D-I-TASSER Q96Q07

D-I-TASSER results for Q96Q07

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

Summary of the Protein

Uniprot ID: Q96Q07
Protein Name: BTB/POZ domain-containing protein 9
Gene Name: BTBD9

Input Sequence in FASTA format

>Q96Q07 (612 residues)
MSNSHPLRPFTAVGEIDHVHILSEHIGALLIGEEYGDVTFVVEKKRFPAHRVILAARCQY
FRALLYGGMRESQPEAEIPLQDTTAEAFTMLLKYIYTGRATLTDEKEEVLLDFLSLAHKY
GFPELEDSTSEYLCTILNIQNVCMTFDVASLYSLPKLTCMCCMFMDRNAQEVLSSEGFLS
LSKTALLNIVLRDSFAAPEKDIFLALLNWCKHNSKENHAEIMQAVRLPLMSLTELLNVVR
PSGLLSPDAILDAIKVRSESRDMDLNYRGMLIPEENIATMKYGAQVVKGELKSALLDGDT
QNYDLDHGFSRHPIDDDCRSGIEIKLGQPSIINHIRILLWDRDSRSYSYFIEVSMDELDW
VRVIDHSQYLCRSWQKLYFPARVCRYIRIVGTHNTVNKIFHIVAFECMFTNKTFTLEKGL
IVPMENVATIADCASVIEGVSRSRNALLNGDTKNYDWDSGYTCHQLGSGAIVVQLAQPYM
IGSIRLLLWDCDDRSYSYYVEVSTNQQQWTMVADRTKVSCKSWQSVTFERQPASFIRIVG
THNTANEVFHCVHFECPEQQSSQKEENSEESGTGDTSLAGQQLDSHALRAPSGSSLPSSP
GSNSRSPNRQHQ

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 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.

Information of Domain

No. of Domain	Domain	Domain Boundary	Length of Domain	Models of Domain	Sequence
1	Q96Q07-D1	1-263	263		MSNSHPLRPFTAVGEIDHVHILSEHIGALLIGEEYGDVTFVVEKKRFPAHRVILAARCQYFRALLYGGMRESQPEAEIPLQDTTAEAFTMLLKYIYTGRATLTDEKEEVLLDFLSLAHKYGFPELEDSTSEYLCTILNIQNVCMTFDVASLYSLPKLTCMCCMFMDRNAQEVLSSEGFLSLSKTALLNIVLRDSFAAPEKDIFLALLNWCKHNSKENHAEIMQAVRLPLMSLTELLNVVRPSGLLSPDAILDAIKVRSESRDM
2	Q96Q07-D2	264-379	116		DLNYRGMLIPEENIATMKYGAQVVKGELKSALLDGDTQNYDLDHGFSRHPIDDDCRSGIEIKLGQPSIINHIRILLWDRDSRSYSYFIEVSMDELDWVRVIDHSQYLCRSWQKLYF
3	Q96Q07-D3	380-459	80		PARVCRYIRIVGTHNTVNKIFHIVAFECMFTNKTFTLEKGLIVPMENVATIADCASVIEGVSRSRNALLNGDTKNYDWDS
4	Q96Q07-D4	460-612	153		GYTCHQLGSGAIVVQLAQPYMIGSIRLLLWDCDDRSYSYYVEVSTNQQQWTMVADRTKVSCKSWQSVTFERQPASFIRIVGTHNTANEVFHCVHFECPEQQSSQKEENSEESGTGDTSLAGQQLDSHALRAPSGSSLPSSPGSNSRSPNRQHQ

Top 1 final models from D-I-TASSER

Click to view	Rank^a	Download	Estimated TM-score^b
	1	model1.pdb.gz	0.48

(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	3s4wB	0.41	7.82	0.050	0.672	model1_3s4wB.pdb.gz
2	7kpxC	0.40	7.87	0.066	0.663	model1_7kpxC.pdb.gz
3	5yz0A	0.40	7.37	0.033	0.613	model1_5yz0A.pdb.gz
4	3iytA	0.39	7.63	0.063	0.618	model1_3iytA.pdb.gz
5	3i3nB	0.39	1.55	0.219	0.399	model1_3i3nB.pdb.gz
6	6tnfB	0.39	7.98	0.046	0.637	model1_6tnfB.pdb.gz
7	4zhjA	0.38	8.14	0.053	0.642	model1_4zhjA.pdb.gz
8	3s4wA	0.38	8.63	0.050	0.667	model1_3s4wA.pdb.gz
9	7emfW2	0.38	7.79	0.051	0.611	model1_7emfW2.pdb.gz
10	5l4kZ	0.38	7.47	0.062	0.585	model1_5l4kZ.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:0003824	0.90	catalytic activity
GO:0016740	0.89	transferase activity
GO:0004842	0.88	ubiquitin-protein transferase 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:0071704	0.74	organic substance metabolic process
GO:0044237	0.73	cellular metabolic process
GO:0044238	0.71	primary metabolic process
GO:0043170	0.71	macromolecule metabolic process
GO:0044260	0.70	cellular macromolecule metabolic process
GO:0019538	0.66	protein metabolic process
GO:0065007	0.65	biological regulation
GO:0006464	0.64	cellular protein modification process
GO:0070647	0.62	protein modification by small protein conjugation or removal
GO:0050789	0.62	regulation of biological process
GO:0016567	0.61	protein ubiquitination
GO:0050794	0.57	regulation of cellular process
GO:0044699	0.53	single-organism process
GO:0042787	0.52	protein ubiquitination involved in ubiquitin-dependent protein catabolic 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:0044424	1.00	intracellular part
GO:0032991	0.94	macromolecular complex
GO:0043234	0.93	protein complex
GO:0031461	0.92	cullin-RING ubiquitin ligase complex
GO:0031463	0.88	Cul3-RING ubiquitin ligase 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	1sliA	0.312	8.05	0.044	0.515	4.2.2.15 3.2.1.18	NA
2	0.060	2qf7B	0.304	7.94	0.042	0.502	6.4.1.1	NA
3	0.060	2x42A	0.316	7.86	0.056	0.513	3.2.1.21	NA
4	0.060	2pffD	0.295	7.67	0.035	0.467	2.3.1.86	29
5	0.060	2fhbA	0.330	7.40	0.055	0.503	3.2.1.41	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	2np0A	0.333	8.10	0.027	0.549	0.15	III	complex1.pdb.gz	30,121,122
2	0.01	2bptA	0.337	7.48	0.060	0.528	0.19	III	complex2.pdb.gz	50,53,54,93
3	0.01	1xmvA	0.194	6.24	0.037	0.276	0.18	ADP	complex3.pdb.gz	34,36,37,50
4	0.01	3cmvE	0.311	8.17	0.029	0.516	0.14	ANP	complex4.pdb.gz	50,51,52,53
5	0.01	2nm1A	0.230	6.99	0.051	0.346	0.16	III	complex5.pdb.gz	36,37,38,61,75,76,77
6	0.01	3izaA	0.387	7.83	0.050	0.627	0.11	ATP	complex6.pdb.gz	85,111,114,115,116
7	0.01	3cmvG	0.317	8.02	0.025	0.520	0.15	ANP	complex7.pdb.gz	35,36,37,51
8	0.01	3cmvA	0.306	8.38	0.036	0.526	0.16	ANP	complex8.pdb.gz	34,35,37,51
9	0.01	3cmvB	0.309	8.20	0.021	0.513	0.14	ANP	complex9.pdb.gz	51,52,53,54

	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.