D-I-TASSER O15178-D2

D-I-TASSER results for O15178-D2

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

Input Sequence in FASTA format

>O15178 (136 residues)
SPTYSDNSPACLSMLQSHDNWSSLGMPAHPSMLPVSHNASPPTSSSQYPSLWSVSNGAVT
PGSQAAAVSNGLGAQFFRGSPAHYTPLTHPVSAPSSSGSPLYEGAAAATDIVDSQYDAAA
QGRLIASWTPVSPPSM

Predicted Secondary Structure

Sequence	20 40 60 80 100 120 \| \| \| \| \| \| SPTYSDNSPACLSMLQSHDNWSSLGMPAHPSMLPVSHNASPPTSSSQYPSLWSVSNGAVTPGSQAAAVSNGLGAQFFRGSPAHYTPLTHPVSAPSSSGSPLYEGAAAATDIVDSQYDAAAQGRLIASWTPVSPPSM
Prediction	CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC
Confidence	9866688876554666888888778888877555688889998988888765667887888888887778878654358888778878888888899987558888877777777677755567778767899999
	H:Helix; S:Strand; C:Coil

Predicted Solvent Accessibility

Sequence	20 40 60 80 100 120 \| \| \| \| \| \| SPTYSDNSPACLSMLQSHDNWSSLGMPAHPSMLPVSHNASPPTSSSQYPSLWSVSNGAVTPGSQAAAVSNGLGAQFFRGSPAHYTPLTHPVSAPSSSGSPLYEGAAAATDIVDSQYDAAAQGRLIASWTPVSPPSM
Prediction	8453476444324324435524524344443324144444465544433312314446444444444344434343234444434434443544444433334454454625544344434443454234344478
	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

                   |                   |                   |                   |                   |                   |

SS
Seq

CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC
SPTYSDNSPACLSMLQSHDNWSSLGMPAHPSMLPVSHNASPPTSSSQYPSLWSVSNGAVTPGSQAAAVSNGLGAQFFRGSPAHYTPLTHPVSAPSSSGSPLYEGAAAATDIVDSQYDAAAQGRLIASWTPVSPPSM

2o3iA2

0.11

0.09

3.19

0.56

CEthreader

LDFLRRELDIKGKLLFGEDGERRCTVLYQNESLLAWDSALSHPLATAPDAISYFVDLSGNDHGLDPSVRGRKAAVIALPAAAPLSEGLILQSFADELAQLGYLGPYAPVD--------------------------

7cq5C1

0.10

3.78

0.55

EigenThreader

IEPVAAGSGIPQIKCFLNGHVVREGPMIHSGSVIAAGISQRDFVSAGAAAGVSAAFGAPVGGVLFSLEEGFASMISTFTLNSPGLINFLHWEAPVTSHSLTAREVMSTPVTCLRRREKVGVIVDVLSDTASNHNGF

5lqwX2

0.06

0.04

1.88

0.33

FFAS-3D

------------------------------------SNLISTSLPPNATKLWLIPDPTTGDNNTLLFITFPKKTMILQIDNTPDEATRSAFLSQDTTIHTCLMGSHSIIQVCTAELRHITGKSRYSNWVP------

7jjvA

0.11

0.10

3.44

1.03

SPARKS-K

GLDGADGTSNG----QAGASGLAGGPNCNGGKGGKGAPGVGTAGGAGGVGGAGGTNGGAGGSGGNSDVAAGGAGAAGGAAGGAGTGGTGGNGGAGKPGGAPGAGGAGTPAGAGSPGQTTVL---------------

1litA

0.13

0.03

1.01

0.24

CNFpred

--------GYCVSLTSGFQKWKDVPCEDK------------------FSFVCKFKN--------------------------------------------------------------------------------

3eg9A2

0.08

0.06

2.36

0.83

DEthreader

EFIQQ--------------N-----EERDG-VRFSWVWPEARMVVPVAALFAIGPCVSLGTGGTCQWKICGLSP-TTL---AIY--FEVVRISFDQEAAAIMLAIRAPLQVFNSPDESSYYRHHFMRQDLT-----

4jspD2

0.06

0.04

1.57

0.76

MapAlign

----VGSDPVILATAGYDHTVRFWQQHQDSQVNALEVTPDRSMIAAAGIVTASSDNLARLWEIKREYGGHQKAVVCLAFNDS------------------------------------------------------

4k0mC

0.13

4.56

0.71

MUSTER

GEKIKEAEEAGADYVGGEEIIQAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA--

6q9mA2

0.22

0.05

1.62

0.51

HHsearch

-TK----------------------------------------------------------------------------------------------G--LPDP---PQEIQLEAGPQD--GTILVTWQPVN--PV

3zf7W

0.08

0.06

2.29

0.48

CEthreader

LPVGAVVNCANLYIISVKGYHGLPAAALGDMVMASVKKGKPELRRKVLNAVIIRQNAGVIVNPKGEMKGSGIAGPVAKEAAELWPKISTHAPAIV-----------------------------------------

(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	0.4827

(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	4zhjA	0.45	5.27	0.016	0.853	model1_4zhjA.pdb.gz
2	5fifA	0.45	4.79	0.041	0.787	model1_5fifA.pdb.gz
3	5jk4A	0.44	5.15	0.085	0.853	model1_5jk4A.pdb.gz
4	1pc3A	0.44	5.33	0.063	0.875	model1_1pc3A.pdb.gz
5	6y795	0.44	4.69	0.056	0.743	model1_6y795.pdb.gz
6	4lvqA	0.41	5.56	0.080	0.846	model1_4lvqA.pdb.gz
7	4exlA	0.38	4.65	0.058	0.669	model1_4exlA.pdb.gz
8	1cvrA1	0.37	5.21	0.028	0.728	model1_1cvrA1.pdb.gz
9	2v3qA2	0.37	5.26	0.048	0.743	model1_2v3qA2.pdb.gz
10	4ecfA	0.37	5.24	0.057	0.699	model1_4ecfA.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	0.64	heterocyclic compound binding
GO:0097159	0.64	organic cyclic compound binding
GO:0003677	0.61	DNA binding
GO:0008134	0.60	transcription factor binding
GO:0001102	0.59	RNA polymerase II activating transcription factor binding
GO:0043565	0.58	sequence-specific DNA binding
GO:0044212	0.57	transcription regulatory region DNA binding
GO:0003700	0.53	transcription factor activity, sequence-specific 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:0065007	0.87	biological regulation
GO:0050789	0.86	regulation of biological process
GO:0050794	0.85	regulation of cellular process
GO:0044699	0.85	single-organism process
GO:0060255	0.81	regulation of macromolecule metabolic process
GO:0031323	0.81	regulation of cellular metabolic process
GO:0009987	0.81	cellular process
GO:2001141	0.80	regulation of RNA biosynthetic process
GO:2000112	0.80	regulation of cellular macromolecule biosynthetic process
GO:0010468	0.80	regulation of gene expression
GO:0006355	0.79	regulation of transcription, DNA-templated
GO:0044707	0.78	single-multicellular organism process
GO:0006357	0.78	regulation of transcription from RNA polymerase II promoter
GO:0007389	0.77	pattern specification process
GO:0048518	0.73	positive regulation of biological process
GO:0048522	0.72	positive regulation of cellular process
GO:0009893	0.71	positive regulation of metabolic process
GO:0032502	0.70	developmental process
GO:0031325	0.70	positive regulation of cellular metabolic process
GO:0010604	0.70	positive regulation of macromolecule metabolic process
GO:0045893	0.69	positive regulation of transcription, DNA-templated
GO:0044767	0.69	single-organism developmental process
GO:0045944	0.68	positive regulation of transcription from RNA polymerase II promoter
GO:0048856	0.67	anatomical structure development
GO:0009653	0.64	anatomical structure morphogenesis
GO:0048646	0.62	anatomical structure formation involved in morphogenesis
GO:0009888	0.62	tissue development
GO:0007498	0.61	mesoderm development
GO:0007165	0.55	signal transduction
GO:0048523	0.54	negative regulation of cellular process
GO:0003257	0.51	positive regulation of transcription from RNA polymerase II promoter involved in myocardial precursor cell differentiation
GO:0003007	0.51	heart morphogenesis
GO:0000122	0.51	negative regulation of transcription from RNA polymerase II promoter

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:0005634	1.00	nucleus
GO:0032991	0.54	macromolecular 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	3ma8A	0.420	4.61	0.031	0.728	2.7.1.40	NA
2	0.060	1maaD	0.362	4.81	0.048	0.632	3.1.1.7	NA
3	0.060	1qgxA	0.435	5.27	0.057	0.787	3.1.3.7	NA
4	0.060	3gpdR	0.424	5.51	0.050	0.809	1.2.1.12	128
5	0.060	1zxiC	0.435	4.99	0.044	0.765	1.2.99.2	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	1qo9A	0.427	4.91	0.072	0.728	0.11	UUU	complex1.pdb.gz	57,61,80
2	0.01	1pc3A	0.441	5.33	0.063	0.875	0.23	PO4	complex2.pdb.gz	92,94,100,101,133
3	0.01	1n60C	0.430	4.79	0.044	0.750	0.15	FAD	complex3.pdb.gz	17,37,38
4	0.01	1h18B	0.432	4.88	0.076	0.772	0.21	PYR	complex4.pdb.gz	53,77,80,83
5	0.01	1h17A	0.429	4.67	0.045	0.757	0.27	COA	complex5.pdb.gz	32,103,106
6	0.01	2ychA	0.431	4.94	0.089	0.765	0.14	ATP	complex6.pdb.gz	3,6,32,33
7	0.01	1w1i2	0.374	5.04	0.051	0.691	0.17	III	complex7.pdb.gz	50,53,54,101,103
8	0.01	1p8j0	0.427	4.88	0.056	0.779	0.30	III	complex8.pdb.gz	101,102,103
9	0.01	1ka0A	0.434	5.30	0.057	0.787	0.15	AMP	complex9.pdb.gz	63,82,88
10	0.01	3rkoM	0.430	4.83	0.047	0.743	0.24	CA7	complex10.pdb.gz	100,101,104,105

	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.