D-I-TASSER Q15195-D1

D-I-TASSER results for Q15195-D1

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

Input Sequence in FASTA format

>Q15195 (96 residues)
MEHKEVVLLLLLFLKSGQGEPLDDYVNAQGASLFSVTKKQLGAGSREECAAKCEEDKEFT
CRAFQYHSKEQQCVIMAENKKSSIIIRMRDVVLFEK

Predicted Secondary Structure

Sequence	20 40 60 80 \| \| \| \| MEHKEVVLLLLLFLKSGQGEPLDDYVNAQGASLFSVTKKQLGAGSREECAAKCEEDKEFTCRAFQYHSKEQQCVIMAENKKSSIIIRMRDVVLFEK
Prediction	CCHHHHHHHHHHHHCCCCCCHHHCHSSSCCSSSSSCCCCSSSCCCHHHHHHHHHHCCCCCCCSSSSCCCCCSSSSSCCCCCCCCSSSSHCHHHHCC
Confidence	961343556677643578850121044177587612652451389999999985224863012786178753775336776643222000122139
	H:Helix; S:Strand; C:Coil

Predicted Solvent Accessibility

Sequence	20 40 60 80 \| \| \| \| MEHKEVVLLLLLFLKSGQGEPLDDYVNAQGASLFSVTKKQLGAGSREECAAKCEEDKEFTCRAFQYHSKEQQCVIMAENKKSSIIIRMRDVVLFEK
Prediction	752320000111123424464055244264230322445424443364015305765614143241465544043244444354334444242358
	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

                   |                   |                   |                   |

SS
Seq

CCHHHHHHHHHHHHCCCCCCHHHCHSSSCCSSSSSCCCCSSSCCCHHHHHHHHHHCCCCCCCSSSSCCCCCSSSSSCCCCCCCCSSSSHCHHHHCC
MEHKEVVLLLLLFLKSGQGEPLDDYVNAQGASLFSVTKKQLGAGSREECAAKCEEDKEFTCRAFQYHSKEQQCVIMAENKKSSIIIRMRDVVLFEK

1i8nA

0.19

0.16

5.06

1.17

DEthreader

-------ET-I--T---AGNED-CWSKRPGWKLPDNLLTKTEFTSVDECRKMCEESAVPSCYILQINTETNECYRNEDV-TWSSLQYQPNVVQWHL

4durA5

0.95

0.74

20.75

2.68

SPARKS-K

---------------------LDDYVNTQGASLFSVTKKQLGAGSIEECAAKCEEDEEFTCRAFQYHSKEQQCVIMAENRKSSIIIRMRDVVLFEK

1bhtA1

0.21

0.17

5.29

1.05

MapAlign

--------------------TIHEFKKSAKTTLIKLKIKTKKVNTADQCANRCTRNKGLTCKAFVFDKARKQCLWFPFNSMSGVKKEFGEFDLYEN

1bhtA1

0.20

0.17

5.32

0.92

CEthreader

-----------------RRNTIHEFKKSAKTTLIKLKIKTKKVNTADQCANRCTRNKGLPCKAFVFDKARKQCLWFPFNSMSSGVKKEFEFDLYEN

4durA5

0.95

0.74

20.75

2.09

MUSTER

---------------------LDDYVNTQGASLFSVTKKQLGAGSIEECAAKCEEDEEFTCRAFQYHSKEQQCVIMAENRKSSIIIRMRDVVLFEK

3hn4A1

0.21

0.18

5.61

3.11

HHsearch

----------------KRRNTIHEFKKSAKTTLIKIDPATKKVNTADQCANRCTRNKGFTCKAFVFDKARKQCLWFPFNSMSSGVKKGHEFDLYEN

4durA5

0.95

0.74

20.75

1.04

FFAS-3D

---------------------LDDYVNTQGASLFSVTKKQLGAGSIEECAAKCEEDEEFTCRAFQYHSKEQQCVIMAENRKSSIIIRMRDVVLFEK

4a5vA

0.12

0.11

4.06

0.98

EigenThreader

VHSDNLEQCAAQCKAVDGCSCDRSCFEQH-VSYEGAPDVMMVTSQSADCQAACAADPSC--EIFTYNEHDQKCTFKGRGFSAFKERGVLGVTSGPK

4a5tS

0.95

0.76

21.33

1.83

CNFpred

-------------------EPLDDYVNTQGASLFSVTKKQLGAGSIEECAAKCEEDEEFTCRAFQYHSKEQQCVIMAENRKSSIIIRMRDVVLFEK

3hn4A

0.21

0.17

5.31

1.00

DEthreader

------------------RNTIHEFKKSAKTTLIKLKIKTKKVNTADQCANRCTRGLPFTCKAFVFDKARKQCLWFPFNSMSGVKKEFGHFDLYEN

(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	0.7419

(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	3hn4A1	0.76	1.33	0.200	0.833	model1_3hn4A1.pdb.gz
2	1bhtA	0.75	1.30	0.228	0.823	model1_1bhtA.pdb.gz
3	4durA5	0.72	1.10	0.947	0.781	model1_4durA5.pdb.gz
4	3cd2A	0.32	4.67	0.022	0.604	model1_3cd2A.pdb.gz
5	2qj2B2	0.29	4.27	0.052	0.521	model1_2qj2B2.pdb.gz
6	1ki0A2	0.28	4.24	0.018	0.510	model1_1ki0A2.pdb.gz
7	3e6pL	0.28	4.60	0.111	0.531	model1_3e6pL.pdb.gz
8	3dp7A	0.26	4.85	0.044	0.510	model1_3dp7A.pdb.gz
9	1jfnA	0.26	4.78	0.048	0.521	model1_1jfnA.pdb.gz
10	2knfA	0.26	5.22	0.032	0.573	model1_2knfA.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:0005102	0.83	receptor binding
GO:0019904	0.82	protein domain specific binding
GO:0003824	0.61	catalytic activity
GO:0004175	0.52	endopeptidase 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:0065007	0.82	biological regulation
GO:0050789	0.80	regulation of biological process
GO:0050794	0.75	regulation of cellular process
GO:0048519	0.75	negative regulation of biological process
GO:0048523	0.69	negative regulation of cellular process
GO:0051239	0.68	regulation of multicellular organismal process
GO:0048518	0.68	positive regulation of biological process
GO:0051241	0.66	negative regulation of multicellular organismal process
GO:0044699	0.61	single-organism process
GO:2000026	0.54	regulation of multicellular organismal development
GO:0042127	0.52	regulation of cell proliferation
GO:0009987	0.51	cellular process
GO:0032501	0.50	multicellular organismal process
GO:0008152	0.50	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:0044421	0.81	extracellular region part
GO:0044464	0.80	cell part
GO:0005615	0.80	extracellular space
GO:0043226	0.72	organelle
GO:0005576	0.72	extracellular region
GO:0043227	0.71	membrane-bounded organelle
GO:0044424	0.61	intracellular part
GO:0044425	0.58	membrane part
GO:0016020	0.58	membrane
GO:0044459	0.52	plasma membrane part
GO:0009986	0.51	cell surface
GO:0005886	0.50	plasma 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	0.066	2j8lB	0.563	2.53	0.151	0.729	3.4.21.27	49,66
2	0.060	3e2zB	0.457	4.31	0.098	0.771	2.6.1.63 2.6.1.7 4.4.1.13	NA
3	0.060	2d6fA	0.472	3.46	0.022	0.708	6.3.5.-	NA
4	0.060	2gqdA	0.540	3.35	0.064	0.802	2.3.1.179	NA
5	0.060	2zjgA	0.456	4.49	0.096	0.781	2.6.1.7 2.6.1.64	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	0.02	1amaA	0.477	3.93	0.134	0.760	0.15	PLA	complex1.pdb.gz	33,67,69,70
2	0.01	3h0lP	0.469	4.15	0.042	0.802	0.11	ASN	complex2.pdb.gz	28,29,31
3	0.01	3c23B	0.484	3.59	0.065	0.802	0.14	3AT	complex3.pdb.gz	29,30,31
4	0.01	3h0lA	0.468	4.48	0.052	0.833	0.23	ASN	complex4.pdb.gz	28,30,31,32,67,90
5	0.01	3c23A	0.471	4.25	0.085	0.854	0.22	3AT	complex5.pdb.gz	30,66,67,72
6	0.01	3h0rJ	0.469	4.15	0.042	0.802	0.17	ASN	complex6.pdb.gz	29,30,32,65,66

	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.