D-I-TASSER Q96FF7

D-I-TASSER results for Q96FF7

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

Summary of the Protein

Uniprot ID: Q96FF7
Protein Name: Uncharacterized protein MISP3
Gene Name: MISP3

Input Sequence in FASTA format

>Q96FF7 (219 residues)
METPIEREIRRSCEREESLRRSRGLSPGRAGRELVELRVRPVLNLPGPGPALPRALERAR
AGAQMQRDIEREAHRQAALARPAVPEPRARSPPQPLGELKRFFEAAAGSGSSAGAGDGAG
PQRLPEPGGRPRSAVQGGCRVLGSAPPPFTPSLLEQEVRAVREREQELQRQRRSVYGTAE
FKEPTPSLTASRGDGKLVVIWPPRRKVSENGLEQEERKP

Predicted Contact and Distance Map Used in D-I-TASSER simulation

Contact Map

Distance Map

D-I-TASSER simulation is guided by the consensus contact map (left figure) and distance map (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.

Information of Domain

No. of Domain	Domain	Domain Boundary	Length of Domain	Models of Domain	Sequence
1	Q96FF7-D1	1-219	219		METPIEREIRRSCEREESLRRSRGLSPGRAGRELVELRVRPVLNLPGPGPALPRALERARAGAQMQRDIEREAHRQAALARPAVPEPRARSPPQPLGELKRFFEAAAGSGSSAGAGDGAGPQRLPEPGGRPRSAVQGGCRVLGSAPPPFTPSLLEQEVRAVREREQELQRQRRSVYGTAEFKEPTPSLTASRGDGKLVVIWPPRRKVSENGLEQEERKP

Top 1 final models from D-I-TASSER

Click to view	Rank^a	Download	Estimated TM-score^b
	1	model1.pdb.gz	0.4202

(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	7jroa	0.52	5.14	0.046	0.817	model1_7jroa.pdb.gz
2	1m56A	0.52	5.18	0.041	0.836	model1_1m56A.pdb.gz
3	4a01A	0.51	5.27	0.040	0.845	model1_4a01A.pdb.gz
4	2yevA	0.51	5.04	0.046	0.831	model1_2yevA.pdb.gz
5	1fftA	0.51	5.25	0.042	0.822	model1_1fftA.pdb.gz
6	3mk7A	0.50	5.03	0.080	0.767	model1_3mk7A.pdb.gz
7	1xmeA	0.46	5.58	0.043	0.785	model1_1xmeA.pdb.gz
8	3o0rB	0.45	6.00	0.034	0.790	model1_3o0rB.pdb.gz
9	3capA	0.42	4.83	0.047	0.630	model1_3capA.pdb.gz
10	1ocrN1	0.30	4.92	0.047	0.457	model1_1ocrN1.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	0.73	heterocyclic compound binding
GO:0097159	0.73	organic cyclic compound binding
GO:0022890	0.71	inorganic cation transmembrane transporter activity
GO:0003824	0.71	catalytic activity
GO:0046872	0.61	metal ion binding
GO:0046914	0.60	transition metal ion binding
GO:0005506	0.56	iron ion binding
GO:0020037	0.55	heme binding
GO:0004129	0.55	cytochrome-c oxidase 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:0009987	0.91	cellular process
GO:0006812	0.82	cation transport
GO:0008152	0.72	metabolic process
GO:0044763	0.71	single-organism cellular process
GO:0044237	0.70	cellular metabolic process
GO:0044710	0.63	single-organism metabolic process
GO:0006816	0.60	calcium ion transport
GO:0071704	0.59	organic substance metabolic process
GO:0044238	0.59	primary metabolic process
GO:1902600	0.55	hydrogen ion transmembrane transport
GO:0009060	0.55	aerobic respiration

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:0016020	0.97	membrane
GO:0044424	0.95	intracellular part
GO:0005886	0.88	plasma membrane
GO:0043231	0.87	intracellular membrane-bounded organelle
GO:0044425	0.82	membrane part
GO:0016021	0.80	integral component of membrane
GO:0030054	0.72	cell junction
GO:0005925	0.71	focal adhesion
GO:0044444	0.56	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	2fenD	0.433	5.18	0.033	0.667	5.5.1.2	98
2	0.060	1m56A	0.515	5.18	0.041	0.836	1.9.3.1	NA
3	0.060	2dkiA	0.429	5.92	0.066	0.744	1.14.13.23	NA
4	0.060	2pfmA	0.425	4.70	0.058	0.621	4.3.2.2	NA
5	0.060	1fftA	0.510	5.25	0.042	0.822	1.10.3.-	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	3ehbA	0.512	5.06	0.062	0.808	0.14	HEA	complex1.pdb.gz	5,9,16,19,22,23,156,160,164,168,195
2	0.01	3hb3A	0.515	4.97	0.058	0.799	0.16	HEA	complex2.pdb.gz	58,65,66,68,138
3	0.01	1m56A	0.515	5.18	0.041	0.836	0.16	HEA	complex3.pdb.gz	65,69,70,73,74,105,137,138
4	0.01	3omaC	0.516	5.13	0.041	0.836	0.23	DMU	complex4.pdb.gz	64,68,72,96,97
5	0.01	1m56A	0.515	5.18	0.041	0.836	0.13	PEH	complex5.pdb.gz	45,57,60
6	0.01	3dtuC	0.509	4.93	0.042	0.799	0.20	HEA	complex6.pdb.gz	38,62,69,70,73,138
7	0.01	1m56A	0.515	5.18	0.041	0.836	0.16	PEH	complex7.pdb.gz	24,39,64
8	0.01	1fftA	0.510	5.25	0.042	0.822	0.15	HEM	complex8.pdb.gz	23,54,55,161
9	0.01	1m57G	0.514	5.19	0.041	0.840	0.30	PEH	complex9.pdb.gz	62,64,65,72,98
10	0.01	1m57A	0.511	4.95	0.048	0.790	0.20	PEH	complex10.pdb.gz	66,67,68,71,75

	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.