D-I-TASSER Q7Z2Z2-D2

D-I-TASSER results for Q7Z2Z2-D2

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

Input Sequence in FASTA format

>Q7Z2Z2 (215 residues)
IDRLIVELKFTPQEAYSHLKNILEQINALTGTLFTSKVLEERAERETESQVNPNSEQGEQ
VYDWSTGLEDTDDSHLYFSPEQGNVVFTSAIDGWGFGIEHFARIYSQKIGIKKEVLMKTL
WGDYYINMKAKKIMKGDQAKGKKPLFVQLILENIWSLYDAVLKKDKDKIDKIVTSLGLKI
GAREARHSDPKVQINAICSQWLPISHAVLAMVCQK

Predicted Secondary Structure

Sequence	20 40 60 80 100 120 140 160 180 200 \| \| \| \| \| \| \| \| \| \| IDRLIVELKFTPQEAYSHLKNILEQINALTGTLFTSKVLEERAERETESQVNPNSEQGEQVYDWSTGLEDTDDSHLYFSPEQGNVVFTSAIDGWGFGIEHFARIYSQKIGIKKEVLMKTLWGDYYINMKAKKIMKGDQAKGKKPLFVQLILENIWSLYDAVLKKDKDKIDKIVTSLGLKIGAREARHSDPKVQINAICSQWLPISHAVLAMVCQK
Prediction	CCHHHHHHCCCHHHHHHHHHHHHHHHHHHHHHHCCHHHHHHHHHHHHHHHHCCCCCCCCCCCCCCCCCCCCCCCCSSSSCCCCCSSSSSCCCCCSSSHHHHHHHHHHHHCCCHHHHHHHHHCCCSCCCCCCSSCCCCCCCCCCCSSSHHHHHHHHHHHHHHHCCCHHHHHHHHHHHCCCCCHHHHHHCCHHHHHHHHHHHHCCCHHHHHHHHHCC
Confidence	82337872999999999999999999999999624035667888877643012332211223333333456778559804789389984266827769999999999839999999998425110077667231478888888532013799999999999658713799999996888898898623818999999998649705899998519
	H:Helix; S:Strand; C:Coil

Predicted Solvent Accessibility

Sequence	20 40 60 80 100 120 140 160 180 200 \| \| \| \| \| \| \| \| \| \| IDRLIVELKFTPQEAYSHLKNILEQINALTGTLFTSKVLEERAERETESQVNPNSEQGEQVYDWSTGLEDTDDSHLYFSPEQGNVVFTSAIDGWGFGIEHFARIYSQKIGIKKEVLMKTLWGDYYINMKAKKIMKGDQAKGKKPLFVQLILENIWSLYDAVLKKDKDKIDKIVTSLGLKIGAREARHSDPKVQINAICSQWLPISHAVLAMVCQK
Prediction	62200311614354014203410430131023125442145335445555455555555444544453455755412020442100000133100010330042016425252530152012220023744413445637734200010004002400320365554414400452615145622554412400230043014314000300177
	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

                   |                   |                   |                   |                   |                   |                   |                   |                   |                   |

SS
Seq

CCHHHHHHCCCHHHHHHHHHHHHHHHHHHHHHHCCHHHHHHHHHHHHHHHHCCCCCCCCCCCCCCCCCCCCCCCCSSSSCCCCCSSSSSCCCCCSSSHHHHHHHHHHHHCCCHHHHHHHHHCCCSCCCCCCSSCCCCCCCCCCCSSSHHHHHHHHHHHHHHHCCCHHHHHHHHHHHCCCCCHHHHHHCCHHHHHHHHHHHHCCCHHHHHHHHHCC
IDRLIVELKFTPQEAYSHLKNILEQINALTGTLFTSKVLEERAERETESQVNPNSEQGEQVYDWSTGLEDTDDSHLYFSPEQGNVVFTSAIDGWGFGIEHFARIYSQKIGIKKEVLMKTLWGDYYINMKAKKIMKGDQAKGKKPLFVQLILENIWSLYDAVLKKDKDKIDKIVTSLGLKIGAREARHSDPKVQINAICSQWLPISHAVLAMVCQK

2e1rA4

0.28

0.24

7.24

1.17

DEthreader

VDRALLELQVSKEDLYQTFARTVESVNVIVSTYAD--E--------------------------------VLGD-VQVYPARGTVAFGSGLHGWAFTIRQFATRYAKKFGVDKAKMMDRLWGDSFFNPKTKKWTNKDTDKPLERAFNMFILDPIFRLFTAIMNFKKDEIPVLLEKLEIVLKGDEKDLE-GKALLKVVMRKFLPAADALLEMIVLH

2e1rA4

0.29

0.24

7.36

3.13

SPARKS-K

VDRALLELQVSKEDLYQTFARTVESVNVIVSTYA-----------------------------------DEVLGDVQVYPARGTVAFGSGLHGWAFTIRQFATRYAKKFGVDKAKMMDRLWGDSFFNPKTKKWTNKDEGKPLERAFNMFILDPIFRLFTAIMNFKKDEIPVLLEKLEIVLKGDEKDL-EGKALLKVVMRKFLPAADALLEMIVLH

2e1rA

0.28

0.24

7.24

1.18

MapAlign

VDRALLELQVSKEDLYQTFARTVESVNVIVSTYADEVLG-----------------------------------DVQVYPARGTVAFGSGLHGWAFTIRQFATRYAKKFGVDKAKMMDRLWGDSFFNPKTKKWTNKDTDKPLERAFNMFILDPIFRLFTAIMNFKKDEIPVLLEKLEIVLKGDEKDLE-GKALLKVVMRKFLPAADALLEMIVLH

2e1rA4

0.29

0.24

7.36

1.00

CEthreader

VDRALLELQVSKEDLYQTFARTVESVNVIVSTYA-----------------------------------DEVLGDVQVYPARGTVAFGSGLHGWAFTIRQFATRYAKKFGVDKAKMMDRLWGDSFFNPKTKKWTNKDTDKPLERAFNMFILDPIFRLFTAIMNFKKDEIPVLLEKLEIVLKGDEKDLE-GKALLKVVMRKFLPAADALLEMIVLH

5anbK1

1.00

28.00

2.15

MUSTER

IDRLIVELKFTPQEAYSHLKNILEQINALTGTLFTSKVLEERAERETESQVNPNSEQGEQVYDWSTGLEDTDDSHLYFSPEQGNVVFTSAIDGWGFGIEHFARIYSQKIGIKKEVLMKTLWGDYYINMKAKKIMKGDQAKGKKPLFVQLILENIWSLYDAVLKKDKDKIDKIVTSLGLKIGAREARHSDPKVQINAICSQWLPISHAVLAMVCQK

5anbK1

1.00

28.00

3.82

HHsearch

IDRLIVELKFTPQEAYSHLKNILEQINALTGTLFTSKVLEERAERETESQVNPNSEQGEQVYDWSTGLEDTDDSHLYFSPEQGNVVFTSAIDGWGFGIEHFARIYSQKIGIKKEVLMKTLWGDYYINMKAKKIMKGDQAKGKKPLFVQLILENIWSLYDAVLKKDKDKIDKIVTSLGLKIGAREARHSDPKVQINAICSQWLPISHAVLAMVCQK

3j38z1

0.28

0.24

7.24

2.61

FFAS-3D

MDRALLELQLDAEELYQTFQRIVENVNVIIATYND---------------------------------DGGPMGEVRVDPSKGSVGFGSGLHGWAFTLKQFSEMYSEKFKIDVVKLMNRLWGENFFNAKTKKWQKQKE-ADNKRSFCMYILDPIYKVFDAIMNYKKEEIGTLLEKIGVTLKHED-KDKDGKALLKTVMRTWLPAGEALLQMIAIH

2e1rA4

0.23

0.19

5.98

1.55

EigenThreader

VDRALLELQVSKEDLYQTFARTVESVNVIVSTYADE----------------------------------VLGDVQVYPARGTVAFGSG--LHGWAFTRQFATRYAKKFGVDKAKMMDRLWGDSFFNPKKKWTNKDTDGKPLERAFNMFILDPIFRLFTAIMNFKKDEIPVLLEKLEIVLKGDEKDLE-GKALLKVVMRKFLPAADALLEMIVLH

5anbK

1.00

28.00

1.94

CNFpred

IDRLIVELKFTPQEAYSHLKNILEQINALTGTLFTSKVLEERAERETESQVNPNSEQGEQVYDWSTGLEDTDDSHLYFSPEQGNVVFTSAIDGWGFGIEHFARIYSQKIGIKKEVLMKTLWGDYYINMKAKKIMKGDQAKGKKPLFVQLILENIWSLYDAVLKKDKDKIDKIVTSLGLKIGAREARHSDPKVQINAICSQWLPISHAVLAMVCQK

2e1rA

0.28

0.24

7.24

1.17

DEthreader

VDRALLELQVSKEDLYQTFARTVESVNVIVSTYAD--E--------------------------------VLGD-VQVYPARGTVAFGSGLHGWAFTIRQFATRYAKKFGVDKAKMMDRLWGDSFFNPKTKKWTNKDTDKPLERAFNMFILDPIFRLFTAIMNFKKDEIPVLLEKLEIVLKGDEKDLE-GKALLKVVMRKFLPAADALLEMIVLH

(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	0.7829

(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	2e1rA4	0.78	1.61	0.285	0.833	model1_2e1rA4.pdb.gz
2	5anbK	0.78	3.22	0.962	0.986	model1_5anbK.pdb.gz
3	3j38z1	0.77	1.87	0.283	0.837	model1_3j38z1.pdb.gz
4	3jb9B1	0.73	2.09	0.282	0.823	model1_3jb9B1.pdb.gz
5	3jcrB	0.73	2.10	0.282	0.823	model1_3jcrB.pdb.gz
6	5ganC4	0.71	2.00	0.253	0.791	model1_5ganC4.pdb.gz
7	1r5bA	0.32	5.64	0.013	0.572	model1_1r5bA.pdb.gz
8	1g7cA	0.32	6.31	0.029	0.605	model1_1g7cA.pdb.gz
9	1s0uA	0.32	6.22	0.070	0.581	model1_1s0uA.pdb.gz
10	1wb1C	0.31	6.17	0.064	0.572	model1_1wb1C.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:0003924	1.00	GTPase activity
GO:1901363	0.58	heterocyclic compound binding
GO:0097159	0.58	organic cyclic compound 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:0009987	0.99	cellular process
GO:0071704	0.98	organic substance metabolic process
GO:0044237	0.98	cellular metabolic process
GO:1901576	0.97	organic substance biosynthetic process
GO:0044260	0.97	cellular macromolecule metabolic process
GO:0044249	0.97	cellular biosynthetic process
GO:0044238	0.97	primary metabolic process
GO:0006807	0.97	nitrogen compound metabolic process
GO:1901564	0.96	organonitrogen compound metabolic process
GO:0044267	0.96	cellular protein metabolic process
GO:0034645	0.96	cellular macromolecule biosynthetic process
GO:0034641	0.96	cellular nitrogen compound metabolic process
GO:0006412	0.95	translation

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:0044464	1.00	cell part
GO:0005622	0.93	intracellular
GO:0044424	0.82	intracellular part
GO:0044444	0.50	cytoplasmic 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	3dlaD	0.416	5.30	0.063	0.670	6.3.5.1	NA
2	0.060	3czkA	0.412	5.73	0.056	0.721	3.2.1.48	NA
3	0.060	1d8yA	0.426	4.92	0.061	0.660	2.7.7.7	NA
4	0.060	2e1rA	0.782	1.61	0.285	0.833	3.6.5.3	NA
5	0.060	2azdB	0.410	5.50	0.038	0.702	2.4.1.1	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	0.01	1gz7D	0.488	5.38	0.037	0.814	0.43	GOL	complex1.pdb.gz	89,94,96
2	0.01	3c46A	0.341	6.15	0.036	0.642	0.65	2HP	complex2.pdb.gz	83,97,98,100
3	0.01	3jv2B	0.314	6.02	0.044	0.572	0.46	III	complex3.pdb.gz	83,96,97,98,102,103
4	0.01	3t05B	0.429	6.12	0.053	0.781	0.53	PO4	complex4.pdb.gz	89,90,92,93,94,95

	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.