D-I-TASSER Q9H8G2

D-I-TASSER results for Q9H8G2

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

Summary of the Protein

Uniprot ID: Q9H8G2
Protein Name: Caspase activity and apoptosis inhibitor 1
Gene Name: CAAP1

Input Sequence in FASTA format

>Q9H8G2 (361 residues)
MTGKKSSREKRRKRSSQEAAAALAAPDIVPALASGSSGSTSGCGSAGGCGSVSCCGNANF
SGSVTGGGSGGSCWGGSSVERSERRKRRSTDSSSVSGSLQQETKYILPTLEKELFLAEHS
DLEEGGLDLTVSLKPVSFYISDKKEMLQQCFCIIGEKKLQKMLPDVLKNCSIEEIKKLCQ
EQLELLSEKKILKILEGDNGMDSDMEEEADDGSKMGSDLVSQQDICIDSASSVRENKQPE
GLELKQGKGEDSDVLSINADAYDSDIEGPCNEEAAAPEAPENTVQSEAGQIDDLEKDIEK
SVNEILGLAESSPNEPKAATLAVPPPEDVQPSAQQLELLELEMRARAIKALMKAGDIKKP
A

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	Q9H8G2-D1	1-361	361		MTGKKSSREKRRKRSSQEAAAALAAPDIVPALASGSSGSTSGCGSAGGCGSVSCCGNANFSGSVTGGGSGGSCWGGSSVERSERRKRRSTDSSSVSGSLQQETKYILPTLEKELFLAEHSDLEEGGLDLTVSLKPVSFYISDKKEMLQQCFCIIGEKKLQKMLPDVLKNCSIEEIKKLCQEQLELLSEKKILKILEGDNGMDSDMEEEADDGSKMGSDLVSQQDICIDSASSVRENKQPEGLELKQGKGEDSDVLSINADAYDSDIEGPCNEEAAAPEAPENTVQSEAGQIDDLEKDIEKSVNEILGLAESSPNEPKAATLAVPPPEDVQPSAQQLELLELEMRARAIKALMKAGDIKKPA

Top 1 final models from D-I-TASSER

Click to view	Rank^a	Download	Estimated TM-score^b
	1	model1.pdb.gz	0.3885

(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	5vhaA	0.43	7.04	0.052	0.748	model1_5vhaA.pdb.gz
2	4kx7A	0.41	6.60	0.047	0.670	model1_4kx7A.pdb.gz
3	3se6A	0.40	7.04	0.052	0.706	model1_3se6A.pdb.gz
4	6sytA	0.40	6.83	0.042	0.681	model1_6sytA.pdb.gz
5	4f5cA	0.40	6.86	0.028	0.687	model1_4f5cA.pdb.gz
6	5aorA	0.40	6.94	0.037	0.684	model1_5aorA.pdb.gz
7	5dmyA	0.40	6.58	0.039	0.643	model1_5dmyA.pdb.gz
8	5kdvA	0.39	6.43	0.049	0.654	model1_5kdvA.pdb.gz
9	6z2wE	0.39	7.34	0.031	0.698	model1_6z2wE.pdb.gz
10	7bwmA2	0.39	7.03	0.026	0.676	model1_7bwmA2.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:0046872	0.63	metal ion binding
GO:0016787	0.62	hydrolase activity
GO:0046914	0.50	transition metal ion 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	0.80	cellular process
GO:0071704	0.71	organic substance metabolic process
GO:0044238	0.71	primary metabolic process
GO:0043170	0.67	macromolecule metabolic process
GO:0044237	0.61	cellular metabolic process
GO:0034641	0.56	cellular nitrogen compound metabolic process
GO:0019538	0.56	protein metabolic process
GO:0044699	0.51	single-organism 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:0044464	1.00	cell part
GO:0044424	0.99	intracellular part
GO:0044446	0.93	intracellular organelle part
GO:0044444	0.84	cytoplasmic part
GO:0043227	0.80	membrane-bounded organelle
GO:0043229	0.78	intracellular organelle
GO:0043231	0.77	intracellular membrane-bounded organelle
GO:0016020	0.74	membrane
GO:0005886	0.68	plasma membrane
GO:0044425	0.65	membrane part
GO:0005634	0.64	nucleus
GO:0005737	0.57	cytoplasm

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	2hg2A	0.358	6.55	0.038	0.587	1.2.1.21 1.2.1.22	NA
2	0.060	2ve5H	0.362	6.60	0.035	0.596	1.2.1.8	308
3	0.060	1qksB	0.381	6.45	0.048	0.615	1.7.2.1	111
4	0.060	3k2wB	0.360	6.62	0.048	0.593	1.2.1.8	NA
5	0.060	2dqmA	0.386	6.47	0.047	0.637	3.4.11.2	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	1aofA	0.296	7.12	0.057	0.521	0.36	HEM	complex1.pdb.gz	154,190,194
2	0.01	1aorA	0.370	7.03	0.060	0.654	0.16	SF4	complex2.pdb.gz	175,176,348
3	0.01	2zw9B	0.378	6.53	0.049	0.626	0.11	SAM	complex3.pdb.gz	42,43,75,76,78
4	0.01	1n7qA	0.371	6.10	0.029	0.579	0.10	UUU	complex4.pdb.gz	122,140,265
5	0.01	1gq1B	0.381	6.50	0.052	0.618	0.12	HEC	complex5.pdb.gz	146,154,198
6	0.01	1aofB	0.377	6.42	0.045	0.607	0.17	HEM	complex6.pdb.gz	149,150,153,154,195
7	0.01	3b34A	0.378	7.20	0.055	0.681	0.17	PHE	complex7.pdb.gz	143,187,188,196
8	0.01	1dy7B	0.293	7.05	0.057	0.512	0.29	HEC	complex8.pdb.gz	163,190,195,310
9	0.01	2zw9A	0.388	6.58	0.063	0.643	0.10	SAM	complex9.pdb.gz	71,72,75,76
10	0.01	2zxgA	0.387	6.67	0.061	0.651	0.16	S23	complex10.pdb.gz	183,188,336

	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.