D-I-TASSER Q9NPA2

D-I-TASSER results for Q9NPA2

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

Summary of the Protein

Uniprot ID: Q9NPA2
Protein Name: Matrix metalloproteinase-25
Gene Name: MMP25

Input Sequence in FASTA format

>Q9NPA2 (562 residues)
MRLRLRLLALLLLLLAPPARAPKPSAQDVSLGVDWLTRYGYLPPPHPAQAQLQSPEKLRD
AIKVMQRFAGLPETGRMDPGTVATMRKPRCSLPDVLGVAGLVRRRRRYALSGSVWKKRTL
TWRVRSFPQSSQLSQETVRVLMSYALMAWGMESGLTFHEVDSPQGQEPDILIDFARAFHQ
DSYPFDGLGGTLAHAFFPGEHPISGDTHFDDEETWTFGSKDGEGTDLFAVAVHEFGHALG
LGHSSAPNSIMRPFYQGPVGDPDKYRLSQDDRDGLQQLYGKAPQTPYDKPTRKPLAPPPQ
PPASPTHSPSFPIPDRCEGNFDAIANIRGETFFFKGPWFWRLQPSGQLVSPRPARLHRFW
EGLPAQVRVVQAAYARHRDGRILLFSGPQFWVFQDRQLEGGARPLTELGLPPGEEVDAVF
SWPQNGKTYLVRGRQYWRYDEAAARPDPGYPRDLSLWEGAPPSPDDVTVSNAGDTYFFKG
AHYWRFPKNSIKTEPDAPQPMGPNWLDCPAPSSGPRAPRPPKATPVSETCDCQCELNQAA
GRWPAPIPLLLLPLLVGGVASR

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	Q9NPA2-D1	1-283	283		MRLRLRLLALLLLLLAPPARAPKPSAQDVSLGVDWLTRYGYLPPPHPAQAQLQSPEKLRDAIKVMQRFAGLPETGRMDPGTVATMRKPRCSLPDVLGVAGLVRRRRRYALSGSVWKKRTLTWRVRSFPQSSQLSQETVRVLMSYALMAWGMESGLTFHEVDSPQGQEPDILIDFARAFHQDSYPFDGLGGTLAHAFFPGEHPISGDTHFDDEETWTFGSKDGEGTDLFAVAVHEFGHALGLGHSSAPNSIMRPFYQGPVGDPDKYRLSQDDRDGLQQLYGKAP
2	Q9NPA2-D2	284-562	279		QTPYDKPTRKPLAPPPQPPASPTHSPSFPIPDRCEGNFDAIANIRGETFFFKGPWFWRLQPSGQLVSPRPARLHRFWEGLPAQVRVVQAAYARHRDGRILLFSGPQFWVFQDRQLEGGARPLTELGLPPGEEVDAVFSWPQNGKTYLVRGRQYWRYDEAAARPDPGYPRDLSLWEGAPPSPDDVTVSNAGDTYFFKGAHYWRFPKNSIKTEPDAPQPMGPNWLDCPAPSSGPRAPRPPKATPVSETCDCQCELNQAAGRWPAPIPLLLLPLLVGGVASR

Top 1 final models from D-I-TASSER

Click to view	Rank^a	Download	Estimated TM-score^b
	1	model1.pdb.gz	0.68

(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	1gxdA	0.44	3.81	0.249	0.496	model1_1gxdA.pdb.gz
2	1vw1A	0.42	6.14	0.050	0.591	model1_1vw1A.pdb.gz
3	7lhtA	0.41	7.09	0.054	0.637	model1_7lhtA.pdb.gz
4	6rw9A	0.41	6.59	0.035	0.601	model1_6rw9A.pdb.gz
5	6rw8A	0.41	6.52	0.042	0.594	model1_6rw8A.pdb.gz
6	6xr4A	0.41	6.71	0.043	0.607	model1_6xr4A.pdb.gz
7	1l6jA	0.41	1.15	0.397	0.413	model1_1l6jA.pdb.gz
8	5nrlP	0.41	6.96	0.056	0.617	model1_5nrlP.pdb.gz
9	1su3B	0.39	2.59	0.221	0.416	model1_1su3B.pdb.gz
10	1slmA	0.39	1.31	0.434	0.402	model1_1slmA.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	0.95	catalytic activity
GO:0008233	0.94	peptidase activity
GO:0070011	0.92	peptidase activity, acting on L-amino acid peptides
GO:0008237	0.86	metallopeptidase activity
GO:0004175	0.82	endopeptidase activity
GO:0004222	0.75	metalloendopeptidase activity
GO:0046872	0.51	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:0044699	0.88	single-organism process
GO:0009987	0.81	cellular process
GO:0044763	0.74	single-organism cellular process
GO:0065007	0.61	biological regulation
GO:0071704	0.58	organic substance metabolic process
GO:0032502	0.57	developmental process
GO:0043170	0.56	macromolecule metabolic process
GO:0032501	0.56	multicellular organismal process
GO:0050789	0.55	regulation of biological process
GO:0044707	0.55	single-multicellular organism process
GO:0044767	0.53	single-organism developmental process
GO:0044238	0.51	primary metabolic 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	0.77	cell part
GO:0044421	0.62	extracellular region part
GO:0044424	0.58	intracellular part
GO:0005576	0.45	extracellular region
GO:0043226	0.38	organelle
GO:0044444	0.37	cytoplasmic part
GO:0043227	0.36	membrane-bounded organelle
GO:0031012	0.35	extracellular matrix
GO:0016020	0.33	membrane
GO:0005615	0.31	extracellular space

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	0.232	1fblA	0.340	2.92	0.152	0.368	3.4.24.7	234,251
2	0.229	1slmA	0.394	1.31	0.434	0.402	3.4.24.17	234,251
3	0.093	3hdaP	0.313	5.86	0.121	0.409	3.4.24.-	234
4	0.060	1gxdA	0.440	3.81	0.249	0.496	3.4.24.24	251
5	0.060	1b0pA	0.274	8.12	0.054	0.473	1.2.7.1	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	0.37	2ovzA	0.279	1.08	0.415	0.283	0.19	5MR	complex1.pdb.gz	40,41,42,76,79
2	0.36	2srtA	0.295	1.95	0.434	0.308	0.23	INH	complex2.pdb.gz	40,41,71,75,81
3	0.23	3usnA	0.286	1.87	0.446	0.299	0.22	ATT	complex3.pdb.gz	58,73,76
4	0.22	1b8yA	0.291	1.38	0.449	0.297	0.22	IN7	complex4.pdb.gz	36,73,75,76,77,82
5	0.22	2ow1B	0.272	1.00	0.426	0.276	0.25	7MR	complex5.pdb.gz	67,75,81,86
6	0.21	2ovxB	0.278	1.25	0.415	0.283	0.23	4MR	complex6.pdb.gz	40,41,67,77,85
7	0.19	2usnA	0.284	1.58	0.451	0.292	0.24	IN8	complex7.pdb.gz	41,58,73,76,78,79
8	0.19	1g4kA	0.293	1.40	0.452	0.299	0.40	HQQ	complex8.pdb.gz	33,36,37,40,66,76,77
9	0.16	1c3iB	0.299	1.66	0.445	0.308	0.18	TR1	complex9.pdb.gz	39,40,41,68,83
10	0.16	1cizA	0.292	1.42	0.452	0.299	0.13	DPS	complex10.pdb.gz	52,53,76,77,83

	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.