D-I-TASSER Q96MT1-D2

D-I-TASSER results for Q96MT1-D2

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

Input Sequence in FASTA format

>Q96MT1 (107 residues)
VVPVLFMVFWLVLFALQIYSYFSTRDQPASRERLLFLFLTSIAECCSTPYSLLGLVFTVS
FVALGVLTLCKFYLQGYRAFMNDPAMNRGMTEGVTLLILAVQTGLIE

Predicted Secondary Structure

Sequence	20 40 60 80 100 \| \| \| \| \| VVPVLFMVFWLVLFALQIYSYFSTRDQPASRERLLFLFLTSIAECCSTPYSLLGLVFTVSFVALGVLTLCKFYLQGYRAFMNDPAMNRGMTEGVTLLILAVQTGLIE
Prediction	CCCHHHHHHHHHHHHHHHHHHHCCCCCCHHHHHHHHHHHHHHHHHCCCHHHHHHHHHHHHHHHHHHHHHHHHHHHCHHHHCCCCCCCCCHHHHHHHHHHHHHHCCCC
Confidence	97525899999999999999955898742345799999999987337889999999999999999999999998124543035544445568999999999937999
	H:Helix; S:Strand; C:Coil

Predicted Solvent Accessibility

Sequence	20 40 60 80 100 \| \| \| \| \| VVPVLFMVFWLVLFALQIYSYFSTRDQPASRERLLFLFLTSIAECCSTPYSLLGLVFTVSFVALGVLTLCKFYLQGYRAFMNDPAMNRGMTEGVTLLILAVQTGLIE
Prediction	72223033203230332012212446443444301110022134315232202232310123043224203010213423445544333212112020013324348
	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

                   |                   |                   |                   |                   |

SS
Seq

CCCHHHHHHHHHHHHHHHHHHHCCCCCCHHHHHHHHHHHHHHHHHCCCHHHHHHHHHHHHHHHHHHHHHHHHHHHCHHHHCCCCCCCCCHHHHHHHHHHHHHHCCCC
VVPVLFMVFWLVLFALQIYSYFSTRDQPASRERLLFLFLTSIAECCSTPYSLLGLVFTVSFVALGVLTLCKFYLQGYRAFMNDPAMNRGMTEGVTLLILAVQTGLIE

7khra

0.09

0.08

3.22

1.00

DEthreader

PFF-AVGDTGLIYNS---SS-WSVRPMFTPVLQATNKLTFLNSFKMKSLLWALSLAHAQLSEVLWTMVIHIGLVLALALFFAATLTVAILLMEGLSAFLHALRLHEF

5a63C

0.05

2.26

1.00

MapAlign

PLRVIILVAGAFFWLVSLLLASVVWFILVGAAVSVLLQEVFRFAYLSIRQMAYVSGLSFGIISGVFSVINILADAPYYFLTSAFLTAAIILLHTFWGVVFFDAWALG

6idpA1

0.09

3.52

0.64

CEthreader

GKTEYAKQLGGLVIVIGGIGVALIAWLWWLASAWTGAMLYFYYSVCRANTLLPGTLMMVTSVLNLILDPIFIFTFDLGIDGAAIATIIAFGVGIAIVAPKVAQRQWT

6y7fA

0.05

2.26

0.57

EigenThreader

SFRCDIVDTCWLYYFSKFIEFVLRKKNQVTFLHVFHHTIMPWWFGVKFAAGGLGTFHALLNTAVHVVMYSYYGLSALQKKYLTSLQLVQFVIVAIHISQFFFMYQFP

3hfxA

0.09

0.08

3.25

0.66

FFAS-3D

LGLTASTWILWTVLGSNTLLLIDKNIINIEQYGVARAIIETWAALPSTATMWGFFILCFIATVTLVNACSYTLAMSTCREVRDGEEPPSILVGIIGIVLLALGGL--

6w2wA2

0.06

2.51

0.74

SPARKS-K

AAKECLKAVRAALEAALLALLLLAKHPGSQAAQDAVQLATAALRAVEAACQLAKQAKKCIKAASEAAEEASKAAEEAQRHPDSQKARDEIKEASQKAEEVKERCERA

3rkoC

0.15

0.14

4.70

0.76

CNFpred

GILLKTAAYGLLRFSLPLFPNASAE----FAPIAMWLGVIGIFYGA-DIKRLIAYTSVMGFVLIAIYTGSQLAYQGAVIQM----IAHGLSAAGLFILCGQLYERIH

6xbwa

0.07

2.72

1.00

DEthreader

FPLFAVGSYTGLIYN---GSSWSPAVFIWATN-KLTFLNSFKMKMSVYLRLWALSLAHALSEVLWTMVIHIGLKVALALFFAATLTVAILIMEGLSAFLHAL-RLHF

4q65A

0.06

2.51

0.68

MapAlign

TPILGGFLAAVMLGALLMAIGHVVLGASEFLYLSLAIIVCGYGLFRTVRIWGKFALGLGLMSAGFCILTLSARWSAMYGLPLMVLGLAVMGFAELFIYMLLSGAIAN

2vpyC2

0.18

5.78

0.62

MUSTER

NRPLMAGLFPLTALVLALGLAALLK-SPWALFPLRVLAGASLLLALLYPLTL-PPEARGHLLEEAGFWYGLFLLLGLGTFWQERLAPAGLLAAAGLRALLVLAGQWQ

(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	0.6584

(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	4av3A	0.61	3.68	0.093	0.944	model1_4av3A.pdb.gz
2	5zw0A	0.60	3.56	0.059	0.935	model1_5zw0A.pdb.gz
3	6es9A	0.59	3.39	0.060	0.906	model1_6es9A.pdb.gz
4	6tjvP	0.59	3.94	0.070	0.906	model1_6tjvP.pdb.gz
5	2d29A	0.59	3.89	0.088	0.935	model1_2d29A.pdb.gz
6	5af7A	0.59	3.72	0.040	0.925	model1_5af7A.pdb.gz
7	6m2lA	0.59	3.91	0.078	0.897	model1_6m2lA.pdb.gz
8	1jqiA	0.59	3.63	0.040	0.916	model1_1jqiA.pdb.gz
9	1bucA	0.58	3.60	0.039	0.897	model1_1bucA.pdb.gz
10	1udyA	0.58	3.67	0.078	0.916	model1_1udyA.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:0061630	1.00	ubiquitin protein ligase 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:0043161	1.00	proteasome-mediated ubiquitin-dependent protein catabolic process
GO:0042787	1.00	protein ubiquitination involved in ubiquitin-dependent protein catabolic process
GO:0000209	1.00	protein polyubiquitination

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	0.97	cytoplasmic part
GO:0043229	0.80	intracellular organelle
GO:0043231	0.78	intracellular membrane-bounded organelle
GO:0044446	0.72	intracellular organelle part
GO:0044425	0.60	membrane part
GO:0044432	0.59	endoplasmic reticulum part
GO:0032991	0.58	macromolecular complex
GO:0043234	0.57	protein complex
GO:0098796	0.53	membrane protein complex
GO:0000151	0.51	ubiquitin ligase complex
GO:0000838	0.50	Hrd1p ubiquitin ligase ERAD-M 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	3mddA	0.585	3.66	0.078	0.916	1.3.99.3	100
2	0.060	1t7lA	0.541	4.61	0.088	0.925	2.1.1.14	NA
3	0.060	3lmdA	0.529	3.95	0.076	0.841	2.5.1.30	97
4	0.060	1ah7A	0.526	4.29	0.048	0.888	3.1.4.3	NA
5	0.060	2ix6A	0.520	4.43	0.057	0.906	1.3.3.6	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	3mddA	0.585	3.66	0.078	0.916	0.47	FAD	complex1.pdb.gz	56,94,102,104
2	0.02	1t9gB	0.583	3.76	0.078	0.925	0.53	FAD	complex2.pdb.gz	56,92,98
3	0.01	1udyB	0.582	3.68	0.069	0.916	0.46	UUU	complex3.pdb.gz	53,59,89,90,92
4	0.01	3mdeA	0.584	3.76	0.078	0.925	0.44	FAD	complex4.pdb.gz	59,89,90
5	0.01	1egdA	0.585	3.75	0.069	0.925	0.43	FAD	complex5.pdb.gz	48,53,100
6	0.01	1egcC	0.588	3.63	0.049	0.916	0.50	FAD	complex6.pdb.gz	56,92,99
7	0.01	1ub44	0.286	3.45	0.076	0.393	0.50	III	complex7.pdb.gz	54,56,94,95,97,102
8	0.01	1egcD	0.485	4.45	0.030	0.906	0.50	FAD	complex8.pdb.gz	48,55,57,99,100,103,104

	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.