D-I-TASSER Q9H7Y0

D-I-TASSER results for Q9H7Y0

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

Summary of the Protein

Uniprot ID: Q9H7Y0
Protein Name: Divergent protein kinase domain 2B
Gene Name: DIPK2B

Input Sequence in FASTA format

>Q9H7Y0 (433 residues)
MEPQLGPEAAALRPGWLALLLWVSALSCSFSLPASSLSSLVPQVRTSYNFGRTFLGLDKC
NACIGTSICKKFFKEEIRSDNWLASHLGLPPDSLLSYPANYSDDSKIWRPVEIFRLVSKY
QNEISDRRICASASAPKTCSIERVLRKTERFQKWLQAKRLTPDLVQGLASPLLRCPSQRL
LDRVVRRYAEVADAGSIFMDHFTDRDKLRLLYTLAVNSHPILLQIFPGAEGWPLPKYLGS
CGRFLVSTSTRPLQEFYDAPPDQAADLAYQLLGVLESLRSNDLNYFFYFTHIDAGMFGVF
NNGHLFIRDASAVGVIDKQEGSQEANRAGENKDIFSCLVSGCQAQLPSCESISEKQSLVL
VCQKLLPRLLQGRFPSPVQDDIDSILVQCGDSIRPDPEVLGAASQLKDILRPLRTCDSRF
AYRYPDCKYNDKF

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	Q9H7Y0-D1	1-139,236-249	153		MEPQLGPEAAALRPGWLALLLWVSALSCSFSLPASSLSSLVPQVRTSYNFGRTFLGLDKCNACIGTSICKKFFKEEIRSDNWLASHLGLPPDSLLSYPANYSDDSKIWRPVEIFRLVSKYQNEISDRRICASASAPKTCKYLGSCGRFLVSTS
2	Q9H7Y0-D2	140-235	96		SIERVLRKTERFQKWLQAKRLTPDLVQGLASPLLRCPSQRLLDRVVRRYAEVADAGSIFMDHFTDRDKLRLLYTLAVNSHPILLQIFPGAEGWPLP
3	Q9H7Y0-D3	250-433	184		TRPLQEFYDAPPDQAADLAYQLLGVLESLRSNDLNYFFYFTHIDAGMFGVFNNGHLFIRDASAVGVIDKQEGSQEANRAGENKDIFSCLVSGCQAQLPSCESISEKQSLVLVCQKLLPRLLQGRFPSPVQDDIDSILVQCGDSIRPDPEVLGAASQLKDILRPLRTCDSRFAYRYPDCKYNDKF

Top 1 final models from D-I-TASSER

Click to view	Rank^a	Download	Estimated TM-score^b
	1	model1.pdb.gz	0.54

(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	7nurA	0.47	5.73	0.064	0.644	model1_7nurA.pdb.gz
2	7lhtA	0.46	5.57	0.061	0.624	model1_7lhtA.pdb.gz
3	1koaA	0.45	4.97	0.087	0.577	model1_1koaA.pdb.gz
4	1kobA	0.44	4.67	0.062	0.552	model1_1kobA.pdb.gz
5	2fo0A	0.44	5.19	0.077	0.575	model1_2fo0A.pdb.gz
6	6ygnA	0.44	5.20	0.048	0.559	model1_6ygnA.pdb.gz
7	3mdyA	0.44	4.84	0.099	0.557	model1_3mdyA.pdb.gz
8	6wppA	0.44	4.38	0.083	0.536	model1_6wppA.pdb.gz
9	7kpvA	0.43	4.35	0.089	0.531	model1_7kpvA.pdb.gz
10	4tnbA	0.43	5.06	0.093	0.557	model1_4tnbA.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	0.91	catalytic activity
GO:0016772	0.90	transferase activity, transferring phosphorus-containing groups
GO:0016773	0.89	phosphotransferase activity, alcohol group as acceptor
GO:0016301	0.73	kinase activity
GO:0004672	0.68	protein kinase activity
GO:1901363	0.67	heterocyclic compound binding
GO:0097159	0.67	organic cyclic compound binding
GO:0000166	0.60	nucleotide binding
GO:0004715	0.58	non-membrane spanning protein tyrosine kinase activity
GO:0035639	0.57	purine ribonucleoside triphosphate binding
GO:0032555	0.57	purine ribonucleotide binding
GO:0032550	0.57	purine ribonucleoside binding
GO:0032559	0.54	adenyl ribonucleotide 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:0009966	1.00	regulation of signal transduction

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	0.95	cytoplasmic part
GO:0044422	0.93	organelle part
GO:0044446	0.92	intracellular organelle part
GO:0044425	0.89	membrane part
GO:0032991	0.88	macromolecular complex
GO:0043234	0.86	protein complex
GO:0016020	0.83	membrane
GO:0098796	0.81	membrane protein complex
GO:0044431	0.81	Golgi apparatus part
GO:0044421	0.81	extracellular region part
GO:0030126	0.80	COPI vesicle coat
GO:0005615	0.80	extracellular space
GO:0043226	0.75	organelle
GO:0043229	0.71	intracellular organelle
GO:0043227	0.69	membrane-bounded organelle
GO:0043231	0.64	intracellular membrane-bounded organelle
GO:0005737	0.63	cytoplasm
GO:0005886	0.54	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	0.060	2wtkC	0.423	4.40	0.117	0.522	2.7.11.1	NA
2	0.060	2pziA	0.425	5.22	0.101	0.554	2.7.11.1	NA
3	0.060	3a7hB	0.422	4.48	0.097	0.517	2.7.11.1	NA
4	0.060	1yrpA	0.409	4.16	0.081	0.492	2.7.11.1	NA
5	0.060	3ggfA	0.397	4.45	0.084	0.494	2.7.11.1	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	0.11	3dk6A	0.397	4.37	0.093	0.490	0.27	SX7	complex1.pdb.gz	64,114,239,242,243
2	0.01	2qohA	0.404	4.37	0.086	0.496	0.20	P3Y	complex2.pdb.gz	21,65,238,239,242,243
3	0.01	2g2fA	0.408	4.56	0.085	0.506	0.10	112	complex3.pdb.gz	49,51,276
4	0.01	2hiwB	0.388	4.37	0.096	0.478	0.11	7MP	complex4.pdb.gz	10,116,219,244
5	0.01	1iepA	0.385	4.47	0.088	0.478	0.11	STI	complex5.pdb.gz	39,42,43
6	0.01	3oy3A	0.396	4.72	0.079	0.499	0.27	XY3	complex6.pdb.gz	21,250,298,307,308,309
7	0.01	1m52A	0.406	4.26	0.085	0.494	0.14	P17	complex7.pdb.gz	219,223,242,243
8	0.01	2g2hA	0.404	4.34	0.077	0.494	0.14	P16	complex8.pdb.gz	235,237,238
9	0.01	2z60A	0.409	4.75	0.082	0.515	0.24	P3Y	complex9.pdb.gz	18,235,236,237,238,239,242,243
10	0.01	3qrjB	0.381	4.48	0.088	0.473	0.16	919	complex10.pdb.gz	298,308,309

	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.