEQVVNELFRDGVNWGRIVAFFSFGGALCVESVDKEMQVLVSRIAAWMATYLNDHLEPWIQENGGWDTFVELYGNNAAAESRKGQER------------------------

1g5mA

0.56

0.38

10.87

1.00

DEthreader

TGYDNREIVMKYIHYKLSQRGYEWDAGDD-VE--E-------------------------------------RTEAPEG-TESEVVHLALRQAGDDFSRRYRGDFAEMSSQLHLTPFTARGRFATVVEELFRDGVNWGRIVAFFEFGGVMCVESVNREMSPLVDNIALWMTEYLNRHLHTWIQDNGGWDAFVELYG--PS---------------------------------

(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	0.6911

(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	1lxlA	0.85	1.76	0.963	0.910	model1_1lxlA.pdb.gz
2	1g5mA	0.61	2.29	0.556	0.669	model1_1g5mA.pdb.gz
3	1o0lA	0.58	3.14	0.451	0.687	model1_1o0lA.pdb.gz
4	2a5yA	0.57	3.20	0.189	0.674	model1_2a5yA.pdb.gz
5	3qbrA	0.56	2.57	0.204	0.644	model1_3qbrA.pdb.gz
6	1wsxA	0.56	2.54	0.230	0.635	model1_1wsxA.pdb.gz
7	1f16A	0.54	3.56	0.195	0.674	model1_1f16A.pdb.gz
8	2vohA	0.51	2.64	0.236	0.588	model1_2vohA.pdb.gz
9	2imsA	0.50	2.79	0.221	0.588	model1_2imsA.pdb.gz
10	4b4sA	0.48	3.29	0.223	0.584	model1_4b4sA.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:0046983	0.96	protein dimerization activity
GO:0046982	0.95	protein heterodimerization activity
GO:0042803	0.93	protein homodimerization 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:0050794	0.99	regulation of cellular process
GO:0009987	0.98	cellular process
GO:0050896	0.93	response to stimulus
GO:0007165	0.92	signal transduction
GO:0035556	0.91	intracellular signal transduction
GO:0097193	0.90	intrinsic apoptotic signaling pathway
GO:0033554	0.90	cellular response to stress
GO:0008630	0.87	intrinsic apoptotic signaling pathway in response to DNA damage
GO:0007166	0.87	cell surface receptor signaling pathway
GO:0097191	0.86	extrinsic apoptotic signaling pathway
GO:0042981	0.86	regulation of apoptotic process
GO:0097192	0.85	extrinsic apoptotic signaling pathway in absence of ligand
GO:0048523	0.73	negative regulation of cellular process
GO:0048583	0.70	regulation of response to stimulus
GO:0043066	0.70	negative regulation of apoptotic process
GO:0023051	0.69	regulation of signaling
GO:0010646	0.69	regulation of cell communication
GO:0009966	0.68	regulation of signal transduction
GO:2001233	0.67	regulation of apoptotic signaling pathway
GO:1902531	0.67	regulation of intracellular signal transduction
GO:2001242	0.66	regulation of intrinsic apoptotic signaling pathway
GO:2001234	0.62	negative regulation of apoptotic signaling pathway
GO:1902532	0.62	negative regulation of intracellular signal transduction
GO:2001243	0.61	negative regulation of intrinsic apoptotic signaling pathway
GO:0044699	0.55	single-organism 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:0044444	1.00	cytoplasmic part
GO:0044446	0.97	intracellular organelle part
GO:0044429	0.96	mitochondrial part
GO:0016020	0.96	membrane
GO:0031090	0.93	organelle membrane
GO:0005741	0.92	mitochondrial outer membrane

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	3la4A	0.397	6.21	0.066	0.721	3.5.1.5	88,92
2	0.060	1ofdA	0.390	6.25	0.041	0.712	1.4.7.1	NA
3	0.060	2yr4A	0.392	6.26	0.062	0.717	1.13.12.9	135
4	0.060	2e8yA	0.391	6.18	0.042	0.708	3.2.1.41	NA
5	0.060	1zefA	0.409	5.28	0.053	0.618	3.1.3.1	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	0.80	2ponB	0.573	2.48	0.851	0.635	1.72	III	complex1.pdb.gz	96,97,100,101,113,114,122,126,129,130,133,136,137,138,139,142,146,185,190,193,194,195
2	0.57	1bxlA	0.614	2.90	0.824	0.708	1.63	III	complex2.pdb.gz	97,100,101,125,126,129,130,132,142,146,194,195
3	0.50	2xa0B	0.547	1.73	0.630	0.579	1.56	III	complex3.pdb.gz	96,97,100,101,126,129,130,133,136,137,138,139,141,142,146,193,194,195
4	0.49	2yxjB	0.585	1.20	0.979	0.609	1.95	N3C	complex4.pdb.gz	96,97,100,101,105,108,130,138,139,141,142,146,191,195
5	0.46	3qkdA	0.579	1.14	0.986	0.601	1.95	HI0	complex5.pdb.gz	93,96,97,100,101,105,126,129,130,138,139,141,142,145,146,191,195
6	0.45	3pl7B	0.580	1.22	0.965	0.605	1.91	III	complex6.pdb.gz	101,103,104,108,129,130,136,138,139,194,195
7	0.44	1ysgA	0.629	2.60	0.881	0.712	1.71	4FC	complex7.pdb.gz	97,101,104,105,138,139,142
8	0.42	1ysgA	0.629	2.60	0.881	0.712	1.92	TN1	complex8.pdb.gz	93,96,97,141,191,195
9	0.41	2w3lB	0.567	1.74	0.606	0.609	1.41	DRO	complex9.pdb.gz	97,101,126,129,130,142,146
10	0.38	3fdmC	0.494	2.52	0.830	0.541	1.92	III	complex10.pdb.gz	93,96,97,100,101,103,104,108,111,126,129,130,136,138,139,194,195

	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.